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Yun Li - Publications

Affiliations: 
Biostatistics University of North Carolina, Chapel Hill, Chapel Hill, NC 
Area:
Biostatistics
Website:
http://www.unc.edu/~yunmli/people.html#YunLi

211 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
2022 Shan Y, Cole SA, Haack K, Melton PE, Best LG, Bizon C, Kobes S, Köroğlu Ç, Baier LJ, Hanson RL, Sanna S, Li Y, Franceschini N. Association of protein function-altering variants with cardiometabolic traits: the strong heart study. Scientific Reports. 12: 9317. PMID 35665752 DOI: 10.1038/s41598-022-12866-2  0.385
2022 Mahajan A, Spracklen CN, Zhang W, Ng MCY, Petty LE, Kitajima H, Yu GZ, Rüeger S, Speidel L, Kim YJ, Horikoshi M, Mercader JM, Taliun D, Moon S, Kwak SH, ... ... Li Y, et al. Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation. Nature Genetics. PMID 35551307 DOI: 10.1038/s41588-022-01058-3  0.661
2022 Huang L, Rosen JD, Sun Q, Chen J, Wheeler MM, Zhou Y, Min YI, Kooperberg C, Conomos MP, Stilp AM, Rich SS, Rotter JI, Manichaikul A, Loos RJF, Kenny EE, ... ... Li Y, et al. TOP-LD: A tool to explore linkage disequilibrium with TOPMed whole-genome sequence data. American Journal of Human Genetics. PMID 35504290 DOI: 10.1016/j.ajhg.2022.04.006  0.318
2022 Holliday KM, Gondalia R, Baldassari A, Justice AE, Stewart JD, Liao D, Yanosky JD, Jordahl KM, Bhatti P, Assimes TL, Pankow JS, Guan W, Fornage M, Bressler J, North KE, ... ... Li Y, et al. Gaseous air pollutants and DNA methylation in a methylome-wide association study of an ethnically and environmentally diverse population of U.S. adults. Environmental Research. 113360. PMID 35500859 DOI: 10.1016/j.envres.2022.113360  0.654
2022 Rowland B, Venkatesh S, Tardaguila M, Wen J, Rosen JD, Tapia AL, Sun Q, Graff M, Vuckovic D, Lettre G, Sankaran VG, Voloudakis G, Roussos P, Huffman JE, Reiner AP, ... ... Li Y, et al. Transcriptome-wide association study in UK biobank Europeans identifies associations with blood cell traits. Human Molecular Genetics. PMID 35138379 DOI: 10.1093/hmg/ddac011  0.36
2022 Sun Q, Crowley CA, Huang L, Wen J, Chen J, Bao EL, Auer PL, Lettre G, Reiner AP, Sankaran VG, Raffield LM, Li Y. From GWAS variant to function: A study of ∼148,000 variants for blood cell traits. Hgg Advances. 3: 100063. PMID 35047852 DOI: 10.1016/j.xhgg.2021.100063  0.338
2021 Tapia AL, Rowland BT, Rosen JD, Preuss M, Young K, Graff M, Choquet H, Couper DJ, Buyske S, Bien SA, Jorgenson E, Kooperberg C, Loos RJF, Morrison AC, North KE, ... ... Li Y, et al. Full title: A large-scale transcriptome-wide association study (TWAS) of 10 blood cell phenotypes reveals complexities of TWAS fine-mapping. Genetic Epidemiology. PMID 34779012 DOI: 10.1002/gepi.22436  0.364
2021 Mikhaylova AV, McHugh CP, Polfus LM, Raffield LM, Boorgula MP, Blackwell TW, Brody JA, Broome J, Chami N, Chen MH, Conomos MP, Cox C, Curran JE, Daya M, Ekunwe L, ... ... Li Y, et al. Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program. American Journal of Human Genetics. PMID 34582791 DOI: 10.1016/j.ajhg.2021.08.007  0.57
2021 Little A, Hu Y, Sun Q, Jain D, Broome J, Chen MH, Thibord F, McHugh C, Surendran P, Blackwell TW, Brody JA, Bhan A, Chami N, Vries PS, Ekunwe L, ... ... Li Y, et al. Whole genome sequence analysis of platelet traits in the NHLBI trans-omics for precision medicine initiative. Human Molecular Genetics. PMID 34553764 DOI: 10.1093/hmg/ddab252  0.528
2021 Sun Q, Graff M, Rowland B, Wen J, Huang L, Miller-Fleming TW, Haessler J, Preuss MH, Chai JF, Lee MP, Avery CL, Cheng CY, Franceschini N, Sim X, Cox NJ, ... ... Li Y, et al. Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Journal of Human Genetics. PMID 34376796 DOI: 10.1038/s10038-021-00968-0  0.313
2021 Wen J, Xie M, Rowland B, Rosen JD, Sun Q, Chen J, Tapia AL, Qian H, Kowalski MH, Shan Y, Young KL, Graff M, Argos M, Avery CL, Bien SA, ... ... Li Y, et al. Transcriptome-Wide Association Study of Blood Cell Traits in African Ancestry and Hispanic/Latino Populations. Genes. 12. PMID 34356065 DOI: 10.3390/genes12071049  0.312
2021 Hu Y, Stilp AM, McHugh CP, Rao S, Jain D, Zheng X, Lane J, Méric de Bellefon S, Raffield LM, Chen MH, Yanek LR, Wheeler M, Yao Y, Ren C, Broome J, ... ... Li Y, et al. Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program. American Journal of Human Genetics. 108: 1165. PMID 34087167 DOI: 10.1016/j.ajhg.2021.04.015  0.468
2021 Zhao B, Shan Y, Yang Y, Yu Z, Li T, Wang X, Luo T, Zhu Z, Sullivan P, Zhao H, Li Y, Zhu H. Transcriptome-wide association analysis of brain structures yields insights into pleiotropy with complex neuropsychiatric traits. Nature Communications. 12: 2878. PMID 34001886 DOI: 10.1038/s41467-021-23130-y  0.319
2021 Gondalia R, Baldassari A, Holliday KM, Justice AE, Stewart JD, Liao D, Yanosky JD, Engel SM, Sheps D, Jordahl KM, Bhatti P, Horvath S, Assimes TL, Demerath EW, Guan W, ... ... Li Y, et al. Epigenetically mediated electrocardiographic manifestations of sub-chronic exposures to ambient particulate matter air pollution in the Women's Health Initiative and Atherosclerosis Risk in Communities Study. Environmental Research. 111211. PMID 33895111 DOI: 10.1016/j.envres.2021.111211  0.605
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, ... ... Li Y, 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  0.575
2021 Graff M, Justice AE, Young KL, Marouli E, Zhang X, Fine RS, Lim E, Buchanan V, Rand K, Feitosa MF, Wojczynski MK, Yanek LR, Shao Y, Rohde R, Adeyemo AA, ... ... Li Y, et al. Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry. American Journal of Human Genetics. PMID 33713608 DOI: 10.1016/j.ajhg.2021.02.011  0.355
2021 Bhattacharya A, Li Y, Love MI. MOSTWAS: Multi-Omic Strategies for Transcriptome-Wide Association Studies. Plos Genetics. 17: e1009398. PMID 33684137 DOI: 10.1371/journal.pgen.1009398  0.305
2020 Do WL, Whitsel EA, Costeira R, Masachs OM, Le Roy CI, Bell JT, RStaimez L, Stein AD, Smith AK, Horvath S, Assimes TL, Liu S, Manson JE, Shadyab AH, Li Y, et al. Epigenome-wide association study of diet quality in the Women's Health Initiative and TwinsUK cohort. International Journal of Epidemiology. PMID 33354722 DOI: 10.1093/ije/dyaa215  0.542
2020 Spracklen CN, Iyengar AK, Vadlamudi S, Raulerson CK, Jackson AU, Brotman SM, Wu Y, Cannon ME, Davis JP, Crain AT, Currin KW, Perrin HJ, Narisu N, Stringham HM, Fuchsberger C, ... ... Li Y, et al. Adiponectin GWAS loci harboring extensive allelic heterogeneity exhibit distinct molecular consequences. Plos Genetics. 16: e1009019. PMID 32915782 DOI: 10.1371/Journal.Pgen.1009019  0.724
2020 Justice AE, Chittoor G, Gondalia R, Melton PE, Lim E, Grove ML, Whitsel EA, Liu CT, Cupples LA, Fernandez-Rhodes L, Guan W, Bressler J, Fornage M, Boerwinkle E, Li Y, et al. Methylome-wide association study of central adiposity implicates genes involved in immune and endocrine systems. Epigenomics. PMID 32901515 DOI: 10.2217/Epi-2019-0276  0.685
2020 Vuckovic D, Bao EL, Akbari P, Lareau CA, Mousas A, Jiang T, Chen MH, Raffield LM, Tardaguila M, Huffman JE, Ritchie SC, Megy K, Ponstingl H, Penkett CJ, Albers PK, ... ... Li Y, et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell. 182: 1214-1231.e11. PMID 32888494 DOI: 10.1016/J.Cell.2020.08.008  0.382
2020 Chen MH, Raffield LM, Mousas A, Sakaue S, Huffman JE, Moscati A, Trivedi B, Jiang T, Akbari P, Vuckovic D, Bao EL, Zhong X, Manansala R, Laplante V, Chen M, ... ... Li Y, et al. Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Cell. 182: 1198-1213.e14. PMID 32888493 DOI: 10.1016/J.Cell.2020.06.045  0.413
2020 Matoba N, Liang D, Sun H, Aygün N, McAfee JC, Davis JE, Raffield LM, Qian H, Piven J, Li Y, Kosuri S, Won H, Stein JL. Common genetic risk variants identified in the SPARK cohort support DDHD2 as a candidate risk gene for autism. Translational Psychiatry. 10: 265. PMID 32747698 DOI: 10.1038/S41398-020-00953-9  0.43
2020 Colicino E, Marioni R, Ward-Caviness C, Gondalia R, Guan W, Chen B, Tsai PC, Huan T, Xu G, Golareh A, Schwartz J, Vokonas P, Just A, Starr JM, McRae AF, ... ... Li Y, et al. Blood DNA methylation sites predict death risk in a longitudinal study of 12, 300 individuals. Aging. 12. PMID 32697766 DOI: 10.18632/aging.103408  0.456
2020 Qian H, Kowalski MH, Kramer HJ, Tao R, Lash JP, Stilp AM, Cai J, Li Y, Franceschini N. Genome-wide Association of Kidney Traits in Hispanics/Latinos Using Dense Imputed Whole Genome Sequencing Data: The Hispanic Community Health Study/Study of Latinos. Circulation. Genomic and Precision Medicine. PMID 32600054 DOI: 10.1161/CIRCGEN.119.002891  0.357
2020 Lu L, Liu X, Huang WK, Giusti-Rodríguez P, Cui J, Zhang S, Xu W, Wen Z, Ma S, Rosen JD, Xu Z, Bartels CF, Kawaguchi R, Hu M, Scacheri PC, ... Li Y, ... Li Y, et al. Robust Hi-C Maps of Enhancer-Promoter Interactions Reveal the Function of Non-coding Genome in Neural Development and Diseases. Molecular Cell. PMID 32592681 DOI: 10.1016/J.Molcel.2020.06.007  0.32
2020 Halvorsen M, Huh R, Oskolkov N, Wen J, Netotea S, Giusti-Rodriguez P, Karlsson R, Bryois J, Nystedt B, Ameur A, Kähler AK, Ancalade N, Farrell M, Crowley JJ, Li Y, et al. Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia. Nature Communications. 11: 1842. PMID 32296054 DOI: 10.1038/S41467-020-15707-W  0.369
2020 Hodonsky CJ, Baldassari AR, Bien SA, Raffield LM, Highland HM, Sitlani CM, Wojcik GL, Tao R, Graff M, Tang W, Thyagarajan B, Buyske S, Fornage M, Hindorff LA, Li Y, et al. Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics. Bmc Genomics. 21: 228. PMID 32171239 DOI: 10.1186/S12864-020-6626-9  0.419
2020 Zhong W, Dong L, Poston TB, Darville T, Spracklen CN, Wu D, Mohlke KL, Li Y, Li Q, Zheng X. Inferring Regulatory Networks From Mixed Observational Data Using Directed Acyclic Graphs. Frontiers in Genetics. 11: 8. PMID 32127796 DOI: 10.3389/Fgene.2020.00008  0.308
2020 Li YR, Glessner JT, Coe BP, Li J, Mohebnasab M, Chang X, Connolly J, Kao C, Wei Z, Bradfield J, Kim C, Hou C, Khan M, Mentch F, Qiu H, et al. Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations. Nature Communications. 11: 255. PMID 31937769 DOI: 10.1038/S41467-019-13624-1  0.549
2020 Dong M, Thennavan A, Urrutia E, Li Y, Perou CM, Zou F, Jiang Y. SCDC: bulk gene expression deconvolution by multiple single-cell RNA sequencing references. Briefings in Bioinformatics. PMID 31925417 DOI: 10.1093/Bib/Bbz166  0.301
2020 Gondalia R, Holliday KM, Baldassari A, Justice AE, Stewart JD, Liao D, Yanosky JD, Engel SM, Jordahl KM, Bhatti P, Horvath S, Assimes TL, Pankow JS, Demerath EW, Guan W, ... ... Li Y, et al. Leukocyte Traits and Exposure to Ambient Particulate Matter Air Pollution in the Women's Health Initiative and Atherosclerosis Risk in Communities Study. Environmental Health Perspectives. 128: 17004. PMID 31903802 DOI: 10.1289/Ehp5360  0.638
2020 Nguyen S, Guan W, Bressler J, Grove M, Xia R, Wang Z, Fernandez-rhodes LE, Justice AE, Li Y, Whitsel EA, North KE, Fornage M, Boerwinkle E, Pankow JS, Demerath EW. Abstract P272: Associations of an Epigenetic Biomarker of Aging and Healthspan With BMI Status and Metabolic Health in Adult African Americans: The Atherosclerosis Risk in Communities (ARIC) Study Circulation. 141. DOI: 10.1161/Circ.141.Suppl_1.P272  0.502
2020 Nguyen S, Guan W, Bressler J, Grove M, Palta P, Xia R, Wang Z, Fernandez-Rhodes L, Justice AE, Li Y, Whitsel EA, North KE, Fornage M, Boerwinkle E, Kucharska-Newton A, et al. Abstract P271: Dna Methylation Measures of Aging in Midlife are Associated With Frailty Components in African American and European American Older Adults: The Atherosclerosis Risk in Communities (ARIC) Study Circulation. 141. DOI: 10.1161/Circ.141.Suppl_1.P271  0.515
2019 Raffield LM, Iyengar AK, Wang B, Gaynor SM, Spracklen CN, Zhong X, Kowalski MH, Salimi S, Polfus LM, Benjamin EJ, Bis JC, Bowler R, Cade BE, Choi WJ, Comellas AP, ... ... Li Y, et al. Allelic Heterogeneity at the CRP Locus Identified by Whole-Genome Sequencing in Multi-ancestry Cohorts. American Journal of Human Genetics. PMID 31883642 DOI: 10.1016/J.Ajhg.2019.12.002  0.468
2019 Kowalski MH, Qian H, Hou Z, Rosen JD, Tapia AL, Shan Y, Jain D, Argos M, Arnett DK, Avery C, Barnes KC, Becker LC, Bien SA, Bis JC, Blangero J, ... ... Li Y, et al. Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations. Plos Genetics. 15: e1008500. PMID 31869403 DOI: 10.1371/Journal.Pgen.1008500  0.478
2019 Zhao B, Luo T, Li T, Li Y, Zhang J, Shan Y, Wang X, Yang L, Zhou F, Zhu Z, Zhu H. Genome-wide association analysis of 19,629 individuals identifies variants influencing regional brain volumes and refines their genetic co-architecture with cognitive and mental health traits. Nature Genetics. PMID 31676860 DOI: 10.1038/S41588-019-0516-6  0.438
2019 Zhao B, Zhang J, Ibrahim JG, Luo T, Santelli RC, Li Y, Li T, Shan Y, Zhu Z, Zhou F, Liao H, Nichols TE, Zhu H. Large-scale GWAS reveals genetic architecture of brain white matter microstructure and genetic overlap with cognitive and mental health traits (n = 17,706). Molecular Psychiatry. PMID 31666681 DOI: 10.1038/S41380-019-0569-Z  0.453
2019 Johnson ND, Huang L, Li R, Li Y, Yang Y, Kim HR, Grant C, Wu H, Whitsel EA, Kiel DP, Baccarelli AA, Jin P, Murabito JM, Conneely KN. Age-related DNA hydroxymethylation is enriched for gene expression and immune system processes in human peripheral blood. Epigenetics. PMID 31506003 DOI: 10.1080/15592294.2019.1666651  0.581
2019 Song M, Yang X, Ren X, Maliskova L, Li B, Jones IR, Wang C, Jacob F, Wu K, Traglia M, Tam TW, Jamieson K, Lu SY, Ming GL, Li Y, et al. Mapping cis-regulatory chromatin contacts in neural cells links neuropsychiatric disorder risk variants to target genes. Nature Genetics. 51: 1252-1262. PMID 31367015 DOI: 10.1038/S41588-019-0472-1  0.324
2019 Gondalia R, Baldassari A, Holliday KM, Justice AE, Méndez-Giráldez R, Stewart JD, Liao D, Yanosky JD, Brennan KJM, Engel SM, Jordahl KM, Kennedy E, Ward-Caviness CK, Wolf K, Waldenberger M, ... ... Li Y, et al. Methylome-wide association study provides evidence of particulate matter air pollution-associated DNA methylation. Environment International. 104723. PMID 31208937 DOI: 10.1016/J.Envint.2019.03.071  0.647
2019 Zhong W, Spracklen CN, Mohlke KL, Zheng X, Fine J, Li Y. Multi-SNP mediation intersection-union test. Bioinformatics (Oxford, England). PMID 31099385 DOI: 10.1093/Bioinformatics/Btz285  0.42
2019 Fang Z, Weng C, Li H, Tao R, Mai W, Liu X, Lu L, Lai S, Duan Q, Alvarez C, Arvan P, Wynshaw-Boris A, Li Y, Pei Y, Jin F, Li Y, et al. Single-Cell Heterogeneity Analysis and CRISPR Screen Identify Key β-Cell-Specific Disease Genes. Cell Reports. 26: 3132-3144.e7. PMID 30865899 DOI: 10.1016/J.Celrep.2019.02.043  0.351
2019 Nguyen S, Guan W, Bressler J, Grove ML, Xia R, Wang Z, Fernandez-Rhodes L, Justice AE, Li Y, Whitsel EA, North KE, Fornage M, Boerwinkle E, Pankow JS, Demerath EW. Abstract 002: Adherence to Ideal Life’s Simple 7 Metrics is Associated With Epigenetic Biomarkers of Aging in African Americans: The Atherosclerosis Risk in Communities (ARIC) Study Circulation. 139. DOI: 10.1161/Circ.139.Suppl_1.002  0.489
2019 Giusti-Rodriguez P, Lu L, Crowley C, Bryois J, Liu X, Sariaslan A, Juric I, Martin J, Ancalade N, DeCristo D, Stockmeier C, Hu M, Jin F, Li Y, Sullivan P. A Chromatin Catalog For The Interpretation Of Genetic Associations Of Psychiatric Disorders European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2017.08.251  0.386
2018 Li M, Santpere G, Imamura Kawasawa Y, Evgrafov OV, Gulden FO, Pochareddy S, Sunkin SM, Li Z, Shin Y, Zhu Y, Sousa AMM, Werling DM, Kitchen RR, Kang HJ, Pletikos M, ... ... Li Y, et al. Integrative functional genomic analysis of human brain development and neuropsychiatric risks. Science (New York, N.Y.). 362. PMID 30545854 DOI: 10.1126/Science.Aat7615  0.367
2018 Wang Y, Song F, Zhang B, Zhang L, Xu J, Kuang D, Li D, Choudhary MNK, Li Y, Hu M, Hardison R, Wang T, Yue F. The 3D Genome Browser: a web-based browser for visualizing 3D genome organization and long-range chromatin interactions. Genome Biology. 19: 151. PMID 30286773 DOI: 10.1186/S13059-018-1519-9  0.303
2018 Zhao B, Ibrahim JG, Li Y, Li T, Wang Y, Shan Y, Zhu Z, Zhou F, Zhang J, Huang C, Liao H, Yang L, Thompson PM, Zhu H. Heritability of Regional Brain Volumes in Large-Scale Neuroimaging and Genetic Studies. Cerebral Cortex (New York, N.Y. : 1991). PMID 30010813 DOI: 10.1093/Cercor/Bhy157  0.356
2018 Bi W, Li Y, Smeltzer MP, Gao G, Zhao S, Kang G. STEPS: an efficient prospective likelihood approach to genetic association analyses of secondary traits in extreme phenotype sequencing. Biostatistics (Oxford, England). PMID 30007308 DOI: 10.1093/Biostatistics/Kxy030  0.378
2018 Franceschini N, Kopp JB, Barac A, Martin LW, Li Y, Qian H, Reiner AP, Pollak M, Wallace RB, Rosamond WD, Winkler CA. Association of APOL1 With Heart Failure With Preserved Ejection Fraction in Postmenopausal African American Women. Jama Cardiology. PMID 29971324 DOI: 10.1001/Jamacardio.2018.1827  0.312
2018 Lin Y, Liu L, Yang S, Li Y, Lin D, Zhang X, Yin X. Genotype imputation for Han Chinese population using Haplotype Reference Consortium as reference. Human Genetics. PMID 29855708 DOI: 10.1007/S00439-018-1894-Z  0.414
2018 Li Y, Hu M, Shen Y. Gene Regulation in the 3D Genome. Human Molecular Genetics. PMID 29767704 DOI: 10.1093/Hmg/Ddy164  0.334
2018 Wray NR, Ripke S, Mattheisen M, Trzaskowski M, Byrne EM, Abdellaoui A, Adams MJ, Agerbo E, Air TM, Andlauer TMF, Bacanu SA, Bækvad-Hansen M, Beekman AFT, Bigdeli TB, Binder EB, ... ... Li Y, ... ... Li Y, et al. Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. Nature Genetics. PMID 29700475 DOI: 10.1038/S41588-018-0090-3  0.337
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, 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  0.503
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  0.448
2018 Zhou X, Chen Y, Mok KY, Zhao Q, Chen K, Chen Y, Hardy J, Li Y, Fu AKY, Guo Q, Ip NY. Identification of genetic risk factors in the Chinese population implicates a role of immune system in Alzheimer's disease pathogenesis. Proceedings of the National Academy of Sciences of the United States of America. PMID 29432188 DOI: 10.1073/Pnas.1715554115  0.389
2018 Lu AT, Xue L, Salfati EL, Chen BH, Ferrucci L, Levy D, Joehanes R, Murabito JM, Kiel DP, Tsai PC, Yet I, Bell JT, Mangino M, Tanaka T, McRae AF, ... ... Li Y, et al. GWAS of epigenetic aging rates in blood reveals a critical role for TERT. Nature Communications. 9: 387. PMID 29374233 DOI: 10.1038/S41467-017-02697-5  0.391
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, ... Li Y, 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  0.447
2018 Zhou X, Chen Y, Mok KY, Zhao Q, Chen K, Chen Y, Hardy J, Li Y, Fu AKY, Guo Q, Ip NY, Initiative ADN. P3-104: Identification Of Genetic Risk Factors For Alzheimer'S Disease In The Chinese Population Alzheimers & Dementia. 14. DOI: 10.1016/J.Jalz.2018.06.1461  0.316
2017 Luo Y, Maity A, Wu MC, Smith C, Duan Q, Li Y, Tzeng JY. On the substructure controls in rare variant analysis: Principal components or variance components? Genetic Epidemiology. PMID 29280188 DOI: 10.1002/Gepi.22102  0.375
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  0.441
2017 Richard MA, Huan T, Ligthart S, Gondalia R, Jhun MA, Brody JA, Irvin MR, Marioni R, Shen J, Tsai PC, Montasser ME, Jia Y, Syme C, Salfati EL, Boerwinkle E, ... ... Li Y, et al. DNA Methylation Analysis Identifies Loci for Blood Pressure Regulation. American Journal of Human Genetics. 101: 888-902. PMID 29198723 DOI: 10.1016/J.Ajhg.2017.09.028  0.575
2017 Grant CD, Jafari N, Hou L, Li Y, Stewart JD, Zhang G, Lamichhane A, Manson JE, Baccarelli AA, Whitsel EA, Conneely KN. A longitudinal study of DNA methylation as a potential mediator of age-related diabetes risk. Geroscience. PMID 29159506 DOI: 10.1007/s11357-017-0001-z  0.568
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, ... Li Y, 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  0.342
2017 Du Y, Martin JS, McGee J, Yang Y, Liu EY, Sun Y, Geihs M, Kong X, Zhou EL, Li Y, Huang J. A SNP panel and online tool for checking genotype concordance through comparing QR codes. Plos One. 12: e0182438. PMID 28926565 DOI: 10.1371/Journal.Pone.0182438  0.421
2017 Hui D, Fang Z, Lin J, Duan Q, Li Y, Hu M, Chen W. LAIT: a local ancestry inference toolkit. Bmc Genetics. 18: 83. PMID 28877673 DOI: 10.1186/S12863-017-0546-Y  0.346
2017 Nolte IM, Munoz ML, Tragante V, Amare AT, Jansen R, Vaez A, von der Heyde B, Avery CL, Bis JC, Dierckx B, van Dongen J, Gogarten SM, Goyette P, Hernesniemi J, Huikari V, ... ... Li Y, ... ... Li Y, et al. Erratum: Genetic loci associated with heart rate variability and their effects on cardiac disease risk. Nature Communications. 8: 16140. PMID 28767105 DOI: 10.1038/Ncomms16140  0.323
2017 Cannon ME, Duan Q, Wu Y, Zeynalzadeh M, Xu Z, Kangas AJ, Soininen P, Ala-Korpela M, Civelek M, Lusis AJ, Kuusisto J, Collins FS, Boehnke M, Tang H, Laakso M, ... Li Y, et al. Trans-ancestry Fine Mapping and Molecular Assays Identify Regulatory Variants at the ANGPTL8 HDL-C GWAS Locus. G3 (Bethesda, Md.). PMID 28754724 DOI: 10.1534/G3.117.300088  0.609
2017 Gondalia R, Avery CL, Napier MD, Méndez-Giráldez R, Stewart JD, Sitlani CM, Li Y, Wilhelmsen KC, Duan Q, Roach J, North KE, Reiner AP, Zhang ZM, Tinker LF, Yanosky JD, et al. Genome-wide Association Study of Susceptibility to Particulate Matter-Associated QT Prolongation. Environmental Health Perspectives. 125: 067002. PMID 28749367 DOI: 10.1289/Ehp347  0.342
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