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Human Heredity
|
February 10, 2015
Prioritizing rare variants with conditional likelihood ratios
Weili Li, Sara Dobbins, Ian Tomlinson, et al.
Bioinformatics (Oxford, England)
|
April 16, 2014
Association analysis using next-generation sequence data from publicly available control groups: the robust variance score statistic
Andriy Derkach, Theodore Chiang, Jiafen Gong, et al.
Human Molecular Genetics
|
April 27, 2024
Pathogenic variants in HGF give rise to childhood-to-late onset primary lymphoedema by loss of function
Murat Alpaslan, Elodie Fastré, Sandrine Mestre, et al.
Human Molecular Genetics
|
May 3, 2011
Fine-mapping of colorectal cancer susceptibility loci at 8q23.3, 16q22.1 and 19q13.11: refinement of association signals and use of in silico analysis to suggest functional variation and unexpected candidate target genes
Luis G Carvajal-Carmona, Jean-Baptiste Cazier, Angela M Jones, et al.
Human Molecular Genetics
|
February 13, 2013
Deciphering the 8q24.21 association for glioma
Victor Enciso-Mora, Fay J Hosking, Ben Kinnersley, et al.
Nature Genetics
|
December 25, 2012
Germline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas
Claire Palles, Jean-Baptiste Cazier, Kimberley M Howarth, et al.
Blood
|
July 11, 2024
Germ line ERG haploinsufficiency defines a new syndrome with cytopenia and hematological malignancy predisposition
Jiarna R Zerella, Claire C Homan, Peer Arts, et al.
Scientific Reports
|
November 11, 2015
Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer
Maria N Timofeeva, Ben Kinnersley, Susan M Farrington, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 8) with videos related to
Sort By:
Page
of 1
Human Heredity
|
February 10, 2015
Prioritizing rare variants with conditional likelihood ratios
Weili Li, Sara Dobbins, Ian Tomlinson, et al.
Bioinformatics (Oxford, England)
|
April 16, 2014
Association analysis using next-generation sequence data from publicly available control groups: the robust variance score statistic
Andriy Derkach, Theodore Chiang, Jiafen Gong, et al.
Human Molecular Genetics
|
April 27, 2024
Pathogenic variants in HGF give rise to childhood-to-late onset primary lymphoedema by loss of function
Murat Alpaslan, Elodie Fastré, Sandrine Mestre, et al.
Human Molecular Genetics
|
May 3, 2011
Fine-mapping of colorectal cancer susceptibility loci at 8q23.3, 16q22.1 and 19q13.11: refinement of association signals and use of in silico analysis to suggest functional variation and unexpected candidate target genes
Luis G Carvajal-Carmona, Jean-Baptiste Cazier, Angela M Jones, et al.
Human Molecular Genetics
|
February 13, 2013
Deciphering the 8q24.21 association for glioma
Victor Enciso-Mora, Fay J Hosking, Ben Kinnersley, et al.
Nature Genetics
|
December 25, 2012
Germline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas
Claire Palles, Jean-Baptiste Cazier, Kimberley M Howarth, et al.
Blood
|
July 11, 2024
Germ line ERG haploinsufficiency defines a new syndrome with cytopenia and hematological malignancy predisposition
Jiarna R Zerella, Claire C Homan, Peer Arts, et al.
Scientific Reports
|
November 11, 2015
Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer
Maria N Timofeeva, Ben Kinnersley, Susan M Farrington, et al.
Page
of 1