International Standards for Cytogenomic Arrays

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Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.

David T. Miller, Margaret P. Adam, Margaret P. Adam, et al.. (2010). American journal of human genetics. Cited 2,651 times. https://doi.org/10.1016/j.ajhg.2010.04.006

An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities

E. B. Kaminsky, V. Kaul, J. Paschall, et al.. (2011). Genetics in Medicine. Cited 425 times. https://doi.org/10.1097/GIM.0b013e31822c79f9

Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia.

D. Moreno-De-Luca, J. Mulle, E. B. Kaminsky, et al.. (2010). American journal of human genetics. Cited 335 times. https://doi.org/10.1016/j.ajhg.2010.10.004

Enhanced detection of clinically relevant genomic imbalances using a targeted plus whole genome oligonucleotide microarray

E. L. Baldwin, Jiyun Lee, Douglas M Blake, et al.. (2008). Genetics in Medicine. Cited 188 times. https://doi.org/10.1097/GIM.0b013e318177015c

Using large clinical data sets to infer pathogenicity for rare copy number variants in autism cohorts

D. Moreno-De-Luca, Stephan J Sanders, A. Willsey, et al.. (2012). Molecular Psychiatry. Cited 164 times. https://doi.org/10.1038/mp.2012.138

Towards an evidence‐based process for the clinical interpretation of copy number variation

E. Riggs, Deanna M. Church, K. Hanson, et al.. (2012). Clinical Genetics. Cited 116 times. https://doi.org/10.1111/j.1399-0004.2011.01818.x

Phenotypic information in genomic variant databases enhances clinical care and research: The international standards for cytogenomic arrays consortium experience

E. Riggs, L. Jackson, David T. Miller, et al.. (2012). Human Mutation. Cited 62 times. https://doi.org/10.1002/humu.22052

The Laboratory-Clinician Team: A Professional Call to Action to Improve Communication and Collaboration for Optimal Patient Care in Chromosomal Microarray Testing

K. Wain, E. Riggs, Karen Hanson, et al.. (2012). Journal of Genetic Counseling. Cited 14 times. https://doi.org/10.1007/s10897-012-9507-9
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