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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 4, 2024. (Total: 234082Documents)
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Records 1 - 8 (of 8 Records)

Query Trace: EMX2[original query]
Variants in EMX2 and PTEN do not contribute to risk of endometriosis.
Molecular human reproduction 2007 Aug 13 (8): 587-94.
Treloar Susan A, Zhao Zhen Zhen, Le Lien, Zondervan Krina T, Martin Nicholas G, Kennedy Stephen, Nyholt Dale R, Montgomery Grant
Comprehensive EMX2 genotyping of a large schizencephaly case series.
American journal of medical genetics. Part A 2007 Jun 143A (12): 1313-6.
Tietjen Ian, Bodell Adria, Apse Kira, Mendonza Ashley M, Chang Bernard S, Shaw Gary M, Barkovich A James, Lammer Edward J, Walsh Christopher
Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations. GWAS Catalog
Scientific reports 2018 Jun 8 (1): 8974.
Endo Chihiro, Johnson Todd A, Morino Ryoko, Nakazono Kazuyuki, Kamitsuji Shigeo, Akita Masanori, Kawajiri Maiko, Yamasaki Tatsuya, Kami Azusa, Hoshi Yuria, Tada Asami, Ishikawa Kenichi, Hine Maaya, Kobayashi Miki, Kurume Nami, Tsunemi Yuichiro, Kamatani Naoyuki, Kawashima Mako
Copy number variation and regions of homozygosity analysis in patients with MÜLLERIAN aplasia.
Molecular cytogenetics 2018 2 11 13.
Demir Eksi Durkadin, Shen Yiping, Erman Munire, Chorich Lynn P, Sullivan Megan E, Bilekdemir Meric, Y?lmaz Elanur, Luleci Guven, Kim Hyung-Goo, Alper Ozgul M, Layman Lawrence
Perturbations of genes essential for Müllerian duct and Wölffian duct development in Mayer-Rokitansky-Küster-Hauser syndrome.
American journal of human genetics 2021 Jan .
Chen Na, Zhao Sen, Jolly Angad, Wang Lianlei, Pan Hongxin, Yuan Jian, Chen Shaoke, Koch André, Ma Congcong, Tian Weijie, Jia Ziqi, Kang Jia, Zhao Lina, Qin Chenglu, Fan Xin, Rall Katharina, Coban-Akdemir Zeynep, Chen Zefu, Jhangiani Shalini, Liang Ze, Niu Yuchen, Li Xiaoxin, Yan Zihui, Wu Yong, Dong Shuangshuang, Song Chengcheng, Qiu Guixing, Zhang Shuyang, Liu Pengfei, Posey Jennifer E, Zhang Feng, Luo Guangnan, Wu Zhihong, , Su Jianzhong, Zhang Jianguo, Chen Eugenia Y, Rouskas Konstantinos, Glentis Stavros, Bacopoulou Flora, Deligeoroglou Efthymios, Chrousos George, Lyonnet Stanislas, Polak Michel, Rosenberg Carla, Dingeldein Irene, Bonilla Ximena, Borel Christelle, Gibbs Richard A, Dietrich Jennifer E, Dimas Antigone S, Antonarakis Stylianos E, Brucker Sara Y, Lupski James R, Wu Nan, Zhu L
An Association between EMX2 Variations and Mayer-Rokitansky-Küster-Hauser Syndrome: A Case-Control Study of Chinese Women.
Journal of healthcare engineering 2022 4 2022 9975369.
Li Haiping, Liao Shi, Luo Guangnan, Li Haixia, Wang Shuai, Li Zhimin, Luo Xipi
Ancestry- and sex-specific effects underlying inguinal hernia susceptibility identified in a multiethnic genome-wide association study meta-analysis. GWAS Catalog
Human molecular genetics 2022 1 31 (13): 2279-2293.
Choquet Hélène, Li Weiyu, Yin Jie, Bradley Rachael, Hoffmann Thomas J, Nandakumar Priyanka, , Mostaedi Rouzbeh, Tian Chao, Ahituv Nadav, Jorgenson Er
Role of chromosomal imbalances in the pathogenesis of DSD: A retrospective analysis of 115 prenatal samples.
European journal of medical genetics 2023 3 66 (6): 104748.
Mary L, Fradin M, Pasquier L, Quelin C, Loget P, Le Lous M, Le Bouar G, Nivot-Adamiak S, Lokchine A, Dubourg C, Jauffret V, Nouyou B, Henry C, Launay E, Odent S, Jaillard S, Belaud-Rotureau M
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