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The Lancet. Oncology
|
December 19, 2024
The landscape of primary mismatch repair deficient gliomas in children, adolescents, and young adults: a multi-cohort study
Logine Negm, Jiil Chung, Liana Nobre, et al.
Cell Genomics
|
June 30, 2023
Genome-wide structural variant analysis identifies risk loci for non-Alzheimer's dementias
Karri Kaivola, Ruth Chia, Jinhui Ding, et al.
Brain : a Journal of Neurology
|
September 26, 2018
A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers
Ming Zhang, Raffaele Ferrari, Maria Carmela Tartaglia, et al.
Annals of Neurology
|
September 27, 2018
Prevalence of amyloid-β pathology in distinct variants of primary progressive aphasia
David Bergeron, Maria L Gorno-Tempini, Gil D Rabinovici, et al.
Acta Neuropathologica
|
February 11, 2019
Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD
Cyril Pottier, Yingxue Ren, Ralph B Perkerson, et al.
Nature Communications
|
April 25, 2025
Deciphering distinct genetic risk factors for FTLD-TDP pathological subtypes via whole-genome sequencing
Cyril Pottier, Fahri Küçükali, Matt Baker, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 9, 2024
Deciphering Distinct Genetic Risk Factors for FTLD-TDP Pathological Subtypes via Whole-Genome Sequencing
Cyril Pottier, Fahri Küçükali, Matt Baker, et al.
Nature Genetics
|
March 13, 2026
A repeat expansion in GOLGA8A is a major risk factor for atypical frontotemporal lobar degeneration with ubiquitin-positive inclusions
Wouter De Coster, Marleen Van den Broeck, Matt Baker, et al.
Nature Genetics
|
February 16, 2021
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture
Ruth Chia, Marya S Sabir, Sara Bandres-Ciga, et al.
Page
of 11
Search research articles
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Showing results (101-110 of 109) with videos related to
Sort By:
Page
of 11
You have reached the last page of results.
This site can display upto 109 results.
The Lancet. Oncology
|
December 19, 2024
The landscape of primary mismatch repair deficient gliomas in children, adolescents, and young adults: a multi-cohort study
Logine Negm, Jiil Chung, Liana Nobre, et al.
Cell Genomics
|
June 30, 2023
Genome-wide structural variant analysis identifies risk loci for non-Alzheimer's dementias
Karri Kaivola, Ruth Chia, Jinhui Ding, et al.
Brain : a Journal of Neurology
|
September 26, 2018
A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers
Ming Zhang, Raffaele Ferrari, Maria Carmela Tartaglia, et al.
Annals of Neurology
|
September 27, 2018
Prevalence of amyloid-β pathology in distinct variants of primary progressive aphasia
David Bergeron, Maria L Gorno-Tempini, Gil D Rabinovici, et al.
Acta Neuropathologica
|
February 11, 2019
Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD
Cyril Pottier, Yingxue Ren, Ralph B Perkerson, et al.
Nature Communications
|
April 25, 2025
Deciphering distinct genetic risk factors for FTLD-TDP pathological subtypes via whole-genome sequencing
Cyril Pottier, Fahri Küçükali, Matt Baker, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 9, 2024
Deciphering Distinct Genetic Risk Factors for FTLD-TDP Pathological Subtypes via Whole-Genome Sequencing
Cyril Pottier, Fahri Küçükali, Matt Baker, et al.
Nature Genetics
|
March 13, 2026
A repeat expansion in GOLGA8A is a major risk factor for atypical frontotemporal lobar degeneration with ubiquitin-positive inclusions
Wouter De Coster, Marleen Van den Broeck, Matt Baker, et al.
Nature Genetics
|
February 16, 2021
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture
Ruth Chia, Marya S Sabir, Sara Bandres-Ciga, et al.
Page
of 11