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

by Hunter, Jessica Ezzell, Epstein, Michael P., Tinker, Stuart W., Abramowitz, Ann, Sherman, Stephanie L.
Published 2011

Investigation of Factors Associated With Paternal Nondisjunction of Chromosome 21

by Oliver, Tiffany Renee, Bhise, Archit, Feingold, Eleanor, Tinker, Stuart, Masse, Nirupama, Sherman, Stephanie L.
Published 2009

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

by Hunter, Jessica Ezzell, Epstein, Michael P., Tinker, Stuart W., Charen, Krista H., Sherman, Stephanie L.
Published 2008

New Insights into Human Nondisjunction of Chromosome 21 in Oocytes

by Oliver, Tiffany Renee, Feingold, Eleanor, Yu, Kai, Cheung, Vivian, Tinker, Stuart, Yadav-Shah, Maneesha, Masse, Nirupama, Sherman, Stephanie L.
Published 2008

An Examination of the Relationship between Hotspots and Recombination Associated with Chromosome 21 Nondisjunction

by Oliver, Tiffany Renee, Middlebrooks, Candace D., Tinker, Stuart W., Allen, Emily Graves, Bean, Lora J. H., Begum, Ferdouse, Feingold, Eleanor, Chowdhury, Reshmi, Cheung, Vivian, Sherman, Stephanie L.
Published 2014

Evidence for dysregulation of genome-wide recombination in oocytes with nondisjoined chromosomes 21

by Middlebrooks, Candace D., Mukhopadhyay, Nandita, Tinker, Stuart W., Allen, Emily Graves, Bean, Lora J. H., Begum, Ferdouse, Chowdhury, Reshmi, Cheung, Vivian, Doheny, Kimberly, Adams, Marcia, Feingold, Eleanor, Sherman, Stephanie L.
Published 2014

Altered patterns of multiple recombinant events are associated with nondisjunction of chromosome 21

by Oliver, Tiffany Renee, Tinker, Stuart W., Allen, Emily Graves, Hollis, Natasha, Locke, Adam E., Bean, Lora J. H., Chowdhury, Reshmi, Begum, Ferdouse, Marazita, Mary, Cheung, Vivian, Feingold, Eleanor, Sherman, Stephanie L.
Published 2011

The National Down Syndrome Project: Design and Implementation

by Freeman, Sallie B., Allen, Emily G., Oxford-Wright, Cindy L., Tinker, Stuart W., Druschel, Charlotte, Hobbs, Charlotte A., O'Leary, Leslie A., Romitti, Paul A., Royle, Marjorie H., Torfs, Claudine P., Sherman, Stephanie L.
Published 2007

Preconception folic acid supplementation and risk for chromosome 21 nondisjunction: A report from the National Down Syndrome Project

by HOLLIS, NaTasha D., ALLEN, Emily G., OLIVER, Tiffany Renee, TINKER, Stuart W., DRUSCHEL, Charlotte, HOBBS, Charlotte A., O’LEARY, Leslie A., ROMITTI, Paul A., ROYLE, Marjorie H., TORFS, Claudine P., FREEMAN, Sallie B., SHERMAN, Stephanie L., BEAN, Lora J. H.
Published 2013

Lack of maternal folic acid supplementation is associated with heart defects in Down syndrome: a report from the National Down Syndrome Project

by Bean, Lora J. H., Allen, Emily G., Tinker, Stuart W., Hollis, NaTasha D., Locke, Adam E., Druschel, Charlotte, Hobbs, Charlotte A., O’Leary, Leslie, Romitti, Paul A., Royle, Marjorie H., Torfs, Claudine P., Dooley, Kenneth J., Freeman, Sallie B., Sherman, Stephanie L.
Published 2011

Variation in Folate Pathway Genes Contributes to Risk of Congenital Heart Defects Among Individuals With Down Syndrome

by Locke, Adam E., Dooley, Kenneth J., Tinker, Stuart W., Cheong, Soo Yeon, Feingold, Eleanor, Allen, Emily G., Freeman, Sallie B., Torfs, Claudine P., Cua, Clifford L., Epstein, Michael P., Wu, Michael C., Lin, Xihong, Capone, George, Sherman, Stephanie L., Bean, Lora J. H.
Published 2010