| Increased exonic de novo mutation rate in individuals with schizophrenia SL Girard, J Gauthier, A Noreau, L Xiong, S Zhou, L Jouan, ... Nature genetics 43 (9), 860-863, 2011 | 487 | 2011 |
| Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases Y Chen, T Lu, U Pettersson-Kymmer, ID Stewart, G Butler-Laporte, ... Nature genetics 55 (1), 44-53, 2023 | 414 | 2023 |
| Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors MK Bakker, RAA van der Spek, W van Rheenen, S Morel, R Bourcier, ... Nature genetics 52 (12), 1303-1313, 2020 | 253 | 2020 |
| A Neanderthal OAS1 isoform protects individuals of European ancestry against COVID-19 susceptibility and severity S Zhou, G Butler-Laporte, T Nakanishi, DR Morrison, J Afilalo, M Afilalo, ... Nature medicine 27 (4), 659-667, 2021 | 242 | 2021 |
| Vitamin D and COVID-19 susceptibility and severity in the COVID-19 Host Genetics Initiative: A Mendelian randomization study G Butler-Laporte, T Nakanishi, V Mooser, DR Morrison, T Abdullah, ... PLoS medicine 18 (6), e1003605, 2021 | 151* | 2021 |
| Exome sequencing reveals SPG11 mutations causing juvenile ALS H Daoud, S Zhou, A Noreau, M Sabbagh, V Belzil, A Dionne-Laporte, ... Neurobiology of aging 33 (4), 839. e5-839. e9, 2012 | 124 | 2012 |
| From target discovery to clinical drug development with human genetics K Trajanoska, C Bhérer, D Taliun, S Zhou, JB Richards, V Mooser Nature 620 (7975), 737-745, 2023 | 101 | 2023 |
| De novo variants in sporadic cases of childhood onset schizophrenia A Ambalavanan, SL Girard, K Ahn, S Zhou, A Dionne-Laporte, ... European Journal of Human Genetics 24 (6), 944-948, 2016 | 100 | 2016 |
| The association of mitochondrial aldehyde dehydrogenase gene (ALDH2) polymorphism with susceptibility to late-onset Alzheimer's disease in Chinese B Wang, J Wang, S Zhou, S Tan, X He, Z Yang, YC Xie, S Li, C Zheng, ... Journal of the neurological sciences 268 (1-2), 172-175, 2008 | 97 | 2008 |
| Genetics of intracranial aneurysms S Zhou, PA Dion, GA Rouleau Stroke 49 (3), 780-787, 2018 | 95 | 2018 |
| Rare loss-of-function variants in type I IFN immunity genes are not associated with severe COVID-19 G Povysil, G Butler-Laporte, N Shang, C Wang, A Khan, M Alaamery, ... The Journal of clinical investigation 131 (14), 2021 | 77 | 2021 |
| RNF213 is associated with intracranial aneurysms in the French-Canadian population S Zhou, A Ambalavanan, D Rochefort, P Xie, CV Bourassa, P Hince, ... The American Journal of Human Genetics 99 (5), 1072-1085, 2016 | 75 | 2016 |
| Analyses of growth differentiation factor 9 (GDF9) and bone morphogenetic protein 15 (BMP15) mutation in Chinese women with premature ovarian failure B Wang, Q Wen, F Ni, S Zhou, J Wang, Y Cao, X Ma Clinical endocrinology 72 (1), 135-136, 2010 | 73 | 2010 |
| Life-threatening viral disease in a novel form of autosomal recessive IFNAR2 deficiency in the Arctic CJA Duncan, MK Skouboe, S Howarth, AK Hollensen, R Chen, ... Journal of Experimental Medicine 219 (6), e20212427, 2022 | 62 | 2022 |
| A novel CRYGD mutation (p.Trp43Arg) causing autosomal dominant congenital cataract in a Chinese family B Wang, C Yu, YB Xi, HC Cai, J Wang, S Zhou, S Zhou, Y Wu, YB Yan, ... Human mutation 32 (1), E1939-E1947, 2011 | 61 | 2011 |
| Individuals with common diseases but with a low polygenic risk score could be prioritized for rare variant screening T Lu, S Zhou, H Wu, V Forgetta, CMT Greenwood, JB Richards Genetics in Medicine 23 (3), 508-515, 2021 | 59 | 2021 |
| Association between-238 but not-308 polymorphism of Tumor necrosis factor alpha (TNF-alpha) v and unexplained recurrent spontaneous abortion (URSA) in Chinese population C Liu, J Wang, S Zhou, B Wang, X Ma Reproductive biology and endocrinology 8, 1-4, 2010 | 59 | 2010 |
| A study of TNF-alpha-238 and -308 polymorphisms with different outcomes of persistent hepatitis B virus infection in China B Wang, J Wang, Y Zheng, S Zhou, J Zheng, F Wang, X Ma, Z Zeng, ... Pathology 42 (7), 674-680, 2010 | 58 | 2010 |
| Analysis of FOXO3 mutation in 114 Chinese women with premature ovarian failure B Wang, Y Mu, F Ni, S Zhou, J Wang, Y Cao, X Ma Reproductive biomedicine online 20 (4), 499-503, 2010 | 53 | 2010 |
| Proteome-wide Mendelian randomization implicates nephronectin as an actionable mediator of the effect of obesity on COVID-19 severity S Yoshiji, G Butler-Laporte, T Lu, JDS Willett, CY Su, T Nakanishi, ... Nature Metabolism 5 (2), 248-264, 2023 | 52 | 2023 |
