A multiancestral genome-wide exome array study of Alzheimer disease, frontotemporal dementia, and progressive supranuclear palsy (Q34464088)

2 August 2017

title

A multiancestral genome-wide exome array study of Alzheimer disease, frontotemporal dementia, and progressive supranuclear palsy (English)

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progressive supranuclear palsy

2 August 2017

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frontotemporal dementia

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based on heuristic

inferred from title

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32

Charles DeCarli

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Jeremy Davis-Turak

Jeremy Davis-Turak

3

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Jason A Chen

Jason A Chen

1

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Wayne W Poon

Wayne W Poon

18

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Walter A. Kukull

Walter A Kukull

27

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Tatiana Foroud

24

Tatiana M Foroud

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34

Daniel H Geschwind

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33

Bruce L Miller

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14

Adam Boxer

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15

Kelley M Faber

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2 August 2017

Qing Wang

2

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2 August 2017

Yun Li

4

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Anna M Karydas

5

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Sandy C Hsu

6

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Renee L Sears

7

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Doxa Chatzopoulou

8

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Alden Y Huang

9

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Kevin J Wojta

10

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Eric Klein

11

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Jason Lee

12

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Duane L Beekly

13

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Claudia M Haase

16

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Josh Miller

17

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Ami Rosen

19

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Howard Rosen

20

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Anna Sapozhnikova

21

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Jill Shapira

22

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Arousiak Varpetian

23

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Robert W Levenson

25

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Allan I Levey

26

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Mario F Mendez

28

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John Ringman

29

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Helena Chui

30

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Carl Cotman

31

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Giovanni Coppola

35

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2 August 2017

language of work or name

English

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publication date

1 April 2015

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2 August 2017

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2 August 2017

volume

72

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2 August 2017

issue

4

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2 August 2017

page(s)

414-422

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Frontotemporal dementia and its subtypes: a genome-wide association study

2 August 2017

cites work

1 reference

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6 July 2018

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An epigenetic signature in peripheral blood associated with the haplotype on 17q21.31, a risk factor for neurodegenerative tauopathy

6 July 2018

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Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks

6 July 2018

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Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease

6 July 2018

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6 July 2018

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6 July 2018

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Integrated systems approach identifies genetic nodes and networks in late-onset Alzheimer's disease

6 July 2018

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Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E ϵ4,and the risk of late-onset Alzheimer disease in African Americans

6 July 2018

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Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion

6 July 2018

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Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis

6 July 2018

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TREM2 Variants in Alzheimer's Disease

6 July 2018

1 reference

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Advances in understanding the molecular basis of frontotemporal dementia

6 July 2018

1 reference

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Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases

6 July 2018

1 reference

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Rare-variant association testing for sequencing data with the sequence kernel association test

6 July 2018

1 reference

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Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy

6 July 2018

1 reference

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Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease

6 July 2018

1 reference

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Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

6 July 2018

1 reference

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Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions

6 July 2018

1 reference

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PTIP regulates 53BP1 and SMC1 at the DNA damage sites

6 July 2018

1 reference

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Genetic control of human brain transcript expression in Alzheimer disease

6 July 2018

1 reference

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Phospho-epitope binding by the BRCT domains of hPTIP controls multiple aspects of the cellular response to DNA damage

6 July 2018

1 reference

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Dysferlin and muscle membrane repair.

6 July 2018

1 reference

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The muscle protein dysferlin accumulates in the Alzheimer brain

6 July 2018

1 reference

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Role of Genes and Environments for Explaining Alzheimer Disease

6 July 2018

1 reference

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Linkage and association studies identify a novel locus for Alzheimer disease at 7q36 in a Dutch population-based sample

6 July 2018

1 reference

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Linkage disequilibrium fine mapping and haplotype association analysis of the tau gene in progressive supranuclear palsy and corticobasal degeneration

6 July 2018

1 reference

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Human PTIP facilitates ATM-mediated activation of p53 and promotes cellular resistance to ionizing radiation

6 July 2018

1 reference

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Defective membrane repair in dysferlin-deficient muscular dystrophy

6 July 2018

1 reference

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6 July 2018

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Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy

6 July 2018

1 reference

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Exploring the etiology of Alzheimer disease using molecular genetics

6 July 2018

1 reference

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Linkage studies in familial Alzheimer disease: evidence for chromosome 19 linkage

6 July 2018

1 reference

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Exome array study did not identify novel variants in Alzheimer's disease.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4397175

Dysferlin is a newly identified binding partner of AβPP and it co-aggregates with amyloid-β42 within sporadic inclusion-body myositis (s-IBM) muscle fibers

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4397175

Dysferlin is a new marker for leaky brain blood vessels in multiple sclerosis.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4397175

Association of an extended haplotype in the tau gene with progressive supranuclear palsy

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4397175

10.1001/JAMANEUROL.2014.4040

27 October 2018

Identifiers

DOI

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2 August 2017

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2 August 2017

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