| Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations BJ O’Roak, L Vives, S Girirajan, E Karakoc, N Krumm, BP Coe, R Levy, ... Nature 485 (7397), 246-250, 2012 | 2387 | 2012 |
| Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders BJ O’Roak, L Vives, W Fu, JD Egertson, IB Stanaway, IG Phelps, G Carvill, ... Science 338 (6114), 1619-1622, 2012 | 1394 | 2012 |
| A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose GM Cooper, JA Johnson, TY Langaee, H Feng, IB Stanaway, UI Schwarz, ... Blood, The Journal of the American Society of Hematology 112 (4), 1022-1027, 2008 | 528 | 2008 |
| Identification, replication, and functional fine-mapping of expression quantitative trait loci in primary human liver tissue F Innocenti, GM Cooper, IB Stanaway, ER Gamazon, JD Smith, S Mirkov, ... PLoS genetics 7 (5), e1002078, 2011 | 269 | 2011 |
| Genome-wide modeling of polygenic risk score in colorectal cancer risk M Thomas, LC Sakoda, M Hoffmeister, EA Rosenthal, JK Lee, ... The American journal of human genetics 107 (3), 432-444, 2020 | 137 | 2020 |
| GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network B Namjou, T Lingren, Y Huang, S Parameswaran, BL Cobb, IB Stanaway, ... BMC medicine 17, 1-19, 2019 | 127 | 2019 |
| Large-scale genome-wide association study of coronary artery disease in genetically diverse populations C Tcheandjieu, X Zhu, AT Hilliard, SL Clarke, V Napolioni, S Ma, KM Lee, ... Nature medicine 28 (8), 1679-1692, 2022 | 121 | 2022 |
| Harmonizing clinical sequencing and interpretation for the eMERGE III network H Zouk, E Venner, NJ Lennon, DM Muzny, D Abrams, S Adunyah, ... The American Journal of Human Genetics 105 (3), 588-605, 2019 | 93 | 2019 |
| Frequency of genomic secondary findings among 21,915 eMERGE network participants AS Gordon, H Zouk, E Venner, CM Eng, BH Funke, LM Amendola, ... Genetics in Medicine 22 (9), 1470-1477, 2020 | 76 | 2020 |
| The eMERGE genotype set of 83,717 subjects imputed to~ 40 million variants genome wide and association with the herpes zoster medical record phenotype IB Stanaway, TO Hall, EA Rosenthal, M Palmer, V Naranbhai, R Knevel, ... Genetic epidemiology 43 (1), 63-81, 2019 | 75 | 2019 |
| Burden of potentially pathologic copy number variants is higher in children with isolated congenital heart disease and significantly impairs covariate-adjusted transplant-free … DS Kim, JH Kim, AA Burt, DR Crosslin, N Burnham, CE Kim, ... The Journal of thoracic and cardiovascular surgery 151 (4), 1147-1151. e4, 2016 | 74 | 2016 |
| A genome-wide association study of polycystic ovary syndrome identified from electronic health records Y Zhang, K Ho, JM Keaton, DN Hartzel, F Day, AE Justice, NS Josyula, ... American journal of obstetrics and gynecology 223 (4), 559. e1-559. e21, 2020 | 57 | 2020 |
| An atlas of genetic variation linking pathogen-induced cellular traits to human disease L Wang, KJ Pittman, JR Barker, RE Salinas, IB Stanaway, GD Williams, ... Cell host & microbe 24 (2), 308-323. e6, 2018 | 53 | 2018 |
| A polygenic and phenotypic risk prediction for polycystic ovary syndrome evaluated by phenome-wide association studies YY Joo, KE Actkins, JA Pacheco, AO Basile, R Carroll, DR Crosslin, F Day, ... The Journal of Clinical Endocrinology & Metabolism 105 (6), 1918-1936, 2020 | 51 | 2020 |
| Genomic and functional characterization of a mucosal symbiont involved in early-stage colorectal cancer MC Kordahi, IB Stanaway, M Avril, D Chac, MP Blanc, B Ross, C Diener, ... Cell host & microbe 29 (10), 1589-1598. e6, 2021 | 46 | 2021 |
| IGF1R variants associated with isolated single suture craniosynostosis ML Cunningham, JA Horst, MJ Rieder, AV Hing, IB Stanaway, SS Park, ... American Journal of Medical Genetics Part A 155 (1), 91-97, 2011 | 46 | 2011 |
| Direct detection of null alleles in SNP genotyping data CS Carlson, JD Smith, IB Stanaway, MJ Rieder, DA Nickerson Human molecular genetics 15 (12), 1931-1937, 2006 | 46 | 2006 |
| Genetic candidate variants in two multigenerational families with childhood apraxia of speech B Peter, EM Wijsman, AQ Nato Jr, ... PloS one 11 (4), e0153864, 2016 | 42 | 2016 |
| Medical records-based chronic kidney disease phenotype for clinical care and “big data” observational and genetic studies N Shang, A Khan, F Polubriaginof, F Zanoni, K Mehl, D Fasel, PE Drawz, ... Npj Digital Medicine 4 (1), 70, 2021 | 41 | 2021 |
| Association of rare missense variants in the second intracellular loop of NaV1. 7 sodium channels with familial autism M Rubinstein, A Patowary, IB Stanaway, E McCord, RR Nesbitt, M Archer, ... Molecular psychiatry 23 (2), 231-239, 2018 | 39 | 2018 |
