Lamb, Allen N.
University of Utah · ARUP Laboratories (United States)
5 papers on CoChat
Most cited papers
- Verified
Chromosomal microarray versus karyotyping for prenatal diagnosis
Wapner, R. J., Martin, C. L., Levy, B., Ballif, B. C., Eng, C. M., Zachary, J. M., Savage, M., Platt, L. D., Saltzman, D., Grobman, W. A., et al. (2012) · New England Journal of Medicine
Prenatal Screening and DiagnosticsGenomic variations and chromosomal abnormalities
Cited by 1,412
- Verified
Copy number variations associated with autism spectrum disorders contribute to a spectrum of neurodevelopmental disorders
Rosenfeld, J. A., Ballif, B. C., Torchia, B. S., Sahoo, T., Ravnan, J. B., Schultz, R., Lamb, A., Bejjani, B. A., & Shaffer, L. G. (2010) · Genetics in Medicine
Genomic variations and chromosomal abnormalitiesAutism Spectrum Disorder Research
Cited by 169
- Verified
Copy number variants of schizophrenia susceptibility loci are associated with a spectrum of speech and developmental delays and behavior problems
Sahoo, T., Theisen, A., Rosenfeld, J. A., Lamb, A. N., Ravnan, J. B., Schultz, R. A., Torchia, B. S., Neill, N., Casci, I., Bejjani, B. A., et al. (2011) · Genetics in Medicine
Genomic variations and chromosomal abnormalitiesSchizophrenia research and treatment
Cited by 115
- Verified
MEF2C Haploinsufficiency features consistent hyperkinesis, variable epilepsy, and has a role in dorsal and ventral neuronal developmental pathways
Paciorkowski, A. R., Traylor, R. N., Rosenfeld, J. A., Hoover, J. M., Harris, C. J., Winter, S., Lacassie, Y., Bialer, M., Lamb, A. N., Schultz, R. A., et al. (2013) · neurogenetics
Genetics and Neurodevelopmental DisordersGenomic variations and chromosomal abnormalities
Cited by 109
- Verified
Haploinsufficiency of SOX5 at 12p12.1 is associated with developmental delays with prominent language delay, behavior problems, and mild dysmorphic features
Lamb, A. N., Rosenfeld, J. A., Neill, N. J., Talkowski, M. E., Blumenthal, I., Girirajan, S., Keelean-Fuller, D., Fan, Z., Pouncey, J., Stevens, C., et al. (2012) · Human Mutation
Genomic variations and chromosomal abnormalitiesGenetics and Neurodevelopmental Disorders
Cited by 107
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