Genome-Wide Association Study of Meiotic Recombination Phenotypes

by Ferdouse Begum, Reshmi Chowdhury, Vivian G. Cheung, Stephanie L. Sherman, Eleanor Feingold
Published 2016-12-01

Genetic analysis of variation in human meiotic recombination.

by Reshmi Chowdhury, Philippe R J Bois, Eleanor Feingold, Stephanie L Sherman, Vivian G Cheung
Published 2009-09-01

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

by Emily G. Allen, Wendy E. Grus, Sarayu eNarayan, Whitney eEspinel, Stephanie L. Sherman
Published 2014-08-01

Fragile X Associated Primary Ovarian Insufficiency (FXPOI): Case Report and Literature Review

by Dorothy A. Fink, Lawrence M. Nelson, Reed Pyeritz, Josh Johnson, Stephanie L. Sherman, Yoram Cohen, Shai E. Elizur
Published 2018-11-01

Relationship between Apgar scores and long-term cognitive outcomes in individuals with Down syndrome

by Laura del Hoyo Soriano, Tracie C. Rosser, Debra R. Hamilton, Danielle J. Harvey, Leonard Abbeduto, Stephanie L. Sherman
Published 2021-06-01

A candidate gene analysis and GWAS for genes associated with maternal nondisjunction of chromosome 21.

by Jonathan M Chernus, Emily G Allen, Zhen Zeng, Eva R Hoffman, Terry J Hassold, Eleanor Feingold, Stephanie L Sherman
Published 2019-12-01

New insights into human nondisjunction of chromosome 21 in oocytes.

by Tiffany Renee Oliver, Eleanor Feingold, Kai Yu, Vivian Cheung, Stuart Tinker, Maneesha Yadav-Shah, Nirupama Masse, Stephanie L Sherman
Published 2008-03-01

Spoken language outcome measures for treatment studies in Down syndrome: feasibility, practice effects, test-retest reliability, and construct validity of variables generated from...

by Angela John Thurman, Jamie O. Edgin, Stephanie L. Sherman, Audra Sterling, Andrea McDuffie, Elizabeth Berry-Kravis, Debra Hamilton, Leonard Abbeduto
Published 2021-04-01

Predictors of Comorbid Conditions in Women Who Carry an FMR1 Premutation

by Emily Graves Allen, Krista Charen, Heather S. Hipp, Lisa Shubeck, Ashima Amin, Weiya He, Jessica Ezzell Hunter, Katharine E. Shelly, Stephanie L. Sherman
Published 2021-10-01

FXPOI: Pattern of AGG Interruptions Does not Show an Association With Age at Amenorrhea Among Women With a Premutation

by Emily G. Allen, Anne Glicksman, Nicole Tortora, Krista Charen, Weiya He, Ashima Amin, Heather Hipp, Lisa Shubeck, Sarah L. Nolin, Stephanie L. Sherman
Published 2018-08-01

An examination of the relationship between hotspots and recombination associated with chromosome 21 nondisjunction.

by Tiffany Renee Oliver, Candace D Middlebrooks, Stuart W Tinker, Emily Graves Allen, Lora J H Bean, Ferdouse Begum, Eleanor Feingold, Reshmi Chowdhury, Vivian Cheung, Stephanie L Sherman
Published 2014-01-01

Capturing cognitive and behavioral variability among individuals with Down syndrome: a latent profile analysis

by Marie Moore Channell, Laura J. Mattie, Debra R. Hamilton, George T. Capone, E. Mark Mahone, Stephanie L. Sherman, Tracie C. Rosser, Roger H. Reeves, Luther G. Kalb, The Down Syndrome Cognition Project
Published 2021-04-01

Analysis of Copy Number Variants on Chromosome 21 in Down Syndrome-Associated Congenital Heart Defects

by Benjamin L. Rambo-Martin, Jennifer G. Mulle, David J. Cutler, Lora J. H. Bean, Tracie C. Rosser, Kenneth J. Dooley, Clifford Cua, George Capone, Cheryl L. Maslen, Roger H. Reeves, Stephanie L. Sherman, Michael E. Zwick
Published 2018-01-01

Comparison of COVID-19 and Non-COVID-19 Pneumonia in Down Syndrome

by Diego Real de Asua, Miguel A. Mayer, María del Carmen Ortega, Jose M. Borrel, Teresa de Jesús Bermejo, Domingo González-Lamuño, Coral Manso, Fernando Moldenhauer, María Carmona-Iragui, Anke Hüls, Stephanie L. Sherman, Andre Strydom, Rafael de la Torre, Mara Dierssen
Published 2021-08-01

Medical vulnerability of individuals with Down syndrome to severe COVID-19–data from the Trisomy 21 Research Society and the UK ISARIC4C survey

by Anke Hüls, Alberto C.S. Costa, Mara Dierssen, R. Asaad Baksh, Stefania Bargagna, Nicole T. Baumer, Ana Claudia Brandão, Angelo Carfi, Maria Carmona-Iragui, Brian Allen Chicoine, Sujay Ghosh, Monica Lakhanpaul, Coral Manso, Miguel-Angel Mayer, Maria del Carmen Ortega, Diego Real de Asua, Anne-Sophie Rebillat, Lauren Ashley Russell, Giuseppina Sgandurra, Diletta Valentini, Stephanie L. Sherman, Andre Strydom
Published 2021-03-01

Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome

by Cristina E. Trevino, Aaron M. Holleman, Holly Corbitt, Cheryl L. Maslen, Tracie C. Rosser, David J. Cutler, H. Richard Johnston, Benjamin L. Rambo-Martin, Jai Oberoi, Kenneth J. Dooley, George T. Capone, Roger H. Reeves, Heather J. Cordell, Bernard D. Keavney, A. J. Agopian, Elizabeth Goldmuntz, Peter J. Gruber, James E. O’Brien, Douglas C. Bittel, Lalita Wadhwa, Clifford L. Cua, Ivan P. Moskowitz, Jennifer G. Mulle, Michael P. Epstein, Stephanie L. Sherman, Michael E. Zwick
Published 2021-07-01