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Genes
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January 28, 2026
Transcriptome- and Epigenome-Wide Association Studies of Tic Spectrum Disorder in Discordant Monozygotic Twins
Jonas Dalsberg, Cathrine Jespersgaard, Amanda M Levy, et al.
Cardiovascular Journal of Africa
|
November 13, 2013
Long QT syndrome in South Africa: the results of comprehensive genetic screening
Paula L Hedley, Glenda A Durrheim, Firzana Hendricks, et al.
Inflammatory Bowel Diseases
|
April 3, 2012
Genome-wide peripheral blood leukocyte DNA methylation microarrays identified a single association with inflammatory bowel diseases
R Alan Harris, Dorottya Nagy-Szakal, Natalia Pedersen, et al.
Genes
|
December 23, 2020
Bi-Allelic Pathogenic Variations in <i>MERTK</i> Including Deletions Are Associated with an Early Onset Progressive Form of Retinitis Pigmentosa
Cathrine Jespersgaard, Mette Bertelsen, Farah Arif, et al.
Neurobiology of Aging
|
March 15, 2008
The diagnostic efficiency of biomarkers in sporadic Creutzfeldt-Jakob disease compared to Alzheimer's disease
Justyna Maria Czarna Bahl, Niels H H Heegaard, Gerhard Falkenhorst, et al.
Pain
|
February 23, 2018
Heterozygous mutations in GTP-cyclohydrolase-1 reduce BH4 biosynthesis but not pain sensitivity
Arafat Nasser, Anette Torvin Møller, Vibe Hellmund, et al.
Plos One
|
March 3, 2011
Determination of beta-defensin genomic copy number in different populations: a comparison of three methods
Peder Fode, Cathrine Jespersgaard, Robert J Hardwick, et al.
Digestive Diseases and Sciences
|
June 25, 2011
Alpha-defensin DEFA1A3 gene copy number elevation in Danish Crohn's disease patients
Cathrine Jespersgaard, Peder Fode, Marianne Dybdahl, et al.
Molecular Genetics & Genomic Medicine
|
February 6, 2014
MT-CYB mutations in hypertrophic cardiomyopathy
Christian M Hagen, Frederik H Aidt, Ole Havndrup, et al.
Human Molecular Genetics
|
October 29, 2024
A novel GFAP frameshift variant identified in a family with optico-retinal dysplasia and vision impairment
Menachem V K Sarusie, Cecilia Rönnbäck, Cathrine Jespersgaard, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 37) with videos related to
Sort By:
Page
of 4
Genes
|
January 28, 2026
Transcriptome- and Epigenome-Wide Association Studies of Tic Spectrum Disorder in Discordant Monozygotic Twins
Jonas Dalsberg, Cathrine Jespersgaard, Amanda M Levy, et al.
Cardiovascular Journal of Africa
|
November 13, 2013
Long QT syndrome in South Africa: the results of comprehensive genetic screening
Paula L Hedley, Glenda A Durrheim, Firzana Hendricks, et al.
Inflammatory Bowel Diseases
|
April 3, 2012
Genome-wide peripheral blood leukocyte DNA methylation microarrays identified a single association with inflammatory bowel diseases
R Alan Harris, Dorottya Nagy-Szakal, Natalia Pedersen, et al.
Genes
|
December 23, 2020
Bi-Allelic Pathogenic Variations in <i>MERTK</i> Including Deletions Are Associated with an Early Onset Progressive Form of Retinitis Pigmentosa
Cathrine Jespersgaard, Mette Bertelsen, Farah Arif, et al.
Neurobiology of Aging
|
March 15, 2008
The diagnostic efficiency of biomarkers in sporadic Creutzfeldt-Jakob disease compared to Alzheimer's disease
Justyna Maria Czarna Bahl, Niels H H Heegaard, Gerhard Falkenhorst, et al.
Pain
|
February 23, 2018
Heterozygous mutations in GTP-cyclohydrolase-1 reduce BH4 biosynthesis but not pain sensitivity
Arafat Nasser, Anette Torvin Møller, Vibe Hellmund, et al.
Plos One
|
March 3, 2011
Determination of beta-defensin genomic copy number in different populations: a comparison of three methods
Peder Fode, Cathrine Jespersgaard, Robert J Hardwick, et al.
Digestive Diseases and Sciences
|
June 25, 2011
Alpha-defensin DEFA1A3 gene copy number elevation in Danish Crohn's disease patients
Cathrine Jespersgaard, Peder Fode, Marianne Dybdahl, et al.
Molecular Genetics & Genomic Medicine
|
February 6, 2014
MT-CYB mutations in hypertrophic cardiomyopathy
Christian M Hagen, Frederik H Aidt, Ole Havndrup, et al.
Human Molecular Genetics
|
October 29, 2024
A novel GFAP frameshift variant identified in a family with optico-retinal dysplasia and vision impairment
Menachem V K Sarusie, Cecilia Rönnbäck, Cathrine Jespersgaard, et al.
Page
of 4