Premature Ovarian Failure among Fragile X Premutation Carriers: Parent-of-Origin Effect?

Por Sherman, Stephanie L.
Publicado em 2000

Multipoint Estimation of Genetic Maps for Human Trisomies with One Parent or Other Partial Data

Por Feingold, Eleanor, Brown, Amanda Savage, Sherman, Stephanie L.
Publicado em 2000

Cognitive Aspects of Fragile X syndrome

Por Huddleston, Lillie B., Visootsak, Jeannie, Sherman, Stephanie L.
Publicado no Wiley Interdiscip Rev Cogn Sci (2014)

Multipoint Genetic Mapping with Trisomy Data

Por Li, Jinming, Sherman, Stephanie L., Lamb, Neil, Zhao, Hongyu
Publicado em 2001

Clinical significance of tri-nucleotide repeats in Fragile X testing: A clarification of American College of Medical Genetics guidel...

Por Kronquist, Kathryn E., Sherman, Stephanie L., Spector, Elaine B.
Publicado em 2008

FMR1 and the Fragile X Syndrome: Human Genome Epidemiology Review

Por Crawford, Dana C., Acuña, Juan M., Sherman, Stephanie L.
Publicado no Genet Med (2001)

Is there evidence for neuropsychological and neurobehavioral phenotypes among adults without FXTAS who carry the FMR1 premutation? A review of current literature

Por Hunter, Jessica Ezzell, Abramowitz, Ann, Rusin, Michele, Sherman, Stephanie L.
Publicado em 2009

Association between Maternal Age and Meiotic Recombination for Trisomy 21

Por Lamb, Neil E., Yu, Kai, Shaffer, John, Feingold, Eleanor, Sherman, Stephanie L.
Publicado em 2005

A novel procedure for genotyping of single nucleotide polymorphisms in trisomy with genomic DNA and the invader assay

Por Duffy, Kelly J., Littrell, Jack, Locke, Adam, Sherman, Stephanie L., Olivier, Michael
Publicado em 2008

Genome-Wide Association Study of Meiotic Recombination Phenotypes

Por Begum, Ferdouse, Chowdhury, Reshmi, Cheung, Vivian G., Sherman, Stephanie L., Feingold, Eleanor
Publicado no G3 (Bethesda) (2016)

Examination of FMR1 transcript and protein levels among 74 premutation carriers

Por Peprah, Emmanuel, He, Weiya, Allen, Emily, Oliver, Tiffany, Boyne, Alex, Sherman, Stephanie L
Publicado em 2009

Approaches to identify genetic variants that influence the risk for onset of fragile X-associated primary ovarian insufficiency (FXPOI): a preliminary study

Por Allen, Emily G., Grus, Wendy E., Narayan, Sarayu, Espinel, Whitney, Sherman, Stephanie L.
Publicado em 2014

REGIONALLY SMOOTHED META-ANALYSIS METHODS FOR GWAS DATASETS

Por Begum, Ferdouse, Sharker, Monir H., Sherman, Stephanie L., Tseng, George C., Feingold, Eleanor
Publicado no Genet Epidemiol (2015)

Genetic Analysis of Variation in Human Meiotic Recombination

Por Chowdhury, Reshmi, Bois, Philippe R. J., Feingold, Eleanor, Sherman, Stephanie L., Cheung, Vivian G.
Publicado em 2009

The FMR1 Premutation and Attention-Deficit Hyperactivity Disorder (ADHD): Evidence for a Complex Inheritance

Por Hunter, Jessica Ezzell, Epstein, Michael P., Tinker, Stuart W., Abramowitz, Ann, Sherman, Stephanie L.
Publicado em 2011

Investigation of Factors Associated With Paternal Nondisjunction of Chromosome 21

Por Oliver, Tiffany Renee, Bhise, Archit, Feingold, Eleanor, Tinker, Stuart, Masse, Nirupama, Sherman, Stephanie L.
Publicado em 2009

Reproductive and Gynecologic Care of Women with Fragile X Primary Ovarian Insufficiency (FXPOI)

Por Hipp, Heather S, Charen, Krista H, Spencer, Jessica B, Allen, Emily G, Sherman, Stephanie L
Publicado no Menopause (2016)

Paternally Transmitted FMR1 Alleles Are Less Stable than Maternally Transmitted Alleles in the Common and Intermediate Size Range

Por Sullivan, Amy K., Crawford, Dana C., Scott, Elizabeth H., Leslie, Mary L., Sherman, Stephanie L.
Publicado em 2002

Incidence of Fragile X Syndrome by Newborn Screening for Methylated FMR1 DNA

Por Coffee, Bradford, Keith, Krayton, Albizua, Igor, Malone, Tamika, Mowrey, Julie, Sherman, Stephanie L., Warren, Stephen T.
Publicado em 2009

Fragile X-associated Primary Ovarian Insufficiency: Evidence for Additional Genetic Contributions to Severity

Por Hunter, Jessica Ezzell, Epstein, Michael P., Tinker, Stuart W., Charen, Krista H., Sherman, Stephanie L.
Publicado em 2008