Evidence map›Paper›PMID 22709328›Full record

ArticleFamilies, systems & health : the journal of collaborative family healthcare2012

"My funky genetics": BRCA1/2 mutation carriers' understanding of genetic inheritance and reproductive merger in the context of new reprogenetic technologies.

Allison Werner-Lin, Lisa R Rubin, Maya Doyle, Rikki Stern, Katie Savin, Karen Hurley, Michal Sagi

Abstract read
In one paragraph

Article in Families, systems & health : the journal of collaborative family healthcare, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.7field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 32 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Allison Werner-LinSilver School of Social Work, New York University, New York, NY 10003, USA. awernerlin@nyu.edu
Lisa R Rubin
Maya Doyle
Rikki Stern
Katie Savin
Karen Hurley
Michal Sagi
New York University · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Psychosocial Palliative & Community Research in CancerT32CA009461 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI JENNIFER L HAY, Jamie S. Ostroff · 1985 to 2026
$10.1M
MULTIPLE RISKS, DECISIONS & BEHAVIORS IN THE GENOMIC ERAK07CA109236 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI HURLEY, KAREN E · 2006 to 2010
$672k
Attitudes Regarding Prenatal and Preimplantation Genetic Diagnosis For Inherited R03HG004528 · NHGRI · NEW SCHOOL UNIVERSITY · PI RUBIN, LISA ROBYN · 2008 to 2009
$152k
NCI NIH HHS K07 CA109236NCI NIH HHS P30 CA008748NCI NIH HHS T32 CA009461NCI NIH HHS T32 CA009461-22NHGRI NIH HHS R03 HG0004528NHGRI NIH HHS R03 HG004528
6 · The paper itself

Abstract

Deleterious mutations in the BRCA1/BRCA2 genes elevate lifetime risk of breast and ovarian cancer. Each child of a mutation-positive parent has a 50% chance of inheriting it. Preimplantation genetic diagnosis (PGD) permits prospective parents to avoid the birth of a BRCA-mutation-positive child, introducing predictability into a process historically defined by chance. This investigation explored how BRCA1/2 mutation carriers understand genetic inheritance and consider a child's inheritance of a BRCA1/2 mutation, given the opportunities that exist to pursue PGD. Thirty-nine female and male BRCA1/2 mutation carriers of reproductive age were recruited from urban cancer and reproductive medical centers. Participants completed a standardized educational presentation on PGD and prenatal diagnosis, with pre- and posttest assessments. An interdisciplinary team of qualitative researchers analyzed data using grounded theory techniques. Participants expressed the belief that reproduction yields children with unique genetic strengths and challenges, including the BRCA1/2 mutation, family traits for which predictive tests do not exist, and hypothetical genetic risks. Participants expressed preference for biologically related children, yet stated their genetically "well" partner's lineage would be marred through reproductive merger, requiring the well partner to assume the burden of the BRCA1/2 mutation via their children. Participants expressed diverse views of genetically "well" partners' participation in family planning and risk management decisions. Pressure to use reprogenetic technology may grow as genetic susceptibility testing becomes more widely available. Work with individuals and couples across the disease spectrum must be attuned to the ways beliefs about genetic inheritance play into reproductive decision-making.

Indexed as

Genes, BRCA1Genes, BRCA2Breast NeoplasmsFemaleGenetic Predisposition to DiseaseGenetic TestingHumansInfectious Disease Transmission, VerticalMaleNew York CityOvarian NeoplasmsPolymorphism, GeneticPregnancyPregnancy Complications, NeoplasticPreimplantation DiagnosisReproductive Techniques

Identifiers

PMID22709328
PMCPMC4229842
OpenAlexW2053264391

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.