A candidate gene analysis and GWAS for genes associated with maternal nondisjunction of chromosome 21 von Chernus, Jonathan M, Allen, Emily G, Zeng, Zhen, Hoffman, Eva R, Hassold, Terry J, Feingold, Eleanor, Sherman, Stephanie L

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Genetic analysis of variation in human meiotic recombination von Chowdhury, Reshmi, Bois, Philippe R J, Feingold, Eleanor, Sherman, Stephanie L, Cheung, Vivian G

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An Excess of Deleterious Variants in VEGF-A Pathway Genes in Down-Syndrome-Associated Atrioventricular Septal Defects von ACKERMAN, Christine, LOCKE, Adam E, REEVES, Roger H, SHERMAN, Stephanie L, MASLEN, Cheryl L, FEINGOLD, Eleanor, RESHEY, Benjamin, ESPANA, Karina, THUSBERG, Janita, MOONEY, Sean, BEAN, Lora J. H, DOOLEY, Kenneth J, CUA, Clifford L

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Medical vulnerability of individuals with Down syndrome to severe COVID-19–data from the Trisomy 21 Research Society and the UK ISARIC4C survey von Hüls, Anke, Costa, Alberto C.S., Dierssen, Mara, Baksh, R. Asaad, Bargagna, Stefania, Baumer, Nicole T., Brandão, Ana Claudia, Carfi, Angelo, Carmona-Iragui, Maria, Chicoine, Brian Allen, Ghosh, Sujay, Lakhanpaul, Monica, Manso, Coral, Mayer, Miguel-Angel, Ortega, Maria del Carmen, de Asua, Diego Real, Rebillat, Anne-Sophie, Russell, Lauren Ashley, Sgandurra, Giuseppina, Valentini, Diletta, Sherman, Stephanie L., Strydom, Andre

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The FMR1 premutation and reproduction von Wittenberger, Michael D., M.D, Hagerman, Randi J., M.D, Sherman, Stephanie L., Ph.D, McConkie-Rosell, Allyn, Ph.D, Welt, Corrine K., M.D, Rebar, Robert W., M.D, Corrigan, Emily C., M.D, Simpson, Joe Leigh, M.D, Nelson, Lawrence M., M.D

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Predictors of Comorbid Conditions in Women Who Carry an FMR1 Premutation von Allen, Emily Graves, Charen, Krista, Hipp, Heather S, Shubeck, Lisa, Amin, Ashima, He, Weiya, Hunter, Jessica Ezzell, Shelly, Katharine E, Sherman, Stephanie L

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Relationship between Apgar scores and long-term cognitive outcomes in individuals with Down syndrome von del Hoyo Soriano, Laura, Rosser, Tracie C., Hamilton, Debra R., Harvey, Danielle J., Abbeduto, Leonard, Sherman, Stephanie L.

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Fragile X AGG analysis provides new risk predictions for 45-69 repeat alleles von Nolin, Sarah L., Sah, Sachin, Glicksman, Anne, Sherman, Stephanie L., Allen, Emily, Berry-Kravis, Elizabeth, Tassone, Flora, Yrigollen, Carolyn, Cronister, Amy, Jodah, Marcia, Ersalesi, Nicole, Dobkin, Carl, Brown, W. Ted, Shroff, Raghav, Latham, Gary J., Hadd, Andrew G.

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Spoken language outcome measures for treatment studies in Down syndrome: feasibility, practice effects, test-retest reliability, and construct validity of variables generated from... von Thurman, Angela John, Edgin, Jamie O, Sherman, Stephanie L, Sterling, Audra, McDuffie, Andrea, Berry-Kravis, Elizabeth, Hamilton, Debra, Abbeduto, Leonard

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Capturing cognitive and behavioral variability among individuals with Down syndrome: a latent profile analysis von Channell, Marie Moore, Mattie, Laura J, Hamilton, Debra R, Capone, George T, Mahone, E Mark, Sherman, Stephanie L, Rosser, Tracie C, Reeves, Roger H, Kalb, Luther G

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New insights into human nondisjunction of chromosome 21 in oocytes von Oliver, Tiffany Renee, Feingold, Eleanor, Yu, Kai, Cheung, Vivian, Tinker, Stuart, Yadav-Shah, Maneesha, Masse, Nirupama, Sherman, Stephanie L

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Fragile X analysis of 1112 prenatal samples from 1991 to 2010 von Nolin, Sarah L., Glicksman, Anne, Ding, Xiaohua, Ersalesi, Nicole, Brown, W. Ted, Sherman, Stephanie L., Dobkin, Carl

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Fragile X Associated Primary Ovarian Insufficiency (FXPOI): Case Report and Literature Review von Fink, Dorothy A, Nelson, Lawrence M, Pyeritz, Reed, Johnson, Josh, Sherman, Stephanie L, Cohen, Yoram, Elizur, Shai E

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Ethnicity, sex, and the incidence of congenital heart defects: a report from the National Down Syndrome Project von Freeman, Sallie B., Bean, Lora H., Allen, Emily G., Tinker, Stuart W., Locke, Adam E., Druschel, Charlotte, Hobbs, Charlotte A., Romitti, Paul A., Royle, Marjorie H., Torfs, Claudine P., Dooley, Kenneth J., Sherman, Stephanie L.

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Maternal age and risk for trisomy 21 assessed by the origin of chromosome nondisjunction: a report from the Atlanta and National Down Syndrome Projects von Allen, Emily Graves, Freeman, Sallie B., Druschel, Charlotte, Hobbs, Charlotte A., O’Leary, Leslie A., Romitti, Paul A., Royle, Marjorie H., Torfs, Claudine P., Sherman, Stephanie L.

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Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome von Trevino, Cristina E., Holleman, Aaron M., Corbitt, Holly, Maslen, Cheryl L., Rosser, Tracie C., Cutler, David J., Johnston, H. Richard, Rambo-Martin, Benjamin L., Oberoi, Jai, Dooley, Kenneth J., Capone, George T., Reeves, Roger H., Cordell, Heather J., Keavney, Bernard D., Agopian, A. J., Goldmuntz, Elizabeth, Gruber, Peter J., O’Brien, James E., Bittel, Douglas C., Wadhwa, Lalita, Cua, Clifford L., Moskowitz, Ivan P., Mulle, Jennifer G., Epstein, Michael P., Sherman, Stephanie L., Zwick, Michael E.

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Down syndrome von Antonarakis, Stylianos E., Skotko, Brian G., Rafii, Michael S., Strydom, Andre, Pape, Sarah E., Bianchi, Diana W., Sherman, Stephanie L., Reeves, Roger H.

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Examination of FMR1 transcript and protein levels among 74 premutation carriers von Peprah, Emmanuel, He, Weiya, Allen, Emily, Oliver, Tiffany, Boyne, Alex, Sherman, Stephanie L

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Autism Spectrum Disorder in Fragile X Syndrome: Cooccurring Conditions and Current Treatment von Kaufmann, Walter E, Kidd, Sharon A, Andrews, Howard F, Budimirovic, Dejan B, Esler, Amy, Haas-Givler, Barbara, Stackhouse, Tracy, Riley, Catharine, Peacock, Georgina, Sherman, Stephanie L, Brown, W Ted, Berry-Kravis, Elizabeth

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FXPOI: Pattern of AGG Interruptions Does not Show an Association With Age at Amenorrhea Among Women With a Premutation von Allen, Emily G, Glicksman, Anne, Tortora, Nicole, Charen, Krista, He, Weiya, Amin, Ashima, Hipp, Heather, Shubeck, Lisa, Nolin, Sarah L, Sherman, Stephanie L

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