Journal of Genetic Counseling

Article	Citations
Issue Information	87
Clients' experiences of empathy in genetic counseling for hereditary breast and ovarian cancer: A qualitative study in Japan	59
Barriers in applying to genetic counseling Master's degree programs: Perceptions of prospective applicants when compared with Canadian admissions committee members	57
Acceptability of an online communication training intervention for genetic counseling students	46
Women's thoughts on receiving and sharing genetic information: Considerations for genetic counseling	44
An internship in psychiatric genetic counseling: Impact on genetic counseling graduates' practice and career choices	27
Genetic counseling program remediation practices for students underperforming in clinical skills: An exploratory study	23
Exploring spiritual/religious coping strategies among mothers of children with severe or profound intellectual disability during genetic counseling in Brazil	21
Perinatal palliative care for family with prenatal diagnosis of Matthew‐Wood syndrome	19
Characterization of variant reclassification and patient re‐contact in a cancer genetics clinic	18
Sudden cardiac death in the young: A qualitative study of experiences of family members with cardiogenetic evaluation	18
Misattributed parentage identified through diagnostic exome sequencing: Frequency of detection and reporting practices	17
Supervision for genetic counselors: The role of career‐long supervision to develop resilient practitioners	17
Courtesy stigma of parents of children with Down syndrome: Adaptation process and transcendent stage	17
Women's preferences for NIPT as a first‐line test in England and France: Challenges for genetic counseling practices	16
Narrative review on ethical and psychological issues raised by genetic and genomic testing in pediatric oncology care	16
Genetic testing for Parkinson's disease in an underrepresented population: Knowledge, attitudes, and ethical considerations from a Malaysian perspective	16
Application of motivational interviewing strategies with the extended parallel process model to improve risk communication for parents of children with familial hypercholesterolemia	16
Identifying potential genetic counseling program applicant competencies	15
Incorporating multiracial and multiethnic experiences into genetic counseling practice and research: A necessary opportunity	15
Reply to Rathbun and Paulyson Nuñez	15
Genetic counseling for fetal sex prediction by NIPT: Challenges and opportunities	14
Genetic counseling in diabetes mellitus: A practice resource of the National Society of Genetic Counselors	13
Exploring parental cystic fibrosis disclosure to well children	13
The attitudes of individuals with or at risk of adult‐onset genetic conditions on reproductive genetic testing: A systematic review	13

Invisible diversities, academic capital, and competitiveness of genetic counseling applicants	12
From intention to action: Assessing need and creating a JEDI toolkit for individuals teaching cancer genetics curriculum	12
Issue Information	12
A qualitative study exploring LGBTQ genetic counseling students' relationships with peers and faculty in graduate school	12
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Prospective parents' views on reproductive genetic carrier screening: “You know better, you do better”	12
Pregnant people's views and knowledge on prenatal screening for fetal trisomy in the absence of a national screening program	12
Graduate training, credentialing, and continuing education to prepare genetic counselors for laboratory roles—Results of a national survey	12
Issue Information	11
Correction to “Who is at risk for compassion fatigue? An investigation of genetic counselor demographics, anxiety, compassion satisfaction, and burnout”	11
Clinical Bootcamp: Moving toward competency outside of the clinic	11
Investigating genetic counselors' communication with Lynch syndrome patients about cascade testing: Barriers, facilitators, and strategies	10
The experiences of families receiving a diagnosis of 22q11.2 deletion syndrome in Ireland	10
Issue Information	10
A cross‐professional competency framework for communicating genomic results	10
Uptake rates for non‐invasive prenatal screening for single‐gene disorders associated with advanced paternal age	10
Patient perceptions of genetic counselors' role and emotional support needs in adults with Parkinson's disease	9
Evaluation of face validity and core concepts of a novel knowledge scale for inherited heart disease: A pilot study	9
Assessing and attending to psychosocial concerns in genetic counseling: Proposing the BATHE method	9
The effect of knowledge and person‐related factors on breast cancer susceptibility genes (BRCA1/2) testing perception in Turkish women	9
Beyond multiple choice: Clinical simulation as a rigorous and inclusive method for assessing genetic counseling competencies	8
Strength of the genetic counselor: patient relationship is associated with extent of increased empowerment in patients with arrhythmogenic cardiomyopathy	8
Mothers' reflections on the diagnosis and birth of their child with Down syndrome: Variability based on the timing of the diagnosis	8
Genetic counseling for adult‐onset neurogenetic conditions in Hispanic/Latine communities: A qualitative study of barriers and facilitators from Hispanic/Latine genetic counselors' perspectives	8
Assessing the perspectives of genetic counselors with oncology patients at the end of life	8
Buying my existence. Just $49, free shipping included	8
Workplace perk or pitfall? A qualitative study of genetic counselors' perspectives and experiences with workplace genetic testing	8
Performance of the shared decision‐making process scale for use in evaluation of hereditary cancer genetic testing decisions	8
BIPOC genetic counseling students' perspectives on career‐oriented social media use: Results from a longitudinal qualitative study	8
Genetic Counselors' attitudes & perceptions regarding suicide risk assessment and identification in practice	8
The review of genetic screening services and common BRCA1/2 variants among South African breast cancer patients	8
How parents of children with ataxia‐telangiectasia use dynamic coping to navigate cyclical uncertainty	8
Lessons learned from BRCA1/2 screening in Israel: A cross‐sectional survey comparing experiences and communication	8
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	7
Experiences of genetic counseling students with disabilities and chronic illnesses: A qualitative study	7
Evaluating attributes of a collaborative model of service delivery for hereditary cancer risk assessment	7
Evaluating a general pediatric/adult genetic counseling clinic in a Midwest medical center	7
Genetic testing and counseling for hypertrophic cardiomyopathy: An evidence‐based practice resource of the National Society of Genetic Counselors	7
Cardiac genetic counseling services: Exploring downstream revenue in a pediatric medical center	7
Noninvasive prenatal screening (NIPS) results for participants of the eXtraordinarY babies study: Screening, counseling, diagnosis, and discordance	7
Genetic counselors and congenital heart disease: Clinical roles, genetic testing practices, and perceived genetic testing utility	7
The development and preliminary evaluation of the Genetic Counseling Skills Checklist	7
Current attitudes toward carrier screening for spinal muscular atrophy among pregnant women in Eastern China	7
The long‐term impact of receiving incidental findings on parents undergoing genome‐wide sequencing	7
Changes in acceptability, consideration, intention, and uptake of direct‐to‐consumer genetic tests in the Netherlands from 2017 to 2022	7
Genetic counselors' experience with reimbursement and patient out‐of‐pocket cost for multi‐cancer gene panel testing for hereditary cancer syndromes	7
How should we address the inevitable harms from non‐negligent variant reclassification in predictive genetic testing?	7
Medical students' self‐perceived knowledge and clinical comfort with genetics in Pakistan	7
The goldilocks conundrum: Disclosing discrimination risks in informed consent	7

North American genetic counselors' approach to collecting and using ancestry in clinical practice	7
Primary care patient and clinician attitudes about population genomic screening, informed decision‐making needs, and the potential for Chatbot technology	6
Impacts of student debt on the professional and personal lives of genetic counselors: A 10‐year perspective	6
Examining the communication work of women who have tested BRCA‐positive: “I feel this responsibility to let people know”	6
Both sides now: Changing a long‐standing pedigree tradition of men on the left and women on the right	6
Exploring genetic counselors' interest and role in transitional care discussions for pediatric patients with neurodevelopmental conditions	6
A preliminary adaptation and validation of the genetic counseling outcome scale (GCOS‐24) for use in Greece	6
Experiences of hereditary cancer care among transgender and gender diverse people: “It's gender. It's cancer risk…it's everything”	6
A comment on ‘COVID‐19 vaccine hesitancy and acceptance among pregnant people’	6
Assessing the relationship between patient preferences for recontact after BRCA1 or BRCA2 genetic testing and their monitoring coping style in a Norwegian sample	6
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”	6
Clinical genetic counselors' use of people‐ and identity‐first language in regard to patients' identification with disability	6
Leadership development in genetic counseling graduate programs	6
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Host perspectives on international fieldwork placements for U.S.‐based genetic counseling students	5
Insights into genetic assistant practice and the workforce in North America	5
Role of psychological background in cancer susceptibility genetic testing distress: It is not only about a positive result	5
Issue Information	5
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Development of the Affiliate Stigma Scale for parents of children with genetic conditions	5
Qualitative analysis of the needs of parents of children with rare genetic diseases, following their diagnosis obtained by whole‐exome sequencing	5
Building a foundation in self‐awareness: Genetic counseling students’ experiences with self‐care, reflection, and mindfulness	5
Proposed use of entrustable professional activities (EPAs) in genetic counseling for clinical training and assessment	5
Optimizing risk‐reducing surgery and aspirin decision aids for Lynch syndrome carriers using the person‐based approach: A think‐aloud interview study	5
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	5
Evaluating genetic counseling session duration: A scoping review of patient care time, influencing factors, and impact on patient outcomes	5
Use of digital health tools with point‐of‐care testing improves access to germline genetic testing within a gastrointestinal cancer clinic	5
Exploring the journey to genomic testing and genetic services: A qualitative study of parental perspectives of children with rare conditions	5
Experience with a nurse‐driven genetic counseling pathway of Italian women with uninformative BRCA test result	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
A survey to analyze the need of genetic counseling among doctors in Lahore, Pakistan	5
Perceived cancer risk and genetic counseling: A biopsychological perspective	5
The efficacy of genetic counseling for familial colorectal cancer: A meta‐analysis	5
Adolescents' and young adults' reactions to and perceived utility of carrier screening results in the context of a genomic research study	4
Does the amount of family history matter? Perspectives of adult adoptees	4
Preferences of parents from diverse backgrounds on genomic screening of apparently healthy newborns	4
Elicitation of children’s understanding of information in pediatric genetic counseling encounters: A discourse‐oriented perspective	4
A heartfelt thank you to the 2024 Journal of Genetic Counseling reviewers	4
Need for specially designed educational support groups: Young women's experiences of being identified with BRCA pathogenic variants	4
Ethno‐racial differences in the frequency of cancer reported from family pedigrees in the prenatal genetic counseling setting	4
Evaluating pregnancy termination rates for fetal chromosome and single gene disorders	4
Clinical geneticists' views on and experiences with unsolicited findings in next‐generation sequencing: “A great technology creating new dilemmas”	4
Cross‐cultural validation of the genetic counseling outcome scale in Korea	4
Issue Information	4
Cascade testing for inherited cardiac conditions: Risk perception and screening after a negative genetic test result	4
Reading and writing reviews: A primer on systematic, scoping, and narrative reviews for genetic counselors	4
Transgender patients’ perspectives on their cancer genetic counseling experiences	4
Learning from our patients: Utilizing the expertise of transgender and/or gender diverse educators to build an inclusive learning cycle	4
Race, ethnicity, and ancestry reporting in genetic counseling research: A focused mapping review and synthesis	4
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Expanded carrier screening for inherited genetic disease using exome and genome sequencing	4
Graduate training during the COVID‐19 pandemic: North American genetic counseling students' challenges, intolerance of uncertainty, and psychological well‐being	4
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The erasure of transgender and intersex identities through fetal sex prediction and genetic essentialism	4
Assessing perceived empathy based on genetic counselor gender using a randomized, hypothetical prenatal genetic counseling scenario design	4
Experiences of reproductive genetic counselors with abortion regulations in Ohio	4
Awareness of genetic counseling and genetic testing for hereditary gynecologic cancers among Korean healthcare providers: A survey	4
Assessing genetic counselors’ graduate school education and training in congenital heart defects	4
Association between proband characteristics and CDH1 cascade genetic testing uptake in at‐risk relatives	4
Decision stability among adolescents and young adults making choices about learning genomic research results	4
Evaluation of barriers to referral for cancer predisposition syndromes in pediatric oncology patients in the United States	4
Attitudes and training needs of oncologists and surgeons in mainstreaming breast cancer genetic counseling in a low‐to‐middle income Asian country	4
Unlocking the next phase of development for our profession: Developing and consolidating the recognition of genetic counseling as a rigorous area of academic study	4
Evaluating a communication aid for return of genetic results in families with hypertrophic cardiomyopathy: A randomized controlled trial	4
The impact of cohort relationships on BIPOC genetic counseling students: Results from a longitudinal qualitative study	4
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COVID‐19 vaccine hesitancy and acceptance among pregnant people contacting a teratogen information service	4
Factors associated with US and Canadian genetic counselors' testing decisions during pregnancy	4
Evolving approaches to prenatal genetic counseling for Spinal Muscular Atrophy in the new treatment era	4
2024 National Society of Genetic Counselors presidential address: The path we take	4
Western Australian women's expectations for expanded NIPT—An online survey regarding NIPT for single gene, recessive and chromosomal conditions	4
Exploring genetic counselors' experiences with non‐paternity in clinical settings	4
Research to reduce inequities in cancer risk services: Insights for remote genetic counseling in a pandemic and beyond	4
Uptake of genetic testing among patients seeking cancer genetic counseling in Taiwan	4
Issue Information	4
An investigation of preceptors' perceptions of behavioral elements of “professionalism” among genetic counseling students	4
Navigating complexity: How shifting abortion regulations impacted prenatal genetic counselors practicing in restrictive states from 2020 to 2024	4
Attitudes and beliefs regardingrace‐targetedgenetic testing of Black people: A systematic review	4
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Characterizing the research mentorship experience of genetic counseling students	4
Issues, challenges, and future perspectives of genetic counseling in Republic of Korea: Perspectives of laboratory physicians based on a 2022 survey	4
Influence of genetic counselor medical history on specialty and psychosocial practice in North America	4
The State of National Institute of Health Awards for funding genetic counseling research, resources, and training over the past decade	4
Familial communication and cascade testing following elective genomic testing	4
Understanding and issues related to next‐generation sequencing among educated laypersons in India	4
A report of the AGCPD task force to evaluate associations between select admissions requirements, demographics, and performance on ABGC certification examination	3
Awareness and knowledge of familial breast and ovarian cancer among German general practice patients	3
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	3
Picture this: Evaluating the efficacy of genetic counseling visual aids	3
Group meditation, addressing stigma, and “mental health days”: Recommendations for integrating self‐awareness practices into genetic counseling graduate programs	3
The book is just being written: The enduring journey of parents of children with emerging‐ ultrarare disorders	3
Clinical and laboratory genetic counseling assistants: Comparing background experiences, responsibilities, satisfaction, and career goals	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
Issue Information	3
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	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
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	3
Genetic counseling students' use of patient‐centered communication skills predicts standardized patient satisfaction during virtual simulated sessions	3
Subspecialty neurology genetic counselors—A cost effective solution to substantial time costs associated with genomic testing in the neurology clinic	3
To be or not to be (honest): The persistent problem of misattributed paternity	3
Empathy experiences of Japanese certified genetic counselors: A qualitative investigation and proposed framework	3
Experience conducting a community‐engaged student research project involving an underrepresented community: A reflective essay	3
Application of the RIME framework in genetic counseling fieldwork training to assess practice‐based competencies	3
Experiences of genetic counselors practicing in multiple languages: Progress and places for improvement	3
Perspectives of genetic counseling supervisors regarding genetic counseling students' attainment of practice‐based competencies in clinical care through remote supervision	3
Psychiatric genetic counseling: A survey of Australian genetic counselors' practice and attitudes	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
Ethical concerns surrounding sex prediction using noninvasive prenatal screening from pediatric endocrinologists' perspective	3
Patterns of germline and somatic testing after universal tumor screening for Lynch syndrome: A clinical practice survey of active members of the Collaborative Group of the Americas on Inherited Gastro	3
Outcomes of pregnancies that screened positive for sex chromosome aneuploidy ascertained via cell‐free DNA screening	3
Readiness and leadership for the implementation of polygenic risk scores: Genetic healthcare providers' perspectives in the hereditary cancer context	3
Clinical and laboratory genetic counselor attitudes on the reporting of variants of uncertain significance for multigene cancer panels	3
Exploring the occurrence of microaggressions in the genetic counseling student–supervisor relationship: A mixed‐methods study	3
Issue Information	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
Introduction of the genetic counseling profession by teachers in BIPOC‐majority high schools	3
Promoting the integration of genetic counseling education and research across the spectrum of learners at a large academic institution	3
Links between gender norms and the intergenerational transmission of health information in parents carrying BRCA1/2 pathogenic variants	3
Exploring Canadian genetic counselors' perspectives and experiences with discussing medical assistance in dying (MAiD)	3
A qualitative exploration of experiences of gender identity and gender questioning among adults with Klinefelter syndrome/XXY	3
Pediatric predictive testing to inform preimplantation genetic testing: A case report and review of the literature	3
Creation and beta testing of a “choose your own adventure” digital simulation to reinforce motivational interviewing skills in genetic counseling	3
Investigating factors that influence genetic counselors’ decisions to refer patients to mental health providers	3
Further defining the roles and impact of genetic counselors in the biotechnology and pharmaceutical industry	3
Something to chat about: An analysis of genetic counseling via asynchronous messaging following direct‐to‐consumer genetic testing	3
BRCAShare—Assessment of an animated digital message for intrafamilial communication of pathogenic variant positive test results: A feasibility study	3
Adoptees' experiences of using direct‐to‐consumer genetic testing and determinants of this use: A mixed study in Quebec	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
The Genetic Information Nondiscrimination Act and workplace genetic testing: Knowledge and perceptions of employed adults in the United States	3
Assessing management practices for variants of uncertain significance among genetic counselors in pediatrics	3
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Use of a chatbot to increase uptake of cascade genetic testing	3
Issue Information	3
Exploring United States genetic counselor and healthcare interpreter perspectives: Allocation of roles within the genetic counseling encounter	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
Research methodologies in genetic counseling: Grounded theory	3