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| Leveraging polygenic functional enrichment to improve GWAS power G Kichaev, G Bhatia, PR Loh, S Gazal, K Burch, MK Freund, A Schoech, ... The American Journal of Human Genetics 104 (1), 65-75, 2019 | 890 | 2019 |
| Mixed-model association for biobank-scale datasets PR Loh, G Kichaev, S Gazal, AP Schoech, AL Price Nature genetics 50 (7), 906-908, 2018 | 706 | 2018 |
| COVID-19 tissue atlases reveal SARS-CoV-2 pathology and cellular targets TM Delorey, CGK Ziegler, G Heimberg, R Normand, Y Yang, ... Nature 595 (7865), 107-113, 2021 | 681 | 2021 |
| Linkage disequilibrium-dependent architecture of human complex traits shows action of negative selection S Gazal, HK Finucane, NA Furlotte, PR Loh, PF Palamara, X Liu, ... Nature Genetics 49 (10), 1421-1427, 2017 | 470 | 2017 |
| MUC5B Promoter Variant and Rheumatoid Arthritis with Interstitial Lung Disease PA Juge, JS Lee, E Ebstein, H Furukawa, E Dobrinskikh, S Gazal, ... New England Journal of Medicine 379 (23), 2209-2219, 2018 | 449 | 2018 |
| Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases K Ishigaki, M Akiyama, M Kanai, A Takahashi, E Kawakami, H Sugishita, ... Nature genetics 52 (7), 669-679, 2020 | 426 | 2020 |
| Shared genetic and experimental links between obesity-related traits and asthma subtypes in UK Biobank Z Zhu, Y Guo, H Shi, CL Liu, RA Panganiban, W Chung, LJ O'Connor, ... Journal of Allergy and Clinical Immunology 145 (2), 537-549, 2020 | 305 | 2020 |
| Comparison of methods that use whole genome data to estimate the heritability and genetic architecture of complex traits LM Evans, R Tahmasbi, SI Vrieze, GR Abecasis, S Das, S Gazal, ... Nature genetics 50 (5), 737-745, 2018 | 286 | 2018 |
| Functionally informed fine-mapping and polygenic localization of complex trait heritability O Weissbrod, F Hormozdiari, C Benner, R Cui, J Ulirsch, S Gazal, ... Nature genetics 52 (12), 1355-1363, 2020 | 265 | 2020 |
| Extreme polygenicity of complex traits is explained by negative selection LJ O'Connor, AP Schoech, F Hormozdiari, S Gazal, N Patterson, AL Price The American Journal of Human Genetics 105 (3), 456-476, 2019 | 235 | 2019 |
| Methotrexate and rheumatoid arthritis associated interstitial lung disease PA Juge, JS Lee, J Lau, L Kawano-Dourado, JR Serrano, M Sebastiani, ... European Respiratory Journal 57 (2), 2021 | 216 | 2021 |
| Shared genetic predisposition in rheumatoid arthritis-interstitial lung disease and familial pulmonary fibrosis PA Juge, R Borie, C Kannengiesser, S Gazal, P Revy, ... European Respiratory Journal 49 (5), 2017 | 206 | 2017 |
| Heterozygous HTRA1 mutations are associated with autosomal dominant cerebral small vessel disease E Verdura, D Herve, E Scharrer, MM Amador, L Guyant-Marechal, ... Brain 138 (8), 2347-2358, 2015 | 198 | 2015 |
| Leveraging fine-mapping and multipopulation training data to improve cross-population polygenic risk scores O Weissbrod, M Kanai, H Shi, S Gazal, WJ Peyrot, AV Khera, Y Okada, ... Nature Genetics 54 (4), 450-458, 2022 | 197* | 2022 |
| Juvenile myelomonocytic leukemia displays mutations in components of the RAS pathway and the PRC2 network A Caye, M Strullu, F Guidez, B Cassinat, S Gazal, O Fenneteau, E Lainey, ... Nature genetics 47 (11), 1334-1340, 2015 | 191 | 2015 |
| The MUC5B variant is associated with idiopathic pulmonary fibrosis but not with systemic sclerosis interstitial lung disease in the European Caucasian population R Borie, B Crestani, P Dieude, H Nunes, Y Allanore, C Kannengiesser, ... PloS one 8 (8), e70621, 2013 | 185 | 2013 |
| Leveraging molecular quantitative trait loci to understand the genetic architecture of diseases and complex traits F Hormozdiari, S Gazal, B Van De Geijn, HK Finucane, CJT Ju, PR Loh, ... Nature genetics 50 (7), 1041-1047, 2018 | 174 | 2018 |
| Identification of mutations in TMEM5 and ISPD as a cause of severe cobblestone lissencephaly S Vuillaumier-Barrot, C Bouchet-Séraphin, M Chelbi, L Devisme, ... The American Journal of Human Genetics 91 (6), 1135-1143, 2012 | 174 | 2012 |
| Heterozygous RTEL1 mutations are associated with familial pulmonary fibrosis C Kannengiesser, R Borie, C Ménard, M Réocreux, P Nitschké, S Gazal, ... European Respiratory Journal 46 (2), 474-485, 2015 | 170 | 2015 |
