| 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 | 2405 | 2012 |
| Genome structural variation discovery and genotyping C Alkan, BP Coe, EE Eichler Nature reviews genetics 12 (5), 363-376, 2011 | 1770 | 2011 |
| A copy number variation morbidity map of developmental delay GM Cooper, BP Coe, S Girirajan, JA Rosenfeld, TH Vu, C Baker, ... Nature genetics 43 (9), 838-846, 2011 | 1440 | 2011 |
| 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 | 1416 | 2012 |
| Disruptive CHD8 mutations define a subtype of autism early in development R Bernier, C Golzio, B Xiong, HA Stessman, BP Coe, O Penn, ... Cell 158 (2), 263-276, 2014 | 808 | 2014 |
| A tiling resolution DNA microarray with complete coverage of the human genome AS Ishkanian, CA Malloff, SK Watson, RJ DeLeeuw, B Chi, BP Coe, ... Nature genetics 36 (3), 299-303, 2004 | 802 | 2004 |
| Copy number variation detection and genotyping from exome sequence data N Krumm, PH Sudmant, A Ko, BJ O'Roak, M Malig, BP Coe, AR Quinlan, ... Genome research 22 (8), 1525-1532, 2012 | 709 | 2012 |
| A higher mutational burden in females supports a “female protective model” in neurodevelopmental disorders S Jacquemont, BP Coe, M Hersch, MH Duyzend, N Krumm, S Bergmann, ... The American Journal of Human Genetics 94 (3), 415-425, 2014 | 706 | 2014 |
| Refining analyses of copy number variation identifies specific genes associated with developmental delay BP Coe, K Witherspoon, JA Rosenfeld, BWM Van Bon, ... Nature genetics 46 (10), 1063-1071, 2014 | 657 | 2014 |
| Excess of rare, inherited truncating mutations in autism N Krumm, TN Turner, C Baker, L Vives, K Mohajeri, K Witherspoon, ... Nature genetics 47 (6), 582-588, 2015 | 636 | 2015 |
| Phenotypic heterogeneity of genomic disorders and rare copy-number variants S Girirajan, JA Rosenfeld, BP Coe, S Parikh, N Friedman, A Goldstein, ... New England Journal of Medicine 367 (14), 1321-1331, 2012 | 618 | 2012 |
| Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases HAF Stessman, BO Xiong, BP Coe, T Wang, K Hoekzema, M Fenckova, ... Nature genetics 49 (4), 515-526, 2017 | 534 | 2017 |
| Global diversity, population stratification, and selection of human copy-number variation PH Sudmant, S Mallick, BJ Nelson, F Hormozdiari, N Krumm, ... Science 349 (6253), aab3761, 2015 | 395 | 2015 |
| Relative burden of large CNVs on a range of neurodevelopmental phenotypes S Girirajan, Z Brkanac, BP Coe, C Baker, L Vives, TH Vu, N Shafer, ... PLoS genetics 7 (11), e1002334, 2011 | 369 | 2011 |
| A SWI/SNF-related autism syndrome caused by de novo mutations in ADNP C Helsmoortel, AT Vulto-van Silfhout, BP Coe, G Vandeweyer, L Rooms, ... Nature genetics 46 (4), 380-384, 2014 | 361 | 2014 |
| De novo genic mutations among a Chinese autism spectrum disorder cohort T Wang, H Guo, B Xiong, HAF Stessman, H Wu, BP Coe, TN Turner, Y Liu, ... Nature communications 7 (1), 13316, 2016 | 356 | 2016 |
| Genomic patterns of de novo mutation in simplex autism TN Turner, BP Coe, DE Dickel, K Hoekzema, BJ Nelson, MC Zody, ... Cell 171 (3), 710-722. e12, 2017 | 347 | 2017 |
| Refinement and discovery of new hotspots of copy-number variation associated with autism spectrum disorder S Girirajan, MY Dennis, C Baker, M Malig, BP Coe, CD Campbell, K Mark, ... The American Journal of Human Genetics 92 (2), 221-237, 2013 | 346 | 2013 |
| Estimates of penetrance for recurrent pathogenic copy-number variations JA Rosenfeld, BP Coe, EE Eichler, H Cuckle, LG Shaffer Genetics in Medicine 15 (6), 478-481, 2013 | 343 | 2013 |
| Neurodevelopmental disease genes implicated by de novo mutation and copy number variation morbidity BP Coe, HAF Stessman, A Sulovari, MR Geisheker, TE Bakken, AM Lake, ... Nature genetics 51 (1), 106-116, 2019 | 281 | 2019 |
