Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: EIF4G3[original query] |
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Common variants at 1p36 are associated with superior frontal gyrus volume.
Translational psychiatry 2014 4 e472. Hashimoto R, Ikeda M, Yamashita F, Ohi K, Yamamori H, Yasuda Y, Fujimoto M, Fukunaga M, Nemoto K, Takahashi T, Tochigi M, Onitsuka T, Yamasue H, Matsuo K, Iidaka T, Iwata N, Suzuki M, Takeda M, Kasai K, Ozaki |
De novo and biallelic DEAF1 variants cause a phenotypic spectrum. Genetics in medicine : official journal of the American College of Medical Genetics 2019 3 21 (9): 2059-2069. Nabais Sá Maria J, Jensik Philip J, McGee Stacey R, Parker Michael J, Lahiri Nayana, McNeil Evan P, Kroes Hester Y, Hagerman Randi J, Harrison Rachel E, Montgomery Tara, Splitt Miranda, Palmer Elizabeth E, Sachdev Rani K, Mefford Heather C, Scott Abbey A, Martinez-Agosto Julian A, Lorenz Rüdiger, Orenstein Naama, Berg Jonathan N, Amiel Jeanne, Heron Delphine, Keren Boris, Cobben Jan-Maarten, Menke Leonie A, Marco Elysa J, Graham John M, Pierson Tyler Mark, Karimiani Ehsan Ghayoor, Maroofian Reza, Manzini M Chiara, Cauley Edmund S, Colombo Roberto, Odent Sylvie, Dubourg Christele, Phornphutkul Chanika, de Brouwer Arjan P M, de Vries Bert B A, Vulto-vanSilfhout Anneke |
Whole-exome sequencing identifies somatic mutations and intratumor heterogeneity in inflammatory breast cancer. NPJ breast cancer 2021 6 7 (1): 72. Luo Rui, Chong Weelic, Wei Qiang, Zhang Zhenchao, Wang Chun, Ye Zhong, Abu-Khalaf Maysa M, Silver Daniel P, Stapp Robert T, Jiang Wei, Myers Ronald E, Li Bingshan, Cristofanilli Massimo, Yang Hush |
Identification of distinct genomic features reveals frequent somatic AHNAK and PTEN mutations predominantly in primary malignant melanoma presenting in the ureter. Japanese journal of clinical oncology 2022 5 52 (8): 930-943. Huang Yan, Wei Lai, Huang Yuanbin, Wen Shuang, Liu Tianqing, Duan Xu, Wang Yutong, Zhang Hongshuo, Fan Bo, Hu B |
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- Page last updated:Apr 22, 2024
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