Publications by authors named "Parisa Hemati"

6Publications

Domain-Specific Cognitive Impairments in Humans and Flies With Reduced CYFIP1 Dosage.

Biol Psychiatry 2019 08 17;86(4):306-314. Epub 2019 Apr 17.

Department of Genetics, Albert Einstein College of Medicine, Bronx, New York; Dominick P. Purpura Department of Neuroscience, Albert Einstein College of Medicine, Bronx, New York. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S00063223193127
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http://dx.doi.org/10.1016/j.biopsych.2019.04.008DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6679746PMC
August 2019

Loss-of-function variants in NFIA provide further support that NFIA is a critical gene in 1p32-p31 deletion syndrome: A four patient series.

Am J Med Genet A 2017 Dec 22;173(12):3158-3164. Epub 2017 Sep 22.

Department of Pediatrics, Division of Clinical Genetics, Columbia University Medical Center (CUMC), New York, New York.

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http://dx.doi.org/10.1002/ajmg.a.38460DOI Listing
December 2017

4q12-4q21.21 deletion genotype-phenotype correlation and the absence of piebaldism in presence of KIT haploinsufficiency.

Am J Med Genet A 2015 Jan 29;167A(1):231-7. Epub 2014 Oct 29.

Child and Family Research Institute, Vancouver, Canada; Department of Medical Genetics, University of British Columbia, Vancouver, Canada.

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http://doi.wiley.com/10.1002/ajmg.a.36821
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http://dx.doi.org/10.1002/ajmg.a.36821DOI Listing
January 2015