Daniel L. Koller, Ph.D. - Publications

Affiliations: 
2001 Indiana University, Bloomington, Bloomington, IN, United States 
Area:
Genetics, Biostatistics Biology

93 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 Hsu YH, Estrada K, Evangelou E, Ackert-Bicknell C, Akesson K, Beck T, Brown SJ, Capellini T, Carbone L, Cauley J, Cheung CL, Cummings SR, Czerwinski S, Demissie S, Econs M, ... ... Koller DL, et al. Meta-Analysis of Genomewide Association Studies Reveals Genetic Variants for Hip Bone Geometry. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. e3698. PMID 30888730 DOI: 10.1002/Jbmr.3698  0.363
2018 Budde M, Friedrichs S, Alliey-Rodriguez N, Ament S, Badner JA, Berrettini WH, Bloss CS, Byerley W, Cichon S, Comes AL, Coryell W, Craig DW, Degenhardt F, Edenberg HJ, Foroud T, ... ... Koller DL, et al. Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder. European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology. PMID 30503783 DOI: 10.1016/J.Euroneuro.2018.10.005  0.353
2018 Breuer R, Mattheisen M, Frank J, Krumm B, Treutlein J, Kassem L, Strohmaier J, Herms S, Mühleisen TW, Degenhardt F, Cichon S, Nöthen MM, Karypis G, Kelsoe J, Greenwood T, ... ... Koller D, et al. Detecting significant genotype-phenotype association rules in bipolar disorder: market research meets complex genetics. International Journal of Bipolar Disorders. 6: 24. PMID 30415424 DOI: 10.1186/S40345-018-0132-X  0.397
2017 Zillikens MC, Demissie S, Hsu YH, Yerges-Armstrong LM, Chou WC, Stolk L, Livshits G, Broer L, Johnson T, Koller DL, Kutalik Z, Luan J, Malkin I, Ried JS, Smith AV, et al. Large meta-analysis of genome-wide association studies identifies five loci for lean body mass. Nature Communications. 8: 80. PMID 28724990 DOI: 10.1038/S41467-017-00031-7  0.328
2016 Hou L, Bergen SE, Akula N, Song J, Hultman CM, Landén M, Adli M, Alda M, Ardau R, Arias B, Aubry JM, Backlund L, Badner JA, Barrett TB, Bauer M, ... ... Koller DL, et al. Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder. Human Molecular Genetics. PMID 27329760 DOI: 10.1093/Hmg/Ddw181  0.471
2015 Alam I, Koller DL, Cañete T, Blázquez G, Mont-Cardona C, López-Aumatell R, Martínez-Membrives E, Díaz-Morán S, Tobeña A, Fernández-Teruel A, Stridh P, Diez M, Olsson T, Johannesson M, Baud A, et al. Fine mapping of bone structure and strength QTLs in heterogeneous stock rat. Bone. 81: 417-26. PMID 26297441 DOI: 10.1016/J.Bone.2015.08.013  0.387
2015 Schneider BP, Li L, Radovich M, Shen F, Miller C, Flockhart DA, Jiang G, Vance GH, Gardner L, Vatta M, Bai C, Lai D, Koller D, Zhao F, O'Neill A, et al. Genome-wide association studies for taxane-induced peripheral neuropathy (TIPN) in ECOG-5103 and ECOG-1199. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. PMID 26138065 DOI: 10.1158/1078-0432.Ccr-15-0586  0.308
2015 Farlow JL, Lin H, Sauerbeck L, Lai D, Koller DL, Pugh E, Hetrick K, Ling H, Kleinloog R, van der Vlies P, Deelen P, Swertz MA, Verweij BH, Regli L, Rinkel GJ, et al. Lessons learned from whole exome sequencing in multiplex families affected by a complex genetic disorder, intracranial aneurysm. Plos One. 10: e0121104. PMID 25803036 DOI: 10.1371/Journal.Pone.0121104  0.403
2015 Wetherill L, Agrawal A, Kapoor M, Bertelsen S, Bierut LJ, Brooks A, Dick D, Hesselbrock M, Hesselbrock V, Koller DL, Le N, Nurnberger JI, Salvatore JE, Schuckit M, Tischfield JA, et al. Association of substance dependence phenotypes in the COGA sample. Addiction Biology. 20: 617-27. PMID 24832863 DOI: 10.1111/Adb.12153  0.352
2014 Foroud T, Lai D, Koller D, Van't Hof F, Kurki MI, Anderson CS, Brown RD, Connolly ES, Eriksson JG, Flaherty M, Fornage M, von Und Zu Fraunberg M, Gaál EI, Laakso A, Hernesniemi J, et al. Genome-wide association study of intracranial aneurysm identifies a new association on chromosome 7. Stroke; a Journal of Cerebral Circulation. 45: 3194-9. PMID 25256182 DOI: 10.1161/Strokeaha.114.006096  0.32
2014 Perry JR, Day F, Elks CE, Sulem P, Thompson DJ, Ferreira T, He C, Chasman DI, Esko T, Thorleifsson G, Albrecht E, Ang WQ, Corre T, Cousminer DL, Feenstra B, ... ... Koller DL, et al. Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche. Nature. 514: 92-7. PMID 25231870 DOI: 10.1038/Nature13545  0.408
2014 Kemp JP, Medina-Gomez C, Estrada K, St Pourcain B, Heppe DH, Warrington NM, Oei L, Ring SM, Kruithof CJ, Timpson NJ, Wolber LE, Reppe S, Gautvik K, Grundberg E, Ge B, ... ... Koller DL, et al. Phenotypic dissection of bone mineral density reveals skeletal site specificity and facilitates the identification of novel loci in the genetic regulation of bone mass attainment. Plos Genetics. 10: e1004423. PMID 24945404 DOI: 10.1371/Journal.Pgen.1004423  0.428
2014 Alam I, Padgett LR, Ichikawa S, Alkhouli M, Koller DL, Lai D, Peacock M, Xuei X, Foroud T, Edenberg HJ, Econs MJ. SIBLING family genes and bone mineral density: Association and allele-specific expression in humans Bone. 64: 166-172. PMID 24747200 DOI: 10.1016/J.Bone.2014.04.013  0.381
2014 Alam I, Koller DL, Cañete T, Blázquez G, López-Aumatell R, Martínez-Membrives E, Díaz-Morán S, Tobeña A, Fernández-Teruel A, Stridh P, Diez M, Olsson T, Johannesson M, Baud A, Econs MJ, et al. High-resolution genome screen for bone mineral density in heterogeneous stock rat. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 29: 1619-26. PMID 24643965 DOI: 10.1002/Jbmr.2195  0.468
2013 Lee SH, Ripke S, Neale BM, Faraone SV, Purcell SM, Perlis RH, Mowry BJ, Thapar A, Goddard ME, Witte JS, Absher D, Agartz I, Akil H, Amin F, ... ... Koller DL, et al. Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nature Genetics. 45: 984-94. PMID 23933821 DOI: 10.1038/Ng.2711  0.302
2013 Chen C, Cheng L, Grennan K, Pibiri F, Zhang C, Badner JA, Kelsoe JR, Greenwood TA, Nievergelt CM, Barrett TB, McKinney R, Shilling PD, Schork NJ, Smith EN, Bloss CS, ... ... Koller DL, et al. Two gene co-expression modules differentiate psychotics and controls Molecular Psychiatry. 18: 1308-1314. PMID 23147385 DOI: 10.1038/Mp.2012.146  0.337
2013 Wang JC, Foroud T, Hinrichs AL, Le NX, Bertelsen S, Budde JP, Harari O, Koller DL, Wetherill L, Agrawal A, Almasy L, Brooks AI, Bucholz K, Dick D, Hesselbrock V, et al. A genome-wide association study of alcohol-dependence symptom counts in extended pedigrees identifies C15orf53. Molecular Psychiatry. 18: 1218-24. PMID 23089632 DOI: 10.1038/Mp.2012.143  0.432
2013 Koller DL, Zheng HF, Karasik D, Yerges-Armstrong L, Liu CT, McGuigan F, Kemp JP, Giroux S, Lai D, Edenberg HJ, Peacock M, Czerwinski SA, Choh AC, McMahon G, St Pourcain B, et al. Meta-analysis of genome-wide studies identifies WNT16 and ESR1 SNPs associated with bone mineral density in premenopausal women. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 28: 547-58. PMID 23074152 DOI: 10.1002/Jbmr.1796  0.464
2013 Gamazon ER, Badner JA, Cheng L, Zhang C, Zhang D, Cox NJ, Gershon ES, Kelsoe JR, Greenwood TA, Nievergelt CM, Chen C, McKinney R, Shilling PD, Schork NJ, Smith EN, ... ... Koller DL, et al. Enrichment of cis-regulatory gene expression SNPs and methylation quantitative trait loci among bipolar disorder susceptibility variants. Molecular Psychiatry. 18: 340-6. PMID 22212596 DOI: 10.1038/Mp.2011.174  0.415
2013 White KE, Koller DL, Corbin T. Skeletal Genetics: From Gene Identification to Murine Models of Disease Basic and Applied Bone Biology. 149-171. DOI: 10.1016/B978-0-12-416015-6.00008-3  0.343
2012 Nissen S, Liang S, Shehktman T, Kelsoe JR, Greenwood TA, Nievergelt CM, McKinney R, Shilling PD, Smith EN, Schork NJ, Bloss CS, Nurnberger JI, Edenberg HJ, Foroud T, ... Koller DL, et al. Evidence for association of bipolar disorder to haplotypes in the 22q12.3 region near the genes stargazin, IFT27 and parvalbumin. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 159: 941-50. PMID 23038240 DOI: 10.1002/Ajmg.B.32099  0.348
2012 Meier S, Mattheisen M, Vassos E, Strohmaier J, Treutlein J, Josef F, Breuer R, Degenhardt F, Mühleisen TW, Müller-Myhsok B, Steffens M, Schmael C, McMahon FJ, Nöthen MM, ... ... Koller DL, et al. Genome-wide significant association between a 'negative mood delusions' dimension in bipolar disorder and genetic variation on chromosome 3q26.1. Translational Psychiatry. 2: e165. PMID 23010768 DOI: 10.1038/Tp.2012.81  0.42
2012 Teng M, Ichikawa S, Padgett LR, Wang Y, Mort M, Cooper DN, Koller DL, Foroud T, Edenberg HJ, Econs MJ, Liu Y. regSNPs: a strategy for prioritizing regulatory single nucleotide substitutions. Bioinformatics (Oxford, England). 28: 1879-86. PMID 22611130 DOI: 10.1093/Bioinformatics/Bts275  0.396
2012 Ayalew M, Le-Niculescu H, Levey DF, Jain N, Changala B, Patel SD, Winiger E, Breier A, Shekhar A, Amdur R, Koller D, Nurnberger JI, Corvin A, Geyer M, Tsuang MT, et al. Convergent functional genomics of schizophrenia: from comprehensive understanding to genetic risk prediction. Molecular Psychiatry. 17: 887-905. PMID 22584867 DOI: 10.1038/Mp.2012.37  0.383
2012 Estrada K, Styrkarsdottir U, Evangelou E, Hsu YH, Duncan EL, Ntzani EE, Oei L, Albagha OM, Amin N, Kemp JP, Koller DL, Li G, Liu CT, Minster RL, Moayyeri A, et al. Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture. Nature Genetics. 44: 491-501. PMID 22504420 DOI: 10.1038/Ng.2249  0.445
2012 Badner JA, Koller D, Foroud T, Edenberg H, Nurnberger JI, Zandi PP, Willour VL, McMahon FJ, Potash JB, Hamshere M, Grozeva D, Green E, Kirov G, Jones I, Jones L, et al. Genome-wide linkage analysis of 972 bipolar pedigrees using single-nucleotide polymorphisms. Molecular Psychiatry. 17: 818-26. PMID 21769101 DOI: 10.1038/Mp.2011.89  0.448
2011 Sklar P, Ripke S, Scott LJ, Andreassen OA, Cichon S, Craddock N, Edenberg HJ, Nurnberger JI, Rietschel M, Blackwood D, Corvin A, Flickinger M, Guan W, Mattingsdal M, McQuillin A, ... ... Koller DL, et al. Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4 Nature Genetics. 43: 977-985. PMID 21926972 DOI: 10.1038/Ng.943  0.367
2011 Smith EN, Koller DL, Panganiban C, Szelinger S, Zhang P, Badner JA, Barrett TB, Berrettini WH, Bloss CS, Byerley W, Coryell W, Edenberg HJ, Foroud T, Gershon ES, Greenwood TA, et al. Genome-wide association of bipolar disorder suggests an enrichment of replicable associations in regions near genes. Plos Genetics. 7: e1002134. PMID 21738484 DOI: 10.1371/Journal.Pgen.1002134  0.461
2011 Alam I, Koller DL, Sun Q, Roeder RK, Cañete T, Blázquez G, López-Aumatell R, Martínez-Membrives E, Vicens-Costa E, Mont C, Díaz S, Tobeña A, Fernández-Teruel A, Whitley A, Strid P, et al. Heterogeneous stock rat: a unique animal model for mapping genes influencing bone fragility. Bone. 48: 1169-77. PMID 21334473 DOI: 10.1016/J.Bone.2011.02.009  0.392
2011 Zlojutro M, Manz N, Rangaswamy M, Xuei X, Flury-Wetherill L, Koller D, Bierut LJ, Goate A, Hesselbrock V, Kuperman S, Nurnberger J, Rice JP, Schuckit MA, Foroud T, Edenberg HJ, et al. Genome-wide association study of theta band event-related oscillations identifies serotonin receptor gene HTR7 influencing risk of alcohol dependence. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 156: 44-58. PMID 21184583 DOI: 10.1002/Ajmg.B.31136  0.473
2011 Wang TJ, Zhang F, Richards JB, Kestenbaum B, Van Meurs JB, Berry D, Kiel DP, Streeten EA, Ohlsson C, Koller DL, Peltonen L, Cooper JD, O'Reilly PF, Houston DK, Glazer NL, et al. Common genetic determinants of vitamin D insufficiency: A genome-wide association study Obstetrical and Gynecological Survey. 66: 91-93. DOI: 10.1097/Ogx.0B013E318216B03D  0.342
2011 Estrada K, Evangelou E, Hsu Y, Styrkarsdottir U, Liu C, Moayyeri A, Kaptoge S, Duncan E, Amin N, Kiel D, Karasik D, Albagha O, Brown M, Spector T, Zillikens M, ... ... Koller D, et al. Association analyses of 47,500 individuals identifies six fracture loci and 82 BMD loci clustering in biological pathways that regulate osteoblast and osteoclast activity Bone. 48: S69. DOI: 10.1016/J.Bone.2011.03.070  0.348
2010 Elks CE, Perry JR, Sulem P, Chasman DI, Franceschini N, He C, Lunetta KL, Visser JA, Byrne EM, Cousminer DL, Gudbjartsson DF, Esko T, Feenstra B, Hottenga JJ, Koller DL, et al. Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. Nature Genetics. 42: 1077-85. PMID 21102462 DOI: 10.1038/Ng.714  0.419
2010 Patel SD, Le-Niculescu H, Koller DL, Green SD, Lahiri DK, McMahon FJ, Nurnberger JI, Niculescu AB. Coming to grips with complex disorders: genetic risk prediction in bipolar disorder using panels of genes identified through convergent functional genomics. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 850-77. PMID 20468069 DOI: 10.1002/Ajmg.B.31087  0.442
2010 Edenberg HJ, Koller DL, Xuei X, Wetherill L, McClintick JN, Almasy L, Bierut LJ, Bucholz KK, Goate A, Aliev F, Dick D, Hesselbrock V, Hinrichs A, Kramer J, Kuperman S, et al. Genome-wide association study of alcohol dependence implicates a region on chromosome 11. Alcoholism, Clinical and Experimental Research. 34: 840-52. PMID 20201924 DOI: 10.1111/J.1530-0277.2010.01156.X  0.43
2010 Ichikawa S, Koller DL, Padgett LR, Lai D, Hui SL, Peacock M, Foroud T, Econs MJ. Replication of previous genome-wide association studies of bone mineral density in premenopausal American women. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 25: 1821-9. PMID 20200978 DOI: 10.1002/Jbmr.62  0.445
2010 Koller DL, Ichikawa S, Lai D, Padgett LR, Doheny KF, Pugh E, Paschall J, Hui SL, Edenberg HJ, Xuei X, Peacock M, Econs MJ, Foroud T. Genome-wide association study of bone mineral density in premenopausal European-American women and replication in African-American women. The Journal of Clinical Endocrinology and Metabolism. 95: 1802-9. PMID 20164292 DOI: 10.1210/Jc.2009-1903  0.389
2009 Smith EN, Bloss CS, Badner JA, Barrett T, Belmonte PL, Berrettini W, Byerley W, Coryell W, Craig D, Edenberg HJ, Eskin E, Foroud T, Gershon E, Greenwood TA, Hipolito M, ... Koller DL, et al. Genome-wide association study of bipolar disorder in European American and African American individuals. Molecular Psychiatry. 14: 755-63. PMID 19488044 DOI: 10.1038/Mp.2009.43  0.427
2009 Peacock M, Koller DL, Lai D, Hui S, Foroud T, Econs MJ. Bone mineral density variation in men is influenced by sex-specific and non sex-specific quantitative trait loci. Bone. 45: 443-8. PMID 19427925 DOI: 10.1016/J.Bone.2009.05.002  0.456
2009 Koller DL, Liu L, Alam I, Sun Q, Econs MJ, Foroud T, Turner CH. Epistasis between QTLs for bone density variation in Copenhagen x dark agouti F2 rats. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 20: 180-6. PMID 19153792 DOI: 10.1007/S00335-008-9161-6  0.499
2009 Foroud T, Sauerbeck L, Brown R, Anderson C, Woo D, Kleindorfer D, Flaherty ML, Deka R, Hornung R, Meissner I, Bailey-Wilson JE, Langefeld C, Rouleau G, Connolly ES, Lai D, ... Koller DL, et al. Genome screen in familial intracranial aneurysm. Bmc Medical Genetics. 10: 3. PMID 19144135 DOI: 10.1186/1471-2350-10-3  0.331
2009 Zhang D, Cheng L, Qian Y, Alliey-Rodriguez N, Kelsoe JR, Greenwood T, Nievergelt C, Barrett TB, McKinney R, Schork N, Smith EN, Bloss C, Nurnberger J, Edenberg HJ, Foroud T, ... ... Koller D, et al. Singleton deletions throughout the genome increase risk of bipolar disorder. Molecular Psychiatry. 14: 376-80. PMID 19114987 DOI: 10.1038/Mp.2008.144  0.374
2009 Ichikawa S, Koller DL, Curry LR, Lai D, Xuei X, Edenberg HJ, Hui SL, Peacock M, Foroud T, Econs MJ. Association of adenylate cyclase 10 (ADCY10) polymorphisms and bone mineral density in healthy adults. Calcified Tissue International. 84: 97-102. PMID 19093065 DOI: 10.1007/S00223-008-9200-Z  0.423
2009 Jung J, Sun B, Kwon D, Koller DL, Foroud TM. Allelic-based gene-gene interaction associated with quantitative traits. Genetic Epidemiology. 33: 332-43. PMID 19058262 DOI: 10.1002/Gepi.20385  0.414
2008 Chu K, Koller DL, Ichikawa S, Snyder R, Curry L, Lai D, Austin A, Xuei X, Edenberg HJ, Hui SL, Foroud TM, Peacock M, Econs MJ. CLCN7 polymorphisms and bone mineral density in healthy premenopausal white women and in white men. Bone. 43: 995-8. PMID 18755304 DOI: 10.1016/J.Bone.2008.07.249  0.4
2008 Alam I, Sun Q, Liu L, Koller DL, Liu Y, Edenberg HJ, Econs MJ, Foroud T, Turner CH. Genomic expression analysis of rat chromosome 4 for skeletal traits at femoral neck. Physiological Genomics. 35: 191-6. PMID 18728226 DOI: 10.1152/Physiolgenomics.90237.2008  0.365
2008 Koller DL, Liu L, Alam I, Sun Q, Econs MJ, Foroud T, Turner CH. Linkage screen for BMD phenotypes in male and female COP and DA rat strains. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 23: 1382-8. PMID 18707222 DOI: 10.1359/Jbmr.080401  0.321
2008 Ichikawa S, Koller DL, Curry LR, Lai D, Xuei X, Pugh EW, Tsai YY, Doheny KF, Edenberg HJ, Hui SL, Foroud T, Peacock M, Econs MJ. Identification of a linkage disequilibrium block in chromosome 1q associated with BMD in premenopausal white women. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 23: 1680-8. PMID 18505370 DOI: 10.1359/Jbmr.080509  0.477
2008 Foroud T, Sauerbeck L, Brown R, Anderson C, Woo D, Kleindorfer D, Flaherty ML, Deka R, Hornung R, Meissner I, Bailey-Wilson JE, Rouleau G, Connolly ES, Lai D, Koller DL, et al. Genome screen to detect linkage to intracranial aneurysm susceptibility genes: the Familial Intracranial Aneurysm (FIA) study. Stroke; a Journal of Cerebral Circulation. 39: 1434-40. PMID 18323491 DOI: 10.1161/Strokeaha.107.502930  0.411
2008 Alam I, Sun Q, Liu L, Koller DL, Carr LG, Econs MJ, Foroud T, Turner CH. Sex-specific genetic loci for femoral neck bone mass and strength identified in inbred COP and DA rats. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 23: 850-9. PMID 18282130 DOI: 10.1359/Jbmr.080221  0.416
2008 Sun Q, Alam I, Liu L, Koller DL, Carr LG, Econs MJ, Foroud T, Turner CH. Genetic loci affecting bone structure and strength in inbred COP and DA rats. Bone. 42: 547-53. PMID 18158281 DOI: 10.1016/J.Bone.2007.11.004  0.421
2008 Foroud T, Ichikawa S, Koller D, Lai D, Curry L, Xuei X, Edenberg HJ, Hui S, Peacock M, Econs MJ. Association studies of ALOX5 and bone mineral density in healthy adults Osteoporosis International. 19: 637-643. PMID 17909879 DOI: 10.1007/S00198-007-0484-Z  0.472
2008 Koller DL, Liu L, Alam I, Sun Q, Econs MJ, Foroud T, Turner CH. Epistatic effects contribute to variation in BMD in Fischer 344 x Lewis F2 rats. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 23: 41-7. PMID 17907919 DOI: 10.1359/Jbmr.071001  0.376
2007 Ioannidis JP, Ng MY, Sham PC, Zintzaras E, Lewis CM, Deng HW, Econs MJ, Karasik D, Devoto M, Kammerer CM, Spector T, Andrew T, Cupples LA, Duncan EL, Foroud T, ... ... Koller D, et al. Meta-analysis of genome-wide scans provides evidence for sex- and site-specific regulation of bone mass. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 22: 173-83. PMID 17228994 DOI: 10.1359/Jbmr.060806  0.431
2006 Hui SL, Koller DL, Foroud TM, Econs MJ, Johnston CC, Peacock M. Heritability of changes in bone size and bone mass with age in premenopausal white sisters. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 21: 1121-5. PMID 16813533 DOI: 10.1359/Jbmr.060412  0.303
2006 Ichikawa S, Koller DL, Johnson ML, Lai D, Xuei X, Edenberg HJ, Klein RF, Orwoll ES, Hui SL, Foroud TM, Peacock M, Econs MJ. Human ALOX12, but not ALOX15, is associated with BMD in white men and women. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 21: 556-64. PMID 16598376 DOI: 10.1359/Jbmr.051212  0.348
2006 Alam I, Sun Q, Liu L, Koller DL, Fishburn T, Carr LG, Econs MJ, Foroud T, Turner CH. Identification of a quantitative trait locus on rat chromosome 4 that is strongly linked to femoral neck structure and strength Bone. 39: 93-99. PMID 16461031 DOI: 10.1016/J.Bone.2005.12.009  0.468
2006 Ichikawa S, Johnson ML, Koller DL, Lai D, Xuei X, Edenberg HJ, Hui SL, Foroud TM, Peacock M, Econs MJ. Polymorphisms in the bone morphogenetic protein 2 (BMP2) gene do not affect bone mineral density in white men or women Osteoporosis International. 17: 587-592. PMID 16432645 DOI: 10.1007/S00198-005-0018-5  0.464
2005 Koller DL, Alam I, Sun Q, Liu L, Fishburn T, Carr LG, Econs MJ, Foroud T, Turner CH. Genome screen for bone mineral density phenotypes in Fisher 344 and Lewis rat strains. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 16: 578-86. PMID 16180139 DOI: 10.1007/S00335-004-2459-0  0.44
2005 Chu K, Koller DL, Snyder R, Fishburn T, Lai D, Waguespack SG, Foroud T, Econs MJ. Analysis of variation in expression of autosomal dominant osteopetrosis type 2: searching for modifier genes. Bone. 37: 655-61. PMID 16120485 DOI: 10.1016/J.Bone.2005.06.003  0.458
2005 Ichikawa S, Koller DL, Peacock M, Johnson ML, Lai D, Hui SL, Johnston CC, Foroud TM, Econs MJ. Polymorphisms in the estrogen receptor beta (ESR2) gene are associated with bone mineral density in Caucasian men and women. The Journal of Clinical Endocrinology and Metabolism. 90: 5921-7. PMID 16118344 DOI: 10.1210/Jc.2004-2253  0.463
2005 Alam I, Sun Q, Liu L, Koller DL, Fishburn T, Carr LG, Econs MJ, Foroud T, Turner CH. Whole-genome scan for linkage to bone strength and structure in inbred Fischer 344 and Lewis rats. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 20: 1589-96. PMID 16059631 DOI: 10.1359/Jbmr.050512  0.423
2005 Peacock M, Koller DL, Lai D, Hui S, Foroud T, Econs MJ. Sex-specific quantitative trait loci contribute to normal variation in bone structure at the proximal femur in men. Bone. 37: 467-73. PMID 16046210 DOI: 10.1016/J.Bone.2005.05.005  0.465
2005 Peacock M, Koller DL, Fishburn T, Krishnan S, Lai D, Hui S, Johnston CC, Foroud T, Econs MJ. Sex-specific and non-sex-specific quantitative trait loci contribute to normal variation in bone mineral density in men. The Journal of Clinical Endocrinology and Metabolism. 90: 3060-6. PMID 15741260 DOI: 10.1210/Jc.2004-2143  0.411
2005 Koller DL, Ichikawa S, Johnson ML, Lai D, Xuei X, Edenberg HJ, Conneally PM, Hui SL, Johnston CC, Peacock M, Foroud T, Econs MJ. Contribution of the LRP5 gene to normal variation in peak BMD in women. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 20: 75-80. PMID 15619672 DOI: 10.1359/Jbmr.041019  0.64
2004 Koller DL, Peacock M, Lai D, Foroud T, Econs MJ. False positive rates in association studies as a function of degree of stratification. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 19: 1291-5. PMID 15231016 DOI: 10.1359/Jbmr.040409  0.435
2004 Peacock M, Koller DL, Hui S, Johnston CC, Foroud T, Econs MJ. Peak bone mineral density at the hip is linked to chromosomes 14q and 15q. Osteoporosis International : a Journal Established as Result of Cooperation Between the European Foundation For Osteoporosis and the National Osteoporosis Foundation of the Usa. 15: 489-96. PMID 15205721 DOI: 10.1007/S00198-003-1560-7  0.444
2004 Econs MJ, Koller DL, Hui SL, Fishburn T, Conneally PM, Johnston CC, Peacock M, Foroud TM. Confirmation of linkage to chromosome 1q for peak vertebral bone mineral density in premenopausal white women. American Journal of Human Genetics. 74: 223-8. PMID 14730478 DOI: 10.1086/381401  0.648
2003 Liu Y, Xu F, Recker RR, Deng HW, Koller DL, White KE, Liu G, Hui SL, Conneally PM, Johnston CC, Econs MJ, Foroud T, Peacock M. Interpretation of Genetic Linkage Findings (multiple letters) Journal of Bone and Mineral Research. 18: 2077-2080. PMID 14606522 DOI: 10.1359/Jbmr.2003.18.11.2077  0.579
2003 Koller DL, Schriefer J, Sun Q, Shultz KL, Donahue LR, Rosen CJ, Foroud T, Beamer WG, Turner CH. Genetic effects for femoral biomechanics, structure, and density in C57BL/6J and C3H/HeJ inbred mouse strains. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 18: 1758-65. PMID 14584885 DOI: 10.1359/Jbmr.2003.18.10.1758  0.36
2003 Waguespack SG, Koller DL, White KE, Fishburn T, Carn G, Buckwalter KA, Johnson M, Kocisko M, Evans WE, Foroud T, Econs MJ. Chloride channel 7 (ClCN7) gene mutations and autosomal dominant osteopetrosis, type II. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 18: 1513-8. PMID 12929941 DOI: 10.1359/Jbmr.2003.18.8.1513  0.375
2003 Koller DL, White KE, Liu G, Hui SL, Conneally PM, Johnston CC, Econs MJ, Foroud T, Peacock M. Linkage of structure at the proximal femur to chromosomes 3, 7, 8, and 19. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 18: 1057-65. PMID 12817759 DOI: 10.1359/Jbmr.2003.18.6.1057  0.63
2003 Song J, Koller DL, Foroud T, Carr K, Zhao J, Rice J, Nurnberger JI, Begleiter H, Porjesz B, Smith TL, Schuckit MA, Edenberg HJ. Association of GABA(A) receptors and alcohol dependence and the effects of genetic imprinting. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 117: 39-45. PMID 12555233 DOI: 10.1002/Ajmg.B.10022  0.382
2002 Dowsett SA, Archila L, Foroud T, Koller D, Eckert GJ, Kowolik MJ. The effect of shared genetic and environmental factors on periodontal disease parameters in untreated adult siblings in Guatemala. Journal of Periodontology. 73: 1160-8. PMID 12416774 DOI: 10.1902/Jop.2002.73.10.1160  0.372
2002 Carn G, Koller DL, Peacock M, Hui SL, Evans WE, Conneally PM, Johnston CC, Foroud T, Econs MJ. Sibling pair linkage and association studies between peak bone mineral density and the gene locus for the osteoclast-specific subunit (OC116) of the vacuolar proton pump on chromosome 11p12-13. The Journal of Clinical Endocrinology and Metabolism. 87: 3819-24. PMID 12161516 DOI: 10.1210/Jcem.87.8.8740  0.674
2001 Pankratz N, Kirkwood SC, Flury L, Koller DL, Foroud T. Use of variable marker density, principal components, and neural networks in the dissection of disease etiology Genetic Epidemiology. 21: S732-737. PMID 11793770 DOI: 10.1002/Gepi.2001.21.S1.S732  0.729
2001 McClintick J, Koller DL, Pankratz N, Kirkwood SC, Naughton B, Foroud T. Parametric linkage analysis and disequilibrium methods to identify loci for complex disease Genetic Epidemiology. 21: S528-S533. PMID 11793731 DOI: 10.1002/Gepi.2001.21.S1.S528  0.741
2001 Koller DL, Liu G, Econs MJ, Hui SL, Morin PA, Joslyn G, Rodriguez LA, Conneally PM, Christian JC, Johnston CC, Foroud T, Peacock M. Genome screen for quantitative trait loci underlying normal variation in femoral structure. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 16: 985-91. PMID 11393795 DOI: 10.1359/Jbmr.2001.16.6.985  0.644
2000 Koller DL, Econs MJ, Morin PA, Christian JC, Hui SL, Parry P, Curran ME, Rodriguez LA, Conneally PM, Joslyn G, Peacock M, Johnston CC, Foroud T. Genome screen for QTLs contributing to normal variation in bone mineral density and osteoporosis. The Journal of Clinical Endocrinology and Metabolism. 85: 3116-20. PMID 10999795 DOI: 10.1210/Jcem.85.9.6778  0.654
2000 Foroud T, Edenberg HJ, Goate A, Rice J, Flury L, Koller DL, Bierut LJ, Conneally PM, Nurnberger JI, Bucholz KK, Li TK, Hesselbrock V, Crowe R, Schuckit M, Porjesz B, et al. Alcoholism susceptibility loci: confirmation studies in a replicate sample and further mapping. Alcoholism, Clinical and Experimental Research. 24: 933-45. PMID 10923994  0.588
2000 Takacs I, Koller DL, Peacock M, Christian JC, Evans WE, Hui SL, Conneally PM, Johnston CC, Foroud T, Econs MJ. Sib pair linkage and association studies between bone mineral density and the interleukin-6 gene locus. Bone. 27: 169-73. PMID 10865225 DOI: 10.1016/S8756-3282(00)00296-9  0.597
2000 Foroud T, Castelluccio PF, Koller DL, Edenberg HJ, Miller M, Bowman E, Rau NL, Smiley C, Rice JP, Goate A, Armstrong C, Bierut LJ, Reich T, Detera-Wadleigh SD, Goldin LR, et al. Suggestive evidence of a locus on chromosome 10p using the NIMH genetics initiative bipolar affective disorder pedigrees. American Journal of Medical Genetics. 96: 18-23. PMID 10686547 DOI: 10.1002/(Sici)1096-8628(20000207)96:1<18::Aid-Ajmg6>3.0.Co;2-G  0.422
2000 Foroud T, Edenberg HJ, Goate A, Rice J, Flury L, Koller DL, Bierut LJ, Conneally PM, Nurnberger JI, Bucholz KK, Li T, Hesselbrock V, Crowe R, Schuckit M, Porjesz B, et al. Alcoholism Susceptibility Loci: Confirmation Studies in a Replicate Sample and Further Mapping Alcoholism: Clinical and Experimental Research. 24: 933-945. DOI: 10.1111/J.1530-0277.2000.Tb04634.X  0.625
1999 Takacs I, Koller DL, Peacock M, Christian JC, Hui SL, Conneally PM, Johnston CC, Foroud T, Econs MJ. Sibling pair linkage and association studies between bone mineral density and the insulin-like growth factor I gene locus. The Journal of Clinical Endocrinology and Metabolism. 84: 4467-71. PMID 10599704 DOI: 10.1210/Jcem.84.12.6179  0.617
1999 Koller DL, Balding J, Foroud T. Nonparametric linkage and family-based association studies of a simulated complex disorder Genetic Epidemiology. 17: S627-S632. PMID 10597504 DOI: 10.1002/Gepi.13701707102  0.48
1999 White KE, Koller DL, Takacs I, Buckwalter KA, Foroud T, Econs MJ. Locus heterogeneity of autosomal dominant osteopetrosis (ADO) Journal of Clinical Endocrinology and Metabolism. 84: 1047-1051. PMID 10084593 DOI: 10.1210/Jcem.84.3.5578  0.44
1998 Foroud T, Bucholz KK, Edenberg HJ, Goate A, Neuman RJ, Porjesz B, Koller DL, Rice J, Reich T, Bierut LJ, Cloninger CR, Nurnberger JI, Li TK, Conneally PM, Tischfield JA, et al. Linkage of an alcoholism-related severity phenotype to chromosome 16. Alcoholism, Clinical and Experimental Research. 22: 2035-42. PMID 9884148 DOI: 10.1097/00000374-199812000-00020  0.546
1998 Koller DL, Rodriguez LA, Christian JC, Slemenda CW, Econs MJ, Hui SL, Morin P, Conneally PM, Joslyn G, Curran ME, Peacock M, Johnston CC, Foroud T. Linkage of a QTL contributing to normal variation in bone mineral density to chromosome 11q12-13. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 13: 1903-8. PMID 9844108 DOI: 10.1359/Jbmr.1998.13.12.1903  0.661
1998 Edenberg HJ, Reynolds J, Koller DL, Begleiter H, Bucholz KK, Conneally PM, Crowe R, Goate A, Hesselbrock V, Li TK, Nurnberger JI, Porjesz B, Reich T, Rice JP, Schuckit M, et al. A family-based analysis of whether the functional promoter alleles of the serotonin transporter gene HTT affect the risk for alcohol dependence. Alcoholism, Clinical and Experimental Research. 22: 1080-5. PMID 9726278  0.516
1998 Edenberg HJ, Foroud T, Koller DL, Goate A, Rice J, Van Eerdewegh P, Reich T, Cloninger CR, Nurnberger JI, Kowalczuk M, Wu B, Li TK, Conneally PM, Tischfield JA, Wu W, et al. A family-based analysis of the association of the dopamine D2 receptor (DRD2) with alcoholism. Alcoholism, Clinical and Experimental Research. 22: 505-12. PMID 9581660  0.513
1997 Murrell JR, Koller D, Foroud T, Goedert M, Spillantini MG, Edenberg HJ, Farlow MR, Ghetti B. Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17. American Journal of Human Genetics. 61: 1131-8. PMID 9345089 DOI: 10.1086/301594  0.367
1997 Nichols WC, Koller DL, Slovis B, Foroud T, Terry VH, Arnold ND, Siemieniak DR, Wheeler L, Phillips JA, Newman JH, Conneally PM, Ginsburg D, Loyd JE. Localization of the gene for familial primary pulmonary hypertension to chromosome 2q31-32. Nature Genetics. 15: 277-80. PMID 9054941 DOI: 10.1038/Ng0397-277  0.584
1997 Murrell L, Koller D, Foroud T, Goedert M, Spillantini MG, Farlow MR, Ghetti B. GENE MAP OF THE MSTD (MULTIPLE SYSTEM TAUOPATHY WITH PRESENILE DEMENTIA) REGION ON HUMAN CHROMOSOME 17q21–22 Journal of Neuropathology and Experimental Neurology. 56: 610. DOI: 10.1097/00005072-199705000-00171  0.37
Show low-probability matches.