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Predictors of Comorbid Conditions in Women Who Carry an FMR1 Premutation.
Front Psychiatry. 2021 Oct 1;12:715922. doi: 10.3389/fpsyt.2021.715922. eCollection 2021.
Front Psychiatry. 2021.
PMID: 34658954
Free PMC article.
Ectopic expression of CGG-repeats alters ovarian response to gonadotropins and leads to infertility in a murine FMR1 premutation model.
Shelly KE, Candelaria NR, Li Z, Allen EG, Jin P, Nelson DL.
Shelly KE, et al.
Hum Mol Genet. 2021 May 29;30(10):923-938. doi: 10.1093/hmg/ddab083.
Hum Mol Genet. 2021.
PMID: 33856019
Free PMC article.
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Refining the risk for fragile X-associated primary ovarian insufficiency (FXPOI) by FMR1 CGG repeat size.
Allen EG, Charen K, Hipp HS, Shubeck L, Amin A, He W, Nolin SL, Glicksman A, Tortora N, McKinnon B, Shelly KE, Sherman SL.
Allen EG, et al. Among authors: shelly ke.
Genet Med. 2021 Sep;23(9):1648-1655. doi: 10.1038/s41436-021-01177-y. Epub 2021 Apr 29.
Genet Med. 2021.
PMID: 33927378
Free PMC article.
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Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on FMR1 Premutation.
Tassone F, Protic D, Allen EG, Archibald AD, Baud A, Brown TW, Budimirovic DB, Cohen J, Dufour B, Eiges R, Elvassore N, Gabis LV, Grudzien SJ, Hall DA, Hessl D, Hogan A, Hunter JE, Jin P, Jiraanont P, Klusek J, Kooy RF, Kraan CM, Laterza C, Lee A, Lipworth K, Losh M, Loesch D, Lozano R, Mailick MR, Manolopoulos A, Martinez-Cerdeno V, McLennan Y, Miller RM, Montanaro FAM, Mosconi MW, Potter SN, Raspa M, Rivera SM, Shelly K, Todd PK, Tutak K, Wang JY, Wheeler A, Winarni TI, Zafarullah M, Hagerman RJ.
Tassone F, et al.
Cells. 2023 Sep 21;12(18):2330. doi: 10.3390/cells12182330.
Cells. 2023.
PMID: 37759552
Free PMC article.
Review.
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VCAM1 Is Induced in Ovarian Theca and Stromal Cells in a Mouse Model of Androgen Excess.
Candelaria NR, Padmanabhan A, Stossi F, Ljungberg MC, Shelly KE, Pew BK, Solis M, Rossano AM, McAllister JM, Wu S, Richards JS.
Candelaria NR, et al. Among authors: shelly ke.
Endocrinology. 2019 Jun 1;160(6):1377-1393. doi: 10.1210/en.2018-00731.
Endocrinology. 2019.
PMID: 30951142
Free PMC article.
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Identification of critical regions and candidate genes for cardiovascular malformations and cardiomyopathy associated with deletions of chromosome 1p36.
Zaveri HP, Beck TF, Hernández-García A, Shelly KE, Montgomery T, van Haeringen A, Anderlid BM, Patel C, Goel H, Houge G, Morrow BE, Cheung SW, Lalani SR, Scott DA.
Zaveri HP, et al. Among authors: shelly ke.
PLoS One. 2014 Jan 15;9(1):e85600. doi: 10.1371/journal.pone.0085600. eCollection 2014.
PLoS One. 2014.
PMID: 24454898
Free PMC article.
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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 S, Rubin J, Chakchouk I, Sharif M, Mahadevan SK, Erfani H, Shelly K, Liao L, Lorenzo I, Ramakrishnan R, Van den Veyver IB.
Arian S, et al.
Reprod Sci. 2021 Jul;28(7):1850-1865. doi: 10.1007/s43032-020-00360-x. Epub 2020 Oct 22.
Reprod Sci. 2021.
PMID: 33090377
Free PMC article.
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