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Aparna Prasad
Aparna Prasad
Invitae
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Cited by
Year
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
23112010
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
7182010
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
4762011
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
3892012
Pan-cancer analysis of whole genomes
ITPCAWG Consortium
Nature 578 (7793), 82-93, 2020
272*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
2562012
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
2132012
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
1832013
Methods and compositions for screening and treating developmental disorders
E Hatchwell, PS Eis, S Scherer, A Prasad
US Patent 10,233,495, 2019
131*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
1202009
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
1022008
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
942008
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
932016
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
732016
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
522008
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
382006
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
342017
Methods and compositions for screening and treating developmental disorders
E Hatchwell, PS Eis, S Scherer, A Prasad
US Patent 10,407,724, 2019
332019
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
292010
High resolution radiation hybrid maps of bovine chromosomes 19 and 29: comparison with the bovine genome sequence assembly
A Prasad, T Schiex, S McKay, B Murdoch, Z Wang, JE Womack, ...
BMC genomics 8 (1), 310, 2007
262007
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