ABCA7 rare variants and Alzheimer disease risk (Q36982034)

17 August 2017

0 references

ABCA7 rare variants and Alzheimer disease risk (English)

1 reference

17 August 2017

0 references

28

1 reference

17 August 2017

20

Mark Lathrop

1 reference

17 August 2017

Kilan Le Guennec

1

0 references

Richard Redon

Richard Redon

22

0 references

Céline Bellenguez

Céline Bellenguez

6

0 references

Luc Letenneur

Luc Letenneur

23

0 references

Philippe Amouyel

Philippe Amouyel

17

0 references

Florence Pasquier

Florence Pasquier

25

0 references

Guillaume Bourque

19

Guillaume Bourque

1 reference

17 August 2017

Adeline Rollin-Sillaire

26

Adeline Rollin-Sillaire

1 reference

17 August 2017

29

Didier Hannequin

1 reference

17 August 2017

30

Dominique Campion

1 reference

17 August 2017

5

David Wallon

1 reference

17 August 2017

Benjamin Grenier-Boley

7

Benjamin Grenier-Boley

1 reference

17 August 2017

10

Anne Rovelet-Lecrux

1 reference

17 August 2017

21

Thierry Frebourg

1 reference

17 August 2017

3

Olivier Quenez

1 reference

17 August 2017

4

Camille Charbonnier

1 reference

17 August 2017

13

Robert Olaso

1 reference

17 August 2017

Jean-François Deleuze

16

Jean-François Deleuze

1 reference

17 August 2017

18

Hans Markus Munter

1 reference

17 August 2017

27

Emmanuelle Génin

1 reference

17 August 2017

CNR-MAJ collaborators

31

CNR-MAJ collaborators

1 reference

17 August 2017

Jean-François Dartigues

24

Jean-François Dartigues

1 reference

17 August 2017

Gaël Nicolas

2

1 reference

17 August 2017

Stéphane Rousseau

8

1 reference

17 August 2017

Anne-Claire Richard

9

1 reference

17 August 2017

Delphine Bacq

11

1 reference

17 August 2017

Jean-Guillaume Garnier

12

1 reference

17 August 2017

Anne Boland

14

1 reference

17 August 2017

Vincent Meyer

15

1 reference

17 August 2017

language of work or name

English

0 references

publication date

1 April 2016

1 reference

17 August 2017

1 reference

17 August 2017

86

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17 August 2017

2134-2137

1 reference

17 August 2017

23

1 reference

Rare Variants in PLD3 Do Not Affect Risk for Early-Onset Alzheimer Disease in a European Consortium Cohort

17 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4898320

ATP-binding cassette transporter A7 (ABCA7) loss of function alters Alzheimer amyloid processing

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4898320

Screening of dementia genes by whole-exome sequencing in early-onset Alzheimer disease: input and lessons

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4898320

Loss-of-function variants in ABCA7 confer risk of Alzheimer's disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4898320

Second-generation PLINK: rising to the challenge of larger and richer datasets

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4898320

A rare mutation in UNC5C predisposes to late-onset Alzheimer's disease and increases neuronal cell death

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4898320

Variant association tools for quality control and analysis of large-scale sequence and genotyping array data

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4898320

Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer's disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4898320

Deletion of Abca7 increases cerebral amyloid-β accumulation in the J20 mouse model of Alzheimer's disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4898320

TREM2 Variants in Alzheimer's Disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4898320

Variant of TREM2 Associated with the Risk of Alzheimer's Disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4898320

Detecting and estimating contamination of human DNA samples in sequencing and array-based genotype data

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4898320

A mutation in APP protects against Alzheimer’s disease and age-related cognitive decline

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4898320

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4898320

The diagnosis of dementia due to Alzheimer's disease: recommendations from the National Institute on Aging-Alzheimer's Association workgroups on diagnostic guidelines for Alzheimer's disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4898320

Data quality control in genetic case-control association studies.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4898320

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4898320

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4898320

Fast and accurate long-read alignment with Burrows-Wheeler transform

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4898320

APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4898320

PLD3 variants in population studies

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4898320

SORL1 rare variants: a major risk factor for familial early-onset Alzheimer's disease.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4898320

Mutations in ABCA7 in a Belgian cohort of Alzheimer's disease patients: a targeted resequencing study.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4898320

PLD3 gene variants and Alzheimer's disease.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4898320

PLD3 in non-familial Alzheimer's disease.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4898320

PLD3 and sporadic Alzheimer's disease risk.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4898320

High frequency of potentially pathogenic SORL1 mutations in autosomal dominant early-onset Alzheimer disease.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4898320

10.1212/WNL.0000000000002627

4 September 2018

Identifiers

DOI

1 reference

17 August 2017

1 reference

17 August 2017

1 reference