Ethan Lange - Publications

Affiliations: 
Bioinformatics & Computational Biology University of North Carolina, Chapel Hill, Chapel Hill, NC 
Area:
Bioinformatics, Genetics, Oncology

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Year Citation  Score
2018 Raffield LM, Ellis J, Olson NC, Duan Q, Li J, Durda P, Pankratz N, Keating BJ, Wassel CL, Cushman M, Wilson JG, Gross MD, Tracy RP, Rich SS, Reiner AP, ... ... Lange EM, et al. Genome-wide association study of homocysteine in African Americans from the Jackson Heart Study, the Multi-Ethnic Study of Atherosclerosis, and the Coronary Artery Risk in Young Adults study. Journal of Human Genetics. PMID 29321517 DOI: 10.1038/S10038-017-0384-9  0.588
2017 Larson NB, McDonnell S, Cannon Albright L, Teerlink C, Stanford J, Ostrander EA, Isaacs WB, Xu J, Cooney KA, Lange E, Schleutker J, Carpten JD, Powell I, Bailey-Wilson JE, Cussenot O, et al. gsSKAT: Rapid gene set analysis and multiple testing correction for rare-variant association studies using weighted linear kernels. Genetic Epidemiology. PMID 28211093 DOI: 10.1002/Gepi.22036  0.37
2016 Tajuddin SM, Schick UM, Eicher JD, Chami N, Giri A, Brody JA, Hill WD, Kacprowski T, Li J, Lyytikäinen LP, Manichaikul A, Mihailov E, O'Donoghue ML, Pankratz N, Pazoki R, ... ... Lange E, et al. Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases. American Journal of Human Genetics. PMID 27346689 DOI: 10.1016/J.Ajhg.2016.05.003  0.374
2016 Eicher JD, Chami N, Kacprowski T, Nomura A, Chen MH, Yanek LR, Tajuddin SM, Schick UM, Slater AJ, Pankratz N, Polfus L, Schurmann C, Giri A, Brody JA, Lange LA, ... ... Lange E, et al. Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals. American Journal of Human Genetics. PMID 27346686 DOI: 10.1016/J.Ajhg.2016.05.005  0.331
2016 Chami N, Chen MH, Slater AJ, Eicher JD, Evangelou E, Tajuddin SM, Love-Gregory L, Kacprowski T, Schick UM, Nomura A, Giri A, Lessard S, Brody JA, Schurmann C, Pankratz N, ... ... Lange E, et al. Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits. American Journal of Human Genetics. PMID 27346685 DOI: 10.1016/J.Ajhg.2016.05.007  0.399
2016 Larson NB, McDonnell S, Albright LC, Teerlink C, Stanford J, Ostrander EA, Isaacs WB, Xu J, Cooney KA, Lange E, Schleutker J, Carpten JD, Powell I, Bailey-Wilson J, Cussenot O, et al. Post hoc Analysis for Detecting Individual Rare Variant Risk Associations Using Probit Regression Bayesian Variable Selection Methods in Case-Control Sequencing Studies. Genetic Epidemiology. PMID 27312771 DOI: 10.1002/Gepi.21983  0.389
2016 Teerlink CC, Leongamornlert D, Dadaev T, Thomas A, Farnham J, Stephenson RA, Riska S, McDonnell SK, Schaid DJ, Catalona WJ, Zheng SL, Cooney KA, Ray AM, Zuhlke KA, Lange EM, et al. Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21. Human Genetics. PMID 27262462 DOI: 10.1007/S00439-016-1690-6  0.418
2015 Lange EM, Ribado J, Zuhlke KA, Johnson A, Keele G, Li J, Wang Y, Duan Q, Li G, Gao Z, Li Y, Xu J, Zheng SL, Cooney KA. Assessing the Cumulative Contribution of New and Established Common Genetic Risk Factors to Early-Onset Prostate Cancer. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. PMID 26671023 DOI: 10.1158/1055-9965.Epi-14-0995  0.386
2014 Zuhlke KA, Johnson AM, Tomlins SA, Palanisamy N, Carpten JD, Lange EM, Isaacs WB, Cooney KA. Identification of a novel germline SPOP mutation in a family with hereditary prostate cancer. The Prostate. 74: 983-90. PMID 24796539 DOI: 10.1002/Pros.22818  0.401
2014 Lange EM, Johnson AM, Wang Y, Zuhlke KA, Lu Y, Ribado JV, Keele GR, Li J, Duan Q, Li G, Gao Z, Li Y, Xu J, Isaacs WB, Zheng S, et al. Genome-wide association scan for variants associated with early-onset prostate cancer. Plos One. 9: e93436. PMID 24740154 DOI: 10.1371/Journal.Pone.0093436  0.447
2014 Ellis J, Lange EM, Li J, Dupuis J, Baumert J, Walston JD, Keating BJ, Durda P, Fox ER, Palmer CD, Meng YA, Young T, Farlow DN, Schnabel RB, Marzi CS, et al. Large multiethnic Candidate Gene Study for C-reactive protein levels: identification of a novel association at CD36 in African Americans. Human Genetics. 133: 985-95. PMID 24643644 DOI: 10.1007/S00439-014-1439-Z  0.594
2014 Teerlink CC, Thibodeau SN, McDonnell SK, Schaid DJ, Rinckleb A, Maier C, Vogel W, Cancel-Tassin G, Egrot C, Cussenot O, Foulkes WD, Giles GG, Hopper JL, Severi G, Eeles R, ... ... Lange EM, et al. Association analysis of 9,560 prostate cancer cases from the International Consortium of Prostate Cancer Genetics confirms the role of reported prostate cancer associated SNPs for familial disease. Human Genetics. 133: 347-56. PMID 24162621 DOI: 10.1007/S00439-013-1384-2  0.445
2014 Lange EM, Johnson AM, Wang Y, Zuhlke KA, Lu Y, Ribado JV, Keele GR, Li J, Duan Q, Li G, Gao Z, Li Y, Xu J, Isaacs WB, Zheng S, et al. Genome-wide association scan for variants associated with early-onset prostate cancer Plos One. 9. DOI: 10.1371/journal.pone.0093436.t001  0.381
2013 Eeles RA, Olama AA, Benlloch S, Saunders EJ, Leongamornlert DA, Tymrakiewicz M, Ghoussaini M, Luccarini C, Dennis J, Jugurnauth-Little S, Dadaev T, Neal DE, Hamdy FC, Donovan JL, Muir K, ... ... Lange E, et al. Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array. Nature Genetics. 45: 385-91, 391e1-2. PMID 23535732 DOI: 10.1038/Ng.2560  0.402
2013 Reiner AP, Lange EM, Jenny NS, Chaves PH, Ellis J, Li J, Walston J, Lange LA, Cushman M, Tracy RP. Soluble CD14: genomewide association analysis and relationship to cardiovascular risk and mortality in older adults. Arteriosclerosis, Thrombosis, and Vascular Biology. 33: 158-64. PMID 23162014 DOI: 10.1161/Atvbaha.112.300421  0.516
2013 Xu J, Lange EM, Lu L, Zheng SL, Wang Z, Thibodeau SN, Cannon-Albright LA, Teerlink CC, Camp NJ, Johnson AM, Zuhlke KA, Stanford JL, Ostrander EA, Wiley KE, Isaacs SD, et al. HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG). Human Genetics. 132: 5-14. PMID 23064873 DOI: 10.1007/S00439-012-1229-4  0.391
2012 Zuhlke KA, Johnson AM, Okoth LA, Stoffel EM, Robbins CM, Tembe WA, Salinas CA, Zheng SL, Xu J, Carpten JD, Lange EM, Isaacs WB, Cooney KA. Identification of a novel NBN truncating mutation in a family with hereditary prostate cancer. Familial Cancer. 11: 595-600. PMID 22864661 DOI: 10.1007/S10689-012-9555-1  0.37
2012 Bailey-Wilson JE, Childs EJ, Cropp CD, Schaid DJ, Xu J, Camp NJ, Cannon-Albright LA, Farnham JM, George A, Powell I, Carpten JD, Giles GG, Hopper JL, Severi G, English DR, ... ... Lange EM, et al. Analysis of Xq27-28 linkage in the international consortium for prostate cancer genetics (ICPCG) families. Bmc Medical Genetics. 13: 46. PMID 22712434 DOI: 10.1186/1471-2350-13-46  0.404
2012 Ewing CM, Ray AM, Lange EM, Zuhlke KA, Robbins CM, Tembe WD, Wiley KE, Isaacs SD, Johng D, Wang Y, Bizon C, Yan G, Gielzak M, Partin AW, Shanmugam V, et al. Germline mutations in HOXB13 and prostate-cancer risk. The New England Journal of Medicine. 366: 141-9. PMID 22236224 DOI: 10.1056/Nejmoa1110000  0.414
2012 Jin G, Lu L, Cooney KA, Ray AM, Zuhlke KA, Lange EM, Cannon-Albright LA, Camp NJ, Teerlink CC, Fitzgerald LM, Stanford JL, Wiley KE, Isaacs SD, Walsh PC, Foulkes WD, et al. Validation of prostate cancer risk-related loci identified from genome-wide association studies using family-based association analysis: evidence from the International Consortium for Prostate Cancer Genetics (ICPCG). Human Genetics. 131: 1095-103. PMID 22198737 DOI: 10.1007/S00439-011-1136-0  0.438
2012 Lu L, Cancel-Tassin G, Valeri A, Cussenot O, Lange EM, Cooney KA, Farnham JM, Camp NJ, Cannon-Albright LA, Tammela TL, Schleutker J, Hoegel J, Herkommer K, Maier C, Vogel W, et al. Chromosomes 4 and 8 implicated in a genome wide SNP linkage scan of 762 prostate cancer families collected by the ICPCG. The Prostate. 72: 410-26. PMID 21748754 DOI: 10.1002/Pros.21443  0.392
2012 Lange EM, Salinas CA, Zuhlke KA, Ray AM, Wang Y, Lu Y, Ho LA, Luo J, Cooney KA. Early onset prostate cancer has a significant genetic component. The Prostate. 72: 147-56. PMID 21538423 DOI: 10.1002/Pros.21414  0.679
2011 Taylor KC, Lange LA, Zabaneh D, Lange E, Keating BJ, Tang W, Smith NL, Delaney JA, Kumari M, Hingorani A, North KE, Kivimaki M, Tracy RP, O'Donnell CJ, Folsom AR, et al. A gene-centric association scan for Coagulation Factor VII levels in European and African Americans: the Candidate Gene Association Resource (CARe) Consortium. Human Molecular Genetics. 20: 3525-34. PMID 21676895 DOI: 10.1093/Hmg/Ddr264  0.324
2011 Wassel CL, Lange LA, Keating BJ, Taylor KC, Johnson AD, Palmer C, Ho LA, Smith NL, Lange EM, Li Y, Yang Q, Delaney JA, Tang W, Tofler G, Redline S, et al. Association of genomic loci from a cardiovascular gene SNP array with fibrinogen levels in European Americans and African-Americans from six cohort studies: the Candidate Gene Association Resource (CARe). Blood. 117: 268-75. PMID 20978265 DOI: 10.1182/Blood-2010-06-289546  0.65
2011 Wang Y, Ray AM, Johnson EK, Zuhlke KA, Cooney KA, Lange EM. Evidence for an association between prostate cancer and chromosome 8q24 and 10q11 genetic variants in African American men: the Flint Men's Health Study. The Prostate. 71: 225-31. PMID 20717903 DOI: 10.1002/Pros.21234  0.461
2010 Ho LA, Lange EM. Using public control genotype data to increase power and decrease cost of case-control genetic association studies. Human Genetics. 128: 597-608. PMID 20821337 DOI: 10.1007/S00439-010-0880-X  0.619
2010 Beebe-Dimmer JL, Zuhlke KA, Ray AM, Lange EM, Cooney KA. Genetic variation in adiponectin (ADIPOQ) and the type 1 receptor (ADIPOR1), obesity and prostate cancer in African Americans. Prostate Cancer and Prostatic Diseases. 13: 362-8. PMID 20697428 DOI: 10.1038/Pcan.2010.27  0.406
2010 Christensen GB, Baffoe-Bonnie AB, George A, Powell I, Bailey-Wilson JE, Carpten JD, Giles GG, Hopper JL, Severi G, English DR, Foulkes WD, Maehle L, Moller P, Eeles R, Easton D, ... ... Lange EM, et al. Genome-wide linkage analysis of 1,233 prostate cancer pedigrees from the International Consortium for Prostate Cancer Genetics using novel sumLINK and sumLOD analyses. The Prostate. 70: 735-44. PMID 20333727 DOI: 10.1002/Pros.21106  0.419
2010 Cooney KA, Salinas CA, Ray AM, Wang Y, Lange EM, Zuhlke KA. Evaluation of the genetic component of early-onset prostate cancer. Journal of Clinical Oncology. 28: 4502-4502. DOI: 10.1200/Jco.2010.28.15_Suppl.4502  0.352
2009 Ray AM, Zuhlke KA, Johnson GR, Levin AM, Douglas JA, Lange EM, Cooney KA. Absence of truncating BRIP1 mutations in chromosome 17q-linked hereditary prostate cancer families. British Journal of Cancer. 101: 2043-7. PMID 19935797 DOI: 10.1038/Sj.Bjc.6605433  0.376
2009 Eeles RA, Kote-Jarai Z, Al Olama AA, Giles GG, Guy M, Severi G, Muir K, Hopper JL, Henderson BE, Haiman CA, Schleutker J, Hamdy FC, Neal DE, Donovan JL, Stanford JL, ... ... Lange EM, et al. Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. Nature Genetics. 41: 1116-21. PMID 19767753 DOI: 10.1038/Ng.450  0.427
2009 Frazier-Bowers S, Rincon-Rodriguez R, Zhou J, Alexander K, Lange E. Evidence of linkage in a Hispanic cohort with a Class III dentofacial phenotype. Journal of Dental Research. 88: 56-60. PMID 19131318 DOI: 10.1177/0022034508327817  0.387
2009 Lange EM, Beebe-Dimmer JL, Ray AM, Zuhlke KA, Ellis J, Wang Y, Walters S, Cooney KA. Genome-wide linkage scan for prostate cancer susceptibility from the University of Michigan Prostate Cancer Genetics Project: suggestive evidence for linkage at 16q23. The Prostate. 69: 385-91. PMID 19035517 DOI: 10.1002/Pros.20891  0.667
2008 Lange EM, Sun J, Lange LA, Zheng SL, Duggan D, Carpten JD, Gronberg H, Isaacs WB, Xu J, Chang BL. Family-based samples can play an important role in genetic association studies. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 17: 2208-14. PMID 18768484 DOI: 10.1158/1055-9965.Epi-08-0183  0.336
2008 Tischkowitz M, Sabbaghian N, Ray AM, Lange EM, Foulkes WD, Cooney KA. Analysis of the gene coding for the BRCA2-interacting protein PALB2 in hereditary prostate cancer. The Prostate. 68: 675-8. PMID 18288683 DOI: 10.1002/Pros.20729  0.391
2008 Lange EM, Sarma AV, Ray A, Wang Y, Ho LA, Anderson SA, Cunningham JM, Cooney KA. The androgen receptor CAG and GGN repeat polymorphisms and prostate cancer susceptibility in African-American men: results from the Flint Men's Health Study. Journal of Human Genetics. 53: 220-6. PMID 18217192 DOI: 10.1007/S10038-007-0240-4  0.684
2008 Sun J, Lange EM, Isaacs SD, Liu W, Wiley KE, Lange L, Gronberg H, Duggan D, Carpten JD, Walsh PC, Xu J, Chang BL, Isaacs WB, Zheng SL. Chromosome 8q24 risk variants in hereditary and non-hereditary prostate cancer patients. The Prostate. 68: 489-97. PMID 18213635 DOI: 10.1002/Pros.20695  0.418
2008 Sarma AV, Dunn RL, Lange LA, Ray A, Wang Y, Lange EM, Cooney KA. Genetic polymorphisms in CYP17, CYP3A4, CYP19A1, SRD5A2, IGF-1, and IGFBP-3 and prostate cancer risk in African-American men: the Flint Men's Health Study. The Prostate. 68: 296-305. PMID 18163429 DOI: 10.1002/Pros.20696  0.412
2007 Douglas JA, Levin AM, Zuhlke KA, Ray AM, Johnson GR, Lange EM, Wood DP, Cooney KA. Common variation in the BRCA1 gene and prostate cancer risk. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 16: 1510-6. PMID 17585057 DOI: 10.1158/1055-9965.Epi-07-0137  0.454
2007 Camp NJ, Cannon-Albright LA, Farnham JM, Baffoe-Bonnie AB, George A, Powell I, Bailey-Wilson JE, Carpten JD, Giles GG, Hopper JL, Severi G, English DR, Foulkes WD, Maehle L, Moller P, ... ... Lange EM, et al. Compelling evidence for a prostate cancer gene at 22q12.3 by the International Consortium for Prostate Cancer Genetics. Human Molecular Genetics. 16: 1271-8. PMID 17478474 DOI: 10.1093/Hmg/Ddm075  0.401
2007 Graham RR, Ortmann W, Rodine P, Espe K, Langefeld C, Lange E, Williams A, Beck S, Kyogoku C, Moser K, Gaffney P, Gregersen PK, Criswell LA, Harley JB, Behrens TW. Specific combinations of HLA-DR2 and DR3 class II haplotypes contribute graded risk for disease susceptibility and autoantibodies in human SLE. European Journal of Human Genetics : Ejhg. 15: 823-30. PMID 17406641 DOI: 10.1038/Sj.Ejhg.5201827  0.306
2007 Lange EM, Robbins CM, Gillanders EM, Zheng SL, Xu J, Wang Y, White KA, Chang BL, Ho LA, Trent JM, Carpten JD, Isaacs WB, Cooney KA. Fine-mapping the putative chromosome 17q21-22 prostate cancer susceptibility gene to a 10 cM region based on linkage analysis. Human Genetics. 121: 49-55. PMID 17120048 DOI: 10.1007/S00439-006-0274-2  0.702
2007 Sarma AV, Lange L, Ray A, Lange E, Dunn RL, Cooney KA. 456: Genetic Polymorphisms in CYP17, CYPJA4, CYP19 and SRD5A2 and Prostate Cancer Risk in African American Men: the Flint Men's Health Study Journal of Urology. 177: 153-153. DOI: 10.1016/S0022-5347(18)30709-2  0.461
2006 Schaid DJ, McDonnell SK, Zarfas KE, Cunningham JM, Hebbring S, Thibodeau SN, Eeles RA, Easton DF, Foulkes WD, Simard J, Giles GG, Hopper JL, Mahle L, Moller P, Badzioch M, ... ... Lange EM, et al. Pooled genome linkage scan of aggressive prostate cancer: results from the International Consortium for Prostate Cancer Genetics. Human Genetics. 120: 471-85. PMID 16932970 DOI: 10.1007/s00439-006-0219-9  0.714
2006 White KA, Lange EM, Ray AM, Wojno KJ, Cooney KA. Prohibitin mutations are uncommon in prostate cancer families linked to chromosome 17q. Prostate Cancer and Prostatic Diseases. 9: 298-302. PMID 16733518 DOI: 10.1038/Sj.Pcan.4500878  0.357
2006 Li T, Lange LA, Li X, Susswein L, Bryant B, Malone R, Lange EM, Huang TY, Stafford DW, Evans JP. Polymorphisms in the VKORC1 gene are strongly associated with warfarin dosage requirements in patients receiving anticoagulation. Journal of Medical Genetics. 43: 740-4. PMID 16611750 DOI: 10.1136/Jmg.2005.040410  0.317
2006 Kuhlenbäumer G, Berger K, Huge A, Lange E, Kessler C, John U, Funke H, Nabavi DG, Stögbauer F, Ringelstein EB, Stoll M. Evaluation of single nucleotide polymorphisms in the phosphodiesterase 4D gene (PDE4D) and their association with ischaemic stroke in a large German cohort. Journal of Neurology, Neurosurgery, and Psychiatry. 77: 521-4. PMID 16543535 DOI: 10.1136/Jnnp.2005.073577  0.305
2006 Lange EM, Ho LA, Beebe-Dimmer JL, Wang Y, Gillanders EM, Trent JM, Lange LA, Wood DP, Cooney KA. Genome-wide linkage scan for prostate cancer susceptibility genes in men with aggressive disease: significant evidence for linkage at chromosome 15q12. Human Genetics. 119: 400-7. PMID 16508751 DOI: 10.1007/S00439-006-0149-6  0.72
2006 Chang BL, Lange EM, Dimitrov L, Valis CJ, Gillanders EM, Lange LA, Wiley KE, Isaacs SD, Wiklund F, Baffoe-Bonnie A, Langefeld CD, Zheng SL, Matikainen MP, Ikonen T, Fredriksson H, et al. Two-locus genome-wide linkage scan for prostate cancer susceptibility genes with an interaction effect. Human Genetics. 118: 716-24. PMID 16328469 DOI: 10.1007/S00439-005-0099-4  0.422
2006 Beebe-Dimmer JL, Lange LA, Cain JE, Lewis RC, Ray AM, Sarma AV, Lange EM, Cooney KA. Polymorphisms in the prostate-specific antigen gene promoter do not predict serum prostate-specific antigen levels in African-American men. Prostate Cancer and Prostatic Diseases. 9: 50-5. PMID 16247489 DOI: 10.1038/Sj.Pcan.4500840  0.37
2006 Slager SL, Zarfas KE, Brown WM, Lange EM, McDonnell SK, Wojno KJ, Cooney KA. Genome-wide linkage scan for prostate cancer aggressiveness loci using families from the University of Michigan Prostate Cancer Genetics Project. The Prostate. 66: 173-9. PMID 16173044 DOI: 10.1002/Pros.20332  0.384
2005 Xu J, Dimitrov L, Chang BL, Adams TS, Turner AR, Meyers DA, Eeles RA, Easton DF, Foulkes WD, Simard J, Giles GG, Hopper JL, Mahle L, Moller P, Bishop T, ... ... Lange EM, et al. A combined genomewide linkage scan of 1,233 families for prostate cancer-susceptibility genes conducted by the international consortium for prostate cancer genetics. American Journal of Human Genetics. 77: 219-29. PMID 15988677 DOI: 10.1086/432377  0.395
2004 Zuhlke KA, Madeoy JJ, Beebe-Dimmer J, White KA, Griffin A, Lange EM, Gruber SB, Ostrander EA, Cooney KA. Truncating BRCA1 mutations are uncommon in a cohort of hereditary prostate cancer families with evidence of linkage to 17q markers. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. 10: 5975-80. PMID 15447980 DOI: 10.1158/1078-0432.Ccr-04-0554  0.405
2004 Gillanders EM, Xu J, Chang BL, Lange EM, Wiklund F, Bailey-Wilson JE, Baffoe-Bonnie A, Jones M, Gildea D, Riedesel E, Albertus J, Isaacs SD, Wiley KE, Mohai CE, Matikainen MP, et al. Combined genome-wide scan for prostate cancer susceptibility genes. Journal of the National Cancer Institute. 96: 1240-7. PMID 15316059 DOI: 10.1093/Jnci/Djh228  0.41
2004 Brown WM, Lange EM, Chen H, Zheng SL, Chang B, Wiley KE, Isaacs SD, Walsh PC, Isaacs WB, Xu J, Cooney KA. Hereditary prostate cancer in African American families: linkage analysis using markers that map to five candidate susceptibility loci. British Journal of Cancer. 90: 510-4. PMID 14735201 DOI: 10.1038/Sj.Bjc.6601417  0.421
2004 Blumenthal MN, Langefeld CD, Beaty TH, Bleecker ER, Ober C, Lester L, Lange E, Barnes KC, Wolf R, King RA, Solway J, Oetting W, Meyers DA, Rich SS. A genome-wide search for allergic response (atopy) genes in three ethnic groups: Collaborative Study on the Genetics of Asthma. Human Genetics. 114: 157-64. PMID 14586638 DOI: 10.1007/S00439-003-1030-5  0.394
2003 Lange EM, Gillanders EM, Davis CC, Brown WM, Campbell JK, Jones M, Gildea D, Riedesel E, Albertus J, Freas-Lutz D, Markey C, Giri V, Dimmer JB, Montie JE, Trent JM, et al. Genome-wide scan for prostate cancer susceptibility genes using families from the University of Michigan prostate cancer genetics project finds evidence for linkage on chromosome 17 near BRCA1. The Prostate. 57: 326-34. PMID 14601029 DOI: 10.1002/Pros.10307  0.441
2003 Miller DC, Zheng SL, Dunn RL, Sarma AV, Montie JE, Lange EM, Meyers DA, Xu J, Cooney KA. Germ-line mutations of the macrophage scavenger receptor 1 gene: association with prostate cancer risk in African-American men. Cancer Research. 63: 3486-9. PMID 12839931  0.384
2003 Huang SK, Mathias RA, Ehrlich E, Plunkett B, Liu X, Cutting GR, Wang XJ, Li XD, Togias A, Barnes KC, Malveaux F, Rich S, Mellen B, Lange E, Beaty TH, et al. Evidence for asthma susceptibility genes on chromosome 11 in an African-American population. Human Genetics. 113: 71-5. PMID 12664305 DOI: 10.1007/S00439-003-0934-4  0.381
2003 Chen H, Griffin AR, Wu YQ, Tomsho LP, Zuhlke KA, Lange EM, Gruber SB, Cooney KA. RNASEL mutations in hereditary prostate cancer Journal of Medical Genetics. 40. PMID 12624150 DOI: 10.1136/Jmg.40.3.E21  0.399
2002 Xu J, Zheng SL, Komiya A, Mychaleckyj JC, Isaacs SD, Hu JJ, Sterling D, Lange EM, Hawkins GA, Turner A, Ewing CM, Faith DA, Johnson JR, Suzuki H, Bujnovszky P, et al. Germline mutations and sequence variants of the macrophage scavenger receptor 1 gene are associated with prostate cancer risk. Nature Genetics. 32: 321-5. PMID 12244320 DOI: 10.1038/Ng994  0.393
2001 Bock CH, Cunningham JM, McDonnell SK, Schaid DJ, Peterson BJ, Pavlic RJ, Schroeder JJ, Klein J, French AJ, Marks A, Thibodeau SN, Lange EM, Cooney KA. Analysis of the prostate cancer-susceptibility locus HPC20 in 172 families affected by prostate cancer. American Journal of Human Genetics. 68: 795-801. PMID 11179028 DOI: 10.1086/318797  0.422
1998 Cerosaletti KM, Lange E, Stringham HM, Weemaes CMR, Smeets D, Sölder B, Belohradsky BH, Taylor AMR, Karnes P, Elliott A, Komatsu K, Gatti RA, Boehnke M, Concannon P. Fine localization of the Nijmegen breakage syndrome gene to 8q21: Evidence for a common founder haplotype American Journal of Human Genetics. 63: 125-134. PMID 9634525 DOI: 10.1086/301927  0.396
1998 Cooney K, McCarthy J, Lange E, Huang L, Miesfeldt S, Montie J, Oesterling J, Sandler H, Lange K. Prostate Cancer Susceptibility Locus on Chromosome 1q: A Confirmatory Study Journal of Urology. 160: 264-265. DOI: 10.1016/S0022-5347(01)63103-3  0.475
1997 Cooney KA, McCarthy JD, Lange E, Huang L, Miesfeldt S, Montie JE, Oesterling JE, Sandler HM, Lange K. Prostate cancer susceptibility locus on chromosome 1q: A confirmatory study Journal of the National Cancer Institute. 89: 955-959. PMID 9214675 DOI: 10.1093/Jnci/89.13.955  0.513
1996 Xia YR, Welch CL, Warden CH, Lange E, Fukao T, Lusis AJ, Gatti RA. Assignment of the mouse ataxia-telangiectasia gene (Atm) to mouse Chromosome 9 Mammalian Genome. 7: 554-555. PMID 8672141 DOI: 10.1007/S003359900165  0.311
1994 Gatti RA, Lange E, Rotman G, Chen X, Uhrhammer N, Liang T, Chiplunkar S, Yang L, Udar N, Dandekar S, Sheikhavandi S, Wang Z, Yang HM, Polikow J, Elashoff M, et al. Genetic haplotyping of ataxia-telangiectasia families localizes the major gene to an ∼ 850 kb region on chromosome 11q23.1 International Journal of Radiation Biology. 66: S57-S62. PMID 7836853 DOI: 10.1080/09553009414551861  0.349
1993 Johnson B, Brooks BA, Heinzmann C, Diep A, Mohandas T, Sparkes RS, Reyes H, Hoffman E, Lange E, Gatti A, Xia YR, Lusis AJ, Hankinson O. The Ah Receptor Nuclear Translocator Gene (ARNT) Is Located on q21 of Human Chromosome 1 and on Mouse Chromosome 3 near Cf-3 Genomics. 17: 592-598. PMID 8244375 DOI: 10.1006/Geno.1993.1377  0.318
1992 Sanal O, Lange E, Telatar M, Sobel E, Salazar-Novak J, Ersoy F, Morrison A, Concannon P, Tolun A, Gatti RA. Ataxia-telangiectasia: linkage analysis of chromosome 11q22-23 markers in Turkish families. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 6: 2848-52. PMID 1634048 DOI: 10.1096/Fasebj.6.10.1634048  0.416
Low-probability matches (unlikely to be authored by this person)
1995 Telatar M, Lange E, Uhrhammer N, Gatti RA. New localization of NCAM, proximal to DRD2 at Chromosome 11q23 Mammalian Genome. 6: 59-60. PMID 7719033 DOI: 10.1007/Bf00350901  0.298
2015 Lunetta KL, Day FR, Sulem P, Ruth KS, Tung JY, Hinds DA, Esko T, Elks CE, Altmaier E, He C, Huffman JE, Mihailov E, Porcu E, Robino A, Rose LM, ... ... Lange EM, et al. Rare coding variants and X-linked loci associated with age at menarche. Nature Communications. 6: 7756. PMID 26239645 DOI: 10.1038/Ncomms8756  0.284
2022 Durda P, Raffield LM, Lange EM, Olson NC, Jenny NS, Cushman M, Deichgraeber P, Grarup N, Jonsson A, Hansen T, Mychaleckyj JC, Psaty BM, Reiner AP, Tracy RP, Lange LA. Circulating Soluble CD163, Associations With Cardiovascular Outcomes and Mortality, and Identification of Genetic Variants in Older Individuals: The Cardiovascular Health Study. Journal of the American Heart Association. e024374. PMID 36314488 DOI: 10.1161/JAHA.121.024374  0.278
1995 Nair RP, Guo SW, Jenisch S, Henseler T, Lange EM, Terhune M, Westphal E, Christophers E, Voorhees JJ, Elder JT. Scanning chromosome 17 for psoriasis susceptibility: lack of evidence for a distal 17q locus. Human Heredity. 45: 219-30. PMID 7558055 DOI: 10.1159/000154293  0.277
2012 Beebe-Dimmer JL, Iyer PT, Nriagu JO, Keele GR, Mehta S, Meliker JR, Lange EM, Schwartz AG, Zuhlke KA, Schottenfeld D, Cooney KA. Genetic variation in glutathione S-transferase omega-1, arsenic methyltransferase and methylene-tetrahydrofolate reductase, arsenic exposure and bladder cancer: a case-control study. Environmental Health : a Global Access Science Source. 11: 43. PMID 22747749 DOI: 10.1186/1476-069X-11-43  0.273
2021 Stanislawski MA, Lange LA, Raffield LM, Zakai NA, Meyer M, Ferrier K, Szeto M, Leavitt C, Shortt JA, Thornton TA, Tracy RP, Auer PL, Reiner AP, Lange EM, Olson NC. Soluble CD14 Levels in the Jackson Heart Study: Associations With Cardiovascular Disease Risk and Genetic Variants. Arteriosclerosis, Thrombosis, and Vascular Biology. ATVBAHA121316035. PMID 33910371 DOI: 10.1161/ATVBAHA.121.316035  0.271
2017 Duan Q, Xu Z, Raffield LM, Chang S, Wu D, Lange EM, Reiner AP, Li Y. A robust and powerful two-step testing procedure for local ancestry adjusted allelic association analysis in admixed populations. Genetic Epidemiology. PMID 29226381 DOI: 10.1002/Gepi.22104  0.268
2020 Bick AG, Weinstock JS, Nandakumar SK, Fulco CP, Bao EL, Zekavat SM, Szeto MD, Liao X, Leventhal MJ, Nasser J, Chang K, Laurie C, Burugula BB, Gibson CJ, Lin AE, ... ... Lange E, et al. Inherited causes of clonal haematopoiesis in 97,691 whole genomes. Nature. PMID 33057201 DOI: 10.1038/s41586-020-2819-2  0.266
2015 Li J, Lange LA, Sabourin J, Duan Q, Valdar W, Willis MS, Li Y, Wilson JG, Lange EM. Genome- and exome-wide association study of serum lipoprotein (a) in the Jackson Heart Study. Journal of Human Genetics. PMID 26377243 DOI: 10.1038/Jhg.2015.107  0.265
2011 Wright FA, Strug LJ, Doshi VK, Commander CW, Blackman SM, Sun L, Berthiaume Y, Cutler D, Cojocaru A, Collaco JM, Corey M, Dorfman R, Goddard K, Green D, Kent JW, ... Lange EM, et al. Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2. Nature Genetics. 43: 539-46. PMID 21602797 DOI: 10.1038/Ng.838  0.261
2010 Wu Y, Li Y, Lange EM, Croteau-Chonka DC, Kuzawa CW, McDade TW, Qin L, Curocichin G, Borja JB, Lange LA, Adair LS, Mohlke KL. Genome-wide association study for adiponectin levels in Filipino women identifies CDH13 and a novel uncommon haplotype at KNG1-ADIPOQ. Human Molecular Genetics. 19: 4955-64. PMID 20876611 DOI: 10.1093/Hmg/Ddq423  0.257
2008 Li C, Li M, Lange EM, Watanabe RM. Prioritized subset analysis: improving power in genome-wide association studies. Human Heredity. 65: 129-41. PMID 17934316 DOI: 10.1159/000109730  0.255
2001 Davis CC, Brown WM, Lange EM, Rich SS, Langefeld CD. Nonparametric linkage regression. II: Identification of influential pedigrees in tests for linkage. Genetic Epidemiology. 21: S123-9. PMID 11793654 DOI: 10.1002/gepi.2001.21.s1.s123  0.252
2011 Croteau-Chonka DC, Marvelle AF, Lange EM, Lee NR, Adair LS, Lange LA, Mohlke KL. Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. Obesity (Silver Spring, Md.). 19: 1019-27. PMID 20966902 DOI: 10.1038/Oby.2010.256  0.252
2012 Divaris K, Monda KL, North KE, Olshan AF, Lange EM, Moss K, Barros SP, Beck JD, Offenbacher S. Genome-wide association study of periodontal pathogen colonization. Journal of Dental Research. 91: 21S-28S. PMID 22699663 DOI: 10.1177/0022034512447951  0.251
2012 Auer PL, Johnsen JM, Johnson AD, Logsdon BA, Lange LA, Nalls MA, Zhang G, Franceschini N, Fox K, Lange EM, Rich SS, O'Donnell CJ, Jackson RD, Wallace RB, Chen Z, et al. Imputation of exome sequence variants into population- based samples and blood-cell-trait-associated loci in African Americans: NHLBI GO Exome Sequencing Project. American Journal of Human Genetics. 91: 794-808. PMID 23103231 DOI: 10.1016/J.Ajhg.2012.08.031  0.25
2017 Marouli E, Graff M, Medina-Gomez C, Lo KS, Wood AR, Kjaer TR, Fine RS, Lu Y, Schurmann C, Highland HM, Rüeger S, Thorleifsson G, Justice AE, Lamparter D, Stirrups KE, ... ... Lange EM, et al. Rare and low-frequency coding variants alter human adult height. Nature. PMID 28146470 DOI: 10.1038/Nature21039  0.249
2011 Curocichin G, Wu Y, McDade TW, Kuzawa CW, Borja JB, Qin L, Lange EM, Adair LS, Lange LA, Mohlke KL. Single-nucleotide polymorphisms at five loci are associated with C-reactive protein levels in a cohort of Filipino young adults. Journal of Human Genetics. 56: 823-7. PMID 21937998 DOI: 10.1038/Jhg.2011.106  0.246
2010 Lange LA, Croteau-Chonka DC, Marvelle AF, Qin L, Gaulton KJ, Kuzawa CW, McDade TW, Wang Y, Li Y, Levy S, Borja JB, Lange EM, Adair LS, Mohlke KL. Genome-wide association study of homocysteine levels in Filipinos provides evidence for CPS1 in women and a stronger MTHFR effect in young adults. Human Molecular Genetics. 19: 2050-8. PMID 20154341 DOI: 10.1093/Hmg/Ddq062  0.242
2003 Smith TR, Miller MS, Lohman K, Lange EM, Case LD, Mohrenweiser HW, Hu JJ. Polymorphisms of XRCC1 and XRCC3 genes and susceptibility to breast cancer. Cancer Letters. 190: 183-90. PMID 12565173 DOI: 10.1016/S0304-3835(02)00595-5  0.24
2023 Zhang X, Brody JA, Graff M, Highland HM, Chami N, Xu H, Wang Z, Ferrier K, Chittoor G, Josyula NS, Li X, Li Z, Allison MA, Becker DM, Bielak LF, ... ... Lange EM, et al. WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE. Medrxiv : the Preprint Server For Health Sciences. PMID 37662265 DOI: 10.1101/2023.08.21.23293271  0.239
2019 Fürstenau M, Bahlo J, Fink AM, Lange E, Dreger P, Dreyling M, Hess G, Ritgen M, Kneba M, Döhner H, Stilgenbauer S, Wendtner CM, Goede V, Fischer K, Böttcher S, et al. Residual abdominal lymphadenopathy after intensive frontline chemoimmunotherapy is associated with inferior outcome independently of minimal residual disease status in chronic lymphocytic leukemia. Leukemia. PMID 31611627 DOI: 10.1038/S41375-019-0597-3  0.236
2013 Divaris K, Monda KL, North KE, Olshan AF, Reynolds LM, Hsueh WC, Lange EM, Moss K, Barros SP, Weyant RJ, Liu Y, Newman AB, Beck JD, Offenbacher S. Exploring the genetic basis of chronic periodontitis: a genome-wide association study. Human Molecular Genetics. 22: 2312-24. PMID 23459936 DOI: 10.1093/Hmg/Ddt065  0.233
2019 Schlenk RF, Weber D, Herr W, Wulf G, Salih HR, Derigs HG, Kuendgen A, Ringhoffer M, Hertenstein B, Martens UM, Grießhammer M, Bernhard H, Krauter J, Girschikofsky M, Wolf D, ... Lange E, et al. Randomized phase-II trial evaluating induction therapy with idarubicin and etoposide plus sequential or concurrent azacitidine and maintenance therapy with azacitidine. Leukemia. PMID 30728457 DOI: 10.1038/S41375-019-0395-Y  0.232
2013 Pfeifer H, Wassmann B, Bethge W, Dengler J, Bornhäuser M, Stadler M, Beelen D, Vucinic V, Burmeister T, Stelljes M, Faul C, Dreger P, Kiani A, Schäfer-Eckart K, Schwerdtfeger R, ... Lange E, et al. Randomized comparison of prophylactic and minimal residual disease-triggered imatinib after allogeneic stem cell transplantation for BCR-ABL1-positive acute lymphoblastic leukemia. Leukemia. 27: 1254-62. PMID 23212150 DOI: 10.1038/Leu.2012.352  0.232
2021 Sofer T, Zheng X, Laurie CA, Gogarten SM, Brody JA, Conomos MP, Bis JC, Thornton TA, Szpiro A, O'Connell JR, Lange EM, Gao Y, Cupples LA, Psaty BM, et al. Variant-specific inflation factors for assessing population stratification at the phenotypic variance level. Nature Communications. 12: 3506. PMID 34108454 DOI: 10.1038/s41467-021-23655-2  0.229
2020 Al-Sawaf O, Robrecht S, Bahlo J, Fink AM, Cramer P, V Tresckow J, Lange E, Kiehl M, Dreyling M, Ritgen M, Dürig J, Tausch E, Schneider C, Stilgenbauer S, Wendtner CM, et al. Richter transformation in chronic lymphocytic leukemia (CLL)-a pooled analysis of German CLL Study Group (GCLLSG) front line treatment trials. Leukemia. PMID 32203141 DOI: 10.1038/S41375-020-0797-X  0.229
2022 Raghavan S, Huang J, Tcheandjieu C, Huffman JE, Litkowski E, Liu C, Ho YA, Hunter-Zinck H, Zhao H, Marouli E, North KE, Lange E, Lange LA, Voight BF, Gaziano JM, et al. A multi-population phenome-wide association study of genetically-predicted height in the Million Veteran Program. Plos Genetics. 18: e1010193. PMID 35653334 DOI: 10.1371/journal.pgen.1010193  0.228
2015 Li J, Lange LA, Duan Q, Lu Y, Singleton AB, Zonderman AB, Evans MK, Li Y, Taylor HA, Willis MS, Nalls M, Wilson JG, Lange EM. Genome-wide admixture and association study of serum iron, ferritin, transferrin saturation and total iron binding capacity in African Americans. Human Molecular Genetics. 24: 572-81. PMID 25224454 DOI: 10.1093/Hmg/Ddu454  0.226
2007 Marvelle AF, Lange LA, Qin L, Wang Y, Lange EM, Adair LS, Mohlke KL. Comparison of ENCODE region SNPs between Cebu Filipino and Asian HapMap samples. Journal of Human Genetics. 52: 729-37. PMID 17636361 DOI: 10.1007/S10038-007-0175-9  0.226
2017 Al-Sawaf O, Robrecht S, Bahlo J, Fink AM, Cramer P, von Tresckow J, Maurer C, Bergmann M, Seiler T, Lange E, Kneba M, Stilgenbauer S, Döhner H, Kiehl MG, Jäger U, et al. Impact of gender on outcome after chemoimmunotherapy in patients with chronic lymphocytic leukemia: a meta-analysis by the German CLL study group. Leukemia. PMID 28745332 DOI: 10.1038/Leu.2017.221  0.223
2006 Bell TA, de la Casa-Esperón E, Doherty HE, Ideraabdullah F, Kim K, Wang Y, Lange LA, Wilhemsen K, Lange EM, Sapienza C, de Villena FP. The paternal gene of the DDK syndrome maps to the Schlafen gene cluster on mouse chromosome 11. Genetics. 172: 411-23. PMID 16172501 DOI: 10.1534/Genetics.105.047118  0.222
2012 Croteau-Chonka DC, Wu Y, Li Y, Fogarty MP, Lange LA, Kuzawa CW, McDade TW, Borja JB, Luo J, AbdelBaky O, Combs TP, Adair LS, Lange EM, Mohlke KL. Population-specific coding variant underlies genome-wide association with adiponectin level. Human Molecular Genetics. 21: 463-71. PMID 22010046 DOI: 10.1093/Hmg/Ddr480  0.22
2009 Walston JD, Matteini AM, Nievergelt C, Lange LA, Fallin DM, Barzilai N, Ziv E, Pawlikowska L, Kwok P, Cummings SR, Kooperberg C, LaCroix A, Tracy RP, Atzmon G, Lange EM, et al. Inflammation and stress-related candidate genes, plasma interleukin-6 levels, and longevity in older adults. Experimental Gerontology. 44: 350-5. PMID 19249341 DOI: 10.1016/J.Exger.2009.02.004  0.22
2018 Turcot V, Lu Y, Highland HM, Schurmann C, Justice AE, Fine RS, Bradfield JP, Esko T, Giri A, Graff M, Guo X, Hendricks AE, Karaderi T, Lempradl A, Locke AE, ... ... Lange EM, et al. Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. Nature Genetics. 50: 26-41. PMID 29273807 DOI: 10.1038/S41588-017-0011-X  0.219
2001 Mohlke KL, Lange EM, Valle TT, Ghosh S, Magnuson VL, Silander K, Watanabe RM, Chines PS, Bergman RN, Tuomilehto J, Collins FS, Boehnke M. Linkage disequilibrium between microsatellite markers extends beyond 1 cM on chromosome 20 in Finns. Genome Research. 11: 1221-6. PMID 11435404 DOI: 10.1101/Gr.173201  0.219
1992 Ziv Y, Frydman M, Lange E, Zelnik N, Rotman G, Julier C, Jaspers NG, Dagan Y, Abeliovicz D, Dar H, Borochowitz Z, Lathrop M, Gatti RA, Shiloh Y. Ataxia-telangiectasia: linkage analysis in highly inbred Arab and Druze families and differentiation from an ataxia-microcephaly-cataract syndrome. Human Genetics. 88: 619-26. PMID 1551665 DOI: 10.1007/Bf02265285  0.218
2018 Spracklen CN, Shi J, Vadlamudi S, Wu Y, Zou M, Raulerson CK, Davis JP, Zeynalzadeh M, Jackson K, Yuan W, Wang H, Shou W, Wang Y, Luo J, Lange LA, ... Lange EM, et al. Identification and functional analysis of glycemic trait loci in the China Health and Nutrition Survey. Plos Genetics. 14: e1007275. PMID 29621232 DOI: 10.1371/Journal.Pgen.1007275  0.215
2023 Armstrong ND, Srinivasasainagendra V, Ammous F, Assimes TL, Beitelshees AL, Brody J, Cade BE, Ida Chen YD, Chen H, de Vries PS, Floyd JS, Franceschini N, Guo X, Hellwege JN, House JS, ... ... Lange EM, et al. Whole genome sequence analysis of apparent treatment resistant hypertension status in participants from the Trans-Omics for Precision Medicine program. Frontiers in Genetics. 14: 1278215. PMID 38162683 DOI: 10.3389/fgene.2023.1278215  0.215
2016 Al-Sawaf O, Kluth S, Bahlo J, Hopfinger G, Fink AM, Cramer P, Maurer C, Bergmann M, Dreyling M, Lange E, Kneba M, Stilgenbauer S, Kiehl MG, Jäger U, Wendtner CM, et al. Impact of gender on outcome after chemoimmunotherapy with fludarabine, cyclophosphamide and rituximab (FCR) or bendamustin plus R (BR) in CLL patients: a pooled analysis of the German CLL Study Group (GCLLSG) Onkologie. DOI: 10.1159/000449050  0.21
2015 Xu Z, Duan Q, Yan S, Chen W, Li M, Lange E, Li Y. DISSCO: direct imputation of summary statistics allowing covariates. Bioinformatics (Oxford, England). PMID 25810429 DOI: 10.1093/Bioinformatics/Btv168  0.21
2023 Gupta Y, Friedman DJ, McNulty MT, Khan A, Lane B, Wang C, Ke J, Jin G, Wooden B, Knob AL, Lim TY, Appel GB, Huggins K, Liu L, Mitrotti A, ... ... Lange EM, et al. Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease. Nature Communications. 14: 7836. PMID 38036523 DOI: 10.1038/s41467-023-43020-9  0.206
2004 Lange EM, Boehnke M. The haplotype runs test: the parent-parent-affected offspring trio design. Genetic Epidemiology. 27: 118-30. PMID 15305328 DOI: 10.1002/Gepi.20010  0.206
2014 Lange LA, Hu Y, Zhang H, Xue C, Schmidt EM, Tang ZZ, Bizon C, Lange EM, Smith JD, Turner EH, Jun G, Kang HM, Peloso G, Auer P, Li KP, et al. Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol. American Journal of Human Genetics. 94: 233-45. PMID 24507775 DOI: 10.1016/J.Ajhg.2014.01.010  0.203
2023 Gupta Y, Friedman DJ, McNulty M, Khan A, Lane B, Wang C, Ke J, Jin G, Wooden B, Knob AL, Lim TY, Appel GB, Huggins K, Liu L, Mitrotti A, ... ... Lange EM, et al. Strong protective effect of the p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease. Medrxiv : the Preprint Server For Health Sciences. PMID 37577628 DOI: 10.1101/2023.08.02.23293554  0.203
2011 Cohen SS, Gammon MD, North KE, Millikan RC, Lange EM, Williams SM, Zheng W, Cai Q, Long J, Smith JR, Signorello LB, Blot WJ, Matthews CE. ADIPOQ, ADIPOR1, and ADIPOR2 polymorphisms in relation to serum adiponectin levels and BMI in black and white women. Obesity (Silver Spring, Md.). 19: 2053-62. PMID 21273992 DOI: 10.1038/Oby.2010.346  0.202
2019 Daya M, Rafaels N, Brunetti TM, Chavan S, Levin AM, Shetty A, Gignoux CR, Boorgula MP, Wojcik G, Campbell M, Vergara C, Torgerson DG, Ortega VE, Doumatey A, Johnston HR, ... ... Lange EM, et al. Association study in African-admixed populations across the Americas recapitulates asthma risk loci in non-African populations. Nature Communications. 10: 880. PMID 30787307 DOI: 10.1038/S41467-019-08469-7  0.202
2016 Lange LA, Graff M, Lange EM, Young KL, Richardson AS, Mohlke KL, North KE, Harris KM, Gordon-Larsen P. Evidence for Association between SH2B1 Gene Variants and Glycated Hemoglobin in Nondiabetic European American Young Adults: The Add Health Study. Annals of Human Genetics. 80: 294-305. PMID 27530450 DOI: 10.1111/Ahg.12165  0.202
2021 Armstrong ND, Srinivasasainagendra V, Patki A, Tanner RM, Hidalgo BA, Tiwari HK, Limdi NA, Lange EM, Lange LA, Arnett DK, Irvin MR. Genetic Contributors of Incident Stroke in 10,700 African Americans With Hypertension: A Meta-Analysis From the Genetics of Hypertension Associated Treatments and Reasons for Geographic and Racial Differences in Stroke Studies. Frontiers in Genetics. 12: 781451. PMID 34992631 DOI: 10.3389/fgene.2021.781451  0.201
2017 Haskell GT, Jensen BC, Skrzynia C, Pulikkotil T, Tilley CR, Lu Y, Marchuk DS, Ann Samsa L, Wilhelmsen KC, Lange E, Patterson C, Evans JP, Berg JS. Genetic Complexity of Mitral Valve Prolapse Revealed by Clinical and Genetic Evaluation of a Large Family. The Journal of Heart Valve Disease. 26: 569-580. PMID 29762926  0.2
2023 Hughes O, Bentley AR, Breeze CE, Aguet F, Xu X, Nadkarni G, Sun Q, Lin BM, Gilliland T, Meyer MC, Du J, Raffield LM, Kramer H, Morton RW, Gouveia MH, ... ... Lange EM, et al. Genome-wide study investigating effector genes and polygenic prediction for kidney function in persons with ancestry from Africa and the Americas. Cell Genomics. 100468. PMID 38190104 DOI: 10.1016/j.xgen.2023.100468  0.2
2010 Yan Y, Klein R, Heiss G, Girman CJ, Lange EM, Klein BE, Rose KM, Boerwinkle E, Pankow JS, Brancati FL, Ballantyne CM, Köttgen A, North KE. The transcription factor 7-like 2 (TCF7L2) polymorphism may be associated with focal arteriolar narrowing in Caucasians with hypertension or without diabetes: the ARIC Study. Bmc Endocrine Disorders. 10: 9. PMID 20478041 DOI: 10.1186/1472-6823-10-9  0.194
2020 Van Tassell JC, Shimbo D, Hess R, Kittles R, Wilson JG, Jorde LB, Li M, Lange LA, Lange EM, Muntner P, Bress AP. Association of West African ancestry and blood pressure control among African Americans taking antihypertensive medication in the Jackson Heart Study. Journal of Clinical Hypertension (Greenwich, Conn.). PMID 32049421 DOI: 10.1111/Jch.13824  0.19
2016 Ioannidis NM, Rothstein JH, Pejaver V, Middha S, McDonnell SK, Baheti S, Musolf A, Li Q, Holzinger E, Karyadi D, Cannon-Albright LA, Teerlink CC, Stanford JL, Isaacs WB, Xu J, ... ... Lange EM, et al. REVEL: an Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants. American Journal of Human Genetics. PMID 27666373 DOI: 10.1016/J.Ajhg.2016.08.016  0.188
2020 Raffield LM, Lu AT, Szeto MD, Little A, Grinde KE, Shaw J, Auer PL, Cushman M, Horvath S, Irvin MR, Lange EM, Lange LA, Nickerson DA, Thornton TA, Wilson JG, et al. Coagulation factor VIII: Relationship to Cardiovascular Disease Risk and Whole Genome Sequence and Epigenome-Wide Analysis in African Americans. Journal of Thrombosis and Haemostasis : Jth. PMID 31985870 DOI: 10.1111/Jth.14741  0.188
2010 Joubert BR, North KE, Wang Y, Mwapasa V, Franceschini N, Meshnick SR, Lange EM. Comparison of genome-wide variation between Malawians and African ancestry HapMap populations. Journal of Human Genetics. 55: 366-74. PMID 20485449 DOI: 10.1038/Jhg.2010.41  0.188
2015 Staples J, Ekunwe L, Lange E, Wilson JG, Nickerson DA, Below JE. PRIMUS: Improving Pedigree Reconstruction using Mitochondrial and Y Haplotypes. Bioinformatics (Oxford, England). PMID 26515822 DOI: 10.1093/Bioinformatics/Btv618  0.186
2021 Stanislawski MA, Litkowski E, Fore R, Rifas-Shiman SL, Oken E, Hivert MF, Lange EM, Lange LA, Dabelea D, Raghavan S. Genetic Interactions with Intrauterine Diabetes Exposure in Relation to Obesity: The EPOCH and Project Viva Studies. Pediatric Reports. 13: 279-288. PMID 34205853 DOI: 10.3390/pediatric13020036  0.183
2007 Sullivan PF, Keefe RS, Lange LA, Lange EM, Stroup TS, Lieberman J, Maness PF. NCAM1 and neurocognition in schizophrenia. Biological Psychiatry. 61: 902-10. PMID 17161382 DOI: 10.1016/J.Biopsych.2006.07.036  0.181
2002 Guo SW, Jenisch S, Stuart P, Lange EM, Kukuruga D, Nair R, Henseler T, Voorhees J, Christophers E, Elder JT. Combined segregation and linkage analysis of HLA markers in familial psoriasis. European Journal of Human Genetics : Ejhg. 10: 327-33. PMID 12082508 DOI: 10.1038/sj.ejhg.5200810  0.18
2014 Matteini AM, Li J, Lange EM, Tanaka T, Lange LA, Tracy RP, Wang Y, Biggs ML, Arking DE, Fallin MD, Chakravarti A, Psaty BM, Bandinelli S, Ferrucci L, Reiner AP, et al. Novel gene variants predict serum levels of the cytokines IL-18 and IL-1ra in older adults. Cytokine. 65: 10-6. PMID 24182552 DOI: 10.1016/J.Cyto.2013.10.002  0.179
2014 Richardson AS, North KE, Graff M, Young KM, Mohlke KL, Lange LA, Lange EM, Harris KM, Gordon-Larsen P. Moderate to vigorous physical activity interactions with genetic variants and body mass index in a large US ethnically diverse cohort. Pediatric Obesity. 9: e35-46. PMID 23529959 DOI: 10.1111/J.2047-6310.2013.00152.X  0.179
2004 Lange EM, Lange K. Powerful allele sharing statistics for nonparametric linkage analysis. Human Heredity. 57: 49-58. PMID 15133312 DOI: 10.1159/000077389  0.177
2002 Lange LA, Lange EM, Bielak LF, Langefeld CD, Kardia SL, Royston P, Turner ST, Sheedy PF, Boerwinkle E, Peyser PA. Autosomal genome-wide scan for coronary artery calcification loci in sibships at high risk for hypertension. Arteriosclerosis, Thrombosis, and Vascular Biology. 22: 418-23. PMID 11884284 DOI: 10.1161/Hq0302.105721  0.176
2022 Jones AC, Patki A, Claas SA, Tiwari HK, Chaudhary NS, Absher DM, Lange LA, Lange EM, Zhao W, Ratliff SM, Kardia SLR, Smith JA, Irvin MR, Arnett DK. Differentially Methylated DNA Regions and Left Ventricular Hypertrophy in African Americans: A HyperGEN Study. Genes. 13. PMID 36292585 DOI: 10.3390/genes13101700  0.176
2008 Lange LA, Reiner AP, Carty CL, Jenny NS, Cushman M, Lange EM. Common genetic variants associated with plasma fibrin D-dimer concentration in older European- and African-American adults. Journal of Thrombosis and Haemostasis : Jth. 6: 654-9. PMID 18208536 DOI: 10.1111/J.1538-7836.2008.02906.X  0.17
2018 Raffield LM, Ulirsch JC, Naik RP, Lessard S, Handsaker RE, Jain D, Kang HM, Pankratz N, Auer PL, Bao EL, Smith JD, Lange LA, Lange EM, Li Y, Thornton TA, et al. Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease. Plos Genetics. 14: e1007293. PMID 29590102 DOI: 10.1371/journal.pgen.1007293  0.168
2022 Schubert R, Geoffroy E, Gregga I, Mulford AJ, Aguet F, Ardlie K, Gerszten R, Clish C, Van Den Berg D, Taylor KD, Durda P, Johnson WC, Cornell E, Guo X, Liu Y, ... ... Lange E, et al. Protein prediction for trait mapping in diverse populations. Plos One. 17: e0264341. PMID 35202437 DOI: 10.1371/journal.pone.0264341  0.163
2017 Raffield LM, Zakai NA, Duan Q, Laurie C, Smith JD, Irvin MR, Doyle MF, Naik RP, Song C, Manichaikul AW, Liu Y, Durda P, Rotter JI, Jenny NS, Rich SS, ... ... Lange EM, et al. D-Dimer in African Americans: Whole Genome Sequence Analysis and Relationship to Cardiovascular Disease Risk in the Jackson Heart Study. Arteriosclerosis, Thrombosis, and Vascular Biology. PMID 28912365 DOI: 10.1161/Atvbaha.117.310073  0.163
2015 Lunetta KL, Day FR, Sulem P, Ruth KS, Tung JY, Hinds DA, Esko T, Elks CE, Altmaier E, He C, Huffman JE, Mihailov E, Porcu E, Robino A, Rose LM, ... ... Lange EM, et al. Corrigendum: Rare coding variants and X-linked loci associated with age at menarche. Nature Communications. 6: 10257. PMID 26674845 DOI: 10.1038/Ncomms10257  0.161
2015 Wessel J, Chu AY, Willems SM, Wang S, Yaghootkar H, Brody JA, Dauriz M, Hivert MF, Raghavan S, Lipovich L, Hidalgo B, Fox K, Huffman JE, An P, Lu Y, ... ... Lange EM, et al. Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility. Nature Communications. 6: 5897. PMID 25631608 DOI: 10.1038/Ncomms6897  0.16
2000 Watanabe RM, Ghosh S, Langefeld CD, Valle TT, Hauser ER, Magnuson VL, Mohlke KL, Silander K, Ally DS, Chines P, Blaschak-Harvan J, Douglas JA, Duren WL, Epstein MP, Fingerlin TE, ... ... Lange EM, et al. The Finland–United States Investigation of Non–Insulin-Dependent Diabetes Mellitus Genetics (FUSION) Study. II. An Autosomal Genome Scan for Diabetes-Related Quantitative-Trait Loci The American Journal of Human Genetics. 67: 1186-1200. DOI: 10.1016/S0002-9297(07)62949-8  0.16
2003 Colilla S, Nicolae D, Pluzhnikov A, Blumenthal MN, Beaty TH, Bleecker ER, Lange EM, Rich SS, Meyers DA, Ober C, Cox NJ. Evidence for gene-environment interactions in a linkage study of asthma and smoking exposure. The Journal of Allergy and Clinical Immunology. 111: 840-6. PMID 12704367 DOI: 10.1067/Mai.2003.170  0.159
2021 Olson NC, Raffield LM, Moxley AH, Miller-Fleming TW, Auer PL, Franceschini N, Ngo D, Thornton TA, Lange EM, Li Y, Nickerson DA, Zakai NA, Gerszten RE, Cox NJ, Correa A, et al. Soluble Urokinase Plasminogen Activator Receptor: Genetic Variation and Cardiovascular Disease Risk in Blacks. Circulation. Genomic and Precision Medicine. CIRCGEN121003421. PMID 34706549 DOI: 10.1161/CIRCGEN.121.003421  0.159
2010 Yan Y, North KE, Heiss G, Klein R, Girman CJ, Lange EM, Pankow JS, Brancati FL, Boerwinkle E. Transcription factor 7-like 2 (TCF7L2) polymorphism and context-specific risk of impaired fasting glucose in African American and Caucasian adults: the atherosclerosis risk in communities (ARIC) study. Diabetes/Metabolism Research and Reviews. 26: 371-7. PMID 20578204 DOI: 10.1002/Dmrr.1087  0.157
2017 Olson NC, Raffield LM, Lange LA, Lange EM, Longstreth WT, Chauhan G, Debette S, Seshadri S, Reiner AP, Tracy RP. Associations of activated coagulation factor VII and factor VIIa-antithrombin levels with genome-wide polymorphisms and cardiovascular disease risk. Journal of Thrombosis and Haemostasis : Jth. PMID 29112333 DOI: 10.1111/Jth.13899  0.157
2004 Ambrosius WT, Lange EM, Langefeld CD. Power for genetic association studies with random allele frequencies and genotype distributions. American Journal of Human Genetics. 74: 683-93. PMID 15024689 DOI: 10.1086/383282  0.157
2005 Szalai AJ, Wu J, Lange EM, McCrory MA, Langefeld CD, Williams A, Zakharkin SO, George V, Allison DB, Cooper GS, Xie F, Fan Z, Edberg JC, Kimberly RP. Single-nucleotide polymorphisms in the C-reactive protein (CRP) gene promoter that affect transcription factor binding, alter transcriptional activity, and associate with differences in baseline serum CRP level. Journal of Molecular Medicine (Berlin, Germany). 83: 440-7. PMID 15778807 DOI: 10.1007/S00109-005-0658-0  0.156
2020 Szeto MD, Raffield LM, Nickerson DA, Zakai NA, Klemm DJ, Taylor MR, Yang IV, Correa A, Reiner AP, Lange EM, Lange LA. Abstract 25: Epigenome-Wide DNA Methylation Analysis Reveals Novel Hematologic Trait Associations for African Americans in The Jackson Heart Study Circulation. 141. DOI: 10.1161/Circ.141.Suppl_1.25  0.156
2007 Lange LA, Lange EM, Tracy RP, Reine AP. Polymorphisms in the Jama. 297: 1317. DOI: 10.1001/Jama.297.12.1317-B  0.154
2020 Reiner AP, Raffield LM, Franceschini N, Auer PL, Lange EM, Nickerson DA, Zakai NA, Correa A, Olson N. Effect of Sickle Cell Trait and Genotype on the Association of Soluble uPAR with Kidney Function Measures in Blacks. Clinical Journal of the American Society of Nephrology : Cjasn. PMID 33268503 DOI: 10.2215/CJN.12100720  0.152
2021 Breeze CE, Batorsky A, Lee MK, Szeto MD, Xu X, McCartney DL, Jiang R, Patki A, Kramer HJ, Eales JM, Raffield L, Lange L, Lange E, Durda P, Liu Y, et al. Epigenome-wide association study of kidney function identifies trans-ethnic and ethnic-specific loci. Genome Medicine. 13: 74. PMID 33931109 DOI: 10.1186/s13073-021-00877-z  0.15
2015 Do R, Stitziel NO, Won HH, Jørgensen AB, Duga S, Angelica Merlini P, Kiezun A, Farrall M, Goel A, Zuk O, Guella I, Asselta R, Lange LA, Peloso GM, Auer PL, ... ... Lange EM, et al. Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction. Nature. 518: 102-6. PMID 25487149 DOI: 10.1038/Nature13917  0.149
2019 Zhao X, Geng X, Srinivasasainagendra V, Chaudhary N, Judd S, Wadley V, Gutiérrez OM, Wang H, Lange EM, Lange LA, Woo D, Unverzagt FW, Safford M, Cushman M, Limdi N, et al. A PheWAS study of a large observational epidemiological cohort of African Americans from the REGARDS study. Bmc Medical Genomics. 12: 26. PMID 30704471 DOI: 10.1186/S12920-018-0462-7  0.148
2010 North KE, Graff M, Adair LS, Lange EM, Lange LA, Guo G, Gordon-Larsen P. Genetic epidemiology of BMI and body mass change from adolescence to young adulthood. Obesity (Silver Spring, Md.). 18: 1474-6. PMID 19851309 DOI: 10.1038/Oby.2009.350  0.148
2013 Duan Q, Liu EY, Auer PL, Zhang G, Lange EM, Jun G, Bizon C, Jiao S, Buyske S, Franceschini N, Carlson CS, Hsu L, Reiner AP, Peters U, Haessler J, et al. Imputation of coding variants in African Americans: better performance using data from the exome sequencing project. Bioinformatics (Oxford, England). 29: 2744-9. PMID 23956302 DOI: 10.1093/Bioinformatics/Btt477  0.145
2014 Weiss JM, Schumacher J, Allen GO, Neuman H, Lange EO, Loconte NK, Greenberg CC, Smith MA. Adjuvant chemotherapy for stage II right-sided and left-sided colon cancer: analysis of SEER-medicare data. Annals of Surgical Oncology. 21: 1781-91. PMID 24643898 DOI: 10.1245/S10434-014-3631-8  0.144
2016 Graff M, Richardson AS, Young KL, Mazul AL, Highland H, North KE, Mohlke KL, Lange LA, Lange EM, Harris KM, Gordon-Larsen P. The interaction between physical activity and obesity gene variants in association with BMI: Does the obesogenic environment matter? Health & Place. 42: 159-165. PMID 27771443 DOI: 10.1016/J.Healthplace.2016.09.003  0.144
2020 Stanislawski MA, Shaw J, Litkowski E, Lange EM, Perng W, Dabelea D, Lange LA. Genetic Risk for Hepatic Fat among an Ethnically Diverse Cohort of Youth: The Exploring Perinatal Outcomes among Children Study. The Journal of Pediatrics. PMID 32143931 DOI: 10.1016/J.Jpeds.2020.01.031  0.143
2022 Vargas LB, Lange LA, Ferrier K, Aguet F, Ardlie K, Gabriel S, Gupta N, Smith JD, Blackwell TW, Ding J, Durda P, Tracy RP, Liu Y, Taylor KD, Craig Johnson W, ... ... Lange EM, et al. Gene expression associations with body mass index in the Multi-Ethnic Study of Atherosclerosis. International Journal of Obesity (2005). PMID 36463326 DOI: 10.1038/s41366-022-01240-x  0.143
2021 Stanislawski MA, Litkowski E, Raghavan S, Harrall KK, Shaw J, Glueck DH, Lange EM, Dabelea D, Lange LA. Genetic Risk Score for Type 2 Diabetes and Traits Related to Glucose-Insulin Homeostasis in Youth: The Exploring Perinatal Outcomes Among Children (EPOCH) Study. Diabetes Care. PMID 34257098 DOI: 10.2337/dc21-0464  0.141
2015 Olson NC, Butenas S, Lange LA, Lange EM, Cushman M, Jenny NS, Walston J, Souto JC, Soria JM, Chauhan G, Debette S, Longstreth WT, Seshadri S, Reiner AP, Tracy RP. Coagulation factor XII genetic variation, ex vivo thrombin generation, and stroke risk in the elderly: results from the Cardiovascular Health Study. Journal of Thrombosis and Haemostasis : Jth. 13: 1867-77. PMID 26286125 DOI: 10.1111/Jth.13111  0.14
2020 Leavitt C, Zakai NA, Auer P, Cushman M, Lange EM, Levitan EB, Olson N, Thornton TA, Tracy RP, Wilson JG, Lange LA, Reiner AP, Raffield LM. Interferon gamma-induced protein 10 (IP-10) and cardiovascular disease in African Americans. Plos One. 15: e0231013. PMID 32240245 DOI: 10.1371/Journal.Pone.0231013  0.139
2015 Young KL, Graff M, North KE, Richardson AS, Mohlke KL, Lange LA, Lange EM, Harris KM, Gordon-Larsen P. Interaction of smoking and obesity susceptibility loci on adolescent BMI: The National Longitudinal Study of Adolescent to Adult Health. Bmc Genetics. 16: 131. PMID 26537541 DOI: 10.1186/S12863-015-0289-6  0.138
2015 Young KL, Graff M, North KE, Richardson AS, Bradfield JP, Grant SF, Lange LA, Lange EM, Harris KM, Gordon-Larsen P. Influence of SNP*SNP interaction on BMI in European American adolescents: findings from the National Longitudinal Study of Adolescent Health. Pediatric Obesity. PMID 25893265 DOI: 10.1111/Ijpo.12026  0.137
2010 Joubert BR, Lange EM, Franceschini N, Mwapasa V, North KE, Meshnick SR. A whole genome association study of mother-to-child transmission of HIV in Malawi. Genome Medicine. 2: 17. PMID 20487506 DOI: 10.1186/Gm138  0.135
2019 Daya M, Rafaels N, Brunetti TM, Chavan S, Levin AM, Shetty A, Gignoux CR, Boorgula MP, Wojcik G, Campbell M, Vergara C, Torgerson DG, Ortega VE, Doumatey A, Johnston HR, ... ... Lange EM, et al. Author Correction: Association study in African-admixed populations across the Americas recapitulates asthma risk loci in non-African populations. Nature Communications. 10: 4082. PMID 31484942 DOI: 10.1038/S41467-019-12158-W  0.13
2021 Allman PH, Aban I, Long DM, Patki A, MacKenzie T, Irvin MR, Lange LA, Lange E, Cutter G, Tiwari HK. Mendelian randomization in the multivariate general linear model framework. Genetic Epidemiology. PMID 34672390 DOI: 10.1002/gepi.22435  0.129
2022 Litkowski EM, Logue MW, Zhang R, Charest BR, Lange EM, Hokanson JE, Lynch JA, Vujkovic M, Phillips LS, Lange LA, Hauger RL, Raghavan S. A Diabetes Genetic Risk Score Is Associated With All-Cause Dementia and Clinically Diagnosed Vascular Dementia in the Million Veteran Program. Diabetes Care. PMID 36041056 DOI: 10.2337/dc22-0105  0.127
2021 Bick AG, Weinstock JS, Nandakumar SK, Fulco CP, Bao EL, Zekavat SM, Szeto MD, Liao X, Leventhal MJ, Nasser J, Chang K, Laurie C, Burugula BB, Gibson CJ, Niroula A, ... ... Lange E, et al. Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomes. Nature. PMID 33707633 DOI: 10.1038/s41586-021-03280-1  0.125
2012 Graff M, North KE, Mohlke KL, Lange LA, Luo J, Harris KM, Young KL, Richardson AS, Lange EM, Gordon-Larsen P. Estimation of genetic effects on BMI during adolescence in an ethnically diverse cohort: The National Longitudinal Study of Adolescent Health. Nutrition & Diabetes. 2: e47. PMID 23168566 DOI: 10.1038/Nutd.2012.20  0.125
2018 Booth JN, Li M, Shimbo D, Hess R, Irvin MR, Kittles R, Wilson JG, Jorde LB, Cheung AK, Lange LA, Lange EM, Yano Y, Muntner P, Bress AP. West African ancestry and nocturnal blood pressure in African Americans: the Jackson Heart Study. American Journal of Hypertension. PMID 29528363 DOI: 10.1093/Ajh/Hpy038  0.125
2017 Raghavan S, Zhang W, Yang IV, Lange LA, Lange EM, Fingerlin TE, Dabelea D. Association between gestational diabetes mellitus exposure and childhood adiposity is not substantially explained by offspring genetic risk of obesity. Diabetic Medicine : a Journal of the British Diabetic Association. PMID 29048747 DOI: 10.1111/Dme.13529  0.124
2019 Douce DR, Soliman EZ, Naik R, Hyacinth HI, Cushman M, Winkler CA, Howard G, Lange EM, Lange LA, Irvin MR, Zakai NA. Association of sickle cell trait with atrial fibrillation: The REGARDS cohort. Journal of Electrocardiology. 55: 1-5. PMID 31028976 DOI: 10.1016/J.Jelectrocard.2019.04.010  0.124
2003 Brown WM, Beck SR, Lange EM, Davis CC, Kay CM, Langefeld CD, Rich SS. Age-stratified heritability estimation in the Framingham Heart Study families. Bmc Genetics. 4: S32. PMID 14975100 DOI: 10.1186/1471-2156-4-S1-S32  0.122
2006 Lange LA, Carlson CS, Hindorff LA, Lange EM, Walston J, Durda JP, Cushman M, Bis JC, Zeng D, Lin D, Kuller LH, Nickerson DA, Psaty BM, Tracy RP, Reiner AP. Association of polymorphisms in the CRP gene with circulating C-reactive protein levels and cardiovascular events. Jama. 296: 2703-11. PMID 17164456 DOI: 10.1001/Jama.296.22.2703  0.12
2015 Li J, Shi J, Huang W, Sun J, Wu Y, Duan Q, Luo J, Lange LA, Gordon-Larsen P, Zheng SL, Yuan W, Wang Y, Popkin BM, Mo Z, Xu J, ... ... Lange EM, et al. Variant Near FGF5 Has Stronger Effects on Blood Pressure in Chinese With a Higher Body Mass Index. American Journal of Hypertension. 28: 1031-7. PMID 25618516 DOI: 10.1093/Ajh/Hpu263  0.119
2016 Franceschini N, Fry RC, Balakrishnan P, Navas-Acien A, Oliver-Williams C, Howard AG, Cole SA, Haack K, Lange EM, Howard BV, Best LG, Francesconi KA, Goessler W, Umans JG, Tellez-Plaza M. Cadmium body burden and increased blood pressure in middle-aged American Indians: the Strong Heart Study. Journal of Human Hypertension. PMID 27629244 DOI: 10.1038/Jhh.2016.67  0.119
2015 Durda P, Sabourin J, Lange EM, Nalls MA, Mychaleckyj JC, Jenny NS, Li J, Walston J, Harris TB, Psaty BM, Valdar W, Liu Y, Cushman M, Reiner AP, Tracy RP, et al. Plasma Levels of Soluble IL-2 Receptor α: Associations With Clinical Cardiovascular Events and Genome-Wide Association Scan. Arteriosclerosis, Thrombosis, and Vascular Biology. PMID 26293465 DOI: 10.1161/Atvbaha.115.305289  0.119
2003 Hirakawa S, Lange EM, Colicigno CJ, Freedman BI, Rich SS, Bowden DW. Evaluation of genetic variation and association in the matrix metalloproteinase 9 (MMP9) gene in ESRD patients. American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation. 42: 133-42. PMID 12830465 DOI: 10.1016/S0272-6386(03)00416-5  0.116
2002 Mahadev K, Raval G, Bharadwaj S, Willingham MC, Lange EM, Vonderhaar B, Salomon D, Prasad GL. Suppression of the transformed phenotype of breast cancer by tropomyosin-1. Experimental Cell Research. 279: 40-51. PMID 12213212  0.113
2007 Pinheiro AP, Keefe RS, Skelly T, Olarte M, Leviel K, Lange LA, Lange EM, Stroup TS, Lieberman J, Sullivan PF. AKT1 and neurocognition in schizophrenia. The Australian and New Zealand Journal of Psychiatry. 41: 169-77. PMID 17464696 DOI: 10.1080/00048670601109956  0.109
2002 Shah S, Doyle K, Lange EM, Shen P, Pennell T, Ferree C, Levine EA, Perrier ND. Breast cancer recurrences in elderly patients after lumpectomy. The American Surgeon. 68: 735-9. PMID 12206612  0.104
2011 Graff M, North KE, Monda KL, Lange EM, Lange LA, Guo G, Gordon-Larsen P. The combined influence of genetic factors and sedentary activity on body mass changes from adolescence to young adulthood: the National Longitudinal Adolescent Health Study. Diabetes/Metabolism Research and Reviews. 27: 63-9. PMID 21218509 DOI: 10.1002/Dmrr.1147  0.104
2021 Matías-García PR, Ward-Caviness CK, Raffield LM, Gao X, Zhang Y, Wilson R, Gào X, Nano J, Bostom A, Colicino E, Correa A, Coull B, Eaton C, Hou L, Just AC, ... ... Lange E, et al. DNAm-based signatures of accelerated aging and mortality in blood are associated with low renal function. Clinical Epigenetics. 13: 121. PMID 34078457 DOI: 10.1186/s13148-021-01082-w  0.098
2014 Lange EH, NesvÃ¥g R, Ringen PA, Hartberg CB, Haukvik UK, Andreassen OA, Melle I, Agartz I. One year follow-up of alcohol and illicit substance use in first-episode psychosis: does gender matter? Comprehensive Psychiatry. 55: 274-82. PMID 24262129 DOI: 10.1016/j.comppsych.2013.08.018  0.091
1997 Jöns A, Gerdts V, Lange E, Kaden V, Mettenleiter TC. Attenuation of dUTPase-deficient pseudorabies virus for the natural host Veterinary Microbiology. 56: 47-54. PMID 9228681 DOI: 10.1016/S0378-1135(96)01353-3  0.089
2016 Graff M, North KE, Richardson AS, Young KL, Mazul AL, Highland HM, Mohlke KL, Lange LA, Lange EM, Harris KM, Gordon-Larsen P. BMI loci and longitudinal BMI from adolescence to young adulthood in an ethnically diverse cohort. International Journal of Obesity (2005). PMID 28025578 DOI: 10.1038/Ijo.2016.233  0.088
2023 Hill EB, Konigsberg IR, Ir D, Frank DN, Jambal P, Litkowski EM, Lange EM, Lange LA, Ostendorf DM, Scorsone JJ, Wayland L, Bing K, MacLean PS, Melanson EL, Bessesen DH, et al. The Microbiome, Epigenome, and Diet in Adults with Obesity during Behavioral Weight Loss. Nutrients. 15. PMID 37630778 DOI: 10.3390/nu15163588  0.087
2013 Graff M, North KE, Richardson AS, Young KM, Mohlke KL, Lange LA, Lange EM, Harris KM, Gordon-Larsen P. Screen time behaviours may interact with obesity genes, independent of physical activity, to influence adolescent BMI in an ethnically diverse cohort. Pediatric Obesity. 8: e74-9. PMID 24039247 DOI: 10.1111/J.2047-6310.2013.00195.X  0.083
2005 Nicklas BJ, Mychaleckyj J, Kritchevsky S, Palla S, Lange LA, Lange EM, Messier SP, Bowden D, Pahor M. Physical function and its response to exercise: associations with cytokine gene variation in older adults with knee osteoarthritis. The Journals of Gerontology. Series a, Biological Sciences and Medical Sciences. 60: 1292-8. PMID 16282562 DOI: 10.1093/Gerona/60.10.1292  0.083
2023 Fridman V, Sillau S, Ritchie A, Bockhorst J, Coughlan C, Araya P, Espinosa JM, Smith K, Lange EM, Lange LA, El Ghormli L, Drews KL, Zeitler P, Reusch JEB. Plasma Neurofilament Light Chain Concentrations are Elevated in Youth-onset Type 2 Diabetes and Associate with Neuropathy. Journal of the Peripheral Nervous System : Jpns. PMID 37341347 DOI: 10.1111/jns.12575  0.082
2010 Joubert BR, Lange EM, Franceschini N, Mwapasa V, North KE, Meshnick SR. Correction: A whole genome association study of mother-to-child transmission of HIV in Malawi Genome Medicine. 2. DOI: 10.1186/Gm197  0.081
2019 Turcot V, Lu Y, Highland HM, Schurmann C, Justice AE, Fine RS, Bradfield JP, Esko T, Giri A, Graff M, Guo X, Hendricks AE, Karaderi T, Lempradl A, Locke AE, ... ... Lange EM, et al. Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. Nature Genetics. PMID 31160809 DOI: 10.1038/s41588-019-0447-2  0.08
2011 Cohen SS, Gammon MD, Signorello LB, North KE, Lange EM, Fowke JH, Hargreaves MK, Cai Q, Zheng W, Blot WJ, Matthews CE. Serum adiponectin in relation to body mass index and other correlates in black and white women. Annals of Epidemiology. 21: 86-94. PMID 21109453 DOI: 10.1016/J.Annepidem.2010.10.011  0.077
2009 Bartlett JR, Friedman KJ, Ling SC, Pace RG, Bell SC, Bourke B, Castaldo G, Castellani C, Cipolli M, Colombo C, Colombo JL, Debray D, Fernandez A, Lacaille F, Macek M, ... ... Lange EM, et al. Genetic modifiers of liver disease in cystic fibrosis. Jama. 302: 1076-83. PMID 19738092 DOI: 10.1001/Jama.2009.1295  0.076
2014 Mouchantat S, Haas B, Böhle W, Globig A, Lange E, Mettenleiter TC, Depner K. Proof of principle: non-invasive sampling for early detection of foot-and-mouth disease virus infection in wild boar using a rope-in-a-bait sampling technique. Veterinary Microbiology. 172: 329-33. PMID 24930983 DOI: 10.1016/j.vetmic.2014.05.021  0.076
2013 Harder TC, Grosse Beilage E, Lange E, Meiners C, Döhring S, Pesch S, Noé T, Grund C, Beer M, Starick E. Expanded cocirculation of stable subtypes, emerging lineages, and new sporadic reassortants of porcine influenza viruses in swine populations in Northwest Germany. Journal of Virology. 87: 10460-76. PMID 23824819 DOI: 10.1128/JVI.00381-13  0.074
2015 Lange EO, Jensen CC, Melton GB, Madoff RD, Kwaan MR. Relationship between model for end-stage liver disease score and 30-day outcomes for patients undergoing elective colorectal resections: an American college of surgeons-national surgical quality improvement program study. Diseases of the Colon and Rectum. 58: 494-501. PMID 25850836 DOI: 10.1097/DCR.0000000000000358  0.074
2005 Kritchevsky SB, Nicklas BJ, Visser M, Simonsick EM, Newman AB, Harris TB, Lange EM, Penninx BW, Goodpaster BH, Satterfield S, Colbert LH, Rubin SM, Pahor M. Angiotensin-converting enzyme insertion/deletion genotype, exercise, and physical decline. Jama. 294: 691-8. PMID 16091571 DOI: 10.1001/Jama.294.6.691  0.071
2014 NesvÃ¥g R, Schaer M, Haukvik UK, Westlye LT, Rimol LM, Lange EH, Hartberg CB, Ottet MC, Melle I, Andreassen OA, Jönsson EG, Agartz I, Eliez S. Reduced brain cortical folding in schizophrenia revealed in two independent samples. Schizophrenia Research. 152: 333-8. PMID 24365403 DOI: 10.1016/j.schres.2013.11.032  0.071
2018 Turcot V, Lu Y, Highland HM, Schurmann C, Justice AE, Fine RS, Bradfield JP, Esko T, Giri A, Graff M, Guo X, Hendricks AE, Karaderi T, Lempradl A, Locke AE, ... ... Lange EM, et al. Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. Nature Genetics. PMID 29549330 DOI: 10.1038/s41588-018-0082-3  0.071
2018 Turcot V, Lu Y, Highland HM, Schurmann C, Justice AE, Fine RS, Bradfield JP, Esko T, Giri A, Graff M, Guo X, Hendricks AE, Karaderi T, Lempradl A, Locke AE, ... ... Lange EM, et al. Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. Nature Genetics. PMID 29549329 DOI: 10.1038/S41588-018-0050-Y  0.07
2016 Lange EM, Toledo P, Stariha J, Nixon HC. Anesthetic management for Cesarean delivery in parturients with a diagnosis of dwarfism. Canadian Journal of Anaesthesia = Journal Canadien D'Anesthesie. PMID 27174298 DOI: 10.1007/s12630-016-0671-5  0.068
2014 Klingbeil K, Lange E, Teifke JP, Mettenleiter TC, Fuchs W. Immunization of pigs with an attenuated pseudorabies virus recombinant expressing the haemagglutinin of pandemic swine origin H1N1 influenza A virus. The Journal of General Virology. 95: 948-59. PMID 24431235 DOI: 10.1099/vir.0.059253-0  0.067
2015 Mahjoub N, Dhorne-Pollet S, Fuchs W, Endale Ahanda ML, Lange E, Klupp B, Arya A, Loveland JE, Lefevre F, Mettenleiter TC, Giuffra E. A 2.5-kilobase deletion containing a cluster of nine microRNAs in the latency-associated-transcript locus of the pseudorabies virus affects the host response of porcine trigeminal ganglia during established latency. Journal of Virology. 89: 428-42. PMID 25320324 DOI: 10.1128/JVI.02181-14  0.065
2023 Litkowski EM, Logue MW, Zhang R, Charest BR, Lange EM, Hokanson JE, Lynch JA, Vujkovic M, Phillips LS, Hauger RL, Lange LA, Raghavan S. Mendelian randomization study of diabetes and dementia in the Million Veteran Program. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 37417779 DOI: 10.1002/alz.13373  0.063
2023 Litkowski EM, Logue MW, Zhang R, Charest BR, Lange EM, Hokanson JE, Lynch JA, Vujkovic M, Phillips LS, Hauger RL, Lange LA, Raghavan S. Mendelian randomization study of diabetes and dementia in the Million Veteran Program. Medrxiv : the Preprint Server For Health Sciences. PMID 36945581 DOI: 10.1101/2023.03.07.23286526  0.061
2014 Haukvik UK, McNeil T, Lange EH, Melle I, Dale AM, Andreassen OA, Agartz I. Pre- and perinatal hypoxia associated with hippocampus/amygdala volume in bipolar disorder. Psychological Medicine. 44: 975-85. PMID 23803260 DOI: 10.1017/S0033291713001529  0.061
2015 Lange E, Miranda Pires IM. From “sensed” to “complex”: some reflections on borders throughout history Space and Polity. 19: 293-304. DOI: 10.1080/09700161.2015.1093294  0.06
2015 Lange EO, Ferrari L, Krane M, Fichera A. Ligation of Intersphincteric Fistula Tract: a Sphincter-Sparing Option for Complex Fistula-in-Ano. Journal of Gastrointestinal Surgery : Official Journal of the Society For Surgery of the Alimentary Tract. PMID 26394877 DOI: 10.1007/s11605-015-2947-4  0.058
2016 Shaw EA, Lange E, Shucksmith JD, Lerner DN. Importance of partial barriers and temporal variation in flow when modelling connectivity in fragmented river systems Ecological Engineering. 91: 515-528. DOI: 10.1016/j.ecoleng.2016.01.030  0.055
2014 Proetel U, Pletsch N, Lauseker M, Müller MC, Hanfstein B, Krause SW, Kalmanti L, Schreiber A, Heim D, Baerlocher GM, Hofmann WK, Lange E, Einsele H, Wernli M, Kremers S, et al. Older patients with chronic myeloid leukemia (≥65 years) profit more from higher imatinib doses than younger patients: a subanalysis of the randomized CML-Study IV. Annals of Hematology. 93: 1167-76. PMID 24658964 DOI: 10.1007/s00277-014-2041-0  0.055
2015 Cramer P, Isfort S, Bahlo J, Stilgenbauer S, Döhner H, Bergmann M, Stauch M, Kneba M, Lange E, Langerbeins P, Pflug N, Kovacs G, Goede V, Fink AM, Elter T, et al. OUTCOME OF ADVANCED CHRONIC LYMPHOCYTIC LEUKEMIA FOLLOWING DIFFERENT FIRSTLINE- AND RELAPSE-THERAPIES: A METAANALYSIS OF FIVE PROSPECTIVE TRIALS OF THE GERMAN CLL STUDY GROUP (GCLLSG). Haematologica. PMID 26315931 DOI: 10.3324/haematol.2015.124693  0.053
2014 Schlosser J, Eiden M, Vina-Rodriguez A, Fast C, Dremsek P, Lange E, Ulrich RG, Groschup MH. Natural and experimental hepatitis E virus genotype 3-infection in European wild boar is transmissible to domestic pigs. Veterinary Research. 45: 121. PMID 25421429 DOI: 10.1186/s13567-014-0121-8  0.05
2013 Lange EA, Kerr SG. Accounting and incentives for sustainability in higher education: An interdisciplinary analysis of a needed revolution Social Responsibility Journal. 9: 210-219. DOI: 10.1108/Srj-08-2011-0058  0.05
2015 Peralta F, Higgins N, Lange E, Wong CA, McCarthy RJ. The Relationship of Body Mass Index with the Incidence of Postdural Puncture Headache in Parturients. Anesthesia and Analgesia. PMID 25993388 DOI: 10.1213/ANE.0000000000000802  0.048
2014 Haukvik UK, Rimol LM, Roddey JC, Hartberg CB, Lange EH, Vaskinn A, Melle I, Andreassen OA, Dale A, Agartz I. Normal birth weight variation is related to cortical morphology across the psychosis spectrum. Schizophrenia Bulletin. 40: 410-9. PMID 23419977 DOI: 10.1093/schbul/sbt005  0.047
2015 Steele SR, Varma MG, Prichard D, Bharucha AE, Vogler SA, Erdogan A, Rao SS, Lowry AC, Lange EO, Hall GM, Bleier JI, Senagore AJ, Maykel J, Chan SY, Paquette IM, et al. The evolution of evaluation and management of urinary or fecal incontinence and pelvic organ prolapse. Current Problems in Surgery. 52: 92-136. PMID 25933741 DOI: 10.1067/j.cpsurg.2015.02.001  0.045
2015 Mørch-Johnsen L, Nesvåg R, Faerden A, Haukvik UK, Jørgensen KN, Lange EH, Andreassen OA, Melle I, Agartz I. Brain structure abnormalities in first-episode psychosis patients with persistent apathy. Schizophrenia Research. 164: 59-64. PMID 25818626 DOI: 10.1016/j.schres.2015.03.001  0.043
2014 Best C, Lange E, Buchholz HG, Schreckenberger M, Reuss S, Dieterich M. Left hemispheric dominance of vestibular processing indicates lateralization of cortical functions in rats. Brain Structure & Function. 219: 2141-58. PMID 23979449 DOI: 10.1007/s00429-013-0628-1  0.042
2015 Behringer K, Goergen H, Hitz F, Zijlstra JM, Greil R, Markova J, Sasse S, Fuchs M, Topp MS, Soekler M, Mathas S, Meissner J, Wilhelm M, Koch P, Lindemann HW, ... ... Lange E, et al. Omission of dacarbazine or bleomycin, or both, from the ABVD regimen in treatment of early-stage favourable Hodgkin's lymphoma (GHSG HD13): an open-label, randomised, non-inferiority trial. Lancet (London, England). 385: 1418-27. PMID 25539730 DOI: 10.1016/S0140-6736(14)61469-0  0.041
2016 Pastega DF, Lange E, Ameixa J, Barbosa AS, Blanco F, García G, Bettega MHF, Limão-Vieira P, Ferreira Da Silva F. Combined experimental and theoretical study on the differential elastic scattering cross sections for acetone by electron impact energy of 7.0-50 eV Physical Review a - Atomic, Molecular, and Optical Physics. 93. DOI: 10.1103/PhysRevA.93.032708  0.04
2014 Hasse C, Holz O, Lange E, Pisowodzki L, Rebscher N, Christin Eder M, Hobmayer B, Hassel M. FGFR-ERK signaling is an essential component of tissue separation. Developmental Biology. 395: 154-66. PMID 25149325 DOI: 10.1016/J.Ydbio.2014.08.010  0.039
2014 Downes M, Lange E. What you see is not always what you get: A qualitative, comparative analysis of ex ante visualizations with ex post photography of landscape and architectural projects Landscape and Urban Planning. DOI: 10.1016/j.landurbplan.2014.06.002  0.039
2014 Wang Z, Burwinkel M, Chai W, Lange E, Blohm U, Breithaupt A, Hoffmann B, Twardziok S, Rieger J, Janczyk P, Pieper R, Osterrieder N. Dietary Enterococcus faecium NCIMB 10415 and zinc oxide stimulate immune reactions to trivalent influenza vaccination in pigs but do not affect virological response upon challenge infection. Plos One. 9: e87007. PMID 24489827 DOI: 10.1371/Journal.Pone.0087007  0.039
2014 Engelhard IM, Leer A, Lange E, Olatunji BO. Shaking that icky feeling: effects of extinction and counterconditioning on disgust-related evaluative learning. Behavior Therapy. 45: 708-19. PMID 25022781 DOI: 10.1016/J.Beth.2014.04.003  0.037
2015 Shaw E, Kumar V, Lange E, Lerner DN. Exploring the utility of Bayesian Networks for modelling cultural ecosystem services: A canoeing case study. The Science of the Total Environment. PMID 26345252 DOI: 10.1016/j.scitotenv.2015.08.027  0.037
2014 Lange E. Data center on four wheels | Datenzentrale auf vier Rädern Mechatronik. 122: 28-30.  0.037
2015 Jørgensen KN, Skjærvø I, Mørch-Johnsen L, Haukvik UK, Lange EH, Melle I, Andreassen OA, Agartz I. Cigarette smoking is associated with thinner cingulate and insular cortices in patients with severe mental illness. Journal of Psychiatry & Neuroscience : Jpn. 40: 241-9. PMID 25672482 DOI: 10.1503/jpn.140163  0.037
2015 Haukvik UK, Westlye LT, Mørch-Johnsen L, Jørgensen KN, Lange EH, Dale AM, Melle I, Andreassen OA, Agartz I. In vivo hippocampal subfield volumes in schizophrenia and bipolar disorder. Biological Psychiatry. 77: 581-8. PMID 25127742 DOI: 10.1016/j.biopsych.2014.06.020  0.036
2014 WÅ‚odarek D, GÅ‚abska D, Lange E. The effect of dairy products choice on calcium dietary intake in female university students of nutritional faculty. Roczniki Paå„Stwowego Zakå‚Adu Higieny. 65: 35-9. PMID 24964577  0.035
2015 Klingbeil K, Lange E, Blohm U, Teifke JP, Mettenleiter TC, Fuchs W. Protection of pigs against pandemic swine origin H1N1 influenza A virus infection by hemagglutinin- or neuraminidase-expressing attenuated pseudorabies virus recombinants. Virus Research. 199: 20-30. PMID 25599604 DOI: 10.1016/j.virusres.2015.01.009  0.033
2015 Song IH, Hermann KG, Haibel H, Althoff CE, Poddubnyy D, Listing J, Weiß A, Lange E, Freundlich B, Rudwaleit M, Sieper J. Prevention of new osteitis on magnetic resonance imaging in patients with early axial spondyloarthritis during 3 years of continuous treatment with etanercept: data of the ESTHER trial. Rheumatology (Oxford, England). 54: 257-61. PMID 25140041 DOI: 10.1093/rheumatology/keu263  0.032
2014 Ekberg E, Lange E. Business history and economic globalisation Business History. 56: 101-115. DOI: 10.1080/00076791.2013.818418  0.031
2015 Lange E. (Re)igniting a sociological imagination in adult education: the continuing relevance of classical theory International Journal of Lifelong Education. DOI: 10.1080/02601370.2015.1028574  0.028
2014 Beaudu-Lange C, Lange E. Unusual clinical presentation of leptospirosis in a cat Revue Veterinaire Clinique. 49: 115-122. DOI: 10.1016/j.anicom.2014.05.001  0.028
2014 Lange E, Bertrand S, Holz O, Rebscher N, Hassel M. Dynamic expression of a Hydra FGF at boundaries and termini. Development Genes and Evolution. 224: 235-44. PMID 25311911 DOI: 10.1007/S00427-014-0480-1  0.027
2015 Song IH, Hermann KG, Haibel H, Althoff CE, Poddubnyy D, Listing J, Weiß A, Freundlich B, Lange E, Rudwaleit M, Sieper J. Inflammatory and fatty lesions in the spine and sacroiliac joints on whole-body MRI in early axial spondyloarthritis-3-Year data of the ESTHER trial. Seminars in Arthritis and Rheumatism. PMID 26519007 DOI: 10.1016/j.semarthrit.2015.08.005  0.026
2015 Lange EL. Exchanging without Exploiting: A Critique of Karatani Köjin's the Structure of World History Historical Materialism. 23: 171-200. DOI: 10.1163/1569206X-12341425  0.025
2014 Mosunov AY, Grishkevich OY, Nikolskaya IA, Lange EE. On the influence of the sideholes profile on the initial production rate of wells (by example of Nizhne-Sortimskoye oilfield) Neftyanoe Khozyaystvo - Oil Industry. 90-92.  0.023
2013 Lange E. Saving costs with the cloud: Automation from the cloud will become a trend | Mit der Wolke Kosten sparen: Automation aus der Cloud wird ein Trend Mechatronik. 121: 55-57.  0.022
2013 Riemer B, Lange E, Hameyer K. Calculation of the flux distribution of three phase five limb power transformers considering nonlinear material properties Compel - the International Journal For Computation and Mathematics in Electrical and Electronic Engineering. 32: 1230-1243. DOI: 10.1108/03321641311317059  0.021
2015 Sysoeva OV, Lange EB, Sorokin AB, Campbell T. From pre-attentive processes to durable representation: an ERP index of visual distraction. International Journal of Psychophysiology : Official Journal of the International Organization of Psychophysiology. 95: 310-21. PMID 25523346 DOI: 10.1016/J.Ijpsycho.2014.12.007  0.02
2015 Ferreira da Silva F, Lange E, Limão-Vieira P, Jones NC, Hoffmann SV, Hubin-Franskin MJ, Delwiche J, Brunger MJ, Neves RF, Lopes MC, de Oliveira EM, da Costa RF, Varella MT, Bettega MH, Blanco F, et al. Electronic excitation of furfural as probed by high-resolution vacuum ultraviolet spectroscopy, electron energy loss spectroscopy, and ab initio calculations. The Journal of Chemical Physics. 143: 144308. PMID 26472380 DOI: 10.1063/1.4932603  0.019
2015 Ekberg E, Lange E, Nybo A. Maritime entrepreneurs and policy-makers: A historical approach to contemporary economic globalization Journal of Global History. 10: 171-193. DOI: 10.1017/S1740022814000333  0.019
2015 Lange E. Transformative learning and concepts of the self: insights from immigrant and intercultural journeys International Journal of Lifelong Education. DOI: 10.1080/02601370.2015.1036944  0.016
2015 Beaudu-Lange C, Lange E, Lecoq K. What is your diagnosis? | Quel est votre diagnostic? Pratique Vet. 12-15.  0.016
2015 Beaudu-Lange C, Lange E, Lecoq K. What is your diagnosis? | Quel est votre diagnostic? Pratique Vet. 12-15.  0.016
2014 Guzek D, Glabska D, Lange E, Glabski K, Wierzbicka A. Study of beef blade muscles' differentiation depending on conformation and fat class Turkish Journal of Veterinary and Animal Sciences. 38: 195-199. DOI: 10.3906/vet-1308-25  0.016
2015 Lange E, Meneses G, Cunha T, Krasuska J, Kopyra J, García G, Da Silva FF, Limão-Vieira P. Electron induced fragmentation of sulphur containing biological prototypes: Thiaproline and taurine Journal of Physics: Conference Series. 635. DOI: 10.1088/1742-6596/635/7/072069  0.016
2014 Lange E. Machine data in the cloud | Maschinendaten in der Woike Mechatronik. 122: 36-38.  0.016
2013 Lange E. Industrial service providers: Increasing number of companies trust the service professionals | Immer mehr Unternehmen vertrauen den Serviceprofis Stahl Und Eisen. 133: 68-70.  0.015
2014 Tastsoglou E, Abidi CB, Brigham SM, Lange EA. (En) gendering vulnerability: Immigrant service providers' perceptions of needs, policies, and practices related to gender and women refugee claimants in Atlantic Canada Refuge. 30: 67-78. DOI: 10.25071/1920-7336.39620  0.014
2015 Błaszczyk K, Wilczak J, Harasym J, Gudej S, Suchecka D, Królikowski T, Lange E, Gromadzka-Ostrowska J. Impact of low and high molecular weight oat beta-glucan on oxidative stress and antioxidant defense in spleen of rats with LPS induced enteritis Food Hydrocolloids. 51: 272-280. DOI: 10.1016/j.foodhyd.2015.05.025  0.014
2014 Lange E. An optical measurement picture says more than 1000 numbers | Ein optisches Mess-Bild sagt mehr als 1000 Zahlen Mechatronik. 122: 25-27.  0.014
2015 Lange E. Always keeping pace | Immer am Puls Mechatronik. 123: 38-39.  0.013
2015 Gess B, Röhr D, Lange E, Halfter H, Young P. Desmoplakin is involved in organization of an adhesion complex in peripheral nerve regeneration after injury. Experimental Neurology. 264: 55-66. PMID 25496840 DOI: 10.1016/j.expneurol.2014.12.005  0.013
2016 Lange E. Klein und sicherheitsbedürftig Mechatronik. 124: 37-39.  0.013
2014 Dyke C, Horton H, Peake D, Poole J, Ge L, Biradar S, Boyer T, Boyer L, Yao A, Lange E, Semon N, Chan D, Vajtai R, Ajayan P, Barrera E. Ultrahigh conductivity umbilicals: Polymer nanotube umbilicals Proceedings of the Annual Offshore Technology Conference. 4: 2783-2790.  0.011
2014 Lange E. Battery-free trackers monitor machines | Batterielose Spürhunde überwachen Maschinen Mechatronik. 122: 50-51.  0.01
2016 Lindquist M, Lange E, Kang J. From 3D landscape visualization to environmental simulation: The contribution of sound to the perception of virtual environments Landscape and Urban Planning. 148: 216-231. DOI: 10.1016/j.landurbplan.2015.12.017  0.01
2016 Lange E. Noble Entwicklung Mechatronik. 124: 54-56.  0.01
2015 Lange EM, Shah AM, Braithwaite BA, You WB, Wong CA, Grobman WA, Toledo P. Readability, content, and quality of online patient education materials on preeclampsia. Hypertension in Pregnancy. 1-8. PMID 26153628 DOI: 10.3109/10641955.2015.1053607  0.01
2015 Bauder J, Lange E. Exploratory subject searching in library catalogs: Reclaiming the vision Information Technology and Libraries. 34: 92-102. DOI: 10.6017/ital.v34i3.5888  0.01
2015 Gill L, Lange E. Getting virtual 3D landscapes out of the lab Computers, Environment and Urban Systems. 54: 356-362. DOI: 10.1016/j.compenvurbsys.2015.09.012  0.01
2015 Lange E. Technology lead thanks to innovative thermal process engineering | Technologievorsprung dank innovativer Thermischer Prozesstechnik Stahl Und Eisen. 135: 175-184.  0.01
2015 Lange E. Energy diet makes steel industry future-proof | Energiediät macht stahlindustrie zulcunftsfest Stahl Und Eisen. 135: 74-78.  0.01
2014 Lange EL. Failed abstraction - the problem of uno kozo's reading of marx's theory of the value form Historical Materialism. 22: 3-33. DOI: 10.1163/1569206X-12341336  0.01
2014 Maximov AA, Eremina TR, Lange EK, Litvinchuk LF, Maximova OB. Regime shift in the ecosystem of the eastern Gulf of Finland caused by the invasion of the polychaete Marenzelleria arctia Oceanology. 54: 46-53. DOI: 10.1134/S0001437013060052  0.01
2014 Lange E. Oschatz: Plant construction firm with tradition | Oschatz: Anlagenbauer mit Tradition Stahl Und Eisen. 134: 76-78.  0.01
2014 Lange E. Expanding the dynamic range of current measurement Engineerit. 33-34.  0.01
2014 Lange E. Lightweight design: Innovative joining technology holds material mix together | Innovative Fügetechnik hält Materialmix zusammen Stahl Und Eisen. 134: 104-106.  0.01
2014 Lange E. The city of tomorrow - Challenges for steel. City of tomorrow builds on steel | Stadt der Zukunft baut auf Stahl Stahl Und Eisen. 134: 44-47.  0.01
2014 Lange E. Industrial site Germany in Europe: Challenges and perspectives. Industrial site Germany is the model for Europe | Industriestandort Deutschland ist das Vorbild für Europa Stahl Und Eisen. 134: 40-43.  0.01
2014 Lange E. Golden times for smart robots: Service robotics is in the ascendant | Goldene Zeiten für schlaue Roboter: Die Servicerobotik ist im Aufwind Mechatronik. 122: 24-25.  0.01
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