(Q33678811)

English

Psychological distress in applicants for predictive DNA testing for autosomal dominant, heritable, late onset disorders. The Rotterdam/Leiden Genetics Workgroup.

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scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9152835%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

Psychological distress in applicants for predictive DNA testing for autosomal dominant, heritable, late onset disorders. The Rotterdam/Leiden Genetics Workgroup (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9152835%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

2

1 reference

Europe PubMed Central

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3 November 2019

author name string

A C DudokdeWit

1

1 reference

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3 November 2019

H J Duivenvoorden

3

1 reference

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3 November 2019

P G Frets

4

1 reference

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3 November 2019

M W Zoeteweij

5

1 reference

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3 November 2019

M Losekoot

6

1 reference

Europe PubMed Central

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3 November 2019

A van Haeringen

7

1 reference

Europe PubMed Central

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3 November 2019

M F Niermeijer

8

1 reference

Europe PubMed Central

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3 November 2019

J Passchier

9

1 reference

Europe PubMed Central

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3 November 2019

language of work or name

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publication date

1 May 1997

1 reference

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3 November 2019

Journal of Medical Genetics

1 reference

Europe PubMed Central

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3 November 2019

34

1 reference

Europe PubMed Central

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3 November 2019

5

1 reference

Europe PubMed Central

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3 November 2019

382-390

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9152835%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

Preparing for presymptomatic DNA testing for early onset Alzheimer's disease/cerebral haemorrhage and hereditary Pick disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050945

21 June 2018

Genetic linkage analysis in familial breast and ovarian cancer: results from 214 families. The Breast Cancer Linkage Consortium

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050945

21 June 2018

On attitudes and appreciation 6 months after predictive DNA testing for Huntington disease in the Dutch program

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050945

21 June 2018

Presymptomatic DNA-testing for Huntington disease: pretest attitudes and expectations of applicants and their partners in the Dutch program

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050945

21 June 2018

Presymptomatic DNA testing for Huntington disease: identifying the need for psychological intervention

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050945

21 June 2018

The illusion of mental health

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050945

21 June 2018

Dynamic mutation in Dutch Huntington's disease patients: increased paternal repeat instability extending to within the normal size range

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050945

21 June 2018

Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050945

21 June 2018

Predictive testing for Huntington disease: nonparticipants compared with participants in the Dutch program.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050945

21 June 2018

Risks of cancer in BRCA1-mutation carriers. Breast Cancer Linkage Consortium

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050945

21 June 2018

Borderline repeat expansion in Huntington's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050945

21 June 2018

Breast and ovarian cancer incidence in BRCA1-mutation carriers. Breast Cancer Linkage Consortium.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050945

21 June 2018

Seven new mutations in hMSH2, an HNPCC gene, identified by denaturing gradient-gel electrophoresis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050945

21 June 2018

A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050945

21 June 2018

Uptake of presymptomatic predictive testing for Huntington's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050945

21 June 2018

Predictive testing for Huntington's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050945

21 June 2018

Predictive testing for Huntington disease: II. Demographic characteristics, life-style patterns, attitudes, and psychosocial assessments of the first fifty-one test candidates

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050945

21 June 2018

Partners of Huntington patients: implications of the disease and opinions about predictive testing and prenatal diagnosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050945

21 June 2018

Age at onset in Huntington's disease: effect of line of inheritance and patient's sex.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050945

21 June 2018

DNA diagnosis for hereditary cerebral hemorrhage with amyloidosis (Dutch type)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050945

21 June 2018

Understanding the decision to take the predictive test for Huntington disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050945

21 June 2018

Identification of FAP locus genes from chromosome 5q21

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050945

21 June 2018

Identification and characterization of the familial adenomatous polyposis coli gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050945

21 June 2018

One hundred requests for predictive testing for Huntington's disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050945

21 June 2018

Predictive testing for Huntington disease in Canada: adverse effects and unexpected results in those receiving a decreased risk

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050945

21 June 2018

Predictive testing for Huntington disease in Canada: the experience of those receiving an increased risk

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050945

21 June 2018

The psychological consequences of predictive testing for Huntington's disease. Canadian Collaborative Study of Predictive Testing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050945

21 June 2018

Understanding the low uptake of presymptomatic DNA testing for Huntington's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050945

21 June 2018

Eight novel inactivating germ line mutations at the APC gene identified by denaturing gradient gel electrophoresis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050945

21 June 2018

Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050945

21 June 2018

Ethical issues in genetic testing for Huntington's disease: lessons for the study of familial cancers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050945

21 June 2018

Intrusive and Repetitive Thoughts After Experimental Stress

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050945

21 June 2018

Impact of Event Scale: A Measure of Subjective Stress

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050945

21 June 2018

Three-year follow-up after presymptomatic testing for Huntington's disease in tested individuals and partners

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050945

30 October 2018

Reluctance to undergo predictive testing: the case of Huntington disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050945

30 October 2018

Forgotten person in the Huntington disease family

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050945

30 October 2018

Chromosome 14-encoded Alzheimer's disease: genetic and clinicopathological description.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050945

30 October 2018

Rapid detection of translation-terminating mutations at the adenomatous polyposis coli (APC) gene by direct protein truncation test.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050945

30 October 2018

Self-selection in predictive testing for Huntington's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050945

30 October 2018

Exploration of the effects of predictive testing for Huntington disease on intimate relationships

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050945

30 October 2018

Signs and symptoms of posttraumatic stress disorder.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050945

30 October 2018

Familial Alzheimer's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/9152835

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Age at diagnosis as an indicator of eligibility for BRCA1 DNA testing in familial breast cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/9152835

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic testing in breast/ovarian cancer (BRCA1) families

1 reference

https://pubmed.ncbi.nlm.nih.gov/9152835

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rapid detection of BRCA1 mutations by the protein truncation test

1 reference

https://pubmed.ncbi.nlm.nih.gov/9152835

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

White matter lesions and cognitive deterioration in presymptomatic carriers of the amyloid precursor protein gene codon 693 mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/9152835

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

BRCA1 testing in families with hereditary breast-ovarian cancer. A prospective study of patient decision making and outcomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/9152835

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations and polymorphisms in the familial early-onset breast cancer (BRCA1) gene. Breast Cancer Information Core

1 reference

https://pubmed.ncbi.nlm.nih.gov/9152835

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Impact of Event Scale: a cross-validation study and some empirical evidence supporting a conceptual model of stress response syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/9152835

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Validation of the Impact of Event Scale for psychological sequelae of combat

1 reference

https://pubmed.ncbi.nlm.nih.gov/9152835

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary cerebral hemorrhage with amyloidosis--Dutch type. Research-Group Hereditary Cerebral Amyloid-Angiopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/9152835

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.34.5.382

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9152835%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

release_wqaboemagbd2lasl4fysycmkba

1 reference

https://api.fatcat.wiki/v0/release/wqaboemagbd2lasl4fysycmkba

24 November 2022

based on heuristic

mapped directly with Wikidata item

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9152835%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9152835%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

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