Comprehensive screening of a North American Parkinson's disease cohort for LRRK2 mutation. (Q48109654)

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Language	Label	Description	Also known as
English	Comprehensive screening of a North American Parkinson's disease cohort for LRRK2 mutation.	scientific article

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scholarly article

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/17622782

Comprehensive screening of a North American Parkinson's disease cohort for LRRK2 mutation. (English)

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/17622782

Parkinson's disease

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based on heuristic

inferred from title

Michael S. Okun

16

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Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/17622782

11

object named as

Kelly D Foote

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Europe PubMed Central

8 February 2018

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object named as

Katrina Gwinn-Hardy

1 reference

Europe PubMed Central

8 February 2018

Hubert H Fernandez

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object named as

Hubert H Fernandez

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Europe PubMed Central

8 February 2018

Andrew Singleton

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object named as

Andrew B Singleton

1 reference

Europe PubMed Central

8 February 2018

Coro Paisán-Ruíz

2

object named as

Coro Paisán-Ruíz

0 references

4

object named as

Cynthia Crews

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/17622782

Aideen M McInerney-Leo

object named as

Aideen McInerney-Leo

8

1 reference

ORCID Public Data File 2021

Angela F Britton

5

object named as

Angela Britton

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/17622782

Sharon Reimsnider

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object named as

Sharon Reimsnider

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/17622782

author name string

Janel Johnson

1

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/17622782

Grisel Lopez

3

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/17622782

Roniel Malkani

6

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Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/17622782

E Whitney Evans

7

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/17622782

Shushant Jain

9

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/17622782

Robert L Nussbaum

10

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/17622782

Ronald J Mandel

12

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Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/17622782

Anthony Crawley

13

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/17622782

publication date

6 July 2007

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/17622782

Neurodegenerative Diseases

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/17622782

4

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Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/17622782

5

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Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/17622782

386-391

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Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/17622782

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

1 reference

https://api.crossref.org/works/10.1159%2F000105160

21 January 2018

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

1 reference

https://api.crossref.org/works/10.1159%2F000105160

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1159%2F000105160

21 January 2018

Analysis of the PINK1 gene in a large cohort of cases with Parkinson disease

1 reference

https://api.crossref.org/works/10.1159%2F000105160

21 January 2018

SNCA multiplication is not a common cause of Parkinson disease or dementia with Lewy bodies.

1 reference

https://api.crossref.org/works/10.1159%2F000105160

21 January 2018

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

1 reference

https://api.crossref.org/works/10.1159%2F000105160

21 January 2018

The WD repeat: a common architecture for diverse functions

1 reference

https://api.crossref.org/works/10.1159%2F000105160

21 January 2018

Early-onset Parkinson's disease caused by a compound heterozygous DJ-1 mutation

1 reference

https://api.crossref.org/works/10.1159%2F000105160

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1159%2F000105160

21 January 2018

Identifiers

10.1159/000105160

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/17622782

1 reference

Europe PubMed Central

8 February 2018

http://europepmc.org/abstract/MED/17622782

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