Ethnicity, sex, and the incidence of congenital heart defects: a report from the National Down Syndrome Project
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.
Published in Genetics in medicine (01.03.2008)
Published in Genetics in medicine (01.03.2008)
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An examination of the relationship between hotspots and recombination associated with chromosome 21 nondisjunction
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 in PloS one (13.06.2014)
Published in PloS one (13.06.2014)
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New insights into human nondisjunction of chromosome 21 in oocytes
Oliver, Tiffany Renee, Feingold, Eleanor, Yu, Kai, Cheung, Vivian, Tinker, Stuart, Yadav-Shah, Maneesha, Masse, Nirupama, Sherman, Stephanie L
Published in PLoS genetics (01.03.2008)
Published in PLoS genetics (01.03.2008)
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Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome
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 in Genetic epidemiology (01.09.2010)
Published in Genetic epidemiology (01.09.2010)
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Altered patterns of multiple recombinant events are associated with nondisjunction of chromosome 21
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 in Human genetics (01.07.2012)
Published in Human genetics (01.07.2012)
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Evidence for dysregulation of genome-wide recombination in oocytes with nondisjoined chromosomes 21
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 in Human molecular genetics (15.01.2014)
Published in Human molecular genetics (15.01.2014)
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Lack of maternal folic acid supplementation is associated with heart defects in Down syndrome: a report from the National Down Syndrome Project
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 in Birth defects research. A Clinical and molecular teratology (01.10.2011)
Published in Birth defects research. A Clinical and molecular teratology (01.10.2011)
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Preconception folic acid supplementation and risk for chromosome 21 nondisjunction: A report from the National Down Syndrome Project
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 in American journal of medical genetics. Part A (01.03.2013)
Published in American journal of medical genetics. Part A (01.03.2013)
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The National down Syndrome Project: Design and Implementation
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., Shermanz, Stephanie L.
Published in Public health reports (1974) (01.01.2007)
Published in Public health reports (1974) (01.01.2007)
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New Insights into Human Nondisjunction of Chromosome 21 in Oocytes: e1000033
Oliver, Tiffany Renee, Feingold, Eleanor, Yu, Kai, Cheung, Vivian, Tinker, Stuart, Yadav-Shah, Maneesha, Masse, Nirupama, Sherman, Stephanie L
Published in PLoS genetics (01.03.2008)
Published in PLoS genetics (01.03.2008)
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Linkage disequilibrium mapping in trisomic populations: Analytical approaches and an application to congenital heart defects in Down syndrome
Kerstann, Kimberly F., Feingold, Eleanor, Freeman, Sallie B., Bean, Lora J. H., Pyatt, Robert, Tinker, Stuart, Jewel, Amy H., Capone, George, Sherman, Stephanie L.
Published in Genetic epidemiology (01.11.2004)
Published in Genetic epidemiology (01.11.2004)
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