Brandler, William M
University of California San Diego · Human Longevity (United States)
4 papers on CoChatORCID 0000-0001-5280-325X
Most cited papers
- Verified
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
Marshall, C. R., Howrigan, D. P., Merico, D., Thiruvahindrapuram, B., Wu, W., Greer, D. S., Antaki, D., Shetty, A., Holmans, P. A., Pinto, D., et al. (2017) · Nature Genetics
Genomic variations and chromosomal abnormalitiesSchizophrenia research and treatment
Cited by 1,058
- Verified
Paternally inherited cis-regulatory structural variants are associated with autism
Brandler, W. M., Antaki, D., Gujral, M., Kleiber, M. L., Whitney, J., Maile, M. S., Hong, O., Chapman, T. R., Tan, S., Tandon, P., et al. (2018) · Science
Autism Spectrum Disorder ResearchGenomic variations and chromosomal abnormalities
Cited by 209
- Verified
Frequency and complexity of de novo structural mutation in autism
Brandler, W. M., Antaki, D., Gujral, M., Noor, A., Rosanio, G., Chapman, T. R., Barrera, D. J., Lin, G. N., Malhotra, D., Watts, A. C., et al. (2016) · The American Journal of Human Genetics
Genomic variations and chromosomal abnormalitiesAutism Spectrum Disorder Research
Cited by 104
- Verified
SV2: accurate structural variation genotyping and de novo mutation detection from whole genomes
Antaki, D., Brandler, W. M., & Sebat, J. (2018) · Bioinformatics
Genomic variations and chromosomal abnormalitiesGenomics and Phylogenetic Studies
Cited by 45
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