(Q42675021)

4 November 2017

title

Comprehensive analysis of the LRRK2 gene in sixty families with Parkinson's disease (English)

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4 November 2017

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1

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10

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4 November 2017

Stefano Goldwurm

31

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Joaquim Ferreira

Joaquim Ferreira

5

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Marco Onofrj

Marco Onofrj

18

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Fabrizio Stocchi

Fabrizio Stocchi

17

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Michele Tinazzi

Michele Tinazzi

20

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Angelo Antonini

Angelo Antonini

8

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Nicola Vanacore

23

Nicola Vanacore

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4 November 2017

28

Thomas Gasser

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4 November 2017

26

Ryan J Uitti

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4 November 2017

27

Zbigniew K Wszolek

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4 November 2017

33

Cristina Sampaio

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4 November 2017

32

Gianni Pezzoli

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4 November 2017

21

Giovanni Fabbrini

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4 November 2017

24

Giuseppe Meco

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4 November 2017

13

Leonardo Lopiano

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4 November 2017

37

Vincenzo Bonifati

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4 November 2017

2

Cristina Tassorelli

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4 November 2017

36

Ben A Oostra

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4 November 2017

3

Michele De Mari

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4 November 2017

6

Christan F Rohé

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4 November 2017

11

Roberto Marconi

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4 November 2017

14

Emiliana Fincati

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4 November 2017

15

Marco Guidi

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4 November 2017

19

Vincenzo Toni

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4 November 2017

30

Guido J Breedveld

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4 November 2017

34

Egberto Barbosa

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4 November 2017

35

Emilia Martignoni

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Italian Parkinson's Genetics Network

4 November 2017

38

Italian Parkinson's Genetics Network

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4 November 2017

Hsin F Chien

4

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4 November 2017

Giulio Riboldazzi

7

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4 November 2017

Gianni Albani

9

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4 November 2017

Giovanni Abbruzzese

12

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4 November 2017

Paolo Marini

16

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4 November 2017

Paolo Lamberti

22

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4 November 2017

Petra Leitner

25

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4 November 2017

Erik J Simons

29

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4 November 2017

publication date

1 March 2006

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European Journal of Human Genetics

4 November 2017

published in

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4 November 2017

volume

14

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4 November 2017

issue

3

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4 November 2017

page(s)

322-331

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https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201539

4 November 2017

exact match

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cites work

Unraveling the pathogenesis of Parkinson's disease--the contribution of monogenic forms

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201539

Molecular Pathways of Neurodegeneration in Parkinson's Disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201539

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201539

alpha-Synuclein locus triplication causes Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201539

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201539

Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201539

Hereditary early-onset Parkinson's disease caused by mutations in PINK1

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201539

A new locus for Parkinson's disease (PARK8) maps to chromosome 12p11.2-q13.1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201539

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201539

Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201539

Roc, a Ras/GTPase domain in complex proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201539

Clinical and positron emission tomography of Parkinson's disease caused by LRRK2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201539

Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201539

An LRRK2 mutation as a cause for the parkinsonism in the original PARK8 family.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201539

LRRK2 R1441G in Spanish patients with Parkinson's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201539

The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201539

Clinical features of LRRK2-associated Parkinson's disease in central Norway

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201539

Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201539

The G6055A (G2019S) mutation in LRRK2 is frequent in both early and late onset Parkinson's disease and originates from a common ancestor

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201539

LRRK2 haplotype analyses in European and North African families with Parkinson disease: a common founder for the G2019S mutation dating from the 13th century

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201539

The protein kinase complement of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201539

Regulation of protein kinases; controlling activity through activation segment conformation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201539

Mutations of the BRAF gene in human cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201539

Autosomal dominant parkinsonism associated with variable synuclein and tau pathology

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201539

A clinic-based study of the LRRK2 gene in Parkinson disease yields new mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201539

LRRK2 gene in Parkinson disease: Mutation analysis and case control association study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201539

LRRK2 mutations in Parkinson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201539

A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201539

Genetic and clinical identification of Parkinson's disease patients with LRRK2 G2019S mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201539

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/SJ.EJHG.5201539

1 reference

Dimensions Publication ID

4 November 2017

1024123808

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Fatcat ID

release_lr7dyd2o3jbhjhjpjmguevuh4u

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/lr7dyd2o3jbhjhjpjmguevuh4u

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference