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Emily Allen

Research Profile

Chemicals & Drugs

Disorders

Concepts & Ideas

Anatomy

Chromosomes, Human, Pair 21

Physiology

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Publications

TOP 3
NaTasha D Hollis; Leslie A O'Leary; Tiffany Renee Oliver; Paul A Romitti; Marjorie H Royle; Stephanie L Sherman; Stuart W Tinker; Claudine P Torfs; Emily G Allen; Charlotte M Druschel; Sallie B Freeman; Charlotte A Hobbs; Lora J H Bean
Preconception folic acid supplementation and risk for chromosome 21 nondisjunction: a report from the National Down Syndrome Project.
Jorge L Juncos; Joash T Lazarus; Gloria Novak; Julia Rohr; Emily G Allen; Debra Hamilton; Lisa Shubeck; Stephanie L Sherman
Olfactory dysfunction in fragile X tremor ataxia syndrome.
Tiffany Renee Oliver; Stuart W Tinker; Emily G Allen; Lora J H Bean; Ferdouse Begum; Vivian Cheung; Reshmi Chowdhury; Eleanor Feingold; Natasha Hollis; Adam E Locke; Mary Marazita; Stephanie L Sherman
Altered patterns of multiple recombinant events are associated with nondisjunction of chromosome 21.

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All Publications

2013: NaTasha D Hollis; Leslie A O'Leary; Tiffany Renee Oliver; Paul A Romitti; Marjorie H Royle; Stephanie L Sherman; Stuart W Tinker; Claudine P Torfs; Emily G Allen; Charlotte M Druschel; Sallie B Freeman; Charlotte A Hobbs; Lora J H Bean
Preconception folic acid supplementation and risk for chromosome 21 nondisjunction: a report from the National Down Syndrome Project.
American journal of medical genetics. Part A 2013;161(3):438-44.
2012: Jorge L Juncos; Joash T Lazarus; Gloria Novak; Julia Rohr; Emily G Allen; Debra Hamilton; Lisa Shubeck; Stephanie L Sherman
Olfactory dysfunction in fragile X tremor ataxia syndrome.
Movement disorders : official journal of the Movement Disorder Society 2012;27(12):1556-9.
2012: Tiffany Renee Oliver; Stuart W Tinker; Emily G Allen; Lora J H Bean; Ferdouse Begum; Vivian Cheung; Reshmi Chowdhury; Eleanor Feingold; Natasha Hollis; Adam E Locke; Mary Marazita; Stephanie L Sherman
Altered patterns of multiple recombinant events are associated with nondisjunction of chromosome 21.
Human genetics 2012;131(7):1039-46.
2011: Lora J H Bean; Charlotte A Hobbs; Natasha D Hollis; Adam E Locke; Leslie O'Leary; Paul A Romitti; Marjorie H Royle; Emily G Allen; Kenneth J Dooley; Charlotte M Druschel; Sallie B Freeman; Stuart W Tinker; Claudine P Torfs; Stephanie L Sherman
Lack of maternal folic acid supplementation is associated with heart defects in Down syndrome: a report from the National Down Syndrome Project.
Birth defects research. Part A, Clinical and molecular teratology 2011;91(10):885-93.
2011: Emily G Allen; Jessica E Hunter; Michele Rusin; Jorge L Juncos; Gloria Novak; Debra Hamilton; Lisa Shubeck; Krista Charen; Stephanie L Sherman
Neuropsychological findings from older premutation carrier males and their noncarrier siblings from families with fragile X syndrome.
Neuropsychology 2011;25(3):404-11.
2010: Adam E Locke; Kenneth J Dooley; Stuart W Tinker; Soo Yeon Cheong; Eleanor Feingold; Emily G Allen; Sallie B Freeman; Claudine P Torfs; Clifford L Cua; Michael P Epstein; Michael C Wu; Xihong Lin; George T Capone; Stephanie L Sherman; Lora J H Bean
Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome.
Genetic epidemiology 2010;34(6):613-23.
2010: Emmanuel K Peprah; Emily G Allen; Scott M Williams; Laresa M Woodard; Stephanie L Sherman
Genetic diversity of the fragile X syndrome gene (FMR1) in a large Sub-Saharan West African population.
Annals of human genetics 2010;74(4):316-25.
2009: Emily G Allen; Sallie B Freeman; Charlotte M Druschel; Charlotte A Hobbs; Leslie A O'Leary; Paul A Romitti; Marjorie H Royle; Claudine P Torfs; Stephanie L Sherman
Maternal age and risk for trisomy 21 assessed by the origin of chromosome nondisjunction: a report from the Atlanta and National Down Syndrome Projects.
Human genetics 2009;125(1):41-52.
2008: Jessica Ezzell Hunter; Emily G Allen; Ann Abramowitz; Michele Rusin; Mary Leslie; Gloria Novak; Debra Hamilton; Lisa Shubeck; Krista Charen; Stephanie L Sherman
No evidence for a difference in neuropsychological profile among carriers and noncarriers of the FMR1 premutation in adults under the age of 50.
American journal of human genetics 2008;83(6):692-702.
2008: Jessica Ezzell Hunter; Emily G Allen; Ann Abramowitz; Michele Rusin; Mary Leslie; Gloria Novak; Debra Hamilton; Lisa Shubeck; Krista Charen; Stephanie L Sherman
Investigation of phenotypes associated with mood and anxiety among male and female fragile X premutation carriers.
Behavior genetics 2008;38(5):493-502.
2008: J Rohr; Emily G Allen; K Charen; J Giles; W He; C Dominguez; Stephanie L Sherman
Anti-Mullerian hormone indicates early ovarian decline in fragile X mental retardation (FMR1) premutation carriers: a preliminary study.
Human reproduction (Oxford, England) 2008;23(5):1220-5.
2008: Emily G Allen; Jorge L Juncos; Richard Letz; M Rusin; D Hamilton; G Novak; L Shubeck; S W Tinker; Stephanie L Sherman
Detection of early FXTAS motor symptoms using the CATSYS computerised neuromotor test battery.
Journal of medical genetics 2008;45(5):290-7.
2008: Sallie B Freeman; Lora H Bean; Emily G Allen; Stuart W Tinker; Adam E Locke; Charlotte Druschel; Charlotte A Hobbs; Paul A Romitti; Marjorie H Royle; Claudine P Torfs; Kenneth J Dooley; Stephanie L Sherman
Ethnicity, sex, and the incidence of congenital heart defects: a report from the National Down Syndrome Project.
Genetics in medicine : official journal of the American College of Medical Genetics 2008;10(3):173-80.
2007: Emily G Allen; Amy K Sullivan; Michele Marcus; C Small; C Dominguez; Michael P Epstein; K Charen; W He; K C Taylor; Stephanie L Sherman
Examination of reproductive aging milestones among women who carry the FMR1 premutation.
Human reproduction (Oxford, England) 2007;22(8):2142-52.
2007: Stephanie L Sherman; Emily G Allen; Lora H Bean; Sallie B Freeman
Epidemiology of Down syndrome.
Mental retardation and developmental disabilities research reviews 2007;13(3):221-7.
2007: Sallie B Freeman; Emily G Allen; Cindy L Oxford-Wright; Stuart W Tinker; Charlotte M Druschel; Charlotte A Hobbs; Leslie A O'Leary; Paul A Romitti; Marjorie H Royle; Claudine P Torfs; Stephanie L Sherman
The National Down Syndrome Project: design and implementation.
Public health reports (Washington, D.C. : 1974) 2007;122(1):62-72.
2005: Emily G Allen; Stephanie L Sherman; Ann Abramowitz; Mary Leslie; Gloria Novak; Michele Rusin; Elizabeth Scott; Richard Letz
Examination of the effect of the polymorphic CGG repeat in the FMR1 gene on cognitive performance.
Behavior genetics 2005;35(4):435-45.
2005: Amy K Sullivan; Michele Marcus; Michael P Epstein; Emily G Allen; Aimee Anido; J J Paquin; M Yadav-Shah; Stephanie L Sherman
Association of FMR1 repeat size with ovarian dysfunction.
Human reproduction (Oxford, England) 2005;20(2):402-12.
2005: Stephanie L Sherman; Sallie B Freeman; Emily G Allen; Neil E Lamb
Risk factors for nondisjunction of trisomy 21.
Cytogenetic and genome research 2005;111(3-4):273-80.
2004: Emily G Allen; Weiya He; Maneesha Yadav-Shah; Stephanie L Sherman
A study of the distributional characteristics of FMR1 transcript levels in 238 individuals.
Human genetics 2004;114(5):439-47.