Publications by authors named "Irina R Tikhonova"

9Publications

Mutations disrupting neuritogenesis genes confer risk for cerebral palsy.

Nat Genet 2020 10 28;52(10):1046-1056. Epub 2020 Sep 28.

Pediatric Movement Disorders Program, Division of Pediatric Neurology, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ, USA.

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http://dx.doi.org/10.1038/s41588-020-0695-1DOI Listing
October 2020

Genetic diagnosis of neuroacanthocytosis disorders using exome sequencing.

Mov Disord 2012 Apr 28;27(4):539-43. Epub 2011 Oct 28.

Department of Neurology, James J Peters Veterans Affairs Medical Center, Bronx, New York 10468, USA.

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http://dx.doi.org/10.1002/mds.24020DOI Listing
April 2012

Genetic diagnosis by whole exome capture and massively parallel DNA sequencing.

Proc Natl Acad Sci U S A 2009 Nov 27;106(45):19096-101. Epub 2009 Oct 27.

Department of Genetics, Howard Hughes Medical Institute, Yale University School of Medicine, New Haven, CT 06510, USA.

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http://dx.doi.org/10.1073/pnas.0910672106DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2768590PMC
November 2009