Ravinesh A Kumar

Ravinesh A Kumar

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Ravinesh A Kumar

Ravinesh A Kumar

Publications by authors named "Ravinesh A Kumar"

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15Publications

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The Influence of Microdeletions and Microduplications of 16p11.2 on Global Transcription Profiles.

J Child Neurol 2015 Dec 20;30(14):1947-53. Epub 2015 Sep 20.

Beyster Center for Genomics of Psychiatric Diseases, Department of Psychiatry, and Department of Cellular and Molecular Medicine, University of California, San Diego, La Jolla, CA, USA

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http://dx.doi.org/10.1177/0883073815602066DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4739844PMC
December 2015

Duplication 16p11.2 in a child with infantile seizure disorder.

Am J Med Genet A 2010 Jun;152A(6):1567-74

Department of Pediatrics, The University of Michigan, Ann Arbor, Michigan 48109-5652, USA.

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http://dx.doi.org/10.1002/ajmg.a.33415DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3160635PMC
June 2010

Copy number and sequence variants implicate APBA2 as an autism candidate gene.

Autism Res 2009 Dec;2(6):359-64

Department of Human Genetics, University of Chicago, Chicago, Illinois 60637-5415, USA.

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http://dx.doi.org/10.1002/aur.107DOI Listing
December 2009

Genetics of autism spectrum disorders.

Curr Neurol Neurosci Rep 2009 May;9(3):188-97

Department of Human Genetics, University of Chicago, 920 East 58th Street, MC0077, Chicago, IL 60637, USA.

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May 2009

Recurrent 16p11.2 microdeletions in autism.

Hum Mol Genet 2008 Feb 21;17(4):628-38. Epub 2007 Dec 21.

Department of Human Genetics, University of Chicago, Chicago, IL 60637, USA.

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http://dx.doi.org/10.1093/hmg/ddm376DOI Listing
February 2008

Absence of mutations in NR2E1 and SNX3 in five patients with MMEP (microcephaly, microphthalmia, ectrodactyly, and prognathism) and related phenotypes.

BMC Med Genet 2007 Jul 26;8:48. Epub 2007 Jul 26.

Centre for Molecular Medicine and Therapeutics, Child & Family Research Institute, Department of Medical Genetics, University of British Columbia, 950 West 28th Ave, Vancouver, V5Z 4H4, Canada.

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http://dx.doi.org/10.1186/1471-2350-8-48DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1950490PMC
July 2007

Unexpected embryonic stem (ES) cell mutations represent a concern in gene targeting: lessons from "fierce" mice.

Genesis 2004 Feb;38(2):51-7

Doctorate Program in Medical Genetics, University of British Columbia, Vancouver, British Columbia, V5Z 4H4 Canada.

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http://doi.wiley.com/10.1002/gene.20001
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http://dx.doi.org/10.1002/gene.20001DOI Listing
February 2004