Publications by authors named "Stuart W Tinker"

Claim this Profile
A
An examination of the relationship between hotspots and recombination associated with chromosome 21 nondisjunction.
Tiffany Renee Oliver, Candace D Middlebrooks, Stuart W Tinker, Emily Graves Allen, Lora J H Bean

PLoS One· October 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Evidence for dysregulation of genome-wide recombination in oocytes with nondisjoined chromosomes 21.
Candace D Middlebrooks, Nandita Mukhopadhyay, Stuart W Tinker, Emily Graves Allen, Lora J H Bean

Hum Mol Genet· January 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Free the data: one laboratory's approach to knowledge-based genomic variant classification and preparation for EMR integration of genomic data.
Lora J H Bean, Stuart W Tinker, Cristina da Silva, Madhuri R Hegde

Hum Mutat· September 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Preconception folic acid supplementation and risk for chromosome 21 nondisjunction: a report from the National Down Syndrome Project.
NaTasha D Hollis, Emily G Allen, Tiffany Renee Oliver, Stuart W Tinker, Charlotte Druschel

Am J Med Genet A· March 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Altered patterns of multiple recombinant events are associated with nondisjunction of chromosome 21.
Tiffany Renee Oliver, Stuart W Tinker, Emily Graves Allen, Natasha Hollis, Adam E Locke

Hum Genet· July 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The FMR1 premutation and attention-deficit hyperactivity disorder (ADHD): evidence for a complex inheritance.
Jessica Ezzell Hunter, Michael P Epstein, Stuart W Tinker, Ann Abramowitz, Stephanie L Sherman

Behav Genet· May 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Lack of maternal folic acid supplementation is associated with heart defects in Down syndrome: a report from the National Down Syndrome Project.
Lora J H Bean, Emily G Allen, Stuart W Tinker, Natasha D Hollis, Adam E Locke

Birth Defects Res A Clin Mol Teratol· October 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
V
Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome.
Adam E Locke, Kenneth J Dooley, Stuart W Tinker, Soo Yeon Cheong, Eleanor Feingold

Genet Epidemiol· September 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Fragile X-associated primary ovarian insufficiency: evidence for additional genetic contributions to severity.
Jessica Ezzell Hunter, Michael P Epstein, Stuart W Tinker, Krista H Charen, Stephanie L Sherman

Genet Epidemiol· September 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Ethnicity, sex, and the incidence of congenital heart defects: a report from the National Down Syndrome Project.
Sallie B Freeman, Lora H Bean, Emily G Allen, Stuart W Tinker, Adam E Locke

Genet Med· March 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The National Down Syndrome Project: design and implementation.
Sallie B Freeman, Emily G Allen, Cindy L Oxford-Wright, Stuart W Tinker, Charlotte Druschel

Public Health Rep· February 2007

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis