| DNA testing information on YouTube: Inadequate advice can mislead and harm the public |
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| Pondering the future of genetic counseling: An adolescent field comes of age |
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| Considerations in genetic counseling of transgender patients: Cultural competencies and altered disease risk profiles |
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| GeneLiFT: A novel test to facilitate rapid screening of genetic literacy in a diverse population undergoing genetic testing |
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✓ |
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| Exome sequencing study in a clinical research setting finds general acceptance of study returning secondary genomic findings with little decisional conflict |
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| A survey of aortic disease biorepository participants’ preferences for return of research genetic results |
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| Outcomes of genetic test disclosure and genetic counseling in a large Parkinson's disease research study |
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| Content analysis of Journal of Genetic Counseling research articles: A multi‐year perspective |
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| In Memoriam |
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| Talking to policy makers about genetic counseling: A personal reflection |
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| A review and definition of ‘usual care’ in genetic counseling trials to standardize use in research |
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| Transition to telephone genetic counseling services during the COVID‐19 pandemic |
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| Issue Information |
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| Communication about positive <i>BRCA1</i> and <i>BRCA2</i> genetic test results and uptake of testing in relatives in a diverse Asian setting |
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✓ |
✓ |
Chinese; Indian; Malay; Asian; Western societies; diverse Asian setting |
| Rapid acute care genomics: Challenges and opportunities for genetic counselors |
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| Process evaluation of a culturally targeted video for Latinas at risk of hereditary breast and ovarian cancer |
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| Chatbots & artificial intelligence to scale genetic information delivery |
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| 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’ |
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| Family communication of genetic test results among women with inherited breast cancer genes |
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✓ |
✓ |
non-Hispanic whites (89%) |
| A Delphi study to prioritize genetic counseling outcomes: What matters most |
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| Cancer genetic counseling for childhood cancer predisposition is associated with improved levels of knowledge and high satisfaction in parents |
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| Preparing the genetic counseling workforce for the future in Australasia |
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| State of recent literature on communication about cancer genetic testing among Latinx populations |
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✓ |
✓ |
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 |
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| Preferences of Italian patients for return of secondary findings from clinical genome/exome sequencing |
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| Beyond the disease itself: A cross‐cutting educational initiative for patients and families with rare diseases |
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| Professional regulation for Australasian genetic counselors |
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| A systematic review and meta‐analysis of telephone vs in‐person genetic counseling in <i>BRCA1</i>/<i>BRCA2</i> genetic testing |
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| The Canadian genetic counseling workforce: Perspectives from employers and recent graduates |
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| Assessing clinical education tools for expanded carrier screening |
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| Rapid genome‐wide sequencing in a neonatal intensive care unit: A retrospective qualitative exploration of parental experiences |
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| Knowledge and attitudes about genetic counseling in patients at a major hospital in Addis Ababa, Ethiopia |
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| A narrative literature review: Growing the workforce through increased fieldwork capacity in genetic counseling training programs |
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| Breast cancer polygenic risk scores in the clinical cancer genetic counseling setting: Current practices and impact on patient management |
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✓ |
|
|
non-European ancestry |
| Family genetic result communication in rare and undiagnosed disease communities: Understanding the practice |
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| Evaluating co‐created patient‐facing materials to increase understanding of genetic test results |
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| The impact of genetic counseling on women's grief and coping following termination of pregnancy for fetal anomaly |
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| Parental attitudes regarding the need for genetic services in a pediatric brain tumor survivorship program |
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| Perceptions of provider’s epistemic authority in response to variant of uncertain significance‐related recommendations |
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| Predictive testing for neurodegenerative diseases in the age of next‐generation sequencing |
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| Impact of variant reclassification in the clinical setting of cardiovascular genetics |
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| Characterizing standardized patients and genetic counseling graduate education |
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| <i>BRCA1/2</i> mutations and risk‐reducing bilateral salpingo‐oophorectomy among Latinas: The UPTAKE study |
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| Perceived barriers to paternal expanded carrier screening following a positive maternal result: To screen or not to screen |
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| Positive and negative professionalism experiences of genetic counseling students in the United States and Canada |
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|
✓ |
✓ |
race/ethnicity |
| Issue Information |
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| Implementing innovative service delivery models in genetic counseling: a qualitative analysis of facilitators and barriers |
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| Geographical analysis of the distribution of certified genetic counselors in the United States |
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| Pursuing genetic testing for children with autism spectrum disorders: What do parents think? |
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| Adaptation and validation of the Genetic Counseling Outcome Scale for autism spectrum disorders and related conditions |
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| Advancing the genetic counseling profession through research: Identification of priorities by the National Society of Genetic Counselors research task force |
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| Exploring empathy in genetic counseling students and new genetic counselors |
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| Genetic counseling for advanced paternal age: A survey of genetic counselors' current practice |
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| Research participant understanding and engagement in an institutional, self‐consent biobank model |
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✓ |
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| A pilot randomized trial of an educational intervention to increase genetic counseling and genetic testing among Latina breast cancer survivors |
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| Preconception expanded carrier screening: Impact of information presented by text or video on genetic knowledge and attitudes |
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| Comprehension and personal value of negative non‐diagnostic genetic panel testing |
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| Informing models of cancer genetics care in the era of multigene panel testing with patient‐led recommendations |
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✓ |
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| Fabry Disease practice resource: Focused revision |
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| Genetic counseling service delivery models: A study of genetic counselors’ interests, needs, and barriers to implementation |
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| Issue Information |
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| Changes in genetic variant results over time in pediatric cardiomyopathy and electrophysiology |
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| 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? |
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| 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’ |
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| Open communication of Duchenne muscular dystrophy facilitates disclosure process by parents to unaffected siblings |
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| Genetic counseling student demographics: an empirical comparison of two cohorts |
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✓ |
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✓ |
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| Parental experiences of uncertainty following an abnormal fetal anomaly scan: Insights using Han’s taxonomy of uncertainty |
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| Genetic counseling following direct‐to consumer genetic testing: Consumer perspectives |
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| Social media usage in family communication about genetic information: ‘I no longer speak with my sister but she needed to know’ |
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| A thematic analysis of health information technology use among cancer genetic counselors |
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| 40 years and beyond for the National Society of Genetic Counselors: Reflections on genetic counseling practice |
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| Adult adoptees and their use of direct‐to‐consumer genetic testing: Searching for family, searching for health |
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✓ |
✓ |
"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 |
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| Effects of monitoring versus blunting on the public’s preferences for information in a hypothetical cancer diagnosis scenario |
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| The experience of Preimplantation Genetic Testing (PGT) among Muslim couples in Oman in the Middle East |
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| 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 |
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| Genetic counselors’ perspectives on population‐based screening for <i>BRCA</i>‐related hereditary breast and ovarian cancer and Lynch syndrome |
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| Male–female differences in quality of life and coping style in patients with Marfan syndrome and hereditary thoracic aortic diseases |
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| Issue Information |
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| Genetic counseling graduate training to address religion and spirituality in clinical practice: A qualitative exploration of programs in North America |
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| Corrigendum |
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| Experiences and lessons learned by genetic counselors in returning secondary genetic findings to patients |
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| How do geneticists and prospective parents interpret and negotiate an uncertain prenatal genetic result? An analysis of clinical interactions |
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| Impacts of genesurance considerations on genetic counselors' practice and attitudes |
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| Feasibility, face validity, and sensitivity of a web‐based simulation tool for assessing genetic counseling communication |
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| Use of telephone intake for family history taking at a cancer genetics service in Asia |
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| Genetic testing costs and compliance with clinical best practices |
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| Eliciting culturally and medically informative family health histories from Marshallese patients living in the United States |
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| Understanding the personal and community impact of long QT syndrome: A perspective from Gitxsan women |
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| Genetic Counseling Service Delivery Models in the United States: Assessment of changes in use from 2010 to 2017 |
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| Unanswered Questions: Hereditary breast and gynecological cancer risk assessment in transgender adolescents and young adults |
|
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|
|
| 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 |
|
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|
|
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|
|
| 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 |
|
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|
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|
|
| 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 |
|
|
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|
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|
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| Pre‐genetics clinic resource evaluation for adults with intellectual disability: The pre‐genetics clinic aid |
|
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|
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| Issue Information |
|
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|
|
| Introduction: The state of minority and health disparities in research and practice in genetic counseling and genomic medicine |
|
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|
|
| 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 |
|
|
|
✓ |
|
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|
|
| Efforts of diversity and inclusion, cultural competency, and equity in the genetic counseling profession: A snapshot and reflection |
|
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|
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| Genetic counseling education at the undergraduate level: An outreach initiative to promote professional recruitment and support workforce development |
|
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|
|
| 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 |
|
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|
|
| Assessing the newborn screening education needs of families living in medically underserved areas |
|
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|
|
| Summary report of the 2019 Diversity and Inclusion Task Force of the National Society of Genetic Counselors |
|
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|
|
| 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 |
|
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| Public perception of predictive cancer genetic testing and research in Oregon |
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| Creation and utility of ‘Boston Minority Genetic Counselors’ |
|
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|
✓ |
✓ |
"racial minorities", "social minority backgrounds", "social minority identities", "minority" |
| Recruiting diversity where it exists: The Alabama Genomic Health Initiative |
|
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|
|
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|
|
| Creation of the Minority Genetic Professionals Network to increase diversity in the genetics work force |
|
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|
✓ |
|
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|
|
| Conscripted curriculum: The experiences of minority genetic counseling students |
|
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|
|
✓ |
✓ |
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 |
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| 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 |
|
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|
|
| 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 |
|
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|
|
| Exploring the barriers preventing Indigenous Australians from accessing cancer genetic counseling |
|
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| Patient perspectives on the diagnostic journey to a monogenic diabetes diagnosis: Barriers and facilitators |
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| Psychological reactions to predictive genetic testing for Huntington’s disease: A qualitative study |
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| Reflections on diversity, equity, and inclusion in genetic counseling education |
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|
| A Systematized review of experiences of individuals in Arnett’s emerging adulthood stage who live with or are at‐risk for genetic conditions |
|
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|
|
| Community education to enhance the more equitable use of precision medicine in Northern Manhattan |
|
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|
|
|
✓ |
✓ |
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 |
|
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|
✓ |
|
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|
|
| The importance of <i>personalismo</i>: Navigating obstacles in recruitment strategies for Spanish speakers in marginalized communities |
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|
|
| Genetic counselor implicit bias and its effects on cognitive and affective exchanges in racially discordant simulations |
|
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|
✓ |
|
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|
|
| Understanding genetic learning needs of people affected by rare disease |
|
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| The gendered pay gap in genetic counseling |
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| 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 |
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|
| Psychological correlates of interest in genetic testing among Korean American adoptees and their parents |
|
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| Family health history collected by virtual conversational agents: An empirical study to investigate the efficacy of this approach |
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| It’s not wrong, it’s just different |
|
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|
|
| Practices in synagogues regarding Jewish genetic disease education |
|
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|
|
|
✓ |
✓ |
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 |
|
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|
|
|
|
|
|
| Evaluating a genetic counseling narrative group session for people who have tested positive for the Huntington's disease expansion: An interpretative phenomenological analysis |
|
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|
|
| Issue Highlights |
|
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|
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|
|
| 2020 National Society of Genetic Counselors Presidential Address |
|
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|
|
| A Heartfelt Thank You to the 2019 <i>Journal of Genetic Counseling</i> Reviewers |
|
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|
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| Issue Information |
|
|
|
|
|
|
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|
|
| Impact of hereditary pancreatitis on patients and their families |
|
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|
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|
|
| Adult patients with undiagnosed conditions and their responses to unresolved uncertainty from exome sequencing |
|
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|
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|
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|
|
| Ethical and professional challenges encountered by Japanese healthcare professionals who provide genetic counseling services |
|
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|
|
| Factors that impact risk management decisions among women with pathogenic variants in moderate penetrance genes associated with hereditary breast cancer |
|
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|
|
| Health knowledge of women with a fragile X premutation: Improving understanding with targeted educational material |
|
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|
|
| 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 |
|
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|
|
| Family storytelling about hereditary cancer: Framing shared understandings of risk |
|
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|
|
| Focused revision: An addendum to a National Society of Genetic Counselors (NSGC) practice resource |
|
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|
|
| Consanguineous marriage and its effect on reproductive behavior and uptake of prenatal screening |
|
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| Facing the challenge of genetic counselors' need for rapid continuing education about genomic technologies |
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| Exploring relatives’ perceptions of participation, ethics, and communication in a patient‐driven study for hereditary cancer variant reclassification |
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| The big reveal: Family disclosure patterns of <i>BRCA</i> genetic test results among young Black women with invasive breast cancer |
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| An exploration of genetic counseling information needs and information‐seeking behaviors |
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| Communication of genetic information to at‐risk relatives during the multidisciplinary monitoring of vascular Ehlers–Danlos syndrome in a French referral clinic |
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| Somatic mismatch repair testing in evaluation of Lynch syndrome: The gap between preferred and current practices |
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