Journal of Genetic Counseling

Article	Citations
Telehealth for genetic counseling: A systematic evidence review	37
Genetic testing and counseling for the unexplained epilepsies: An evidence‐based practice guideline of the National Society of Genetic Counselors	34
Benefits and limitations of telegenetics: A literature review	28
Use of a chatbot to increase uptake of cascade genetic testing	28
Genetic counseling service delivery models: A study of genetic counselors’ interests, needs, and barriers to implementation	27
Practice resource‐focused revision: Standardized pedigree nomenclature update centered on sex and gender inclusivity: A practice resource of the National Society of Genetic Counselors	27
Supporting a sense of inclusion and belonging for genetic counseling students who identify as racial or ethnic minorities	25
Chatbots & artificial intelligence to scale genetic information delivery	25
Considerations in genetic counseling of transgender patients: Cultural competencies and altered disease risk profiles	22
Risk assessment and genetic counseling for hereditary breast and ovarian cancer syndromes—Practice resource of the National Society of Genetic Counselors	22
Exploring racial and ethnic minority individuals’ journey to becoming genetic counselors: Mapping paths to diversifying the genetic counseling profession	20
Evaluating co‐created patient‐facing materials to increase understanding of genetic test results	19
Rapid genome‐wide sequencing in a neonatal intensive care unit: A retrospective qualitative exploration of parental experiences	19
Transition to telephone genetic counseling services during the COVID‐19 pandemic	19
Genetic counseling, virtual visits, and equity in the era of COVID‐19 and beyond	19
Parental experiences of uncertainty following an abnormal fetal anomaly scan: Insights using Han’s taxonomy of uncertainty	18
Transitioning to telegenetics in the COVID‐19 era: Patient satisfaction with remote genetic counseling in adult neurology	18
Perceived barriers to paternal expanded carrier screening following a positive maternal result: To screen or not to screen	18
Genetic counselors' experiences with transgender individuals in prenatal and preconception settings	17
Prenatal Genetic Diagnosis of a Sex Chromosome Aneuploidy: Parent Experiences	17
Rapid acute care genomics: Challenges and opportunities for genetic counselors	16
Influence of payer coverage and out‐of‐pocket costs on ordering of NGS panel tests for hereditary cancer in diverse settings	15
Do research participants share genomic screening results with family members?	15
GeneLiFT: A novel test to facilitate rapid screening of genetic literacy in a diverse population undergoing genetic testing	15
A pilot randomized trial of an educational intervention to increase genetic counseling and genetic testing among Latina breast cancer survivors	14

Genetic counselor experiences with telehealth before and after COVID‐19	14
Comprehension and personal value of negative non‐diagnostic genetic panel testing	14
Breast cancer polygenic risk scores in the clinical cancer genetic counseling setting: Current practices and impact on patient management	14
Genetic counseling for congenital heart disease – Practice resource of the National Society of Genetic Counselors	14
Impact of variant reclassification in the clinical setting of cardiovascular genetics	14
Considerations for the use of qualitative methodologies in genetic counseling research	14
Geographical analysis of the distribution of certified genetic counselors in the United States	13
Contributors to and consequences of burnout among clinical genetic counselors in the United States	13
Genetic counseling following direct‐to consumer genetic testing: Consumer perspectives	13
Transgender patients’ perspectives on their cancer genetic counseling experiences	12
After genomic testing results: Parents’ long‐term views	12
“Doctors can read about it, they can know about it, but they've never lived with it”: How parents use social media throughout the diagnostic odyssey	12
A review and definition of ‘usual care’ in genetic counseling trials to standardize use in research	12
Outcomes of genetic test disclosure and genetic counseling in a large Parkinson's disease research study	12
Influence of lived experience on risk perception among women who received a breast cancer polygenic risk score: ‘Another piece of the pie’	12
A systematic review and meta‐analysis of telephone vs in‐person genetic counseling in BRCA1/BRCA2 genetic testing	12
Direct‐to‐consumer genetic testing companies tell their customers to ‘see a genetic counselor'. How do genetic counselors feel about direct‐to‐consumer genetic testing?	12
A narrative literature review: Growing the workforce through increased fieldwork capacity in genetic counseling training programs	12
Reflections of parents of children with 22q11.2 Deletion Syndrome on the experience of receiving psychiatric genetic counseling: ‘Awareness to Act’	11
Expanded carrier screening in the United States: A systematic evidence review exploring client and provider experiences	11
Attitudes toward population screening among people living with fragile X syndrome in the UK: ‘I wouldn’t wish him away, I’d just wish his fragile X syndrome away’	11
Expanded carrier screening for reproductive risk assessment: An evidence‐based practice guideline from the National Society of Genetic Counselors	11
Genetic counseling student demographics: an empirical comparison of two cohorts	11
Pursuing genetic testing for children with autism spectrum disorders: What do parents think?	10
Genetic counselors and legal recognition: A made‐for‐Canada approach	10
Pharmacogenomic education among genetic counseling training programs in North America	10
Family communication of genetic test results among women with inherited breast cancer genes	10
COVID‐19 vaccine hesitancy and acceptance among pregnant people contacting a teratogen information service	10
Characterizing standardized patients and genetic counseling graduate education	10
Improving gender‐affirming care in genetic counseling: Using educational tools that amplify transgender and/or gender non‐binary community voices	10
A family systems approach to genetic counseling: Development of narrative interventions	10
Australian healthcare professionals' perspectives on the ethical and practical issues associated with genomic newborn screening	10
Risk assessment and genetic counseling for Lynch syndrome – Practice resource of the National Society of Genetic Counselors and the Collaborative Group of the Americas on Inherited Gastrointestinal Ca	10
Implementing innovative service delivery models in genetic counseling: a qualitative analysis of facilitators and barriers	10
The current landscape of genetic test stewardship: A multi‐center prospective study	10
Preconception expanded carrier screening: Impact of information presented by text or video on genetic knowledge and attitudes	10
Telehealth genetic services during the COVID‐19 Pandemic: Implementation and patient experiences across multiple specialties in Nebraska	9
The Canadian genetic counseling workforce: Perspectives from employers and recent graduates	9
Pregnant Hispanic women's views and knowledge of prenatal genetic testing	9
Adapting genetic counseling operations amidst the COVID‐19 pandemic	9
Social support networks of adults with sickle cell disease	9
Advancing the genetic counseling profession through research: Identification of priorities by the National Society of Genetic Counselors research task force	9
State of recent literature on communication about cancer genetic testing among Latinx populations	9
Genetic counseling for patients with positive genomic screening results: Considerations for when the genetic test comes first	9
Family planning in carriers of BRCA1 and BRCA2 pathogenic variants	8
The uptake and utility of genetic testing and genetic counseling for hypertrophic cardiomyopathy—A systematic review and meta‐analysis	8
A report of the AGCPD task force to evaluate associations between select admissions requirements, demographics, and performance on ABGC certification examination	8
Understanding patients' views and willingness toward the use of telehealth in a cancer genetics service in Asia	8
Communication about positive BRCA1 and BRCA2 genetic test results and uptake of testing in relatives in a diverse Asian setting	8
Clinical genetic counseling and translation considerations for polygenic scores in personalized risk assessments: A Practice Resource from the National Society of Genetic Counselors	8

An evidence‐based practice guideline of the National Society of Genetic Counselors for telehealth genetic counseling	8
The impact of a cascade testing video on recipients’ knowledge, cognitive message processing, and affective reactions: A formative evaluation	7
Genetic counseling in the time of COVID‐19: The Philippine experience with telegenetics	7
Professional regulation for Australasian genetic counselors	7
Genetic counseling for fetal sex prediction by NIPT: Challenges and opportunities	7
Spanish language concordance in genetic counseling sessions in the United States: Counselor experiences and perceptions of its effects on processes and outcomes	7
Financial constraints on genetic counseling and further risk‐management decisions among U.S. women at elevated breast cancer risk	7
Outcomes from a pilot genetic counseling intervention using motivational interviewing and the extended parallel process model to increase cascade cholesterol screening	7
Examining clinical training through a bicultural lens: Experiences of genetic counseling students who identify with a racial or ethnic minority group	7
Motivational interviewing for genetic counseling: A unified framework for persuasive and equipoise conversations	7
Prenatal genetic counselors' perceptions of the impact of abortion legislation on counseling and access in the United States	7
COVID contingencies: Early epicenter experiences of different genetics clinics at a New York City institution inform emergency adaptation strategies	7
Changes in genetic variant results over time in pediatric cardiomyopathy and electrophysiology	7
Genome sequencing among children with medical complexity: What constitutes value from parents’ perspective?	7
Whether, when, and how to communicate genetic risk to minors: ‘I wanted more information but I think they were scared I couldn’t handle it’	7
Genetic counseling for early onset and familial dementia: Patient perspectives on exome sequencing	7
40 years and beyond for the National Society of Genetic Counselors: Reflections on genetic counseling practice	7
Attitudes and training needs of oncologists and surgeons in mainstreaming breast cancer genetic counseling in a low‐to‐middle income Asian country	7
Parenting a child with Down syndrome: A qualitative study of everyday practices in Danish families	7
Genetic counseling and diagnostic genetic testing for familial amyotrophic lateral sclerosis and/or frontotemporal dementia: A qualitative study of client experiences	7
Diversity training experiences and factors associated with implicit racial bias among recent genetic counselor graduates of accredited programs in the United States and Canada	7
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
Adaptation and validation of the Genetic Counseling Outcome Scale for autism spectrum disorders and related conditions	6
The COVID‐19 pandemic and reproductive genetic counseling: Changes in access and service delivery at an academic medical center in the United States	6
Implicit and explicit racial prejudice and stereotyping toward Black (vs. White) Americans: The prevalence and variation among genetic counselors in North America	6
Disclosure and comfort during genetic counseling sessions with LGBTQ+ patients: An updated assessment	6
Experiences of reproductive genetic counselors with abortion regulations in Ohio	6
Application of motivational interviewing strategies with the extended parallel process model to improve risk communication for parents of children with familial hypercholesterolemia	6
Integrating genetic assistants into the workforce: An 18‐year productivity analysis and development of a staff mix planning tool	6
Experiences of adolescents and their parents after receiving adolescents’ genomic screening results	6
Does a proactive procedure lead to a higher uptake of predictive testing in families with a pathogenic BRCA1/BRCA2 variant? A family cancer clinic evaluation	6
Assessing clinical education tools for expanded carrier screening	6
The long‐term impact of receiving incidental findings on parents undergoing genome‐wide sequencing	6
Newborn screening for Pompe disease: Parental experiences and follow‐up care for a late‐onset diagnosis	6
Utilization of genetic testing: Analysis of 4,499 prior authorization requests for molecular genetic tests at four US regional health plans	6
The impact of genetic counseling on women's grief and coping following termination of pregnancy for fetal anomaly	6
Content analysis of Journal of Genetic Counseling research articles: A multi‐year perspective	6
Process evaluation of a culturally targeted video for Latinas at risk of hereditary breast and ovarian cancer	6
Predictive testing for neurodegenerative diseases in the age of next‐generation sequencing	6
Social media usage in family communication about genetic information: ‘I no longer speak with my sister but she needed to know’	6
Large‐scale group genetic counseling: Evaluation of a novel service delivery model in a Canadian hereditary cancer clinic	6
Characterization of variant reclassification and patient re‐contact in a cancer genetics clinic	6
The experiences of families receiving a diagnosis of 22q11.2 deletion syndrome in Ireland	5
Metaphors and why these are important in all aspects of genetic counseling	5
The erasure of transgender and intersex identities through fetal sex prediction and genetic essentialism	5
Effects of participation in a U.S. trial of newborn genomic sequencing on parents at risk for depression	5
Reasons affecting the uptake of reproductive genetic carrier screening among nonpregnant reproductive‐aged women in Flanders (Belgium)	5
Evaluation of barriers to referral for cancer predisposition syndromes in pediatric oncology patients in the United States	5
Interest in and uptake of genetic counseling for preconception carrier screening when offered to predominantly white reproductive‐age persons seeking gynecologic care at a single U.S. academic medical	5
Between responsibility and desire: Accounts of reproductive decisions from those at risk for or affected by late‐onset neurological diseases	5
Clinical genetic counselor experience in the adoption of telehealth in the United States and Canada during the COVID‐19 pandemic	5
Elective genomic testing: Practice resource of the National Society of Genetic Counselors	5
Informing models of cancer genetics care in the era of multigene panel testing with patient‐led recommendations	5
Conscience clauses in genetic counseling: Awareness and attitudes	5
Understanding and interpretation of a variant of uncertain significance (VUS) genetic test result by pediatric providers who do not specialize in genetics	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
Exome sequencing study in a clinical research setting finds general acceptance of study returning secondary genomic findings with little decisional conflict	5
Young people’s experiences of a CDH1 pathogenic variant: Decision‐making about gastric cancer risk management	5
A survey of aortic disease biorepository participants’ preferences for return of research genetic results	5
The genetic counseling profession in Austria: Stakeholders’ perspectives	5
DNA testing information on YouTube: Inadequate advice can mislead and harm the public	5
Courtesy stigma of parents of children with Down syndrome: Adaptation process and transcendent stage	5
Learning from our patients: Utilizing the expertise of transgender and/or gender diverse educators to build an inclusive learning cycle	5
‘Steep learning curves’ to ‘Smooth Sailing’: A reappraisal of telegenetics amidst the COVID‐19 pandemic	5
Graduate training during the COVID‐19 pandemic: North American genetic counseling students' challenges, intolerance of uncertainty, and psychological well‐being	5
Trends in coverage and reimbursement for reproductive genetic counseling in New Jersey by multiple payers from 2010 to 2018	5
Exploring empathy in genetic counseling students and new genetic counselors	5
Revising the FOCUS framework through a qualitative study assessing self‐reported counseling skills of genetic counselors	5
A Delphi study to prioritize genetic counseling outcomes: What matters most	5
Family genetic result communication in rare and undiagnosed disease communities: Understanding the practice	5
Critical components of genomic medicine practice for non‐genetics healthcare professionals: Genetic counselors' perspectives and implications for medical education	4
Adding a genetic counseling assistant improves efficiency of hereditary cancer genetic counseling without impacting patient experience	4
Need for additional training to be a laboratory genetic counselor—A qualitative exploration	4
Adaptation of the working alliance inventory for the assessment of the therapeutic alliance in genetic counseling	4
Exploring how mothers of a child with a genetic disorder experience their couple relationship in a low socio‐economic setting	4
Genetic counseling student rotations in industry: How COVID‐19 magnified the urgency for virtual learning options in diverse training settings	4
Changes to the genetic counseling workforce as a result of the COVID‐19 pandemic	4
Evolving approaches to prenatal genetic counseling for Spinal Muscular Atrophy in the new treatment era	4
Strength of the genetic counselor: patient relationship is associated with extent of increased empowerment in patients with arrhythmogenic cardiomyopathy	4
CDH1 variants leading to gastric cancer risk management decision‐making experiences in emerging adults: ‘I am not ready yet’	4

Research participant understanding and engagement in an institutional, self‐consent biobank model	4
Attitudes and beliefs regardingrace‐targetedgenetic testing of Black people: A systematic review	4
Adapting to the challenges of the global pandemic on genetic counselor education: Evaluating students’ satisfaction with virtual clinical experiences	4
The evolution of genetic counseling graduate education in New York City during the COVID‐19 pandemic: In the eye of the storm	4
Latinx attitudes, barriers, and experiences with genetic counseling and testing: A systematic review	4
	4
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	4
Medical knowledge and information needs among women with pathogenic variants in moderate‐risk genes for hereditary breast cancer attending genetic counseling at an academic hospital in Germany—A quali	4
Genetic counseling for advanced paternal age: A survey of genetic counselors' current practice	4
No longer “non‐traditional”: Genetic counselors' perceptions towards laboratory and industry roles	4
Management of amended variant classification laboratory reports by genetic counselors in the United States and Canada: An exploratory study	4
Sudden shift to remote genetic counseling during the COVID‐19 pandemic: Experiences of genetics professionals in Italy	4
International genetic counseling: What do genetic counselors actually do?	4
Understanding and perception of direct‐to‐consumer genetic testing in Hong Kong	4
Misattributed parentage identified through diagnostic exome sequencing: Frequency of detection and reporting practices	4
Polygenic risk in familial breast cancer: Changing the dynamics of communicating genetic risk	4
Ethical and moral perspectives of individuals who considered/used preimplantation (embryo) genetic testing	4
Characterization of genetic counselor practices in inpatient care settings	4
A descriptive investigation of clinical practice models used by cardiovascular genetic counselors in North America	4
Cascade testing for inherited arrhythmia conditions: Experiences and attitudes of family communication approaches for a Canadian cohort	4
Stagnation in quality of next‐generation sequencing assays for the diagnosis of hereditary hematopoietic malignancies	4
Medical interpreter‐mediated genetic counseling for Spanish preferring adults at risk for a hereditary cancer syndrome	4
Opinions of adults affected with later‐onset lysosomal storage diseases regarding newborn screening: A qualitative study	4
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
Knowledge and attitudes about genetic counseling in patients at a major hospital in Addis Ababa, Ethiopia	3
The experience of a sample of individuals in the United Kingdom living in the pre‐manifest stage of Huntington’s disease: An interpretative phenomenological analysis	3
Helping young children understand inherited cancer predisposition syndromes using bibliotherapy	3
Western Australian women's expectations for expanded NIPT—An online survey regarding NIPT for single gene, recessive and chromosomal conditions	3
Attitudes toward offering genetic counseling for psychiatric conditions among genetics healthcare practitioners in the United Kingdom: A qualitative study	3
Outcomes of psychiatric genetic counseling in relation to time since diagnosis and symptom onset	3
Views of Israeli healthcare professionals regarding communication of genetic variants of uncertain significance to patients	3
Results of the Genetic Counselor SARS‐CoV‐2 Impact Survey from the National Society of Genetic Counselors: Progress and penalty during the COVID‐19 pandemic	3
Building a foundation in self‐awareness: Genetic counseling students’ experiences with self‐care, reflection, and mindfulness	3
Preferences of Italian patients for return of secondary findings from clinical genome/exome sequencing	3
Experiences of United States genetic counseling supervisors regarding race/ethnicity in supervision: A qualitative investigation	3
Open communication of Duchenne muscular dystrophy facilitates disclosure process by parents to unaffected siblings	3
Ethical concerns surrounding sex prediction using noninvasive prenatal screening from pediatric endocrinologists' perspective	3
BRCA1/2 mutations and risk‐reducing bilateral salpingo‐oophorectomy among Latinas: The UPTAKE study	3
The goldilocks conundrum: Disclosing discrimination risks in informed consent	3
Clinical application of a scale to assess genomic healthcare empowerment (GEmS): Process and illustrative case examples	3
North American genetic counselors' approach to collecting and using ancestry in clinical practice	3
Assessing genetic counselor communication in response to virtual, asynchronous simulated video prompts	3
Telegenetics: The experience of an Indian center (Centre for Human Genetics) during the COVID‐19 pandemic	3
Evaluating a communication aid for return of genetic results in families with hypertrophic cardiomyopathy: A randomized controlled trial	3
Prognostic imagination: Genetic counseling amidst therapeutic innovation and evolving futures	3
Examining the effect of patient personality types and coping styles on outcomes of genetic counseling	3
Effects of genetic counselor disabilities on their professional experiences: A qualitative investigation of North American counselors' perceptions	3
Moral distress in genetic counseling: A study of North American genetic counselors	3
Preparing the genetic counseling workforce for the future in Australasia	3
Toward depathologizing queerness: An analysis of queer oppression in clinical genetics	3
Toward a better understanding of the experience of patients with moderate penetrance breast cancer gene pathogenic/likely pathogenic variants: A focus on ATM and CHEK2	3
Barriers to family history knowledge and family communication among LGBTQ+ individuals in the context of hereditary cancer risk assessment	3
The lived experience of reconstructing identity in response to genetic risk of frontotemporal degeneration and amyotrophic lateral sclerosis	3
Cancer genetic counseling for childhood cancer predisposition is associated with improved levels of knowledge and high satisfaction in parents	3
Healthcare decision makers' perspectives on the creation of new genetic counselor positions in North America: Exploring the case for psychiatric genetic counseling	3
Examining career shadowing in genetic counseling: Perspectives of shadowees, program directors, and genetic counselors	3
Explanatory models for the cause of Fragile X Syndrome in rural Cameroon	3
The role of psychosocial factors in Black women's self‐efficacy in receiving genetic counseling and testing	3
Unraveling non‐participation in genomic research: A complex interplay of barriers, facilitators, and sociocultural factors	3
Genetic counseling clinical documentation: Practice Resource of the National Society of Genetic Counselors	3
Pursuing germline genome sequencing to reduce illness uncertainty may involve additional uncertainties for cancer patients: A mixed‐methods study	3
Implementing genomics in the neonatal period: An assessment of parental decision making and anxiety	3
Clinical geneticists' views on and experiences with unsolicited findings in next‐generation sequencing: “A great technology creating new dilemmas”	3
Advancing health equity: A qualitative study assessing barriers and facilitators of implementing hereditary breast and ovarian cancer risk screening tools in community‐based organizations	3
Barriers in applying to genetic counseling Master's degree programs: Perceptions of prospective applicants when compared with Canadian admissions committee members	3
Challenges and opportunities in the establishment of a hereditary breast cancer clinic at an academic medical center in a low‐middle income country	3
Genetic counseling students' use of patient‐centered communication skills predicts standardized patient satisfaction during virtual simulated sessions	3
Universal access to genetic counseling for women with epithelial ovarian cancer in Nova Scotia: Evaluating a new collaborative care model	2
The impact of converting to telehealth for cancer genetic counseling and testing during the COVID‐19 pandemic	2
Mitochondrial replacement therapy: Genetic counselors' experiences, knowledge, and opinions	2
Research to reduce inequities in cancer risk services: Insights for remote genetic counseling in a pandemic and beyond	2
Prenatal patient perceptions of receiving difficult news over the telephone	2
Rethinking genetic counseling clinical skills training in the time of COVID‐19	2
Assessing barriers to the career ladder and professional development for ethnic minority genetic counselors in the United States	2
A qualitative study exploring LGBTQ genetic counseling students' relationships with peers and faculty in graduate school	2
Reproductive deliberation: Supporting autonomous decision making in prenatal genetic counseling	2
Assessing the acceptability, feasibility, and usefulness of a psychosocial screening tool to patients and clinicians in a clinical genetics service in Australia	2
Health‐related quality of life and fear of progression in individuals with Li‐Fraumeni syndrome	2
Advocating for equitable management of hereditary cancer syndromes	2
Factors that influence genetic counselors' participation in research	2
How are uncertain prenatal genetic results perceived and managed two years after they were received? A qualitative interview study	2
Exploring a brief medical improvisational performing arts intervention for genetic counseling graduate students	2
Public perceived knowledge of, attitude toward, and use of genetic testing in urban China	2
Assessing genetic counselors’ graduate school education and training in congenital heart defects	2
Preferences for and acceptability of receiving pharmacogenomic results by mail: A focus group study with a primarily African‐American cohort	2
U.S. Genetic counselors’ perceptions of inpatient genetic counseling: A valuable model for medically complex patients	2
A qualitative assessment of parental experiences with false‐positive newborn screening for Krabbe disease	2
An internship in psychiatric genetic counseling: Impact on genetic counseling graduates' practice and career choices	2
Psychological characteristics of Japanese patients and their family members receiving genetic counseling: A single‐institute exploratory study	2
What knowledge is required for an informed choice related to non‐invasive prenatal screening?	2
The experiences of adolescent siblings of children with rare genetic conditions: “It's made me who I am”	2
Elicitation of children’s understanding of information in pediatric genetic counseling encounters: A discourse‐oriented perspective	2
Genetic counseling practice for inherited eye diseases in an Israeli medical center during the COVID‐19 pandemic	2
‘Do language and culturereallymatter?’: A trans‐disciplinary investigation of cultural diversity in genetic counseling in Hong Kong	2
A qualitative study of LGBTQIA+ genetic counselors' experiences while applying to graduate school	2