McMahon, William M.
Broad Institute · University of California, Los Angeles · Massachusetts General Hospital · Stanley Center for Psychiatric Research · Massachusetts Institute of Technology
23 papers on CoChat
Most cited papers
- Verified
Functional impact of global rare copy number variation in autism spectrum disorders
Pinto, D., Pagnamenta, A. T., Klei, L., Anney, R., Merico, D., Regan, R., Conroy, J., Magalhaes, T. R., Correia, C., Abrahams, B. S., et al. (2010) · Nature
Autism Spectrum Disorder ResearchGenomic variations and chromosomal abnormalities
Cited by 2,013
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Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
Glessner, J. T., Wang, K., Cai, G., Korvatska, O., Kim, C. E., Wood, S., Zhang, H., Estes, A., Brune, C. W., Bradfield, J. P., et al. (2009) · Nature
Autism Spectrum Disorder ResearchGenomic variations and chromosomal abnormalities
Cited by 1,421
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Common genetic variants on 5p14.1 associate with autism spectrum disorders
Wang, K., Zhang, H., Ma, D., Bucan, M., Glessner, J. T., Abrahams, B. S., Salyakina, D., Imielinski, M., Bradfield, J. P., Sleiman, P. M. A., et al. (2009) · Nature
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 989
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A genome-wide scan for common alleles affecting risk for autism
Anney, R., Klei, L., Pinto, D., Regan, R., Conroy, J., Magalhaes, T. R., Correia, C., Abrahams, B. S., Sykes, N., Pagnamenta, A. T., et al. (2010) · Human Molecular Genetics
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 593
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Twenty‐year outcome for individuals with autism and average or near‐average cognitive abilities
Farley, M. A., McMahon, W. M., Fombonne, E., Jenson, W. R., Miller, J., Gardner, M., Block, H., Pingree, C. B., Ritvo, E. R., Ritvo, R. A., et al. (2009) · Autism Research
Autism Spectrum Disorder ResearchFamily and Disability Support Research
Cited by 515
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Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes
Bucan, M., Abrahams, B. S., Wang, K., Glessner, J. T., Herman, E. I., Sonnenblick, L. I., Alvarez Retuerto, A. I., Imielinski, M., Hadley, D., Bradfield, J. P., et al. (2009) · PLoS Genetics
Autism Spectrum Disorder ResearchGenomic variations and chromosomal abnormalities
Cited by 424
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Repetitive Behavior Profiles in Asperger Syndrome and High-Functioning Autism
South, M., Ozonoff, S., & McMahon, W. M. (2005) · Journal of Autism and Developmental Disorders
Autism Spectrum Disorder ResearchChild Nutrition and Feeding Issues
Cited by 423
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Interrogating the Genetic Determinants of Tourette’s Syndrome and Other Tic Disorders Through Genome-Wide Association Studies
Yu, D., Sul, J. H., Tsetsos, F., Nawaz, M. S., Huang, A. Y., Zelaya, I., Illmann, C., Osiecki, L., Darrow, S. M., Hirschtritt, M. E., et al. (2019) · American Journal of Psychiatry
Obsessive-Compulsive Spectrum DisordersGenetic Associations and Epidemiology
Cited by 410
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Performance on Cambridge Neuropsychological Test Automated Battery subtests sensitive to frontal lobe function in people with autistic disorder: Evidence from the Collaborative Programs of Excellence in Autism network
Ozonoff, S., Cook, I., Coon, H., Dawson, G., Joseph, R. M., Klin, A., McMahon, W. M., Minshew, N., Munson, J. A., Pennington, B. F., et al. (2004) · Journal of Autism and Developmental Disorders
Autism Spectrum Disorder ResearchNeural and Behavioral Psychology Studies
Cited by 391
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Individual common variants exert weak effects on the risk for autism spectrum disorders
Anney, R., Klei, L., Pinto, D., Almeida, J., Bacchelli, E., Baird, G., Bolshakova, N., Bölte, S., Bolton, P. F., Bourgeron, T., et al. (2012) · Human Molecular Genetics
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 375
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Face processing in children with autism: Effects of stimulus contents and type
Speer, L. L., Cook, A. E., McMahon, W. M., & Clark, E. (2007) · Autism
Autism Spectrum Disorder ResearchFace Recognition and Perception
Cited by 342
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Psychiatric Comorbidity and Medication Use in Adults with Autism Spectrum Disorder
Buck, T. R., Viskochil, J., Farley, M., Coon, H., McMahon, W. M., Morgan, J., & Bilder, D. A. (2014) · Journal of Autism and Developmental Disorders
Autism Spectrum Disorder ResearchChild Nutrition and Feeding Issues
Cited by 323
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The UCLA-University of Utah epidemiologic survey of autism: prevalence
RITVO, E. R., Freeman, B. J., Pingree, C., MASON-BROTHERS, A., Jorde, L. B., Jenson, W. R., McMahon, W. M., Petersen, P. B., Mo, A., & Ritvo, A. (1989) · American Journal of Psychiatry
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 273
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A Candidate Gene Approach Identifies the CHRNA5-A3-B4 Region as a Risk Factor for Age-Dependent Nicotine Addiction
Weiss, R. B., Baker, T. B., Cannon, D. S., von Niederhausern, A., Dunn, D. M., Matsunami, N., Singh, N. A., Baird, L., Coon, H., McMahon, W. M., et al. (2008) · PLoS Genetics
Smoking Behavior and CessationGenetic Associations and Epidemiology
Cited by 271
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The relationship between executive functioning, central coherence, and repetitive behaviors in the high-functioning autism spectrum
South, M., Ozonoff, S., & Mcmahon, W. M. (2007) · Autism
Autism Spectrum Disorder ResearchDevelopmental and Educational Neuropsychology
Cited by 260
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The UCLA-University of Utah epidemiologic survey of autism: recurrence risk estimates and genetic counseling
RITVO, E. R., Jorde, L. B., MASON-BROTHERS, A., Freeman, B. J., Pingree, C., Jones, M. B., McMahon, W. M., Petersen, P. B., Jenson, W. R., & Mo, A. (1989) · American Journal of Psychiatry
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 255
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A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder
Casey, J. P., Magalhaes, T., Conroy, J. M., Regan, R., Shah, N., Anney, R., Shields, D. C., Abrahams, B. S., Almeida, J., Bacchelli, E., et al. (2012) · Human Genetics
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 200
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Is There a ‘Regressive Phenotype’ of Autism Spectrum Disorder Associated with the Measles-Mumps-Rubella Vaccine? A CPEA Study
Richler, J., Luyster, R., Risi, S., Hsu, W.-L., Dawson, G., Bernier, R., Dunn, M., Hepburn, S., Hyman, S. L., McMahon, W. M., et al. (2006) · Journal of Autism and Developmental Disorders
Autism Spectrum Disorder ResearchChild Nutrition and Feeding Issues
Cited by 149
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Evidence for multiple loci from a genome scan of autism kindreds
Schellenberg, G. D., Dawson, G., Sung, Y. J., Estes, A., Munson, J., Rosenthal, E., Rothstein, J., Flodman, P., Smith, M., Coon, H., et al. (2006) · Molecular Psychiatry
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 129
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Excess mortality and causes of death in autism spectrum disorders: a follow up of the 1980s Utah/UCLA autism epidemiologic study.
Bilder, D., Botts, E. L., Smith, K. R., Pimentel, R., Farley, M., Viskochil, J., McMahon, W. M., Block, H., Ritvo, E., Ritvo, R.-A., et al. (2013) · Journal of Autism and Developmental Disorders
Autism Spectrum Disorder ResearchDown syndrome and intellectual disability research
Cited by 116
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Confirmation of the association of the C4B null allelle in autism
Odell, D., Maciulis, A., Cutler, A., Warren, L., McMahon, W. M., Coon, H., Stubbs, G., Henley, K., & Torres, A. (2005) · Human Immunology
Autism Spectrum Disorder ResearchComplement system in diseases
Cited by 110
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A high-density SNP genome-wide linkage scan in a large autism extended pedigree
Allen-Brady, K., Miller, J., Matsunami, N., Stevens, J., Block, H., Farley, M., Krasny, L., Pingree, C., Lainhart, J., Leppert, M., et al. (2009) · Molecular Psychiatry
Autism Spectrum Disorder ResearchGenetic Associations and Epidemiology
Cited by 77
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Heterogeneous association between engrailed‐2 and autism in the CPEA network
Brune, C. W., Korvatska, E., Allen‐Brady, K., Cook, E. H., Dawson, G., Devlin, B., Estes, A., Hennelly, M., Hyman, S. L., McMahon, W. M., et al. (2008) · American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 40
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