Journal of Genetic Counseling

Article	Citations
Issue Information	116
Acceptability of an online communication training intervention for genetic counseling students	78
Barriers in applying to genetic counseling Master's degree programs: Perceptions of prospective applicants when compared with Canadian admissions committee members	57
Identifying potential genetic counseling program applicant competencies	53
Narrative review on ethical and psychological issues raised by genetic and genomic testing in pediatric oncology care	35
Factors impacting experience of genetic testing among adults with inherited retinal diseases	30
Reply to Rathbun and Paulyson Nuñez	30
Exploring spiritual/religious coping strategies among mothers of children with severe or profound intellectual disability during genetic counseling in Brazil	27
Characterization of variant reclassification and patient re‐contact in a cancer genetics clinic	26
Women's preferences for NIPT as a first‐line test in England and France: Challenges for genetic counseling practices	25
Provider perceptions and insights on polygenic risk scores for colorectal cancer: A qualitative study	23
Genetic counseling program remediation practices for students underperforming in clinical skills: An exploratory study	22
Perinatal palliative care for family with prenatal diagnosis of Matthew‐Wood syndrome	21
Clients' experiences of empathy in genetic counseling for hereditary breast and ovarian cancer: A qualitative study in Japan	20
Women's thoughts on receiving and sharing genetic information: Considerations for genetic counseling	20
Exploring parental cystic fibrosis disclosure to well children	18
Genetic counseling in diabetes mellitus: A practice resource of the National Society of Genetic Counselors	17
The attitudes of individuals with or at risk of adult‐onset genetic conditions on reproductive genetic testing: A systematic review	15
Sudden cardiac death in the young: A qualitative study of experiences of family members with cardiogenetic evaluation	15
Supervision for genetic counselors: The role of career‐long supervision to develop resilient practitioners	14
Genetic testing for Parkinson's disease in an underrepresented population: Knowledge, attitudes, and ethical considerations from a Malaysian perspective	14
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Incorporating multiracial and multiethnic experiences into genetic counseling practice and research: A necessary opportunity	13
Genetic counseling for fetal sex prediction by NIPT: Challenges and opportunities	13
The effect of knowledge and person‐related factors on breast cancer susceptibility genes (BRCA1/2) testing perception in Turkish women	12

Issue Information	12
Patient perceptions of genetic counselors' role and emotional support needs in adults with Parkinson's disease	12
Assessing and attending to psychosocial concerns in genetic counseling: Proposing the BATHE method	12
The experiences of families receiving a diagnosis of 22q11.2 deletion syndrome in Ireland	12
Uptake rates for non‐invasive prenatal screening for single‐gene disorders associated with advanced paternal age	12
Issue Information	12
Investigating genetic counselors' communication with Lynch syndrome patients about cascade testing: Barriers, facilitators, and strategies	12
Invisible diversities, academic capital, and competitiveness of genetic counseling applicants	11
Issue Information	11
Population‐based hereditary cancer screening in a general endoscopy clinic: Evaluating interest in, uptake, and outcomes of genetic services	11
Pregnant people's views and knowledge on prenatal screening for fetal trisomy in the absence of a national screening program	11
The review of genetic screening services and common BRCA1/2 variants among South African breast cancer patients	11
Prospective parents' views on reproductive genetic carrier screening: “You know better, you do better”	11
Evaluation of face validity and core concepts of a novel knowledge scale for inherited heart disease: A pilot study	11
Clinical Bootcamp: Moving toward competency outside of the clinic	11
Workplace perk or pitfall? A qualitative study of genetic counselors' perspectives and experiences with workplace genetic testing	10
Issue Information	10
A qualitative study exploring LGBTQ genetic counseling students' relationships with peers and faculty in graduate school	10
A cross‐professional competency framework for communicating genomic results	10
From intention to action: Assessing need and creating a JEDI toolkit for individuals teaching cancer genetics curriculum	10
Buying my existence. Just $49, free shipping included	10
Representation of skin tone: The use of medical imagery in the genetic counseling profession	10
Graduate training, credentialing, and continuing education to prepare genetic counselors for laboratory roles—Results of a national survey	10
A qualitative study of US ‐based transgender, nonbinary, and gender diverse individuals' perspectives on preconception and prenatal genetic testing f	9
Performance of the shared decision‐making process scale for use in evaluation of hereditary cancer genetic testing decisions	9
Clinical outcomes after nondiagnostic prenatal exome sequencing: Need for balancing reassurance and residual risks in genetic counseling	9
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Genetic Counselors' attitudes & perceptions regarding suicide risk assessment and identification in practice	9
Correction to “Who is at risk for compassion fatigue? An investigation of genetic counselor demographics, anxiety, compassion satisfaction, and burnout”	9
Genetic counseling for adult‐onset neurogenetic conditions in Hispanic/Latine communities: A qualitative study of barriers and facilitators from Hispanic/Latine genetic counselors' perspectives	9
A SMART framework for equitable supervision: Insights from a longitudinal study with BIPOC genetic	8
Lessons learned from BRCA1/2 screening in Israel: A cross‐sectional survey comparing experiences and communication	8
Cardiac genetic counseling services: Exploring downstream revenue in a pediatric medical center	8
Mothers' reflections on the diagnosis and birth of their child with Down syndrome: Variability based on the timing of the diagnosis	8
Medical students' self‐perceived knowledge and clinical comfort with genetics in Pakistan	8
How parents of children with ataxia‐telangiectasia use dynamic coping to navigate cyclical uncertainty	8
Assessing the perspectives of genetic counselors with oncology patients at the end of life	8
BIPOC genetic counseling students' perspectives on career‐oriented social media use: Results from a longitudinal qualitative study	8
Changes in acceptability, consideration, intention, and uptake of direct‐to‐consumer genetic tests in the Netherlands from 2017 to 2022	8
Impact of barriers and motivators on intention and confidence to undergo hereditary cancer genetic testing	8
Beyond multiple choice: Clinical simulation as a rigorous and inclusive method for assessing genetic counseling competencies	8
Evaluating attributes of a collaborative model of service delivery for hereditary cancer risk assessment	8
Noninvasive prenatal screening ( NIPS ) results for participants of the eXtraordinarY babies study	8
Genetic testing and counseling for hypertrophic cardiomyopathy: An evidence‐based practice resource of the National Society of Genetic Counselors	8
An analysis of direct‐to‐consumer genetic testing portals and their communication of health risk and test limitations	8
Barriers and facilitators to genetic counseling service availability in the Arab world: A genetic counselors' perspective	8
North American genetic counselors' approach to collecting and using ancestry in clinical practice	8
Examining the communication work of women who have tested BRCA‐positive: “I feel this responsibility to let people know”	8
Exploring genetic counselors' interest and role in transitional care discussions for pediatric patients with neurodevelopmental conditions	7
Genetic counselors and congenital heart disease: Clinical roles, genetic testing practices, and perceived genetic testing utility	7

A qualitative study of the experiences of patients with prostate cancer when receiving negative genetic results: “I still don't have a grasp of what it all means”	7
Evaluating a general pediatric/adult genetic counseling clinic in a Midwest medical center	7
The goldilocks conundrum: Disclosing discrimination risks in informed consent	7
To refer or not to refer? Exploring the cognitive process of genetic counselors' decision to refer a patient to another professional	7
Primary care patient and clinician attitudes about population genomic screening, informed decision‐making needs, and the potential for Chatbot technology	7
Impacts of student debt on the professional and personal lives of genetic counselors: A 10‐year perspective	7
Experiences of hereditary cancer care among transgender and gender diverse people: “It's gender. It's cancer risk…it's everything”	7
Leadership development in genetic counseling graduate programs	7
Clinical genetic counselors' use of people‐ and identity‐first language in regard to patients' identification with disability	7
Genetic counselors' experience with reimbursement and patient out‐of‐pocket cost for multi‐cancer gene panel testing for hereditary cancer syndromes	7
Current attitudes toward carrier screening for spinal muscular atrophy among pregnant women in Eastern China	7
How should we address the inevitable harms from non‐negligent variant reclassification in predictive genetic testing?	7
Experiences of genetic counseling students with disabilities and chronic illnesses: A qualitative study	7
Development and acceptability of a support intervention for families after sudden cardiac death in the young	7
The development and preliminary evaluation of the Genetic Counseling Skills Checklist	7
Perspectives of Italian lay persons who would decline genetic risk information: “I think I'd be living in constant worry”	7
A preliminary adaptation and validation of the genetic counseling outcome scale (GCOS‐24) for use in Greece	7
Use of digital health tools with point‐of‐care testing improves access to germline genetic testing within a gastrointestinal cancer clinic	6
Proposed use of entrustable professional activities (EPAs) in genetic counseling for clinical training and assessment	6
A survey to analyze the need of genetic counseling among doctors in Lahore, Pakistan	6
Issue Information	6
Perceived cancer risk and genetic counseling: A biopsychological perspective	6
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Is intermediate risk really intermediate? Comparison of karyotype and non‐invasive prenatal testing results of pregnancies at intermediate risk of trisomy 21 on maternal serum screening	6
Host perspectives on international fieldwork placements for U.S.‐based genetic counseling students	6
A comment on ‘COVID‐19 vaccine hesitancy and acceptance among pregnant people’	6
Development of the Affiliate Stigma Scale for parents of children with genetic conditions	6
The State of National Institute of Health Awards for funding genetic counseling research, resources, and training over the past decade	6
Parents' perspectives of non‐informative germline genetic testing in children with Juvenile Polyposis Syndrome	6
Voices in practice: Exploring genetic counseling ethical, cultural, social, and religious dynamics in the UAE	6
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Exploring the journey to genomic testing and genetic services: A qualitative study of parental perspectives of children with rare conditions	5
Optimizing risk‐reducing surgery and aspirin decision aids for Lynch syndrome carriers using the person‐based approach: A think‐aloud interview study	5
The efficacy of genetic counseling for familial colorectal cancer: A meta‐analysis	5
The impact of cohort relationships on BIPOC genetic counseling students: Results from a longitudinal qualitative study	5
Factors associated with US and Canadian genetic counselors' testing decisions during pregnancy	5
Navigating complexity: How shifting abortion regulations impacted prenatal genetic counselors practicing in restrictive states from 2020 to 2024	5
A Filipinized view of the counselor‐client relationship in genetic counseling	5
Cross‐cultural validation of the genetic counseling outcome scale in Korea	5
The erasure of transgender and intersex identities through fetal sex prediction and genetic essentialism	5
Adolescents' and young adults' reactions to and perceived utility of carrier screening results in the context of a genomic research study	5
Issue Information	5
Qualitative analysis of the needs of parents of children with rare genetic diseases, following their diagnosis obtained by whole‐exome sequencing	5
Experience with a nurse‐driven genetic counseling pathway of Italian women with uninformative BRCA test result	5
Role of psychological background in cancer susceptibility genetic testing distress: It is not only about a positive result	5
Insights into genetic assistant practice and the workforce in North America	5
Exploring genetic counselors' experiences with non‐paternity in clinical settings	5
A heartfelt thank you to the 2024 Journal of Genetic Counseling reviewers	5
Experiences of Dutch parents undergoing prenatal genomic testing for fetal structural anomalies: A prospective qualitative analysis	5
Issue Information	5
2024 National Society of Genetic Counselors presidential address: The path we take	5
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Unlocking the next phase of development for our profession: Developing and consolidating the recognition of genetic counseling as a rigorous area of academic study	5
Association between proband characteristics and CDH1 cascade genetic testing uptake in at‐risk relatives	5
Quality‐of‐life after risk‐reducing mastectomy in women with increased risk of breast cancer: A longitudinal study	5
Evaluating genetic counseling session duration: A scoping review of patient care time, influencing factors, and impact on patient outcomes	5
Both sides now: Changing a long‐standing pedigree tradition of men on the left and women on the right	5
Characterizing the research mentorship experience of genetic counseling students	5
Cascade testing for inherited cardiac conditions: Risk perception and screening after a negative genetic test result	5
Cascade testing in an ovarian cancer traceback genetic testing program: The GRACE study experience	5
Familial communication and cascade testing following elective genomic testing	5
Canadian certification exam pass rates are impacted by genetic counseling program location: A review of Canadian Board of Genetic Counselling data from 2007 to 2025	5
COVID‐19 vaccine hesitancy and acceptance among pregnant people contacting a teratogen information service	5
Preferences of parents from diverse backgrounds on genomic screening of apparently healthy newborns	5
Assessing patient communication preferences for reclassified variants of uncertain significance in a general genetics clinic	5
Learning from our patients: Utilizing the expertise of transgender and/or gender diverse educators to build an inclusive learning cycle	5
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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”	5
Reading and writing reviews: A primer on systematic, scoping, and narrative reviews for genetic counselors	4
Ethno‐racial differences in the frequency of cancer reported from family pedigrees in the prenatal genetic counseling setting	4
Evaluating a communication aid for return of genetic results in families with hypertrophic cardiomyopathy: A randomized controlled trial	4
Implementing genetic screening into primary care for medically actionable conditions: Insights from a precision health pilot program	4
Correction to: Practice resource‐focused revision: Standardized pedigree nomenclature update centered on sex and gender inclusivity: A practice resource of the National Society of Genetic Counselors	4
Psychosocial issues of individuals undergoing surveillance for increased risk of melanoma and pancreatic cancer due to a germline CDKN2A variant: A focus group study	4
How the other half screens: A model for partnerships between student‐run free clinics and genetic counseling programs to address disparities in hereditary cancer evaluation	4
Expanded carrier screening for inherited genetic disease using exome and genome sequencing	4
Research methodologies in genetic counseling: Grounded theory	4
Evaluating pregnancy termination rates for fetal chromosome and single gene disorders	4
Subspecialty neurology genetic counselors—A cost effective solution to substantial time costs associated with genomic testing in the neurology clinic	4
Paternal expanded carrier screening after positive maternal results: Perceptions and barriers to screening	4

Introduction of the genetic counseling profession by teachers in BIPOC‐majority high schools	4
Decision stability among adolescents and young adults making choices about learning genomic research results	4
Clinical geneticists' views on and experiences with unsolicited findings in next‐generation sequencing: “A great technology creating new dilemmas”	4
Uptake of genetic testing among patients seeking cancer genetic counseling in Taiwan	4
Need for specially designed educational support groups: Young women's experiences of being identified with BRCA pathogenic variants	4
Pediatric predictive testing to inform preimplantation genetic testing: A case report and review of the literature	4
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Awareness and knowledge of familial breast and ovarian cancer among German general practice patients	4
A qualitative exploration of experiences of gender identity and gender questioning among adults with Klinefelter syndrome/XXY	4
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Issue Information	4
Does the amount of family history matter? Perspectives of adult adoptees	4
An introduction to Delphi studies and consensus methods for genetic counselors	4
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An investigation of preceptors' perceptions of behavioral elements of “professionalism” among genetic counseling students	4
Western Australian women's expectations for expanded NIPT—An online survey regarding NIPT for single gene, recessive and chromosomal conditions	4
Race, ethnicity, and ancestry reporting in genetic counseling research: A focused mapping review and synthesis	4
Development of genetic assistant competencies using the Delphi consensus building method	4
Understanding and issues related to next‐generation sequencing among educated laypersons in India	4
Assessing perceived empathy based on genetic counselor gender using a randomized, hypothetical prenatal genetic counseling scenario design	4
Application of the RIME framework in genetic counseling fieldwork training to assess practice‐based competencies	4
To be or not to be (honest): The persistent problem of misattributed paternity	4
Genetic counseling students' use of patient‐centered communication skills predicts standardized patient satisfaction during virtual simulated sessions	4
Clinical and laboratory genetic counselor attitudes on the reporting of variants of uncertain significance for multigene cancer panels	4
Group meditation, addressing stigma, and “mental health days”: Recommendations for integrating self‐awareness practices into genetic counseling graduate programs	4
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	4
How genetic counselors in North America describe their professional identity	4
Issue Information	4
Attitudes and beliefs regardingrace‐targetedgenetic testing of Black people: A systematic review	4
Issues, challenges, and future perspectives of genetic counseling in Republic of Korea: Perspectives of laboratory physicians based on a 2022 survey	4
Links between gender norms and the intergenerational transmission of health information in parents carrying BRCA1/2 pathogenic variants	4
Expanding the methodological repertoire: Integrating multimodal approaches in genetic counseling research	3
Psychiatric genetic counseling: A survey of Australian genetic counselors' practice and attitudes	3
Sponsored genetic testing and informed consent implications: Experience and attitudes of genetic counselors	3
Exploring the occurrence of microaggressions in the genetic counseling student–supervisor relationship: A mixed‐methods study	3
Training for the future of the genetic counseling profession: Exploring the assessment and adaptation of graduate programs' didactic curriculum	3
The Genetic Information Nondiscrimination Act and workplace genetic testing: Knowledge and perceptions of employed adults in the United States	3
Paid summer undergraduate internships are one strategy to increase diversity in genetic counseling	3
Issue Information	3
Need for additional training to be a laboratory genetic counselor—A qualitative exploration	3
Further defining the roles and impact of genetic counselors in the biotechnology and pharmaceutical industry	3
Acceptability, consideration, intention, and uptake of six common types of direct‐to‐consumer genetic tests in the Netherlands	3
Exploring Canadian genetic counselors' perspectives and experiences with discussing medical assistance in dying (MAiD)	3
Creation and beta testing of a “choose your own adventure” digital simulation to reinforce motivational interviewing skills in genetic counseling	3
BRCAShare—Assessment of an animated digital message for intrafamilial communication of pathogenic variant positive test results: A feasibility study	3
Survey research in genetic counseling	3
Experiences of genetic counselors practicing in multiple languages: Progress and places for improvement	3
Examining aspects of job satisfaction associated with burnout and factors related to turnover intention in genetic counselors	3
Ethical concerns surrounding sex prediction using noninvasive prenatal screening from pediatric endocrinologists' perspective	3
Genetic counselors' professional identity in North America: A scoping review	3
Experience conducting a community‐engaged student research project involving an underrepresented community: A reflective essay	3
Parent experiences with genetic testing for pediatric hearing loss	3
Promoting the integration of genetic counseling education and research across the spectrum of learners at a large academic institution	3
Cross‐cultural adaptation and validation of a French version of the perceived personal control questionnaire as an outcome measure instrument for genetic counseling	3
Adoptees' experiences of using direct‐to‐consumer genetic testing and determinants of this use: A mixed study in Quebec	3
Leveling the field: Development of an asynchronous interactive module series for genetic counseling trainees on molecular testing and variant interpretation	3
The book is just being written: The enduring journey of parents of children with emerging‐ ultrarare disorders	3
Microlearning: Evidence‐based education that is effective for busy professionals and short attention spans	3
Tension between the need for certainty and numerous uncertainties—A focus group study on various perspectives on a potential genomic newborn screening program in Germany	3
Incidental finding of maternal sex chromosome aneuploidy from DMD carrier screening and single‐nucleotide polymorphism (SNP)‐based prenatal cell‐free DNA screening	3
Assessing management practices for variants of uncertain significance among genetic counselors in pediatrics	3
Views of genetic health professionals, patients, and next of kin on retesting and recontact with results from updated genetic testing	3
Something to chat about: An analysis of genetic counseling via asynchronous messaging following direct‐to‐consumer genetic testing	3
Promotores' perspectives on the virtual adaptation of a hereditary breast cancer education program	3
Bringing Genetics to Mental Health: Integrating Genetic Counseling into a Mental Health Program at Monash Health, Australia	3
Readiness and leadership for the implementation of polygenic risk scores: Genetic healthcare providers' perspectives in the hereditary cancer context	3
A guide to utilizing implementation science for genetic counseling	3
Genetic counseling training program perspectives on delivering disability‐related education	3
Exploring the role of a multidisciplinary hereditary gynecologic oncology clinic in epithelial ovarian cancer risk‐reducing surgical decision‐making practices: A mixed‐methods study	3
Development and evaluation of an educational resource for parents of children with 22q11.2 deletion syndrome about the psychiatric manifestations of the condition	3
A qualitative study of parents' experiences with receiving a prenatal diagnosis of confined placental mosaicism – “We had nothing to rely on, you know?”	3
A cross‐sectional survey‐based exploration of diversity in the admissions committees and student cohorts of genetic counseling programs over time	3
Professional development of certified genetic counselors in Japan: The Japanese Association of Certified Genetic Counselors biennial survey for FY2022	3
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Parent‐reported genetic counselor adherence to the NSGC practice resource for communicating a potential prenatal diagnosis: Impact on the Down syndrome diagnosis experience	3
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Picture this: Evaluating the efficacy of genetic counseling visual aids	3
Counseling supervision for genetic counselors: A proposed outsider witness structure	3
Clinical and laboratory genetic counseling assistants: Comparing background experiences, responsibilities, satisfaction, and career goals	3
Issue Information	3
A qualitative study of unaffected ATM and CHEK2 carriers: How participants make meaning of ‘moderate risk’ genetic results in a population breast cancer screening t	3
Perspectives of genetic counseling supervisors regarding genetic counseling students' attainment of practice‐based competencies in clinical care through remote supervision	3
Outcomes of pregnancies that screened positive for sex chromosome aneuploidy ascertained via cell‐free DNA screening	3
Exploring communication preferences for disclosing breast cancer risk in women with a family history	2
Interpreter style in translating complex terminology and psychosocial aspects of genetic counseling sessions	2
Developing global consensus about core knowledge and skills for genetic counselor education	2
Coping with the challenges of caregiving: A qualitative exploration of the experiences of family caregivers of children with rare diseases in South Africa	2
Genetic health professionals' facilitation of communication between parents and young children about inherited genetic conditions: A scoping review	2
Healthcare professionals' perspectives on supporting individuals with NF1 during pregnancy and decision‐making processes	2
Considerations for the use of qualitative methodologies in genetic counseling research	2
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Interpretation of ambiguous TP53 test results: Mosaicism, clonal hematopoiesis, and variants of uncertain significance	2
Counseling in a different language: An analysis of experiences and resources in multilingual genetic counseling	2
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Issue Information	2