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Jacek Majewski

Showing results (271-280 of 333) with videos related to

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Plos Genetics|October 24, 2014
Germline mutations in MAP3K6 are associated with familial gastric cancerDaniel Gaston, Samantha Hansford, Carla Oliveira, et al.
American Journal of Human Genetics|December 24, 2013
Mutations in CSPP1, encoding a core centrosomal protein, cause a range of ciliopathy phenotypes in humansRanad Shaheen, Hanan E Shamseldin, Catrina M Loucks, et al.
Nature Genetics|January 10, 2017
Impaired H3K36 methylation defines a subset of head and neck squamous cell carcinomasSimon Papillon-Cavanagh, Chao Lu, Tenzin Gayden, et al.
Nature Communications|November 3, 2018
TRPV4 and KRAS and FGFR1 gain-of-function mutations drive giant cell lesions of the jawCarolina Cavalieri Gomes, Tenzin Gayden, Andrea Bajic, et al.
American Journal of Human Genetics|June 7, 2014
FORGE Canada Consortium: outcomes of a 2-year national rare-disease gene-discovery projectChandree L Beaulieu, Jacek Majewski, Jeremy Schwartzentruber, et al.
Nature Genetics|March 30, 2016
Corrigendum: Germline RECQL mutations are associated with breast cancer susceptibilityCezary Cybulski, Jian Carrot-Zhang, Wojciech Kluźniak, et al.
Nature Communications|April 7, 2016
Spatial and temporal homogeneity of driver mutations in diffuse intrinsic pontine gliomaHamid Nikbakht, Eshini Panditharatna, Leonie G Mikael, et al.
Nature Genetics|April 28, 2015
Germline RECQL mutations are associated with breast cancer susceptibilityCezary Cybulski, Jian Carrot-Zhang, Wojciech Kluźniak, et al.
American Journal of Human Genetics|May 1, 2012
Haploinsufficiency of SF3B4, a component of the pre-mRNA spliceosomal complex, causes Nager syndromeFrancois P Bernier, Oana Caluseriu, Sarah Ng, et al.
Nature|September 6, 2019
The histone mark H3K36me2 recruits DNMT3A and shapes the intergenic DNA methylation landscapeDaniel N Weinberg, Simon Papillon-Cavanagh, Haifen Chen, et al.
Pageof 34

Showing results (271-280 of 333) with videos related to

Sort By:
Pageof 34
Plos Genetics|October 24, 2014
Germline mutations in MAP3K6 are associated with familial gastric cancerDaniel Gaston, Samantha Hansford, Carla Oliveira, et al.
American Journal of Human Genetics|December 24, 2013
Mutations in CSPP1, encoding a core centrosomal protein, cause a range of ciliopathy phenotypes in humansRanad Shaheen, Hanan E Shamseldin, Catrina M Loucks, et al.
Nature Genetics|January 10, 2017
Impaired H3K36 methylation defines a subset of head and neck squamous cell carcinomasSimon Papillon-Cavanagh, Chao Lu, Tenzin Gayden, et al.
Nature Communications|November 3, 2018
TRPV4 and KRAS and FGFR1 gain-of-function mutations drive giant cell lesions of the jawCarolina Cavalieri Gomes, Tenzin Gayden, Andrea Bajic, et al.
American Journal of Human Genetics|June 7, 2014
FORGE Canada Consortium: outcomes of a 2-year national rare-disease gene-discovery projectChandree L Beaulieu, Jacek Majewski, Jeremy Schwartzentruber, et al.
Nature Genetics|March 30, 2016
Corrigendum: Germline RECQL mutations are associated with breast cancer susceptibilityCezary Cybulski, Jian Carrot-Zhang, Wojciech Kluźniak, et al.
Nature Communications|April 7, 2016
Spatial and temporal homogeneity of driver mutations in diffuse intrinsic pontine gliomaHamid Nikbakht, Eshini Panditharatna, Leonie G Mikael, et al.
Nature Genetics|April 28, 2015
Germline RECQL mutations are associated with breast cancer susceptibilityCezary Cybulski, Jian Carrot-Zhang, Wojciech Kluźniak, et al.
American Journal of Human Genetics|May 1, 2012
Haploinsufficiency of SF3B4, a component of the pre-mRNA spliceosomal complex, causes Nager syndromeFrancois P Bernier, Oana Caluseriu, Sarah Ng, et al.
Nature|September 6, 2019
The histone mark H3K36me2 recruits DNMT3A and shapes the intergenic DNA methylation landscapeDaniel N Weinberg, Simon Papillon-Cavanagh, Haifen Chen, et al.
Pageof 34