| Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies W Zhou, JB Nielsen, LG Fritsche, R Dey, ME Gabrielsen, BN Wolford, ... Nature genetics 50 (9), 1335-1341, 2018 | 1243 | 2018 |
| LocusZoom. js: interactive and embeddable visualization of genetic association study results AP Boughton, RP Welch, M Flickinger, P VandeHaar, D Taliun, ... Bioinformatics 37 (18), 3017-3018, 2021 | 241 | 2021 |
| Exploring and visualizing large-scale genetic associations by using PheWeb SA Gagliano Taliun, P VandeHaar, AP Boughton, RP Welch, D Taliun, ... Nature genetics 52 (6), 550-552, 2020 | 183 | 2020 |
| Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci X Yin, LS Chan, D Bose, AU Jackson, P VandeHaar, AE Locke, ... Nature communications 13 (1), 1644, 2022 | 122 | 2022 |
| Cancer PRSweb: an online repository with polygenic risk scores for major cancer traits and their evaluation in two independent biobanks LG Fritsche, S Patil, LJ Beesley, P VandeHaar, M Salvatore, Y Ma, ... The American Journal of Human Genetics 107 (5), 815-836, 2020 | 88 | 2020 |
| The Michigan Genomics Initiative: a biobank linking genotypes and electronic clinical records in Michigan Medicine patients M Zawistowski, LG Fritsche, A Pandit, B Vanderwerff, S Patil, EM Schmidt, ... Cell Genomics 3 (2), 2023 | 86 | 2023 |
| UK Biobank whole-exome sequence binary phenome analysis with robust region-based rare-variant test Z Zhao, W Bi, W Zhou, P VandeHaar, LG Fritsche, S Lee The American Journal of Human Genetics 106 (1), 3-12, 2020 | 71 | 2020 |
| Exploring various polygenic risk scores for skin cancer in the phenomes of the Michigan genomics initiative and the UK Biobank with a visual catalog: PRSWeb LG Fritsche, LJ Beesley, P VandeHaar, RB Peng, M Salvatore, ... PLoS genetics 15 (6), e1008202, 2019 | 40 | 2019 |
| FIVEx: an interactive eQTL browser across public datasets A Kwong, AP Boughton, M Wang, P VandeHaar, M Boehnke, G Abecasis, ... Bioinformatics, 2021 | 33 | 2021 |
| A powerful subset-based gene-set analysis method identifies novel associations and improves interpretation in UK Biobank D Dutta, P VandeHaar, LJ Scott, M Boehnke, S Lee bioRxiv, 799791, 2019 | 18* | 2019 |
| Epigenome-wide DNA methylation association study of circulating IgE levels identifies novel targets for asthma K Recto, P Kachroo, T Huan, D Van Den Berg, GY Lee, H Bui, DH Lee, ... EBioMedicine 95, 2023 | 8 | 2023 |
| Rare and common genetic variation underlying atrial fibrillation risk OB Vad, LM Monfort, C Paludan-Müller, K Kahnert, SZ Diederichsen, ... JAMA cardiology 9 (8), 732-740, 2024 | 7 | 2024 |
| False discovery rates for genome-wide association tests in biobanks with thousands of phenotypes A Annis, A Pandit, J LeFaive, SG Taliun, L Fritsche, P VandeHaar, ... | 6 | 2021 |
| FIVEx: an interactive multi-tissue eQTL browser A Kwong, AP Boughton, M Wang, P VandeHaar, M Boehnke, G Abecasis, ... bioRxiv, 2021.01. 22.426874, 2021 | 5 | 2021 |
| Genome-wide association study of 1,391 plasma metabolites in 6,136 finnish men identifies 303 novel signals and provides biological insights into human diseases X Yin, LS Chan, D Bose, AU Jackson, P VandeHaar, AE Locke, ... medRxiv, 2021.10. 19.21265094, 2021 | 3 | 2021 |
| Cancer PRSweb–an online Repository with polygenic risk scores (PRS) for major cancer traits and their Phenome-wide exploration in two independent biobanks LG Fritsche, S Patil, LJ Beesley, P VandeHaar, M Salvatore, RB Peng, ... bioRxiv, 2020.01. 22.915751, 2020 | 3 | 2020 |
| Exploring Various Polygenic Risk Scores for Basal Cell Carcinoma, Cutaneous Squamous Cell Carcinoma and Melanoma in the Phenomes of the Michigan Genomics Initiative and the UK … LG Fritsche, LJ Beesley, P VandeHaar, RB Peng, M Salvatore, ... bioRxiv, 384909, 2018 | 3 | 2018 |
| Simulating evolution of protein complexes through gene duplication and co-option L Haarsma, S Nelesen, E VanAndel, J Lamine, P VandeHaar Journal of Theoretical Biology 399, 22-32, 2016 | 3 | 2016 |
| The Michigan Genomics Initiative: A Model Framework for Genetic Discovery Using Patient Electronic Health Records EM Schmidt, LG Fritsche, S Lee, P VandeHaar, CM Brummett, ... Genetic Epidemiology 41 (7), 676-677, 2017 | 1 | 2017 |