| The complete genome of an individual by massively parallel DNA sequencing DA Wheeler, M Srinivasan, M Egholm, Y Shen, L Chen, A McGuire, W He, ... nature 452 (7189), 872-876, 2008 | 2530 | 2008 |
| Evolutionary and biomedical insights from the rhesus macaque genome RA Gibbs, J Rogers, MG Katze, R Bumgarner, GM Weinstock, ER Mardis, ... science 316 (5822), 222-234, 2007 | 1563 | 2007 |
| The support of human genetic evidence for approved drug indications MR Nelson, H Tipney, JL Painter, J Shen, P Nicoletti, Y Shen, A Floratos, ... Nature genetics 47 (8), 856-860, 2015 | 1518 | 2015 |
| The Genome of the Sea Urchin Strongylocentrotus purpuratus E Sodergren, GM Weinstock, EH Davidson, RA Cameron, RA Gibbs, ... Science 314 (5801), 941-952, 2006 | 1281 | 2006 |
| HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin AK Daly, PT Donaldson, P Bhatnagar, Y Shen, I Pe'er, A Floratos, MJ Daly, ... Nature genetics 41 (7), 816-819, 2009 | 1223 | 2009 |
| Human tissue-resident memory T cells are defined by core transcriptional and functional signatures in lymphoid and mucosal sites BV Kumar, W Ma, M Miron, T Granot, RS Guyer, DJ Carpenter, T Senda, ... Cell reports 20 (12), 2921-2934, 2017 | 1039 | 2017 |
| De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies J Homsy, S Zaidi, Y Shen, JS Ware, KE Samocha, KJ Karczewski, ... Science 350 (6265), 1262-1266, 2015 | 842 | 2015 |
| Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands SC Jin, J Homsy, S Zaidi, Q Lu, S Morton, SR DePalma, X Zeng, H Qi, ... Nature genetics 49 (11), 1593-1601, 2017 | 822 | 2017 |
| Spatial map of human T cell compartmentalization and maintenance over decades of life JJC Thome, N Yudanin, Y Ohmura, M Kubota, B Grinshpun, ... Cell 159 (4), 814-828, 2014 | 617 | 2014 |
| Susceptibility to amoxicillin-clavulanate-induced liver injury is influenced by multiple HLA class I and II alleles MI Lucena, M Molokhia, Y Shen, TJ Urban, GP Aithal, RJ Andrade, ... Gastroenterology 141 (1), 338-347, 2011 | 529 | 2011 |
| The genome sequence of taurine cattle: a window to ruminant biology and evolution TBG Sequencing, CG Elsik, RL Tellam, KC Worley, Analysis Consortium Science (New York, NY) 324 (5926), 522, 2009 | 397 | 2009 |
| SPARK: A US cohort of 50,000 families to accelerate autism research P Feliciano, AM Daniels, LAG Snyder, A Beaumont, A Camba, A Esler, ... Neuron 97 (3), 488-493, 2018 | 391 | 2018 |
| Next-Generation Sequencing of Pulmonary Sarcomatoid Carcinoma Reveals High Frequency of Actionable MET Gene Mutations X Liu, Y Jia, MB Stoopler, Y Shen, H Cheng, J Chen, M Mansukhani, ... Journal of clinical oncology 34 (8), 794-802, 2016 | 373 | 2016 |
| Tissue determinants of human NK cell development, function, and residence P Dogra, C Rancan, W Ma, M Toth, T Senda, DJ Carpenter, M Kubota, ... Cell 180 (4), 749-763. e13, 2020 | 370 | 2020 |
| Long-read sequencing and de novo assembly of a Chinese genome L Shi, Y Guo, C Dong, J Huddleston, H Yang, X Han, A Fu, Q Li, N Li, ... Nature communications 7 (1), 12065, 2016 | 292 | 2016 |
| Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence data JT Glessner, AG Bick, K Ito, JG Homsy, L Rodriguez-Murillo, M Fromer, ... Circulation research 115 (10), 884-896, 2014 | 284 | 2014 |
| Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes X Zhou, P Feliciano, C Shu, T Wang, I Astrovskaya, JB Hall, JU Obiajulu, ... Nature genetics 54 (9), 1305-1319, 2022 | 255 | 2022 |
| Association of liver injury from specific drugs, or groups of drugs, with polymorphisms in HLA and other genes in a genome-wide association study P Nicoletti, GP Aithal, ES Bjornsson, RJ Andrade, A Sawle, M Arrese, ... Gastroenterology 152 (5), 1078-1089, 2017 | 245 | 2017 |
| Tracking donor-reactive T cells: evidence for clonal deletion in tolerant kidney transplant patients H Morris, S DeWolf, H Robins, B Sprangers, SA LoCascio, BA Shonts, ... Science translational medicine 7 (272), 272ra10-272ra10, 2015 | 232 | 2015 |
| A SNP discovery method to assess variant allele probability from next-generation resequencing data Y Shen, Z Wan, C Coarfa, R Drabek, L Chen, EA Ostrowski, Y Liu, ... Genome research 20 (2), 273-280, 2010 | 230 | 2010 |
Wendy ChungBoston Children's Hospital, Harvard Medical Schoolcumc.columbia.edu의 이메일 확인됨