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	39
Telehealth for genetic counseling: A systematic evidence review	38
Use of a chatbot to increase uptake of cascade genetic testing	36
Benefits and limitations of telegenetics: A literature review	31
Genetic counseling service delivery models: A study of genetic counselors’ interests, needs, and barriers to implementation	28
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
Considerations in genetic counseling of transgender patients: Cultural competencies and altered disease risk profiles	23
Exploring racial and ethnic minority individuals’ journey to becoming genetic counselors: Mapping paths to diversifying the genetic counseling profession	22
Rapid genome‐wide sequencing in a neonatal intensive care unit: A retrospective qualitative exploration of parental experiences	22
Risk assessment and genetic counseling for hereditary breast and ovarian cancer syndromes—Practice resource of the National Society of Genetic Counselors	22
Transitioning to telegenetics in the COVID‐19 era: Patient satisfaction with remote genetic counseling in adult neurology	19
Evaluating co‐created patient‐facing materials to increase understanding of genetic test results	19
Perceived barriers to paternal expanded carrier screening following a positive maternal result: To screen or not to screen	19
Considerations for the use of qualitative methodologies in genetic counseling research	19
Genetic counseling, virtual visits, and equity in the era of COVID‐19 and beyond	19
Prenatal Genetic Diagnosis of a Sex Chromosome Aneuploidy: Parent Experiences	19
Transition to telephone genetic counseling services during the COVID‐19 pandemic	19
Rapid acute care genomics: Challenges and opportunities for genetic counselors	18
Genetic counselors' experiences with transgender individuals in prenatal and preconception settings	17
Do research participants share genomic screening results with family members?	16
Influence of payer coverage and out‐of‐pocket costs on ordering of NGS panel tests for hereditary cancer in diverse settings	16
A pilot randomized trial of an educational intervention to increase genetic counseling and genetic testing among Latina breast cancer survivors	16
GeneLiFT: A novel test to facilitate rapid screening of genetic literacy in a diverse population undergoing genetic testing	16

Breast cancer polygenic risk scores in the clinical cancer genetic counseling setting: Current practices and impact on patient management	15
Genetic counseling for congenital heart disease – Practice resource of the National Society of Genetic Counselors	15
Genetic counselor experiences with telehealth before and after COVID‐19	15
Contributors to and consequences of burnout among clinical genetic counselors in the United States	15
Impact of variant reclassification in the clinical setting of cardiovascular genetics	15
Outcomes of genetic test disclosure and genetic counseling in a large Parkinson's disease research study	15
Comprehension and personal value of negative non‐diagnostic genetic panel testing	14
Geographical analysis of the distribution of certified genetic counselors in the United States	14
Expanded carrier screening for reproductive risk assessment: An evidence‐based practice guideline from the National Society of Genetic Counselors	14
Expanded carrier screening in the United States: A systematic evidence review exploring client and provider experiences	14
A review and definition of ‘usual care’ in genetic counseling trials to standardize use in research	13
A narrative literature review: Growing the workforce through increased fieldwork capacity in genetic counseling training programs	13
After genomic testing results: Parents’ long‐term views	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
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
Transgender patients’ perspectives on their cancer genetic counseling experiences	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
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
Australian healthcare professionals' perspectives on the ethical and practical issues associated with genomic newborn screening	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
Pursuing genetic testing for children with autism spectrum disorders: What do parents think?	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
Characterizing standardized patients and genetic counseling graduate education	10
The Canadian genetic counseling workforce: Perspectives from employers and recent graduates	10
Preconception expanded carrier screening: Impact of information presented by text or video on genetic knowledge and attitudes	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
Understanding patients' views and willingness toward the use of telehealth in a cancer genetics service in Asia	10
Pharmacogenomic education among genetic counseling training programs in North America	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
Genetic counseling for fetal sex prediction by NIPT: Challenges and opportunities	9
Telehealth genetic services during the COVID‐19 Pandemic: Implementation and patient experiences across multiple specialties in Nebraska	9
Social support networks of adults with sickle cell disease	9
Communication about positive BRCA1 and BRCA2 genetic test results and uptake of testing in relatives in a diverse Asian setting	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
Advancing the genetic counseling profession through research: Identification of priorities by the National Society of Genetic Counselors research task force	9
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
State of recent literature on communication about cancer genetic testing among Latinx populations	8
Professional regulation for Australasian genetic counselors	8
A report of the AGCPD task force to evaluate associations between select admissions requirements, demographics, and performance on ABGC certification examination	8
The uptake and utility of genetic testing and genetic counseling for hypertrophic cardiomyopathy—A systematic review and meta‐analysis	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
Spanish language concordance in genetic counseling sessions in the United States: Counselor experiences and perceptions of its effects on processes and outcomes	8
Genome sequencing among children with medical complexity: What constitutes value from parents’ perspective?	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
Motivational interviewing for genetic counseling: A unified framework for persuasive and equipoise conversations	7
Characterization of variant reclassification and patient re‐contact in a cancer genetics clinic	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	7
Adaptation and validation of the Genetic Counseling Outcome Scale for autism spectrum disorders and related conditions	7
The long‐term impact of receiving incidental findings on parents undergoing genome‐wide sequencing	7
Genetic counseling for early onset and familial dementia: Patient perspectives on exome sequencing	7
Genetic counseling and diagnostic genetic testing for familial amyotrophic lateral sclerosis and/or frontotemporal dementia: A qualitative study of client experiences	7
Financial constraints on genetic counseling and further risk‐management decisions among U.S. women at elevated breast cancer risk	7
The impact of genetic counseling on women's grief and coping following termination of pregnancy for fetal anomaly	7
Content analysis of Journal of Genetic Counseling research articles: A multi‐year perspective	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
Genetic counseling in the time of COVID‐19: The Philippine experience with telegenetics	7
Examining clinical training through a bicultural lens: Experiences of genetic counseling students who identify with a racial or ethnic minority group	7
Application of motivational interviewing strategies with the extended parallel process model to improve risk communication for parents of children with familial hypercholesterolemia	7
COVID contingencies: Early epicenter experiences of different genetics clinics at a New York City institution inform emergency adaptation strategies	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
Integrating genetic assistants into the workforce: An 18‐year productivity analysis and development of a staff mix planning tool	6
Latinx attitudes, barriers, and experiences with genetic counseling and testing: A systematic review	6
Process evaluation of a culturally targeted video for Latinas at risk of hereditary breast and ovarian cancer	6
Assessing clinical education tools for expanded carrier screening	6
Disclosure and comfort during genetic counseling sessions with LGBTQ+ patients: An updated assessment	6
Large‐scale group genetic counseling: Evaluation of a novel service delivery model in a Canadian hereditary cancer clinic	6
Utilization of genetic testing: Analysis of 4,499 prior authorization requests for molecular genetic tests at four US regional health plans	6
Understanding and interpretation of a variant of uncertain significance (VUS) genetic test result by pediatric providers who do not specialize in genetics	6
Evaluation of barriers to referral for cancer predisposition syndromes in pediatric oncology patients in the United States	6
Trends in coverage and reimbursement for reproductive genetic counseling in New Jersey by multiple payers from 2010 to 2018	6
Between responsibility and desire: Accounts of reproductive decisions from those at risk for or affected by late‐onset neurological diseases	6
Predictive testing for neurodegenerative diseases in the age of next‐generation sequencing	6
Elective genomic testing: Practice resource of the National Society of Genetic Counselors	6
Experiences of reproductive genetic counselors with abortion regulations in Ohio	6
The erasure of transgender and intersex identities through fetal sex prediction and genetic essentialism	6
Experiences of adolescents and their parents after receiving adolescents’ genomic screening results	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
Strength of the genetic counselor: patient relationship is associated with extent of increased empowerment in patients with arrhythmogenic cardiomyopathy	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
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
Graduate training during the COVID‐19 pandemic: North American genetic counseling students' challenges, intolerance of uncertainty, and psychological well‐being	5
Management of amended variant classification laboratory reports by genetic counselors in the United States and Canada: An exploratory study	5
Polygenic risk in familial breast cancer: Changing the dynamics of communicating genetic risk	5
Exploring empathy in genetic counseling students and new genetic counselors	5
Young people’s experiences of a CDH1 pathogenic variant: Decision‐making about gastric cancer risk management	5
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	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
The genetic counseling profession in Austria: Stakeholders’ perspectives	5
Courtesy stigma of parents of children with Down syndrome: Adaptation process and transcendent stage	5
‘Steep learning curves’ to ‘Smooth Sailing’: A reappraisal of telegenetics amidst the COVID‐19 pandemic	5
Adaptation of the working alliance inventory for the assessment of the therapeutic alliance in genetic counseling	5
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
Implementing genomics in the neonatal period: An assessment of parental decision making and anxiety	5
Revising the FOCUS framework through a qualitative study assessing self‐reported counseling skills of genetic counselors	5
Characterization of genetic counselor practices in inpatient care settings	5
Evolving approaches to prenatal genetic counseling for Spinal Muscular Atrophy in the new treatment era	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
Attitudes and beliefs regardingrace‐targetedgenetic testing of Black people: A systematic review	5
Learning from our patients: Utilizing the expertise of transgender and/or gender diverse educators to build an inclusive learning cycle	5
Medical interpreter‐mediated genetic counseling for Spanish preferring adults at risk for a hereditary cancer syndrome	5
Effects of participation in a U.S. trial of newborn genomic sequencing on parents at risk for depression	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
Exome sequencing study in a clinical research setting finds general acceptance of study returning secondary genomic findings with little decisional conflict	5
Ethical and moral perspectives of individuals who considered/used preimplantation (embryo) genetic testing	5
Ethical concerns surrounding sex prediction using noninvasive prenatal screening from pediatric endocrinologists' perspective	5
Clinical genetic counselor experience in the adoption of telehealth in the United States and Canada during the COVID‐19 pandemic	5
Family genetic result communication in rare and undiagnosed disease communities: Understanding the practice	5
Misattributed parentage identified through diagnostic exome sequencing: Frequency of detection and reporting practices	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	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
Genetic counseling for advanced paternal age: A survey of genetic counselors' current practice	4

U.S. Genetic counselors’ perceptions of inpatient genetic counseling: A valuable model for medically complex patients	4
Opinions of adults affected with later‐onset lysosomal storage diseases regarding newborn screening: A qualitative study	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
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
Exploring how mothers of a child with a genetic disorder experience their couple relationship in a low socio‐economic setting	4
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Cascade testing for inherited arrhythmia conditions: Experiences and attitudes of family communication approaches for a Canadian cohort	4
Explanatory models for the cause of Fragile X Syndrome in rural Cameroon	4
Western Australian women's expectations for expanded NIPT—An online survey regarding NIPT for single gene, recessive and chromosomal conditions	4
Stagnation in quality of next‐generation sequencing assays for the diagnosis of hereditary hematopoietic malignancies	4
Research participant understanding and engagement in an institutional, self‐consent biobank model	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
Building a foundation in self‐awareness: Genetic counseling students’ experiences with self‐care, reflection, and mindfulness	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
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
Exploring the role of Islam on the lived experience of patients with Long QT Syndrome in Saudi Arabia	4
A descriptive investigation of clinical practice models used by cardiovascular genetic counselors in North America	4
Reproductive deliberation: Supporting autonomous decision making in prenatal genetic counseling	4
Sudden shift to remote genetic counseling during the COVID‐19 pandemic: Experiences of genetics professionals in Italy	4
No longer “non‐traditional”: Genetic counselors' perceptions towards laboratory and industry roles	4
Toward depathologizing queerness: An analysis of queer oppression in clinical genetics	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