| The power of genetic diversity in genome-wide association studies of lipids SE Graham, SL Clarke, KHH Wu, S Kanoni, GJM Zajac, S Ramdas, ... Nature 600 (7890), 675-679, 2021 | 391 | 2021 |
| A saturated map of common genetic variants associated with human height L Yengo, S Vedantam, E Marouli, J Sidorenko, E Bartell, S Sakaue, ... Nature 610 (7933), 704-712, 2022 | 282 | 2022 |
| Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease W Zhou, M Kanai, KHH Wu, H Rasheed, K Tsuo, JB Hirbo, Y Wang, ... Cell Genomics 2 (10), 2022 | 179 | 2022 |
| Increased proportion of variance explained and prediction accuracy of survival of breast cancer patients with use of whole-genome multiomic profiles AI Vazquez, Y Veturi, M Behring, S Shrestha, M Kirst, MFR Resende Jr, ... Genetics 203 (3), 1425-1438, 2016 | 58 | 2016 |
| Characterizing heterogeneity in neuroimaging, cognition, clinical symptoms, and genetics among patients with late-life depression J Wen, CHY Fu, D Tosun, Y Veturi, Z Yang, A Abdulkadir, E Mamourian, ... JAMA psychiatry 79 (5), 464-474, 2022 | 54 | 2022 |
| Meta-analysis fine-mapping is often miscalibrated at single-variant resolution M Kanai, R Elzur, W Zhou, KHH Wu, H Rasheed, K Tsuo, JB Hirbo, ... Cell Genomics 2 (12), 2022 | 47 | 2022 |
| How powerful are summary-based methods for identifying expression-trait associations under different genetic architectures? Y Veturi, MD Ritchie PACIFIC SYMPOSIUM ON BIOCOMPUTING 2018: Proceedings of the Pacific Symposium …, 2018 | 43 | 2018 |
| Evaluation of PrediXcan for prioritizing GWAS associations and predicting gene expression B Li, SS Verma, YC Veturi, A Verma, Y Bradford, DW Haas, MD Ritchie PACIFIC SYMPOSIUM ON BIOCOMPUTING 2018: Proceedings of the Pacific Symposium …, 2018 | 41 | 2018 |
| Incorporating genetic heterogeneity in whole-genome regressions using interactions G de Los Campos, Y Veturi, AI Vazquez, C Lehermeier, ... Journal of agricultural, biological, and environmental statistics 20, 467-490, 2015 | 41 | 2015 |
| Modeling heterogeneity in the genetic architecture of ethnically diverse groups using random effect interaction models Y Veturi, G de Los Campos, N Yi, W Huang, AI Vazquez, B Kühnel Genetics 211 (4), 1395-1407, 2019 | 40 | 2019 |
| Collective feature selection to identify crucial epistatic variants SS Verma, A Lucas, X Zhang, Y Veturi, S Dudek, B Li, R Li, R Urbanowicz, ... BioData mining 11, 1-22, 2018 | 29 | 2018 |
| Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis S Kanoni, SE Graham, Y Wang, I Surakka, S Ramdas, X Zhu, SL Clarke, ... Genome biology 23 (1), 268, 2022 | 27 | 2022 |
| A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids S Ramdas, J Judd, SE Graham, S Kanoni, Y Wang, I Surakka, B Wenz, ... The American Journal of Human Genetics 109 (8), 1366-1387, 2022 | 21 | 2022 |
| Effectiveness of shrinkage and variable selection methods for the prediction of complex human traits using data from distantly related individuals S Berger, P Pérez‐Rodríguez, Y Veturi, H Simianer, G de los Campos Annals of human genetics 79 (2), 122-135, 2015 | 20 | 2015 |
| A unified framework identifies new links between plasma lipids and diseases from electronic medical records across large-scale cohorts Y Veturi, A Lucas, Y Bradford, D Hui, S Dudek, E Theusch, A Verma, ... Nature genetics 53 (7), 972-981, 2021 | 19 | 2021 |
| Rare variants in drug target genes contributing to complex diseases, phenome-wide SS Verma, N Josyula, A Verma, X Zhang, Y Veturi, FE Dewey, DN Hartzel, ... Scientific reports 8 (1), 4624, 2018 | 15 | 2018 |
| Tissue specificity-aware TWAS (TSA-TWAS) framework identifies novel associations with metabolic, immunologic, and virologic traits in HIV-positive adults B Li, Y Veturi, A Verma, Y Bradford, ES Daar, RM Gulick, SA Riddler, ... PLoS genetics 17 (4), e1009464, 2021 | 13 | 2021 |
| Detecting potential pleiotropy across cardiovascular and neurological diseases using univariate, bivariate, and multivariate methods on 43,870 individuals from the eMERGE network X Zhang, Y Veturi, S Verma, W Bone, A Verma, A Lucas, S Hebbring, ... BIOCOMPUTING 2019: Proceedings of the Pacific Symposium, 272-283, 2018 | 13 | 2018 |
| Innovative strategies for annotating the “relationSNP” between variants and molecular phenotypes JE Miller, Y Veturi, MD Ritchie BioData mining 12, 1-22, 2019 | 12 | 2019 |
| Evidence of epistasis in regions of long-range linkage disequilibrium across five complex diseases in the UK Biobank and eMERGE datasets P Singhal, Y Veturi, SM Dudek, A Lucas, A Frase, K Van Steen, ... The American Journal of Human Genetics 110 (4), 575-591, 2023 | 9 | 2023 |
Marylyn D RitchieUniversity of PennsylvaniaVerified email at upenn.edu
