KaraMohamed, S.
University of Chicago
3 papers on CoChat
Most cited papers
- Verified
Recurrent 16p11.2 microdeletions in autism
Kumar, R. A., KaraMohamed, S., Sudi, J., Conrad, D. F., Brune, C., Badner, J. A., Gilliam, T. C., Nowak, N. J., Cook, E. H., Dobyns, W. B., et al. (2007) · Human Molecular Genetics
Genomic variations and chromosomal abnormalitiesAutism Spectrum Disorder Research
Cited by 731
- Verified
Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder.
Christian, S. L., Brune, C. W., Sudi, J., Kumar, R. A., Liu, S., Karamohamed, S., Badner, J. A., Matsui, S., Conroy, J., McQuaid, D., et al. (2008) · Biological Psychiatry
Genomic variations and chromosomal abnormalitiesAutism Spectrum Disorder Research
Cited by 299
- Verified
Association and mutation analyses of 16p11.2 autism candidate genes
Kumar, R. A., Marshall, C. R., Badner, J. A., Babatz, T. D., Mukamel, Z., Aldinger, K. A., Sudi, J., Brune, C. W., Goh, G., KaraMohamed, S., et al. (2009) · PLoS ONE
Autism Spectrum Disorder ResearchGenomic variations and chromosomal abnormalities
Cited by 95
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