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Nature Genetics
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April 8, 2003
C. elegans ORFeome version 1.1: experimental verification of the genome annotation and resource for proteome-scale protein expression
Jérôme Reboul, Philippe Vaglio, Jean-François Rual, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
December 25, 2025
Biomarkers
Julie K Wisch, Ziqiao Jiao, Patrick J Lao, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
June 22, 2025
Longitudinal study of body mass index in relation to Alzheimer's disease pathology and symptomatology in Down syndrome
Victoria L Fleming, Brian C Helsel, Lauren T Ptomey, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 6, 2019
Incidence of mosaicism in 1055 de novo NF2 cases: much higher than previous estimates with high utility of next-generation sequencing
D Gareth Evans, Claire L Hartley, Philip T Smith, et al.
Human Mutation
|
February 19, 2013
Combined NGS approaches identify mutations in the intraflagellar transport gene IFT140 in skeletal ciliopathies with early progressive kidney Disease
Miriam Schmidts, Valeska Frank, Tobias Eisenberger, et al.
Annals of Neurology
|
September 22, 2025
Cross-Sectional FDG in Down Syndrome and Autosomal Dominant Alzheimer's Disease
Omar Abdelmoity, Julie K Wisch, James T Kennedy, et al.
Brain : a Journal of Neurology
|
November 15, 2025
The tau biomarker cascade is condensed in Down syndrome compared to sporadic Alzheimer's disease
Matthew D Zammit, Hailey Bruzzone, Karly A Cody, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
January 19, 2026
Brain volume trajectories in Down syndrome and autosomal dominant Alzheimer's disease
James T Kennedy, Julie K Wisch, Anna H Boerwinkle, et al.
Nucleic Acids Research
|
November 24, 2023
The Monarch Initiative in 2024: an analytic platform integrating phenotypes, genes and diseases across species
Tim E Putman, Kevin Schaper, Nicolas Matentzoglu, et al.
American Journal of Human Genetics
|
October 22, 2013
Defects in the IFT-B component IFT172 cause Jeune and Mainzer-Saldino syndromes in humans
Jan Halbritter, Albane A Bizet, Miriam Schmidts, et al.
Page
of 46
Search research articles
Search
Showing results (441-450 of 451) with videos related to
Sort By:
Page
of 46
Nature Genetics
|
April 8, 2003
C. elegans ORFeome version 1.1: experimental verification of the genome annotation and resource for proteome-scale protein expression
Jérôme Reboul, Philippe Vaglio, Jean-François Rual, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
December 25, 2025
Biomarkers
Julie K Wisch, Ziqiao Jiao, Patrick J Lao, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
June 22, 2025
Longitudinal study of body mass index in relation to Alzheimer's disease pathology and symptomatology in Down syndrome
Victoria L Fleming, Brian C Helsel, Lauren T Ptomey, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 6, 2019
Incidence of mosaicism in 1055 de novo NF2 cases: much higher than previous estimates with high utility of next-generation sequencing
D Gareth Evans, Claire L Hartley, Philip T Smith, et al.
Human Mutation
|
February 19, 2013
Combined NGS approaches identify mutations in the intraflagellar transport gene IFT140 in skeletal ciliopathies with early progressive kidney Disease
Miriam Schmidts, Valeska Frank, Tobias Eisenberger, et al.
Annals of Neurology
|
September 22, 2025
Cross-Sectional FDG in Down Syndrome and Autosomal Dominant Alzheimer's Disease
Omar Abdelmoity, Julie K Wisch, James T Kennedy, et al.
Brain : a Journal of Neurology
|
November 15, 2025
The tau biomarker cascade is condensed in Down syndrome compared to sporadic Alzheimer's disease
Matthew D Zammit, Hailey Bruzzone, Karly A Cody, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
January 19, 2026
Brain volume trajectories in Down syndrome and autosomal dominant Alzheimer's disease
James T Kennedy, Julie K Wisch, Anna H Boerwinkle, et al.
Nucleic Acids Research
|
November 24, 2023
The Monarch Initiative in 2024: an analytic platform integrating phenotypes, genes and diseases across species
Tim E Putman, Kevin Schaper, Nicolas Matentzoglu, et al.
American Journal of Human Genetics
|
October 22, 2013
Defects in the IFT-B component IFT172 cause Jeune and Mainzer-Saldino syndromes in humans
Jan Halbritter, Albane A Bizet, Miriam Schmidts, et al.
Page
of 46