| Genetics of 35 blood and urine biomarkers in the UK Biobank N Sinnott-Armstrong, Y Tanigawa, D Amar, N Mars, C Benner, M Aguirre, ... Nature genetics 53 (2), 185-194, 2021 | 478 | 2021 |
| Large-scale sequencing identifies multiple genes and rare variants associated with Crohn’s disease susceptibility A Sazonovs, CR Stevens, GR Venkataraman, K Yuan, B Avila, MT Abreu, ... Nature genetics 54 (9), 1275-1283, 2022 | 75 | 2022 |
| Significant sparse polygenic risk scores across 813 traits in UK Biobank Y Tanigawa, J Qian, G Venkataraman, JM Justesen, R Li, R Tibshirani, ... PLoS genetics 18 (3), e1010105, 2022 | 58 | 2022 |
| Rare protein-altering variants in ANGPTL7 lower intraocular pressure and protect against glaucoma Y Tanigawa, M Wainberg, J Karjalainen, T Kiiskinen, G Venkataraman, ... PLoS Genetics 16 (5), e1008682, 2020 | 35 | 2020 |
| FasTag: Automatic text classification of unstructured medical narratives GR Venkataraman, AL Pineda, OJ Bear Don’t Walk IV, AM Zehnder, ... PLoS one 15 (6), e0234647, 2020 | 33 | 2020 |
| Cardiac imaging of aortic valve area from 34 287 UK Biobank participants reveals novel genetic associations and shared genetic comorbidity with multiple disease phenotypes A Córdova-Palomera, C Tcheandjieu, JA Fries, P Varma, VS Chen, ... Circulation: Genomic and Precision Medicine 13 (6), e003014, 2020 | 20 | 2020 |
| Polygenic risk modeling with latent trait-related genetic components M Aguirre, Y Tanigawa, GR Venkataraman, R Tibshirani, T Hastie, ... European Journal of Human Genetics 29 (7), 1071-1081, 2021 | 16 | 2021 |
| Rare and common variant discovery in complex disease: the IBD case study GR Venkataraman, MA Rivas Human molecular genetics 28 (R2), R162-R169, 2019 | 16 | 2019 |
| Sequencing of over 100,000 individuals identifies multiple genes and rare variants associated with Crohns disease susceptibility A Sazonovs, CR Stevens, GR Venkataraman, K Yuan, B Avila, MT Abreu, ... medRxiv, 2021.06. 15.21258641, 2021 | 13 | 2021 |
| Pervasive additive and non-additive effects within the HLA region contribute to disease risk in the UK Biobank GR Venkataraman, JE Olivieri, C DeBoever, Y Tanigawa, JM Justesen, ... BioRxiv, 2020.05. 28.119669, 2020 | 9 | 2020 |
| DE NOVO MUTATIONS IN AUTISM IMPLICATE THE SYNAPTIC ELIMINATION NETWORK GR Venkataraman, C O’CONNELL, F Egawa, D Kashef-Haghighi, ... PACIFIC SYMPOSIUM ON BIOCOMPUTING 2017, 521-532, 2017 | 9 | 2017 |
| FinnGen. Rodriguez F, Assimes TL, Agarwala V, Tibshirani R, Hastie T, Ripatti S, Pritchard JK, Daly MJ, Rivas MA. Genetics of 35 blood and urine biomarkers in the UK biobank N Sinnott-Armstrong, Y Tanigawa, D Amar, N Mars, C Benner, M Aguirre, ... Nature Genetics 53, 185-194, 2021 | 8 | 2021 |
| Bayesian model comparison for rare-variant association studies GR Venkataraman, C DeBoever, Y Tanigawa, M Aguirre, AG Ioannidis, ... The American Journal of Human Genetics 108 (12), 2354-2367, 2021 | 5 | 2021 |
| Genetics of 38 blood and urine biomarkers in the UK Biobank. bioRxiv. 2019: 660506 N Sinnott-Armstrong, Y Tanigawa, D Amar, NJ Mars, M Aguirre, ... Preprint posted June 5, 2019 | 4 | 2019 |
| Medical relevance of common protein-altering variants in GPCR genes across 337,205 individuals in the UK Biobank study C DeBoever, AJ Venkatakrishnan, JM Paggi, FM Heydenreich, SA Laurin, ... bioRxiv, 2019.12. 13.876250, 2019 | 3 | 2019 |
| Deep learning facilitates rapid cohort identification using human and veterinary clinical narratives AL Pineda, OJ Bear, GR Venkataraman, AM Zehnder, S Ayyar, RL Page, ... bioRxiv, 429720, 2018 | 3 | 2018 |
| Cardiac imaging of aortic valve area from 26,142 UK Biobank participants reveal novel genetic associations and shared genetic comorbidity with multiple disease phenotypes A Córdova-Palomera, C Tcheandjieu, J Fries, P Varma, VS Chen, ... medRxiv, 2020.04. 09.20060012, 2020 | 2 | 2020 |
| Fastag: automatic text classification of unstructured medical narratives AL Pineda, JB Oliver, RV Guhan, MZ Ashley, S Ayyar, LP Rodney bioRxiv, 429720, 2019 | 2 | 2019 |
| Nanoparticle enrichment mass-spectrometry proteomics identifies protein-altering variants for precise pQTL mapping K Suhre, GR Venkataraman, H Guturu, A Halama, N Stephan, G Thareja, ... Nature Communications 15 (1), 989, 2024 | 1 | 2024 |
| 778 EXOME SEQUENCING IN 30,000 CASES DEFINES NOVEL RISK FACTORS FOR CROHN'S DISEASE C Stevens, K Yuan, A Sazonovs, GR Venkataraman, MA Rivas, JD Rioux, ... Gastroenterology 160 (6), S-156, 2021 | 1 | 2021 |
