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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
SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues
SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues
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SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues

D’Antonio, Matteo ; Chwialkowska, Karolina ; Tenesa, Albert ; D’Mellow, Kenton ; Aprile von Hohenstaufen, Kathrin ; Eltoukhy, Madonna M. ; Yassen, Amr M. ; Moahmed, Hanteera S. ; Tobin, Martin D. ; Guyatt, Anna L. ; Hollox, Edward J. ; Sharififard, Bahareh ; Abdollahi, Hamed ; Puthanakit, Thanyawee ; Suchartlikitwong, Pintip ; Sodsai, Pimpayao ; Alaamery, Manal ; Aljawini, Nora ; Albesher, Nour ; Alahmadey, Ziab Z. ; Suliman, Bandar A. ; Al-Afghani, Hani ; Massadeh, Salam ; Muiño, Elena ; Coto, Eliecer ; Albaiceta, Guillermo M. ; Dietl, Beatriz ; Martí-Fàbregas, Joan ; Villalonga, Joan Montaner ; Menéndez-Valladares, Paloma ; Glessner, Joseph R. ; Forgetta, Vincenzo ; Ghosh, Biswarup ; Guiot, Julien ; Guntz, Julien ; Beguin, Yves ; Claassen, Sabine ; Malaise, Olivier ; Daya, Michelle ; Chavan, Sameer ; Laisk, Triin ; Alavere, Helene ; Metsalu, Kristjan ; Peterson, Pärt ; Cortés, Beatriz ; Torrents, David ; Fallerini, Chiara ; Doddato, Gabriella ; Bruttini, Mirella ; Pinto, Anna Maria ; Bruno, Raffaele ; Picchiotti, Nicola ; Mantovani, Stefania ; Bargagli, Elena ; D’Alessandro, Miriana ; Franchi, Federico ; Cantarini, Luca ; Tacconi, Danilo ; Desanctis, Elena ; Antinori, Andrea ; Vergori, Alessandra ; Baratti, Stefano ; Menatti, Elisabetta ; Trotta, Tullio ; Martinelli, Enrico ; Bachetti, Tiziana ; Ceri, Stefano ; Parati, Gianfranco ; Ravaglia, Sabrina ; Catena, Emanuele ; Pessina, Gloria ; Tumbarello, Mario ; Guarnaccia, Alessandra ; Boughton, Andrew P. ; Annis, Aubrey ; Carey, Dave J. ; Gass, Matthew C. ; Abecasis, Goncalo R. ; Butterworth, Adam S. ; Nivard, Michel (M.G.) ; de geus, Eco (E.J.C.) ; Verma, Anurag ; Ritchie, Marylyn D. ; Verma, Shefali S. ; Lucas, Anastasia ; Karczewski, Konrad J. ; Walters, Raymond K. ; Palmer, Duncan S. ; Sarma, Gopal ; Crook, Derrick W. ; Koelling, Nils ; Moutsianas, Loukas ; Rhodes, Daniel ; Ball, Catherine A. ; Baltzell, Asher Haug ; Gaddis, Michael ; Noto, Keith ; Tang, Lara ; Nadkarni, Girish N. ; Choi, Sam

Cell reports (Cambridge), 2021-11, Vol.37 (7), p.110020-110020, Article 110020 [Periódico revisado por pares]

United States: Elsevier Inc

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3
Exome sequencing of serous endometrial tumors identifies recurrent somatic mutations in chromatin-remodeling and ubiquitin ligase complex genes
Exome sequencing of serous endometrial tumors identifies recurrent somatic mutations in chromatin-remodeling and ubiquitin ligase complex genes
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Exome sequencing of serous endometrial tumors identifies recurrent somatic mutations in chromatin-remodeling and ubiquitin ligase complex genes

LE GALLO, Matthieu ; O'HARA, Andrea J ; SGROI, Dennis C ; HIETER, Philip ; MULLIKIN, James C ; MERINO, Maria J ; BELL, Daphne W ; RUDD, Meghan L ; URICK, Mary Ellen ; HANSEN, Nancy F ; O'NEIL, Nigel J ; PRICE, Jessica C ; SUIYUAN ZHANG ; ENGLAND, Bryant M ; GODWIN, Andrew K

Nature genetics, 2012-12, Vol.44 (12), p.1310-1315 [Periódico revisado por pares]

New York, NY: Nature Publishing Group

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4
Highly effective SNP-based association mapping and management of recessive defects in livestock
Highly effective SNP-based association mapping and management of recessive defects in livestock
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Highly effective SNP-based association mapping and management of recessive defects in livestock

Charlier, Carole ; Coppieters, Wouter ; Rollin, Frédéric ; Desmecht, Daniel ; Agerholm, Jorgen S ; Cambisano, Nadine ; Carta, Eloisa ; Dardano, Sabrina ; Dive, Marc ; Fasquelle, Corinne ; Frennet, Jean-Claude ; Hanset, Roger ; Hubin, Xavier ; Jorgensen, Claus ; Karim, Latifa ; Kent, Matthew ; Harvey, Kirsten ; Pearce, Brian R ; Simon, Patricia ; Tamma, Nico ; Nie, Haisheng ; Vandeputte, Sébastien ; Lien, Sigbjorn ; Longeri, Maria ; Fredholm, Merete ; Harvey, Robert J ; Georges, Michel

Nature genetics, 2008-04, Vol.40 (4), p.449-54 [Periódico revisado por pares]

London: Nature Publishing Group

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5
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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6
Stress response, behavior, and development are shaped by transposable element-induced mutations in Drosophila
Stress response, behavior, and development are shaped by transposable element-induced mutations in Drosophila
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Stress response, behavior, and development are shaped by transposable element-induced mutations in Drosophila

Rech, Gabriel E ; Bogaerts-Márquez, María ; Barrón, Maite G ; Merenciano, Miriam ; Villanueva-Cañas, José Luis ; Horváth, Vivien ; Fiston-Lavier, Anna-Sophie ; Luyten, Isabelle ; Venkataram, Sandeep ; Quesneville, Hadi ; Petrov, Dmitri A ; González, Josefa Schaack, Sarah

PLoS genetics, 2019-02, Vol.15 (2), p.e1007900-e1007900 [Periódico revisado por pares]

United States: Public Library of Science

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7
Apolipoprotein(a) Genetic Sequence Variants Associated With Systemic Atherosclerosis and Coronary Atherosclerotic Burden But Not With Venous Thromboembolism
Apolipoprotein(a) Genetic Sequence Variants Associated With Systemic Atherosclerosis and Coronary Atherosclerotic Burden But Not With Venous Thromboembolism
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Apolipoprotein(a) Genetic Sequence Variants Associated With Systemic Atherosclerosis and Coronary Atherosclerotic Burden But Not With Venous Thromboembolism

Helgadottir, Anna, MD, PhD ; Gretarsdottir, Solveig, PhD ; Thorleifsson, Gudmar, PhD ; Holm, Hilma, MD ; Patel, Riyaz S., MD ; Gudnason, Thorarinn, MD, PhD ; Jones, Gregory T., PhD ; van Rij, Andre M., MD ; Eapen, Danny J., MD ; Baas, Annette F., PhD ; Tregouet, David-Alexandre, PhD ; Morange, Pierre-Emmanuel, MD ; Emmerich, Joseph, MD, PhD ; Lindblad, Bengt, MD, PhD ; Gottsäter, Anders, MD, PhD ; Kiemeny, Lambertus A., PhD ; Lindholt, Jes S., MD, PhD ; Sakalihasan, Natzi, MD, PhD ; Ferrell, Robert E., PhD ; Carey, David J., PhD ; Elmore, James R., MD ; Tsao, Philip S., PhD ; Grarup, Niels, MD, PhD ; Jørgensen, Torben, MD, DMSci ; Witte, Daniel R., MD, PhD ; Hansen, Torben, MD, PhD ; Pedersen, Oluf, MD, DMSci ; Pola, Roberto, MD, PhD ; Gaetani, Eleonora, MD ; Magnadottir, Hulda B., MD ; Wijmenga, Cisca, PhD ; Tromp, Gerard, PhD ; Ronkainen, Antti, MD, PhD ; Ruigrok, Ynte M., MD ; Blankensteijn, Jan D ; Mueller, Thomas, MD ; Wells, Philip S., MD ; Corral, Javier, PhD ; Soria, Jose Manuel, PhD ; Souto, Juan Carlos, MD, PhD ; Peden, John F., PhD ; Jalilzadeh, Shapour, MD, PhD ; Mayosi, Bongani M., DPhil ; Keavney, Bernard, MD ; Strawbridge, Rona J., PhD ; Sabater-Lleal, Maria, PhD ; Gertow, Karl, PhD ; Baldassarre, Damiano, PhD ; Nyyssönen, Kristiina, PhD ; Rauramaa, Rainer, MD, PhD ; Smit, Andries J., MD, PhD ; Mannarino, Elmo, MD ; Giral, Philippe, MD ; Tremoli, Elena, PhD ; de Faire, Ulf, MD, PhD ; Humphries, Steve E., PhD ; Hamsten, Anders, MD, PhD ; Haraldsdottir, Vilhelmina, MD ; Olafsson, Isleifur, MD, PhD ; Magnusson, Magnus K., MD ; Samani, Nilesh J., MD ; Levey, Allan I., MD, PhD ; Markus, Hugh S., MD ; Kostulas, Konstantinos, MD, PhD ; Dichgans, Martin, MD ; Berger, Klaus, MD ; Kuhlenbäumer, Gregor, MD ; Ringelstein, E. Bernd, MD ; Stoll, Monika, PhD ; Seedorf, Udo, PhD ; Rothwell, Peter M., MD, PhD ; Powell, Janet T., MD ; Kuivaniemi, Helena, MD, PhD ; Onundarson, Pall T., MD ; Valdimarsson, Einar, MD ; Matthiasson, Stefan E., MD, PhD ; Gudbjartsson, Daniel F., PhD ; Thorgeirsson, Guðmundur, MD, PhD ; Quyyumi, Arshed A., MD ; Watkins, Hugh, MD, PhD ; Farrall, Martin, MD ; Thorsteinsdottir, Unnur, PhD ; Stefansson, Kari, MD, PhD

Journal of the American College of Cardiology, 2012-08, Vol.60 (8), p.722-729 [Periódico revisado por pares]

New York, NY: Elsevier Inc

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8
Genome-Wide Association Study Identifies African-Specific Susceptibility Loci in African Americans With Inflammatory Bowel Disease
Genome-Wide Association Study Identifies African-Specific Susceptibility Loci in African Americans With Inflammatory Bowel Disease
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Genome-Wide Association Study Identifies African-Specific Susceptibility Loci in African Americans With Inflammatory Bowel Disease

Brant, Steven R ; Okou, David T ; Simpson, Claire L ; Cutler, David J ; Haritunians, Talin ; Bradfield, Jonathan P ; Chopra, Pankaj ; Prince, Jarod ; Begum, Ferdouse ; Kumar, Archana ; Huang, Chengrui ; Venkateswaran, Suresh ; Datta, Lisa W ; Wei, Zhi ; Thomas, Kelly ; Herrinton, Lisa J ; Klapproth, Jan-Micheal A ; Quiros, Antonio J ; Seminerio, Jenifer ; Liu, Zhenqiu ; Alexander, Jonathan S ; Baldassano, Robert N ; Dudley-Brown, Sharon ; Cross, Raymond K ; Dassopoulos, Themistocles ; Denson, Lee A ; Dhere, Tanvi A ; Dryden, Gerald W ; Hanson, John S ; Hou, Jason K ; Hussain, Sunny Z ; Hyams, Jeffrey S ; Isaacs, Kim L ; Kader, Howard ; Kappelman, Michael D ; Katz, Jeffry ; Kellermayer, Richard ; Kirschner, Barbara S ; Kuemmerle, John F ; Kwon, John H ; Lazarev, Mark ; Li, Ellen ; Mack, David ; Mannon, Peter ; Moulton, Dedrick E ; Newberry, Rodney D ; Osuntokun, Bankole O ; Patel, Ashish S ; Saeed, Shehzad A ; Targan, Stephan R ; Valentine, John F ; Wang, Ming-Hsi ; Zonca, Martin ; Rioux, John D ; Duerr, Richard H ; Silverberg, Mark S ; Cho, Judy H ; Hakonarson, Hakon ; Zwick, Michael E ; McGovern, Dermot P.B ; Kugathasan, Subra

Gastroenterology (New York, N.Y. 1943), 2017-01, Vol.152 (1), p.206-217.e2 [Periódico revisado por pares]

United States: Elsevier Inc

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9
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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10
Resequencing of 200 human exomes identifies an excess of low-frequency non-synonymous coding variants
Resequencing of 200 human exomes identifies an excess of low-frequency non-synonymous coding variants
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Resequencing of 200 human exomes identifies an excess of low-frequency non-synonymous coding variants

Pedersen, Oluf ; Nielsen, Rasmus ; Wang, Jun ; Li, Yingrui ; Vinckenbosch, Nicolas ; Tian, Geng ; Huerta-Sanchez, Emilia ; Jiang, Tao ; Jiang, Hui ; Albrechtsen, Anders ; Andersen, Gitte ; Cao, Hongzhi ; Korneliussen, Thorfinn ; Grarup, Niels ; Guo, Yiran ; Hellman, Ines ; Jin, Xin ; Li, Qibin ; Liu, Jiangtao ; Liu, Xiao ; Sparsø, Thomas ; Tang, Meifang ; Wu, Honglong ; Wu, Renhua ; Yu, Chang ; Zheng, Hancheng ; Astrup, Arne ; Bolund, Lars ; Holmkvist, Johan ; Jørgensen, Torben ; Kristiansen, Karsten ; Schmitz, Ole ; Schwartz, Thue W ; Zhang, Xiuqing ; Li, Ruiqiang ; Yang, Huanming ; Wang, Jian ; Hansen, Torben

Nature genetics, 2010-11, Vol.42 (11), p.969-972 [Periódico revisado por pares]

New York, NY: Nature Publishing Group

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