Human Genome Epidemiology Literature Finder
Records 1 - 6 (of 6 Records) |
Query Trace: NXN[original query] |
---|
Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk.
Nature genetics 2014 Jun 46 (6): 533-42. Zhang Ben, Jia Wei-Hua, Matsuda Koichi, Kweon Sun-Seog, Matsuo Keitaro, Xiang Yong-Bing, Shin Aesun, Jee Sun Ha, Kim Dong-Hyun, Cai Qiuyin, Long Jirong, Shi Jiajun, Wen Wanqing, Yang Gong, Zhang Yanfeng, Li Chun, Li Bingshan, Guo Yan, Ren Zefang, Ji Bu-Tian, Pan Zhi-Zhong, Takahashi Atsushi, Shin Min-Ho, Matsuda Fumihiko, Gao Yu-Tang, Oh Jae Hwan, Kim Soriul, Ahn Yoon-Ok, , Chan Andrew T, Chang-Claude Jenny, Slattery Martha L, , Gruber Stephen B, Schumacher Fredrick R, Stenzel Stephanie L, , Casey Graham, Kim Hyeong-Rok, Jeong Jin-Young, Park Ji Won, Li Hong-Lan, Hosono Satoyo, Cho Sang-Hee, Kubo Michiaki, Shu Xiao-Ou, Zeng Yi-Xin, Zheng W |
De novo large rare copy-number variations contribute to conotruncal heart disease in Chinese patients. NPJ genomic medicine 2016 1 16033. Mak Christopher C Y, Chow Pak Cheong, Liu Anthony P Y, Chan Kelvin Y K, Chu Yoyo W Y, Mok Gary T K, Leung Gordon K C, Yeung Kit San, Chau Adolphus K T, Lowther Chelsea, Scherer Stephen W, Marshall Christian R, Bassett Anne S, Chung Brian H |
CYP2D6 basic genotyping as a potential tool to improve the antiemetic efficacy of ondansetron in prophylaxis of postoperative nausea and vomiting. Advances in clinical and experimental medicine : official organ Wroclaw Medical University 2018 Jul . Niewi?ski Przemys?aw A, Wojciechowski Robert, ?liwi?ski Marek, Hurkacz Magdalena E, G?owacka Krystyna, Orzechowska-Juzwenko Krystyna, Wiela-Hoje?ska Anna |
Genetic variation in Charcot-Marie-Tooth genes contributes to sensitivity to paclitaxel-induced peripheral neuropathy. Pharmacogenomics 2020 7 21 (12): 841-851. Chen Yongzhen, Fang Fang, Kidwell Kelley M, Vangipuram Kiran, Marcath Lauren A, Gersch Christina L, Rae James M, Hayes Daniel F, Lavoie Smith Ellen M, Henry N Lynn, Beutler Andreas S, Hertz Daniel |
Novel pathogenic genomic variants leading to autosomal dominant and recessive Robinow syndrome. American journal of medical genetics. Part A 2020 Oct . Zhang Chaofan, Mazzeu Juliana F, Eisfeldt Jesper, Grochowski Christopher M, White Janson, Akdemir Zeynep C, Jhangiani Shalini N, Muzny Donna M, Gibbs Richard A, Lindstrand Anna, Lupski James R, Sutton V Reid, Carvalho Claudia M |
Novel pathogenic variants and quantitative phenotypic analyses of Robinow syndrome: WNT signaling perturbation and phenotypic variability. HGG advances 2022 1 3 (1): 100074. Zhang Chaofan, Jolly Angad, Shayota Brian J, Mazzeu Juliana F, Du Haowei, Dawood Moez, Soper Patricia Celestino, Ramalho de Lima Ariadne, Ferreira Bárbara Merfort, Coban-Akdemir Zeynep, White Janson, Shears Deborah, Thomson Fraser Robert, Douglas Sarah Louise, Wainwright Andrew, Bailey Kathryn, Wordsworth Paul, Oldridge Mike, Lester Tracy, Calder Alistair D, Dumic Katja, Banka Siddharth, Donnai Dian, Jhangiani Shalini N, Potocki Lorraine, Chung Wendy K, Mora Sara, Northrup Hope, Ashfaq Myla, Rosenfeld Jill A, Mason Kati, Pollack Lynda C, McConkie-Rosell Allyn, Kelly Wei, McDonald Marie, Hauser Natalie S, Leahy Peter, Powell Cynthia M, Boy Raquel, Honjo Rachel Sayuri, Kok Fernando, Martelli Lucia R, Filho Vicente Odone, Genomics England Research Consortium , Muzny Donna M, Gibbs Richard A, Posey Jennifer E, Liu Pengfei, Lupski James R, Sutton V Reid, Carvalho Claudia M |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: