Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: HHAT[original query] |
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Whole-genome-wide association study in the Bulgarian population reveals HHAT as schizophrenia susceptibility gene.
Psychiatric genetics 2013 Feb 23 (1): 11-9. Betcheva Elitza T, Yosifova Adelina G, Mushiroda Taisei, Kubo Michiaki, Takahashi Atsushi, Karachanak Sena K, Zaharieva Irina T, Hadjidekova Savina P, Dimova Ivanka I, Vazharova Radoslava V, Stoyanov Drozdstoy S, Milanova Vihra K, Tolev Todor, Kirov George, Kamatani Naoyuki, Toncheva Draga I, Nakamura Yusu |
Genome-wide copy number variation analysis identifies deletion variants associated with ankylosing spondylitis. Arthritis & rheumatology (Hoboken, N.J.) 2014 Aug 66 (8): 2103-12. Jung Seung-Hyun, Yim Seon-Hee, Hu Hae-Jin, Lee Kyu Hoon, Lee Joo-Hyun, Sheen Dong-Hyuk, Lim Mi-Kyoung, Kim Soon-Young, Park Sung-Won, Kim So-Hee, Han Kyudong, Kim Tae-Hwan, Shim Seung-Cheol, Chung Yeun-J |
Exome chip analyses identify genes affecting mortality after HLA-matched unrelated-donor blood and marrow transplantation. Blood 2018 Apr . Zhu Qianqian, Yan Li, Liu Qian, Zhang Chi, Wei Lei, Hu Qiang, Preus Leah, Clay-Gilmour Alyssa I, Onel Kenan, Stram Daniel O, Pooler Loreall, Sheng Xin, Haiman Christopher A, Zhu Xiaochun, Spellman Stephen R, Pasquini Marcelo, McCarthy Philip L, Liu Song, Hahn Theresa, Sucheston-Campbell Lara |
A logical relationship for schizophrenia, bipolar, and major depressive disorder. Part 1: Evidence from chromosome 1 high density association screen. The Journal of comparative neurology 2020 4 528 (15): 2620-2635. Zhang Zhihua, Chen Ga |
Genome-Wide Scan for Parent-of-Origin Effects in a sub-Saharan African Cohort With Nonsyndromic Cleft Lip and/or Cleft Palate (CL/P). The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association 2021 Aug 10556656211036316. Gowans Lord J J, Comnick Carissa L, Mossey Peter A, Eshete Mekonen A, Adeyemo Wasiu L, Naicker Thirona, Awotoye Waheed A, Petrin Aline, Adeleke Chinyere, Donkor Peter, Busch Tamara D, James Olutayo, Ogunlewe Mobolanle O, Li Mary, Olotu Joy, Hassan Mohaned, Adeniyan Oluwole A, Obiri-Yeboah Solomon, Arthur Fareed K N, Agbenorku Pius, Oti Alexander A, Olatosi Olubukola, Adamson Olawale O, Fashina Azeez A, Zeng Erliang, Marazita Mary L, Adeyemo Adebowale A, Murray Jeffrey C, Butali Aze |
Advances in genomic diagnosis of a large cohort of Egyptian patients with disorders of sex development. American journal of medical genetics. Part A 2021 3 185 (6): 1666-1677. Mazen Inas, Mekkawy Mona, Kamel Alaa, Essawi Mona, Hassan Heba, Abdel-Hamid Mohamed, Amr Khalda, Soliman Hala, El-Ruby Mona, Torky Ahmed, El Gammal Mona, Elaidy Aya, Bashamboo Anu, McElreavey Kenne |
Additional evidence for the role of chromosomal imbalances and SOX8, ZNRF3 and HHAT gene variants in early human testis development. Reproductive biology and endocrinology : RB&E 2023 1 21 (1): 2. Rjiba Khouloud, Mougou-Zerelli Soumaya, Hamida Imen Hadj, Saad Ghada, Khadija Bochra, Jelloul Afef, Slimani Wafa, Hasni Yosra, Dimassi Sarra, Khelifa Hela Ben, Sallem Amira, Kammoun Molka, Abdallah Hamza Hadj, Gribaa Moez, Bignon-Topalovic Joelle, Chelly Sami, Khairi Hédi, Bibi Mohamed, Kacem Maha, Saad Ali, Bashamboo Anu, McElreavey Kenne |
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- Page last updated:Apr 22, 2024
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