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JAMA Network Open
|
May 17, 2023
Genetic Associations Between Modifiable Risk Factors and Alzheimer Disease
, Jiao Luo, Jesper Qvist Thomassen, et al.
Neurology
|
April 8, 2021
Plasma Neurofilament Light for Prediction of Disease Progression in Familial Frontotemporal Lobar Degeneration
Julio C Rojas, Ping Wang, Adam M Staffaroni, et al.
Nature Communications
|
July 21, 2025
Machine learning in Alzheimer's disease genetics
Matthew Bracher-Smith, Federico Melograna, Brittany Ulm, et al.
The Lancet. Neurology
|
December 8, 2019
Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study
Katrina M Moore, Jennifer Nicholas, Murray Grossman, et al.
JAMA Neurology
|
May 31, 2022
Association of Rare APOE Missense Variants V236E and R251G With Risk of Alzheimer Disease
Yann Le Guen, Michael E Belloy, Benjamin Grenier-Boley, et al.
Nature Medicine
|
September 22, 2022
Temporal order of clinical and biomarker changes in familial frontotemporal dementia
Adam M Staffaroni, Melanie Quintana, Barbara Wendelberger, 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.
Neurology
|
September 18, 2020
<i>C9orf72</i>, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohorts
Beatrice Costa, Claudia Manzoni, Manuel Bernal-Quiros, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 19, 2025
<i>APOE</i> stratified genome-wide association studies provide novel insights into the genetic etiology of Alzheimers's disease
Jesper Qvist Thomassen, Leonard Hampton, Brittany Ulms, 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.
Page
of 27
Search research articles
Search
Showing results (241-250 of 267) with videos related to
Sort By:
Page
of 27
JAMA Network Open
|
May 17, 2023
Genetic Associations Between Modifiable Risk Factors and Alzheimer Disease
, Jiao Luo, Jesper Qvist Thomassen, et al.
Neurology
|
April 8, 2021
Plasma Neurofilament Light for Prediction of Disease Progression in Familial Frontotemporal Lobar Degeneration
Julio C Rojas, Ping Wang, Adam M Staffaroni, et al.
Nature Communications
|
July 21, 2025
Machine learning in Alzheimer's disease genetics
Matthew Bracher-Smith, Federico Melograna, Brittany Ulm, et al.
The Lancet. Neurology
|
December 8, 2019
Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study
Katrina M Moore, Jennifer Nicholas, Murray Grossman, et al.
JAMA Neurology
|
May 31, 2022
Association of Rare APOE Missense Variants V236E and R251G With Risk of Alzheimer Disease
Yann Le Guen, Michael E Belloy, Benjamin Grenier-Boley, et al.
Nature Medicine
|
September 22, 2022
Temporal order of clinical and biomarker changes in familial frontotemporal dementia
Adam M Staffaroni, Melanie Quintana, Barbara Wendelberger, 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.
Neurology
|
September 18, 2020
<i>C9orf72</i>, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohorts
Beatrice Costa, Claudia Manzoni, Manuel Bernal-Quiros, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 19, 2025
<i>APOE</i> stratified genome-wide association studies provide novel insights into the genetic etiology of Alzheimers's disease
Jesper Qvist Thomassen, Leonard Hampton, Brittany Ulms, 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.
Page
of 27