| Year |
Citation |
Score |
| 2024 |
Jakubek YA, Ma X, Stilp AM, Yu F, Bacon J, Wong JW, Aguet F, Ardlie K, Arnett D, Barnes K, Bis JC, Blackwell T, Becker LC, Boerwinkle E, Bowler RP, ... ... Li Y, et al. Genomic and phenotypic correlates of mosaic loss of chromosome Y in blood. Medrxiv : the Preprint Server For Health Sciences. PMID 38699360 DOI: 10.1101/2024.04.16.24305851 |
0.335 |
|
| 2024 |
Sun Q, Yang Y, Rosen JD, Chen J, Li X, Guan W, Jiang MZ, Wen J, Pace RG, Blackman SM, Bamshad MJ, Gibson RL, Cutting GR, O'Neal WK, Knowles MR, ... ... Li Y, et al. MagicalRsq-X: A cross-cohort transferable genotype imputation quality metric. American Journal of Human Genetics. PMID 38636510 DOI: 10.1016/j.ajhg.2024.04.001 |
0.304 |
|
| 2024 |
Suzuki K, Hatzikotoulas K, Southam L, Taylor HJ, Yin X, Lorenz KM, Mandla R, Huerta-Chagoya A, Melloni GEM, Kanoni S, Rayner NW, Bocher O, Arruda AL, Sonehara K, Namba S, ... ... Li Y, et al. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology. Nature. PMID 38374256 DOI: 10.1038/s41586-024-07019-6 |
0.531 |
|
| 2023 |
Ren X, Yang H, Nierenberg JL, Sun Y, Chen J, Beaman C, Pham T, Nobuhara M, Takagi MA, Narayan V, Li Y, Ziv E, Shen Y. High-throughput PRIME-editing screens identify functional DNA variants in the human genome. Molecular Cell. 83: 4633-4645.e9. PMID 38134886 DOI: 10.1016/j.molcel.2023.11.021 |
0.332 |
|
| 2023 |
Sun Q, Broadaway KA, Edmiston SN, Fajgenbaum K, Miller-Fleming T, Westerkam LL, Melendez-Gonzalez M, Bui H, Blum FR, Levitt B, Lin L, Hao H, Harris KM, Liu Z, Thomas NE, ... ... Li Y, et al. Genetic Variants Associated With Hidradenitis Suppurativa. Jama Dermatology. PMID 37494057 DOI: 10.1001/jamadermatol.2023.2217 |
0.327 |
|
| 2023 |
Buren EV, Radicioni G, Lester S, O'Neal WK, Dang H, Kasela S, Garudadri S, Curtis JL, Han MK, Krishnan JA, Wan ES, Silverman EK, Hastie A, Ortega VE, Lappalainen T, ... ... Li Y, et al. Genetic regulators of sputum mucin concentration and their associations with COPD phenotypes. Plos Genetics. 19: e1010445. PMID 37352370 DOI: 10.1371/journal.pgen.1010445 |
0.327 |
|
| 2023 |
Suzuki K, Hatzikotoulas K, Southam L, Taylor HJ, Yin X, Lorenz KM, Mandla R, Huerta-Chagoya A, Rayner NW, Bocher O, Ana Luiza de SVA, Sonehara K, Namba S, Lee SSK, Preuss MH, ... ... Li Y, et al. Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications. Medrxiv : the Preprint Server For Health Sciences. PMID 37034649 DOI: 10.1101/2023.03.31.23287839 |
0.539 |
|
| 2022 |
Wheeler MM, Stilp AM, Rao S, Halldórsson BV, Beyter D, Wen J, Mihkaylova AV, McHugh CP, Lane J, Jiang MZ, Raffield LM, Jun G, Sedlazeck FJ, Metcalf G, Yao Y, ... ... Li Y, et al. Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program. Nature Communications. 13: 7592. PMID 36481753 DOI: 10.1038/s41467-022-35354-7 |
0.55 |
|
| 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 |
0.374 |
|
| 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 |
0.312 |
|
| 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 |
0.645 |
|
| 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 |
0.361 |
|
| 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 |
0.34 |
|
| 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 |
0.365 |
|
| 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 |
0.572 |
|
| 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 |
0.314 |
|
| 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 |
0.32 |
|
| 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 |
0.594 |
|
| 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 |
0.577 |
|
| 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 |
0.356 |
|
| 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 |
0.304 |
|
| 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 |
0.535 |
|
| 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 |
0.721 |
|
| 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 |
0.679 |
|
| 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 |
0.383 |
|
| 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 |
0.445 |
|
| 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 |
0.356 |
|
| 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 |
0.322 |
|
| 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 |
0.37 |
|
| 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 |
0.42 |
|
| 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 |
0.546 |
|
| 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 |
0.302 |
|
| 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 |
0.63 |
|
| 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 |
0.493 |
|
| 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 |
0.507 |
|
| 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 |
0.467 |
|
| 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 |
0.452 |
|
| 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 |
0.575 |
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| 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 |
0.325 |
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| 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 |
0.639 |
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| 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 |
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| 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 |
0.352 |
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| 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 |
0.48 |
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| 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 |
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| 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 |
0.368 |
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| 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 |
0.304 |
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| 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 |
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| 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 |
0.379 |
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| 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 |
0.311 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
0.445 |
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