Journal of Genetic Counseling

Article	Citations
Issue Information	94
Acceptability of an online communication training intervention for genetic counseling students	63
Barriers in applying to genetic counseling Master's degree programs: Perceptions of prospective applicants when compared with Canadian admissions committee members	62
Factors impacting experience of genetic testing among adults with inherited retinal diseases	48
Provider perceptions and insights on polygenic risk scores for colorectal cancer: A qualitative study	46
The attitudes of individuals with or at risk of adult‐onset genetic conditions on reproductive genetic testing: A systematic review	30
Identifying potential genetic counseling program applicant competencies	22
Narrative review on ethical and psychological issues raised by genetic and genomic testing in pediatric oncology care	21
Genetic testing for Parkinson's disease in an underrepresented population: Knowledge, attitudes, and ethical considerations from a Malaysian perspective	21
Courtesy stigma of parents of children with Down syndrome: Adaptation process and transcendent stage	18
Exploring parental cystic fibrosis disclosure to well children	18
Supervision for genetic counselors: The role of career‐long supervision to develop resilient practitioners	18
Reply to Rathbun and Paulyson Nuñez	18
Genetic counseling program remediation practices for students underperforming in clinical skills: An exploratory study	17
An internship in psychiatric genetic counseling: Impact on genetic counseling graduates' practice and career choices	16
Clients' experiences of empathy in genetic counseling for hereditary breast and ovarian cancer: A qualitative study in Japan	16
Exploring spiritual/religious coping strategies among mothers of children with severe or profound intellectual disability during genetic counseling in Brazil	16
Women's thoughts on receiving and sharing genetic information: Considerations for genetic counseling	16
Perinatal palliative care for family with prenatal diagnosis of Matthew‐Wood syndrome	16
Genetic counseling in diabetes mellitus: A practice resource of the National Society of Genetic Counselors	16
Genetic counseling for fetal sex prediction by NIPT: Challenges and opportunities	15
Characterization of variant reclassification and patient re‐contact in a cancer genetics clinic	14
Sudden cardiac death in the young: A qualitative study of experiences of family members with cardiogenetic evaluation	14
Women's preferences for NIPT as a first‐line test in England and France: Challenges for genetic counseling practices	13
Incorporating multiracial and multiethnic experiences into genetic counseling practice and research: A necessary opportunity	13

Application of motivational interviewing strategies with the extended parallel process model to improve risk communication for parents of children with familial hypercholesterolemia	12
Uptake rates for non‐invasive prenatal screening for single‐gene disorders associated with advanced paternal age	12
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Issue Information	11
The effect of knowledge and person‐related factors on breast cancer susceptibility genes (BRCA1/2) testing perception in Turkish women	10
Assessing and attending to psychosocial concerns in genetic counseling: Proposing the BATHE method	10
A qualitative study exploring LGBTQ genetic counseling students' relationships with peers and faculty in graduate school	10
Evaluation of face validity and core concepts of a novel knowledge scale for inherited heart disease: A pilot study	10
Graduate training, credentialing, and continuing education to prepare genetic counselors for laboratory roles—Results of a national survey	10
Pregnant people's views and knowledge on prenatal screening for fetal trisomy in the absence of a national screening program	10
Patient perceptions of genetic counselors' role and emotional support needs in adults with Parkinson's disease	10
Invisible diversities, academic capital, and competitiveness of genetic counseling applicants	10
Prospective parents' views on reproductive genetic carrier screening: “You know better, you do better”	10
Issue Information	9
Buying my existence. Just $49, free shipping included	9
Population‐based hereditary cancer screening in a general endoscopy clinic: Evaluating interest in, uptake, and outcomes of genetic services	9
From intention to action: Assessing need and creating a JEDI toolkit for individuals teaching cancer genetics curriculum	9
Clinical Bootcamp: Moving toward competency outside of the clinic	9
Correction to “Who is at risk for compassion fatigue? An investigation of genetic counselor demographics, anxiety, compassion satisfaction, and burnout”	9
The experiences of families receiving a diagnosis of 22q11.2 deletion syndrome in Ireland	9
The review of genetic screening services and common BRCA1/2 variants among South African breast cancer patients	9
Issue Information	9
An analysis of direct‐to‐consumer genetic testing portals and their communication of health risk and test limitations	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
How parents of children with ataxia‐telangiectasia use dynamic coping to navigate cyclical uncertainty	8
Beyond multiple choice: Clinical simulation as a rigorous and inclusive method for assessing genetic counseling competencies	8
Genetic Counselors' attitudes & perceptions regarding suicide risk assessment and identification in practice	8
Investigating genetic counselors' communication with Lynch syndrome patients about cascade testing: Barriers, facilitators, and strategies	8
BIPOC genetic counseling students' perspectives on career‐oriented social media use: Results from a longitudinal qualitative study	8
Workplace perk or pitfall? A qualitative study of genetic counselors' perspectives and experiences with workplace genetic testing	8
The long‐term impact of receiving incidental findings on parents undergoing genome‐wide sequencing	8
Assessing the perspectives of genetic counselors with oncology patients at the end of life	8
A cross‐professional competency framework for communicating genomic results	8
Performance of the shared decision‐making process scale for use in evaluation of hereditary cancer genetic testing decisions	8
Changes in acceptability, consideration, intention, and uptake of direct‐to‐consumer genetic tests in the Netherlands from 2017 to 2022	7
North American genetic counselors' approach to collecting and using ancestry in clinical practice	7
Evaluating attributes of a collaborative model of service delivery for hereditary cancer risk assessment	7
The goldilocks conundrum: Disclosing discrimination risks in informed consent	7
Medical students' self‐perceived knowledge and clinical comfort with genetics in Pakistan	7
Lessons learned from BRCA1/2 screening in Israel: A cross‐sectional survey comparing experiences and communication	7
Impact of barriers and motivators on intention and confidence to undergo hereditary cancer genetic testing	7
Current attitudes toward carrier screening for spinal muscular atrophy among pregnant women in Eastern China	7
Genetic counselors' experience with reimbursement and patient out‐of‐pocket cost for multi‐cancer gene panel testing for hereditary cancer syndromes	7
Cardiac genetic counseling services: Exploring downstream revenue in a pediatric medical center	7
Genetic testing and counseling for hypertrophic cardiomyopathy: An evidence‐based practice resource of the National Society of Genetic Counselors	7
Noninvasive prenatal screening ( NIPS ) results for participants of the eXtraordinarY babies study	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
Experiences of hereditary cancer care among transgender and gender diverse people: “It's gender. It's cancer risk…it's everything”	6

Experiences of genetic counseling students with disabilities and chronic illnesses: A qualitative study	6
A preliminary adaptation and validation of the genetic counseling outcome scale (GCOS‐24) for use in Greece	6
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How should we address the inevitable harms from non‐negligent variant reclassification in predictive genetic testing?	6
Primary care patient and clinician attitudes about population genomic screening, informed decision‐making needs, and the potential for Chatbot technology	6
Both sides now: Changing a long‐standing pedigree tradition of men on the left and women on the right	6
Evaluating a general pediatric/adult genetic counseling clinic in a Midwest medical center	6
Clinical genetic counselors' use of people‐ and identity‐first language in regard to patients' identification with disability	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
Leadership development in genetic counseling graduate programs	6
Perspectives of Italian lay persons who would decline genetic risk information: “I think I'd be living in constant worry”	6
A comment on ‘COVID‐19 vaccine hesitancy and acceptance among pregnant people’	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
Exploring genetic counselors' interest and role in transitional care discussions for pediatric patients with neurodevelopmental conditions	6
Evaluating genetic counseling session duration: A scoping review of patient care time, influencing factors, and impact on patient outcomes	5
Perceived cancer risk and genetic counseling: A biopsychological perspective	5
Development of the Affiliate Stigma Scale for parents of children with genetic conditions	5
Issue Information	5
Adolescents' and young adults' reactions to and perceived utility of carrier screening results in the context of a genomic research study	5
A survey to analyze the need of genetic counseling among doctors in Lahore, Pakistan	5
Experience with a nurse‐driven genetic counseling pathway of Italian women with uninformative BRCA test result	5
Association between proband characteristics and CDH1 cascade genetic testing uptake in at‐risk relatives	5
Building a foundation in self‐awareness: Genetic counseling students’ experiences with self‐care, reflection, and mindfulness	5
Exploring the journey to genomic testing and genetic services: A qualitative study of parental perspectives of children with rare conditions	5
Role of psychological background in cancer susceptibility genetic testing distress: It is not only about a positive result	5
The efficacy of genetic counseling for familial colorectal cancer: A meta‐analysis	5
Qualitative analysis of the needs of parents of children with rare genetic diseases, following their diagnosis obtained by whole‐exome sequencing	5
Insights into genetic assistant practice and the workforce in North America	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 State of National Institute of Health Awards for funding genetic counseling research, resources, and training over the past decade	5
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2024 National Society of Genetic Counselors presidential address: The path we take	5
Evaluation of barriers to referral for cancer predisposition syndromes in pediatric oncology patients in the United States	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
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Use of digital health tools with point‐of‐care testing improves access to germline genetic testing within a gastrointestinal cancer clinic	5
Proposed use of entrustable professional activities (EPAs) in genetic counseling for clinical training and assessment	5
Host perspectives on international fieldwork placements for U.S.‐based genetic counseling students	5
Parents' perspectives of non‐informative germline genetic testing in children with Juvenile Polyposis Syndrome	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
Cross‐cultural validation of the genetic counseling outcome scale in Korea	5
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Voices in practice: Exploring genetic counseling ethical, cultural, social, and religious dynamics in the UAE	5
Assessing genetic counselors’ graduate school education and training in congenital heart defects	4
Uptake of genetic testing among patients seeking cancer genetic counseling in Taiwan	4
Familial communication and cascade testing following elective genomic testing	4
Does the amount of family history matter? Perspectives of adult adoptees	4
An investigation of preceptors' perceptions of behavioral elements of “professionalism” among genetic counseling students	4
Evolving approaches to prenatal genetic counseling for Spinal Muscular Atrophy in the new treatment era	4
Attitudes and beliefs regardingrace‐targetedgenetic testing of Black people: A systematic review	4
Links between gender norms and the intergenerational transmission of health information in parents carrying BRCA1/2 pathogenic variants	4
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An introduction to Delphi studies and consensus methods for genetic counselors	4
Issue Information	4
Ethno‐racial differences in the frequency of cancer reported from family pedigrees in the prenatal genetic counseling setting	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
Issues, challenges, and future perspectives of genetic counseling in Republic of Korea: Perspectives of laboratory physicians based on a 2022 survey	4
Navigating complexity: How shifting abortion regulations impacted prenatal genetic counselors practicing in restrictive states from 2020 to 2024	4
Evaluating a communication aid for return of genetic results in families with hypertrophic cardiomyopathy: A randomized controlled trial	4
Transgender patients’ perspectives on their cancer genetic counseling experiences	4
Introduction of the genetic counseling profession by teachers in BIPOC‐majority high schools	4
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Research methodologies in genetic counseling: Grounded theory	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
A heartfelt thank you to the 2024 Journal of Genetic Counseling reviewers	4
Use of a chatbot to increase uptake of cascade genetic testing	4
Evaluating pregnancy termination rates for fetal chromosome and single gene disorders	4
Exploring United States genetic counselor and healthcare interpreter perspectives: Allocation of roles within the genetic counseling encounter	4
Attitudes and training needs of oncologists and surgeons in mainstreaming breast cancer genetic counseling in a low‐to‐middle income Asian country	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
Race, ethnicity, and ancestry reporting in genetic counseling research: A focused mapping review and synthesis	4
Understanding and issues related to next‐generation sequencing among educated laypersons in India	4
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
Characterizing the research mentorship experience of genetic counseling students	4
Reading and writing reviews: A primer on systematic, scoping, and narrative reviews for genetic counselors	4
Learning from our patients: Utilizing the expertise of transgender and/or gender diverse educators to build an inclusive learning cycle	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

COVID‐19 vaccine hesitancy and acceptance among pregnant people contacting a teratogen information service	4
Clinical geneticists' views on and experiences with unsolicited findings in next‐generation sequencing: “A great technology creating new dilemmas”	4
Issue Information	4
Factors associated with US and Canadian genetic counselors' testing decisions during pregnancy	4
Expanded carrier screening for inherited genetic disease using exome and genome sequencing	4
Decision stability among adolescents and young adults making choices about learning genomic research results	4
Empathy experiences of Japanese certified genetic counselors: A qualitative investigation and proposed framework	4
Issue Information	4
Pediatric predictive testing to inform preimplantation genetic testing: A case report and review of the literature	4
Cascade testing in an ovarian cancer traceback genetic testing program: The GRACE study experience	4
Application of the RIME framework in genetic counseling fieldwork training to assess practice‐based competencies	4
The impact of cohort relationships on BIPOC genetic counseling students: Results from a longitudinal qualitative study	4
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Issue Information	4
Need for specially designed educational support groups: Young women's experiences of being identified with BRCA pathogenic variants	4
Cascade testing for inherited cardiac conditions: Risk perception and screening after a negative genetic test result	4
Subspecialty neurology genetic counselors—A cost effective solution to substantial time costs associated with genomic testing in the neurology clinic	4
Preferences of parents from diverse backgrounds on genomic screening of apparently healthy newborns	4