| Elective genetic testing: Genetics professionals’ perspectives and practices |
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| Prognostic imagination: Genetic counseling amidst therapeutic innovation and evolving futures |
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| The experiences of families receiving a diagnosis of 22q11.2 deletion syndrome in Ireland |
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| Genetic counseling students' use of patient‐centered communication skills predicts standardized patient satisfaction during virtual simulated sessions |
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| Both sides now: Changing a <scp>long‐standing</scp> pedigree tradition of men on the left and women on the right |
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| Prenatal genetic counseling in states hostile to abortion in the final days of <i>Roe v. Wade</i>: A qualitative study |
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| Psychiatric genetic counseling: A survey of Australian genetic counselors' practice and attitudes |
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| Healthcare decision makers' perspectives on the creation of new genetic counselor positions in North America: Exploring the case for psychiatric genetic counseling |
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| Patient uptake of updated genetic testing following uninformative <scp><i>BRCA1</i></scp> and <scp><i>BRCA2</i></scp> results |
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| Patient‐reported outcomes associated with reflex <i><scp>BRCA1</scp>/2</i> tumor and subsequent germline panel genetic testing for high‐grade serous ovarian cancer |
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| Issue Information |
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| Exploring parental cystic fibrosis disclosure to well children |
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| North American genetic counselors' approach to collecting and using ancestry in clinical practice |
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Ashkenazi Jewish ancestry |
| <scp>BRCAShare</scp>—Assessment of an animated digital message for intrafamilial communication of pathogenic variant positive test results: A feasibility study |
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| Evaluating a communication aid for return of genetic results in families with hypertrophic cardiomyopathy: A randomized controlled trial |
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| Measuring quality and value in genetic counseling: The current landscape and future directions |
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| Clinical geneticists' views on and experiences with unsolicited findings in next‐generation sequencing: “A great technology creating new dilemmas” |
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| Implicit and explicit racial prejudice and stereotyping toward Black (vs. White) Americans: The prevalence and variation among genetic counselors in North America |
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| Introduction of the genetic counseling profession by teachers in <scp>BIPOC</scp>‐majority high schools |
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BIPOC; BIPOC‐identifying; Black, Indigenous, and people of color (BIPOC); white‐identifying |
| Latinx attitudes, barriers, and experiences with genetic counseling and testing: A systematic review |
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| Genetic testing and counseling for the unexplained epilepsies: An evidence‐based practice guideline of the National Society of Genetic Counselors |
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| Considerations for the use of qualitative methodologies in genetic counseling research |
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| How should we address the inevitable harms from non‐negligent variant reclassification in predictive genetic testing? |
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| Australian healthcare professionals' perspectives on the ethical and practical issues associated with genomic newborn screening |
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| Summary of the experiences, knowledge, medical management, and family communication of monoallelic <scp><i>MUTYH</i></scp> carriers |
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| A descriptive investigation of clinical practice models used by cardiovascular genetic counselors in North America |
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| Factors that influence genetic counselors' participation in research |
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| Noninvasive prenatal screening (<scp>NIPS</scp>) results for participants of the <scp>eXtraordinarY</scp> babies study: Screening, counseling, diagnosis, and discordance |
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| An investigation of preceptors' perceptions of behavioral elements of “professionalism” among genetic counseling students |
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| Issue Information |
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| Genetic counselors' response types to prenatal patient deferring or attributing religious/spiritual statements: An exploratory study of <scp>US</scp> genetic counselors |
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| Experiences of receiving an increased chance of sex chromosome aneuploidy result from non‐invasive prenatal testing in Australia: “A more complicated scenario than what I had ever realized” |
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| Effects of genetic counselor disabilities on their professional experiences: A qualitative investigation of North American counselors' perceptions |
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| The experiences of adolescent siblings of children with rare genetic conditions: “It's made me who I am” |
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| Perspectives on Spanish language concordant cancer genetic counseling sessions from the <scp>Spanish‐speaking</scp> population |
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| Implementation and outcome evaluations of a <scp>multi‐site</scp> improvement program in cancer genetics |
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| Practice resource‐focused revision: Standardized pedigree nomenclature update centered on sex and gender inclusivity: A practice resource of the National Society of Genetic Counselors |
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| The effects of an online decision aid to support the reproductive decision‐making process of genetically at risk couples—A pilot study |
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| An <scp>evidence‐based</scp> practice guideline of the National Society of Genetic Counselors for telehealth genetic counseling |
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| Experience with a nurse‐driven genetic counseling pathway of Italian women with uninformative <scp><i>BRCA</i></scp> test result |
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Italian women |
| Psychological characteristics of Japanese patients and their family members receiving genetic counseling: A single‐institute exploratory study |
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| Factors associated with pediatric genetic counselors' practices related to bullying screening |
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| Genetic variants with discordant classifications: An assessment of genetic counselor attitudes and practices |
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| Are genetic counselors prepared to counsel active‐duty service members? A survey of genetic counselors' self‐efficacy, counseling techniques, and knowledge of military policy |
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| Motivation and family communication in hereditary prostate cancer genetic testing: Survey of patients from a <scp>US</scp> tertiary medical center |
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| Issue Information |
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| The goldilocks conundrum: Disclosing discrimination risks in informed consent |
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| Attitudes towards and sociodemographic determinants of genetic test usage in the <scp>USA</scp>; data from the Health Information National Trend Survey, 2020 |
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| Newborn screening for Pompe disease: Parental experiences and follow‐up care for a late‐onset diagnosis |
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| Ethical implications of early genetic diagnosis in an infant with <scp>Lesch–Nyhan</scp> syndrome |
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| Motivational interviewing for genetic counseling: A unified framework for persuasive and equipoise conversations |
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| Examining the effect of patient personality types and coping styles on outcomes of genetic counseling |
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| Impact of <i>BRCA1/2</i> cascade testing on anxiety, depression, and cancer worry levels among unaffected relatives in a multiethnic Asian cohort |
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| Dilemmas when talking about Huntington's disease: A qualitative study of offspring and caregiver experiences in Norway |
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| Genetic counselors' experience with reimbursement and patient out‐of‐pocket cost for multi‐cancer gene panel testing for hereditary cancer syndromes |
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| Assessing the impact of pre‐test education on patient knowledge, perceptions, and expectations of pharmacogenomic testing to guide antidepressant use |
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| A qualitative study of unaffected <scp><i>ATM</i></scp> and <scp><i>CHEK2</i></scp> carriers: How participants make meaning of ‘moderate risk’ genetic results in a population breast cancer screening t |
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| Danish heritable retinoblastoma survivors' perspectives on reproductive choices: “It's important for me, not to pass on this condition” |
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| A comment on ‘<scp>COVID</scp>‐19 vaccine hesitancy and acceptance among pregnant people’ |
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| Lack of consensus among healthcare professionals at a large academic medical center on the use of exome sequencing for prenatal diagnosis |
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| The uptake and utility of genetic testing and genetic counseling for hypertrophic cardiomyopathy—A systematic review and meta‐analysis |
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| Women's thoughts on receiving and sharing genetic information: Considerations for genetic counseling |
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| Factors associated with <scp>US</scp> and Canadian genetic counselors' testing decisions during pregnancy |
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| <scp>Evaluating</scp> a general pediatric/adult genetic counseling clinic in a Midwest medical center |
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| A qualitative interview study of the attitudes toward reproductive options of people with genetic visual loss |
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| Characterization of variant reclassification and patient re‐contact in a cancer genetics clinic |
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non-White patients |
| Cascade testing for inherited cardiac conditions: Risk perception and screening after a negative genetic test result |
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| <scp>COVID</scp>‐19 vaccine hesitancy and acceptance among pregnant people contacting a teratogen information service |
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| Implementing genomics in the neonatal period: An assessment of parental decision making and anxiety |
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| Issue Information |
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| Genetic counseling and diagnostic genetic testing for familial amyotrophic lateral sclerosis and/or frontotemporal dementia: A qualitative study of client experiences |
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| Exploring a brief medical improvisational performing arts intervention for genetic counseling graduate students |
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| Use of a chatbot to increase uptake of cascade genetic testing |
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| Cross‐sectional clinical cancer genomics community of practice survey analysis of provider attitudes and beliefs regarding the use of deceased family member tissue to guide living family member geneti |
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| Integrating genetic assistants into the workforce: An 18‐year productivity analysis and development of a staff mix planning tool |
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| Assessing barriers to the career ladder and professional development for ethnic minority genetic counselors in the United States |
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| Genetics providers’ experiences using telehealth: A grounded theory approach |
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| Effects of diet education on empowerment for individuals who have an increased risk of developing breast or colon cancer: A pilot study |
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| Perceptions of motivational interviewing in genetic counseling practice and training |
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| Outcomes of psychiatric genetic counseling in relation to time since diagnosis and symptom onset |
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| Attitudes and training needs of oncologists and surgeons in mainstreaming breast cancer genetic counseling in a low‐to‐middle income Asian country |
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| Cardiology clinic patient attitudes toward and potential personal utility of genetic testing: Findings from a unique multiracial clinical sample |
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| Improving gender‐affirming care in genetic counseling: Using educational tools that amplify transgender and/or gender non‐binary community voices |
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| Investigating factors that influence genetic counselors’ decisions to refer patients to mental health providers |
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| Mental models about heredity among immigrant Latinx adults with limited education from Mexico and Central America |
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| Empathy experiences of Japanese certified genetic counselors: A qualitative investigation and proposed framework |
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"Western countries"; "non‐Western country"; "Japanese culture"; "Japanese certified genetic counselo |
| An internship in psychiatric genetic counseling: Impact on genetic counseling graduates' practice and career choices |
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| Prenatal genetic counseling practices regarding recommendations for cancer genetic counseling: A retrospective chart review from two academic institutions |
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| Exploring United States genetic counselor and healthcare interpreter perspectives: Allocation of roles within the genetic counseling encounter |
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| Examining the role of language competency in genetic testing awareness among adults in the United States |
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| Reasons affecting the uptake of reproductive genetic carrier screening among nonpregnant reproductive‐aged women in Flanders (Belgium) |
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| Issue Information |
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| COVID‐19 and the adaptive evolution of genetic counseling |
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| Retrospective comparison of parent‐reported genetics knowledge, empowerment, and familial uptake of cardiac screening between parents who received genetic counseling by a certified genetic counselor a |
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| National Society of Genetic Counselors' Board of Directors response to Myers et al. ‘A report of the AGCPD task force to evaluate associations between select admissions requirements, demographics, and |
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| Toward a better understanding of the experience of patients with moderate penetrance breast cancer gene pathogenic/likely pathogenic variants: A focus on <i>ATM</i> and <i>CHEK2</i> |
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| Patterns of germline and somatic testing after universal tumor screening for Lynch syndrome: A clinical practice survey of active members of the Collaborative Group of the Americas on Inherited Gastro |
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| Expanded carrier screening in the United States: A systematic evidence review exploring client and provider experiences |
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ancestry‐based screening |
| Exploring the role of Islam on the lived experience of patients with Long QT Syndrome in Saudi Arabia |
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| Genetic counseling certificate program: A program evaluation of undergraduate exposure to genetic counseling |
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| Leveraging electronic health records to inform genetic counseling practice surrounding psychiatric disorders |
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| Application of motivational interviewing strategies with the extended parallel process model to improve risk communication for parents of children with familial hypercholesterolemia |
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| Accreditation Council for Genetic Counseling Board of Directors Response to Myers et al ‘A report of the AGCPD task force to evaluate associations between select admissions requirements, demographics, |
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| Evaluation of barriers to referral for cancer predisposition syndromes in pediatric oncology patients in the United States |
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| Commentary from the Minority Genetic Professionals Network on the AGCPD Taskforce analysis of select criteria and performance on the ABGC certification examination by Myers et al. (2021) |
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| Revising the FOCUS framework through a qualitative study assessing self‐reported counseling skills of genetic counselors |
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| A Heartfelt Thank You to the 2021 <i>Journal of Genetic Counseling</i> Reviewers |
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| Views of Israeli healthcare professionals regarding communication of genetic variants of uncertain significance to patients |
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| Issue Information |
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| The long‐term impact of receiving incidental findings on parents undergoing genome‐wide sequencing |
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| Perception of genetic testing among patients with inherited retinal disease: Benefits and challenges in a Japanese population |
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| Challenges and opportunities in the establishment of a hereditary breast cancer clinic at an academic medical center in a low‐middle income country |
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| 2021 National Society of Genetic Counselors Presidential Address: The Dance of Genetic Counseling |
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| Diversity training experiences and factors associated with implicit racial bias among recent genetic counselor graduates of accredited programs in the United States and Canada |
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| Moral distress in genetic counseling: A study of North American genetic counselors |
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| Advocating for equitable management of hereditary cancer syndromes |
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| Cascade testing for inherited arrhythmia conditions: Experiences and attitudes of family communication approaches for a Canadian cohort |
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| Evolving approaches to prenatal genetic counseling for Spinal Muscular Atrophy in the new treatment era |
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| Risk assessment and genetic counseling for Lynch syndrome – Practice resource of the National Society of Genetic Counselors and the Collaborative Group of the Americas on Inherited Gastrointestinal Ca |
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| A call for unity in DEIJ efforts using a proposed framework for Education, Recruitment, Retainment, Research, and Active outreach (ERA) for genetic counselors in the United States |
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