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Movement Disorders : Official Journal of the Movement Disorder Society
|
November 2, 2004
Pilot association study of the beta-glucocerebrosidase N370S allele and Parkinson's disease in subjects of Jewish ethnicity
Lorraine N Clark, Angelique Nicolai, Shehla Afridi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 16, 2004
Analysis of an early-onset Parkinson's disease cohort for DJ-1 mutations
Lorraine N Clark, Shehla Afridi, Helen Mejia-Santana, et al.
Nature Genetics
|
January 26, 2002
Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features
Sergey Kalachikov, Oleg Evgrafov, Barbara Ross, et al.
Alzheimer'S & Dementia (New York, N. Y.)
|
January 3, 2025
Designing and implementing the IDEAL Study: A randomized clinical trial of <i>APOE</i> genotype disclosure for late-onset Alzheimer's disease in an urban Latino population
John B Wetmore, Sophia Rodriguez, Daniela Diaz Caro, et al.
JAMA Neurology
|
January 16, 2014
Age-specific incidence rates for dementia and Alzheimer disease in NIA-LOAD/NCRAD and EFIGA families: National Institute on Aging Genetics Initiative for Late-Onset Alzheimer Disease/National Cell Repository for Alzheimer Disease (NIA-LOAD/NCRAD) and Estudio Familiar de Influencia Genetica en Alzheimer (EFIGA)
Badri N Vardarajan, Kelley M Faber, Thomas D Bird, et al.
Ebiomedicine
|
May 31, 2022
Common risk variants for epilepsy are enriched in families previously targeted for rare monogenic variant discovery
Karen L Oliver, Colin A Ellis, Ingrid E Scheffer, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 7, 2007
Construction and validation of a Parkinson's disease mutation genotyping array for the Parkin gene
Lorraine N Clark, Eneli Haamer, Helen Mejia-Santana, et al.
American Journal of Human Genetics
|
June 6, 2015
Heterozygous reelin mutations cause autosomal-dominant lateral temporal epilepsy
Emanuela Dazzo, Manuela Fanciulli, Elena Serioli, et al.
JAMA Neurology
|
August 18, 2016
The Role of Cardiovascular Risk Factors and Stroke in Familial Alzheimer Disease
Giuseppe Tosto, Thomas D Bird, David A Bennett, et al.
Neurology
|
February 19, 2017
Polygenic risk scores in familial Alzheimer disease
Giuseppe Tosto, Thomas D Bird, Debby Tsuang, et al.
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Search research articles
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Showing results (101-110 of 124) with videos related to
Sort By:
Page
of 13
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 2, 2004
Pilot association study of the beta-glucocerebrosidase N370S allele and Parkinson's disease in subjects of Jewish ethnicity
Lorraine N Clark, Angelique Nicolai, Shehla Afridi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 16, 2004
Analysis of an early-onset Parkinson's disease cohort for DJ-1 mutations
Lorraine N Clark, Shehla Afridi, Helen Mejia-Santana, et al.
Nature Genetics
|
January 26, 2002
Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features
Sergey Kalachikov, Oleg Evgrafov, Barbara Ross, et al.
Alzheimer'S & Dementia (New York, N. Y.)
|
January 3, 2025
Designing and implementing the IDEAL Study: A randomized clinical trial of <i>APOE</i> genotype disclosure for late-onset Alzheimer's disease in an urban Latino population
John B Wetmore, Sophia Rodriguez, Daniela Diaz Caro, et al.
JAMA Neurology
|
January 16, 2014
Age-specific incidence rates for dementia and Alzheimer disease in NIA-LOAD/NCRAD and EFIGA families: National Institute on Aging Genetics Initiative for Late-Onset Alzheimer Disease/National Cell Repository for Alzheimer Disease (NIA-LOAD/NCRAD) and Estudio Familiar de Influencia Genetica en Alzheimer (EFIGA)
Badri N Vardarajan, Kelley M Faber, Thomas D Bird, et al.
Ebiomedicine
|
May 31, 2022
Common risk variants for epilepsy are enriched in families previously targeted for rare monogenic variant discovery
Karen L Oliver, Colin A Ellis, Ingrid E Scheffer, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 7, 2007
Construction and validation of a Parkinson's disease mutation genotyping array for the Parkin gene
Lorraine N Clark, Eneli Haamer, Helen Mejia-Santana, et al.
American Journal of Human Genetics
|
June 6, 2015
Heterozygous reelin mutations cause autosomal-dominant lateral temporal epilepsy
Emanuela Dazzo, Manuela Fanciulli, Elena Serioli, et al.
JAMA Neurology
|
August 18, 2016
The Role of Cardiovascular Risk Factors and Stroke in Familial Alzheimer Disease
Giuseppe Tosto, Thomas D Bird, David A Bennett, et al.
Neurology
|
February 19, 2017
Polygenic risk scores in familial Alzheimer disease
Giuseppe Tosto, Thomas D Bird, Debby Tsuang, et al.
Page
of 13