Journal of Genetic Counseling

Article	Citations
An internship in psychiatric genetic counseling: Impact on genetic counseling graduates' practice and career choices	69
Women's thoughts on receiving and sharing genetic information: Considerations for genetic counseling	54
Issue Information	50
Women's preferences for NIPT as a first‐line test in England and France: Challenges for genetic counseling practices	39
Application of motivational interviewing strategies with the extended parallel process model to improve risk communication for parents of children with familial hypercholesterolemia	39
Acceptability of an online communication training intervention for genetic counseling students	32
Clients' experiences of empathy in genetic counseling for hereditary breast and ovarian cancer: A qualitative study in Japan	24
Supervision for genetic counselors: The role of career‐long supervision to develop resilient practitioners	22
Narrative review on ethical and psychological issues raised by genetic and genomic testing in pediatric oncology care	22
Barriers in applying to genetic counseling Master's degree programs: Perceptions of prospective applicants when compared with Canadian admissions committee members	20
Perinatal palliative care for family with prenatal diagnosis of Matthew‐Wood syndrome	20
Characterization of variant reclassification and patient re‐contact in a cancer genetics clinic	20
Exploring parental cystic fibrosis disclosure to well children	20
Exploring spiritual/religious coping strategies among mothers of children with severe or profound intellectual disability during genetic counseling in Brazil	19
Reply to Rathbun and Paulyson Nuñez	19
Sudden cardiac death in the young: A qualitative study of experiences of family members with cardiogenetic evaluation	17
Misattributed parentage identified through diagnostic exome sequencing: Frequency of detection and reporting practices	16
Incorporating multiracial and multiethnic experiences into genetic counseling practice and research: A necessary opportunity	16
Genetic counseling program remediation practices for students underperforming in clinical skills: An exploratory study	16
Metaphors and why these are important in all aspects of genetic counseling	16
Genetic counseling in diabetes mellitus: A practice resource of the National Society of Genetic Counselors	16
Courtesy stigma of parents of children with Down syndrome: Adaptation process and transcendent stage	16
Genetic counseling for fetal sex prediction by NIPT: Challenges and opportunities	15
From intention to action: Assessing need and creating a JEDI toolkit for individuals teaching cancer genetics curriculum	15
Clinical Bootcamp: Moving toward competency outside of the clinic	15

Public perceived knowledge of, attitude toward, and use of genetic testing in urban China	14
	14
A qualitative study exploring LGBTQ genetic counseling students' relationships with peers and faculty in graduate school	13
Genetic counseling practice for inherited eye diseases in an Israeli medical center during the COVID‐19 pandemic	12
Pregnant women's experiences of non‐invasive prenatal testing (NIPT) in Japan: A qualitative study	12
Pregnant people's views and knowledge on prenatal screening for fetal trisomy in the absence of a national screening program	12
Correction to “Who is at risk for compassion fatigue? An investigation of genetic counselor demographics, anxiety, compassion satisfaction, and burnout”	12
Buying my existence. Just $49, free shipping included	12
Uptake rates for non‐invasive prenatal screening for single‐gene disorders associated with advanced paternal age	12
Graduate training, credentialing, and continuing education to prepare genetic counselors for laboratory roles—Results of a national survey	12
A cross‐professional competency framework for communicating genomic results	12
The review of genetic screening services and common BRCA1/2 variants among South African breast cancer patients	11
Evaluation of face validity and core concepts of a novel knowledge scale for inherited heart disease: A pilot study	11
Issue Information	11
Workplace perk or pitfall? A qualitative study of genetic counselors' perspectives and experiences with workplace genetic testing	10
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
U.S. Genetic counselors’ perceptions of inpatient genetic counseling: A valuable model for medically complex patients	10
Patient perceptions of genetic counselors' role and emotional support needs in adults with Parkinson's disease	10
Assessing and attending to psychosocial concerns in genetic counseling: Proposing the BATHE method	10
The effect of knowledge and person‐related factors on breast cancer susceptibility genes (BRCA1/2) testing perception in Turkish women	10
How parents of children with ataxia‐telangiectasia use dynamic coping to navigate cyclical uncertainty	9
The long‐term impact of receiving incidental findings on parents undergoing genome‐wide sequencing	9
Impact of barriers and motivators on intention and confidence to undergo hereditary cancer genetic testing	9
Genetic Counselors' attitudes & perceptions regarding suicide risk assessment and identification in practice	9
Beyond multiple choice: Clinical simulation as a rigorous and inclusive method for assessing genetic counseling competencies	9
Noninvasive prenatal screening (NIPS) results for participants of the eXtraordinarY babies study: Screening, counseling, diagnosis, and discordance	9
Cardiac genetic counseling services: Exploring downstream revenue in a pediatric medical center	9
North American genetic counselors' approach to collecting and using ancestry in clinical practice	9
Standardized applications for genetic counseling graduate programs: Opinions of program directors	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	8
Genetic counselor use of self‐involving responses in a clinical setting: A qualitative investigation	8
Lessons learned from BRCA1/2 screening in Israel: A cross‐sectional survey comparing experiences and communication	8
Strength of the genetic counselor: patient relationship is associated with extent of increased empowerment in patients with arrhythmogenic cardiomyopathy	8
How should we address the inevitable harms from non‐negligent variant reclassification in predictive genetic testing?	8
Outcomes from a pilot genetic counseling intervention using motivational interviewing and the extended parallel process model to increase cascade cholesterol screening	8
Mothers' reflections on the diagnosis and birth of their child with Down syndrome: Variability based on the timing of the diagnosis	8
Performance of the shared decision‐making process scale for use in evaluation of hereditary cancer genetic testing decisions	8
Current attitudes toward carrier screening for spinal muscular atrophy among pregnant women in Eastern China	8
Genetic testing and counseling for hypertrophic cardiomyopathy: An evidence‐based practice resource of the National Society of Genetic Counselors	8
Changes in acceptability, consideration, intention, and uptake of direct‐to‐consumer genetic tests in the Netherlands from 2017 to 2022	8
An analysis of direct‐to‐consumer genetic testing portals and their communication of health risk and test limitations	8
Assessing the relationship between patient preferences for recontact after BRCA1 or BRCA2 genetic testing and their monitoring coping style in a Norwegian sample	7
Experiences of hereditary cancer care among transgender and gender diverse people: “It's gender. It's cancer risk…it's everything”	7
Examining the communication work of women who have tested BRCA‐positive: “I feel this responsibility to let people know”	7
The goldilocks conundrum: Disclosing discrimination risks in informed consent	7
Exploring genetic counselors' interest and role in transitional care discussions for pediatric patients with neurodevelopmental conditions	7
Experiences of genetic counseling students with disabilities and chronic illnesses: A qualitative study	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

Barriers to family history knowledge and family communication among LGBTQ+ individuals in the context of hereditary cancer risk assessment	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
Genetic counseling student rotations in industry: How COVID‐19 magnified the urgency for virtual learning options in diverse training settings	7
Ethical and moral perspectives of individuals who considered/used preimplantation (embryo) genetic testing	7
Medical students' self‐perceived knowledge and clinical comfort with genetics in Pakistan	7
Genetic counselors' experience with reimbursement and patient out‐of‐pocket cost for multi‐cancer gene panel testing for hereditary cancer syndromes	7
Evaluating attributes of a collaborative model of service delivery for hereditary cancer risk assessment	7
Host perspectives on international fieldwork placements for U.S.‐based genetic counseling students	6
Experience with a nurse‐driven genetic counseling pathway of Italian women with uninformative BRCA test result	6
	6
Impacts of student debt on the professional and personal lives of genetic counselors: A 10‐year perspective	6
Issue Information	6
The State of National Institute of Health Awards for funding genetic counseling research, resources, and training over the past decade	6
Building a foundation in self‐awareness: Genetic counseling students’ experiences with self‐care, reflection, and mindfulness	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 comment on ‘COVID‐19 vaccine hesitancy and acceptance among pregnant people’	6
Evaluating a general pediatric/adult genetic counseling clinic in a Midwest medical center	6
Offering preimplantation genetic testing for monogenic disorders (PGT‐M) for conditions with reduced penetrance or variants of uncertain significance: Ethical insight from U.S. laboratory genetic coun	6
A survey to analyze the need of genetic counseling among doctors in Lahore, Pakistan	6
Evaluation of barriers to referral for cancer predisposition syndromes in pediatric oncology patients in the United States	6
Proposed use of entrustable professional activities (EPAs) in genetic counseling for clinical training and assessment	6
	6
Both sides now: Changing a long‐standing pedigree tradition of men on the left and women on the right	6
Polygenic risk in familial breast cancer: Changing the dynamics of communicating genetic risk	6
Insights into genetic assistant practice and the workforce in North America	5
Genetic counseling delivery, outcomes, training, and practice in response to COVID‐19: Introduction to the special issue	5
	5
Analysis of the reported use of practice‐based competencies by North American genetic counselors during the COVID‐19 pandemic	5
Cascade testing for inherited cardiac conditions: Risk perception and screening after a negative genetic test result	5
Qualitative analysis of the needs of parents of children with rare genetic diseases, following their diagnosis obtained by whole‐exome sequencing	5
Role of psychological background in cancer susceptibility genetic testing distress: It is not only about a positive result	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
Influence of genetic counselor medical history on specialty and psychosocial practice in North America	5
Understanding and interpretation of a variant of uncertain significance (VUS) genetic test result by pediatric providers who do not specialize in genetics	5
Characterizing the research mentorship experience of genetic counseling students	5
Exploring genetic counselors' experiences with non‐paternity in clinical settings	5
Transgender patients’ perspectives on their cancer genetic counseling experiences	5
Evaluating genetic counseling session duration: A scoping review of patient care time, influencing factors, and impact on patient outcomes	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
Learning from our patients: Utilizing the expertise of transgender and/or gender diverse educators to build an inclusive learning cycle	5
Management of amended variant classification laboratory reports by genetic counselors in the United States and Canada: An exploratory study	5
‘Steep learning curves’ to ‘Smooth Sailing’: A reappraisal of telegenetics amidst the COVID‐19 pandemic	5
Preferences of parents from diverse backgrounds on genomic screening of apparently healthy newborns	5
Knowledge and perceptions of the genetic counseling profession among a national cross‐sectional sample of U.S. adults	5
Perceived cancer risk and genetic counseling: A biopsychological perspective	5
Exploring the journey to genomic testing and genetic services: A qualitative study of parental perspectives of children with rare conditions	5
Transitioning to telegenetics in the COVID‐19 era: Patient satisfaction with remote genetic counseling in adult neurology	5
Graduate training during the COVID‐19 pandemic: North American genetic counseling students' challenges, intolerance of uncertainty, and psychological well‐being	4
Understanding and perception of direct‐to‐consumer genetic testing in Hong Kong	4
Familial communication and cascade testing following elective genomic testing	4
Assessing genetic counselors’ graduate school education and training in congenital heart defects	4
Issues, challenges, and future perspectives of genetic counseling in Republic of Korea: Perspectives of laboratory physicians based on a 2022 survey	4
Issue Information	4
Decision stability among adolescents and young adults making choices about learning genomic research results	4
Issue Information	4
Issue Information	4
Research to reduce inequities in cancer risk services: Insights for remote genetic counseling in a pandemic and beyond	4
	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
Following NCCN guidelines within one hospital system in the United States: Comparison between cancer centers and genetic counselor utilization	4
Factors associated with US and Canadian genetic counselors' testing decisions during pregnancy	4
Clinical geneticists' views on and experiences with unsolicited findings in next‐generation sequencing: “A great technology creating new dilemmas”	4
	4
Explanatory models for the cause of Fragile X Syndrome in rural Cameroon	4
Uptake of genetic testing among patients seeking cancer genetic counseling in Taiwan	4
Attitudes and training needs of oncologists and surgeons in mainstreaming breast cancer genetic counseling in a low‐to‐middle income Asian country	4
A qualitative assessment of parental experiences with false‐positive newborn screening for Krabbe disease	4
Awareness of genetic counseling and genetic testing for hereditary gynecologic cancers among Korean healthcare providers: A survey	4
Adolescents' and young adults' reactions to and perceived utility of carrier screening results in the context of a genomic research study	4
Cross‐cultural validation of the genetic counseling outcome scale in Korea	4
2024 National Society of Genetic Counselors presidential address: The path we take	4
The impact of cohort relationships on BIPOC genetic counseling students: Results from a longitudinal qualitative study	4
Race, ethnicity, and ancestry reporting in genetic counseling research: A focused mapping review and synthesis	4
Need for specially designed educational support groups: Young women's experiences of being identified with BRCA pathogenic variants	4
	4
Elicitation of children’s understanding of information in pediatric genetic counseling encounters: A discourse‐oriented perspective	4
Attitudes and beliefs regardingrace‐targetedgenetic testing of Black people: A systematic review	4
Association between proband characteristics and CDH1 cascade genetic testing uptake in at‐risk relatives	4
A heartfelt thank you to the 2024 Journal of Genetic Counseling reviewers	4

An investigation of preceptors' perceptions of behavioral elements of “professionalism” among genetic counseling students	4
COVID‐19 vaccine hesitancy and acceptance among pregnant people contacting a teratogen information service	4
The erasure of transgender and intersex identities through fetal sex prediction and genetic essentialism	4
Adoptees' experiences of using direct‐to‐consumer genetic testing and determinants of this use: A mixed study in Quebec	3
Exploring United States genetic counselor and healthcare interpreter perspectives: Allocation of roles within the genetic counseling encounter	3
Exploring the occurrence of microaggressions in the genetic counseling student–supervisor relationship: A mixed‐methods study	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
Issue Information	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
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
Genetic counseling students' use of patient‐centered communication skills predicts standardized patient satisfaction during virtual simulated sessions	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
Experiences of genetic counselors practicing in multiple languages: Progress and places for improvement	3
Genetic counseling in the time of COVID‐19: The Philippine experience with telegenetics	3
Ethical concerns surrounding sex prediction using noninvasive prenatal screening from pediatric endocrinologists' perspective	3
Expanded carrier screening for inherited genetic disease using exome and genome sequencing	3
Ethno‐racial differences in the frequency of cancer reported from family pedigrees in the prenatal genetic counseling setting	3
Western Australian women's expectations for expanded NIPT—An online survey regarding NIPT for single gene, recessive and chromosomal conditions	3
Clinical and laboratory genetic counseling assistants: Comparing background experiences, responsibilities, satisfaction, and career goals	3
Genetic counselor experiences with telehealth before and after COVID‐19	3
Issue Information	3
Exploring Canadian genetic counselors' perspectives and experiences with discussing medical assistance in dying (MAiD)	3
Clinical and laboratory genetic counselor attitudes on the reporting of variants of uncertain significance for multigene cancer panels	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
Parent‐reported genetic counselor adherence to the NSGC practice resource for communicating a potential prenatal diagnosis: Impact on the Down syndrome diagnosis experience	3
BRCAShare—Assessment of an animated digital message for intrafamilial communication of pathogenic variant positive test results: A feasibility study	3
Young people’s experiences of a CDH1 pathogenic variant: Decision‐making about gastric cancer risk management	3
Changes to the genetic counseling workforce as a result of the COVID‐19 pandemic	3
Use of a chatbot to increase uptake of cascade genetic testing	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
Evolving approaches to prenatal genetic counseling for Spinal Muscular Atrophy in the new treatment era	3
A qualitative exploration of experiences of gender identity and gender questioning among adults with Klinefelter syndrome/XXY	3
Understanding and issues related to next‐generation sequencing among educated laypersons in India	3
Links between gender norms and the intergenerational transmission of health information in parents carrying BRCA1/2 pathogenic variants	3
Experiences of reproductive genetic counselors with abortion regulations in Ohio	3
A report of the AGCPD task force to evaluate associations between select admissions requirements, demographics, and performance on ABGC certification examination	3
Empathy experiences of Japanese certified genetic counselors: A qualitative investigation and proposed framework	3
Picture this: Evaluating the efficacy of genetic counseling visual aids	3
Application of the RIME framework in genetic counseling fieldwork training to assess practice‐based competencies	3
Further defining the roles and impact of genetic counselors in the biotechnology and pharmaceutical industry	3
Promoting the integration of genetic counseling education and research across the spectrum of learners at a large academic institution	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
Experience conducting a community‐engaged student research project involving an underrepresented community: A reflective essay	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
Group meditation, addressing stigma, and “mental health days”: Recommendations for integrating self‐awareness practices into genetic counseling graduate programs	3
To be or not to be (honest): The persistent problem of misattributed paternity	3
The COVID‐19 pandemic and reproductive genetic counseling: Changes in access and service delivery at an academic medical center in the United States	3
	3
Introduction of the genetic counseling profession by teachers in BIPOC‐majority high schools	3
Issue Information	3
Examining clinical training through a bicultural lens: Experiences of genetic counseling students who identify with a racial or ethnic minority group	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
Evaluating a communication aid for return of genetic results in families with hypertrophic cardiomyopathy: A randomized controlled trial	3
Does the amount of family history matter? Perspectives of adult adoptees	3
Assessing management practices for variants of uncertain significance among genetic counselors in pediatrics	3
Should genes for non‐syndromic hearing loss be included in reproductive genetic carrier screening: Views of people with a personal or family experience of deafness	2
A cross‐sectional survey‐based exploration of diversity in the admissions committees and student cohorts of genetic counseling programs over time	2
Differences in genetic counseling student responses to intense patient affect: A study of students in North American programs	2
Clinical genetic counselor experience in the adoption of telehealth in the United States and Canada during the COVID‐19 pandemic	2
Accreditation Council for Genetic Counseling Board of Directors Response to Myers et al ‘A report of the AGCPD task force to evaluate associations between select admissions requirements, demographics,	2
Dilemmas when talking about Huntington's disease: A qualitative study of offspring and caregiver experiences in Norway	2
Processing the process: Reflections on genetic counselor‐led student supervision groups and practical tips for future facilitators	2
Interpreter use in telehealth genetic counseling sessions	2
Research participants' perspectives about the return of uninformative genomic test results in a clinical research setting	2
“It becomes your whole life”—Exploring experiences of reciprocal translocation carriers and their partners	2
Patient uptake of updated genetic testing following uninformative BRCA1 and BRCA2 results	2
Creation and beta testing of a “choose your own adventure” digital simulation to reinforce motivational interviewing skills in genetic counseling	2
Script concordance testing in genetic counseling training: A pilot study	2
The Genetic Information Nondiscrimination Act and workplace genetic testing: Knowledge and perceptions of employed adults in the United States	2
Enhancing the didactic learning experience for Laboratory Genetics and Genomics fellows through a multi‐institutional lecture series	2
Cardiology clinic patient attitudes toward and potential personal utility of genetic testing: Findings from a unique multiracial clinical sample	2
Research participants' perspectives regarding the feedback of secondary findings–A cohort from the DDD‐Africa study, South Africa	2
Factors influencing applicants' rank order in the Genetic Counseling Admissions Match	2
	2
Establishing a mentorship program for prospective genetic counseling graduate students: Two cycles of program experience	2
Examining the effect of patient personality types and coping styles on outcomes of genetic counseling	2
Elective genomic testing: Practice resource of the National Society of Genetic Counselors	2
Conducting inclusive research in genetics for transgender, gender‐diverse, and sex‐diverse individuals: Case analyses and recommendations from a clinical genomics study	2
The multigenerational impact of long QT syndrome: A Gitxsan perspective	2
Issue Information	2
Psychiatric genetic counseling: A survey of Australian genetic counselors' practice and attitudes	2
Commentary from a commercial laboratory: The unexpected benefits of a more virtual world during the COVID‐19 pandemic	2
A Heartfelt Thank You to the 2021 Journal of Genetic Counseling Reviewers	2
Stagnation in quality of next‐generation sequencing assays for the diagnosis of hereditary hematopoietic malignancies	2
Attitudes of parents of children with ADHD towards genetic testing: Data from a Turkish sample	2
Navigating sexual orientation and gender identity data privacy concerns in United States genetics practices	2
Referral networks for pediatric patients with genetic conditions: The perspective of occupational therapists	2
Assessing barriers to the career ladder and professional development for ethnic minority genetic counselors in the United States	2
Landscape of genetic counseling in the Philippines	2
Understanding patients' views and willingness toward the use of telehealth in a cancer genetics service in Asia	2
A qualitative study of LGBTQIA+ genetic counselors' experiences while applying to graduate school	2
Policy and laboratory practice: How quality control procedures for genetic testing perpetuate biological essentialism and discrimination against transgender, gender diverse, and intersex people	2
Disability education and implications for genetic counselor training	2
Issue Information	2