Maternal age and risk for trisomy 21 assessed by the origin of chromosome nondisjunction: a report from the Atlanta and National Down Syndrome Projects
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.
Published in Human genetics (01.02.2009)
Published in Human genetics (01.02.2009)
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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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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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Susceptible chiasmate configurations of chromosome 21 predispose to non-disjunction in both maternal meiosis I and meiosis II
Lamb, Neil E, Freeman, Sallie B, Savage-Austin, Amanda, Pettay, Dorothy, Taft, Lisa, Hersey, Jane, Gu, Yuanchao, Shen, Joe, Saker, Denise, May, Kristen M, Avramopoulos, Dimitris, Petersen, Michael B, Hallberg, Anni, Mikkelsen, Margareta, Hassold, Terry J, Sherman, Stephanie L
Published in Nature genetics (01.12.1996)
Published in Nature genetics (01.12.1996)
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Epidemiology of Down syndrome
Sherman, Stephanie L., Allen, Emily G., Bean, Lora H., Freeman, Sallie B.
Published in Mental retardation and developmental disabilities research reviews (2007)
Published in Mental retardation and developmental disabilities research reviews (2007)
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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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The association of low socioeconomic status and the risk of having a child with Down syndrome: a report from the National Down Syndrome Project
Hunter, Jessica Ezzell, Allen, Emily Graves, Shin, Mikyong, Bean, Lora J.H., Correa, Adolfo, Druschel, Charlotte, Hobbs, Charlotte A., O’Leary, Leslie A., Romitti, Paul A., Royle, Marjorie H., Torfs, Claudine P., Freeman, Sallie B., Sherman, Stephanie L.
Published in Genetics in medicine (01.09.2013)
Published in Genetics in medicine (01.09.2013)
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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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Journal Article
Non-disjunction of chromosome 21 in maternal meiosis I: evidence for a maternal age-dependent mechanism involving reduced recombination
Sherman, S L, Petersen, M B, Freeman, S B, Hersey, J, Pettay, D, Taft, L, Frantzen, M, Mikkelsen, M, Hassold, T J
Published in Human molecular genetics (01.09.1994)
Published in Human molecular genetics (01.09.1994)
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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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Journal Article
Population-based study of congenital heart defects in Down syndrome
Freeman, S B, Taft, L F, Dooley, K J, Allran, K, Sherman, S L, Hassold, T J, Khoury, M J, Saker, D M
Published in American journal of medical genetics (16.11.1998)
Published in American journal of medical genetics (16.11.1998)
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Women with a Reduced Ovarian Complement May Have an Increased Risk for a Child with Down Syndrome
Freeman, Sallie B., Yang, Quanhe, Allran, Katherine, Taft, Lisa F., Sherman, Stephanie L.
Published in American journal of human genetics (01.05.2000)
Published in American journal of human genetics (01.05.2000)
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Journal Article
Conference Proceeding
Advanced maternal age and the risk of Down syndrome characterized by the meiotic stage of the chromosomal error : A population-based study
YOON, P. W, FREEMAN, S. B, SHERMAN, S. L, TAFT, L. F, YUANCHAO GU, PETTAY, D, FLANDERS, W. D, KHOURY, M. J, HASSOLD, T. J
Published in American journal of human genetics (01.03.1996)
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Published in American journal of human genetics (01.03.1996)
Journal Article
Elucidating the Mechanisms of Paternal Non-Disjunction of Chromosome 21 in Humans
Savage, Amanda R., Petersen, Michael B., Pettay, Dorothy, Taft, Lisa, Allran, Katherine, Freeman, Sallie B., Karadima, Georgia, Avramopoulos, Dimitris, Torfs, Claudine, Mikkelsen, Margareta, Hassold, Terry J., Sherman, Stephanie L.
Published in Human molecular genetics (01.08.1998)
Published in Human molecular genetics (01.08.1998)
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Journal Article
Sialic acid in egg capsules and oviducts of the newt, Notophthalmus viridescens
Humphries, Jr, A A, Freeman, S B, Workman, W M
Published in The Biological bulletin (Lancaster) (01.04.1968)
Published in The Biological bulletin (Lancaster) (01.04.1968)
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Risk factors for trisomy 21: Maternal cigarette smoking and oral contraceptive use in a spopulation-based case-control study
Yang, Quanhe, Sherman, Stephanie L., Hassold, Terry J., Allran, Katherine, Taft, Lisa, Pettay, Dorothy, Khoury, Muin J., Erickson, J. David, Freeman, Sallie B.
Published in Genetics in medicine (01.03.1999)
Published in Genetics in medicine (01.03.1999)
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Assignment of X-linked hydrocephalus to Xq28 by linkage analysis
Willems, Patrick J., Dijkstra, Irene, Van der Auwera, Bart J., Vits, Lieve, Coucke, Paul, Raeymaekers, Peter, Van Broeckhoven, Christine, Consalez, Giacomo G., Freeman, Sallie B., Warren, Stephen T., Brouwer, Oebele F., Brunner, Han G., Renier, Willy O., Van Elsen, August F., Dumon, Jan E.
Published in Genomics (San Diego, Calif.) (01.10.1990)
Published in Genomics (San Diego, Calif.) (01.10.1990)
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Journal Article
Characterization and molecular analysis of nondisjunction in 18 cases of trisomy 21 and leukemia
Lorber, B J, Freeman, S B, Hassold, T, Ragab, A H, Vega, R A, Cockwell, A E, Jacobs, P A, Radford, M, Doyle, J, Dubé, I D
Published in Genes chromosomes & cancer (01.04.1992)
Published in Genes chromosomes & cancer (01.04.1992)
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