Journal of Genetic Counseling

Article	Citations
Issue Information	114
Acceptability of an online communication training intervention for genetic counseling students	77
Barriers in applying to genetic counseling Master's degree programs: Perceptions of prospective applicants when compared with Canadian admissions committee members	73
Genetic counseling for fetal sex prediction by NIPT: Challenges and opportunities	54
Identifying potential genetic counseling program applicant competencies	52
Genetic testing for Parkinson's disease in an underrepresented population: Knowledge, attitudes, and ethical considerations from a Malaysian perspective	34
Narrative review on ethical and psychological issues raised by genetic and genomic testing in pediatric oncology care	29
Reply to Rathbun and Paulyson Nuñez	27
Factors impacting experience of genetic testing among adults with inherited retinal diseases	25
Women's preferences for NIPT as a first‐line test in England and France: Challenges for genetic counseling practices	25
Characterization of variant reclassification and patient re‐contact in a cancer genetics clinic	24
Incorporating multiracial and multiethnic experiences into genetic counseling practice and research: A necessary opportunity	23
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
Genetic counseling program remediation practices for students underperforming in clinical skills: An exploratory study	20
Perinatal palliative care for family with prenatal diagnosis of Matthew‐Wood syndrome	20
Provider perceptions and insights on polygenic risk scores for colorectal cancer: A qualitative study	18
Exploring parental cystic fibrosis disclosure to well children	18
Exploring spiritual/religious coping strategies among mothers of children with severe or profound intellectual disability during genetic counseling in Brazil	17
Supervision for genetic counselors: The role of career‐long supervision to develop resilient practitioners	15
Sudden cardiac death in the young: A qualitative study of experiences of family members with cardiogenetic evaluation	14
The attitudes of individuals with or at risk of adult‐onset genetic conditions on reproductive genetic testing: A systematic review	14
Uptake rates for non‐invasive prenatal screening for single‐gene disorders associated with advanced paternal age	13
Genetic counseling in diabetes mellitus: A practice resource of the National Society of Genetic Counselors	13
Issue Information	13

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Prospective parents' views on reproductive genetic carrier screening: “You know better, you do better”	12
Investigating genetic counselors' communication with Lynch syndrome patients about cascade testing: Barriers, facilitators, and strategies	12
The effect of knowledge and person‐related factors on breast cancer susceptibility genes (BRCA1/2) testing perception in Turkish women	12
The experiences of families receiving a diagnosis of 22q11.2 deletion syndrome in Ireland	12
Assessing and attending to psychosocial concerns in genetic counseling: Proposing the BATHE method	12
Issue Information	12
Patient perceptions of genetic counselors' role and emotional support needs in adults with Parkinson's disease	12
The review of genetic screening services and common BRCA1/2 variants among South African breast cancer patients	11
Issue Information	11
Invisible diversities, academic capital, and competitiveness of genetic counseling applicants	11
Evaluation of face validity and core concepts of a novel knowledge scale for inherited heart disease: A pilot study	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
Clinical Bootcamp: Moving toward competency outside of the clinic	11
Representation of skin tone: The use of medical imagery in the genetic counseling profession	10
A qualitative study exploring LGBTQ genetic counseling students' relationships with peers and faculty in graduate school	10
Buying my existence. Just $49, free shipping included	10
Issue Information	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
Workplace perk or pitfall? A qualitative study of genetic counselors' perspectives and experiences with workplace genetic testing	9
A qualitative study of US ‐based transgender, nonbinary, and gender diverse individuals' perspectives on preconception and prenatal genetic testing f	9
Genetic Counselors' attitudes & perceptions regarding suicide risk assessment and identification in practice	9
Graduate training, credentialing, and continuing education to prepare genetic counselors for laboratory roles—Results of a national survey	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
Correction to “Who is at risk for compassion fatigue? An investigation of genetic counselor demographics, anxiety, compassion satisfaction, and burnout”	9
Clinical outcomes after nondiagnostic prenatal exome sequencing: Need for balancing reassurance and residual risks in genetic counseling	9
Performance of the shared decision‐making process scale for use in evaluation of hereditary cancer genetic testing decisions	9
An analysis of direct‐to‐consumer genetic testing portals and their communication of health risk and test limitations	8
Impact of barriers and motivators on intention and confidence to undergo hereditary cancer genetic testing	8
North American genetic counselors' approach to collecting and using ancestry in clinical practice	8
Evaluating attributes of a collaborative model of service delivery for hereditary cancer risk assessment	8
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
Noninvasive prenatal screening ( NIPS ) results for participants of the eXtraordinarY babies study	8
Cardiac genetic counseling services: Exploring downstream revenue in a pediatric medical center	8
Genetic counselors' experience with reimbursement and patient out‐of‐pocket cost for multi‐cancer gene panel testing for hereditary cancer syndromes	8
Beyond multiple choice: Clinical simulation as a rigorous and inclusive method for assessing genetic counseling competencies	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
Mothers' reflections on the diagnosis and birth of their child with Down syndrome: Variability based on the timing of the diagnosis	8
How parents of children with ataxia‐telangiectasia use dynamic coping to navigate cyclical uncertainty	8
Medical students' self‐perceived knowledge and clinical comfort with genetics in Pakistan	8
Assessing the perspectives of genetic counselors with oncology patients at the end of life	8
Genetic testing and counseling for hypertrophic cardiomyopathy: An evidence‐based practice resource of the National Society of Genetic Counselors	8
Experiences of hereditary cancer care among transgender and gender diverse people: “It's gender. It's cancer risk…it's everything”	7
Development and acceptability of a support intervention for families after sudden cardiac death in the young	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

Perceived cancer risk and genetic counseling: A biopsychological perspective	7
How should we address the inevitable harms from non‐negligent variant reclassification in predictive genetic testing?	7
Perspectives of Italian lay persons who would decline genetic risk information: “I think I'd be living in constant worry”	7
Examining the communication work of women who have tested BRCA‐positive: “I feel this responsibility to let people know”	7
The development and preliminary evaluation of the Genetic Counseling Skills Checklist	7
Genetic counselors and congenital heart disease: Clinical roles, genetic testing practices, and perceived genetic testing utility	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
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Primary care patient and clinician attitudes about population genomic screening, informed decision‐making needs, and the potential for Chatbot technology	7
Current attitudes toward carrier screening for spinal muscular atrophy among pregnant women in Eastern China	7
Impacts of student debt on the professional and personal lives of genetic counselors: A 10‐year perspective	7
Experiences of genetic counseling students with disabilities and chronic illnesses: A qualitative study	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
Exploring genetic counselors' interest and role in transitional care discussions for pediatric patients with neurodevelopmental conditions	7
Development of the Affiliate Stigma Scale for parents of children with genetic conditions	7
A comment on ‘COVID‐19 vaccine hesitancy and acceptance among pregnant people’	7
A preliminary adaptation and validation of the genetic counseling outcome scale (GCOS‐24) for use in Greece	7
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
A survey to analyze the need of genetic counseling among doctors in Lahore, Pakistan	6
Role of psychological background in cancer susceptibility genetic testing distress: It is not only about a positive result	6
Insights into genetic assistant practice and the workforce in North America	6
Issue Information	6
Use of digital health tools with point‐of‐care testing improves access to germline genetic testing within a gastrointestinal cancer clinic	6
The State of National Institute of Health Awards for funding genetic counseling research, resources, and training over the past decade	6
Both sides now: Changing a long‐standing pedigree tradition of men on the left and women on the right	6
Parents' perspectives of non‐informative germline genetic testing in children with Juvenile Polyposis Syndrome	6
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Proposed use of entrustable professional activities (EPAs) in genetic counseling for clinical training and assessment	6
The efficacy of genetic counseling for familial colorectal cancer: A meta‐analysis	6
Optimizing risk‐reducing surgery and aspirin decision aids for Lynch syndrome carriers using the person‐based approach: A think‐aloud interview study	6
Evaluating genetic counseling session duration: A scoping review of patient care time, influencing factors, and impact on patient outcomes	6
Host perspectives on international fieldwork placements for U.S.‐based genetic counseling students	6
Voices in practice: Exploring genetic counseling ethical, cultural, social, and religious dynamics in the UAE	6
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
Learning from our patients: Utilizing the expertise of transgender and/or gender diverse educators to build an inclusive learning cycle	5
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
Decision stability among adolescents and young adults making choices about learning genomic research results	5
A heartfelt thank you to the 2024 Journal of Genetic Counseling reviewers	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
Cross‐cultural validation of the genetic counseling outcome scale in Korea	5
Preferences of parents from diverse backgrounds on genomic screening of apparently healthy newborns	5
Cascade testing for inherited cardiac conditions: Risk perception and screening after a negative genetic test result	5
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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
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
Assessing patient communication preferences for reclassified variants of uncertain significance in a general genetics clinic	5
A Filipinized view of the counselor‐client relationship in genetic counseling	5
An investigation of preceptors' perceptions of behavioral elements of “professionalism” among genetic counseling students	5
Familial communication and cascade testing following elective genomic testing	5
Factors associated with US and Canadian genetic counselors' testing decisions during pregnancy	5
The impact of cohort relationships on BIPOC genetic counseling students: Results from a longitudinal qualitative study	5
Experiences of Dutch parents undergoing prenatal genomic testing for fetal structural anomalies: A prospective qualitative analysis	5
Characterizing the research mentorship experience of genetic counseling students	5
Adolescents' and young adults' reactions to and perceived utility of carrier screening results in the context of a genomic research study	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
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The erasure of transgender and intersex identities through fetal sex prediction and genetic essentialism	5
Exploring genetic counselors' experiences with non‐paternity in clinical settings	5
Issue Information	5
COVID‐19 vaccine hesitancy and acceptance among pregnant people contacting a teratogen information service	5
2024 National Society of Genetic Counselors presidential address: The path we take	5
Navigating complexity: How shifting abortion regulations impacted prenatal genetic counselors practicing in restrictive states from 2020 to 2024	5
Issue Information	5
Pediatric predictive testing to inform preimplantation genetic testing: A case report and review of the literature	4
Need for specially designed educational support groups: Young women's experiences of being identified with BRCA pathogenic variants	4
Issues, challenges, and future perspectives of genetic counseling in Republic of Korea: Perspectives of laboratory physicians based on a 2022 survey	4
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	4
Evaluating a communication aid for return of genetic results in families with hypertrophic cardiomyopathy: A randomized controlled trial	4
Bringing Genetics to Mental Health: Integrating Genetic Counseling into a Mental Health Program at Monash Health, Australia	4
Development of genetic assistant competencies using the Delphi consensus building method	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
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Issue Information	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
Clinical and laboratory genetic counselor attitudes on the reporting of variants of uncertain significance for multigene cancer panels	4
Ethno‐racial differences in the frequency of cancer reported from family pedigrees in the prenatal genetic counseling setting	4
Paternal expanded carrier screening after positive maternal results: Perceptions and barriers to screening	4

Attitudes and beliefs regardingrace‐targetedgenetic testing of Black people: A systematic review	4
Assessing perceived empathy based on genetic counselor gender using a randomized, hypothetical prenatal genetic counseling scenario design	4
Expanded carrier screening for inherited genetic disease using exome and genome sequencing	4
Understanding and issues related to next‐generation sequencing among educated laypersons in India	4
Assessing management practices for variants of uncertain significance among genetic counselors in pediatrics	4
Western Australian women's expectations for expanded NIPT—An online survey regarding NIPT for single gene, recessive and chromosomal conditions	4
Awareness and knowledge of familial breast and ovarian cancer among German general practice patients	4
Clinical geneticists' views on and experiences with unsolicited findings in next‐generation sequencing: “A great technology creating new dilemmas”	4
A qualitative exploration of experiences of gender identity and gender questioning among adults with Klinefelter syndrome/XXY	4
Outcomes of pregnancies that screened positive for sex chromosome aneuploidy ascertained via cell‐free DNA screening	4
Use of a chatbot to increase uptake of cascade genetic testing	4
Does the amount of family history matter? Perspectives of adult adoptees	4
Research methodologies in genetic counseling: Grounded theory	4
Uptake of genetic testing among patients seeking cancer genetic counseling in Taiwan	4
Race, ethnicity, and ancestry reporting in genetic counseling research: A focused mapping review and synthesis	4
Cascade testing in an ovarian cancer traceback genetic testing program: The GRACE study experience	4
Links between gender norms and the intergenerational transmission of health information in parents carrying BRCA1/2 pathogenic variants	4
Application of the RIME framework in genetic counseling fieldwork training to assess practice‐based competencies	4
An introduction to Delphi studies and consensus methods for genetic counselors	4
Introduction of the genetic counseling profession by teachers in BIPOC‐majority high schools	4
Implementing genetic screening into primary care for medically actionable conditions: Insights from a precision health pilot program	4
Reading and writing reviews: A primer on systematic, scoping, and narrative reviews for genetic counselors	4
To be or not to be (honest): The persistent problem of misattributed paternity	4
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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
Group meditation, addressing stigma, and “mental health days”: Recommendations for integrating self‐awareness practices into genetic counseling graduate programs	4
How genetic counselors in North America describe their professional identity	4
Subspecialty neurology genetic counselors—A cost effective solution to substantial time costs associated with genomic testing in the neurology clinic	4
Issue Information	4
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Evaluating pregnancy termination rates for fetal chromosome and single gene disorders	4
Picture this: Evaluating the efficacy of genetic counseling visual aids	3
Microlearning: Evidence‐based education that is effective for busy professionals and short attention spans	3
BRCAShare—Assessment of an animated digital message for intrafamilial communication of pathogenic variant positive test results: A feasibility study	3
Acceptability, consideration, intention, and uptake of six common types of direct‐to‐consumer genetic tests in the Netherlands	3
Genetic counseling students' use of patient‐centered communication skills predicts standardized patient satisfaction during virtual simulated sessions	3
The book is just being written: The enduring journey of parents of children with emerging‐ ultrarare disorders	3
Something to chat about: An analysis of genetic counseling via asynchronous messaging following direct‐to‐consumer genetic testing	3
Sponsored genetic testing and informed consent implications: Experience and attitudes of genetic counselors	3
Evaluation of prenatal genetic counselors' abortion education and training as variables associated with self‐efficacy	3
Exploring the occurrence of microaggressions in the genetic counseling student–supervisor relationship: A mixed‐methods study	3
A cross‐sectional survey‐based exploration of diversity in the admissions committees and student cohorts of genetic counseling programs over time	3
Adoptees' experiences of using direct‐to‐consumer genetic testing and determinants of this use: A mixed study in Quebec	3
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Examining aspects of job satisfaction associated with burnout and factors related to turnover intention in genetic counselors	3
Genetics providers’ experiences using telehealth: A grounded theory approach	3
Further defining the roles and impact of genetic counselors in the biotechnology and pharmaceutical industry	3
Issue Information	3
Exploring Canadian genetic counselors' perspectives and experiences with discussing medical assistance in dying (MAiD)	3
A guide to utilizing implementation science for genetic counseling	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
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
Readiness and leadership for the implementation of polygenic risk scores: Genetic healthcare providers' perspectives in the hereditary cancer context	3
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Parent experiences with genetic testing for pediatric hearing loss	3
Experience conducting a community‐engaged student research project involving an underrepresented community: A reflective essay	3
Training for the future of the genetic counseling profession: Exploring the assessment and adaptation of graduate programs' didactic curriculum	3
Promoting the integration of genetic counseling education and research across the spectrum of learners at a large academic institution	3
Paid summer undergraduate internships are one strategy to increase diversity in genetic counseling	3
The Genetic Information Nondiscrimination Act and workplace genetic testing: Knowledge and perceptions of employed adults in the United States	3
Genetic counseling training program perspectives on delivering disability‐related education	3
Issue Information	3
Creation and beta testing of a “choose your own adventure” digital simulation to reinforce motivational interviewing skills in genetic counseling	3
Ethical concerns surrounding sex prediction using noninvasive prenatal screening from pediatric endocrinologists' perspective	3
Promotores' perspectives on the virtual adaptation of a hereditary breast cancer education program	3
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	3
Views of genetic health professionals, patients, and next of kin on retesting and recontact with results from updated genetic testing	3
Experiences of genetic counselors practicing in multiple languages: Progress and places for improvement	3
Psychosocial issues of individuals undergoing surveillance for increased risk of melanoma and pancreatic cancer due to a germline CDKN2A variant: A focus group study	3
Psychiatric genetic counseling: A survey of Australian genetic counselors' practice and attitudes	3
Survey research in genetic counseling	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
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
Cross‐cultural adaptation and validation of a French version of the perceived personal control questionnaire as an outcome measure instrument for genetic counseling	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
Leveling the field: Development of an asynchronous interactive module series for genetic counseling trainees on molecular testing and variant interpretation	3
Expanding the methodological repertoire: Integrating multimodal approaches in genetic counseling research	3
Incidental finding of maternal sex chromosome aneuploidy from DMD carrier screening and single‐nucleotide polymorphism (SNP)‐based prenatal cell‐free DNA screening	3
Parent‐reported genetic counselor adherence to the NSGC practice resource for communicating a potential prenatal diagnosis: Impact on the Down syndrome diagnosis experience	3
Perspectives of genetic counseling supervisors regarding genetic counseling students' attainment of practice‐based competencies in clinical care through remote supervision	3
Dilemmas when talking about Huntington's disease: A qualitative study of offspring and caregiver experiences in Norway	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
Issue Information	2
Healthcare professionals' perspectives on supporting individuals with NF1 during pregnancy and decision‐making processes	2
Australasian genetic counselors' attitudes toward disability and prenatal testing: Findings from a cross‐sectional survey	2
Referral networks for pediatric patients with genetic conditions: The perspective of occupational therapists	2
Genetic counselors providing care to inpatients experience moral distress	2
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Embedding simulation in genetic counselor education from the first week of training: Learning outcomes, standardized clients, and students' satisfaction	2
Genetic health professionals' facilitation of communication between parents and young children about inherited genetic conditions: A scoping review	2
Navigating sexual orientation and gender identity data privacy concerns in United States genetics practices	2
Attitudes of parents of children with ADHD towards genetic testing: Data from a Turkish sample	2
Counseling in a different language: An analysis of experiences and resources in multilingual genetic counseling	2
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