Ectopic expression of CGG-repeats alters ovarian response to gonadotropins and leads to infertility in a murine FMR1 premutation model
Shelly, Katharine E, Candelaria, Nicholes R, Li, Ziyi, Allen, Emily G, Jin, Peng, Nelson, David L
Published in Human molecular genetics (29.05.2021)
Published in Human molecular genetics (29.05.2021)
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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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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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VCAM1 Is Induced in Ovarian Theca and Stromal Cells in a Mouse Model of Androgen Excess
Candelaria, Nicholes R, Padmanabhan, Achuth, Stossi, Fabio, Ljungberg, M Cecilia, Shelly, Katharine E, Pew, Braden K, Solis, Minerva, Rossano, Ayane M, McAllister, Jan M, Wu, Sheng, Richards, JoAnne S
Published in Endocrinology (Philadelphia) (01.06.2019)
Published in Endocrinology (Philadelphia) (01.06.2019)
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Identification of critical regions and candidate genes for cardiovascular malformations and cardiomyopathy associated with deletions of chromosome 1p36
Zaveri, Hitisha P, Beck, Tyler F, Hernández-García, Andrés, Shelly, Katharine E, Montgomery, Tara, van Haeringen, Arie, Anderlid, Britt-Marie, Patel, Chirag, Goel, Himanshu, Houge, Gunnar, Morrow, Bernice E, Cheung, Sau Wai, Lalani, Seema R, Scott, Daryl A
Published in PloS one (15.01.2014)
Published in PloS one (15.01.2014)
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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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Reproductive Outcomes from Maternal Loss of Nlrp2 Are Not Improved by IVF or Embryo Transfer Consistent with Oocyte-Specific Defect
Arian, Sara, Rubin, Jessica, Chakchouk, Imen, Sharif, Momal, Mahadevan, Sangeetha K., Erfani, Hadi, Shelly, Katharine, Liao, Lan, Lorenzo, Isabel, Ramakrishnan, Rajesh, Van den Veyver, Ignatia B.
Published in Reproductive sciences (Thousand Oaks, Calif.) (01.07.2021)
Published in Reproductive sciences (Thousand Oaks, Calif.) (01.07.2021)
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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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Identification of Critical Regions and Candidate Genes for Cardiovascular Malformations and Cardiomyopathy Associated with Deletions of Chromosome 1p36: e85600
Zaveri, Hitisha P, Beck, Tyler F, Hernandez-Garcia, Andres, Shelly, Katharine E, Montgomery, Tara, Haeringen, Arie van, Anderlid, Britt-Marie, Patel, Chirag, Goel, Himanshu, Houge, Gunnar
Published in PloS one (01.01.2014)
Published in PloS one (01.01.2014)
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