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William Brandler
William Brandler
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Year
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
935*2016
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
2072018
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
1752013
The genetic relationship between handedness and neurodevelopmental disorders
WM Brandler, S Paracchini
Trends in molecular medicine 20 (2), 83-90, 2014
1722014
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
1622011
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
1412014
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
1112016
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), 77, 2019
1042019
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
852020
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
552018
From de novo mutations to personalized therapeutic interventions in autism
WM Brandler, J Sebat
Annual review of medicine 66, 487-507, 2015
522015
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
502014
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
92016
Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions
EA Maury, MA Sherman, G Genovese, TG Gilgenast, T Kamath, SJ Burris, ...
Cell Genomics 3 (8), 2023
42023
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
12011
Advancements in somatic variant calling from UG100 whole genome and whole exome sequencing data
D Shem-Tov, M Levy, G Hornung, I Soifer, H Benjamin, A Jaimovich, ...
Cancer Research 84 (6_Supplement), 4926-4926, 2024
2024
Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia
G Alessandro, MS Nazanin, K Moll, J Becker, P Hoffmann, KU Ludwig, ...
Translational Psychiatry 9 (1), 2019
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
2018
SV2: Accurate Structural Variation Genotyping andDe NovoMutation Detection from Whole Genomes
D Antaki, WM Brandler, J Sebat
2017
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Articles 1–19