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Orphanet Journal of Rare Diseases
|
June 12, 2016
The rare and undiagnosed diseases diagnostic service - application of massively parallel sequencing in a state-wide clinical service
Gareth Baynam, Nicholas Pachter, Fiona McKenzie, et al.
NPJ Genomic Medicine
|
December 11, 2020
A flexible computational pipeline for research analyses of unsolved clinical exome cases
Timo Lassmann, Richard W Francis, Alexia Weeks, et al.
Plos One
|
June 5, 2008
Genetic and epigenetic factors at COL2A1 and ABCA4 influence clinical outcome in congenital toxoplasmosis
Sarra E Jamieson, Lee-Anne de Roubaix, Mario Cortina-Borja, et al.
Scientific Reports
|
May 29, 2019
Publisher Correction: Toxoplasma Modulates Signature Pathways of Human Epilepsy, Neurodegeneration & Cancer
Huân M Ngô, Ying Zhou, Hernan Lorenzi, et al.
Scientific Reports
|
September 15, 2017
Toxoplasma Modulates Signature Pathways of Human Epilepsy, Neurodegeneration & Cancer
Huân M Ngô, Ying Zhou, Hernan Lorenzi, et al.
Nature Genetics
|
November 17, 2009
Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region
, Jeffrey C Barrett, James C Lee, et al.
Nature Genetics
|
January 8, 2013
Common variants in the HLA-DRB1-HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis
, , Michaela Fakiola, et al.
Nature Genetics
|
December 28, 2010
Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes
, , Kaixin Zhou, et al.
Nature Communications
|
July 9, 2014
The correlation between reading and mathematics ability at age twelve has a substantial genetic component
Oliver S P Davis, Gavin Band, Matti Pirinen, et al.
American Journal of Human Genetics
|
May 31, 2016
Polymorphism in a lincRNA Associates with a Doubled Risk of Pneumococcal Bacteremia in Kenyan Children
, , Anna Rautanen, et al.
Page
of 11
Search research articles
Search
Showing results (91-100 of 108) with videos related to
Sort By:
Page
of 11
Orphanet Journal of Rare Diseases
|
June 12, 2016
The rare and undiagnosed diseases diagnostic service - application of massively parallel sequencing in a state-wide clinical service
Gareth Baynam, Nicholas Pachter, Fiona McKenzie, et al.
NPJ Genomic Medicine
|
December 11, 2020
A flexible computational pipeline for research analyses of unsolved clinical exome cases
Timo Lassmann, Richard W Francis, Alexia Weeks, et al.
Plos One
|
June 5, 2008
Genetic and epigenetic factors at COL2A1 and ABCA4 influence clinical outcome in congenital toxoplasmosis
Sarra E Jamieson, Lee-Anne de Roubaix, Mario Cortina-Borja, et al.
Scientific Reports
|
May 29, 2019
Publisher Correction: Toxoplasma Modulates Signature Pathways of Human Epilepsy, Neurodegeneration & Cancer
Huân M Ngô, Ying Zhou, Hernan Lorenzi, et al.
Scientific Reports
|
September 15, 2017
Toxoplasma Modulates Signature Pathways of Human Epilepsy, Neurodegeneration & Cancer
Huân M Ngô, Ying Zhou, Hernan Lorenzi, et al.
Nature Genetics
|
November 17, 2009
Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region
, Jeffrey C Barrett, James C Lee, et al.
Nature Genetics
|
January 8, 2013
Common variants in the HLA-DRB1-HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis
, , Michaela Fakiola, et al.
Nature Genetics
|
December 28, 2010
Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes
, , Kaixin Zhou, et al.
Nature Communications
|
July 9, 2014
The correlation between reading and mathematics ability at age twelve has a substantial genetic component
Oliver S P Davis, Gavin Band, Matti Pirinen, et al.
American Journal of Human Genetics
|
May 31, 2016
Polymorphism in a lincRNA Associates with a Doubled Risk of Pneumococcal Bacteremia in Kenyan Children
, , Anna Rautanen, et al.
Page
of 11