(Q27315546)

26 June 2017

title

"Is It Worth Knowing?" Focus Group Participants' Perceived Utility of Genomic Preconception Carrier Screening (English)

1 reference

26 June 2017

4

Benjamin Wilfond

1 reference

26 June 2017

11

Carmit McMullen

1 reference

26 June 2017

Jennifer L Schneider

1

1 reference

26 June 2017

Katrina A B Goddard

2

1 reference

26 June 2017

James Davis

3

1 reference

26 June 2017

Tia L Kauffman

5

1 reference

26 June 2017

Jacob A Reiss

6

1 reference

26 June 2017

Marian Gilmore

7

1 reference

26 June 2017

Patricia Himes

8

1 reference

26 June 2017

Frances L Lynch

9

1 reference

26 June 2017

Michael C Leo

10

1 reference

26 June 2017

language of work or name

English

0 references

publication date

21 June 2015

1 reference

Journal of Genetic Counseling

26 June 2017

published in

1 reference

26 June 2017

volume

25

1 reference

26 June 2017

issue

1

1 reference

26 June 2017

page(s)

135-145

1 reference

Screening and prevention in Tay-Sachs disease: origins, update, and impact

26 June 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4726717

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4726717

It's complicated: criteria for policy decisions for the clinical integration of genome-scale sequencing for reproductive decision making

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4726717

Preferences for return of incidental findings from genome sequencing among women diagnosed with breast cancer at a young age.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4726717

Societal preferences for the return of incidental findings from clinical genomic sequencing: a discrete-choice experiment

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4726717

Diagnostic clinical genome and exome sequencing

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4726717

Population-based carrier screening for cystic fibrosis: a systematic review of 23 years of research.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4726717

Growing up in the genomic era: implications of whole-genome sequencing for children, families, and pediatric practice

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4726717

Return of incidental findings in genomic medicine: measuring what patients value--development of an instrument to measure preferences for information from next-generation testing (IMPRINT).

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4726717

ACMG position statement on prenatal/preconception expanded carrier screening

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4726717

An empirical estimate of carrier frequencies for 400+ causal Mendelian variants: results from an ethnically diverse clinical sample of 23,453 individuals

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4726717

Public preferences regarding the return of individual genetic research results: findings from a qualitative focus group study

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4726717

ACOG Committee Opinion No. 486: Update on carrier screening for cystic fibrosis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4726717

Preconceptional genetic carrier testing and the commercial offer directly-to-consumers

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4726717

Carrier testing for severe childhood recessive diseases by next-generation sequencing

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4726717

Ethical considerations in choosing a model for population‐based cystic fibrosis carrier screening

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4726717

Carrier screening for beta-thalassaemia: a review of international practice

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4726717

Debating clinical utility

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4726717

ACOG Committee Opinion No. 442: Preconception and prenatal carrier screening for genetic diseases in individuals of Eastern European Jewish descent

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4726717

Women's motives for not participating in preconception counseling: qualitative study.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4726717

Disclosing individual genetic results to research participants

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4726717

Screening for thalassemia: a model of success.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4726717

Prevalence and patterns of presentation of genetic disorders in a pediatric emergency department

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4726717

Birth weight-specific infant mortality due to congenital anomalies, 1960 and 1980.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4726717

The effect of Mendelian disease on human health: a measurement.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4726717

Categorizing genetic tests to identify their ethical, legal, and social implications

31 May 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10897-015-9851-7

Laboratory standards and guidelines for population-based cystic fibrosis carrier screening

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10897-015-9851-7

The quest for the perfect baby: why do Israeli women seek prenatal genetic testing?

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4726717

"It's something I need to consider": decisions about carrier screening for fragile X syndrome in a population of non-pregnant women

28 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26093606

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A model for offering carrier screening for fragile X syndrome to nonpregnant women: results from a pilot study

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26093606

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

"It's about having the choice": stakeholder perceptions of population-based genetic carrier screening for fragile X syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26093606

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S10897-015-9851-7

1 reference

OpenCitations bibliographic resource ID

26 June 2017

4845028

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

4845028

1 reference