Paper Details

Paper Title

Genetic Variation in Genes Underlying Diverse Dementias May Explain a Small Proportion of Cases in the Alzheimer's Disease Sequencing Project.

Paper Journal Title

Dement Geriatr Cogn Disord

Paper Citation Count

Paper Publication Year

2018

Bio Mention

AD, ADSP, APOE, ARSA, Alzheimer's Disease, Alzheimer's disease, CHMP2B, CSF1R, Dementias, GRN, MAPT, PSEN1, TREM2, dementia, dementia genes, dementias, dementing disorders, novel genes, participants, rare variants

Mesh Descriptor

Author Name	Affiliation
Elizabeth E Blue	University of Washington
Elizabeth E Blue	University of Washington
Joshua C Bis	University of Washington
Michael O Dorschner	University of Washington
Michael O Dorschner	University of Washington
Jennifer E Below	Vanderbilt University Medical Center
Jennifer E Below	Vanderbilt University Medical Center
William S Bush	Case Western Reserve University
Lindsay A Farrer	Boston University
Alison M Goate	Mount Sinai School of Medicine
Jonathan L Haines	Case Western Reserve University
Jonathan L Haines	Case Western Reserve University
Kathryn L Lunetta	Boston University
Patrick A Navas	University of Washington
Patrick A Navas	University of Washington
Gerard D Schellenberg	University of Pennsylvania
Timothy A Thornton	University of Washington
Cornelia M van Duijn	Erasmus Medical University
Cornelia M van Duijn	Erasmus Medical University
Badri N Vardarajan	Columbia University
Li-San Wang	University of Pennsylvania
Eric Boerwinkle	Baylor College of Medicine
Eric Boerwinkle	University of Texas Health Sciences Center at Houston
Eric Boerwinkle	Baylor College of Medicine
Eric Boerwinkle	University of Texas Health Sciences Center at Houston
JosÃ©e Dupuis	Boston University
Margaret A Pericak-Vance	University of Miami

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Dataset	Description	Source Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link

1 - 15

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