Volume 49; Issue 2

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Nature Genetics
Volume 49; Issue 2

Nature Genetics

Volume 49; Issue 2

1

Dynamics of BAF–Polycomb complex opposition on heterochromatin in normal and oncogenic states

Kadoch, Cigall, Williams, Robert T, Calarco, Joseph P, Miller, Erik L, Weber, Christopher M, Braun, Simon M G, Pulice, John L, Chory, Emma J, Crabtree, Gerald R

Journal:

Nature Genetics

Year:

2016

Language:

english

File:

PDF, 2.27 MB

english, 2016

2

Smarca4 ATPase mutations disrupt direct eviction of PRC1 from chromatin

Stanton, Benjamin Z, Hodges, Courtney, Calarco, Joseph P, Braun, Simon M G, Ku, Wai Lim, Kadoch, Cigall, Zhao, Keji, Crabtree, Gerald R

Journal:

Nature Genetics

Year:

2016

Language:

english

File:

PDF, 2.45 MB

english, 2016

3

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

Journal:

Nature Genetics

Year:

2016

Language:

english

File:

PDF, 9.27 MB

english, 2016

4

SMARCB1-mediated SWI/SNF complex function is essential for enhancer regulation

Wang, Xiaofeng, Lee, Ryan S, Alver, Burak H, Haswell, Jeffrey R, Wang, Su, Mieczkowski, Jakub, Drier, Yotam, Gillespie, Shawn M, Archer, Tenley C, Wu, Jennifer N, Tzvetkov, Evgeni P, Troisi, Emma C, P

Journal:

Nature Genetics

Year:

2016

Language:

english

File:

PDF, 3.18 MB

english, 2016

5

Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia

Meyer, Esther, Carss, Keren J, Rankin, Julia, Nichols, John M E, Grozeva, Detelina, Joseph, Agnel P, Mencacci, Niccolo E, Papandreou, Apostolos, Ng, Joanne, Barral, Serena, Ngoh, Adeline, Ben-Pazi, Hi

Journal:

Nature Genetics

Year:

2016

Language:

english

File:

PDF, 4.31 MB

english, 2016

6

A genome-wide CRISPR screen identifies a restricted set of HIV host dependency factors

Park, Ryan J, Wang, Tim, Koundakjian, Dylan, Hultquist, Judd F, Lamothe-Molina, Pedro, Monel, Blandine, Schumann, Kathrin, Yu, Haiyan, Krupzcak, Kevin M, Garcia-Beltran, Wilfredo, Piechocka-Trocha, Al

Journal:

Nature Genetics

Year:

2016

Language:

english

File:

PDF, 2.07 MB

english, 2016

7

Dynamics of clonal evolution in myelodysplastic syndromes

Makishima, Hideki, Yoshizato, Tetsuichi, Yoshida, Kenichi, Sekeres, Mikkael A, Radivoyevitch, Tomas, Suzuki, Hiromichi, Przychodzen, Bartlomiej, Nagata, Yasunobu, Meggendorfer, Manja, Sanada, Masashi,

Journal:

Nature Genetics

Year:

2016

Language:

english

File:

PDF, 1.41 MB

english, 2016

8

Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel disease

Ji, Sun-Gou, Juran, Brian D, Mucha, Sören, Folseraas, Trine, Jostins, Luke, Melum, Espen, Kumasaka, Natsuhiko, Atkinson, Elizabeth J, Schlicht, Erik M, Liu, Jimmy Z, Shah, Tejas, Gutierrez-Achury, Jav

Journal:

Nature Genetics

Year:

2016

Language:

english

File:

PDF, 493 KB

english, 2016

9

Genome-wide association analyses of sleep disturbance traits identify new loci and highlight shared genetics with neuropsychiatric and metabolic traits

Lane, Jacqueline M, Liang, Jingjing, Vlasac, Irma, Anderson, Simon G, Bechtold, David A, Bowden, Jack, Emsley, Richard, Gill, Shubhroz, Little, Max A, Luik, Annemarie I, Loudon, Andrew, Scheer, Frank

Journal:

Nature Genetics

Year:

2016

Language:

english

File:

PDF, 1.48 MB

english, 2016

10

Robust and scalable inference of population history from hundreds of unphased whole genomes

Terhorst, Jonathan, Kamm, John A, Song, Yun S

Journal:

Nature Genetics

Year:

2016

Language:

english

File:

PDF, 1.17 MB

english, 2016

11

A method for identifying genetic heterogeneity within phenotypically defined disease subgroups

Liley, James, Todd, John A, Wallace, Chris

Journal:

Nature Genetics

Year:

2016

Language:

english

File:

PDF, 21.05 MB

english, 2016

12

SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome

Shaw, Natalie D, Brand, Harrison, Kupchinsky, Zachary A, Bengani, Hemant, Plummer, Lacey, Jones, Takako I, Erdin, Serkan, Williamson, Kathleen A, Rainger, Joe, Stortchevoi, Alexei, Samocha, Kaitlin, C

Journal:

Nature Genetics

Year:

2017

Language:

english

File:

PDF, 2.93 MB

english, 2017

13

Genome-wide association study identifies distinct genetic contributions to prognosis and susceptibility in Crohn's disease

Lee, James C, Biasci, Daniele, Roberts, Rebecca, Gearry, Richard B, Mansfield, John C, Ahmad, Tariq, Prescott, Natalie J, Satsangi, Jack, Wilson, David C, Jostins, Luke, Anderson, Carl A, Traherne, Ja

Journal:

Nature Genetics

Year:

2017

Language:

english

File:

PDF, 1.54 MB

english, 2017

14

Impaired H3K36 methylation defines a subset of head and neck squamous cell carcinomas

Papillon-Cavanagh, Simon, Lu, Chao, Gayden, Tenzin, Mikael, Leonie G, Bechet, Denise, Karamboulas, Christina, Ailles, Laurie, Karamchandani, Jason, Marchione, Dylan M, Garcia, Benjamin A, Weinreb, Ila

Journal:

Nature Genetics

Year:

2017

Language:

english

File:

PDF, 2.62 MB

english, 2017

15

Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease

de Lange, Katrina M, Moutsianas, Loukas, Lee, James C, Lamb, Christopher A, Luo, Yang, Kennedy, Nicholas A, Jostins, Luke, Rice, Daniel L, Gutierrez-Achury, Javier, Ji, Sun-Gou, Heap, Graham, Nimmo, E

Journal:

Nature Genetics

Year:

2017

Language:

english

File:

PDF, 1.39 MB

english, 2017

16

Exploring the genetic architecture of inflammatory bowel disease by whole-genome sequencing identifies association at ADCY7

Luo, Yang, de Lange, Katrina M, Jostins, Luke, Moutsianas, Loukas, Randall, Joshua, Kennedy, Nicholas A, Lamb, Christopher A, McCarthy, Shane, Ahmad, Tariq, Edwards, Cathryn, Serra, Eva Goncalves, Har

Journal:

Nature Genetics

Year:

2017

Language:

english

File:

PDF, 5.19 MB

english, 2017

17

De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development

Gordon, Christopher T, Xue, Shifeng, Yigit, Gökhan, Filali, Hicham, Chen, Kelan, Rosin, Nadine, Yoshiura, Koh-ichiro, Oufadem, Myriam, Beck, Tamara J, McGowan, Ruth, Magee, Alex C, Altmüller, Janine,

Journal:

Nature Genetics

Year:

2017

Language:

english

File:

PDF, 2.77 MB

english, 2017

18

CIViC is a community knowledgebase for expert crowdsourcing the clinical interpretation of variants in cancer

Griffith, Malachi, Spies, Nicholas C, Krysiak, Kilannin, McMichael, Joshua F, Coffman, Adam C, Danos, Arpad M, Ainscough, Benjamin J, Ramirez, Cody A, Rieke, Damian T, Kujan, Lynzey, Barnell, Erica K,

Journal:

Nature Genetics

Year:

2017

Language:

english

File:

PDF, 348 KB

english, 2017

19

Many faces of SMCHD1

Wilkie, Andrew O M

Journal:

Nature Genetics

Year:

2017

Language:

english

File:

PDF, 697 KB

english, 2017

20

Finding host targets for HIV therapy

Tsui, C Kimberly, Gupta, Amita, Bassik, Michael C

Journal:

Nature Genetics

Year:

2017

Language:

english

File:

PDF, 226 KB

english, 2017

21

SWI/SNF complex in cancer

Lu, Chao, Allis, C David

Journal:

Nature Genetics

Year:

2017

Language:

english

File:

PDF, 399 KB

english, 2017

22

It's all druggable

Journal:

Nature Genetics

Year:

2017

Language:

english

File:

PDF, 89 KB

english, 2017

23

Corrigendum: Mutational signatures in esophageal adenocarcinoma define etiologically distinct subgroups with therapeutic relevance

Secrier, Maria, Li, Xiaodun, de Silva, Nadeera, Eldridge, Matthew D, Contino, Gianmarco, Bornschein, Jan, MacRae, Shona, Grehan, Nicola, O'Donovan, Maria, Miremadi, Ahmad, Yang, Tsun-Po, Bower, Lawren

Journal:

Nature Genetics

Year:

2017

Language:

english

File:

PDF, 62 KB

english, 2017

24

Corrigendum: Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts

Jenkinson, Emma M, Rodero, Mathieu P, Kasher, Paul R, Uggenti, Carolina, Oojageer, Anthony, Goosey, Laurence C, Rose, Yoann, Kershaw, Christopher J, Urquhart, Jill E, Williams, Simon G, Bhaskar, Sanje

Journal:

Nature Genetics

Year:

2017

Language:

english

File:

PDF, 64 KB

english, 2017

25

Corrigendum: Integrative genomic analysis implicates limited peripheral adipose storage capacity in the pathogenesis of human insulin resistance

Lotta, Luca A, Gulati, Pawan, Day, Felix R, Payne, Felicity, Ongen, Halit, van de Bunt, Martijn, Gaulton, Kyle J, Eicher, John D, Sharp, Stephen J, Luan, Jian'an, Rolfe, Emanuella De Lucia, Stewart, I

Journal:

Nature Genetics

Year:

2017

Language:

english

File:

PDF, 62 KB

english, 2017

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