| Year |
Citation |
Score |
| 2022 |
Taub MA, Conomos MP, Keener R, Iyer KR, Weinstock JS, Yanek LR, Lane J, Miller-Fleming TW, Brody JA, Raffield LM, McHugh CP, Jain D, Gogarten SM, Laurie CA, Keramati A, ... ... Laurie CC, et al. Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed. Cell Genomics. 2. PMID 35530816 DOI: 10.1016/j.xgen.2021.100084 |
0.389 |
|
| 2022 |
Wainschtein P, Jain D, Zheng Z, Cupples LA, Shadyab AH, McKnight B, Shoemaker BM, Mitchell BD, Psaty BM, Kooperberg C, Liu CT, Albert CM, Roden D, Chasman DI, Darbar D, ... ... Laurie CA, ... ... Laurie CC, et al. Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data. Nature Genetics. PMID 35256806 DOI: 10.1038/s41588-021-00997-7 |
0.324 |
|
| 2021 |
Hu Y, Stilp AM, McHugh CP, Rao S, Jai D, Zheng X, Lane J, Méric de Bellefon S, Raffield LM, Chen MH, Yanek LR, Wheeler M, Yao Y, Ren C, Broome J, ... ... Laurie CC, ... ... Laurie CA, et al. Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program. American Journal of Human Genetics. PMID 33887194 DOI: 10.1016/j.ajhg.2021.04.003 |
0.313 |
|
| 2021 |
Natarajan P, Pampana A, Graham SE, Ruotsalainen SE, Perry JA, de Vries PS, Broome JG, Pirruccello JP, Honigberg MC, Aragam K, Wolford B, Brody JA, Antonacci-Fulton L, Arden M, Aslibekyan S, ... ... Laurie CC, et al. Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices. Nature Communications. 12: 2182. PMID 33846329 DOI: 10.1038/s41467-021-22339-1 |
0.306 |
|
| 2021 |
Taliun D, Harris DN, Kessler MD, Carlson J, Szpiech ZA, Torres R, Taliun SAG, Corvelo A, Gogarten SM, Kang HM, Pitsillides AN, LeFaive J, Lee SB, Tian X, Browning BL, ... ... Laurie CC, et al. Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program. Nature. 590: 290-299. PMID 33568819 DOI: 10.1038/s41586-021-03205-y |
0.319 |
|
| 2020 |
Feofanova EV, Chen H, Dai Y, Jia P, Grove ML, Morrison AC, Qi Q, Daviglus M, Cai J, North KE, Laurie CC, Kaplan RC, Boerwinkle E, Yu B. A Genome-wide Association Study Discovers 46 Loci of the Human Metabolome in the Hispanic Community Health Study/Study of Latinos. American Journal of Human Genetics. PMID 33031748 DOI: 10.1016/j.ajhg.2020.09.003 |
0.301 |
|
| 2018 |
Butali A, Mossey PA, Adeyemo WL, Eshete MA, Gowans LJJ, Busch TD, Jain D, Yu W, Huan L, Laurie CA, Laurie CC, Nelson S, Li M, Sanchez-Lara PA, Magee WP, et al. Genomic analyses in african populations identify novel risk loci for cleft palate. Human Molecular Genetics. PMID 30452639 DOI: 10.1093/Hmg/Ddy402 |
0.357 |
|
| 2018 |
Wang H, Cade BE, Sofer T, Sands SA, Chen H, Browning S, Stilp AM, Louie TL, Thornton TA, Craig Johnson W, Below JE, Conomos MP, Evans DS, Gharib SA, Guo X, ... ... Laurie CC, et al. Admixture mapping identifies novel loci for obstructive sleep apnea in hispanic/latino americans. Human Molecular Genetics. PMID 30403821 DOI: 10.1093/Hmg/Ddy387 |
0.346 |
|
| 2018 |
Oseni GO, Jain D, Mossey PA, Busch TD, Gowans LJJ, Eshete MA, Adeyemo WL, Laurie CA, Laurie CC, Owais A, Olaitan PB, Aregbesola BS, Oginni F, Bello SA, Donkor P, et al. Identification of paternal uniparental disomy on chromosome 22 and a de novo deletion on chromosome 18 in individuals with orofacial clefts. Molecular Genetics & Genomic Medicine. PMID 30141273 DOI: 10.1002/Mgg3.459 |
0.35 |
|
| 2018 |
Wyss AB, Sofer T, Lee MK, Terzikhan N, Nguyen JN, Lahousse L, Latourelle JC, Smith AV, Bartz TM, Feitosa MF, Gao W, Ahluwalia TS, Tang W, Oldmeadow C, Duan Q, ... ... Laurie CC, et al. Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function. Nature Communications. 9: 2976. PMID 30061609 DOI: 10.1038/S41467-018-05369-0 |
0.318 |
|
| 2018 |
Byun J, Schwartz AG, Lusk C, Wenzlaff AS, de Andrade M, Mandal D, Gaba C, Yang P, You M, Kupert EY, Anderson MW, Han Y, Li Y, Qian D, Stilp A, ... Laurie C, et al. Genome-Wide Association Study of Familial Lung Cancer. Carcinogenesis. PMID 29924316 DOI: 10.1093/Carcin/Bgy080 |
0.365 |
|
| 2018 |
Napier MD, Franceschini N, Gondalia R, Stewart JD, Méndez-Giráldez R, Sitlani CM, Seyerle AA, Highland HM, Li Y, Wilhelmsen KC, Yan S, Duan Q, Roach J, Yao J, Guo X, ... ... Laurie CC, et al. Genome-wide association study and meta-analysis identify loci associated with ventricular and supraventricular ectopy. Scientific Reports. 8: 5675. PMID 29618737 DOI: 10.1038/S41598-018-23843-Z |
0.364 |
|
| 2018 |
Sung YJ, Winkler TW, de Las Fuentes L, Bentley AR, Brown MR, Kraja AT, Schwander K, Ntalla I, Guo X, Franceschini N, Lu Y, Cheng CY, Sim X, Vojinovic D, Marten J, ... ... Laurie CC, et al. A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure. American Journal of Human Genetics. PMID 29455858 DOI: 10.1016/J.Ajhg.2018.01.015 |
0.329 |
|
| 2018 |
Jian X, Sofer T, Tarraf W, Laurie C, González HM, Fornage M. P3-118: Tissue-Specific Genome-Wide Prediction Of Genetically Regulated Gene Expression And Its Association With Neurocognitive Function In U.S. Hispanics/Latinos Alzheimers & Dementia. 14. DOI: 10.1016/J.Jalz.2018.06.1475 |
0.354 |
|
| 2017 |
Graff M, Emery LS, Justice AE, Parra E, Below JE, Palmer ND, Gao C, Duan Q, Valladares-Salgado A, Cruz M, Morrison AC, Boerwinkle E, Whitsel EA, Kooperberg C, Reiner A, ... ... Laurie C, et al. Genetic architecture of lipid traits in the Hispanic community health study/study of Latinos. Lipids in Health and Disease. 16: 200. PMID 29025430 DOI: 10.1186/S12944-017-0591-6 |
0.326 |
|
| 2017 |
Hodonsky CJ, Jain D, Schick UM, Morrison JV, Brown L, McHugh CP, Schurmann C, Chen DD, Liu YM, Auer PL, Laurie CA, Taylor KD, Browning BL, Li Y, Papanicolaou G, ... ... Laurie CC, et al. Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos. Plos Genetics. 13: e1006760. PMID 28453575 DOI: 10.1371/Journal.Pgen.1006760 |
0.33 |
|
| 2017 |
Jain D, Hodonsky CJ, Schick UM, Morrison JV, Minnerath S, Brown L, Schurmann C, Liu Y, Auer PL, Laurie CA, Taylor KD, Browning B, Papanicolaou G, Browning S, Loos RJ, ... ... Laurie CC, et al. Genome-Wide Association of White Blood Cell Counts in Hispanic/Latino Americans: The Hispanic Community Health Study/Study of Latinos. Human Molecular Genetics. PMID 28158719 DOI: 10.1093/Hmg/Ddx024 |
0.318 |
|
| 2017 |
Brown LA, Sofer T, Stilp AM, Baier LJ, Kramer HJ, Masindova I, Levy D, Hanson RL, Moncrieft AE, Redline S, Rosas SE, Lash JP, Cai J, Laurie CC, Browning S, et al. Admixture Mapping Identifies an Amerindian Ancestry Locus Associated with Albuminuria in Hispanics in the United States. Journal of the American Society of Nephrology : Jasn. PMID 28137830 DOI: 10.1681/Asn.2016091010 |
0.358 |
|
| 2017 |
Taylor KE, Wong Q, Levine DM, McHugh C, Laurie C, Doheny K, Lam MY, Baer AN, Challacombe S, Lanfranchi H, Schiødt M, Srinivasan M, Umehara H, Vivino FB, Zhao Y, et al. Genome-Wide Association Analysis Reveals Genetic Heterogeneity of Sjögren's Syndrome According to Ancestry. Arthritis & Rheumatology (Hoboken, N.J.). PMID 28076899 DOI: 10.1002/art.40040 |
0.369 |
|
| 2017 |
Fornage M, Jian X, Sofer T, Tarraf W, Laurie C, Gonzalez HM. Genome-Wide Association Study Identifies Novel Genetic Variants For Neurocognitive Function Among Hispanics/Latinos: The Hchs/Sol Study Alzheimers & Dementia. 13. DOI: 10.1016/J.Jalz.2017.07.047 |
0.425 |
|
| 2016 |
Shaffer JR, Orlova E, Lee MK, Leslie EJ, Raffensperger ZD, Heike CL, Cunningham ML, Hecht JT, Kau CH, Nidey NL, Moreno LM, Wehby GL, Murray JC, Laurie CA, Laurie CC, et al. Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology. Plos Genetics. 12: e1006149. PMID 27560520 DOI: 10.1371/Journal.Pgen.1006149 |
0.37 |
|
| 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, ... ... Laurie C, ... ... Laurie C, 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 |
0.359 |
|
| 2016 |
Leslie EJ, Carlson JC, Shaffer JR, Feingold E, Wehby G, Laurie CA, Jain D, Laurie CC, Doheny KF, McHenry T, Resick J, Sanchez C, Jacobs J, Emanuele B, Vieira AR, et al. A multi-ethnic genome-wide association study identifies novel loci for nonsyndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q31. Human Molecular Genetics. PMID 27033726 DOI: 10.1093/Hmg/Ddw104 |
0.312 |
|
| 2016 |
Chen H, Wang C, Conomos MP, Stilp AM, Li Z, Sofer T, Szpiro AA, Chen W, Brehm JM, Celedón JC, Redline S, Papanicolaou GJ, Thornton TA, Laurie CC, Rice K, et al. Control for Population Structure and Relatedness for Binary Traits in Genetic Association Studies via Logistic Mixed Models. American Journal of Human Genetics. PMID 27018471 DOI: 10.1016/J.Ajhg.2016.02.012 |
0.304 |
|
| 2015 |
Schumacher FR, Schmit SL, Jiao S, Edlund CK, Wang H, Zhang B, Hsu L, Huang SC, Fischer CP, Harju JF, Idos GE, Lejbkowicz F, Manion FJ, McDonnell K, McNeil CE, ... ... Laurie CC, ... ... Laurie CA, et al. Corrigendum: Genome-wide association study of colorectal cancer identifies six new susceptibility loci. Nature Communications. 6: 8739. PMID 26498495 DOI: 10.1038/Ncomms9739 |
0.363 |
|
| 2014 |
Mitchell BD, Fornage M, McArdle PF, Cheng YC, Pulit SL, Wong Q, Dave T, Williams SR, Corriveau R, Gwinn K, Doheny K, Laurie CC, Rich SS, de Bakker PI. Using previously genotyped controls in genome-wide association studies (GWAS): application to the Stroke Genetics Network (SiGN). Frontiers in Genetics. 5: 95. PMID 24808905 DOI: 10.3389/Fgene.2014.00095 |
0.314 |
|
| 2013 |
Nelson SC, Doheny KF, Pugh EW, Romm JM, Ling H, Laurie CA, Browning SR, Weir BS, Laurie CC. Imputation-based genomic coverage assessments of current human genotyping arrays. G3 (Bethesda, Md.). 3: 1795-807. PMID 23979933 DOI: 10.1534/G3.113.007161 |
0.315 |
|
| 2013 |
Desch KC, Ozel AB, Siemieniak D, Kalish Y, Shavit JA, Thornburg CD, Sharathkumar AA, McHugh CP, Laurie CC, Crenshaw A, Mirel DB, Kim Y, Cropp CD, Molloy AM, Kirke PN, et al. Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association. Proceedings of the National Academy of Sciences of the United States of America. 110: 588-93. PMID 23267103 DOI: 10.1073/Pnas.1219885110 |
0.39 |
|
| 2013 |
Peters U, Jiao S, Schumacher FR, Hutter CM, Aragaki AK, Baron JA, Berndt SI, Bézieau S, Brenner H, Butterbach K, Caan BJ, Campbell PT, Carlson CS, Casey G, Chan AT, ... ... Laurie CC, ... ... Laurie CA, et al. Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis. Gastroenterology. 144: 799-807.e24. PMID 23266556 DOI: 10.1053/J.Gastro.2012.12.020 |
0.32 |
|
| 2012 |
Zheng X, Levine D, Shen J, Gogarten SM, Laurie C, Weir BS. A high-performance computing toolset for relatedness and principal component analysis of SNP data. Bioinformatics (Oxford, England). 28: 3326-8. PMID 23060615 DOI: 10.1093/Bioinformatics/Bts606 |
0.343 |
|
| 2012 |
Wiggs JL, Yaspan BL, Hauser MA, Kang JH, Allingham RR, Olson LM, Abdrabou W, Fan BJ, Wang DY, Brodeur W, Budenz DL, Caprioli J, Crenshaw A, Crooks K, Delbono E, ... ... Laurie C, et al. Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma. Plos Genetics. 8: e1002654. PMID 22570617 DOI: 10.1371/Journal.Pgen.1002654 |
0.338 |
|
| 2012 |
Rice JP, Hartz SM, Agrawal A, Almasy L, Bennett S, Breslau N, Bucholz KK, Doheny KF, Edenberg HJ, Goate AM, Hesselbrock V, Howells WB, Johnson EO, Kramer J, Krueger RF, ... ... Laurie C, et al. CHRNB3 is more strongly associated with Fagerström test for cigarette dependence-based nicotine dependence than cigarettes per day: phenotype definition changes genome-wide association studies results. Addiction (Abingdon, England). 107: 2019-28. PMID 22524403 DOI: 10.1111/J.1360-0443.2012.03922.X |
0.394 |
|
| 2011 |
Landi MT, Chatterjee N, Yu K, Goldin LR, Goldstein AM, Rotunno M, Mirabello L, Jacobs K, Wheeler W, Yeager M, Bergen AW, Li Q, Consonni D, Pesatori AC, Wacholder S, ... ... Laurie C, et al. A Genome-wide Association Study of Lung Cancer Identifies a Region of Chromosome 5p15 Associated with Risk for Adenocarcinoma. American Journal of Human Genetics. 88: 861. PMID 28472664 DOI: 10.1016/J.Ajhg.2011.05.003 |
0.39 |
|
| 2011 |
Shaffer JR, Wang X, Feingold E, Lee M, Begum F, Weeks DE, Cuenco KT, Barmada MM, Wendell SK, Crosslin DR, Laurie CC, Doheny KF, Pugh EW, Zhang Q, Feenstra B, et al. Genome-wide association scan for childhood caries implicates novel genes. Journal of Dental Research. 90: 1457-62. PMID 21940522 DOI: 10.1177/0022034511422910 |
0.31 |
|
| 2011 |
Amos CI, Wang LE, Lee JE, Gershenwald JE, Chen WV, Fang S, Kosoy R, Zhang M, Qureshi AA, Vattathil S, Schacherer CW, Gardner JM, Wang Y, Bishop DT, Barrett JH, ... ... Laurie CC, et al. Genome-wide association study identifies novel loci predisposing to cutaneous melanoma. Human Molecular Genetics. 20: 5012-23. PMID 21926416 DOI: 10.1093/Hmg/Ddr415 |
0.339 |
|
| 2011 |
Wiggs JL, Kang JH, Yaspan BL, Mirel DB, Laurie C, Crenshaw A, Brodeur W, Gogarten S, Olson LM, Abdrabou W, DelBono E, Loomis S, Haines JL, Pasquale LR. Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma in Caucasians from the USA. Human Molecular Genetics. 20: 4707-13. PMID 21873608 DOI: 10.1093/Hmg/Ddr382 |
0.403 |
|
| 2011 |
Landi MT, Chatterjee N, Yu K, Goldin LR, Goldstein AM, Rotunno M, Mirabello L, Jacobs K, Wheeler W, Yeager M, Bergen AW, Li Q, Consonni D, Pesatori AC, Wacholder S, ... ... Laurie C, et al. A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma (The American Journal of Human Genetics (2009) 85 (679-691)) American Journal of Human Genetics. 88: 861. DOI: 10.1016/j.ajhg.2011.05.003 |
0.334 |
|
| 2010 |
Laurie CC, Doheny KF, Mirel DB, Pugh EW, Bierut LJ, Bhangale T, Boehm F, Caporaso NE, Cornelis MC, Edenberg HJ, Gabriel SB, Harris EL, Hu FB, Jacobs KB, Kraft P, et al. Quality control and quality assurance in genotypic data for genome-wide association studies. Genetic Epidemiology. 34: 591-602. PMID 20718045 DOI: 10.1002/Gepi.20516 |
0.325 |
|
| 2010 |
Cornelis MC, Agrawal A, Cole JW, Hansel NN, Barnes KC, Beaty TH, Bennett SN, Bierut LJ, Boerwinkle E, Doheny KF, Feenstra B, Feingold E, Fornage M, Haiman CA, Harris EL, ... ... Laurie CC, et al. The Gene, Environment Association Studies consortium (GENEVA): maximizing the knowledge obtained from GWAS by collaboration across studies of multiple conditions. Genetic Epidemiology. 34: 364-72. PMID 20091798 DOI: 10.1002/Gepi.20492 |
0.308 |
|
| 2009 |
Landi MT, Chatterjee N, Yu K, Goldin LR, Goldstein AM, Rotunno M, Mirabello L, Jacobs K, Wheeler W, Yeager M, Bergen AW, Li Q, Consonni D, Pesatori AC, Wacholder S, ... ... Laurie C, et al. A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma. American Journal of Human Genetics. 85: 679-91. PMID 19836008 DOI: 10.1016/J.Ajhg.2009.09.012 |
0.382 |
|
| 2009 |
Cervino AC, Li G, Edwards S, Zhu J, Laurie C, Tokiwa G, Lum PY, Wang S, Castellani LW, Lusis AJ, Carlson S, Sachs AB, Schadt EE. Corrigendum to "Integrating QTL and high-density SNP analyses in mice to identify Insig2 as a susceptibility gene for plasma cholesterol levels" [Genomics 86 (2005) 505-517] (DOI:10.1016/j.ygeno.2005.07.010) Genomics. 93: 399. DOI: 10.1016/J.Ygeno.2008.12.005 |
0.333 |
|
| 2005 |
Cervino AC, Li G, Edwards S, Zhu J, Laurie C, Tokiwa G, Lum PY, Wang S, Castellani LW, Castellini LW, Lusis AJ, Carlson S, Sachs AB, Schadt EE. Integrating QTL and high-density SNP analyses in mice to identify Insig2 as a susceptibility gene for plasma cholesterol levels. Genomics. 86: 505-17. PMID 16126366 DOI: 10.1016/J.Ygeno.2005.07.010 |
0.31 |
|
| 2003 |
Tao Y, Zeng ZB, Li J, Hartl DL, Laurie CC. Genetic dissection of hybrid incompatibilities between Drosophila simulans and D. mauritiana. II. Mapping hybrid male sterility loci on the third chromosome. Genetics. 164: 1399-418. PMID 12930748 |
0.577 |
|
| 2003 |
Tao Y, Chen S, Hartl DL, Laurie CC. Genetic dissection of hybrid incompatibilities between Drosophila simulans and D. mauritiana. I. Differential accumulation of hybrid male sterility effects on the X and autosomes. Genetics. 164: 1383-97. PMID 12930747 |
0.548 |
|
| 2001 |
Tao Y, Hartl DL, Laurie CC. Sex-ratio segregation distortion associated with reproductive isolation in Drosophila. Proceedings of the National Academy of Sciences of the United States of America. 98: 13183-8. PMID 11687638 DOI: 10.1073/Pnas.231478798 |
0.551 |
|
| 2000 |
Zeng ZB, Liu J, Stam LF, Kao CH, Mercer JM, Laurie CC. Genetic architecture of a morphological shape difference between two Drosophila species. Genetics. 154: 299-310. PMID 10628989 |
0.373 |
|
| 1997 |
True JR, Liu J, Stam LF, Zeng ZB, Laurie CC. QUANTITATIVE GENETIC ANALYSIS OF DIVERGENCE IN MALE SECONDARY SEXUAL TRAITS BETWEEN DROSOPHILA SIMULANS AND DROSOPHILA MAURITIANA. Evolution; International Journal of Organic Evolution. 51: 816-832. PMID 28568599 DOI: 10.1111/J.1558-5646.1997.Tb03664.X |
0.603 |
|
| 1997 |
Laurie CC, True JR, Liu J, Mercer JM. An introgression analysis of quantitative trait loci that contribute to a morphological difference between Drosophila simulans and D. mauritiana. Genetics. 145: 339-48. PMID 9071588 |
0.618 |
|
| 1996 |
True JR, Mercer JM, Laurie CC. Differences in crossover frequency and distribution among three sibling species of Drosophila. Genetics. 142: 507-23. PMID 8852849 |
0.586 |
|
| 1996 |
True JR, Weir BS, Laurie CC. A genome-wide survey of hybrid incompatibility factors by the introgression of marked segments of Drosophila mauritiana chromosomes into Drosophila simulans. Genetics. 142: 819-37. PMID 8849890 |
0.58 |
|
| 1996 |
Liu J, Mercer JM, Stam LF, Gibson GC, Zeng ZB, Laurie CC. Genetic analysis of a morphological shape difference in the male genitalia of Drosophila simulans and D. mauritiana. Genetics. 142: 1129-45. PMID 8846893 |
0.397 |
|
| 1992 |
Aquadro CF, Jennings RM, Bland MM, Laurie CC, Langley CH. Patterns of naturally occurring restriction map variation, dopa decarboxylase activity variation and linkage disequilibrium in the Ddc gene region of Drosophila melanogaster. Genetics. 132: 443-52. PMID 1358752 |
0.542 |
|
| Show low-probability matches. |