(Q35850713)

10 August 2017

Age-specific penetrance of LRRK2 G2019S in the Michael J. Fox Ashkenazi Jewish LRRK2 Consortium (English)

1 reference

10 August 2017

8

Anat Mirelman

1 reference

10 August 2017

Rachel Saunders-Pullman

series ordinal

9

object named as

Rachel Saunders-Pullman

1 reference

10 August 2017

13

Nir Giladi

1 reference

10 August 2017

12

Avi Orr-Urtreger

1 reference

10 August 2017

3

Roy N Alcalay

1 reference

10 August 2017

11

Laurie Ozelius

1 reference

10 August 2017

7

Deborah Raymond

1 reference

10 August 2017

4

Helen Mejia-Santana

1 reference

10 August 2017

1

Karen Marder

1 reference

LRRK2 Ashkenazi Jewish Consortium

10 August 2017

series ordinal

15

object named as

LRRK2 Ashkenazi Jewish Consortium

1 reference

10 August 2017

2

Yuanjia Wang

1 reference

10 August 2017

10

Lorraine Clark

1 reference

10 August 2017

14

Susan Bressman

1 reference

10 August 2017

5

Ming-Xin Tang

1 reference

10 August 2017

Annie Lee

6

1 reference

10 August 2017

language of work or name

English

0 references

publication date

10 June 2015

1 reference

10 August 2017

1 reference

10 August 2017

85

1 reference

10 August 2017

1

1 reference

10 August 2017

89-95

1 reference

Efficient Estimation of Nonparametric Genetic Risk Function with Censored Data

10 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4501942

Nonmotor symptoms in healthy Ashkenazi Jewish carriers of the G2019S mutation in the LRRK2 gene

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4501942

Olfactory identification in LRRK2 G2019S mutation carriers: a relevant marker?

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4501942

Neuropsychological performance in LRRK2 G2019S carriers with Parkinson's disease

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4501942

Interest in genetic testing in Ashkenazi Jewish Parkinson's disease patients and their unaffected relatives

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4501942

LRRK2 parkinsonism in Tunisia and Norway: a comparative analysis of disease penetrance.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4501942

LRRK2 mutations in Parkinson's disease: confirmation of a gender effect in the Italian population

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4501942

The complexities of hormonal influences and risk of Parkinson's disease

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4501942

Parkinson disease phenotype in Ashkenazi Jews with and without LRRK2 G2019S mutations

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4501942

Age-specific Parkinson disease risk in GBA mutation carriers: information for genetic counseling

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4501942

Risk factors for Parkinson's disease may differ in men and women: an exploratory study

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4501942

Gender differences in the risk of familial parkinsonism: beyond LRRK2?

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4501942

Frequency of known mutations in early-onset Parkinson disease: implication for genetic counseling: the consortium on risk for early onset Parkinson disease study

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4501942

Nonmotor symptoms in genetic Parkinson disease

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4501942

LRRK2 Gly2019Ser penetrance in Arab-Berber patients from Tunisia: a case-control genetic study

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4501942

Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4501942

Risk of Parkinson disease in carriers of parkin mutations: estimation using the kin-cohort method

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4501942

The LRRK2 G2019S mutation in Ashkenazi Jews with Parkinson disease: is there a gender effect?

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4501942

Mutations in the glucocerebrosidase gene are associated with early-onset Parkinson disease

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4501942

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4501942

Are men at greater risk for Parkinson's disease than women?

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4501942

Accuracy of family history data on Parkinson's disease

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4501942

The risk of cancer associated with specific mutations of BRCA1 and BRCA2 among Ashkenazi Jews

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4501942

What features improve the accuracy of clinical diagnosis in Parkinson's disease: A clinicopathologic study

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4501942

Comparative study of Parkinson's disease and leucine-rich repeat kinase 2 p.G2019S parkinsonism

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4501942

Kin-cohort analysis of LRRK2-G2019S penetrance in Parkinson's disease.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4501942

Frequency of LRRK2 mutations in early- and late-onset Parkinson disease.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4501942

LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4501942

LRRK2 G2019S mutation and Parkinson's disease: a clinical, neuropsychological and neuropsychiatric study in a large Italian sample

24 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26062626

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The Kin-Cohort Study for Estimating Penetrance

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26062626

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1212/WNL.0000000000001708

1 reference

10 August 2017

1 reference

10 August 2017

PubMed publication ID

26062626

1 reference