Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: NAV3[original query] |
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Antiphospholipid antibodies in a large population-based cohort: genome-wide associations and effects on monocyte gene expression.
Thrombosis and haemostasis 2016 Apr 116 (1): . Müller-Calleja Nadine, Rossmann Heidi, Müller Christian, Wild Philipp, Blankenberg Stefan, Pfeiffer Norbert, Binder Harald, Beutel Manfred E, Manukyan Davit, Zeller Tanja, Lackner Karl |
Exome and deep sequencing of clinically aggressive neuroblastoma reveal somatic mutations that affect key pathways involved in cancer progression. Oncotarget 2016 Mar . Lasorsa Vito Alessandro, Formicola Daniela, Pignataro Piero, Cimmino Flora, Calabrese Francesco Maria, Mora Jaume, Esposito Maria Rosaria, Pantile Marcella, Zanon Carlo, De Mariano Marilena, Longo Luca, Hogarty Michael D, de Torres Carmen, Tonini Gian Paolo, Iolascon Achille, Capasso Mar |
Analysis of differential ß variable region of T cell receptor expression and NAV3/TNFRSF1B gene mutation in mycosis fungoides. Oncotarget 2016 Feb . Hongzhou Cui, Jie Liu, Li Li, Jingyu Ren, Shuping Guo, Li B |
Nature vs. nurture in human sociality: multi-level genomic analyses of social conformity. Journal of human genetics 2018 2 63 (5): 605-619. Chen Biqing, Zhu Zijian, Wang Yingying, Ding Xiaohu, Guo Xiaobo, He Mingguang, Fang Wan, Zhou Qin, Zhou Shanbi, Lei Han, Huang Ailong, Chen Tingmei, Ni Dongsheng, Gu Yuping, Liu Jianing, Rao |
Exome and copy number variation analyses of Mayer-Rokitansky-Küster- Hauser syndrome. Human genome variation 2018 10 5 27. Takahashi Kazumi, Hayano Takahide, Sugimoto Ryota, Kashiwagi Hirofumi, Shinoda Mari, Nishijima Yoshihiro, Suzuki Takahiro, Suzuki Shingo, Ohnuki Yuko, Kondo Akane, Shiina Takashi, Nakaoka Hirofumi, Inoue Ituro, Izumi Shun-Ichi |
A mutational signature associated with alcohol consumption and prognostically significantly mutated driver genes in esophageal squamous cell carcinoma. Annals of oncology : official journal of the European Society for Medical Oncology 2018 Jan . Li X C, Wang M Y, Yang M, Dai H J, Zhang B F, Wang W, Chu X L, Wang X, Zheng H, Niu R F, Zhang W, Chen K |
The association between genome-wide polymorphisms and chronic postoperative pain: a prospective observational study.
Anaesthesia 2020 01 75 Suppl 1 e111-e120. van Reij R R I, Hoofwijk D M N, Rutten B P F, Weinhold L, Leber M, Joosten E A J, Ramirez A, van den Hoogen N J, |
Genomic Analysis of Response to Neoadjuvant Chemotherapy in Esophageal Adenocarcinoma. Cancers 2021 7 13 (14): . Izadi Fereshteh, Sharpe Benjamin P, Breininger Stella P, Secrier Maria, Gibson Jane, Walker Robert C, Rahman Saqib, Devonshire Ginny, Lloyd Megan A, Walters Zoë S, Fitzgerald Rebecca C, Rose-Zerilli Matthew J J, Underwood Tim J, On Behalf Of Occam |
Genomic Mutation Profile of Primary Gastrointestinal Diffuse Large B-Cell Lymphoma. Frontiers in oncology 2021 3 11 622648. Li Peifeng, Chai Jia, Chen Zi, Liu Yang, Wei Jie, Liu Yixiong, Zhao Danhui, Ma Jing, Wang Kaijing, Li Xia, Shao Yang, Gong Li, Zhang Wei, Guo Shuangping, Yan Qingguo, Li Mingyang, Fan Linni, Wang Z |
Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes. Nature genetics 2022 Sep 54 (9): 1305-1319. Zhou Xueya, Feliciano Pamela, Shu Chang, Wang Tianyun, Astrovskaya Irina, Hall Jacob B, Obiajulu Joseph U, Wright Jessica R, Murali Shwetha C, Xu Simon Xuming, Brueggeman Leo, Thomas Taylor R, Marchenko Olena, Fleisch Christopher, Barns Sarah D, Snyder LeeAnne Green, Han Bing, Chang Timothy S, Turner Tychele N, Harvey William T, Nishida Andrew, O'Roak Brian J, Geschwind Daniel H, , Michaelson Jacob J, Volfovsky Natalia, Eichler Evan E, Shen Yufeng, Chung Wendy |
The impact of blood MCP-1 levels on Alzheimer's disease with genetic variation of UNC5C and NAV3 loci. Research square 2023 10 . Jinghan Huang, Yixuan Wang, Thor D Stein, Ting Fang Alvin Ang, Yibo Zhu, Qiushan Tao, Kathryn L Lunetta, Jesse Mez, Rhoda Au, Lindsay A Farrer, Wei Qiao Qiu, Xiaoling Zha |
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- Page last updated:Apr 22, 2024
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