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1
Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections
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Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections

Tian, Chao ; Hromatka, Bethann S ; Kiefer, Amy K ; Eriksson, Nicholas ; Noble, Suzanne M ; Tung, Joyce Y ; Hinds, David A

Nature communications, 2017-09, Vol.8 (1), p.599-13, Article 599 [Periódico revisado por pares]

England: Nature Publishing Group

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2
Genome-wide association study in Asian populations identifies variants in ETS1 and WDFY4 associated with systemic lupus erythematosus
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Genome-wide association study in Asian populations identifies variants in ETS1 and WDFY4 associated with systemic lupus erythematosus

Yang, Wanling ; Shen, Nan ; Ye, Dong-Qing ; Liu, Qiji ; Zhang, Yan ; Qian, Xiao-Xia ; Hirankarn, Nattiya ; Ying, Dingge ; Pan, Hai-Feng ; Mok, Chi Chiu ; Chan, Tak Mao ; Wong, Raymond Woon Sing ; Lee, Ka Wing ; Mok, Mo Yin ; Wong, Sik Nin ; Leung, Alexander Moon Ho ; Li, Xiang-Pei ; Avihingsanon, Yingyos ; Wong, Chun-Ming ; Lee, Tsz Leung ; Ho, Marco Hok Kung ; Lee, Pamela Pui Wah ; Chang, Yuk Kwan ; Li, Philip H ; Li, Ruo-Jie ; Zhang, Lu ; Wong, Wilfred Hing Sang ; Ng, Irene Oi Lin ; Lau, Chak Sing ; Sham, Pak Chung ; Lau, Yu Lung Flint, Jonathan

PLoS genetics, 2010-02, Vol.6 (2), p.e1000841-e1000841 [Periódico revisado por pares]

United States: Public Library of Science

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3
Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways
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Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways

Duffy, David L ; Zhu, Gu ; Li, Xin ; Sanna, Marianna ; Iles, Mark M ; Jacobs, Leonie C ; Evans, David M ; Yazar, Seyhan ; Beesley, Jonathan ; Law, Matthew H ; Kraft, Peter ; Visconti, Alessia ; Taylor, John C ; Liu, Fan ; Wright, Margaret J ; Henders, Anjali K ; Bowdler, Lisa ; Glass, Dan ; Ikram, M Arfan ; Uitterlinden, André G ; Madden, Pamela A ; Heath, Andrew C ; Nelson, Elliot C ; Green, Adele C ; Chanock, Stephen ; Barrett, Jennifer H ; Brown, Matthew A ; Hayward, Nicholas K ; MacGregor, Stuart ; Sturm, Richard A ; Hewitt, Alex W ; Kayser, Manfred ; Hunter, David J ; Newton Bishop, Julia A ; Spector, Timothy D ; Montgomery, Grant W ; Mackey, David A ; Smith, George Davey ; Nijsten, Tamar E ; Bishop, D Timothy ; Bataille, Veronique ; Falchi, Mario ; Han, Jiali ; Martin, Nicholas G

Nature communications, 2018-11, Vol.9 (1), p.4774-10, Article 4774 [Periódico revisado por pares]

England: Nature Publishing Group

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4
Quantifying the polygenic contribution to variable expressivity in eleven rare genetic disorders
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Quantifying the polygenic contribution to variable expressivity in eleven rare genetic disorders

Oetjens, M T ; Kelly, M A ; Sturm, A C ; Martin, C L ; Ledbetter, D H

Nature communications, 2019-10, Vol.10 (1), p.4897-10, Article 4897 [Periódico revisado por pares]

England: Nature Publishing Group

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5
Genomic Analyses Reveal Mutational Signatures and Frequently Altered Genes in Esophageal Squamous Cell Carcinoma
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Genomic Analyses Reveal Mutational Signatures and Frequently Altered Genes in Esophageal Squamous Cell Carcinoma

Zhang, Ling ; Zhou, Yong ; Cheng, Caixia ; Cui, Heyang ; Cheng, Le ; Kong, Pengzhou ; Wang, Jiaqian ; Li, Yin ; Chen, Wenliang ; Song, Bin ; Wang, Fang ; Jia, Zhiwu ; Li, Lin ; Li, Yaoping ; Yang, Bin ; Liu, Jing ; Shi, Ruyi ; Bi, Yanghui ; Zhang, Yanyan ; Wang, Juan ; Zhao, Zhenxiang ; Hu, Xiaoling ; Yang, Jie ; Li, Hongyi ; Gao, Zhibo ; Chen, Gang ; Huang, Xuanlin ; Yang, Xukui ; Wan, Shengqing ; Chen, Chao ; Li, Bin ; Tan, Yongkai ; Chen, Longyun ; He, Minghui ; Xie, Sha ; Li, Xiangchun ; Zhuang, Xuehan ; Wang, Mengyao ; Xia, Zhi ; Luo, Longhai ; Ma, Jie ; Dong, Bing ; Zhao, Jiuzhou ; Song, Yongmei ; Ou, Yunwei ; Li, Enming ; Xu, Liyan ; Wang, Jinfen ; Xi, Yanfeng ; Li, Guodong ; Xu, Enwei ; Liang, Jianfang ; Yang, Xiaofeng ; Guo, Jiansheng ; Chen, Xing ; Zhang, Yanbo ; Li, Qingshan ; Liu, Lixin ; Li, Yingrui ; Zhang, Xiuqing ; Yang, Huanming ; Lin, Dongxin ; Cheng, Xiaolong ; Guo, Yongjun ; Wang, Jun ; Zhan, Qimin ; Cui, Yongping

American journal of human genetics, 2015-04, Vol.96 (4), p.597-611 [Periódico revisado por pares]

United States: Elsevier Inc

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6
Integrated genetic and epigenetic analysis defines novel molecular subgroups in rhabdomyosarcoma
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Integrated genetic and epigenetic analysis defines novel molecular subgroups in rhabdomyosarcoma

Seki, Masafumi ; Nishimura, Riki ; Yoshida, Kenichi ; Shimamura, Teppei ; Shiraishi, Yuichi ; Sato, Yusuke ; Kato, Motohiro ; Chiba, Kenichi ; Tanaka, Hiroko ; Hoshino, Noriko ; Nagae, Genta ; Shiozawa, Yusuke ; Okuno, Yusuke ; Hosoi, Hajime ; Tanaka, Yukichi ; Okita, Hajime ; Miyachi, Mitsuru ; Souzaki, Ryota ; Taguchi, Tomoaki ; Koh, Katsuyoshi ; Hanada, Ryoji ; Kato, Keisuke ; Nomura, Yuko ; Akiyama, Masaharu ; Oka, Akira ; Igarashi, Takashi ; Miyano, Satoru ; Aburatani, Hiroyuki ; Hayashi, Yasuhide ; Ogawa, Seishi ; Takita, Junko

Nature communications, 2015-07, Vol.6 (1), p.7557-7557, Article 7557 [Periódico revisado por pares]

England: Nature Publishing Group

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7
Runx1 is a central regulator of osteogenesis for bone homeostasis by orchestrating BMP and WNT signaling pathways
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Runx1 is a central regulator of osteogenesis for bone homeostasis by orchestrating BMP and WNT signaling pathways

Tang, Chen-Yi ; Wu, Mengrui ; Zhao, Dongfeng ; Edwards, Diep ; McVicar, Abigail ; Luo, Yuan ; Zhu, Guochun ; Wang, Yongjun ; Zhou, Hou-De ; Chen, Wei ; Li, Yi-Ping LONG, FANXIN

PLoS genetics, 2021-01, Vol.17 (1), p.e1009233-e1009233 [Periódico revisado por pares]

United States: Public Library of Science

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8
Whole-exome sequencing of pancreatic cancer defines genetic diversity and therapeutic targets
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Whole-exome sequencing of pancreatic cancer defines genetic diversity and therapeutic targets

Witkiewicz, Agnieszka K ; McMillan, Elizabeth A ; Balaji, Uthra ; Baek, GuemHee ; Lin, Wan-Chi ; Mansour, John ; Mollaee, Mehri ; Wagner, Kay-Uwe ; Koduru, Prasad ; Yopp, Adam ; Choti, Michael A ; Yeo, Charles J ; McCue, Peter ; White, Michael A ; Knudsen, Erik S

Nature communications, 2015-04, Vol.6 (1), p.6744-6744, Article 6744 [Periódico revisado por pares]

England: Nature Publishing Group

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9
Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients
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Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients

Inoue, Takanobu ; Nakamura, Akie ; Iwahashi-Odano, Megumi ; Tanase-Nakao, Kanako ; Matsubara, Keiko ; Nishioka, Junko ; Maruo, Yoshihiro ; Hasegawa, Yukihiro ; Suzumura, Hiroshi ; Sato, Seiji ; Kobayashi, Yoshiyuki ; Murakami, Nobuyuki ; Nakabayashi, Kazuhiko ; Yamazawa, Kazuki ; Fuke, Tomoko ; Narumi, Satoshi ; Oka, Akira ; Ogata, Tsutomu ; Fukami, Maki ; Kagami, Masayo

Clinical epigenetics, 2020-06, Vol.12 (1), p.86-86, Article 86 [Periódico revisado por pares]

Germany: BioMed Central Ltd

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10
A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease loci
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A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease loci

Liu, Ying ; Helms, Cynthia ; Liao, Wilson ; Zaba, Lisa C ; Duan, Shenghui ; Gardner, Jennifer ; Wise, Carol ; Miner, Andrew ; Malloy, M J ; Pullinger, Clive R ; Kane, John P ; Saccone, Scott ; Worthington, Jane ; Bruce, Ian ; Kwok, Pui-Yan ; Menter, Alan ; Krueger, James ; Barton, Anne ; Saccone, Nancy L ; Bowcock, Anne M Leal, Suzanne M.

PLoS genetics, 2008-04, Vol.4 (3), p.e1000041-e1000041 [Periódico revisado por pares]

United States: Public Library of Science

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