Ian Stanaway
Cited by
Cited by
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
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
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 112 (4), 1022-1027, 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 Genet 7 (5), e1002078, 2011
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
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
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
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), 1-19, 2019
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
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
The environmental genome project: reference polymorphisms for drug metabolism genes and genome-wide association studies
MJ Rieder, RJ Livingston, IB Stanaway, DA Nickerson
Drug metabolism reviews 40 (2), 241-261, 2008
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
Patient genotypes impact survival after surgery for isolated congenital heart disease
DS Kim, JH Kim, AA Burt, DR Crosslin, N Burnham, ...
The Annals of thoracic surgery 98 (1), 104-111, 2014
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
Association of rare missense variants in the second intracellular loop of Na V 1.7 sodium channels with familial autism
M Rubinstein, A Patowary, IB Stanaway, E McCord, RR Nesbitt, M Archer, ...
Molecular psychiatry 23 (2), 231-239, 2018
Human oral buccal microbiomes are associated with farmworker status and azinphos-methyl agricultural pesticide exposure
IB Stanaway, JC Wallace, A Shojaie, WC Griffith, S Hong, CS Wilder, ...
Applied and environmental microbiology 83 (2), 2017
Identification of rare variants from exome sequence in a large pedigree with autism
EE Marchani, NH Chapman, CYK Cheung, K Ankenman, IB Stanaway, ...
Human heredity 74 (3-4), 153-164, 2012
Atlas-CNV: a validated approach to call single-exon CNVs in the eMERGESeq gene panel
T Chiang, X Liu, TJ Wu, J Hu, FJ Sedlazeck, S White, D Schaid, ...
Genetics in Medicine 21 (9), 2135-2144, 2019
Results of genome-wide analyses on neurodevelopmental phenotypes at four-year follow-up following cardiac surgery in infancy
DS Kim, IB Stanaway, R Rajagopalan, JC Bernbaum, CB Solot, ...
PLoS One 7 (9), e45936, 2012
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
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