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1
Qki deficiency maintains stemness of glioma stem cells in suboptimal environment by downregulating endolysosomal degradation
Qki deficiency maintains stemness of glioma stem cells in suboptimal environment by downregulating endolysosomal degradation
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Qki deficiency maintains stemness of glioma stem cells in suboptimal environment by downregulating endolysosomal degradation

Shingu, Takashi ; Ho, Allen L ; Yuan, Liang ; Zhou, Xin ; Dai, Congxin ; Zheng, Siyuan ; Wang, Qianghu ; Zhong, Yi ; Chang, Qing ; Horner, James W ; Liebelt, Brandon D ; Yao, Yu ; Hu, Baoli ; Chen, Yiwen ; Fuller, Gregory N ; Verhaak, Roeland G W ; Heimberger, Amy B ; Hu, Jian

Nature genetics, 2017-01, Vol.49 (1), p.75-86 [Periódico revisado por pares]

United States: Nature Publishing Group

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2
Hearing Impairment and Incident Dementia and Cognitive Decline in Older Adults: The Health ABC Study
Hearing Impairment and Incident Dementia and Cognitive Decline in Older Adults: The Health ABC Study
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Hearing Impairment and Incident Dementia and Cognitive Decline in Older Adults: The Health ABC Study

Deal, Jennifer A. ; Betz, Josh ; Yaffe, Kristine ; Harris, Tamara ; Purchase-Helzner, Elizabeth ; Satterfield, Suzanne ; Pratt, Sheila ; Govil, Nandini ; Simonsick, Eleanor M. ; Lin, Frank R.

The journals of gerontology. Series A, Biological sciences and medical sciences, 2016-04, Vol.72 (5), p.glw069-709 [Periódico revisado por pares]

US: Oxford University Press

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3
ARID1A loss impairs enhancer-mediated gene regulation and drives colon cancer in mice
ARID1A loss impairs enhancer-mediated gene regulation and drives colon cancer in mice
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ARID1A loss impairs enhancer-mediated gene regulation and drives colon cancer in mice

Mathur, Radhika ; Alver, Burak H ; San Roman, Adrianna K ; Wilson, Boris G ; Wang, Xiaofeng ; Agoston, Agoston T ; Park, Peter J ; Shivdasani, Ramesh A ; Roberts, Charles W M

Nature genetics, 2017-02, Vol.49 (2), p.296-302 [Periódico revisado por pares]

United States: Nature Publishing Group

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4
Genome-wide enhancer maps link risk variants to disease genes
Genome-wide enhancer maps link risk variants to disease genes
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Genome-wide enhancer maps link risk variants to disease genes

Nasser, Joseph ; Bergman, Drew T ; Fulco, Charles P ; Guckelberger, Philine ; Doughty, Benjamin R ; Patwardhan, Tejal A ; Jones, Thouis R ; Nguyen, Tung H ; Ulirsch, Jacob C ; Lekschas, Fritz ; Mualim, Kristy ; Natri, Heini M ; Weeks, Elle M ; Munson, Glen ; Kane, Michael ; Kang, Helen Y ; Cui, Ang ; Ray, John P ; Eisenhaure, Thomas M ; Collins, Ryan L ; Dey, Kushal ; Pfister, Hanspeter ; Price, Alkes L ; Epstein, Charles B ; Kundaje, Anshul ; Xavier, Ramnik J ; Daly, Mark J ; Huang, Hailiang ; Finucane, Hilary K ; Hacohen, Nir ; Lander, Eric S ; Engreitz, Jesse M

Nature (London), 2021-05, Vol.593 (7858), p.238-243 [Periódico revisado por pares]

England: Nature Publishing Group

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5
Melanomas acquire resistance to B-RAF(V600E) inhibition by RTK or N-RAS upregulation
Melanomas acquire resistance to B-RAF(V600E) inhibition by RTK or N-RAS upregulation
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Melanomas acquire resistance to B-RAF(V600E) inhibition by RTK or N-RAS upregulation

Shi, Hubing ; Sazegar, Hooman ; Nazarian, Ramin ; Chodon, Thinle ; Lee, Hane ; Sosman, Jeffrey A ; Lo, Roger S ; Koya, Richard C ; Lee, Mi-Kyung ; Attar, Narsis ; Kong, Xiangju ; Nelson, Stanley F ; Ribas, Antoni ; Chen, Zugen ; McArthur, Grant ; Wang, Qi

Nature (London), 2010-12, Vol.468 (7326), p.973-977 [Periódico revisado por pares]

London: Nature Publishing Group

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6
A genome-wide scan for common alleles affecting risk for autism
A genome-wide scan for common alleles affecting risk for autism
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A genome-wide scan for common alleles affecting risk for autism

Pinto, Dalila ; Regan, Regina ; Magalhaes, Tiago R. ; Abrahams, Brett S. ; Pagnamenta, Alistair T. ; Almeida, Joana ; Bailey, Anthony J. ; Baird, Gillian ; Battaglia, Agatino ; Bolshakova, Nadia ; Bölte, Sven ; Bolton, Patrick F. ; Brennan, Sean ; Carson, Andrew R. ; Casallo, Guillermo ; Chu, Su H. ; Cochrane, Lynne ; Dawson, Geraldine ; de Jonge, Maretha ; Delorme, Richard ; Duketis, Eftichia ; Duque, Frederico ; Estes, Annette ; Fernandez, Bridget A. ; Fombonne, Eric ; Freitag, Christine M. ; Glessner, Joseph T. ; Goldberg, Jeremy ; Green, Jonathan ; Heron, Elizabeth A. ; Holt, Richard ; Hughes, Gillian ; Hus, Vanessa ; Kim, Cecilia ; Korvatska, Olena ; Kustanovich, Vlad ; Lajonchere, Clara M. ; Leboyer, Marion ; Leventhal, Bennett L. ; Liu, Xiao-Qing ; Lord, Catherine ; Lotspeich, Linda ; Marshall, Christian R. ; McConachie, Helen ; McMahon, William M. ; Melhem, Nadine M. ; Merikangas, Alison ; Migita, Ohsuke ; Munson, Jeff ; Nelson, Stanley F. ; Noakes, Carolyn ; Noor, Abdul ; Nygren, Gudrun ; Papanikolaou, Katerina ; Parr, Jeremy R. ; Poustka, Annemarie ; Poustka, Fritz ; Prasad, Aparna ; Renshaw, Katy ; Rickaby, Jessica ; Roberts, Wendy ; Roge, Bernadette ; Bierut, Laura J. ; Rice, John P. ; Salt, Jeff ; Sansom, Katherine ; Sato, Daisuke ; Segurado, Ricardo ; Shah, Naisha ; Sheffield, Val C. ; Soorya, Latha ; Stoppioni, Vera ; Tancredi, Raffaella ; Thompson, Ann P. ; Thomson, Susanne ; Tryfon, Ana ; Van Engeland, Herman ; Wang, Kai ; Wang, Zhouzhi ; Wassink, Thomas H. ; Wittemeyer, Kerstin ; Wood, Shawn ; Yaspan, Brian L. ; Zurawiecki, Danielle ; Buxbaum, Joseph D. ; Cantor, Rita M. ; Cook, Edwin H. ; Coon, Hilary ; Cuccaro, Michael L. ; Gallagher, Louise ; Geschwind, Daniel H. ; Gill, Michael ; Haines, Jonathan L. ; Paterson, Andrew D. ; Sutcliffe, James S. ; Szatmari, Peter ; Vicente, Astrid M. ; Wijsman, Ellen M. ; Devlin, Bernie ; Hallmayer, Joachim

Human molecular genetics, 2010-10, Vol.19 (20), p.4072-4082 [Periódico revisado por pares]

Oxford: Oxford University Press

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7
Exome sequencing identifies the cause of a mendelian disorder
Exome sequencing identifies the cause of a mendelian disorder
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Exome sequencing identifies the cause of a mendelian disorder

Huff, Chad D ; Jabs, Ethylin Wang ; Shendure, Jay ; Tabor, Holly K ; Nickerson, Deborah A ; Bamshad, Michael J ; Buckingham, Kati J ; Bigham, Abigail W ; Shannon, Paul T ; Lee, Choli ; Dent, Karin M ; Ng, Sarah B

Nature genetics, 2010-01, Vol.42 (1), p.30-35 [Periódico revisado por pares]

New York, NY: Nature Publishing Group

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8
FORGE Canada Consortium: Outcomes of a 2-Year National Rare-Disease Gene-Discovery Project
FORGE Canada Consortium: Outcomes of a 2-Year National Rare-Disease Gene-Discovery Project
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FORGE Canada Consortium: Outcomes of a 2-Year National Rare-Disease Gene-Discovery Project

Beaulieu, Chandree L. ; Majewski, Jacek ; Schwartzentruber, Jeremy ; Samuels, Mark E. ; Fernandez, Bridget A. ; Bernier, Francois P. ; Brudno, Michael ; Knoppers, Bartha ; Marcadier, Janet ; Dyment, David ; Adam, Shelin ; Bulman, Dennis E. ; Jones, Steve J.M. ; Avard, Denise ; Nguyen, Minh Thu ; Rousseau, Francois ; Marshall, Christian ; Wintle, Richard F. ; Shen, Yaoqing ; Scherer, Stephen W. ; Friedman, Jan M. ; Michaud, Jacques L. ; Boycott, Kym M.

American journal of human genetics, 2014-06, Vol.94 (6), p.809-817 [Periódico revisado por pares]

United States: Elsevier Inc

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9
A comprehensive 1000 Genomes–based genome-wide association meta-analysis of coronary artery disease
A comprehensive 1000 Genomes–based genome-wide association meta-analysis of coronary artery disease
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A comprehensive 1000 Genomes–based genome-wide association meta-analysis of coronary artery disease

Nikpay, Majid ; Goel, Anuj ; Won, Hong-Hee ; Hall, Leanne M ; Willenborg, Christina ; Kanoni, Stavroula ; Kyriakou, Theodosios ; Nelson, Christopher P ; Harris, Tamara B ; Hazen, Stanley L ; Hengstenberg, Christian ; Hofman, Albert ; Ingelsson, Erik ; Iribarren, Carlos ; Jukema, J Wouter ; Karhunen, Pekka J ; Kim, Bong-Jo ; Webb, Thomas R ; Kullo, Iftikhar J ; Loos, Ruth JF ; Melander, Olle ; Metspalu, Andres ; Palmer, Colin N ; Quertermous, Thomas ; Rader, Daniel J ; Zeng, Lingyao ; Ridker, Paul M ; Roberts, Robert ; Schwartz, Stephen M ; Stewart, Alexandre F ; Stott, David J ; Thiery, Joachim ; Dehghan, Abbas ; Zalloua, Pierre A ; O'Donnell, Christopher J ; Thompson, John R ; Erdmann, Jeanette ; Clarke, Robert ; Kathiresan, Sekar ; McPherson, Ruth ; Alver, Maris ; Deloukas, Panos ; Samani, Nilesh J ; Farrall, Martin ; Auro, Kirsi ; Bjonnes, Andrew ; Chasman, Daniel I ; Chen, Shufeng ; Ford, Ian ; Franceschini, Nora ; Gieger, Christian ; Grace, Christopher ; Gustafsson, Stefan ; Huang, Jie ; Kim, Yun Kyoung ; Lau, King Wai ; Lyytikäinen, Leo-Pekka ; Morrison, Alanna C ; Pervjakova, Natalia ; Rose, Lynda M ; Salfati, Elias ; Saxena, Richa ; Scholz, Markus ; Tikkanen, Emmi ; Uitterlinden, Andre ; Zhang, Weihua ; de Andrade, Mariza ; van Zuydam, Natalie R ; Dedoussis, George ; Frossard, Philippe ; Gauguier, Dominique ; Goodall, Alison H ; Gottesman, Omri ; Haber, Marc ; Huang, Jianfeng ; König, Inke R ; Lannfelt, Lars ; Lind, Lars ; Lindgren, Cecilia M ; Magnusson, Patrik K ; Mallick, Nadeem H ; Meitinger, Thomas ; Memon, Fazal-ur-Rehman ; Morris, Andrew P ; Nieminen, Markku S ; Rallidis, Loukianos S ; Rasheed, Asif ; Sinisalo, Juha ; Stirrups, Kathleen E ; Wang, Laiyuan ; Ardissino, Diego ; Boerwinkle, Eric ; Bottinger, Erwin P ; Buring, Julie E ; Chambers, John C ; Cupples, L Adrienne ; Danesh, John ; Demuth, Ilja ; Gudnason, Roberto ; Hamsten, Anders

Nature genetics, 2015-10, Vol.47 (10), p.1121-1130 [Periódico revisado por pares]

New York: Nature Publishing Group

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10
Exome sequencing of extreme phenotypes identifies DCTN4 as a modifier of chronic Pseudomonas aeruginosa infection in cystic fibrosis
Exome sequencing of extreme phenotypes identifies DCTN4 as a modifier of chronic Pseudomonas aeruginosa infection in cystic fibrosis
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Exome sequencing of extreme phenotypes identifies DCTN4 as a modifier of chronic Pseudomonas aeruginosa infection in cystic fibrosis

EMOND, Mary J ; LOUIE, Tin ; BARNES, Kathleen C ; GIBSON, Ronald L ; BAMSHAD, Michael J ; EMERSON, Julia ; WEI ZHAO ; MATHIAS, Rasika A ; KNOWLES, Michael R ; WRIGHT, Fred A ; RIEDER, Mark J ; TABOR, Holly K ; NICKERSON, Deborah A

Nature genetics, 2012-08, Vol.44 (8), p.886-889 [Periódico revisado por pares]

New York, NY: Nature Publishing Group

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