Journal of Genetic Counseling

Article	Citations
Telehealth for genetic counseling: A systematic evidence review	34
Genetic counseling service delivery models: A study of genetic counselors’ interests, needs, and barriers to implementation	27
Benefits and limitations of telegenetics: A literature review	27
Genetic testing and counseling for the unexplained epilepsies: An evidence‐based practice guideline of the National Society of Genetic Counselors	27
Use of a chatbot to increase uptake of cascade genetic testing	26
Supporting a sense of inclusion and belonging for genetic counseling students who identify as racial or ethnic minorities	24
Chatbots & artificial intelligence to scale genetic information delivery	24
Risk assessment and genetic counseling for hereditary breast and ovarian cancer syndromes—Practice resource of the National Society of Genetic Counselors	20
Considerations in genetic counseling of transgender patients: Cultural competencies and altered disease risk profiles	20
Practice resource‐focused revision: Standardized pedigree nomenclature update centered on sex and gender inclusivity: A practice resource of the National Society of Genetic Counselors	20
Evaluating co‐created patient‐facing materials to increase understanding of genetic test results	19
Transitioning to telegenetics in the COVID‐19 era: Patient satisfaction with remote genetic counseling in adult neurology	18
Exploring racial and ethnic minority individuals’ journey to becoming genetic counselors: Mapping paths to diversifying the genetic counseling profession	18
Genetic counseling, virtual visits, and equity in the era of COVID‐19 and beyond	18
Parental experiences of uncertainty following an abnormal fetal anomaly scan: Insights using Han’s taxonomy of uncertainty	18
Transition to telephone genetic counseling services during the COVID‐19 pandemic	18
Perceived barriers to paternal expanded carrier screening following a positive maternal result: To screen or not to screen	18
Rapid genome‐wide sequencing in a neonatal intensive care unit: A retrospective qualitative exploration of parental experiences	17
Prenatal Genetic Diagnosis of a Sex Chromosome Aneuploidy: Parent Experiences	16
GeneLiFT: A novel test to facilitate rapid screening of genetic literacy in a diverse population undergoing genetic testing	15
Male–female differences in quality of life and coping style in patients with Marfan syndrome and hereditary thoracic aortic diseases	15
Genetic counselors' experiences with transgender individuals in prenatal and preconception settings	15
Rapid acute care genomics: Challenges and opportunities for genetic counselors	15
Genetic testing costs and compliance with clinical best practices	15
Do research participants share genomic screening results with family members?	14

Influence of payer coverage and out‐of‐pocket costs on ordering of NGS panel tests for hereditary cancer in diverse settings	14
Breast cancer polygenic risk scores in the clinical cancer genetic counseling setting: Current practices and impact on patient management	14
Genetic counseling following direct‐to consumer genetic testing: Consumer perspectives	13
A pilot randomized trial of an educational intervention to increase genetic counseling and genetic testing among Latina breast cancer survivors	13
Impact of variant reclassification in the clinical setting of cardiovascular genetics	13
Comprehension and personal value of negative non‐diagnostic genetic panel testing	13
Genetic counselor experiences with telehealth before and after COVID‐19	13
Considerations for the use of qualitative methodologies in genetic counseling research	13
Genetic Counseling for Neurofibromatosis 1, Neurofibromatosis 2, and Schwannomatosis—Practice Resource of the National Society of Genetic Counselors	13
A systematic review and meta‐analysis of telephone vs in‐person genetic counseling in BRCA1/BRCA2 genetic testing	12
A review and definition of ‘usual care’ in genetic counseling trials to standardize use in research	12
Influence of lived experience on risk perception among women who received a breast cancer polygenic risk score: ‘Another piece of the pie’	12
Geographical analysis of the distribution of certified genetic counselors in the United States	12
A narrative literature review: Growing the workforce through increased fieldwork capacity in genetic counseling training programs	12
Transgender patients’ perspectives on their cancer genetic counseling 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
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?	11
Genetic counseling student demographics: an empirical comparison of two cohorts	11
Reflections of parents of children with 22q11.2 Deletion Syndrome on the experience of receiving psychiatric genetic counseling: ‘Awareness to Act’	10
After genomic testing results: Parents’ long‐term views	10
Implementing innovative service delivery models in genetic counseling: a qualitative analysis of facilitators and barriers	10
Contributors to and consequences of burnout among clinical genetic counselors in the United States	10
Pharmacogenomic education among genetic counseling training programs in North America	10
“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	10
Genetic counseling for congenital heart disease – Practice resource of the National Society of Genetic Counselors	10
Characterizing standardized patients and genetic counseling graduate education	10
Adult adoptees and their use of direct‐to‐consumer genetic testing: Searching for family, searching for health	10
Outcomes of genetic test disclosure and genetic counseling in a large Parkinson's disease research study	9
Genetic counseling for patients with positive genomic screening results: Considerations for when the genetic test comes first	9
Family communication of genetic test results among women with inherited breast cancer genes	9
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	9
State of recent literature on communication about cancer genetic testing among Latinx populations	9
Advancing the genetic counseling profession through research: Identification of priorities by the National Society of Genetic Counselors research task force	9
Expanded carrier screening in the United States: A systematic evidence review exploring client and provider experiences	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
Social support networks of adults with sickle cell disease	9
Preconception expanded carrier screening: Impact of information presented by text or video on genetic knowledge and attitudes	9
COVID‐19 vaccine hesitancy and acceptance among pregnant people contacting a teratogen information service	9
Adapting genetic counseling operations amidst the COVID‐19 pandemic	8
Communication about positive BRCA1 and BRCA2 genetic test results and uptake of testing in relatives in a diverse Asian setting	8
Genetic counselors and legal recognition: A made‐for‐Canada approach	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
The current landscape of genetic test stewardship: A multi‐center prospective study	8
Australian healthcare professionals' perspectives on the ethical and practical issues associated with genomic newborn screening	8
Family planning in carriers of BRCA1 and BRCA2 pathogenic variants	8
Experiences and lessons learned by genetic counselors in returning secondary genetic findings to patients	8
An evidence‐based practice guideline of the National Society of Genetic Counselors for telehealth genetic counseling	8
A family systems approach to genetic counseling: Development of narrative interventions	8
Telehealth genetic services during the COVID‐19 Pandemic: Implementation and patient experiences across multiple specialties in Nebraska	8

Pursuing genetic testing for children with autism spectrum disorders: What do parents think?	8
A report of the AGCPD task force to evaluate associations between select admissions requirements, demographics, and performance on ABGC certification examination	8
Improving gender‐affirming care in genetic counseling: Using educational tools that amplify transgender and/or gender non‐binary community voices	8
Expanded carrier screening for reproductive risk assessment: An evidence‐based practice guideline from the National Society of Genetic Counselors	8
Spanish language concordance in genetic counseling sessions in the United States: Counselor experiences and perceptions of its effects on processes and outcomes	7
How do geneticists and prospective parents interpret and negotiate an uncertain prenatal genetic result? An analysis of clinical interactions	7
Examining clinical training through a bicultural lens: Experiences of genetic counseling students who identify with a racial or ethnic minority group	7
Financial constraints on genetic counseling and further risk‐management decisions among U.S. women at elevated breast cancer risk	7
Genetic counselors’ perspectives on population‐based screening for BRCA‐related hereditary breast and ovarian cancer and Lynch syndrome	7
The impact of a cascade testing video on recipients’ knowledge, cognitive message processing, and affective reactions: A formative evaluation	7
Effects of monitoring versus blunting on the public’s preferences for information in a hypothetical cancer diagnosis scenario	7
Changes in genetic variant results over time in pediatric cardiomyopathy and electrophysiology	7
COVID contingencies: Early epicenter experiences of different genetics clinics at a New York City institution inform emergency adaptation strategies	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
Outcomes from a pilot genetic counseling intervention using motivational interviewing and the extended parallel process model to increase cascade cholesterol screening	7
Genetic counseling for early onset and familial dementia: Patient perspectives on exome sequencing	7
Prenatal genetic counselors' perceptions of the impact of abortion legislation on counseling and access in the United States	7
Integrating genetic assistants into the workforce: An 18‐year productivity analysis and development of a staff mix planning tool	6
Content analysis of Journal of Genetic Counseling research articles: A multi‐year perspective	6
Diversity training experiences and factors associated with implicit racial bias among recent genetic counselor graduates of accredited programs in the United States and Canada	6
Genome sequencing among children with medical complexity: What constitutes value from parents’ perspective?	6
The long‐term impact of receiving incidental findings on parents undergoing genome‐wide sequencing	6
40 years and beyond for the National Society of Genetic Counselors: Reflections on genetic counseling practice	6
Large‐scale group genetic counseling: Evaluation of a novel service delivery model in a Canadian hereditary cancer clinic	6
Application of motivational interviewing strategies with the extended parallel process model to improve risk communication for parents of children with familial hypercholesterolemia	6
The impact of genetic counseling on women's grief and coping following termination of pregnancy for fetal anomaly	6
Parenting a child with Down syndrome: A qualitative study of everyday practices in Danish families	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
Assessing clinical education tools for expanded carrier screening	6
Experiences of reproductive genetic counselors with abortion regulations in Ohio	6
Genetic counseling and diagnostic genetic testing for familial amyotrophic lateral sclerosis and/or frontotemporal dementia: A qualitative study of client experiences	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
The COVID‐19 pandemic and reproductive genetic counseling: Changes in access and service delivery at an academic medical center in the United States	6
Adaptation and validation of the Genetic Counseling Outcome Scale for autism spectrum disorders and related conditions	6
Social media usage in family communication about genetic information: ‘I no longer speak with my sister but she needed to know’	6
Understanding patients' views and willingness toward the use of telehealth in a cancer genetics service in Asia	6
Motivational interviewing for genetic counseling: A unified framework for persuasive and equipoise conversations	6
Utilization of genetic testing: Analysis of 4,499 prior authorization requests for molecular genetic tests at four US regional health plans	6
A survey of aortic disease biorepository participants’ preferences for return of research genetic results	5
Disclosure and comfort during genetic counseling sessions with LGBTQ+ patients: An updated assessment	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
Effects of participation in a U.S. trial of newborn genomic sequencing on parents at risk for depression	5
Feasibility, face validity, and sensitivity of a web‐based simulation tool for assessing genetic counseling communication	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
The uptake and utility of genetic testing and genetic counseling for hypertrophic cardiomyopathy—A systematic review and meta‐analysis	5
Family genetic result communication in rare and undiagnosed disease communities: Understanding the practice	5
DNA testing information on YouTube: Inadequate advice can mislead and harm the public	5
Characterization of variant reclassification and patient re‐contact in a cancer genetics clinic	5
Reasons affecting the uptake of reproductive genetic carrier screening among nonpregnant reproductive‐aged women in Flanders (Belgium)	5
Understanding and interpretation of a variant of uncertain significance (VUS) genetic test result by pediatric providers who do not specialize in genetics	5
Exome sequencing study in a clinical research setting finds general acceptance of study returning secondary genomic findings with little decisional conflict	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
Clinical genetic counselor experience in the adoption of telehealth in the United States and Canada during the COVID‐19 pandemic	5
A Delphi study to prioritize genetic counseling outcomes: What matters most	5
Professional regulation for Australasian genetic counselors	5
Genetic counseling for fetal sex prediction by NIPT: Challenges and opportunities	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
Graduate training during the COVID‐19 pandemic: North American genetic counseling students' challenges, intolerance of uncertainty, and psychological well‐being	5
Genetic counseling graduate training to address religion and spirituality in clinical practice: A qualitative exploration of programs in North America	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
Experiences of adolescents and their parents after receiving adolescents’ genomic screening results	5
Genetic counseling in the time of COVID‐19: The Philippine experience with telegenetics	5
The experiences of families receiving a diagnosis of 22q11.2 deletion syndrome in Ireland	4
CDH1 variants leading to gastric cancer risk management decision‐making experiences in emerging adults: ‘I am not ready yet’	4
Newborn screening for Pompe disease: Parental experiences and follow‐up care for a late‐onset diagnosis	4
Attitudes and training needs of oncologists and surgeons in mainstreaming breast cancer genetic counseling in a low‐to‐middle income Asian country	4
Adapting to the challenges of the global pandemic on genetic counselor education: Evaluating students’ satisfaction with virtual clinical experiences	4
Trends in coverage and reimbursement for reproductive genetic counseling in New Jersey by multiple payers from 2010 to 2018	4
Exploring how mothers of a child with a genetic disorder experience their couple relationship in a low socio‐economic setting	4
Ethical and moral perspectives of individuals who considered/used preimplantation (embryo) genetic testing	4
Genetic counseling student rotations in industry: How COVID‐19 magnified the urgency for virtual learning options in diverse training settings	4
Implicit and explicit racial prejudice and stereotyping toward Black (vs. White) Americans: The prevalence and variation among genetic counselors in North America	4
Evolving approaches to prenatal genetic counseling for Spinal Muscular Atrophy in the new treatment era	4
Stagnation in quality of next‐generation sequencing assays for the diagnosis of hereditary hematopoietic malignancies	4
The genetic counseling profession in Austria: Stakeholders’ perspectives	4
Research participant understanding and engagement in an institutional, self‐consent biobank model	4

Misattributed parentage identified through diagnostic exome sequencing: Frequency of detection and reporting practices	4
Metaphors and why these are important in all aspects of genetic counseling	4
Adaptation of the working alliance inventory for the assessment of the therapeutic alliance in genetic counseling	4
Latinx attitudes, barriers, and experiences with genetic counseling and testing: A systematic review	4
Polygenic risk in familial breast cancer: Changing the dynamics of communicating genetic risk	4
Between responsibility and desire: Accounts of reproductive decisions from those at risk for or affected by late‐onset neurological diseases	4
	4
A descriptive investigation of clinical practice models used by cardiovascular genetic counselors in North America	4
Genetic counseling for advanced paternal age: A survey of genetic counselors' current practice	4
Opinions of adults affected with later‐onset lysosomal storage diseases regarding newborn screening: A qualitative study	4
Sudden shift to remote genetic counseling during the COVID‐19 pandemic: Experiences of genetics professionals in Italy	4
Use of telephone intake for family history taking at a cancer genetics service in Asia	4
The evolution of genetic counseling graduate education in New York City during the COVID‐19 pandemic: In the eye of the storm	4
Medical interpreter‐mediated genetic counseling for Spanish preferring adults at risk for a hereditary cancer syndrome	4
Exploring empathy in genetic counseling students and new genetic counselors	4
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	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
Strength of the genetic counselor: patient relationship is associated with extent of increased empowerment in patients with arrhythmogenic cardiomyopathy	4