| Functional impact of global rare copy number variation in autism spectrum disorder D Pinto, AT Pagnamenta, L Klei, R Anney, D Merico, R Regan, J Conroy, ... Nature 466 (7304), 368, 2010 | 2335 | 2010 |
| A genome-wide scan for common alleles affecting risk for autism R Anney, L Klei, D Pinto, R Regan, J Conroy, TR Magalhaes, C Correia, ... Human molecular genetics 19 (20), 4072-4082, 2010 | 729 | 2010 |
| Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants D Pinto, K Darvishi, X Shi, D Rajan, D Rigler, T Fitzgerald, AC Lionel, ... Nature biotechnology 29 (6), 512-520, 2011 | 482 | 2011 |
| SHANK1 deletions in males with autism spectrum disorder D Sato, AC Lionel, CS Leblond, A Prasad, D Pinto, S Walker, I O'Connor, ... The American Journal of Human Genetics 90 (5), 879-887, 2012 | 391 | 2012 |
| Pan-cancer analysis of whole genomes ITPCAWG Consortium Nature 578 (7793), 82-93, 2020 | 293* | 2020 |
| Rare deletions at the neurexin 3 locus in autism spectrum disorder AK Vaags, AC Lionel, D Sato, MK Goodenberger, QP Stein, S Curran, ... The American Journal of Human Genetics 90 (1), 133-141, 2012 | 260 | 2012 |
| A discovery resource of rare copy number variations in individuals with autism spectrum disorder A Prasad, D Merico, B Thiruvahindrapuram, J Wei, AC Lionel, D Sato, ... G3: Genes| Genomes| Genetics 2 (12), 1665-1685, 2012 | 219 | 2012 |
| Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures AC Lionel, AK Vaags, D Sato, MJ Gazzellone, EB Mitchell, HY Chen, ... Human molecular genetics 22 (10), 2055-2066, 2013 | 183 | 2013 |
| Methods and compositions for screening and treating developmental disorders E Hatchwell, PS Eis, S Scherer, A Prasad US Patent 10,233,495, 2019 | 136* | 2019 |
| A whole genome scan to map QTL for milk production traits and somatic cell score in Canadian Holstein bulls D Kolbehdari, Z Wang, JR Grant, B Murdoch, A Prasad, Z Xiu, E Marques, ... Journal of animal breeding and genetics 126 (3), 216-227, 2009 | 124 | 2009 |
| A first generation whole genome RH map of the river buffalo with comparison to domestic cattle MEJ Amaral, JR Grant, PK Riggs, NB Stafuzza, EA Rodrigues Filho, ... BMC genomics 9 (1), 631, 2008 | 99 | 2008 |
| A whole-genome scan to map quantitative trait loci for conformation and functional traits in Canadian Holstein bulls D Kolbehdari, Z Wang, JR Grant, B Murdoch, A Prasad, Z Xiu, E Marques, ... Journal of dairy science 91 (7), 2844-2856, 2008 | 96 | 2008 |
| Identification of gene mutations and fusion genes in patients with Sezary Syndrome A Prasad, R Rabionet, B Espinet, L Zapata, A Puiggros, C Melero, A Puig, ... Journal of Investigative Dermatology 136 (7), 1490-1499, 2016 | 94 | 2016 |
| Chromosomal Microarray Analysis of Consecutive Individuals with Autism Spectrum Disorders Using an Ultra-High Resolution Chromosomal Microarray Optimized for Neurodevelopmental … KS Ho, ER Wassman, AL Baxter, CH Hensel, MM Martin, A Prasad, ... International Journal of Molecular Sciences 17 (12), 2070, 2016 | 76 | 2016 |
| Linkage disequilibrium and signatures of selection on chromosomes 19 and 29 in beef and dairy cattle A Prasad, RD Schnabel, SD McKay, B Murdoch, P Stothard, D Kolbehdari, ... Animal genetics 39 (6), 597-605, 2008 | 52 | 2008 |
| A second generation radiation hybrid map to aid the assembly of the bovine genome sequence OC Jann, J Aerts, M Jones, N Hastings, A Law, S McKay, E Marques, ... BMC genomics 7 (1), 283, 2006 | 40 | 2006 |
| Methods and compositions for screening and treating developmental disorders E Hatchwell, PS Eis, S Scherer, A Prasad US Patent 10,407,724, 2019 | 35 | 2019 |
| Germline determinants of the somatic mutation landscape in 2,642 cancer genomes SM Waszak, G Tiao, B Zhu, T Rausch, F Muyas, B Rodriguez-Martin, ... bioRxiv, 208330, 2017 | 34 | 2017 |
| A 2cM genome-wide scan of European Holstein cattle affected by classical BSE BM Murdoch, ML Clawson, WW Laegreid, P Stothard, M Settles, S McKay, ... BMC genetics 11 (1), 20, 2010 | 29 | 2010 |
| Clinical utility of exome sequencing in individuals with large homozygous regions detected by chromosomal microarray analysis A Prasad, MA Sdano, RJ Vanzo, PA Mowery-Rushton, MA Serrano, ... BMC Medical Genetics 19 (1), 46, 2018 | 27 | 2018 |
