Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: MSH4[original query] |
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Genetic investigation of four meiotic genes in women with premature ovarian failure. European journal of endocrinology / European Federation of Endocrine Societies 2008 Jan 158 (1): 107-15. Mandon-Pépin Béatrice, Touraine Philippe, Kuttenn Frédérique, Derbois Céline, Rouxel Agnes, Matsuda Fumihiko, Nicolas Alain, Cotinot Corinne, Fellous Ma |
Common variants in mismatch repair genes associated with increased risk of sperm DNA damage and male infertility. BMC medicine 2012 10 (1): 49. Ji Guixiang, Long Yan, Zhou Yong, Huang Cong, Gu Aihua, Wang Xin |
Mismatch repair single nucleotide polymorphisms and thyroid cancer susceptibility. Oncology letters 2018 May 15 (5): 6715-6726. Santos Luís S, Silva Susana N, Gil Octávia M, Ferreira Teresa C, Limbert Edward, Rueff Jo |
Micronuclei Formation upon Radioiodine Therapy for Well-Differentiated Thyroid Cancer: The Influence of DNA Repair Genes Variants. Genes 2020 9 11 (9): . S Santos Luís, M Gil Octávia, N Silva Susana, C Gomes Bruno, C Ferreira Teresa, Limbert Edward, Rueff Jo |
Genetic dissection of spermatogenic arrest through exome analysis: clinical implications for the management of azoospermic men. Genetics in medicine : official journal of the American College of Medical Genetics 2020 Aug . Krausz Csilla, Riera-Escamilla Antoni, Moreno-Mendoza Daniel, Holleman Kaylee, Cioppi Francesca, Algaba Ferran, Pybus Marc, Friedrich Corinna, Wyrwoll Margot J, Casamonti Elena, Pietroforte Sara, Nagirnaja Liina, Lopes Alexandra M, Kliesch Sabine, Pilatz Adrian, Carrell Douglas T, Conrad Donald F, Ars Elisabet, Ruiz-Castañé Eduard, Aston Kenneth I, Baarends Willy M, Tüttelmann Fra |
Novel LRRK2 mutations and other rare, non-BAP1-related candidate tumor predisposition gene variants in high-risk cancer families with mesothelioma and other tumors. Human molecular genetics 2021 5 30 (18): 1750-1761. Cheung Mitchell, Kadariya Yuwaraj, Sementino Eleonora, Hall Michael J, Cozzi Ilaria, Ascoli Valeria, Ohar Jill A, Testa Joseph |
A novel homozygous mutation in the meiotic gene MSH4 leading to male infertility due to non-obstructive azoospermia. American journal of translational research 2021 1 12 (12): 8185-8191. Tang Dongdong, Xu Chuan, Geng Hao, Gao Yang, Cheng Huiru, Ni Xiaoqing, He Xiaojin, Cao Yunx |
Next-generation sequencing of 500 POI patients identified novel responsible monogenic and oligogenic variants. Journal of ovarian research 2023 2 16 (1): 39. Luo Wei, Ke Hanni, Tang Shuyan, Jiao Xue, Li Zhuqing, Zhao Shidou, Zhang Feng, Guo Ting, Qin Yingyi |
Novel Candidate loci and Pathogenic Germline Variants Involved in Familial Hematological Malignancies Revealed by Whole-Exome Sequencing. Cancers 2023 2 15 (3): . Andrés-Zayas Cristina, Suárez-González Julia, Chicano-Lavilla María, Bastos Oreiro Mariana, Rodríguez-Macías Gabriela, Font López Patricia, Osorio Prendes Santiago, Oarbeascoa Royuela Gillen, García Ramírez Patricia, Nieves Salgado Rocío, Gómez-Centurión Ignacio, Carbonell Muñoz Diego, Muñiz Paula, Kwon Mi, Díez-Martín José Luis, Buño Ismael, Martínez-Laperche Caroli |
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- Page last updated:Apr 29, 2024
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