Journal of Genetic Counseling - 2020

166 articles | Last updated: 2025-12-03 14:12:57
Caucasian
2
White
17
European
4
Other
22
Article Title Cauc. White Euro. Other Phrases Used
T A T A T A T A
DNA testing information on YouTube: Inadequate advice can mislead and harm the public
Pondering the future of genetic counseling: An adolescent field comes of age
Considerations in genetic counseling of transgender patients: Cultural competencies and altered disease risk profiles
GeneLiFT: A novel test to facilitate rapid screening of genetic literacy in a diverse population undergoing genetic testing
Exome sequencing study in a clinical research setting finds general acceptance of study returning secondary genomic findings with little decisional conflict
A survey of aortic disease biorepository participants’ preferences for return of research genetic results
Outcomes of genetic test disclosure and genetic counseling in a large Parkinson's disease research study
Content analysis of Journal of Genetic Counseling research articles: A multi‐year perspective
In Memoriam
Talking to policy makers about genetic counseling: A personal reflection
A review and definition of ‘usual care’ in genetic counseling trials to standardize use in research
Transition to telephone genetic counseling services during the COVID‐19 pandemic
Issue Information
Communication about positive <i>BRCA1</i> and <i>BRCA2</i> genetic test results and uptake of testing in relatives in a diverse Asian setting Chinese; Indian; Malay; Asian; Western societies; diverse Asian setting
Rapid acute care genomics: Challenges and opportunities for genetic counselors
Process evaluation of a culturally targeted video for Latinas at risk of hereditary breast and ovarian cancer
Chatbots &amp; artificial intelligence to scale genetic information delivery
Attitudes toward population screening among people living with fragile X syndrome in the UK: ‘I wouldn’t wish him away, I’d just wish his fragile X syndrome away’
Family communication of genetic test results among women with inherited breast cancer genes non-Hispanic whites (89%)
A Delphi study to prioritize genetic counseling outcomes: What matters most
Cancer genetic counseling for childhood cancer predisposition is associated with improved levels of knowledge and high satisfaction in parents
Preparing the genetic counseling workforce for the future in Australasia
State of recent literature on communication about cancer genetic testing among Latinx populations racial and ethnic minority populations; Latinx; sub-ethnicities
The impact of a cascade testing video on recipients’ knowledge, cognitive message processing, and affective reactions: A formative evaluation
Preferences of Italian patients for return of secondary findings from clinical genome/exome sequencing
Beyond the disease itself: A cross‐cutting educational initiative for patients and families with rare diseases
Professional regulation for Australasian genetic counselors
A systematic review and meta‐analysis of telephone vs in‐person genetic counseling in <i>BRCA1</i>/<i>BRCA2</i> genetic testing
The Canadian genetic counseling workforce: Perspectives from employers and recent graduates
Assessing clinical education tools for expanded carrier screening
Rapid genome‐wide sequencing in a neonatal intensive care unit: A retrospective qualitative exploration of parental experiences
Knowledge and attitudes about genetic counseling in patients at a major hospital in Addis Ababa, Ethiopia
A narrative literature review: Growing the workforce through increased fieldwork capacity in genetic counseling training programs
Breast cancer polygenic risk scores in the clinical cancer genetic counseling setting: Current practices and impact on patient management non-European ancestry
Family genetic result communication in rare and undiagnosed disease communities: Understanding the practice
Evaluating co‐created patient‐facing materials to increase understanding of genetic test results
The impact of genetic counseling on women's grief and coping following termination of pregnancy for fetal anomaly
Parental attitudes regarding the need for genetic services in a pediatric brain tumor survivorship program
Perceptions of provider’s epistemic authority in response to variant of uncertain significance‐related recommendations
Predictive testing for neurodegenerative diseases in the age of next‐generation sequencing
Impact of variant reclassification in the clinical setting of cardiovascular genetics
Characterizing standardized patients and genetic counseling graduate education
<i>BRCA1/2</i> mutations and risk‐reducing bilateral salpingo‐oophorectomy among Latinas: The UPTAKE study
Perceived barriers to paternal expanded carrier screening following a positive maternal result: To screen or not to screen
Positive and negative professionalism experiences of genetic counseling students in the United States and Canada race/ethnicity
Issue Information
Implementing innovative service delivery models in genetic counseling: a qualitative analysis of facilitators and barriers
Geographical analysis of the distribution of certified genetic counselors in the United States
Pursuing genetic testing for children with autism spectrum disorders: What do parents think?
Adaptation and validation of the Genetic Counseling Outcome Scale for autism spectrum disorders and related conditions
Advancing the genetic counseling profession through research: Identification of priorities by the National Society of Genetic Counselors research task force
Exploring empathy in genetic counseling students and new genetic counselors
Genetic counseling for advanced paternal age: A survey of genetic counselors' current practice
Research participant understanding and engagement in an institutional, self‐consent biobank model
A pilot randomized trial of an educational intervention to increase genetic counseling and genetic testing among Latina breast cancer survivors
Preconception expanded carrier screening: Impact of information presented by text or video on genetic knowledge and attitudes
Comprehension and personal value of negative non‐diagnostic genetic panel testing
Informing models of cancer genetics care in the era of multigene panel testing with patient‐led recommendations
Fabry Disease practice resource: Focused revision
Genetic counseling service delivery models: A study of genetic counselors’ interests, needs, and barriers to implementation
Issue Information
Changes in genetic variant results over time in pediatric cardiomyopathy and electrophysiology
Direct‐to‐consumer genetic testing companies tell their customers to ‘see a genetic counselor'. How do genetic counselors feel about direct‐to‐consumer genetic testing?
Whether, when, and how to communicate genetic risk to minors: ‘I wanted more information but I think they were scared I couldn’t handle it’
Open communication of Duchenne muscular dystrophy facilitates disclosure process by parents to unaffected siblings
Genetic counseling student demographics: an empirical comparison of two cohorts
Parental experiences of uncertainty following an abnormal fetal anomaly scan: Insights using Han’s taxonomy of uncertainty
Genetic counseling following direct‐to consumer genetic testing: Consumer perspectives
Social media usage in family communication about genetic information: ‘I no longer speak with my sister but she needed to know’
A thematic analysis of health information technology use among cancer genetic counselors
40 years and beyond for the National Society of Genetic Counselors: Reflections on genetic counseling practice
Adult adoptees and their use of direct‐to‐consumer genetic testing: Searching for family, searching for health "verify race and ethnicity", "confirm their ethnicity and ancestry", "find out where ancestors came
Genetic Counseling for Neurofibromatosis 1, Neurofibromatosis 2, and Schwannomatosis—Practice Resource of the National Society of Genetic Counselors
Effects of monitoring versus blunting on the public’s preferences for information in a hypothetical cancer diagnosis scenario
The experience of Preimplantation Genetic Testing (PGT) among Muslim couples in Oman in the Middle East
Who we are, what we do, and how we add value: The role of the genetic counseling ‘philosophy of practice’ statement in a changing time
Genetic counselors’ perspectives on population‐based screening for <i>BRCA</i>‐related hereditary breast and ovarian cancer and Lynch syndrome
Male–female differences in quality of life and coping style in patients with Marfan syndrome and hereditary thoracic aortic diseases
Issue Information
Genetic counseling graduate training to address religion and spirituality in clinical practice: A qualitative exploration of programs in North America
Corrigendum
Experiences and lessons learned by genetic counselors in returning secondary genetic findings to patients
How do geneticists and prospective parents interpret and negotiate an uncertain prenatal genetic result? An analysis of clinical interactions
Impacts of genesurance considerations on genetic counselors' practice and attitudes
Feasibility, face validity, and sensitivity of a web‐based simulation tool for assessing genetic counseling communication
Use of telephone intake for family history taking at a cancer genetics service in Asia
Genetic testing costs and compliance with clinical best practices
Eliciting culturally and medically informative family health histories from Marshallese patients living in the United States
Understanding the personal and community impact of long QT syndrome: A perspective from Gitxsan women
Genetic Counseling Service Delivery Models in the United States: Assessment of changes in use from 2010 to 2017
Unanswered Questions: Hereditary breast and gynecological cancer risk assessment in transgender adolescents and young adults
Exploring experiences and expectations of prenatal health care and genetic counseling/testing in immigrant Latinas Latino, Latinas, Latin American
Diagnostic uncertainties, ethical tensions, and accounts of role responsibilities in genetic counseling communication
The incidence and carrier frequency of Tay‐Sachs disease in the French‐Canadian population of Quebec based on retrospective data from 24 years, 1992–2015 French-Canadian
A qualitative study of Latinx parents' experiences of clinical exome sequencing Latinx; non‐Latinx; ethnically, linguistically, and culturally diverse
A road map for the future: An exploration of attitudes, perceptions, and beliefs among African Americans to tailor health promotion of cancer‐related genetic counseling and testing
Understanding access to genomics in an ethnically diverse south Florida population: A comparison of demographics in odyssey and rapid whole genome sequencing programs Black; Latinx; ethnically diverse; underrepresented groups
Corrigendum
Financial barriers in a county genetics clinic: Problems and solutions minority status; underserved
Hinduism and reproductive decision‐making:<i>Karma</i>,<i>Samsara,</i>and the in‐between
Pre‐genetics clinic resource evaluation for adults with intellectual disability: The pre‐genetics clinic aid
Issue Information
Introduction: The state of minority and health disparities in research and practice in genetic counseling and genomic medicine
Enhancing inclusion of diverse populations in genomics: A competence framework white European ancestry; Pakistani population; ethnic minority
Perspectives from individuals with familial hypercholesterolemia on direct contact in cascade screening
Ethnic disparities in the frequency of cancer reported in family histories non-Hispanic White; Hispanic; Asian; Ashkenazi Jewish
Associations of sociodemographic and clinical factors with gastrointestinal cancer risk assessment appointment completion
Increasing diversity in the genetic counseling profession: Development of recruitment tools for African American undergraduate students
Efforts of diversity and inclusion, cultural competency, and equity in the genetic counseling profession: A snapshot and reflection
Genetic counseling education at the undergraduate level: An outreach initiative to promote professional recruitment and support workforce development
Ancestry‐specific hereditary cancer panel yields: Moving toward more personalized risk assessment European ancestry; African American, Asian, Hispanic, Ashkenazi Jewish, Middle Eastern
Assessing the availability and quality of Spanish‐language genetic resources for patients on the internet
Assessing the newborn screening education needs of families living in medically underserved areas
Summary report of the 2019 Diversity and Inclusion Task Force of the National Society of Genetic Counselors
The <i>CFTR</i> variant profile of Hispanic patients with cystic fibrosis: Impact on access to effective screening, diagnosis, and personalized medicine Hispanic; non-Hispanic white; Ecuadorian ancestry; Mexican ancestry; racial and ethnic disparities
Assessing transgender and gender non‐conforming pedigree nomenclature in current genetic counselors’ practice: The case for geometric inclusivity
Public perception of predictive cancer genetic testing and research in Oregon
Creation and utility of ‘Boston Minority Genetic Counselors’ "racial minorities", "social minority backgrounds", "social minority identities", "minority"
Recruiting diversity where it exists: The Alabama Genomic Health Initiative
Creation of the Minority Genetic Professionals Network to increase diversity in the genetics work force
Conscripted curriculum: The experiences of minority genetic counseling students racial and ethnic minorities (also: minority, non-minority, non-majority groups, cultural groups, ra
Comparing prenatal screening experiences of Icelandic women who received false‐positive and true‐negative first‐trimester combined screening results in Iceland in 2012–2016
Education on cancer risk assessment and genetic counseling to address cancer health disparities among racial/ethnic groups and rural populations: Implementing culturally tailored outreach through comm
Racial disparities in breast cancer hereditary risk assessment referrals Black non-Hispanic (BNH); White non-Hispanic (WNH)
Factors associated with parental knowledge of neurofibromatosis type 1 (NF1): Parental affected status and genetic counseling
Exploring the barriers preventing Indigenous Australians from accessing cancer genetic counseling
Patient perspectives on the diagnostic journey to a monogenic diabetes diagnosis: Barriers and facilitators
Psychological reactions to predictive genetic testing for Huntington’s disease: A qualitative study
Reflections on diversity, equity, and inclusion in genetic counseling education
A Systematized review of experiences of individuals in Arnett’s emerging adulthood stage who live with or are at‐risk for genetic conditions
Community education to enhance the more equitable use of precision medicine in Northern Manhattan Hispanic
Interpreters’ perceptions of culture bumps in genetic counseling Spanish; Polish
Racial and ethnic differences in genetic counseling experiences and outcomes in the United States: A systematic review
The importance of <i>personalismo</i>: Navigating obstacles in recruitment strategies for Spanish speakers in marginalized communities
Genetic counselor implicit bias and its effects on cognitive and affective exchanges in racially discordant simulations
Understanding genetic learning needs of people affected by rare disease
The gendered pay gap in genetic counseling
Social and cultural influences on genetic screening programme acceptability: A mixed‐methods study of the views of adults, carriers, and family members living with thalassemia in the UK
Psychological correlates of interest in genetic testing among Korean American adoptees and their parents
Family health history collected by virtual conversational agents: An empirical study to investigate the efficacy of this approach
It’s not wrong, it’s just different
Practices in synagogues regarding Jewish genetic disease education Ashkenazi Jews; Jews
Predictors of genetic beliefs toward cancer risk perceptions among adults in the United States: Implications for prevention or early detection African Americans; Non-White Hispanics; Non-Hispanic Asians; minority populations
Beyond circles and squares: A commentary on updating pedigree nomenclature to better represent patient diversity
Evaluating a genetic counseling narrative group session for people who have tested positive for the Huntington's disease expansion: An interpretative phenomenological analysis
Issue Highlights
2020 National Society of Genetic Counselors Presidential Address
A Heartfelt Thank You to the 2019 <i>Journal of Genetic Counseling</i> Reviewers
Issue Information
Impact of hereditary pancreatitis on patients and their families
Adult patients with undiagnosed conditions and their responses to unresolved uncertainty from exome sequencing
Ethical and professional challenges encountered by Japanese healthcare professionals who provide genetic counseling services
Factors that impact risk management decisions among women with pathogenic variants in moderate penetrance genes associated with hereditary breast cancer
Health knowledge of women with a fragile X premutation: Improving understanding with targeted educational material
Relationships of health information orientation and cancer history on preferences for consent and control over biospecimens in a biobank: A race‐stratified analysis European American; African American
Referencing <i>BRCA</i> in hereditary cancer risk discussions: In search of an anchor in a sea of uncertainty
Organizational readiness to implement population‐based screening and genetic service delivery for hereditary cancer prevention and control
Family storytelling about hereditary cancer: Framing shared understandings of risk
Focused revision: An addendum to a National Society of Genetic Counselors (NSGC) practice resource
Consanguineous marriage and its effect on reproductive behavior and uptake of prenatal screening
Facing the challenge of genetic counselors' need for rapid continuing education about genomic technologies
Exploring relatives’ perceptions of participation, ethics, and communication in a patient‐driven study for hereditary cancer variant reclassification
The big reveal: Family disclosure patterns of <i>BRCA</i> genetic test results among young Black women with invasive breast cancer
An exploration of genetic counseling information needs and information‐seeking behaviors
Communication of genetic information to at‐risk relatives during the multidisciplinary monitoring of vascular Ehlers–Danlos syndrome in a French referral clinic
Somatic mismatch repair testing in evaluation of Lynch syndrome: The gap between preferred and current practices