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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Journal Article
Clustering of comorbid conditions among women who carry an FMR1 premutation
Allen, Emily Graves, Charen, Krista, Hipp, Heather S., Shubeck, Lisa, Amin, Ashima, He, Weiya, Hunter, Jessica Ezzell, Sherman, Stephanie L.
Published in Genetics in medicine (01.04.2020)
Published in Genetics in medicine (01.04.2020)
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Journal Article
Refining the risk for fragile X–associated primary ovarian insufficiency (FXPOI) by FMR1 CGG repeat size
Allen, Emily Graves, Charen, Krista, Hipp, Heather S., Shubeck, Lisa, Amin, Ashima, He, Weiya, Nolin, Sarah L., Glicksman, Anne, Tortora, Nicole, McKinnon, Bonnie, Shelly, Katharine E., Sherman, Stephanie L.
Published in Genetics in medicine (01.09.2021)
Published in Genetics in medicine (01.09.2021)
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Journal Article
No Evidence for a Difference in Neuropsychological Profile among Carriers and Noncarriers of the FMR1 Premutation in Adults under the Age of 50
Hunter, Jessica Ezzell, Allen, Emily Graves, Abramowitz, Ann, Rusin, Michele, Leslie, Mary, Novak, Gloria, Hamilton, Debra, Shubeck, Lisa, Charen, Krista, Sherman, Stephanie L.
Published in American journal of human genetics (12.12.2008)
Published in American journal of human genetics (12.12.2008)
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Journal Article
Predictors of Comorbid Conditions in Women Who Carry an FMR1 Premutation
Allen, Emily Graves, Charen, Krista, Hipp, Heather S, Shubeck, Lisa, Amin, Ashima, He, Weiya, Hunter, Jessica Ezzell, Shelly, Katharine E, Sherman, Stephanie L
Published in Frontiers in psychiatry (01.10.2021)
Published in Frontiers in psychiatry (01.10.2021)
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Journal Article
New clinical findings in the fragile X-associated tremor ataxia syndrome (FXTAS)
Juncos, Jorge L., Lazarus, Joash T., Graves-Allen, Emily, Shubeck, Lisa, Rusin, Michelle, Novak, Gloria, Hamilton, Deborah, Rohr, Julia, Sherman, Stephanie L.
Published in Neurogenetics (01.05.2011)
Published in Neurogenetics (01.05.2011)
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Journal Article
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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Journal Article
Neuropsychological findings from older premutation carrier males and their noncarrier siblings from families with fragile X syndrome
Allen, Emily Graves, Hunter, Jessica E, Rusin, Michele, Juncos, Jorge, Novak, Gloria, Hamilton, Debra, Shubeck, Lisa, Charen, Krista, Sherman, Stephanie L
Published in Neuropsychology (01.05.2011)
Published in Neuropsychology (01.05.2011)
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Journal Article
Examination of the effect of the polymorphic CGG repeat in the FMR1 gene on cognitive performance
Allen, Emily Graves, Sherman, Stephanie, Abramowitz, Ann, Leslie, Mary, Novak, Gloria, Rusin, Michele, Scott, Elizabeth, Letz, Richard
Published in Behavior genetics (01.07.2005)
Published in Behavior genetics (01.07.2005)
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Journal Article
The association between maternal occupation and down syndrome: A report from the national Down syndrome project
Keen, Colleen, Hunter, Jessica Ezzell, Allen, Emily Graves, Rocheleau, Carissa, Waters, Martha, Sherman, Stephanie L.
Published in International journal of hygiene and environmental health (01.01.2020)
Published in International journal of hygiene and environmental health (01.01.2020)
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Journal Article
Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on FMR1 Premutation
Tassone, Flora, Protic, Dragana, Allen, Emily Graves, Archibald, Alison D, Baud, Anna, Brown, Ted W, Budimirovic, Dejan B, Cohen, Jonathan, Dufour, Brett, Eiges, Rachel, Elvassore, Nicola, Gabis, Lidia V, Grudzien, Samantha J, Hall, Deborah A, Hessl, David, Hogan, Abigail, Hunter, Jessica Ezzell, Jin, Peng, Jiraanont, Poonnada, Klusek, Jessica, Kooy, R Frank, Kraan, Claudine M, Laterza, Cecilia, Lee, Andrea, Lipworth, Karen, Losh, Molly, Loesch, Danuta, Lozano, Reymundo, Mailick, Marsha R, Manolopoulos, Apostolos, Martinez-Cerdeno, Veronica, McLennan, Yingratana, Miller, Robert M, Montanaro, Federica Alice Maria, Mosconi, Matthew W, Potter, Sarah Nelson, Raspa, Melissa, Rivera, Susan M, Shelly, Katharine, Todd, Peter K, Tutak, Katarzyna, Wang, Jun Yi, Wheeler, Anne, Winarni, Tri Indah, Zafarullah, Marwa, Hagerman, Randi J
Published in Cells (Basel, Switzerland) (21.09.2023)
Published in Cells (Basel, Switzerland) (21.09.2023)
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Journal Article
Investigation of Phenotypes Associated with Mood and Anxiety Among Male and Female Fragile X Premutation Carriers
Hunter, Jessica Ezzell, Allen, Emily Graves, Abramowitz, Ann, Rusin, Michele, Leslie, Mary, Novak, Gloria, Hamilton, Debra, Shubeck, Lisa, Charen, Krista, Sherman, Stephanie L.
Published in Behavior genetics (01.09.2008)
Published in Behavior genetics (01.09.2008)
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Journal Article
Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on IFMR1/I Premutation
Tassone, Flora, Protic, Dragana, Allen, Emily Graves, Archibald, Alison D, Baud, Anna, Brown, Ted W, Budimirovic, Dejan B, Cohen, Jonathan, Dufour, Brett, Eiges, Rachel, Elvassore, Nicola, Gabis, Lidia V, Grudzien, Samantha J, Hall, Deborah A, Hessl, David, Hogan, Abigail, Hunter, Jessica Ezzell, Jin, Peng, Jiraanont, Poonnada, Klusek, Jessica, Kooy, R. Frank, Kraan, Claudine M, Laterza, Cecilia, Lee, Andrea, Lipworth, Karen, Losh, Molly, Loesch, Danuta, Lozano, Reymundo, Mailick, Marsha R, Manolopoulos, Apostolos, Ma, McLennan, Yingratana, Miller, Robert M, Montanaro, Federica Alice Maria, Mosconi, Matthew W, Potter, Sarah Nelson, Raspa, Melissa, Rivera, Susan M, Shelly, Katharine, Todd, Peter K, Tutak, Katarzyna, Wang, Jun Yi, Wheeler, Anne, Winarni, Tri Indah, Zafarullah, Marwa, Hagerman, Randi J
Published in Cells (Basel, Switzerland) (01.09.2023)
Published in Cells (Basel, Switzerland) (01.09.2023)
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Journal Article
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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Journal Article
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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Journal Article
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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Journal Article