The relationship between obsessive-compulsive symptoms and PARKIN genotype: The CORE-PD study (Q35054613)

6 August 2017

title

The relationship between obsessive-compulsive symptoms and PARKIN genotype: The CORE-PD study (English)

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6 August 2017

15

Stanley Fahn

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8

Elan D Louis

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John Nutt

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Joseph H Friedman

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Caroline Tanner

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1

Madeleine E Sharp

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31

Roy N Alcalay

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11

Susan Bressman

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3

Helen Mejia-Santana

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Martha Orbe Reilly

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Karen S Marder

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Lucien Cote

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Lorraine N Clark

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9

Cynthia Comella

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12

William K Scott

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Elise Caccappolo

2

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Ming-X Tang

4

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Llency Rosado

5

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Diana Ruiz

7

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Martha Nance

10

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Cheryl Waters

14

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Blair Ford

17

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Michael Rezak

18

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Kevin Novak

19

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Ronald Pfeiffer

21

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Haydeh Payami

22

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Eric Molho

23

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Stuart A Factor

24

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Carmen Serrano

26

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Maritza Arroyo

27

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Michael W Pauciulo

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6 August 2017

William C Nichols

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6 August 2017

language of work or name

English

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publication date

12 November 2014

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6 August 2017

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6 August 2017

volume

30

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6 August 2017

issue

2

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6 August 2017

page(s)

278-283

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Global resting-state functional magnetic resonance imaging analysis identifies frontal cortex, striatal, and cerebellar dysconnectivity in obsessive-compulsive disorder.

6 August 2017

cites work

1 reference

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Cognitive and motor function in long-duration PARKIN-associated Parkinson disease

8 July 2018

1 reference

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Repeated cortico-striatal stimulation generates persistent OCD-like behavior

8 July 2018

1 reference

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Parkin disease: a clinicopathologic entity?

8 July 2018

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Genome-wide association study of obsessive-compulsive disorder.

8 July 2018

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The relation between depression and parkin genotype: the CORE-PD study

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4318772

Olfaction in Parkin heterozygotes and compound heterozygotes: the CORE-PD study.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4318772

Predictors of parkin mutations in early-onset Parkinson disease: the consortium on risk for early-onset Parkinson disease study

8 July 2018

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Self-report of cognitive impairment and mini-mental state examination performance in PRKN, LRRK2, and GBA carriers with early onset Parkinson's disease

8 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4318772

Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutations

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4318772

Obsessive and compulsive symptoms in prediagnosed Huntington's disease

8 July 2018

2 references

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8 July 2018

A multidisciplinary study of patients with early-onset PD with and without parkin mutations

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4318772

An item response theory analysis of DSM-IV personality disorder criteria across younger and older age groups

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4318772

How much phenotypic variation can be attributed to parkin genotype?

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4318772

Positron emission tomographic analysis of the nigrostriatal dopaminergic system in familial parkinsonism associated with mutations in the parkin gene

8 July 2018

1 reference

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Toward a neurobiology of obsessive-compulsive disorder

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4318772

Nonmotor symptoms in Parkin gene-related parkinsonism.

8 July 2018

1 reference

The striatal dopaminergic deficit is dependent on the number of mutant alleles in a family with mutations in the parkin gene: evidence for enzymatic parkin function in humans

21 January 2018

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Construction and validation of a Parkinson's disease mutation genotyping array for the Parkin gene

21 January 2018

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Case-control study of the parkin gene in early-onset Parkinson disease

21 January 2018

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Motor reorganization in asymptomatic carriers of a single mutant Parkin allele: a human model for presymptomatic parkinsonism

21 January 2018

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Morphometric fingerprint of asymptomatic Parkin and PINK1 mutation carriers in the basal ganglia.

21 January 2018

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Parkin and PINK1 parkinsonism may represent nigral mitochondrial cytopathies distinct from Lewy body Parkinson's disease

21 January 2018

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Parkinson's disease with Lewy bodies associated with a heterozygous PARKIN dosage mutation

21 January 2018

1 reference

Parkin disease: a phenotypic study of a large case series

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4318772

Clinical analysis of 17 patients in 12 Japanese families with autosomal-recessive type juvenile parkinsonism.

25 October 2018

1 reference

12 December 2020

Development and validation of the Schedule of Compulsions, Obsessions, and Pathological Impulses (SCOPI)

1 reference

12 December 2020

Reliability and validity of the Beck depression inventory in patients with Parkinson's disease

1 reference

12 December 2020

Lewy body pathology and typical Parkinson disease in a patient with a heterozygous (R275W) mutation in the Parkin gene (PARK2)

1 reference

12 December 2020

Identifiers

DOI

10.1002/MDS.26065

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6 August 2017

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6 August 2017

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