William Brandler
William Brandler
Verified email at databricks.com
Cited by
Cited by
A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects
C Marshall, D Howrigan, D Merico, B Thiruvahindrapuram, W Wu, D Greer, ...
Nature Genetics 49 (11), 27–35, 2016
Common variants in left/right asymmetry genes and pathways are associated with relative hand skill
WM Brandler, AP Morris, DM Evans, TS Scerri, JP Kemp, NJ Timpson, ...
PLoS genetics 9 (9), e1003751, 2013
PCSK6 is associated with handedness in individuals with dyslexia
TS Scerri, WM Brandler, S Paracchini, AP Morris, SM Ring, AJ Richardson, ...
Human molecular genetics 20 (3), 608-614, 2011
The genetic relationship between handedness and neurodevelopmental disorders
WM Brandler, S Paracchini
Trends in molecular medicine 20 (2), 83-90, 2014
Paternally inherited cis-regulatory structural variants are associated with autism
WM Brandler, D Antaki, M Gujral, ML Kleiber, J Whitney, MS Maile, ...
Science 360 (6386), 327-331, 2018
Genome‐wide screening for DNA variants associated with reading and language traits
A Gialluisi, DF Newbury, EG Wilcutt, RK Olson, JC DeFries, WM Brandler, ...
Genes, Brain and Behavior 13 (7), 686-701, 2014
Frequency and complexity of de novo structural mutation in autism
WM Brandler, D Antaki, M Gujral, A Noor, G Rosanio, TR Chapman, ...
The American Journal of Human Genetics 98 (4), 667-679, 2016
Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia
A Gialluisi, TFM Andlauer, N Mirza-Schreiber, K Moll, J Becker, ...
Translational psychiatry 9 (1), 1-15, 2019
From de novo mutations to personalized therapeutic interventions in autism
WM Brandler, J Sebat
Annual review of medicine 66, 487-507, 2015
Autism risk in offspring can be assessed through quantification of male sperm mosaicism
MW Breuss, D Antaki, RD George, M Kleiber, KN James, LL Ball, O Hong, ...
Nature medicine 26 (1), 143-150, 2020
SV2: accurate structural variation genotyping and de novo mutation detection from whole genomes
D Antaki, WM Brandler, J Sebat
Bioinformatics 34 (10), 1774-1777, 2018
Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia
NH Simpson, L Addis, WM Brandler, V Slonims, A Clark, J Watson, ...
Developmental Medicine & Child Neurology 56 (4), 346-353, 2014
The handedness-associated PCSK6 locus spans an intronic promoter regulating novel transcripts
R Shore, L Covill, KA Pettigrew, WM Brandler, R Diaz, Y Xu, JA Tello, ...
Human molecular genetics 25 (9), 1771-1779, 2016
The Genetic Revolution: Implications for our health, children, and gym attendance: Science Communication Competition Winning Article
W Brandler
The Biochemist 33 (4), 42-44, 2011
Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia
G Alessandro, AT FM, MS Nazanin, K Moll, J Becker, P Hoffmann, ...
Translational Psychiatry 9 (1), 2019
Methods for assessing risk of or diagnosing genetic defects by identifying de novo mutations or somatic mosaic variants in sperm or somatic tissues
J Gleeson, M Breuss, J Kiely, J Sebat, M Kleiber, D Antaki, W Brandler
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