Journal of Genetic Counseling

Article	Citations
Issue Information	91
Acceptability of an online communication training intervention for genetic counseling students	62
Barriers in applying to genetic counseling Master's degree programs: Perceptions of prospective applicants when compared with Canadian admissions committee members	58
Misattributed parentage identified through diagnostic exome sequencing: Frequency of detection and reporting practices	47
Genetic counseling for fetal sex prediction by NIPT: Challenges and opportunities	45
Sudden cardiac death in the young: A qualitative study of experiences of family members with cardiogenetic evaluation	29
Supervision for genetic counselors: The role of career‐long supervision to develop resilient practitioners	22
The attitudes of individuals with or at risk of adult‐onset genetic conditions on reproductive genetic testing: A systematic review	21
Application of motivational interviewing strategies with the extended parallel process model to improve risk communication for parents of children with familial hypercholesterolemia	20
Identifying potential genetic counseling program applicant competencies	18
Incorporating multiracial and multiethnic experiences into genetic counseling practice and research: A necessary opportunity	18
Narrative review on ethical and psychological issues raised by genetic and genomic testing in pediatric oncology care	17
Genetic testing for Parkinson's disease in an underrepresented population: Knowledge, attitudes, and ethical considerations from a Malaysian perspective	17
Reply to Rathbun and Paulyson Nuñez	17
Exploring parental cystic fibrosis disclosure to well children	16
Genetic counseling program remediation practices for students underperforming in clinical skills: An exploratory study	16
Genetic counseling in diabetes mellitus: A practice resource of the National Society of Genetic Counselors	16
Perinatal palliative care for family with prenatal diagnosis of Matthew‐Wood syndrome	15
Exploring spiritual/religious coping strategies among mothers of children with severe or profound intellectual disability during genetic counseling in Brazil	15
Clients' experiences of empathy in genetic counseling for hereditary breast and ovarian cancer: A qualitative study in Japan	14
An internship in psychiatric genetic counseling: Impact on genetic counseling graduates' practice and career choices	14
Women's thoughts on receiving and sharing genetic information: Considerations for genetic counseling	14
Women's preferences for NIPT as a first‐line test in England and France: Challenges for genetic counseling practices	13
Courtesy stigma of parents of children with Down syndrome: Adaptation process and transcendent stage	13
Characterization of variant reclassification and patient re‐contact in a cancer genetics clinic	12

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

Experiences of hereditary cancer care among transgender and gender diverse people: “It's gender. It's cancer risk…it's everything”	6
Both sides now: Changing a long‐standing pedigree tradition of men on the left and women on the right	6
A survey to analyze the need of genetic counseling among doctors in Lahore, Pakistan	6
The development and preliminary evaluation of the Genetic Counseling Skills Checklist	6
Exploring genetic counselors' interest and role in transitional care discussions for pediatric patients with neurodevelopmental conditions	6
Primary care patient and clinician attitudes about population genomic screening, informed decision‐making needs, and the potential for Chatbot technology	6
How should we address the inevitable harms from non‐negligent variant reclassification in predictive genetic testing?	6
A comment on ‘COVID‐19 vaccine hesitancy and acceptance among pregnant people’	6
Qualitative analysis of the needs of parents of children with rare genetic diseases, following their diagnosis obtained by whole‐exome sequencing	6
Experiences of genetic counseling students with disabilities and chronic illnesses: A qualitative study	6
Examining the communication work of women who have tested BRCA‐positive: “I feel this responsibility to let people know”	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
A preliminary adaptation and validation of the genetic counseling outcome scale (GCOS‐24) for use in Greece	6
Evaluating a general pediatric/adult genetic counseling clinic in a Midwest medical center	6
The impact of cohort relationships on BIPOC genetic counseling students: Results from a longitudinal qualitative study	5
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Building a foundation in self‐awareness: Genetic counseling students’ experiences with self‐care, reflection, and mindfulness	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
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Proposed use of entrustable professional activities (EPAs) in genetic counseling for clinical training and assessment	5
Preferences of parents from diverse backgrounds on genomic screening of apparently healthy newborns	5
The State of National Institute of Health Awards for funding genetic counseling research, resources, and training over the past decade	5
Optimizing risk‐reducing surgery and aspirin decision aids for Lynch syndrome carriers using the person‐based approach: A think‐aloud interview study	5
Exploring the journey to genomic testing and genetic services: A qualitative study of parental perspectives of children with rare conditions	5
Perceived cancer risk and genetic counseling: A biopsychological perspective	5
The efficacy of genetic counseling for familial colorectal cancer: A meta‐analysis	5
Evaluation of barriers to referral for cancer predisposition syndromes in pediatric oncology patients in the United States	5
Insights into genetic assistant practice and the workforce in North America	5
Influence of genetic counselor medical history on specialty and psychosocial practice in North America	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
Host perspectives on international fieldwork placements for U.S.‐based genetic counseling students	5
Experience with a nurse‐driven genetic counseling pathway of Italian women with uninformative BRCA test result	5
Development of the Affiliate Stigma Scale for parents of children with genetic conditions	5
Issue Information	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
Role of psychological background in cancer susceptibility genetic testing distress: It is not only about a positive result	5
Application of the RIME framework in genetic counseling fieldwork training to assess practice‐based competencies	4
Factors associated with US and Canadian genetic counselors' testing decisions during pregnancy	4
Subspecialty neurology genetic counselors—A cost effective solution to substantial time costs associated with genomic testing in the neurology clinic	4
Decision stability among adolescents and young adults making choices about learning genomic research results	4
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Navigating complexity: How shifting abortion regulations impacted prenatal genetic counselors practicing in restrictive states from 2020 to 2024	4
2024 National Society of Genetic Counselors presidential address: The path we take	4
Clinical geneticists' views on and experiences with unsolicited findings in next‐generation sequencing: “A great technology creating new dilemmas”	4
Exploring genetic counselors' experiences with non‐paternity in clinical settings	4
Uptake of genetic testing among patients seeking cancer genetic counseling in Taiwan	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
Cross‐cultural validation of the genetic counseling outcome scale in Korea	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
Empathy experiences of Japanese certified genetic counselors: A qualitative investigation and proposed framework	4
Evolving approaches to prenatal genetic counseling for Spinal Muscular Atrophy in the new treatment era	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
An investigation of preceptors' perceptions of behavioral elements of “professionalism” among genetic counseling students	4
Does the amount of family history matter? Perspectives of adult adoptees	4
Attitudes and training needs of oncologists and surgeons in mainstreaming breast cancer genetic counseling in a low‐to‐middle income Asian country	4
Experiences of reproductive genetic counselors with abortion regulations in Ohio	4
Evaluating pregnancy termination rates for fetal chromosome and single gene disorders	4
The erasure of transgender and intersex identities through fetal sex prediction and genetic essentialism	4
Need for specially designed educational support groups: Young women's experiences of being identified with BRCA pathogenic variants	4
COVID‐19 vaccine hesitancy and acceptance among pregnant people contacting a teratogen information service	4
Elicitation of children’s understanding of information in pediatric genetic counseling encounters: A discourse‐oriented perspective	4
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Assessing perceived empathy based on genetic counselor gender using a randomized, hypothetical prenatal genetic counseling scenario design	4
Association between proband characteristics and CDH1 cascade genetic testing uptake in at‐risk relatives	4
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Issues, challenges, and future perspectives of genetic counseling in Republic of Korea: Perspectives of laboratory physicians based on a 2022 survey	4
Links between gender norms and the intergenerational transmission of health information in parents carrying BRCA1/2 pathogenic variants	4
Issue Information	4
Pediatric predictive testing to inform preimplantation genetic testing: A case report and review of the literature	4
A heartfelt thank you to the 2024 Journal of Genetic Counseling reviewers	4
Introduction of the genetic counseling profession by teachers in BIPOC‐majority high schools	4
Attitudes and beliefs regardingrace‐targetedgenetic testing of Black people: A systematic review	4
Research methodologies in genetic counseling: Grounded theory	4
Issue Information	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

Transgender patients’ perspectives on their cancer genetic counseling experiences	4
Ethno‐racial differences in the frequency of cancer reported from family pedigrees in the prenatal genetic counseling setting	4
Cascade testing for inherited cardiac conditions: Risk perception and screening after a negative genetic test result	4
Assessing genetic counselors’ graduate school education and training in congenital heart defects	4
Adolescents' and young adults' reactions to and perceived utility of carrier screening results in the context of a genomic research study	4
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Exploring United States genetic counselor and healthcare interpreter perspectives: Allocation of roles within the genetic counseling encounter	4
Expanded carrier screening for inherited genetic disease using exome and genome sequencing	4
Use of a chatbot to increase uptake of cascade genetic testing	4
Race, ethnicity, and ancestry reporting in genetic counseling research: A focused mapping review and synthesis	4