Journal of Genetic Counseling

Article	Citations
Genetic testing and counseling for the unexplained epilepsies: An evidence‐based practice guideline of the National Society of Genetic Counselors	41
Telehealth for genetic counseling: A systematic evidence review	40
Use of a chatbot to increase uptake of cascade genetic testing	37
Benefits and limitations of telegenetics: A literature review	31
Chatbots & artificial intelligence to scale genetic information delivery	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
Exploring racial and ethnic minority individuals’ journey to becoming genetic counselors: Mapping paths to diversifying the genetic counseling profession	24
Considerations in genetic counseling of transgender patients: Cultural competencies and altered disease risk profiles	23
Risk assessment and genetic counseling for hereditary breast and ovarian cancer syndromes—Practice resource of the National Society of Genetic Counselors	23
Rapid genome‐wide sequencing in a neonatal intensive care unit: A retrospective qualitative exploration of parental experiences	22
Considerations for the use of qualitative methodologies in genetic counseling research	20
Transition to telephone genetic counseling services during the COVID‐19 pandemic	19
Prenatal Genetic Diagnosis of a Sex Chromosome Aneuploidy: Parent Experiences	19
Genetic counseling, virtual visits, and equity in the era of COVID‐19 and beyond	19
Transitioning to telegenetics in the COVID‐19 era: Patient satisfaction with remote genetic counseling in adult neurology	19
Rapid acute care genomics: Challenges and opportunities for genetic counselors	18
Genetic counselors' experiences with transgender individuals in prenatal and preconception settings	17
Influence of payer coverage and out‐of‐pocket costs on ordering of NGS panel tests for hereditary cancer in diverse settings	16
Do research participants share genomic screening results with family members?	16
Outcomes of genetic test disclosure and genetic counseling in a large Parkinson's disease research study	16
GeneLiFT: A novel test to facilitate rapid screening of genetic literacy in a diverse population undergoing genetic testing	16
Expanded carrier screening for reproductive risk assessment: An evidence‐based practice guideline from the National Society of Genetic Counselors	16
Contributors to and consequences of burnout among clinical genetic counselors in the United States	15
Genetic counselor experiences with telehealth before and after COVID‐19	15

Genetic counseling for congenital heart disease – Practice resource of the National Society of Genetic Counselors	15
Expanded carrier screening in the United States: A systematic evidence review exploring client and provider experiences	14
Transgender patients’ perspectives on their cancer genetic counseling experiences	13
After genomic testing results: Parents’ long‐term views	13
A review and definition of ‘usual care’ in genetic counseling trials to standardize use in research	13
Genetic counselors and legal recognition: A made‐for‐Canada approach	13
A systematic review and meta‐analysis of telephone vs in‐person genetic counseling in BRCA1/BRCA2 genetic testing	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
Reflections of parents of children with 22q11.2 Deletion Syndrome on the experience of receiving psychiatric genetic counseling: ‘Awareness to Act’	12
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’	12
Influence of lived experience on risk perception among women who received a breast cancer polygenic risk score: ‘Another piece of the pie’	12
COVID‐19 vaccine hesitancy and acceptance among pregnant people contacting a teratogen information service	11
Pregnant Hispanic women's views and knowledge of prenatal genetic testing	11
Improving gender‐affirming care in genetic counseling: Using educational tools that amplify transgender and/or gender non‐binary community voices	11
The current landscape of genetic test stewardship: A multi‐center prospective study	11
Australian healthcare professionals' perspectives on the ethical and practical issues associated with genomic newborn screening	11
Genetic counseling for patients with positive genomic screening results: Considerations for when the genetic test comes first	11
A family systems approach to genetic counseling: Development of narrative interventions	11
Social support networks of adults with sickle cell disease	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
Clinical genetic counseling and translation considerations for polygenic scores in personalized risk assessments: A Practice Resource from the National Society of Genetic Counselors	10
Family communication of genetic test results among women with inherited breast cancer genes	10
Pharmacogenomic education among genetic counseling training programs in North America	10
Understanding patients' views and willingness toward the use of telehealth in a cancer genetics service in Asia	10
The Canadian genetic counseling workforce: Perspectives from employers and recent graduates	10
Communication about positive BRCA1 and BRCA2 genetic test results and uptake of testing in relatives in a diverse Asian setting	9
State of recent literature on communication about cancer genetic testing among Latinx populations	9
Telehealth genetic services during the COVID‐19 Pandemic: Implementation and patient experiences across multiple specialties in Nebraska	9
An evidence‐based practice guideline of the National Society of Genetic Counselors for telehealth genetic counseling	9
Adapting genetic counseling operations amidst the COVID‐19 pandemic	9
Genetic counseling for fetal sex prediction by NIPT: Challenges and opportunities	9
Latinx attitudes, barriers, and experiences with genetic counseling and testing: A systematic review	8
Family planning in carriers of BRCA1 and BRCA2 pathogenic variants	8
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	8
The impact of a cascade testing video on recipients’ knowledge, cognitive message processing, and affective reactions: A formative evaluation	8
Prenatal genetic counselors' perceptions of the impact of abortion legislation on counseling and access in the United States	8
Spanish language concordance in genetic counseling sessions in the United States: Counselor experiences and perceptions of its effects on processes and outcomes	8
A report of the AGCPD task force to evaluate associations between select admissions requirements, demographics, and performance on ABGC certification examination	8
Genetic counseling in the time of COVID‐19: The Philippine experience with telegenetics	8
Newborn screening for Pompe disease: Parental experiences and follow‐up care for a late‐onset diagnosis	8
Attitudes and training needs of oncologists and surgeons in mainstreaming breast cancer genetic counseling in a low‐to‐middle income Asian country	8
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	8
Genome sequencing among children with medical complexity: What constitutes value from parents’ perspective?	8
The uptake and utility of genetic testing and genetic counseling for hypertrophic cardiomyopathy—A systematic review and meta‐analysis	8
Professional regulation for Australasian genetic counselors	8
Courtesy stigma of parents of children with Down syndrome: Adaptation process and transcendent stage	8
Elective genomic testing: Practice resource of the National Society of Genetic Counselors	7
Application of motivational interviewing strategies with the extended parallel process model to improve risk communication for parents of children with familial hypercholesterolemia	7
The erasure of transgender and intersex identities through fetal sex prediction and genetic essentialism	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

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
Financial constraints on genetic counseling and further risk‐management decisions among U.S. women at elevated breast cancer risk	7
Parenting a child with Down syndrome: A qualitative study of everyday practices in Danish families	7
Outcomes from a pilot genetic counseling intervention using motivational interviewing and the extended parallel process model to increase cascade cholesterol screening	7
The long‐term impact of receiving incidental findings on parents undergoing genome‐wide sequencing	7
Genetic counseling and diagnostic genetic testing for familial amyotrophic lateral sclerosis and/or frontotemporal dementia: A qualitative study of client experiences	7
Characterization of variant reclassification and patient re‐contact in a cancer genetics clinic	7
COVID contingencies: Early epicenter experiences of different genetics clinics at a New York City institution inform emergency adaptation strategies	7
Content analysis of Journal of Genetic Counseling research articles: A multi‐year perspective	7
Genetic counseling for early onset and familial dementia: Patient perspectives on exome sequencing	7
The COVID‐19 pandemic and reproductive genetic counseling: Changes in access and service delivery at an academic medical center in the United States	6
Assessing clinical education tools for expanded carrier screening	6
The genetic counseling profession in Austria: Stakeholders’ perspectives	6
Large‐scale group genetic counseling: Evaluation of a novel service delivery model in a Canadian hereditary cancer clinic	6
International genetic counseling: What do genetic counselors actually do?	6
Reasons affecting the uptake of reproductive genetic carrier screening among nonpregnant reproductive‐aged women in Flanders (Belgium)	6
Experiences of adolescents and their parents after receiving adolescents’ genomic screening results	6
Evaluation of barriers to referral for cancer predisposition syndromes in pediatric oncology patients in the United States	6
Process evaluation of a culturally targeted video for Latinas at risk of hereditary breast and ovarian cancer	6
Implicit and explicit racial prejudice and stereotyping toward Black (vs. White) Americans: The prevalence and variation among genetic counselors in North America	6
DNA testing information on YouTube: Inadequate advice can mislead and harm the public	6
Experiences of reproductive genetic counselors with abortion regulations in Ohio	6
Utilization of genetic testing: Analysis of 4,499 prior authorization requests for molecular genetic tests at four US regional health plans	6
Integrating genetic assistants into the workforce: An 18‐year productivity analysis and development of a staff mix planning tool	6
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	6
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	6
Between responsibility and desire: Accounts of reproductive decisions from those at risk for or affected by late‐onset neurological diseases	6
Strength of the genetic counselor: patient relationship is associated with extent of increased empowerment in patients with arrhythmogenic cardiomyopathy	6
Disclosure and comfort during genetic counseling sessions with LGBTQ+ patients: An updated assessment	6
Effects of participation in a U.S. trial of newborn genomic sequencing on parents at risk for depression	6
Understanding and interpretation of a variant of uncertain significance (VUS) genetic test result by pediatric providers who do not specialize in genetics	6
Trends in coverage and reimbursement for reproductive genetic counseling in New Jersey by multiple payers from 2010 to 2018	6
Conscience clauses in genetic counseling: Awareness and attitudes	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
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	5
Characterization of genetic counselor practices in inpatient care settings	5
Clinical genetic counselor experience in the adoption of telehealth in the United States and Canada during the COVID‐19 pandemic	5
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
Medical interpreter‐mediated genetic counseling for Spanish preferring adults at risk for a hereditary cancer syndrome	5
Learning from our patients: Utilizing the expertise of transgender and/or gender diverse educators to build an inclusive learning cycle	5
Adaptation of the working alliance inventory for the assessment of the therapeutic alliance in genetic counseling	5
Implementing genomics in the neonatal period: An assessment of parental decision making and anxiety	5
Young people’s experiences of a CDH1 pathogenic variant: Decision‐making about gastric cancer risk management	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
A survey of aortic disease biorepository participants’ preferences for return of research genetic results	5
Misattributed parentage identified through diagnostic exome sequencing: Frequency of detection and reporting practices	5
Attitudes and beliefs regardingrace‐targetedgenetic testing of Black people: A systematic review	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
Polygenic risk in familial breast cancer: Changing the dynamics of communicating genetic risk	5
Advancing health equity: A qualitative study assessing barriers and facilitators of implementing hereditary breast and ovarian cancer risk screening tools in community‐based organizations	5
Ethical concerns surrounding sex prediction using noninvasive prenatal screening from pediatric endocrinologists' perspective	5
Ethical and moral perspectives of individuals who considered/used preimplantation (embryo) genetic testing	5
Evolving approaches to prenatal genetic counseling for Spinal Muscular Atrophy in the new treatment era	5
Stagnation in quality of next‐generation sequencing assays for the diagnosis of hereditary hematopoietic malignancies	5
Toward depathologizing queerness: An analysis of queer oppression in clinical genetics	5
Management of amended variant classification laboratory reports by genetic counselors in the United States and Canada: An exploratory study	5
Exploring how mothers of a child with a genetic disorder experience their couple relationship in a low socio‐economic setting	4
Evaluating a general pediatric/adult genetic counseling clinic in a Midwest medical center	4
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A descriptive investigation of clinical practice models used by cardiovascular genetic counselors in North America	4
Explanatory models for the cause of Fragile X Syndrome in rural Cameroon	4
No longer “non‐traditional”: Genetic counselors' perceptions towards laboratory and industry roles	4
Opinions of adults affected with later‐onset lysosomal storage diseases regarding newborn screening: A qualitative study	4
Adding a genetic counseling assistant improves efficiency of hereditary cancer genetic counseling without impacting patient experience	4
The evolution of genetic counseling graduate education in New York City during the COVID‐19 pandemic: In the eye of the storm	4
Telegenetics: The experience of an Indian center (Centre for Human Genetics) during the COVID‐19 pandemic	4
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	4
Genetic counseling student rotations in industry: How COVID‐19 magnified the urgency for virtual learning options in diverse training settings	4
Exploring the role of Islam on the lived experience of patients with Long QT Syndrome in Saudi Arabia	4
Helping young children understand inherited cancer predisposition syndromes using bibliotherapy	4
U.S. Genetic counselors’ perceptions of inpatient genetic counseling: A valuable model for medically complex patients	4
CDH1 variants leading to gastric cancer risk management decision‐making experiences in emerging adults: ‘I am not ready yet’	4
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	4
Understanding and perception of direct‐to‐consumer genetic testing in Hong Kong	4
Adapting to the challenges of the global pandemic on genetic counselor education: Evaluating students’ satisfaction with virtual clinical experiences	4

Prognostic imagination: Genetic counseling amidst therapeutic innovation and evolving futures	4
Building a foundation in self‐awareness: Genetic counseling students’ experiences with self‐care, reflection, and mindfulness	4
Changes to the genetic counseling workforce as a result of the COVID‐19 pandemic	4
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	4
Cascade testing for inherited arrhythmia conditions: Experiences and attitudes of family communication approaches for a Canadian cohort	4
Sudden shift to remote genetic counseling during the COVID‐19 pandemic: Experiences of genetics professionals in Italy	4
Western Australian women's expectations for expanded NIPT—An online survey regarding NIPT for single gene, recessive and chromosomal conditions	4
Reproductive deliberation: Supporting autonomous decision making in prenatal genetic counseling	4
Critical components of genomic medicine practice for non‐genetics healthcare professionals: Genetic counselors' perspectives and implications for medical education	4
Need for additional training to be a laboratory genetic counselor—A qualitative exploration	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
A qualitative interview study of the attitudes toward reproductive options of people with genetic visual loss	3
Value of whole‐genome sequencing to Australian cancer patients and their first‐degree relatives participating in a genomic sequencing study	3
Examining career shadowing in genetic counseling: Perspectives of shadowees, program directors, and genetic counselors	3
Genetic counseling clinical documentation: Practice Resource of the National Society of Genetic Counselors	3
Landscape of genetic counseling in the Philippines	3
Attitudes toward offering genetic counseling for psychiatric conditions among genetics healthcare practitioners in the United Kingdom: A qualitative study	3
Effects of genetic counselor disabilities on their professional experiences: A qualitative investigation of North American counselors' perceptions	3
Evaluating a communication aid for return of genetic results in families with hypertrophic cardiomyopathy: A randomized controlled trial	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
Examining the effect of patient personality types and coping styles on outcomes of genetic counseling	3
Medical students' self‐perceived knowledge and clinical comfort with genetics in Pakistan	3
Easing the burden of multi‐state genetic counseling licensure in the United States: Process, pitfalls, and possible solutions	3
Clinical geneticists' views on and experiences with unsolicited findings in next‐generation sequencing: “A great technology creating new dilemmas”	3
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The goldilocks conundrum: Disclosing discrimination risks in informed consent	3
Establishing a mentorship program for prospective genetic counseling graduate students: Two cycles of program experience	3
Assessing genetic counselor communication in response to virtual, asynchronous simulated video prompts	3
Investigating factors that influence genetic counselors’ decisions to refer patients to mental health providers	3
Noninvasive prenatal screening (NIPS) results for participants of the eXtraordinarY babies study: Screening, counseling, diagnosis, and discordance	3
A systematic review of psycho‐social interventions for individuals with a BRCA1/2 pathogenic variant	3
Utilization of breast cancer risk prediction models by cancer genetic counselors in clinical practice predominantly in the United States	3
Pregnant women's experiences of non‐invasive prenatal testing (NIPT) in Japan: A qualitative study	3
Attitudes towards and sociodemographic determinants of genetic test usage in the USA; data from the Health Information National Trend Survey, 2020	3
Pursuing germline genome sequencing to reduce illness uncertainty may involve additional uncertainties for cancer patients: A mixed‐methods study	3
Views of Israeli healthcare professionals regarding communication of genetic variants of uncertain significance to patients	3
Individuals' experiences in genetic counseling and predictive testing for familial amyotrophic lateral sclerosis	3
Unraveling non‐participation in genomic research: A complex interplay of barriers, facilitators, and sociocultural factors	3
Clinical application of a scale to assess genomic healthcare empowerment (GEmS): Process and illustrative case examples	3
Barriers in applying to genetic counseling Master's degree programs: Perceptions of prospective applicants when compared with Canadian admissions committee members	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
North American genetic counselors' approach to collecting and using ancestry in clinical practice	3
Analysis of the reported use of practice‐based competencies by North American genetic counselors during the COVID‐19 pandemic	3
A qualitative study of LGBTQIA+ genetic counselors' experiences while applying to graduate school	3
The role of psychosocial factors in Black women's self‐efficacy in receiving genetic counseling and testing	3
Preparing the genetic counseling workforce for the future in Australasia	3
Genetic counseling practice for inherited eye diseases in an Israeli medical center during the COVID‐19 pandemic	3
Experiences of United States genetic counseling supervisors regarding race/ethnicity in supervision: A qualitative investigation	3
Outcomes of psychiatric genetic counseling in relation to time since diagnosis and symptom onset	3
Reproductive decision‐making and the utilization of preimplantation genetic testing among individuals with inherited aortic or vascular disease	3
Genetic counseling students' use of patient‐centered communication skills predicts standardized patient satisfaction during virtual simulated sessions	3
Moral distress in genetic counseling: A study of North American genetic counselors	3
Barriers to family history knowledge and family communication among LGBTQ+ individuals in the context of hereditary cancer risk assessment	3
Preferences of Italian patients for return of secondary findings from clinical genome/exome sequencing	3