Search research articles
Contact Us
Filters
Showing results (1-10 of 15) with videos related to
Page
of 2
Sort By:
European Journal of Medical Genetics
|
July 15, 2014
Raine syndrome: an overview
Víctor Faundes, Silvia Castillo-Taucher, Patricio Gonzalez-Hormazabal, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
December 24, 2025
Biomarkers
Martyn Frith, Barry Chioza, Rosemary Bamford, et al.
Annals of Human Genetics
|
January 15, 2010
Founder mutation(s) in the RSPH9 gene leading to primary ciliary dyskinesia in two inbred Bedouin families
Orit Reish, Montgomery Slatkin, Daphne Chapman-Shimshoni, et al.
European Journal of Human Genetics : EJHG
|
December 4, 2002
Haplotype and linkage disequilibrium analysis to characterise a region in the calcium channel gene CACNA1A associated with idiopathic generalised epilepsy
Barry Chioza, Abena Osei-Lah, Lina Nashef, et al.
Briefings in Bioinformatics
|
August 21, 2025
Guidance for the design and analysis of cell-type-specific DNA methylation epidemiology studies
Emma M Walker, Emma L Dempster, Alice Franklin, et al.
BMC Biology
|
January 25, 2024
Quantifying the proportion of different cell types in the human cortex using DNA methylation profiles
Eilis Hannon, Emma L Dempster, Jonathan P Davies, et al.
Cell Genomics
|
September 25, 2025
Cell-type-specific DNA methylation dynamics in the prenatal and postnatal human cortex
Alice Franklin, Jonathan P Davies, Nicholas E Clifton, et al.
Nature Communications
|
August 2, 2024
Long-read transcript sequencing identifies differential isoform expression in the entorhinal cortex in a transgenic model of tau pathology
Szi Kay Leung, Rosemary A Bamford, Aaron R Jeffries, et al.
Nature Communications
|
September 24, 2022
DNA methylation signatures of Alzheimer's disease neuropathology in the cortex are primarily driven by variation in non-neuronal cell-types
Gemma Shireby, Emma L Dempster, Stefania Policicchio, et al.
American Journal of Human Genetics
|
November 13, 2012
Defective presynaptic choline transport underlies hereditary motor neuropathy
Katy E S Barwick, Jane Wright, Saeed Al-Turki, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 15) with videos related to
Sort By:
Page
of 2
European Journal of Medical Genetics
|
July 15, 2014
Raine syndrome: an overview
Víctor Faundes, Silvia Castillo-Taucher, Patricio Gonzalez-Hormazabal, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
December 24, 2025
Biomarkers
Martyn Frith, Barry Chioza, Rosemary Bamford, et al.
Annals of Human Genetics
|
January 15, 2010
Founder mutation(s) in the RSPH9 gene leading to primary ciliary dyskinesia in two inbred Bedouin families
Orit Reish, Montgomery Slatkin, Daphne Chapman-Shimshoni, et al.
European Journal of Human Genetics : EJHG
|
December 4, 2002
Haplotype and linkage disequilibrium analysis to characterise a region in the calcium channel gene CACNA1A associated with idiopathic generalised epilepsy
Barry Chioza, Abena Osei-Lah, Lina Nashef, et al.
Briefings in Bioinformatics
|
August 21, 2025
Guidance for the design and analysis of cell-type-specific DNA methylation epidemiology studies
Emma M Walker, Emma L Dempster, Alice Franklin, et al.
BMC Biology
|
January 25, 2024
Quantifying the proportion of different cell types in the human cortex using DNA methylation profiles
Eilis Hannon, Emma L Dempster, Jonathan P Davies, et al.
Cell Genomics
|
September 25, 2025
Cell-type-specific DNA methylation dynamics in the prenatal and postnatal human cortex
Alice Franklin, Jonathan P Davies, Nicholas E Clifton, et al.
Nature Communications
|
August 2, 2024
Long-read transcript sequencing identifies differential isoform expression in the entorhinal cortex in a transgenic model of tau pathology
Szi Kay Leung, Rosemary A Bamford, Aaron R Jeffries, et al.
Nature Communications
|
September 24, 2022
DNA methylation signatures of Alzheimer's disease neuropathology in the cortex are primarily driven by variation in non-neuronal cell-types
Gemma Shireby, Emma L Dempster, Stefania Policicchio, et al.
American Journal of Human Genetics
|
November 13, 2012
Defective presynaptic choline transport underlies hereditary motor neuropathy
Katy E S Barwick, Jane Wright, Saeed Al-Turki, et al.
Page
of 2