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Genome-wide association study in Asian populations identifies variants in ETS1 and WDFY4 associated with systemic lupus erythematosus
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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2
A genome-wide association study of anorexia nervosa
A genome-wide association study of anorexia nervosa
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A genome-wide association study of anorexia nervosa

Floyd, J A B ; Southam, L ; Rayner, N W ; Treasure, J ; Schmidt, U ; Tozzi, F ; Gorwood, P ; Adan, R A H ; Favaro, A ; Santonastaso, P ; Gratacos, M ; Keski-Rahkonen, A ; Van Furth, E F ; Slof-Op 't Landt, M C T ; Reichborn-Kjennerud, T ; Knudsen, G P S ; Monteleone, P ; Kaplan, A S ; Karwautz, A ; Li, D ; Schork, N J ; Komaki, G ; Inoko, H ; Esko, T ; Baker, J H ; Hilliard, C E ; O'Toole, J K ; Pantel, J ; Szatkiewicz, J P ; Taico, C ; Burghardt, R ; de Zwaan, M ; Egberts, K ; Imgart, H ; Scherag, A ; Zipfel, S ; Versini, A ; Brandys, M K ; de Kovel, C ; Hendriks, J ; Koeleman, B P C ; Ophoff, R A ; Strengman, E ; Bruson, A ; Escaramís, G ; Jiménez-Murcia, S ; Rajewski, A ; Szeszenia-Dabrowska, N ; Slopien, A ; Hauser, J ; Slagboom, P E ; Maj, M ; Dedoussis, G ; Dikeos, D ; Tziouvas, K ; Papezova, H ; Slachtova, L ; Martaskova, D ; Kennedy, J L ; Levitan, R D ; Koubek, D ; Merl, E ; Wagner, G ; Lichtenstein, P ; Breen, G ; Farmer, A ; McGuffin, P ; Giegling, I ; Herms, S ; Wichmann, H-E ; Dina, C ; Sladek, R ; Gambaro, G ; Julia, A ; Gaborieau, V ; Dick, D M ; Ripatti, S ; Widén, E ; Espeseth, T ; Lundervold, A ; Reinvang, I ; Steen, V M ; Ntalla, I ; Foretova, L ; Navratilova, M ; Pinto, D ; Scherer, S W ; Aschauer, H ; Schosser, A ; Courtet, P ; Guillaume, S ; Jaussent, I ; Finan, C ; Kalsi, G ; Roberts, M ; Logan, D W ; Peltonen, L ; Ritchie, G R S ; Barrett, J C ; Sullivan, P F

Molecular psychiatry, 2014-10, Vol.19 (10), p.1085-1094 [Periódico revisado por pares]

England: Nature Publishing Group

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3
Runx1 is a central regulator of osteogenesis for bone homeostasis by orchestrating BMP and WNT signaling pathways
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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4
Multiplex Targeted Sequencing Identifies Recurrently Mutated Genes in Autism Spectrum Disorders
Multiplex Targeted Sequencing Identifies Recurrently Mutated Genes in Autism Spectrum Disorders
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Multiplex Targeted Sequencing Identifies Recurrently Mutated Genes in Autism Spectrum Disorders

O'Roak, Brian J. ; Vives, Laura ; Fu, Wenqing ; Egertson, Jarrett D. ; Stanaway, Ian B. ; Phelps, Ian G. ; Carvill, Gemma ; Kumar, Akash ; Lee, Choli ; Ankenman, Katy ; Munson, Jeff ; Hiatt, Joseph B. ; Turner, Emily H. ; Levy, Roie ; O'Day, Diana R. ; Krumm, Niklas ; Coe, Bradley P. ; Martin, Beth K. ; Borenstein, Elhanan ; Nickerson, Deborah A. ; Mefford, Heather C. ; Doherty, Dan ; Akey, Joshua M. ; Bernier, Raphael ; Eichler, Evan E. ; Shendure, Jay

Science (American Association for the Advancement of Science), 2012-12, Vol.338 (6114), p.1619-1622 [Periódico revisado por pares]

Washington, DC: American Association for the Advancement of Science

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5
Germline BAP1 mutation predisposes to uveal melanoma, lung adenocarcinoma, meningioma, and other cancers
Germline BAP1 mutation predisposes to uveal melanoma, lung adenocarcinoma, meningioma, and other cancers
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Germline BAP1 mutation predisposes to uveal melanoma, lung adenocarcinoma, meningioma, and other cancers

Abdel-Rahman, Mohamed H ; Pilarski, Robert ; Cebulla, Colleen M ; Massengill, James B ; Christopher, Benjamin N ; Boru, Getachew ; Hovland, Peter ; Davidorf, Frederick H

Journal of medical genetics, 2011-12, Vol.48 (12), p.856-859 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd

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6
Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients
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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7
A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease loci
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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8
The role of nucleosome positioning in the evolution of gene regulation
The role of nucleosome positioning in the evolution of gene regulation
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The role of nucleosome positioning in the evolution of gene regulation

Tsankov, Alexander M ; Thompson, Dawn Anne ; Socha, Amanda ; Regev, Aviv ; Rando, Oliver J Becker, Peter B.

PLoS biology, 2010-07, Vol.8 (7), p.e1000414 [Periódico revisado por pares]

United States: Public Library of Science

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9
Bacterial genes in the aphid genome: absence of functional gene transfer from Buchnera to its host
Bacterial genes in the aphid genome: absence of functional gene transfer from Buchnera to its host
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Bacterial genes in the aphid genome: absence of functional gene transfer from Buchnera to its host

Nikoh, Naruo ; McCutcheon, John P ; Kudo, Toshiaki ; Miyagishima, Shin-ya ; Moran, Nancy A ; Nakabachi, Atsushi Copenhaver, Gregory P.

PLoS genetics, 2010-02, Vol.6 (2), p.e1000827-e1000827 [Periódico revisado por pares]

United States: Public Library of Science

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10
RNA-directed DNA Methylation
RNA-directed DNA Methylation
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RNA-directed DNA Methylation

Erdmann, Robert M ; Picard, Colette L

PLoS genetics, 2020-10, Vol.16 (10), p.e1009034-e1009034 [Periódico revisado por pares]

United States: Public Library of Science

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