| Year |
Citation |
Score |
| 2018 |
Wu K, Chen C, Moyzis RK, Nuno M, Yu Z, Greenberger E. More than skin deep: Major histocompatibility complex (MHC)-based attraction among Asian American speed-daters Evolution and Human Behavior. 39: 447-456. DOI: 10.1016/J.Evolhumbehav.2018.04.001 |
0.314 |
|
| 2017 |
Leung PW, Chan JK, Chen LH, Lee CC, Hung SF, Ho TP, Tang CP, Moyzis RK, Swanson JM. Family-based association study of DRD4 gene in methylphenidate-responded Attention Deficit/Hyperactivity Disorder. Plos One. 12: e0173748. PMID 28282463 DOI: 10.1371/Journal.Pone.0173748 |
0.316 |
|
| 2015 |
Li J, Chen C, Wu K, Zhang M, Zhu B, Chen C, Moyzis RK, Dong Q. Genetic variations in the serotonergic system contribute to amygdala volume in humans. Frontiers in Neuroanatomy. 9: 129. PMID 26500508 DOI: 10.3389/Fnana.2015.00129 |
0.338 |
|
| 2015 |
Chen C, Xiu D, Chen C, Moyzis R, Xia M, He Y, Xue G, Li J, He Q, Lei X, Wang Y, Liu B, Chen W, Zhu B, Dong Q. Regional Homogeneity of Resting-State Brain Activity Suppresses the Effect of Dopamine-Related Genes on Sensory Processing Sensitivity. Plos One. 10: e0133143. PMID 26308205 DOI: 10.1371/Journal.Pone.0133143 |
0.308 |
|
| 2014 |
Zhu B, Chen C, Xue G, Lei X, Li J, Moyzis RK, Dong Q, Lin C. The GABRB1 gene is associated with thalamus volume and modulates the association between thalamus volume and intelligence. Neuroimage. 102: 756-63. PMID 25192656 DOI: 10.1016/J.Neuroimage.2014.08.048 |
0.325 |
|
| 2014 |
Zhu B, Chen C, Moyzis RK, Dong Q, Lin C. Educational attainment-related loci identified by GWAS are associated with select personality traits and mathematics and language abilities Personality and Individual Differences. 72: 96-100. DOI: 10.1016/J.Paid.2014.08.028 |
0.309 |
|
| 2013 |
Zhu B, Chen C, Xue G, Moyzis RK, Dong Q, Chen C, Li J, He Q, Lei X, Wang Y, Lin C. The SEMA5A gene is associated with hippocampal volume, and their interaction is associated with performance on Raven's Progressive Matrices. Neuroimage. 88: 181-187. PMID 24291503 DOI: 10.1016/J.Neuroimage.2013.11.035 |
0.33 |
|
| 2013 |
Grady DL, Thanos PK, Corrada MM, Barnett JC, Ciobanu V, Shustarovich D, Napoli A, Moyzis AG, Grandy D, Rubinstein M, Wang GJ, Kawas CH, Chen C, Dong Q, Wang E, ... ... Moyzis RK, et al. DRD4 genotype predicts longevity in mouse and human. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 33: 286-91. PMID 23283341 DOI: 10.1523/Jneurosci.3515-12.2013 |
0.322 |
|
| 2013 |
Zhu B, Chen C, Moyzis RK, Dong Q, Chen C, He Q, Li J, Li J, Lei X, Lin C. The DOPA decarboxylase (DDC) gene is associated with alerting attention. Progress in Neuro-Psychopharmacology & Biological Psychiatry. 43: 140-5. PMID 23276884 DOI: 10.1016/J.Pnpbp.2012.12.020 |
0.321 |
|
| 2013 |
Li J, Chen C, Lei X, Wang Y, Chen C, He Q, Moyzis RK, Xue G, Zhu B, Cao Z, Dong Q. The NTSR1 gene modulates the association between hippocampal structure and working memory performance. Neuroimage. 75: 79-86. PMID 23110888 DOI: 10.1016/J.Neuroimage.2012.09.077 |
0.342 |
|
| 2012 |
Lei X, Chen C, He Q, Chen C, Moyzis RK, Xue G, Chen X, Cao Z, Li J, Li H, Zhu B, Chun Hsu AS, Li S, Li J, Dong Q. Sex determines which section of the SLC6A4 gene is linked to obsessive-compulsive symptoms in normal Chinese college students. Journal of Psychiatric Research. 46: 1153-60. PMID 22727904 DOI: 10.1016/J.Jpsychires.2012.05.002 |
0.342 |
|
| 2012 |
Lei X, Chen C, He Q, Moyzis R, Xue G, Chen C, Cao Z, Li J, Li H, Zhu B, Zhang M, Li J, Dong Q. Haplotype polymorphism in the alpha-2B-adrenergic receptor gene influences response inhibition in a large Chinese sample. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. 37: 1115-21. PMID 22218095 DOI: 10.1038/Npp.2011.266 |
0.317 |
|
| 2012 |
Zhu B, Chen C, Moyzis RK, Dong Q, He Q, Li J, Lei X, Lin C. Association between the HTR2B gene and the personality trait of fun seeking Personality and Individual Differences. 53: 1029-1033. DOI: 10.1016/J.Paid.2012.07.026 |
0.322 |
|
| 2011 |
Chen C, Chen C, Moyzis R, Stern H, He Q, Li H, Li J, Zhu B, Dong Q. Contributions of dopamine-related genes and environmental factors to highly sensitive personality: a multi-step neuronal system-level approach. Plos One. 6: e21636. PMID 21765900 DOI: 10.1371/Journal.Pone.0021636 |
0.321 |
|
| 2010 |
McEvoy BP, Lind JM, Wang ET, Moyzis RK, Visscher PM, van Holst Pellekaan SM, Wilton AN. Whole-genome genetic diversity in a sample of Australians with deep Aboriginal ancestry. American Journal of Human Genetics. 87: 297-305. PMID 20691402 DOI: 10.1016/J.Ajhg.2010.07.008 |
0.31 |
|
| 2009 |
Saccone SF, Bierut LJ, Chesler EJ, Kalivas PW, Lerman C, Saccone NL, Uhl GR, Li CY, Philip VM, Edenberg HJ, Sherry ST, Feolo M, Moyzis RK, Rutter JL. Supplementing high-density SNP microarrays for additional coverage of disease-related genes: addiction as a paradigm. Plos One. 4: e5225. PMID 19381300 DOI: 10.1371/Journal.Pone.0005225 |
0.369 |
|
| 2007 |
Hawks J, Wang ET, Cochran GM, Harpending HC, Moyzis RK. Recent acceleration of human adaptive evolution. Proceedings of the National Academy of Sciences of the United States of America. 104: 20753-8. PMID 18087044 DOI: 10.1073/Pnas.0707650104 |
0.306 |
|
| 2007 |
Swanson JM, Moyzis RK, McGough JJ, McCracken JT, Riddle MA, Kollins SH, Greenhill LL, Abikoff HB, Wigal T, Wigal SB, Posner K, Skrobala AM, Davies M, Ghuman JK, Cunningham C, et al. Effects of source of DNA on genotyping success rates and allele percentages in the Preschoolers with Attention-Deficit/Hyperactivity Disorder Treatment Study (PATS). Journal of Child and Adolescent Psychopharmacology. 17: 635-46. PMID 17979583 DOI: 10.1089/Cap.2007.0076 |
0.34 |
|
| 2007 |
Reist C, Ozdemir V, Wang E, Hashemzadeh M, Mee S, Moyzis R. Novelty seeking and the dopamine D4 receptor gene (DRD4) revisited in Asians: Haplotype characterization and relevance of the 2-repeat allele American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 144: 453-457. PMID 17474081 DOI: 10.1002/Ajmg.B.30473 |
0.322 |
|
| 2007 |
Wang ET, Moyzis RK. Genetic evidence for ongoing balanced selection at human DNA repair genes ERCC8, FANCC, and RAD51C Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis. 616: 165-174. PMID 17257630 DOI: 10.1016/J.Mrfmmm.2006.11.030 |
0.386 |
|
| 2006 |
Wang ET, Kodama G, Baldi P, Moyzis RK. Global landscape of recent inferred Darwinian selection for Homo sapiens. Proceedings of the National Academy of Sciences of the United States of America. 103: 135-40. PMID 16371466 DOI: 10.1073/Pnas.0509691102 |
0.344 |
|
| 2005 |
Grady DL, Harxhi A, Smith M, Flodman P, Spence MA, Swanson JM, Moyzis RK. Sequence variants of the DRD4 gene in autism: Further evidence that rare DRD4 7R haplotypes are ADHD specific American Journal of Medical Genetics - Neuropsychiatric Genetics. 136: 33-35. PMID 15892149 DOI: 10.1002/Ajmg.B.30182 |
0.329 |
|
| 2005 |
Leung PW, Lee CC, Hung SF, Ho TP, Tang CP, Kwong SL, Leung SY, Yuen ST, Lieh-Mak F, Oosterlaan J, Grady D, Harxhi A, Ding YC, Chi HC, Flodman P, ... ... Moyzis R, et al. Dopamine receptor D4 (DRD4) gene in Han Chinese children with attention-deficit/hyperactivity disorder (ADHD): increased prevalence of the 2-repeat allele. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 133: 54-6. PMID 15578612 DOI: 10.1002/Ajmg.B.30129 |
0.311 |
|
| 2005 |
Grady D, Moyzis R, Swanson JM. Molecular genetics and attention in ADHD Clinical Neuroscience Research. 5: 265-272. DOI: 10.1016/J.Cnr.2005.09.012 |
0.326 |
|
| 2004 |
Martin J, Han C, Gordon LA, Terry A, Prabhakar S, She X, Xie G, Hellsten U, Chan YM, Altherr M, Couronne O, Aerts A, Bajorek E, Black S, Blumer H, ... ... Moyzis RK, et al. The sequence and analysis of duplication-rich human chromosome 16. Nature. 432: 988-94. PMID 15616553 DOI: 10.1038/Nature03187 |
0.403 |
|
| 2004 |
Wang E, Ding YC, Flodman P, Kidd JR, Kidd KK, Grady DL, Ryder OA, Spence MA, Swanson JM, Moyzis RK. The genetic architecture of selection at the human dopamine receptor D4 (DRD4) gene locus. American Journal of Human Genetics. 74: 931-44. PMID 15077199 DOI: 10.1086/420854 |
0.346 |
|
| 2002 |
Ding YC, Chi HC, Grady DL, Morishima A, Kidd JR, Kidd KK, Flodman P, Spence MA, Schuck S, Swanson JM, Zhang YP, Moyzis RK. Evidence of positive selection acting at the human dopamine receptor D4 gene locus. Proceedings of the National Academy of Sciences of the United States of America. 99: 309-14. PMID 11756666 DOI: 10.1073/Pnas.012464099 |
0.37 |
|
| 2001 |
Riethman HC, Xiang Z, Paul S, Morse E, Hu XL, Flint J, Chi HC, Grady DL, Moyzis RK. Integration of telomere sequences with the draft human genome sequence Nature. 409: 948-951. PMID 11237019 DOI: 10.1038/35057180 |
0.404 |
|
| 2001 |
Swanson J, Deutsch C, Cantwell D, Posner M, Kennedy JL, Barr CL, Moyzis R, Schuck S, Flodman P, Spence MA, Wasdell M. Genes and attention-deficit hyperactivity disorder Clinical Neuroscience Research. 1: 207-216. DOI: 10.1016/S1566-2772(01)00007-X |
0.314 |
|
| 2000 |
Swanson J, Oosterlaan J, Murias M, Schuck S, Flodman P, Spence MA, Wasdell M, Ding Y, Chi HC, Smith M, Mann M, Carlson C, Kennedy JL, Sergeant JA, Leung P, ... ... Moyzis R, et al. Attention deficit/hyperactivity disorder children with a 7-repeat allele of the dopamine receptor D4 gene have extreme behavior but normal performance on critical neuropsychological tests of attention. Proceedings of the National Academy of Sciences of the United States of America. 97: 4754-9. PMID 10781080 DOI: 10.1073/Pnas.080070897 |
0.317 |
|
| 2000 |
Swanson JM, Flodman P, Kennedy J, Spence MA, Moyzis R, Schuck S, Murias M, Moriarity J, Barr C, Smith M, Posner M. Dopamine genes and ADHD. Neuroscience and Biobehavioral Reviews. 24: 21-5. PMID 10654656 DOI: 10.1016/S0149-7634(99)00062-7 |
0.32 |
|
| 1998 |
Bisoffi M, Chakerian AE, Fore ML, Bryant JE, Hernandez JP, Moyzis RK, Griffith JK. Inhibition of human telomerase by a retrovirus expressing telomeric antisense RNA. European Journal of Cancer (Oxford, England : 1990). 34: 1242-9. PMID 9849487 DOI: 10.1016/S0959-8049(98)00049-5 |
0.303 |
|
| 1998 |
Centola M, Chen X, Sood R, Deng Z, Aksentijevich I, Blake T, Ricke DO, Chen X, Wood G, Zaks N, Richards N, Krizman D, Mansfield E, Apostolou S, Liu J, ... ... Moyzis RK, et al. Construction of an approximately 700-kb transcript map around the familial Mediterranean fever locus on human chromosome 16p13.3. Genome Research. 8: 1172-91. PMID 9847080 DOI: 10.1101/Gr.8.11.1172 |
0.404 |
|
| 1998 |
Kouprina N, Campbell M, Graves J, Campbell E, Meincke L, Tesmer J, Grady DL, Doggett NA, Moyzis RK, Deaven LL, Larionov V. Construction of human chromosome 16- and 5-specific circular YAC/BAC libraries by in vivo recombination in yeast (TAR cloning) Genomics. 53: 21-28. PMID 9787074 DOI: 10.1006/Geno.1998.5469 |
0.384 |
|
| 1998 |
Kostrzewa M, Krings BW, Dixon MJ, Eppelt K, Köhler A, Grady DL, Steinberger D, Fairweather ND, Moyzis RK, Monaco AP, Müller U. Integrated physical and transcript map of 5q31.3-qter. European Journal of Human Genetics : Ejhg. 6: 266-74. PMID 9781031 DOI: 10.1038/Sj.Ejhg.5200188 |
0.364 |
|
| 1998 |
Mariappan SV, Silks LA, Chen X, Springer PA, Wu R, Moyzis RK, Bradbury EM, Garcia AE, Gupta G. Solution structures of the Huntington's disease DNA triplets, (CAG)n. Journal of Biomolecular Structure & Dynamics. 15: 723-44. PMID 9514249 DOI: 10.1080/07391102.1998.10508988 |
0.32 |
|
| 1997 |
McPherson JD, Apostol B, Wagner-McPherson CB, Hakim S, Del Mastro RG, Aziz N, Baer E, Gonzales G, Krane MC, Markovich R, Masny P, Ortega M, Vu J, Vujicic M, Church DM, ... ... Moyzis RK, et al. A radiation hybrid map of human chromosome 5 with integration of cytogenetic, genetic, and transcript maps. Genome Research. 7: 897-909. PMID 9314495 DOI: 10.1101/Gr.7.9.897 |
0.341 |
|
| 1997 |
Aksentijevich I, Centola M, Deng Z, Sood R, Balow J.E. J, Wood G, Zaks N, Mansfield E, Chen X, Eisenberg S, Vedula A, Shafran N, Raben N, Pras E, Pras M, ... ... Moyzis RK, et al. Ancient missense mutations in a new member of the RoRet gene family are likely to cause familial Mediterranean fever Cell. 90: 797-807. PMID 9288758 DOI: 10.1016/S0092-8674(00)80539-5 |
0.317 |
|
| 1997 |
Mitchison HM, Munroe PB, O'Rawe AM, Taschner PE, de Vos N, Kremmidiotis G, Lensink I, Munk AC, D'Arigo KL, Anderson JW, Lerner TJ, Moyzis RK, Callen DF, Breuning MH, Doggett NA, et al. Genomic structure and complete nucleotide sequence of the Batten disease gene, CLN3. Genomics. 40: 346-50. PMID 9119403 DOI: 10.1006/Geno.1996.4576 |
0.359 |
|
| 1996 |
Catasti P, Chen X, Moyzis RK, Bradbury EM, Gupta G. Structure-function correlations of the insulin-linked polymorphic region. Journal of Molecular Biology. 264: 534-45. PMID 8969303 DOI: 10.1006/Jmbi.1996.0659 |
0.306 |
|
| 1996 |
Shen Z, Pardington-Purtymun PE, Comeaux JC, Moyzis RK, Chen DJ. Associations of UBE2I with RAD52, UBL1, p53, and RAD51 proteins in a yeast two-hybrid system Genomics. 37: 183-186. PMID 8921390 DOI: 10.1006/Geno.1996.0540 |
0.302 |
|
| 1996 |
Apostolou S, Whitmore SA, Crawford J, Lennon G, Sutherland GR, Callen DF, Ianzano L, Savino M, D'apolito M, Notarangelo A, Memeo E, Piemontese MR, Zelante L, Savoia A, Gibson RA, ... ... Moyzis RK, et al. Positional cloning of the fanconi anaemia group A gene Nature Genetics. 14: 324-328. PMID 8896564 DOI: 10.1038/Ng1196-324 |
0.388 |
|
| 1996 |
Shen Z, Peterson SR, Comeaux JC, Zastrow D, Moyzis RK, Bradbury EM, Chen DJ. Self-association of human RAD52 protein. Mutation Research. 364: 81-9. PMID 8879274 DOI: 10.1016/0921-8777(96)00025-0 |
0.311 |
|
| 1996 |
Eichler EE, Lu F, Shen Y, Antonacci R, Jurecic V, Doggett NA, Moyzis RK, Baldini A, Gibbs RA, Nelson DL. Duplication of a gene-rich cluster between 16p11.1 and Xq28: a novel pericentromeric-directed mechanism for paralogous genome evolution. Human Molecular Genetics. 5: 899-912. PMID 8817324 DOI: 10.1093/Hmg/5.7.899 |
0.415 |
|
| 1996 |
Shen Z, Pardington-Purtymun PE, Comeaux JC, Moyzis RK, Chen DJ. UBL1, a human ubiquitin-like protein associating with human RAD51/RAD52 proteins Genomics. 36: 271-279. PMID 8812453 DOI: 10.1006/Geno.1996.0462 |
0.348 |
|
| 1996 |
Grady DL, Robinson DL, Gersh M, Nickerson E, McPherson J, Wasmuth JJ, Overhauser J, Deaven LL, Moyzis RK. The generation and regional localization of 303 new chromosome 5 sequence-tagged sites. Genomics. 32: 91-6. PMID 8786125 DOI: 10.1006/Geno.1996.0080 |
0.406 |
|
| 1996 |
Kostrzewa M, Grady DL, Moyzis RK, Flöter L, Müller U. Integration of four genes, a pseudogene, thirty-one STSs, and a highly polymorphic STRP into the 7-10 Mb YAC contig of 5q34-q35 Human Genetics. 97: 399-403. PMID 8786091 DOI: 10.1007/Bf02185781 |
0.35 |
|
| 1996 |
Takiguchi Y, Kurimasa A, Chen F, Pardington PE, Kuriyama T, Okinaka RT, Moyzis R, Chen DJ. Genomic structure and chromosomal assignment of the mouse Ku70 gene. Genomics. 35: 129-135. PMID 8661113 DOI: 10.1006/Geno.1996.0331 |
0.441 |
|
| 1994 |
Kouprina N, Eldarov M, Moyzis R, Resnick M, Larionov V. A model system to assess the integrity of mammalian YACs during transformation and propagation in yeast Genomics. 21: 7-17. PMID 8088818 DOI: 10.1006/Geno.1994.1218 |
0.37 |
|
| 1994 |
Meyne J, Goodwin EH, Moyzis RK. Chromosome localization and orientation of the simple sequence repeat of human satellite I DNA Chromosoma. 103: 99-103. PMID 8055716 DOI: 10.1007/Bf00352318 |
0.381 |
|
| 1994 |
Goodart SA, Simmons AD, Grady D, Rojas K, Moyzis RK, Lovett M, Overhauser J. A yeast artificial chromosome contig of the critical region for cri-du-chat syndrome. Genomics. 24: 63-8. PMID 7896290 DOI: 10.1006/Geno.1994.1582 |
0.33 |
|
| 1994 |
Meyne J, Moyzis RK. In situ hybridization using synthetic oligomers as probes for centromere and telomere repeats Methods in Molecular Biology (Clifton, N.J.). 33: 63-74. PMID 7894593 DOI: 10.1385/0-89603-280-9:63 |
0.318 |
|
| 1993 |
McCormick MK, Campbell E, Deaven L, Moyzis R. Low-frequency chimeric yeast artificial chromosome libraries from flow-sorted human chromosomes 16 and 21. Proceedings of the National Academy of Sciences of the United States of America. 90: 1063-1067. PMID 8430075 DOI: 10.1073/Pnas.90.3.1063 |
0.376 |
|
| 1993 |
McCormick MK, Buckler A, Bruno W, Campbell E, Shera K, Torney D, Deaven L, Moyzis R. Construction and characterization of a YAC library with a low frequency of chimeric clones from flow-sorted human chromosome 9. Genomics. 18: 553-8. PMID 8307565 DOI: 10.1016/S0888-7543(05)80355-6 |
0.378 |
|
| 1993 |
Longmire JL, Brown NC, Meincke LJ, Campbell ML, Albright KL, Fawcett JJ, Campbell EW, Moyzis RK, Hildebrand CE, Evans GA. Construction and characterization of partial digest DNA libraries made from flow-sorted human chromosome 16. Genetic Analysis, Techniques and Applications. 10: 69-76. PMID 8110480 DOI: 10.1016/1050-3862(93)90037-J |
0.384 |
|
| 1993 |
Mitchison HM, Williams RE, McKay TR, Callen DF, Thompson AD, Mulley JC, Stallings RL, Hildebrand CE, Moyzis RK, Järvelä I, Peltonen L, Haines J, Sutherland GR, Gardiner RM. Refined genetic mapping of juvenile-onset neuronal ceroid-lipofuscinosis on chromosome 16 Journal of Inherited Metabolic Disease. 16: 339-341. PMID 8105142 DOI: 10.1007/Bf00710278 |
0.38 |
|
| 1992 |
Grady DL, Ratliff RL, Robinson DL, McCanlies EC, Meyne J, Moyzis RK. Highly conserved repetitive DNA sequences are present at human centromeres. Proceedings of the National Academy of Sciences of the United States of America. 89: 1695-9. PMID 1542662 DOI: 10.1073/Pnas.89.5.1695 |
0.373 |
|
| 1992 |
Fields CA, Grady DL, Moyzis RK. The human THE-LTR(O) and MstII interspersed repeats are subfamilies of a single widely distributed highly variable repeat family Genomics. 13: 431-436. PMID 1319393 DOI: 10.1016/0888-7543(92)90264-S |
0.353 |
|
| 1991 |
Stallings RL, Ford AF, Nelson D, Torney DC, Hildebrand CE, Moyzis RK. Evolution and distribution of (GT)n repetitive sequences in mammalian genomes Genomics. 10: 807-815. PMID 1909685 DOI: 10.1016/0888-7543(91)90467-S |
0.337 |
|
| 1991 |
Moyzis RK. The human telomere Scientific American. 265: 48-55. PMID 1862331 DOI: 10.1038/Scientificamerican0891-48 |
0.383 |
|
| 1991 |
Meyne J, Moyzis RK. C-band minus (CM) chromosomes of SEWA have telomeric (TTAGGG)n sequences Cancer Genetics and Cytogenetics. 56: 98-99. DOI: 10.1016/0165-4608(91)90378-8 |
0.315 |
|
| 1990 |
Lin CC, Meyne J, Sasi R, Moyzis RK. Apparent lack of telomere sequences on double minute chromosomes Cancer Genetics and Cytogenetics. 48: 271-274. PMID 2397458 DOI: 10.1016/0165-4608(90)90131-S |
0.365 |
|
| 1990 |
Stallings RL, Torney DC, Hildebrand CE, Longmire JL, Deaven LL, Jett JH, Doggett NA, Moyzis RK. Physical mapping of human chromosomes by repetitive sequence fingerprinting Proceedings of the National Academy of Sciences of the United States of America. 87: 6218-6222. PMID 2385591 DOI: 10.1073/Pnas.87.16.6218 |
0.377 |
|
| 1990 |
Meyne J, Baker RJ, Hobart HH, Hsu TC, Ryder OA, Ward OG, Wiley JE, Wurster-Hill DH, Yates TL, Moyzis RK. Distribution of non-telomeric sites of the (TTAGGG)n telomeric sequence in vertebrate chromosomes. Chromosoma. 99: 3-10. PMID 2340757 DOI: 10.1007/Bf01737283 |
0.342 |
|
| 1989 |
Meyne J, Ratliff RL, Moyzis RK. Conservation of the human telomere sequence (TTAGGG)(n) among vertebrates Proceedings of the National Academy of Sciences of the United States of America. 86: 7049-7053. PMID 2780561 DOI: 10.1073/Pnas.86.18.7049 |
0.344 |
|
| 1989 |
Meyne J, Moyzis RK. Human chromosome-specific repetitive DNA probes: Targeting in situ hybridization to chromosome 17 with a 42-base-pair alphoid DNA oligomer Genomics. 4: 472-478. PMID 2744759 DOI: 10.1016/0888-7543(89)90270-X |
0.381 |
|
| 1989 |
Meyne J, Littlefield LG, Moyzis RK. Labeling of human centromeres using an alphoid DNA consensus sequence: application to the scoring of chromosome aberrations Mutation Research Letters. 226: 75-79. PMID 2733720 DOI: 10.1016/0165-7992(89)90046-8 |
0.389 |
|
| 1989 |
Moyzis RK, Torney DC, Meyne J, Buckingham JM, Wu JR, Burks C, Sirotkin KM, Goad WB. The distribution of interspersed repetitive DNA sequences in the human genome Genomics. 4: 273-289. PMID 2714792 DOI: 10.1016/0888-7543(89)90331-5 |
0.36 |
|
| 1989 |
Jett JH, Keller RA, Martin JC, Marrone BL, Moyzis RK, Ratliff RL, Seitzinger NK, Shera EB, Stewart CC. High-speed DNA sequencing: an approach based upon fluorescence detection of single molecules. Journal of Biomolecular Structure & Dynamics. 7: 301-9. PMID 2557861 DOI: 10.1080/07391102.1989.10507773 |
0.328 |
|
| 1989 |
Cornforth MN, Meyne J, Littlefield LG, Bailey SM, Moyzis RK. Telomere staining of human chromosomes and the mechanism of radiation-induced dicentric formation Radiation Research. 120: 205-212. PMID 2482516 DOI: 10.2307/3577708 |
0.344 |
|
| 1988 |
Moyzis RK, Buckingham JM, Cram LS, Dani M, Deaven LL, Jones MD, Meyne J, Ratliff RL, Wu JR. A highly conserved repetitive DNA sequence, (TTAGGG)(n), present at the telomeres of human chromosomes Proceedings of the National Academy of Sciences of the United States of America. 85: 6622-6626. PMID 3413114 DOI: 10.1073/Pnas.85.18.6622 |
0.409 |
|
| 1987 |
Moyzis RK, Albright KL, Bartholdi MF, Cram LS, Deaven LL, Hildebrand CE, Joste NE, Longmire JL, Meyne J, Schwarzacher-Robinson T. Human chromosome-specific repetitive DNA sequences: novel markers for genetic analysis Chromosoma. 95: 375-386. PMID 3677921 DOI: 10.1007/Bf00333988 |
0.417 |
|
| 1986 |
Deaven LL, van Dilla MA, Bartholdi MF, Carrano AV, Cram LS, Fuscoe JC, Gray JW, Hildebrand CE, Moyzis RK, Perlman J. Construction of human chromosome-specific DNA libraries from flow-sorted chromosomes Cold Spring Harbor Symposia On Quantitative Biology. 51: 159-167. PMID 3472712 DOI: 10.1101/Sqb.1986.051.01.019 |
0.363 |
|
| 1986 |
Van Dilla MA, Deaven LL, Albright KL, Allen NA, Aubuchon MR, Bartholdi MF, Brown NC, Campbell EW, Carrano AV, Clark LM, Cram LS, Crawford BD, Fuscoe JC, Gray JW, Hildebrand CE, ... ... Moyzis RK, et al. Human chromosome–specific DNA libraries: Construction and availability Bio/Technology. 4: 537-552. DOI: 10.1038/Nbt0686-537 |
0.393 |
|
| 1986 |
Kuo CH, Yamagata K, Moyzis RK, Bitensky MW, Miki N. Multiple opsin mRNA species in bovine retina Molecular Brain Research. 1: 251-260. DOI: 10.1016/0169-328X(86)90031-8 |
0.3 |
|
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