| Genetic counseling for early onset and familial dementia: Patient perspectives on exome sequencing |
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| Transgender patients’ perspectives on their cancer genetic counseling experiences |
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| Courtesy stigma of parents of children with Down syndrome: Adaptation process and transcendent stage |
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| Parenting a child with Down syndrome: A qualitative study of everyday practices in Danish families |
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| Utilization of genetic testing: Analysis of 4,499 prior authorization requests for molecular genetic tests at four US regional health plans |
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| Assessing genetic counselors’ graduate school education and training in congenital heart defects |
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| The role of emotional sensitivity to probability in the decision to choose genetic testing |
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| Issue Information |
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| A report of the AGCPD task force to evaluate associations between select admissions requirements, demographics, and performance on ABGC certification examination |
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| Building a foundation in self‐awareness: Genetic counseling students’ experiences with self‐care, reflection, and mindfulness |
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| Genetic counseling students' and recent graduates' attitudes toward psychiatric illness |
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| Medical knowledge and information needs among women with pathogenic variants in moderate‐risk genes for hereditary breast cancer attending genetic counseling at an academic hospital in Germany—A quali |
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| Influence of genetic counselor medical history on specialty and psychosocial practice in North America |
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| Misattributed parentage identified through diagnostic exome sequencing: Frequency of detection and reporting practices |
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| Characteristics associated with the perceived likelihood to become parents among young adults with sickle cell disease or sickle cell trait in the USA |
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| Issue Information |
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| Elicitation of children’s understanding of information in pediatric genetic counseling encounters: A discourse‐oriented perspective |
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| Assessing the acceptability, feasibility, and usefulness of a psychosocial screening tool to patients and clinicians in a clinical genetics service in Australia |
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| Clinical genetic counselor experience in the adoption of telehealth in the United States and Canada during the COVID‐19 pandemic |
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| Experiences of reproductive genetic counselors with abortion regulations in Ohio |
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| Assessing the relationship between patient preferences for recontact after <i>BRCA1</i> or <i>BRCA2</i> genetic testing and their monitoring coping style in a Norwegian sample |
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| The impact of Marfan syndrome on an Aboriginal Australian family: ‘I don’t like it as much as I don’t like cancer’ |
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| Experiences of United States genetic counseling supervisors regarding race/ethnicity in supervision: A qualitative investigation |
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| Research to reduce inequities in cancer risk services: Insights for remote genetic counseling in a pandemic and beyond |
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| Strength of the genetic counselor: patient relationship is associated with extent of increased empowerment in patients with arrhythmogenic cardiomyopathy |
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| Awareness of genetic counseling and genetic testing for hereditary gynecologic cancers among Korean healthcare providers: A survey |
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| Graduate training during the COVID‐19 pandemic: North American genetic counseling students' challenges, intolerance of uncertainty, and psychological well‐being |
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| Do research participants share genomic screening results with family members? |
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| Japanese women's reasons for accompaniment status to hereditary breast and ovarian cancer‐focused genetic counseling |
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Japanese / Japan |
| Genome sequencing among children with medical complexity: What constitutes value from parents’ perspective? |
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| Evaluating the experiences of individuals with personal health risks identified through expanded carrier screening |
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| Experiences of adolescents and their parents after receiving adolescents’ genomic screening results |
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| Assessing genetic counselor communication in response to virtual, asynchronous simulated video prompts |
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| Telehealth genetic services during the COVID‐19 Pandemic: Implementation and patient experiences across multiple specialties in Nebraska |
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| Telegenetics: The experience of an Indian center (Centre for Human Genetics) during the COVID‐19 pandemic |
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| Large‐scale group genetic counseling: Evaluation of a novel service delivery model in a Canadian hereditary cancer clinic |
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| Genetic counseling experiences at the University of Cape Town during COVID‐19 |
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| Adapting skills from genetic counseling to wearables technology research during the COVID‐19 pandemic: Poised for the pivot |
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lack of ethnic diversity |
| Incorporating genetic counseling into the evaluation of pediatric bone marrow failure |
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| Genetic counseling in the time of COVID‐19: The Philippine experience with telegenetics |
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| Management of amended variant classification laboratory reports by genetic counselors in the United States and Canada: An exploratory study |
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| Uptake of genetic counseling and multi‐gene panel testing among women in the Intermountain West with previous negative <i>BRCA1</i> and <i>BRCA2</i> results contacted for updated testing |
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| Standardized applications for genetic counseling graduate programs: Opinions of program directors |
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| Rethinking genetic counseling clinical skills training in the time of COVID‐19 |
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| Examining clinical training through a bicultural lens: Experiences of genetic counseling students who identify with a racial or ethnic minority group |
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| Genetic counseling for congenital heart disease – Practice resource of the National Society of Genetic Counselors |
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| Genetic counseling research and COVID‐19: A lesson in resiliency |
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| Analysis of the reported use of practice‐based competencies by North American genetic counselors during the COVID‐19 pandemic |
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| Differences in genetic counseling student responses to intense patient affect: A study of students in North American programs |
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race/ethnicity |
| Genetic counseling student rotations in industry: How COVID‐19 magnified the urgency for virtual learning options in diverse training settings |
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| Pregnant women's experiences of non‐invasive prenatal testing (NIPT) in Japan: A qualitative study |
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| Genetic counseling clinical documentation: Practice Resource of the National Society of Genetic Counselors |
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| Clinical utility and cost‐effectiveness analysis of chromosome testing concomitant with chromosomal microarray of patients with constitutional disorders in a U.S. academic medical center |
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| Issue Information |
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| Genetic counseling delivery, outcomes, training, and practice in response to COVID‐19: Introduction to the special issue |
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| Attitudes toward offering genetic counseling for psychiatric conditions among genetics healthcare practitioners in the United Kingdom: A qualitative study |
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| Genetic counselor roles in the undiagnosed diseases network research study: Clinical care, collaboration, and curation |
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| The experience of a sample of individuals in the United Kingdom living in the pre‐manifest stage of Huntington’s disease: An interpretative phenomenological analysis |
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| Following NCCN guidelines within one hospital system in the United States: Comparison between cancer centers and genetic counselor utilization |
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| ‘Steep learning curves’ to ‘Smooth Sailing’: A reappraisal of telegenetics amidst the COVID‐19 pandemic |
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| Telehealth for genetic counseling: A systematic evidence review |
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| Offering preimplantation genetic testing for monogenic disorders (PGT‐M) for conditions with reduced penetrance or variants of uncertain significance: Ethical insight from U.S. laboratory genetic coun |
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| Changes to the genetic counseling workforce as a result of the COVID‐19 pandemic |
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| Contributors to and consequences of burnout among clinical genetic counselors in the United States |
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| Barriers to family history knowledge and family communication among LGBTQ+ individuals in the context of hereditary cancer risk assessment |
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| Effects of participation in a U.S. trial of newborn genomic sequencing on parents at risk for depression |
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| Genetic counseling and screening of consanguineous couples and their offspring practice resource: Focused Revision |
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| Adapting to the challenges of the global pandemic on genetic counselor education: Evaluating students’ satisfaction with virtual clinical experiences |
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| Results of the Genetic Counselor SARS‐CoV‐2 Impact Survey from the National Society of Genetic Counselors: Progress and penalty during the COVID‐19 pandemic |
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| Commentary from a commercial laboratory: The unexpected benefits of a more virtual world during the COVID‐19 pandemic |
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| Genetic counseling, virtual visits, and equity in the era of COVID‐19 and beyond |
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| Spanish language concordance in genetic counseling sessions in the United States: Counselor experiences and perceptions of its effects on processes and outcomes |
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Latina, non‑Latina, Latinx, Spanish-speaking |
| Knowledge and perceptions of the genetic counseling profession among a national cross‐sectional sample of U.S. adults |
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| Ethical and moral perspectives of individuals who considered/used preimplantation (embryo) genetic testing |
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"Hispanic or non‑White"; "mostly White" |
| Genetic counseling practice for inherited eye diseases in an Israeli medical center during the COVID‐19 pandemic |
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| Adapting genetic counseling operations amidst the COVID‐19 pandemic |
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| A proposal to promote diversity in journal research article titles |
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| A qualitative assessment of parental experiences with false‐positive newborn screening for Krabbe disease |
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| Transitioning to telegenetics in the COVID‐19 era: Patient satisfaction with remote genetic counseling in adult neurology |
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| Genesurance counseling: Current training practices of genetic counseling graduate programs in the United States |
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| Genetic counselors and legal recognition: A made‐for‐Canada approach |
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| Young people’s experiences of a <i>CDH1</i> pathogenic variant: Decision‐making about gastric cancer risk management |
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| Outcomes from a pilot genetic counseling intervention using motivational interviewing and the extended parallel process model to increase cascade cholesterol screening |
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| Easing the burden of multi‐state genetic counseling licensure in the United States: Process, pitfalls, and possible solutions |
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| Exploring genetic counselors’ use of pedigree symbols to represent assisted reproductive technology |
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| Metaphors and why these are important in all aspects of genetic counseling |
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| The evolution of genetic counseling graduate education in New York City during the COVID‐19 pandemic: In the eye of the storm |
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| Further validation and psychometric properties of the Spanish adaptation of the Genetic Counseling Outcome Scale |
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| Value of whole‐genome sequencing to Australian cancer patients and their first‐degree relatives participating in a genomic sequencing study |
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| Caregivers of individuals with Rubinstein–Taybi syndrome: Perspectives, experiences, and relationships with medical professionals |
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| Genetic counselor experiences with telehealth before and after COVID‐19 |
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| Influence of payer coverage and out‐of‐pocket costs on ordering of NGS panel tests for hereditary cancer in diverse settings |
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| The Accreditation Council for Genetic Counseling’s response to COVID‐19 impact on genetic counseling programs |
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| The COVID‐19 pandemic and reproductive genetic counseling: Changes in access and service delivery at an academic medical center in the United States |
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| Interest in and uptake of genetic counseling for preconception carrier screening when offered to predominantly white reproductive‐age persons seeking gynecologic care at a single U.S. academic medical |
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| Reflections of parents of children with 22q11.2 Deletion Syndrome on the experience of receiving psychiatric genetic counseling: ‘Awareness to Act’ |
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| Gender imbalance in the genetic counseling profession: An Australasian perspective |
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| Trends in coverage and reimbursement for reproductive genetic counseling in New Jersey by multiple payers from 2010 to 2018 |
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| Polygenic risk in familial breast cancer: Changing the dynamics of communicating genetic risk |
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| After genomic testing results: <i>Parents’ long‐term views</i> |
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| Explanatory models for the cause of Fragile X Syndrome in rural Cameroon |
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| Interventions aiming to improve informed decision on prenatal screening and testing: A scoping review of the literature |
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| U.S. Genetic counselors’ perceptions of inpatient genetic counseling: A valuable model for medically complex patients |
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| Clinical application of a scale to assess genomic healthcare empowerment (GEmS): Process and illustrative case examples |
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| Issue Information |
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| Prenatal genetic counselors' perceptions of the impact of abortion legislation on counseling and access in the United States |
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| Sudden shift to remote genetic counseling during the COVID‐19 pandemic: Experiences of genetics professionals in Italy |
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| “Doctors can read about it, they can know about it, but they've never lived with it”: How parents use social media throughout the diagnostic odyssey |
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| The role of psychosocial factors in Black women's self‐efficacy in receiving genetic counseling and testing |
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Black |
| Utilization of breast cancer risk prediction models by cancer genetic counselors in clinical practice predominantly in the United States |
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| A systematic review of psycho‐social interventions for individuals with a <i>BRCA1/2</i> pathogenic variant |
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| Understanding and interpretation of a variant of uncertain significance (VUS) genetic test result by pediatric providers who do not specialize in genetics |
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| Awareness of genetic counseling services among allied healthcare professionals in South Africa |
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| Understanding patients' views and willingness toward the use of telehealth in a cancer genetics service in Asia |
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| Assessing sensitivity to change of the genomics outcome scale (GOS) |
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| Public perceived knowledge of, attitude toward, and use of genetic testing in urban China |
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| Physician awareness, preparedness, and opinions toward consumer‐initiated genetic testing in Thailand: Views from a changing landscape |
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| Opinions of adults affected with later‐onset lysosomal storage diseases regarding newborn screening: A qualitative study |
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| Understanding and perception of direct‐to‐consumer genetic testing in Hong Kong |
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| Genetic counselor use of self‐involving responses in a clinical setting: A qualitative investigation |
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| Family planning in carriers of <i>BRCA1</i> and <i>BRCA2</i> pathogenic variants |
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| Between responsibility and desire: Accounts of reproductive decisions from those at risk for or affected by late‐onset neurological diseases |
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| Pharmacogenomic education among genetic counseling training programs in North America |
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| Genetic counselors, patients', and carers’ views on an Australian clinical genetics service information system |
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| Value of a genetics clinic evaluation in identifying women at risk for hereditary breast‐ovarian cancer syndrome |
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| Preferences for and acceptability of receiving pharmacogenomic results by mail: A focus group study with a primarily African‐American cohort |
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African‐American |
| Universal access to genetic counseling for women with epithelial ovarian cancer in Nova Scotia: Evaluating a new collaborative care model |
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| Genetic discrimination views in online discussion forums: Perspectives from Canadian forumites |
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| Social support networks of adults with sickle cell disease |
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| How are uncertain prenatal genetic results perceived and managed two years after they were received? A qualitative interview study |
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| Conscience clauses in genetic counseling: Awareness and attitudes |
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| Issue Information |
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| Benefits and limitations of telegenetics: A literature review |
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| Under‐referral of Plain community members for genetic services despite being qualified for genetic evaluation |
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| The genetic counseling profession in Austria: Stakeholders’ perspectives |
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| Helping young children understand inherited cancer predisposition syndromes using bibliotherapy |
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| Education in youth‐friendly genetic counseling |
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| Examining career shadowing in genetic counseling: Perspectives of shadowees, program directors, and genetic counselors |
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| Pursuing germline genome sequencing to reduce illness uncertainty may involve additional uncertainties for cancer patients: A mixed‐methods study |
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| Men with an <i>FMR1</i> premutation and their health education needs |
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| Comparison of methodologies to detect hemoglobinopathy carriers in a multi‐ethnic sperm donor population |
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multi-ethnic; mixed ethnicity; multi‐ethnic sperm donor population |
| 6 feet apart but working together |
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| Genetic counseling for patients with positive genomic screening results: Considerations for when the genetic test comes first |
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| Exploring racial and ethnic minority individuals’ journey to becoming genetic counselors: Mapping paths to diversifying the genetic counseling profession |
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"racial/ethnic minority", "racially/ethnically diverse patient populations", "racial and ethnic mino |
| Germline evaluation of patients undergoing tumor genomic profiling: An academic cancer center’s experience with implementing a germline review protocol |
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| Financial constraints on genetic counseling and further risk‐management decisions among U.S. women at elevated breast cancer risk |
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| The current landscape of genetic test stewardship: A multi‐center prospective study |
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| Exploring parents’ perceptions of the value of pediatric genetic counseling patient letters: A qualitative study presenting lessons learned |
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| Prenatal Genetic Diagnosis of a Sex Chromosome Aneuploidy: Parent Experiences |
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| Evaluating parental genetic knowledge of hearing loss with and without pre‐test genetic counseling in a pediatric otolaryngology clinic |
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| Preparing genetic counselors to serve Native American communities |
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Native American, North America |
| COVID contingencies: Early epicenter experiences of different genetics clinics at a New York City institution inform emergency adaptation strategies |
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| Characterization of genetic counselor practices in inpatient care settings |
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| <i>CDH1</i> variants leading to gastric cancer risk management decision‐making experiences in emerging adults: ‘I am not ready yet’ |
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| Genetic counselors' experiences with transgender individuals in prenatal and preconception settings |
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| Genetic testing for pheochromocytoma and paraganglioma: <i>SDHx</i> carriers’ experiences |
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| Exploring how mothers of a child with a genetic disorder experience their couple relationship in a low socio‐economic setting |
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| Second World Congress on Genetic Counseling: An introduction to the special issue |
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| Issue Information |
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| A Heartfelt Thank You to the 2020 <i>Journal of Genetic Counseling</i> Reviewers |
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| 2021 National Society of Genetic Counselors Presidential Address: Seeking opportunities for growth and leading each other |
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| Genetic counselor approaches to <i>BRCA1/2</i> direct‐to‐consumer genetic testing results |
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Ashkenazi Jewish |
| Supporting a sense of inclusion and belonging for genetic counseling students who identify as racial or ethnic minorities |
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Black/African American; non-white; racial and ethnic minority; underrepresented minorities |
| Adaptation of the working alliance inventory for the assessment of the therapeutic alliance in genetic counseling |
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| ‘Do language and culture<i>really</i>matter?’: A trans‐disciplinary investigation of cultural diversity in genetic counseling in Hong Kong |
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| Pregnant Hispanic women's views and knowledge of prenatal genetic testing |
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| Mitochondrial replacement therapy: Genetic counselors' experiences, knowledge, and opinions |
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| Influence of lived experience on risk perception among women who received a breast cancer polygenic risk score: ‘Another piece of the pie’ |
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| A family systems approach to genetic counseling: Development of narrative interventions |
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| Risk assessment and genetic counseling for hereditary breast and ovarian cancer syndromes—Practice resource of the National Society of Genetic Counselors |
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| ‘LEADERS’: A culturally tailored approach to genetic counseling for minority populations |
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