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Plos One
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May 9, 2009
Genetic structure of Europeans: a view from the North-East
Mari Nelis, Tõnu Esko, Reedik Mägi, et al.
Human Molecular Genetics
|
January 9, 2013
Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot
Heather J Cordell, Ana Töpf, Chrysovalanto Mamasoula, et al.
Nature Genetics
|
December 14, 2011
Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia
Víctor Quesada, Laura Conde, Neus Villamor, et al.
Nature Genetics
|
June 9, 2015
Whole-genome fingerprint of the DNA methylome during human B cell differentiation
Marta Kulis, Angelika Merkel, Simon Heath, et al.
Nature Genetics
|
May 28, 2013
Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16
Heather J Cordell, Jamie Bentham, Ana Topf, et al.
Nature Genetics
|
September 8, 2009
Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease
Jean-Charles Lambert, Simon Heath, Gael Even, et al.
Nature Communications
|
November 30, 2016
Increased DNA methylation variability in type 1 diabetes across three immune effector cell types
Dirk S Paul, Andrew E Teschendorff, Mary A N Dang, et al.
International Journal of Epidemiology
|
September 25, 2009
Association between a 15q25 gene variant, smoking quantity and tobacco-related cancers among 17 000 individuals
Esther H Lips, Valerie Gaborieau, James D McKay, et al.
Scientific Reports
|
June 19, 2021
Gender specific airway gene expression in COPD sub-phenotypes supports a role of mitochondria and of different types of leukocytes
Anna Esteve-Codina, Thomas P Hofer, Dorothe Burggraf, et al.
Nature Medicine
|
May 23, 2018
The reference epigenome and regulatory chromatin landscape of chronic lymphocytic leukemia
Renée Beekman, Vicente Chapaprieta, Núria Russiñol, et al.
Page
of 11
Search research articles
Search
Showing results (81-90 of 110) with videos related to
Sort By:
Page
of 11
Plos One
|
May 9, 2009
Genetic structure of Europeans: a view from the North-East
Mari Nelis, Tõnu Esko, Reedik Mägi, et al.
Human Molecular Genetics
|
January 9, 2013
Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot
Heather J Cordell, Ana Töpf, Chrysovalanto Mamasoula, et al.
Nature Genetics
|
December 14, 2011
Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia
Víctor Quesada, Laura Conde, Neus Villamor, et al.
Nature Genetics
|
June 9, 2015
Whole-genome fingerprint of the DNA methylome during human B cell differentiation
Marta Kulis, Angelika Merkel, Simon Heath, et al.
Nature Genetics
|
May 28, 2013
Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16
Heather J Cordell, Jamie Bentham, Ana Topf, et al.
Nature Genetics
|
September 8, 2009
Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease
Jean-Charles Lambert, Simon Heath, Gael Even, et al.
Nature Communications
|
November 30, 2016
Increased DNA methylation variability in type 1 diabetes across three immune effector cell types
Dirk S Paul, Andrew E Teschendorff, Mary A N Dang, et al.
International Journal of Epidemiology
|
September 25, 2009
Association between a 15q25 gene variant, smoking quantity and tobacco-related cancers among 17 000 individuals
Esther H Lips, Valerie Gaborieau, James D McKay, et al.
Scientific Reports
|
June 19, 2021
Gender specific airway gene expression in COPD sub-phenotypes supports a role of mitochondria and of different types of leukocytes
Anna Esteve-Codina, Thomas P Hofer, Dorothe Burggraf, et al.
Nature Medicine
|
May 23, 2018
The reference epigenome and regulatory chromatin landscape of chronic lymphocytic leukemia
Renée Beekman, Vicente Chapaprieta, Núria Russiñol, et al.
Page
of 11