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Human Mutation
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March 21, 2020
Damaging de novo missense variants in EEF1A2 lead to a developmental and degenerative epileptic-dyskinetic encephalopathy
Gemma L Carvill, Katherine L Helbig, Candace T Myers, et al.
Nature Genetics
|
February 8, 2020
Author Correction: Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk
Iris E Jansen, Jeanne E Savage, Kyoko Watanabe, et al.
Eclinicalmedicine
|
December 5, 2022
Individualised prediction of drug resistance and seizure recurrence after medication withdrawal in people with juvenile myoclonic epilepsy: A systematic review and individual participant data meta-analysis
Remi Stevelink, Dania Al-Toma, Floor E Jansen, et al.
Nature Genetics
|
January 9, 2019
Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk
Iris E Jansen, Jeanne E Savage, Kyoko Watanabe, et al.
Acta Neuropathologica
|
March 14, 2020
PLCG2 protective variant p.P522R modulates tau pathology and disease progression in patients with mild cognitive impairment
Luca Kleineidam, Vincent Chouraki, Tomasz Próchnicki, et al.
Nature Genetics
|
June 21, 2022
Author Correction: A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's disease
Douglas P Wightman, Iris E Jansen, Jeanne E Savage, et al.
Nature Genetics
|
September 8, 2021
A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's disease
Douglas P Wightman, Iris E Jansen, Jeanne E Savage, et al.
Nature Genetics
|
November 13, 2021
Author Correction: A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's disease
Douglas P Wightman, Iris E Jansen, Jeanne E Savage, et al.
Neurology
|
January 2, 2024
Molecular and Phenotypic Characterization of the <i>RORB</i>-Related Disorder
Zeynep Gokce-Samar, Annalisa Vetro, Julitta De Bellescize, et al.
Neuron
|
September 28, 2011
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
Alan E Renton, Elisa Majounie, Adrian Waite, et al.
Page
of 77
Search research articles
Search
Showing results (591-600 of 767) with videos related to
Sort By:
Page
of 77
Human Mutation
|
March 21, 2020
Damaging de novo missense variants in EEF1A2 lead to a developmental and degenerative epileptic-dyskinetic encephalopathy
Gemma L Carvill, Katherine L Helbig, Candace T Myers, et al.
Nature Genetics
|
February 8, 2020
Author Correction: Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk
Iris E Jansen, Jeanne E Savage, Kyoko Watanabe, et al.
Eclinicalmedicine
|
December 5, 2022
Individualised prediction of drug resistance and seizure recurrence after medication withdrawal in people with juvenile myoclonic epilepsy: A systematic review and individual participant data meta-analysis
Remi Stevelink, Dania Al-Toma, Floor E Jansen, et al.
Nature Genetics
|
January 9, 2019
Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk
Iris E Jansen, Jeanne E Savage, Kyoko Watanabe, et al.
Acta Neuropathologica
|
March 14, 2020
PLCG2 protective variant p.P522R modulates tau pathology and disease progression in patients with mild cognitive impairment
Luca Kleineidam, Vincent Chouraki, Tomasz Próchnicki, et al.
Nature Genetics
|
June 21, 2022
Author Correction: A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's disease
Douglas P Wightman, Iris E Jansen, Jeanne E Savage, et al.
Nature Genetics
|
September 8, 2021
A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's disease
Douglas P Wightman, Iris E Jansen, Jeanne E Savage, et al.
Nature Genetics
|
November 13, 2021
Author Correction: A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's disease
Douglas P Wightman, Iris E Jansen, Jeanne E Savage, et al.
Neurology
|
January 2, 2024
Molecular and Phenotypic Characterization of the <i>RORB</i>-Related Disorder
Zeynep Gokce-Samar, Annalisa Vetro, Julitta De Bellescize, et al.
Neuron
|
September 28, 2011
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
Alan E Renton, Elisa Majounie, Adrian Waite, et al.
Page
of 77