Publications by authors named "Kira Apse"

Claim this Profile
E
Expanded mutational spectrum in Cohen syndrome, tissue expression, and transcript variants of COH1.
Wenke Seifert, Muriel Holder-Espinasse, Jirko Kühnisch, Kimia Kahrizi, Andreas Tzschach, Kira Apse

Hum Mutat· February 2009

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Identifying autism loci and genes by tracing recent shared ancestry.
Eric M Morrow, Seung-Yun Yoo, Steven W Flavell, Tae-Kyung Kim, Yingxi Lin, Kira A Apse

Science· July 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Comprehensive EMX2 genotyping of a large schizencephaly case series.
Ian Tietjen, Adria Bodell, Kira Apse, Ashley M Mendonza, Bernard S Chang

Am J Med Genet A· June 2007

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The role of RELN in lissencephaly and neuropsychiatric disease.
Bernard S Chang, Fusun Duzcan, Seonhee Kim, Mine Cinbis, Abha Aggarwal, Kira A Apse

Am J Med Genet B Neuropsychiatr Genet· January 2007

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
Deletion of chromosome 1p36 is associated with periventricular nodular heterotopia.
Jason Neal, Kira Apse, Mustafa Sahin, Christopher A Walsh, Volney L Sheen

Am J Med Genet A· August 2006

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Periventricular nodular heterotopia and Williams syndrome.
Russell J Ferland, John N Gaitanis, Kira Apse, Umadevi Tantravahi, Christopher A Walsh

Am J Med Genet A· June 2006

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
B
Bilateral periventricular heterotopias in an X-linked dominant transmission in a family with two affected males.
Marion Gérard-Blanluet, Volney Sheen, Kalotina Machinis, Jason Neal, Kira Apse

Am J Med Genet A· May 2006

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Cerebellar ataxia with progressive improvement.
Jack W Tsao, Jason Neal, Kira Apse, Mark J Stephan, William B Dobyns

Arch Neurol· April 2006

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
EMX2-independent familial schizencephaly: clinical and genetic analyses.
Ian Tietjen, Füsun Erdogan, Sophie Currier, Kira Apse, Bernard S Chang

Am J Med Genet A· June 2005

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Perceptions of genetic discrimination among at-risk relatives of colorectal cancer patients.
Kira A Apse, Barbara B Biesecker, Francis M Giardiello, Barbara P Fuller, Barbara A Bernhardt

Genet Med· February 2005

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Community involvement in developing policies for genetic testing: assessing the interests and experiences of individuals affected by genetic conditions.
Sarah E Gollust, Kira Apse, Barbara P Fuller, Paul Steven Miller, Barbara B Biesecker

Am J Public Health· January 2005

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis