| Identification of deleterious mutations within three human genomes S Chun, JC Fay Genome research 19 (9), 1553-1561, 2009 | 1156 | 2009 |
| Genome-wide patterns and properties of de novo mutations in humans LC Francioli, PP Polak, A Koren, A Menelaou, S Chun, I Renkens, ... Nature genetics 47 (7), 822-826, 2015 | 405 | 2015 |
| Minke whale genome and aquatic adaptation in cetaceans HS Yim, YS Cho, X Guang, SG Kang, JY Jeong, SS Cha, HM Oh, JH Lee, ... Nature genetics 46 (1), 88-92, 2014 | 277 | 2014 |
| Limited statistical evidence for shared genetic effects of eQTLs and autoimmune-disease-associated loci in three major immune-cell types S Chun, A Casparino, NA Patsopoulos, DC Croteau-Chonka, BA Raby, ... Nature Genetics 49 (4), 600-605, 2017 | 226 | 2017 |
| Genetic associations with obstructive sleep apnea traits in Hispanic/Latino Americans BE Cade, H Chen, AM Stilp, KJ Gleason, T Sofer, S Ancoli-Israel, R Arens, ... American journal of respiratory and critical care medicine 194 (7), 886-897, 2016 | 124 | 2016 |
| Evidence for hitchhiking of deleterious mutations within the human genome S Chun, JC Fay PLoS genetics 7 (8), e1002240, 2011 | 94 | 2011 |
| Genes with monoallelic expression contribute disproportionately to genetic diversity in humans V Savova, S Chun, M Sohail, RB McCole, R Witwicki, L Gai, TL Lenz, ... Nature genetics 48 (3), 231-237, 2016 | 79 | 2016 |
| Multiethnic Meta-Analysis Identifies RAI1 as a Possible Obstructive Sleep Apnea–related Quantitative Trait Locus in Men H Chen, BE Cade, KJ Gleason, AC Bjonnes, AM Stilp, T Sofer, ... American journal of respiratory cell and molecular biology 58 (3), 391-401, 2018 | 75 | 2018 |
| The missing link between genetic association and regulatory function NJ Connally, S Nazeen, D Lee, H Shi, J Stamatoyannopoulos, S Chun, ... Elife 11, e74970, 2022 | 62 | 2022 |
| Using whole-genome sequences of the LG/J and SM/J inbred mouse strains to prioritize quantitative trait genes and nucleotides I Nikolskiy, DF Conrad, S Chun, JC Fay, JM Cheverud, HA Lawson BMC genomics 16 (1), 415, 2015 | 32 | 2015 |
| Non-parametric polygenic risk prediction via partitioned gwas summary statistics S Chun, M Imakaev, D Hui, NA Patsopoulos, BM Neale, S Kathiresan, ... The American Journal of Human Genetics 107 (1), 46-59, 2020 | 31 | 2020 |
| Mitigating False‐Positive Associations in Rare Disease Gene Discovery S Akle, S Chun, DM Jordan, CA Cassa Human mutation 36 (10), 998-1003, 2015 | 21 | 2015 |
| Fine-Mapping an Association of FSHR with Preterm Birth in a Finnish Population S Chun, J Plunkett, K Teramo, LJ Muglia, JC Fay PLOS ONE 8 (10), e78032, 2013 | 15 | 2013 |
| An argument for early genomic sequencing in atypical cases: a WISP3 variant leads to diagnosis of progressive pseudorheumatoid arthropathy of childhood CA Cassa, SE Smith, W Docken, E Hoffman, H McLaughlin, S Chun, ... Rheumatology 55 (3), 586-589, 2016 | 11 | 2016 |
| A polygenic risk score for idiopathic pulmonary fibrosis and interstitial lung abnormalities M Moll, AL Peljto, JS Kim, H Xu, CL Debban, X Chen, A Menon, ... American Journal of Respiratory and Critical Care Medicine 208 (7), 791-801, 2023 | 10 | 2023 |
| Joint analysis reveals shared autoimmune disease associations and identifies common mechanisms MR Lincoln, N Connally, PP Axisa, C Gasperi, M Mitrovic, D van Heel, ... medRxiv, 2021 | 10 | 2021 |
| Non-parametric polygenic risk prediction using partitioned GWAS summary statistics S Chun, M Imakaev, D Hui, NA Patsopoulos, BM Neale, S Kathiresan, ... BioRxiv, 370064, 2020 | 10 | 2020 |
| Leveraging pleiotropy to discover and interpret GWAS results for sleep-associated traits S Chun, S Akle, A Teodosiadis, BE Cade, H Wang, T Sofer, DS Evans, ... PLoS genetics 18 (12), e1010557, 2022 | 8 | 2022 |
| Polygenic risk score validation using Korean genomes of 265 early-onset acute myocardial infarction patients and 636 healthy controls Y Bhak, Y Jeon, S Jeon, C Yoon, M Kim, A Blazyte, Y Kim, Y Kang, C Kim, ... PloS one 16 (2), e0246538, 2021 | 8 | 2021 |
| FGF20 and PGM2 variants are associated with childhood asthma in family-based whole-genome sequencing studies J Hecker, S Chun, A Samiei, C Liu, C Laurie, P Kachroo, SM Lutz, S Lee, ... Human Molecular Genetics, 2022 | 3 | 2022 |
Shamil SunyaevProfessor of Biomedical Informatics and of Medicine (BWH), Harvard Medical Schoolכתובת אימייל מאומתת בדומיין rics.bwh.harvard.edu
