(Q48251025)

10 February 2018

title

PLD3 in non-familial Alzheimer's disease (English)

1 reference

10 February 2018

Stefanie Heilmann-Heimbach

main subject

Alzheimer's disease

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author

1

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10 February 2018

André Lacour

5

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10 February 2018

Johannes Kornhuber

14

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10 February 2018

Markus M Nöthen

31

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10 February 2018

Alfredo Ramirez

32

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10 February 2018

Montserrat Alegret

Montserrat Alegret

10

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Dmitriy Drichel

Dmitriy Drichel

2

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Steffi G. Riedel-Heller

21

Steffi Riedel-Heller

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10 February 2018

Martin Scherer

22

Martin Scherer

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10 February 2018

Frank Jessen

24

Frank Jessen

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10 February 2018

author name string

Jordi Clarimon

3

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10 February 2018

Victoria Fernández

4

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10 February 2018

Holger Wagner

6

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10 February 2018

Mathias Thelen

7

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10 February 2018

Isabel Hernández

8

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10 February 2018

Juan Fortea

9

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Rafael Blesa

11

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10 February 2018

Ana Mauleón

12

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10 February 2018

Maitée Rosende Roca

13

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10 February 2018

Oliver Peters

15

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Reinhard Heun

16

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Lutz Frölich

17

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10 February 2018

Michael Hüll

18

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Michael T Heneka

19

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Eckart Rüther

20

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Jens Wiltfang

23

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Tim Becker

25

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Lluís Tárraga

26

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Mercè Boada

27

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Wolfgang Maier

28

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Alberto Lleó

29

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10 February 2018

Agustin Ruiz

30

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10 February 2018

language of work or name

English

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publication date

1 April 2015

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10 February 2018

published in

Nature

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10 February 2018

volume

520

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10 February 2018

issue

7545

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10 February 2018

page(s)

E3-5

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10 February 2018

TREM2 Variants in Alzheimer's Disease

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNATURE14039

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE14039

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE14039

Follow-up of loci from the International Genomics of Alzheimer's Disease Project identifies TRIP4 as a novel susceptibility gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE14039

Assessing the role of the TREM2 p.R47H variant as a risk factor for Alzheimer's disease and frontotemporal dementia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE14039

Early and differential diagnosis of dementia and mild cognitive impairment: design and cohort baseline characteristics of the German Dementia Competence Network

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE14039

Prediction of dementia in primary care patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE14039

Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE14039

An evaluation of statistical approaches to rare variant analysis in genetic association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE14039

INTERSNP: genome-wide interaction analysis guided by a priori information

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE14039

PLD3 gene variants and Alzheimer's disease.

21 January 2018

1 reference

12 December 2020

PLD3 and sporadic Alzheimer's disease risk.

1 reference

12 December 2020

SUCLG2 identified as both a determinator of CSF Aβ1-42 levels and an attenuator of cognitive decline in Alzheimer's disease

1 reference

12 December 2020

PLD3 variants in population studies

1 reference

12 December 2020

Identifiers

DOI

10.1038/NATURE14039

1 reference

10 February 2018

Dimensions Publication ID

1010773188

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10 February 2018