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Publications by Stephanie L. Sherman
A Candidate Gene Analysis and GWAS for Genes Associated With Maternal Nondisjunction of Chromosome 21
PLoS Genetics
Evolution
Ecology
Genetics
Molecular Biology
Cancer Research
Systematics
Behavior
Depression and Anxiety Symptoms Among Women Who Carry the FMR1 Premutation: Impact of Raising a Child With Fragile X Syndrome Is Moderated by CRHR1 Polymorphisms
American Journal of Medical Genetics, Part B, Neuropsychiatric Genetics
Psychiatry
Molecular Neuroscience
Mental Health
Genetics
Cellular
Approaches to Identify Genetic Variants That Influence the Risk for Onset of Fragile X-Associated Primary Ovarian Insufficiency (FXPOI): A Preliminary Study
Frontiers in Genetics
Genetics
Molecular Medicine
An Examination of the Relationship Between Hotspots and Recombination Associated With Chromosome 21 Nondisjunction
PLoS ONE
Multidisciplinary
Expansion of the Fragile X CGG Repeat in Females With Premutation or Intermediate Alleles
American Journal of Human Genetics
Genetics
Investigation of Phenotypes Associated With Mood and Anxiety Among Male and Female Fragile X Premutation Carriers
Behavior Genetics
Genetics
Evolution
Ecology
Systematics
Behavior
