Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 31 Records) |
| Query Trace: Primary Ovarian Insufficiency and FMR1[original query] |
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| No evidence for a difference in neuropsychological profile among carriers and noncarriers of the FMR1 premutation in adults under the age of 50. American journal of human genetics 2008 Dec 83 (6): 692-702. Hunter Jessica Ezzell, Allen Emily Graves, Abramowitz Ann, Rusin Michele, Leslie Mary, Novak Gloria, Hamilton Debra, Shubeck Lisa, Charen Krista, Sherman Stephanie |
| Intermediate and premutation FMR1 alleles in women with occult primary ovarian insufficiency. Fertility and sterility 2009 Aug 92 (2): 464-70. Streuli Isabelle, Fraisse Timothée, Ibecheole Victoria, Moix Isabelle, Morris Michael A, de Ziegler Dominiq |
| FMR1 premutation carrier frequency in patients undergoing routine population-based carrier screening: insights into the prevalence of fragile X syndrome, fragile X-associated tremor/ataxia syndrome, and fragile X-associated primary ovarian insufficiency in the United States. Genetics in medicine : official journal of the American College of Medical Genetics 2011 Jan 13 (1): 39-45. Hantash Feras M, Goos Dana M, Crossley Beryl, Anderson Ben, Zhang Ke, Sun Weimin, Strom Charles |
| Co-occurring diagnoses among FMR1 premutation allele carriers. Clinical genetics 2010 Apr 77 (4): 374-81. Hunter J E, Rohr J K, Sherman S |
| Number of CGG repeats in the FMR1 gene of Japanese patients with primary ovarian insufficiency. Fertility and sterility 2011 Nov 96 (5): 1170-4. Ishizuka Bunpei, Okamoto Naoki, Hamada Naomi, Sugishita Yodo, Saito Juichiro, Takahashi Noriyuki, Ogata Tsutomu, Itoh Masanori |
| Increased frequency of occult fragile X-associated primary ovarian insufficiency in infertile women with evidence of impaired ovarian function. Human reproduction (Oxford, England) 2011 Aug 26 (8): 2077-83. Karimov C B, Moragianni V A, Cronister A, Srouji S, Petrozza J, Racowsky C, Ginsburg E, Thornton K L, Welt C |
| A mouse model of the fragile X premutation: effects on behavior, dendrite morphology, and regional rates of cerebral protein synthesis. Neurobiology of disease 2011 1 42 (1): 85-98. Qin Mei, Entezam Ali, Usdin Karen, Huang Tianjian, Liu Zhong-Hua, Hoffman Gloria E, Smith Carolyn |
| Prevalence of CGG expansions of the FMR1 gene in a US population-based sample. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2012 Jul 159B (5): 589-97. Seltzer Marsha Mailick, Baker Mei Wang, Hong Jinkuk, Maenner Matthew, Greenberg Jan, Mandel Dani |
| FMR1 low sub-genotype does not rescue BRCA1/2-mutated human embryos and does not explain primary ovarian insufficiency among BRCA1/2-carriers. Human reproduction (Oxford, England) 2013 Aug 28 (8): 2308-11. Brandão R D, van Roozendaal K, Tserpelis D, Blok M |
| Population-based estimates of the prevalence of FMR1 expansion mutations in women with early menopause and primary ovarian insufficiency. Genetics in medicine : official journal of the American College of Medical Genetics 2013 May . Murray A, Schoemaker MJ, Bennett CE, Ennis S, Macpherson JN, Jones M, Morris DH, Orr N, Ashworth A, Jacobs PA, Swerdlow AJ |
| Association of BRCA1/2 mutations with FMR1 genotypes: effects on menarcheal and menopausal age. Maturitas 2013 Jun 75 (2): 148-51. Tea Muy-Kheng M, Weghofer Andrea, Wagner Klaus, Singer Christian |
| Prevalence and risk of migraine headaches in adult fragile X premutation carriers. Clinical genetics 2013 Feb . Au J, Scott Akins R, Berkowitz-Sutherland L, Tang HT, Chen Y, Boyd A, Tassone F, Nguyen DV, Hagerman R |
| Genomic studies in fragile X premutation carriers. Journal of neurodevelopmental disorders 2014 6 (1): 27. Lozano Reymundo, Hagerman Randi J, Duyzend Michael, Budimirovic Dejan B, Eichler Evan E, Tassone Flo |
| AMH in women with diminished ovarian reserve: potential differences by FMR1 CGG repeat level. Journal of assisted reproduction and genetics 2014 Oct 31 (10): 1295-301. Pastore Lisa M, McMurry Timothy L, Williams Christopher D, Baker Valerie L, Young Steven |
| The significance of fragile X mental retardation gene 1 CGG repeat sizes in the normal and intermediate range in women with primary ovarian insufficiency. Human reproduction (Oxford, England) 2014 Jul 29 (7): 1585-93. Voorhuis M, Onland-Moret N C, Janse F, Ploos van Amstel H K, Goverde A J, Lambalk C B, Laven J S E, van der Schouw Y T, Broekmans F J M, Fauser B C J M, |
| FMR1 gene mutation screening by TP-PCR in patients with premature ovarian failure and fragile-X. Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology 2015 Mar 31 (3): 191-5. Tural Sengul, Tekcan Ak?n, Kara Nurten, Elbistan Mehmet, Güven Davut, Ali Tasdemir Hayd |
| Curvilinear association of CGG repeats and age at menopause in women with FMR1 premutation expansions. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2014 Dec 165B (8): 705-11. Mailick Marsha R, Hong Jinkuk, Greenberg Jan, Smith Leann, Sherman Stephan |
| Diminished ovarian reserve is not observed in infertility patients with high normal CGG repeats on the fragile X mental retardation 1 (FMR1) gene. Human reproduction (Oxford, England) 2015 Sep . Schufreider Ann, McQueen Dana B, Lee Sang Mee, Allon Rachel, Uhler Meike L, Davie Jocelyn, Feinberg Eve |
| Women who carry a fragile X premutation are biologically older than noncarriers as measured by telomere length. American journal of medical genetics. Part A 2017 Sep . Albizua Igor, Rambo-Martin Benjamin L, Allen Emily G, He Weiya, Amin Ashima S, Sherman Stephanie |
| Distribution of FMR1 and FMR2 Repeats in Argentinean Patients with Primary Ovarian Insufficiency. Genes 2017 Aug 8 (8): . Espeche Lucía Daniela, Chiauzzi Violeta, Ferder Ianina, Arrar Mehrnoosh, Solari Andrea Paula, Bruque Carlos David, Delea Marisol, Belli Susana, Fernández Cecilia Soledad, Buzzalino Noemí Delia, Charreau Eduardo Hernán, Dain Liliana Beatr |
| Association of skewed X-chromosome inactivation with FMR1 CGG repeat length and anti-Mullerian hormone levels: a cohort study. Reproductive biology and endocrinology : RB&E 2017 Apr 15 (1): 34. Barad David H, Darmon Sarah, Weghofer Andrea, Latham Gary J, Filipovic-Sadic , Wang Qi, Kushnir Vitaly A, Albertini David F, Gleicher Norbe |
| Study of patterns of inheritance of premature ovarian failure syndrome carrying maternal and paternal premutations. BMC medical genetics 2018 7 19 (1): 113. Beke Artur, Piko Henriett, Haltrich Iren, Karcagi Veronika, Rigo Janos, Molnar Maria Judit, Fekete Györ |
| Clinical implication of FMR1 intermediate alleles in a Spanish population. Clinical genetics 2018 Mar . Alvarez-Mora M I, Madrigal I, Martinez F, Tejada M-I, Izquierdo-Alvarez S, Sanchez-Villar de Saz P, Caro-Llopis A, Villate O, Rodríguez-Santiago B, Pérez Jurado L A, Rodriguez-Revenga L, Milà |
| Tremor-Ataxia syndrome and primary ovarian insufficiency in an null premutation carrier. Colombia medica (Cali, Colombia) 2018 1 48 (3): 148-151. Saldarriaga-Gil Wilmar, Rodriguez-Guerrero Tatiana, Fandiño-Losada Andres, Ramirez-Cheyne Juli |
| Association between the FMR1 CGG repeat lengths and the severity of idiopathic primary ovarian insufficiency: a meta analysis. Artificial cells, nanomedicine, and biotechnology 2019 7 47 (1): 3116-3122. Huang Jing, Zhang Wenxiang, Liu Yingchun, Liu Ying, Wang Jing, Jiang Ho |
| First custom next-generation sequencing infertility panel in Latin America: design and first results. JBRA assisted reproduction 2020 3 24 (2): 104-114. Lorenzi Daniela, Fernández Cecilia, Bilinski Melina, Fabbro Mónica, Galain Micaela, Menazzi Sebastián, Miguens Mariana, Perassi Pamela Nicotra, Fulco María Florencia, Kopelman Susana, Fiszbajn Gabriel, Nodar Florencia, Papier Serg |
| Assessment of FMR1 triplet repeats in patients affected with mental retardation, fragile X syndrome and primary ovarian insufficiency. Journal of genetics 2020 2 99 . Salimy Zeinab, Akbari Mohammad Taghi, Deilamani Faravareh Khordadpo |
| Association analysis of FMR1 genetic variants and primary ovarian insufficiency in South Indian women with a novel approach of CGG repeats classification. European journal of medical genetics 2020 Oct 104081. Komaravalli Prasanna Latha, Rani S Vasantha, Dalal Ashwin, Jahan Parve |
| Both cis and trans-acting genetic factors drive somatic instability in female carriers of the FMR1 premutation. Scientific reports 2022 6 12 (1): 10419. Hwang Ye Hyun, Hayward Bruce Eliot, Zafarullah Marwa, Kumar Jay, Durbin Johnson Blythe, Holmans Peter, Usdin Karen, Tassone Flo |
| FMR1 gene CGG repeat distribution among the three individual cohorts with intellectual disability, autism, and primary ovarian insufficiency from Tamil Nadu, Southern India. Advanced genetics (Hoboken, N.J.) 2023 1 2 (2): e10048. Nagarathinam Indhumathi, Chong Samuel S, B K Thelma, Justin Margret Jeffrey, Venkataraman Viswanathan, Natarajan Padmavathy Karthikeyen, Srisailapathy C R Srikuma |
- Page last reviewed:Feb 1, 2023
- Page last updated:Sep 29, 2023
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