Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: PDHB[original query] |
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Spectrum of diverse genomic alterations define non-clear cell renal carcinoma subtypes. Nature genetics 2015 Jan 47 (1): 13-21. Durinck Steffen, Stawiski Eric W, Pavía-Jiménez Andrea, Modrusan Zora, Kapur Payal, Jaiswal Bijay S, Zhang Na, Toffessi-Tcheuyap Vanina, Nguyen Thong T, Pahuja Kanika Bajaj, Chen Ying-Jiun, Saleem Sadia, Chaudhuri Subhra, Heldens Sherry, Jackson Marlena, Peña-Llopis Samuel, Guillory Joseph, Toy Karen, Ha Connie, Harris Corissa J, Holloman Eboni, Hill Haley M, Stinson Jeremy, Rivers Celina Sanchez, Janakiraman Vasantharajan, Wang Weiru, Kinch Lisa N, Grishin Nick V, Haverty Peter M, Chow Bernard, Gehring Julian S, Reeder Jens, Pau Gregoire, Wu Thomas D, Margulis Vitaly, Lotan Yair, Sagalowsky Arthur, Pedrosa Ivan, de Sauvage Frederic J, Brugarolas James, Seshagiri Somasek |
Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels.
Circulation 2019 Jan 139 (5): 620-635. Sabater-Lleal Maria, Huffman Jennifer E, de Vries Paul S, Marten Jonathan, Mastrangelo Michael A, Song Ci, Pankratz Nathan, Ward-Caviness Cavin K, Yanek Lisa R, Trompet Stella, Delgado Graciela E, Guo Xiuqing, Bartz Traci M, Martinez-Perez Angel, Germain Marine, de Haan Hugoline G, Ozel Ayse B, Polasek Ozren, Smith Albert V, Eicher John D, Reiner Alex P, Tang Weihong, Davies Neil M, Stott David J, Rotter Jerome I, Tofler Geoffrey H, Boerwinkle Eric, de Maat Moniek P M, Kleber Marcus E, Welsh Paul, Brody Jennifer A, Chen Ming-Huei, Vaidya Dhananjay, Soria José Manuel, Suchon Pierre, van Hylckama Vlieg Astrid, Desch Karl C, Kolcic Ivana, Joshi Peter K, Launer Lenore J, Harris Tamara B, Campbell Harry, Rudan Igor, Becker Diane M, Li Jun Z, Rivadeneira Fernando, Uitterlinden André G, Hofman Albert, Franco Oscar H, Cushman Mary, Psaty Bruce M, Morange Pierre-Emmanuel, McKnight Barbara, Chong Michael R, Fernandez-Cadenas Israel, Rosand Jonathan, Lindgren Arne, , Gudnason Vilmundur, Wilson James F, Hayward Caroline, Ginsburg David, Fornage Myriam, Rosendaal Frits R, Souto Juan Carlos, Becker Lewis C, Jenny Nancy S, März Winfried, Jukema J Wouter, Dehghan Abbas, Trégouët David-Alexandre, Morrison Alanna C, Johnson Andrew D, O'Donnell Christopher J, Strachan David P, Lowenstein Charles J, Smith Nicholas |
Identification of non-HLA genes associated with development of islet autoimmunity and type 1 diabetes in the prospective TEDDY cohort.
Journal of autoimmunity 2018 Jan . Sharma Ashok, Liu Xiang, Hadley David, Hagopian William, Chen Wei-Min, Onengut-Gumuscu Suna, Törn Carina, Steck Andrea K, Frohnert Brigitte I, Rewers Marian, Ziegler Anette-G, Lernmark Åke, Toppari Jorma, Krischer Jeffrey P, Akolkar Beena, Rich Stephen S, She Jin-Xiong, |
Transcriptome-wide association study identifies susceptibility genes for rheumatoid arthritis. Arthritis research & therapy 2021 Jan 23 (1): 38. Wu Cuiyan, Tan Sijian, Liu Li, Cheng Shiqiang, Li Peilin, Li Wenyu, Liu Huan, Zhang Feng'e, Wang Sen, Ning Yujie, Wen Yan, Zhang Fe |
Complex hereditary peripheral neuropathies caused by novel variants in mitochondrial-related nuclear genes. Journal of neurology 2022 3 269 (8): 4129-4140. Hiramatsu Yu, Okamoto Yuji, Yoshimura Akiko, Yuan Jun-Hui, Ando Masahiro, Higuchi Yujiro, Hashiguchi Akihiro, Matsuura Eiji, Nozaki Fumihito, Kumada Tomohiro, Murayama Kei, Suzuki Mikiya, Yamamoto Yuki, Matsui Naoko, Miyazaki Yoshimichi, Yamaguchi Masamitsu, Suzuki Youji, Mitsui Jun, Ishiura Hiroyuki, Tanaka Masaki, Morishita Shinichi, Nishino Ichizo, Tsuji Shoji, Takashima Hiros |
A novel cuproptosis-related gene signature of prognosis and immune microenvironment in head and neck squamous cell carcinoma cancer. Journal of cancer research and clinical oncology 2022 11 149 (1): 203-218. Jiang Xu, Ke Jing, Jia Lifeng, An Xiang, Ma Haiyu, Li Zhongwan, Yuan W |
Potential impact of cuproptosis-related genes on tumor immunity in esophageal carcinoma. Aging 2023 12 15 (24): 15535-15556. Pengfei Guo, Zemiao Niu, Dengfeng Zhang, Fangchao Zhao, Jing Li, Tianxing Lu, Xuebo Qin, Shiquan Liu, Zhirong Li, Yishuai Li, Shujun |
Leigh Syndrome: Spectrum of Molecular Defects and Clinical Features in Russia. International journal of molecular sciences 2023 1 24 (2): . Kistol Denis, Tsygankova Polina, Krylova Tatiana, Bychkov Igor, Itkis Yulia, Nikolaeva Ekaterina, Mikhailova Svetlana, Sumina Maria, Pechatnikova Natalia, Kurbatov Sergey, Bostanova Fatima, Migiaev Ochir, Zakharova Ekateri |
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