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Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
May 15, 2021
TMEM106B and CPOX are genetic determinants of cerebrospinal fluid Alzheimer's disease biomarker levels
Shengjun Hong, Valerija Dobricic, Olena Ohlei, et al.
Nature Genetics
|
October 21, 2015
A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis
Stephan Buch, Felix Stickel, Eric Trépo, et al.
Human Molecular Genetics
|
September 1, 2012
Immunochip analyses identify a novel risk locus for primary biliary cirrhosis at 13q14, multiple independent associations at four established risk loci and epistasis between 1p31 and 7q32 risk variants
Brian D Juran, Gideon M Hirschfield, Pietro Invernizzi, et al.
Nature Genetics
|
December 15, 2010
Genome-wide association analysis in primary sclerosing cholangitis identifies two non-HLA susceptibility loci
Espen Melum, Andre Franke, Christoph Schramm, et al.
Nature Genetics
|
August 11, 2015
Widespread non-additive and interaction effects within HLA loci modulate the risk of autoimmune diseases
Tobias L Lenz, Aaron J Deutsch, Buhm Han, et al.
Nature Methods
|
September 6, 2011
Toward the blood-borne miRNome of human diseases
Andreas Keller, Petra Leidinger, Andrea Bauer, et al.
The Journal of Allergy and Clinical Immunology
|
November 11, 2019
Protein-coding variants contribute to the risk of atopic dermatitis and skin-specific gene expression
Sören Mucha, Hansjörg Baurecht, Natalija Novak, et al.
American Journal of Human Genetics
|
December 3, 2015
Genome-wide Association Analysis of Psoriatic Arthritis and Cutaneous Psoriasis Reveals Differences in Their Genetic Architecture
Philip E Stuart, Rajan P Nair, Lam C Tsoi, et al.
Immunity
|
September 3, 2024
Autoantigen-specific CD4<sup>+</sup> T cells acquire an exhausted phenotype and persist in human antigen-specific autoimmune diseases
Carina Saggau, Petra Bacher, Daniela Esser, et al.
Human Molecular Genetics
|
May 3, 2011
Chromosome 7p11.2 (EGFR) variation influences glioma risk
Marc Sanson, Fay J Hosking, Sanjay Shete, et al.
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of 68
Search research articles
Search
Showing results (551-560 of 678) with videos related to
Sort By:
Page
of 68
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
May 15, 2021
TMEM106B and CPOX are genetic determinants of cerebrospinal fluid Alzheimer's disease biomarker levels
Shengjun Hong, Valerija Dobricic, Olena Ohlei, et al.
Nature Genetics
|
October 21, 2015
A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis
Stephan Buch, Felix Stickel, Eric Trépo, et al.
Human Molecular Genetics
|
September 1, 2012
Immunochip analyses identify a novel risk locus for primary biliary cirrhosis at 13q14, multiple independent associations at four established risk loci and epistasis between 1p31 and 7q32 risk variants
Brian D Juran, Gideon M Hirschfield, Pietro Invernizzi, et al.
Nature Genetics
|
December 15, 2010
Genome-wide association analysis in primary sclerosing cholangitis identifies two non-HLA susceptibility loci
Espen Melum, Andre Franke, Christoph Schramm, et al.
Nature Genetics
|
August 11, 2015
Widespread non-additive and interaction effects within HLA loci modulate the risk of autoimmune diseases
Tobias L Lenz, Aaron J Deutsch, Buhm Han, et al.
Nature Methods
|
September 6, 2011
Toward the blood-borne miRNome of human diseases
Andreas Keller, Petra Leidinger, Andrea Bauer, et al.
The Journal of Allergy and Clinical Immunology
|
November 11, 2019
Protein-coding variants contribute to the risk of atopic dermatitis and skin-specific gene expression
Sören Mucha, Hansjörg Baurecht, Natalija Novak, et al.
American Journal of Human Genetics
|
December 3, 2015
Genome-wide Association Analysis of Psoriatic Arthritis and Cutaneous Psoriasis Reveals Differences in Their Genetic Architecture
Philip E Stuart, Rajan P Nair, Lam C Tsoi, et al.
Immunity
|
September 3, 2024
Autoantigen-specific CD4<sup>+</sup> T cells acquire an exhausted phenotype and persist in human antigen-specific autoimmune diseases
Carina Saggau, Petra Bacher, Daniela Esser, et al.
Human Molecular Genetics
|
May 3, 2011
Chromosome 7p11.2 (EGFR) variation influences glioma risk
Marc Sanson, Fay J Hosking, Sanjay Shete, et al.
Page
of 68