Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: BCL9[original query] |
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Wnt pathway genes in osteoporosis and osteoarthritis: differential expression and genetic association study. Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA 2010 Jan 21 (1): 109-18. Velasco J, Zarrabeitia M T, Prieto J R, Perez-Castrillon J L, Perez-Aguilar M D, Perez-Nuñez M I, Sañudo C, Hernandez-Elena J, Calvo I, Ortiz F, Gonzalez-Macias J, Riancho J |
Common variants in the BCL9 gene conferring risk of schizophrenia. Archives of general psychiatry 2011 Mar 68 (3): 232-40. Li Junyan, Zhou Guoquan, Ji Weidong, Feng Guoyin, Zhao Qian, Liu Jie, Li Tao, Li You, Chen Peng, Zeng Zhen, Wang Ti, Hu Zhiwei, Zheng Linqing, Wang Yang, Shen Yifeng, He Lin, Shi Yongyo |
Human gene copy number spectra analysis in congenital heart malformations. Physiological genomics 2012 Feb . Tomita-Mitchell A, Mahnke DK, Struble CA, Tuffnell ME, Stamm KD, Hidestrand M, Harris SE, Goetsch MA, Simpson PM, Bick DP, Broeckel U, Pelech AN, Tweddell JS, Mitchell ME |
Wnt-related genes and large-joint osteoarthritis: association study and replication. Rheumatology international 2013 Nov 33 (11): 2875-80. García-Ibarbia Carmen, Pérez-Castrillón José L, Ortiz Fernando, Velasco Javier, Zarrabeitia María T, Sumillera Manuel, Riancho José |
BCL9 and C9orf5 are associated with negative symptoms in schizophrenia: meta-analysis of two genome-wide association studies.
PloS one 2013 8 (1): 1. Xu C, Aragam N, Li X, Villla EC, Wang L, Briones D, Petty L, Posada Y, Arana TB, Cruz G, Mao C, Camarillo C, Su BB, Escamilla MA, Wang K |
First genome-wide association study in an Australian aboriginal population provides insights into genetic risk factors for body mass index and type 2 diabetes.
PloS one 2015 10 (3): e0119333. Anderson Denise, Cordell Heather J, Fakiola Michaela, Francis Richard W, Syn Genevieve, Scaman Elizabeth S H, Davis Elizabeth, Miles Simon J, McLeay Toby, Jamieson Sarra E, Blackwell Jenefer |
Genetic alterations in endometrial cancer by targeted next-generation sequencing. Experimental and molecular pathology 2015 Nov . Chang Ya-Sian, Huang Hsien-Da, Yeh Kun-Tu, Chang Jan-Gow |
Association study of BCL9 gene polymorphism rs583583 with schizophrenia and negative symptoms in Japanese population. Scientific reports 2015 5 15705. Kimura Hiroki, Tanaka Satoshi, Kushima Itaru, Koide Takayoshi, Banno Masahiro, Kikuchi Tsutomu, Nakamura Yukako, Shiino Tomoko, Yoshimi Akira, Oya-Ito Tomoko, Xing Jingrui, Wang Chenyao, Takasaki Yuto, Aleksic Branko, Okada Takashi, Ikeda Masashi, Inada Toshiya, Iidaka Tetsuya, Iwata Nakao, Ozaki Nor |
Multilevel genomics of colorectal cancers with microsatellite instability-clinical impact of JAK1 mutations and consensus molecular subtype 1. Genome medicine 2017 May 9 (1): 46. Sveen Anita, Johannessen Bjarne, Tengs Torstein, Danielsen Stine A, Eilertsen Ina A, Lind Guro E, Berg Kaja C G, Leithe Edward, Meza-Zepeda Leonardo A, Domingo Enric, Myklebost Ola, Kerr David, Tomlinson Ian, Nesbakken Arild, Skotheim Rolf I, Lothe Ragnhild |
Clinical and molecular characteristics of MEF2D fusion-positive B-cell precursor acute lymphoblastic leukemia in childhood, including a novel translocation resulting in MEF2D-HNRNPH1 gene fusion. Haematologica 2018 9 104 (1): 128-137. Ohki Kentaro, Kiyokawa Nobutaka, Saito Yuya, Hirabayashi Shinsuke, Nakabayashi Kazuhiko, Ichikawa Hitoshi, Momozawa Yukihide, Okamura Kohji, Yoshimi Ai, Ogata-Kawata Hiroko, Sakamoto Hiromi, Kato Motohiro, Fukushima Keitaro, Hasegawa Daisuke, Fukushima Hiroko, Imai Masako, Kajiwara Ryosuke, Koike Takashi, Komori Isao, Matsui Atsushi, Mori Makiko, Moriwaki Koichi, Noguchi Yasushi, Park Myoung-Ja, Ueda Takahiro, Yamamoto Shohei, Matsuda Koichi, Yoshida Teruhiko, Matsumoto Kenji, Hata Kenichiro, Kubo Michiaki, Matsubara Yoichi, Takahashi Hiroyuki, Fukushima Takashi, Hayashi Yasuhide, Koh Katsuyoshi, Manabe Atsushi, Ohara Akira, |
The role of BCL9 genetic variation as a biomarker for hepatitis C-related hepatocellular carcinoma in Egyptian patients. Journal, genetic engineering & biotechnology 2022 1 20 (1): 4. Abbas Eman Abd El Razek, Barakat Ahmed Barakat, Hassany Mohamed, Youssef Samar Sam |
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- Page last updated:Apr 16, 2024
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