Journal of Genetic Counseling

Article	Citations
Issue Information	125
Acceptability of an online communication training intervention for genetic counseling students	83
Barriers in applying to genetic counseling Master's degree programs: Perceptions of prospective applicants when compared with Canadian admissions committee members	64
Identifying potential genetic counseling program applicant competencies	55
Reply to Rathbun and Paulyson Nuñez	43
Factors impacting experience of genetic testing among adults with inherited retinal diseases	38
Women's preferences for NIPT as a first‐line test in England and France: Challenges for genetic counseling practices	32
Provider perceptions and insights on polygenic risk scores for colorectal cancer: A qualitative study	28
Genetic counseling program remediation practices for students underperforming in clinical skills: An exploratory study	26
Perinatal palliative care for family with prenatal diagnosis of Matthew‐Wood syndrome	25
Exploring parental cystic fibrosis disclosure to well children	23
Genetic counseling in diabetes mellitus: A practice resource of the National Society of Genetic Counselors	22
Sudden cardiac death in the young: A qualitative study of experiences of family members with cardiogenetic evaluation	21
The attitudes of individuals with or at risk of adult‐onset genetic conditions on reproductive genetic testing: A systematic review	21
Genetic counseling for fetal sex prediction by NIPT: Challenges and opportunities	19
Clients' experiences of empathy in genetic counseling for hereditary breast and ovarian cancer: A qualitative study in Japan	18
Incorporating multiracial and multiethnic experiences into genetic counseling practice and research: A necessary opportunity	18
Genetic testing for Parkinson's disease in an underrepresented population: Knowledge, attitudes, and ethical considerations from a Malaysian perspective	14
Narrative review on ethical and psychological issues raised by genetic and genomic testing in pediatric oncology care	14
Supervision for genetic counselors: The role of career‐long supervision to develop resilient practitioners	14
Exploring spiritual/religious coping strategies among mothers of children with severe or profound intellectual disability during genetic counseling in Brazil	14
Uptake rates for non‐invasive prenatal screening for single‐gene disorders associated with advanced paternal age	13
Investigating genetic counselors' communication with Lynch syndrome patients about cascade testing: Barriers, facilitators, and strategies	13
Issue Information	13
The effect of knowledge and person‐related factors on breast cancer susceptibility genes (BRCA1/2) testing perception in Turkish women	13

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

Experiences of genetic counseling students with disabilities and chronic illnesses: A qualitative study	7
To refer or not to refer? Exploring the cognitive process of genetic counselors' decision to refer a patient to another professional	7
Current attitudes toward carrier screening for spinal muscular atrophy among pregnant women in Eastern China	7
A qualitative investigation of genetic counselors' experiences working with incarcerated patients	7
Evaluating attributes of a collaborative model of service delivery for hereditary cancer risk assessment	7
Experiences of hereditary cancer care among transgender and gender diverse people: “It's gender. It's cancer risk…it's everything”	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
Clinical genetic counselors' use of people‐ and identity‐first language in regard to patients' identification with disability	7
Perspectives of Italian lay persons who would decline genetic risk information: “I think I'd be living in constant worry”	7
The goldilocks conundrum: Disclosing discrimination risks in informed consent	7
The expected utility and psychological impacts of exome sequencing results in the DDD ‐Africa study	7
Leadership development in genetic counseling graduate programs	7
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Genetic counselors and congenital heart disease: Clinical roles, genetic testing practices, and perceived genetic testing utility	7
Medical students' self‐perceived knowledge and clinical comfort with genetics in Pakistan	7
A preliminary adaptation and validation of the genetic counseling outcome scale (GCOS‐24) for use in Greece	7
How should we address the inevitable harms from non‐negligent variant reclassification in predictive genetic testing?	7
Primary care patient and clinician attitudes about population genomic screening, informed decision‐making needs, and the potential for Chatbot technology	7
Providing space in genetic counseling: Reflexive thematic analysis of long and short sessions across clinical specialties	7
The development and preliminary evaluation of the Genetic Counseling Skills Checklist	7
Role of psychological background in cancer susceptibility genetic testing distress: It is not only about a positive result	6
Parents' perspectives of non‐informative germline genetic testing in children with Juvenile Polyposis Syndrome	6
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”	6
Use of digital health tools with point‐of‐care testing improves access to germline genetic testing within a gastrointestinal cancer clinic	6
Establishment of the genetic counselor profession in Ukraine: Present challenges and prospective pathways	6
The Clinical Pathway Initiative: Identifying role relevant competencies in genomic pathways	6
Voices in practice: Exploring genetic counseling ethical, cultural, social, and religious dynamics in the UAE	6
Evaluating genetic counseling session duration: A scoping review of patient care time, influencing factors, and impact on patient outcomes	6
The efficacy of genetic counseling for familial colorectal cancer: A meta‐analysis	6
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
Issue Information	6
Proposed use of entrustable professional activities (EPAs) in genetic counseling for clinical training and assessment	6
Insights into genetic assistant practice and the workforce in North America	6
A survey to analyze the need of genetic counseling among doctors in Lahore, Pakistan	6
Assessing patient communication preferences for reclassified variants of uncertain significance in a general genetics clinic	6
Optimizing risk‐reducing surgery and aspirin decision aids for Lynch syndrome carriers using the person‐based approach: A think‐aloud interview study	6
Host perspectives on international fieldwork placements for U.S.‐based genetic counseling students	6
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Both sides now: Changing a long‐standing pedigree tradition of men on the left and women on the right	6
Qualitative analysis of the needs of parents of children with rare genetic diseases, following their diagnosis obtained by whole‐exome sequencing	6
Quality‐of‐life after risk‐reducing mastectomy in women with increased risk of breast cancer: A longitudinal study	6
Perceived cancer risk and genetic counseling: A biopsychological perspective	6
Experience with a nurse‐driven genetic counseling pathway of Italian women with uninformative BRCA test result	6
Exploring the journey to genomic testing and genetic services: A qualitative study of parental perspectives of children with rare conditions	6
Cross‐cultural validation of the genetic counseling outcome scale in Korea	5
Characterizing the research mentorship experience of genetic counseling students	5
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Navigating complexity: How shifting abortion regulations impacted prenatal genetic counselors practicing in restrictive states from 2020 to 2024	5
Experiences of Dutch parents undergoing prenatal genomic testing for fetal structural anomalies: A prospective qualitative analysis	5
Ethno‐racial differences in the frequency of cancer reported from family pedigrees in the prenatal genetic counseling setting	5
Uptake of genetic testing among patients seeking cancer genetic counseling in Taiwan	5
Factors That Influence Genetic Counselors' Professional Identity—A Qualitative Study	5
Attitudes and beliefs regardingrace‐targetedgenetic testing of Black people: A systematic review	5
Understanding shared and sex‐specific considerations in hereditary breast and ovarian cancer ( HBOC ) testing decision‐making in Singapore	5
An investigation of preceptors' perceptions of behavioral elements of “professionalism” among genetic counseling students	5
Learning from our patients: Utilizing the expertise of transgender and/or gender diverse educators to build an inclusive learning cycle	5
Familial communication and cascade testing following elective genomic testing	5
2024 National Society of Genetic Counselors presidential address: The path we take	5
Issue Information	5
The State of National Institute of Health Awards for funding genetic counseling research, resources, and training over the past decade	5
The erasure of transgender and intersex identities through fetal sex prediction and genetic essentialism	5
Issue Information	5
Evaluating a communication aid for return of genetic results in families with hypertrophic cardiomyopathy: A randomized controlled trial	5
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Decision stability among adolescents and young adults making choices about learning genomic research results	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
Paternal expanded carrier screening after positive maternal results: Perceptions and barriers to screening	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
Cascade testing in an ovarian cancer traceback genetic testing program: The GRACE study experience	5
Exploring genetic counselors' experiences with non‐paternity in clinical settings	5
Race, ethnicity, and ancestry reporting in genetic counseling research: A focused mapping review and synthesis	5
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Association between proband characteristics and CDH1 cascade genetic testing uptake in at‐risk relatives	5
Development of the Affiliate Stigma Scale for parents of children with genetic conditions	5
Preferences of parents from diverse backgrounds on genomic screening of apparently healthy newborns	5
Adolescents' and young adults' reactions to and perceived utility of carrier screening results in the context of a genomic research study	5
Western Australian women's expectations for expanded NIPT—An online survey regarding NIPT for single gene, recessive and chromosomal conditions	5
Issue Information	5
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The impact of cohort relationships on BIPOC genetic counseling students: Results from a longitudinal qualitative study	5

Evaluating pregnancy termination rates for fetal chromosome and single gene disorders	5
A Filipinized view of the counselor‐client relationship in genetic counseling	5
A heartfelt thank you to the 2024 Journal of Genetic Counseling reviewers	5
Issue Information	4
Expanded carrier screening for inherited genetic disease using exome and genome sequencing	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
Reading and writing reviews: A primer on systematic, scoping, and narrative reviews for genetic counselors	4
A pilot qualitative study of patient understanding and perceptions of genetic counselors and cascade testing in the context of transthyretin cardiac amyloidosis	4
Consumer Experiences and Perceptions of Genetic Counseling in Provider‐Mediated Genetic Testing	4
A qualitative exploration of experiences of gender identity and gender questioning among adults with Klinefelter syndrome/XXY	4
Need for specially designed educational support groups: Young women's experiences of being identified with BRCA pathogenic variants	4
Exploring Canadian genetic counselors' perspectives and experiences with discussing medical assistance in dying (MAiD)	4
Group meditation, addressing stigma, and “mental health days”: Recommendations for integrating self‐awareness practices into genetic counseling graduate programs	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
Genetic Counselors as Research Leaders: A Pragmatic Pathway to Becoming a Federally Funded Principal Investigator in the United States	4
To be or not to be (honest): The persistent problem of misattributed paternity	4
Clinical and laboratory genetic counselor attitudes on the reporting of variants of uncertain significance for multigene cancer panels	4
Assessing management practices for variants of uncertain significance among genetic counselors in pediatrics	4
How genetic counselors in North America describe their professional identity	4
An introduction to Delphi studies and consensus methods for genetic counselors	4
Does the amount of family history matter? Perspectives of adult adoptees	4
Implementing genetic screening into primary care for medically actionable conditions: Insights from a precision health pilot program	4
Links between gender norms and the intergenerational transmission of health information in parents carrying BRCA1/2 pathogenic variants	4
BRCAShare—Assessment of an animated digital message for intrafamilial communication of pathogenic variant positive test results: A feasibility study	4
Development of genetic assistant competencies using the Delphi consensus building method	4
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	4
Clinical geneticists' views on and experiences with unsolicited findings in next‐generation sequencing: “A great technology creating new dilemmas”	4
Outcomes of pregnancies that screened positive for sex chromosome aneuploidy ascertained via cell‐free DNA screening	4
Understanding and issues related to next‐generation sequencing among educated laypersons in India	4
Awareness and knowledge of familial breast and ovarian cancer among German general practice patients	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
Clinical and laboratory genetic counseling assistants: Comparing background experiences, responsibilities, satisfaction, and career goals	4
Pediatric predictive testing to inform preimplantation genetic testing: A case report and review of the literature	4
Research methodologies in genetic counseling: Grounded theory	4
Subspecialty neurology genetic counselors—A cost effective solution to substantial time costs associated with genomic testing in the neurology clinic	4
Application of the RIME framework in genetic counseling fieldwork training to assess practice‐based competencies	4
Repercussions of Diagnostic Delay in Rare Diseases	4
Introduction of the genetic counseling profession by teachers in BIPOC‐majority high schools	4
Something to chat about: An analysis of genetic counseling via asynchronous messaging following direct‐to‐consumer genetic testing	4
Assessing perceived empathy based on genetic counselor gender using a randomized, hypothetical prenatal genetic counseling scenario design	4
Experiences of genetic counselors practicing in multiple languages: Progress and places for improvement	4
Issues, challenges, and future perspectives of genetic counseling in Republic of Korea: Perspectives of laboratory physicians based on a 2022 survey	4
Ethical concerns surrounding sex prediction using noninvasive prenatal screening from pediatric endocrinologists' perspective	4
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Genetic counseling students' use of patient‐centered communication skills predicts standardized patient satisfaction during virtual simulated sessions	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
Bringing Genetics to Mental Health: Integrating Genetic Counseling into a Mental Health Program at Monash Health, Australia	4