| Computationally efficient whole-genome regression for quantitative and binary traits J Mbatchou, L Barnard, J Backman, A Marcketta, JA Kosmicki, ... Nature genetics 53 (7), 1097-1103, 2021 | 604 | 2021 |
| Exome sequencing and analysis of 454,787 UK Biobank participants JD Backman, AH Li, A Marcketta, D Sun, J Mbatchou, MD Kessler, ... Nature 599 (7886), 628-634, 2021 | 480 | 2021 |
| Exome sequencing and characterization of 49,960 individuals in the UK Biobank CV Van Hout, I Tachmazidou, JD Backman, JD Hoffman, D Liu, ... Nature 586 (7831), 749-756, 2020 | 398 | 2020 |
| Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations CG Boer, K Hatzikotoulas, L Southam, L Stefánsdóttir, Y Zhang, ... Cell 184 (18), 4784-4818. e17, 2021 | 301 | 2021 |
| GlycReSoft: A Software Package for Automated Recognition of Glycans from LC/MS Data E Maxwell, Y Tan, Y Tan, H Hu, G Benson, K Aizikov, S Conley, ... PLOS ONE 7 (9), e45474, 2012 | 157 | 2012 |
| Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease JE Horowitz, JA Kosmicki, A Damask, D Sharma, GHL Roberts, AE Justice, ... Nature genetics 54 (4), 382-392, 2022 | 113 | 2022 |
| Whole exome sequencing and characterization of coding variation in 49,960 individuals in the UK Biobank CV Van Hout, I Tachmazidou, JD Backman, JX Hoffman, B Ye, AK Pandey, ... BioRxiv, 572347, 2019 | 110 | 2019 |
| CLAMMS: a scalable algorithm for calling common and rare copy number variants from exome sequencing data JS Packer, EK Maxwell, C O’Dushlaine, AE Lopez, FE Dewey, ... Bioinformatics 32 (1), 133-135, 2016 | 100 | 2016 |
| Global gene expression analysis of murine limb development L Taher, NM Collette, D Murugesh, E Maxwell, I Ovcharenko, GG Loots PloS one 6 (12), e28358, 2011 | 100 | 2011 |
| An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs HJ Cordell, JJ Fryett, K Ueno, R Darlay, Y Aiba, Y Hitomi, M Kawashima, ... Journal of hepatology 75 (3), 572-581, 2021 | 94 | 2021 |
| Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals JA Kosmicki, JE Horowitz, N Banerjee, R Lanche, A Marcketta, E Maxwell, ... The American Journal of Human Genetics 108 (7), 1350-1355, 2021 | 83 | 2021 |
| Diagnosing memory leaks using graph mining on heap dumps EK Maxwell, G Back, N Ramakrishnan Proceedings of the 16th ACM SIGKDD international conference on Knowledge …, 2010 | 72 | 2010 |
| Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline M Gorski, B Jung, Y Li, PR Matias-Garcia, M Wuttke, S Coassin, CHL Thio, ... Kidney international 99 (4), 926-939, 2021 | 58 | 2021 |
| Identification of neuropsychiatric copy number variants in a health care system population CL Martin, KE Wain, MT Oetjens, K Tolwinski, E Palen, A Hare-Harris, ... JAMA psychiatry 77 (12), 1276-1285, 2020 | 54 | 2020 |
| Profiling and leveraging relatedness in a precision medicine cohort of 92,455 exomes J Staples, EK Maxwell, N Gosalia, C Gonzaga-Jauregui, C Snyder, ... The American Journal of Human Genetics 102 (5), 874-889, 2018 | 53 | 2018 |
| MicroRNAs and essential components of the microRNA processing machinery are not encoded in the genome of the ctenophore Mnemiopsis leidyi EK Maxwell, JF Ryan, CE Schnitzler, WE Browne, AD Baxevanis BMC genomics 13, 1-11, 2012 | 53 | 2012 |
| Evolutionary profiling reveals the heterogeneous origins of classes of human disease genes: implications for modeling disease genetics in animals EK Maxwell, CE Schnitzler, P Havlak, NH Putnam, AD Nguyen, ... BMC evolutionary biology 14, 1-18, 2014 | 48 | 2014 |
| Polygenic risk of psychiatric disorders exhibits cross-trait associations in electronic health record data from European ancestry individuals RL Kember, AK Merikangas, SS Verma, A Verma, R Judy, G Abecasis, ... Biological psychiatry 89 (3), 236-245, 2021 | 34 | 2021 |
| Common genetic variants identify therapeutic targets for COVID-19 and individuals at high risk of severe disease JE Horowitz, JA Kosmicki, A Damask, D Sharma, GHL Roberts, AE Justice, ... MedRxiv, 2020 | 23 | 2020 |
| SubmiRine: assessing variants in microRNA targets using clinical genomic data sets EK Maxwell, JD Campbell, A Spira, AD Baxevanis Nucleic Acids Research 43 (8), 3886-3898, 2015 | 21 | 2015 |
