Journal of Genetic Counseling

Article	Citations
Translation, cross‐cultural adaptation, and preliminary validation of a patient‐reported outcome measure for genetic counseling outcomes in Sweden	67
The experience of “at‐risk” status for familial frontotemporal dementia (fFTD) and its impact on reproductive decision‐making: A qualitative study	50
Clients' experiences of empathy in genetic counseling for hereditary breast and ovarian cancer: A qualitative study in Japan	50
Is it time for a paradigm shift? Inclusion of APOE on genetic dyslipidemia panels	38
Status of abortion curriculum in genetic counseling: Survey of graduate programs and recent graduates in the United States	37
Race, ethnicity, and ancestry reporting in genetic counseling research: A focused mapping review and synthesis	32
Familial communication and cascade testing following elective genomic testing	28
Understanding the psychological impact of identifying carrier status on young adults: A qualitative study exploring peer reactions	22
Health‐related quality of life and fear of progression in individuals with Li‐Fraumeni syndrome	22
Training for the future of the genetic counseling profession: Exploring the assessment and adaptation of graduate programs' didactic curriculum	20
Predictive genetic testing for Huntington's disease: Exploring participant experiences of uncertainty and ambivalence between clinic appointments	20
Supervision for genetic counselors: The role of career‐long supervision to develop resilient practitioners	19
A heartfelt thank you to the 2024 Journal of Genetic Counseling reviewers	19
Transfer of embryos with positive PGT‐M results: Genetic Counselors' perspectives and ethical considerations	18
Issue Information	16
Small programs, big challenges: Reimagining the evaluation of clinical teaching in genetic counseling	16
Factors that influence genetic counselors' participation in research	16
Genetic counselors' professional identity in North America: A scoping review	16
Genetic counseling certificate program: A program evaluation of undergraduate exposure to genetic counseling	15
The effect of a prior e‐learning tool on genetic counseling outcomes in diverse ethnic couples with abnormal Down syndrome screening tests: A randomized controlled trial	15
Advocating for equitable management of hereditary cancer syndromes	15
Factors associated with US and Canadian genetic counselors' testing decisions during pregnancy	14
Women's thoughts on receiving and sharing genetic information: Considerations for genetic counseling	14
An internship in psychiatric genetic counseling: Impact on genetic counseling graduates' practice and career choices	14
Mental models about heredity among immigrant Latinx adults with limited education from Mexico and Central America	13

Barriers in applying to genetic counseling Master's degree programs: Perceptions of prospective applicants when compared with Canadian admissions committee members	12
Understanding type and quality of relationships between individuals with chromosome 18 syndromes and their siblings	12
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Research to reduce inequities in cancer risk services: Insights for remote genetic counseling in a pandemic and beyond	11
Issue Information	11
Acceptability of an online communication training intervention for genetic counseling students	11
Awareness of genetic counseling services among allied healthcare professionals in South Africa	10
Genetic counselors' perceptions of student supervision across service delivery models	10
Incorporating telehealth education into the genetic counseling curriculum	10
Exploring genetic counselors’ use of pedigree symbols to represent assisted reproductive technology	10
Paid summer undergraduate internships are one strategy to increase diversity in genetic counseling	10
Fellowships for genetic counselors: An emerging opportunity for additional training and specialization	10
Genetic counselors, patients', and carers’ views on an Australian clinical genetics service information system	10
Awareness of genetic counseling and genetic testing for hereditary gynecologic cancers among Korean healthcare providers: A survey	10
Need for additional training to be a laboratory genetic counselor—A qualitative exploration	10
The evolution of genetic counseling graduate education in New York City during the COVID‐19 pandemic: In the eye of the storm	9
Development and evaluation of an educational resource for parents of children with 22q11.2 deletion syndrome about the psychiatric manifestations of the condition	9
An exploration of cultural competency training and genetic counselors' racial biases	9
Genetic counseling program remediation practices for students underperforming in clinical skills: An exploratory study	9
The impact of converting to telehealth for cancer genetic counseling and testing during the COVID‐19 pandemic	9
Psychological characteristics of Japanese patients and their family members receiving genetic counseling: A single‐institute exploratory study	9
Universal access to genetic counseling for women with epithelial ovarian cancer in Nova Scotia: Evaluating a new collaborative care model	9
Exploring spiritual/religious coping strategies among mothers of children with severe or profound intellectual disability during genetic counseling in Brazil	9
Perinatal palliative care for family with prenatal diagnosis of Matthew‐Wood syndrome	9
Effects of diet education on empowerment for individuals who have an increased risk of developing breast or colon cancer: A pilot study	9
Need for integration of genetic counselors in the Portuguese healthcare: Their added value from the medical geneticists perspective	9
Prenatal patient perceptions of receiving difficult news over the telephone	8
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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	8
Genetic variants with discordant classifications: An assessment of genetic counselor attitudes and practices	8
A heartfelt thank you to the 2022 Journal of Genetic Counseling reviewers	8
The impact of Marfan syndrome on an Aboriginal Australian family: ‘I don’t like it as much as I don’t like cancer’	8
Comparison of genetic testing documentation between genetic counselors and non‐genetic counselors	8
Interventions to support decision making in people considering germline genetic testing for BRCA 1/2 pathogenic and likely pathogenic variants: A scoping review	8
An investigation of preceptors' perceptions of behavioral elements of “professionalism” among genetic counseling students	8
Application of motivational interviewing strategies with the extended parallel process model to improve risk communication for parents of children with familial hypercholesterolemia	8
What knowledge is required for an informed choice related to non‐invasive prenatal screening?	8
Sudden cardiac death in the young: A qualitative study of experiences of family members with cardiogenetic evaluation	8
Issue Information	8
Issue Information	7
Critical components of genomic medicine practice for non‐genetics healthcare professionals: Genetic counselors' perspectives and implications for medical education	7
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	7
What next for “counseling” in genetic counseling training: A reflection on how CBT and ACT approaches can contribute to the genetic counseling toolkit	7
Utilization of genetic testing: Analysis of 4,499 prior authorization requests for molecular genetic tests at four US regional health plans	7
Exploring parental cystic fibrosis disclosure to well children	7
Pregnant individuals' genetic literacy and decisional conflict about prenatal screening tests: A cross‐sectional study	7
Leveling the field: Development of an asynchronous interactive module series for genetic counseling trainees on molecular testing and variant interpretation	7
Characterization of variant reclassification and patient re‐contact in a cancer genetics clinic	7
Attitudes and beliefs regardingrace‐targetedgenetic testing of Black people: A systematic review	7
Genetic counseling in diabetes mellitus: A practice resource of the National Society of Genetic Counselors	7

Women's preferences for NIPT as a first‐line test in England and France: Challenges for genetic counseling practices	6
Generative AI and the profession of genetic counseling	6
An examination of psychosocial and professional effects of the COVID‐19 pandemic on genetic counselors	6
Issue Information	6
Discussions of personal identity in genetic counseling supervision	6
The experiences and support needs of applicants who go unmatched to genetic counseling graduate programs: An exploratory qualitative study	6
Metaphors and why these are important in all aspects of genetic counseling	6
Courtesy stigma of parents of children with Down syndrome: Adaptation process and transcendent stage	6
Cross‐cultural adaptation of the Genetic Counseling Outcome Scale (GCOS‐24) for use in Canada: A qualitative study	6
Attitudes and training needs of oncologists and surgeons in mainstreaming breast cancer genetic counseling in a low‐to‐middle income Asian country	6
Trauma‐informed practice for genetic counselors: Insights from a workshop evaluation	6
Following NCCN guidelines within one hospital system in the United States: Comparison between cancer centers and genetic counselor utilization	6
Parent experiences with genetic testing for pediatric hearing loss	6
Narrative review on ethical and psychological issues raised by genetic and genomic testing in pediatric oncology care	6
Genetic counseling for fetal sex prediction by NIPT: Challenges and opportunities	6
Adding a genetic counseling assistant improves efficiency of hereditary cancer genetic counseling without impacting patient experience	6
Reply to Rathbun and Paulyson Nuñez	6
Misattributed parentage identified through diagnostic exome sequencing: Frequency of detection and reporting practices	6
Understanding and perception of direct‐to‐consumer genetic testing in Hong Kong	6
Maintaining psychological well‐being when living at risk of Huntington's disease: An interpretative phenomenological analysis	5
A Heartfelt Thank You to the 2021 Journal of Genetic Counseling Reviewers	5
Experiences of reproductive genetic counselors with abortion regulations in Ohio	5
Rethinking genetic counseling clinical skills training in the time of COVID‐19	5
International genetic counseling: What do genetic counselors actually do?	5
Toward depathologizing queerness: An analysis of queer oppression in clinical genetics	5
A qualitative assessment of parental experiences with false‐positive newborn screening for Krabbe disease	5
Expanded carrier screening in the United States: A systematic evidence review exploring client and provider experiences	5
Cross‐cultural adaptation and validation of a French version of the perceived personal control questionnaire as an outcome measure instrument for genetic counseling	5
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Clinical geneticists' views on and experiences with unsolicited findings in next‐generation sequencing: “A great technology creating new dilemmas”	5
Psychosocial impact on individuals who received negative test results from predictive testing for Huntington's disease: An exploratory qualitative study	5
A cross‐sectional survey‐based exploration of diversity in the admissions committees and student cohorts of genetic counseling programs over time	5
Expanded carrier screening for reproductive risk assessment: An evidence‐based practice guideline from the National Society of Genetic Counselors	5
Adapting to the challenges of the global pandemic on genetic counselor education: Evaluating students’ satisfaction with virtual clinical experiences	5
Incorporating multiracial and multiethnic experiences into genetic counseling practice and research: A necessary opportunity	5
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Evaluation of face validity and core concepts of a novel knowledge scale for inherited heart disease: A pilot study	5
Genetic counseling processes and strategies for racially and ethnically diverse populations: A systematic review	5
Cancer genetic counseling via telegenetics and telephone: A qualitative study exploring the experience of patients and genetic counselors in an Australian cancer genetics context	5
Enhancing intersex healthcare: A qualitative study of parental perspectives on the role of genetics	5
Gender imbalance in the genetic counseling profession: An Australasian perspective	5
How are uncertain prenatal genetic results perceived and managed two years after they were received? A qualitative interview study	5
Processing the process: Reflections on genetic counselor‐led student supervision groups and practical tips for future facilitators	4
Experiences of young people growing up in a family with Huntington's disease: A meta‐ethnography of qualitative research	4
Moral distress in genetic counseling: A study of North American genetic counselors	4
An eMERGEing definition of patient engagement in genetic counseling	4
Elicitation of children’s understanding of information in pediatric genetic counseling encounters: A discourse‐oriented perspective	4
Defining orienting language in the genetic counseling process	4
Assessing genetic counselors’ graduate school education and training in congenital heart defects	4
Prenatal genetic counselors' perceptions of the impact of abortion legislation on counseling and access in the United States	4
Social support networks of adults with sickle cell disease	4
The experiences of families receiving a diagnosis of 22q11.2 deletion syndrome in Ireland	4
What next for “counseling” in genetic counseling training: A co‐production workshop exploring how CBT and ACT approaches can contribute to the genetic counseling toolkit	4
Identifying potential LGBTQIA+ competencies for genetic counseling student training	4
Graduate training, credentialing, and continuing education to prepare genetic counselors for laboratory roles—Results of a national survey	4
Disability training for genetic counseling students: The advocates' perspective	4
Pregnant people's views and knowledge on prenatal screening for fetal trisomy in the absence of a national screening program	4
Summary of the experiences, knowledge, medical management, and family communication of monoallelic MUTYH carriers	4
The experiences of adolescent siblings of children with rare genetic conditions: “It's made me who I am”	4
Applying the practice‐based competencies to evaluate and characterize the contracting process within genetic counseling sessions	4
Use of gender‐inclusive language in genetic counseling to optimize patient care	4
Issue Information	4
A team‐based approach to cardiogenomic education	4
Clinical Bootcamp: Moving toward competency outside of the clinic	4
From intention to action: Assessing need and creating a JEDI toolkit for individuals teaching cancer genetics curriculum	4
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Examining the effect of patient personality types and coping styles on outcomes of genetic counseling	4
Conducting inclusive research in genetics for transgender, gender‐diverse, and sex‐diverse individuals: Case analyses and recommendations from a clinical genomics study	4
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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	4
The multigenerational impact of long QT syndrome: A Gitxsan perspective	4
Policy and laboratory practice: How quality control procedures for genetic testing perpetuate biological essentialism and discrimination against transgender, gender diverse, and intersex people	4
iKNOWgynetics – A web‐based learning concept to empower primary care gynecologists to participate in the care of patients with a family history of breast and ovarian cancer	4
Disclosure and comfort during genetic counseling sessions with LGBTQ+ patients: An updated assessment	3
Misunderstood terms and concepts identified through user testing of educational materials for fragile X premutation: “Not weak or fragile?”	3
Explanatory models for the cause of Fragile X Syndrome in rural Cameroon	3
Exploring genetic counselors' practice of discussing clinical trials with patients	3
Script concordance testing in genetic counseling training: A pilot study	3
Outcomes of psychiatric genetic counseling in relation to time since diagnosis and symptom onset	3
Newborn screening for Pompe disease: Parental experiences and follow‐up care for a late‐onset diagnosis	3

Enhancing the didactic learning experience for Laboratory Genetics and Genomics fellows through a multi‐institutional lecture series	3
Large‐scale group genetic counseling: Evaluation of a novel service delivery model in a Canadian hereditary cancer clinic	3
Research participants' perspectives about the return of uninformative genomic test results in a clinical research setting	3
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Issue Information	3
Public perceived knowledge of, attitude toward, and use of genetic testing in urban China	3
Issue Information	3
Alleviating the confusion around content analysis: A comment in response to Wainstein, Elliott & Austin 2023	3
Cancer patients' experience of receiving variant of uncertain significance results: An Asian perspective	3
Elective genomic testing: Practice resource of the National Society of Genetic Counselors	3
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	3
A qualitative study exploring LGBTQ genetic counseling students' relationships with peers and faculty in graduate school	3
Pregnant women's experiences of non‐invasive prenatal testing (NIPT) in Japan: A qualitative study	3
Correction to “Who is at risk for compassion fatigue? An investigation of genetic counselor demographics, anxiety, compassion satisfaction, and burnout”	3
Disability education and implications for genetic counselor training	3
An evidence‐based practice guideline of the National Society of Genetic Counselors for telehealth genetic counseling	3
Commentary from a commercial laboratory: The unexpected benefits of a more virtual world during the COVID‐19 pandemic	3
No longer “non‐traditional”: Genetic counselors' perceptions towards laboratory and industry roles	3
Young adults' reasoning for involving a parent in a genomic decision‐making research study	3
Evaluating a communication aid for return of genetic results in families with hypertrophic cardiomyopathy: A randomized controlled trial	3
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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	3
Investigating genetic counselors' communication with Lynch syndrome patients about cascade testing: Barriers, facilitators, and strategies	3
Opinions of adults affected with later‐onset lysosomal storage diseases regarding newborn screening: A qualitative study	3
Issue Information	3
Creation and initial validation of a genetic counseling supervisory self‐efficacy scale	3
Uptake of genetic testing among patients seeking cancer genetic counseling in Taiwan	3
Assessing and attending to psychosocial concerns in genetic counseling: Proposing the BATHE method	3
Genetic testing for children at risk to be hemophilia carriers	3
Genetic counseling practice for inherited eye diseases in an Israeli medical center during the COVID‐19 pandemic	3
A cross‐professional competency framework for communicating genomic results	3
Patient uptake of updated genetic testing following uninformative BRCA1 and BRCA2 results	3
Preferences for and acceptability of receiving pharmacogenomic results by mail: A focus group study with a primarily African‐American cohort	3
Cardiology clinic patient attitudes toward and potential personal utility of genetic testing: Findings from a unique multiracial clinical sample	3
Differences in genetic counseling student responses to intense patient affect: A study of students in North American programs	3
The review of genetic screening services and common BRCA1/2 variants among South African breast cancer patients	3
U.S. Genetic counselors’ perceptions of inpatient genetic counseling: A valuable model for medically complex patients	3
The role of emotional sensitivity to probability in the decision to choose genetic testing	3
Assessing barriers to the career ladder and professional development for ethnic minority genetic counselors in the United States	3
Leveraging electronic health records to inform genetic counseling practice surrounding psychiatric disorders	3
The genetic counseling profession in Austria: Stakeholders’ perspectives	3
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Assessment of attitudes towards the use of preimplantation genetic diagnosis in a single center in Riyadh, Saudi Arabia	2
Telesupervision in genetic counseling education during COVID‐19 and beyond	2
How parents of children with ataxia‐telangiectasia use dynamic coping to navigate cyclical uncertainty	2
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Buying my existence. Just $49, free shipping included	2
Value of whole‐genome sequencing to Australian cancer patients and their first‐degree relatives participating in a genomic sequencing study	2
Sudden shift to remote genetic counseling during the COVID‐19 pandemic: Experiences of genetics professionals in Italy	2
A qualitative focus group analysis: Increasing fieldwork capacity in genetic counseling training programs	2
The effect of knowledge and person‐related factors on breast cancer susceptibility genes (BRCA1/2) testing perception in Turkish women	2
Noninvasive prenatal screening (NIPS) results for participants of the eXtraordinarY babies study: Screening, counseling, diagnosis, and discordance	2
Beyond multiple choice: Clinical simulation as a rigorous and inclusive method for assessing genetic counseling competencies	2
Spanish language opportunities in genetic counseling training programs in the United States	2
Introduction of the genetic counseling profession by teachers in BIPOC‐majority high schools	2
Implementing mainstream genetic counseling within the area‐wide network of the German Consortium Hereditary Breast and Ovarian Cancer (GC‐HBOC): Satisfaction of primary care providers with	2
Issue Information	2
Exploring the role of Islam on the lived experience of patients with Long QT Syndrome in Saudi Arabia	2
Referral networks for pediatric patients with genetic conditions: The perspective of occupational therapists	2
Perception of genetic testing among patients with inherited retinal disease: Benefits and challenges in a Japanese population	2
Examining the role of language competency in genetic testing awareness among adults in the United States	2
Research participants' perspectives regarding the feedback of secondary findings–A cohort from the DDD‐Africa study, South Africa	2
Development and preliminary evaluation of a genetics education booklet for retinoblastoma	2
Application of the RIME framework in genetic counseling fieldwork training to assess practice‐based competencies	2
Need for specially designed educational support groups: Young women's experiences of being identified with BRCA pathogenic variants	2
Lived experiences of undergoing regular tumor screening in patients with multiple endocrine neoplasia types 1 and 2 (MEN1/MEN2)	2
Understanding patients' views and willingness toward the use of telehealth in a cancer genetics service in Asia	2
Issue Information	2
Should genes for non‐syndromic hearing loss be included in reproductive genetic carrier screening: Views of people with a personal or family experience of deafness	2
A proposal to promote diversity in journal research article titles	2
Integrating nutrition and genetic counseling: A case study approach to interprofessional learning	2
Issues, challenges, and future perspectives of genetic counseling in Republic of Korea: Perspectives of laboratory physicians based on a 2022 survey	2
Landscape of genetic counseling in the Philippines	2
Searching for secrets, searching for self: Childhood adversity, self‐concept clarity, and the motivation to uncover family secrets through direct‐to‐consumer genetic testing	2
Assessing the impact of pre‐test education on patient knowledge, perceptions, and expectations of pharmacogenomic testing to guide antidepressant use	2
Genetic testing and counseling for hypertrophic cardiomyopathy: An evidence‐based practice resource of the National Society of Genetic Counselors	2
Performance of the shared decision‐making process scale for use in evaluation of hereditary cancer genetic testing decisions	2
Development and assessment of educational materials for spinal muscular atrophy carrier screening in the Plain community	2
Unraveling non‐participation in genomic research: A complex interplay of barriers, facilitators, and sociocultural factors	2
Attitudes of parents of children with ADHD towards genetic testing: Data from a Turkish sample	2
“It becomes your whole life”—Exploring experiences of reciprocal translocation carriers and their partners	2
Danish heritable retinoblastoma survivors' perspectives on reproductive choices: “It's important for me, not to pass on this condition”	2
A qualitative study of LGBTQIA+ genetic counselors' experiences while applying to graduate school	2
Links between gender norms and the intergenerational transmission of health information in parents carrying BRCA1/2 pathogenic variants	2
Patient perceptions of genetic counselors' role and emotional support needs in adults with Parkinson's disease	2
Genetic discrimination views in online discussion forums: Perspectives from Canadian forumites	2
Stagnation in quality of next‐generation sequencing assays for the diagnosis of hereditary hematopoietic malignancies	2
Genesurance counseling: Current training practices of genetic counseling graduate programs in the United States	2
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Families' experiences accessing care after genomic sequencing in the pediatric cancer context: “It's just been a big juggle”	2
An exploration of knowledge, risk perceptions, and communication in a family with multiple genetic risks for Parkinson's disease	2
North American genetic counselors' approach to collecting and using ancestry in clinical practice	2
Empathy experiences of Japanese certified genetic counselors: A qualitative investigation and proposed framework	2
Commonalities and contrasts: North American program directors' perspectives on genetic counseling education	2
Dilemmas when talking about Huntington's disease: A qualitative study of offspring and caregiver experiences in Norway	2