Journal of Genetic Counseling

Article	Citations
Genetic Counseling Service Delivery Models in the United States: Assessment of changes in use from 2010 to 2017	39
Telehealth for genetic counseling: A systematic evidence review	33
Genetic testing and counseling for the unexplained epilepsies: An evidence‐based practice guideline of the National Society of Genetic Counselors	27
Benefits and limitations of telegenetics: A literature review	27
Genetic counseling service delivery models: A study of genetic counselors’ interests, needs, and barriers to implementation	26
Use of a chatbot to increase uptake of cascade genetic testing	24
Supporting a sense of inclusion and belonging for genetic counseling students who identify as racial or ethnic minorities	23
Chatbots & artificial intelligence to scale genetic information delivery	22
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
Considerations in genetic counseling of transgender patients: Cultural competencies and altered disease risk profiles	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
Unanswered Questions: Hereditary breast and gynecological cancer risk assessment in transgender adolescents and young adults	18
Perceived barriers to paternal expanded carrier screening following a positive maternal result: To screen or not to screen	18
Transition to telephone genetic counseling services during the COVID‐19 pandemic	18
Exploring racial and ethnic minority individuals’ journey to becoming genetic counselors: Mapping paths to diversifying the genetic counseling profession	18
Risk assessment and genetic counseling for hereditary breast and ovarian cancer syndromes—Practice resource of the National Society of Genetic Counselors	18
Parental experiences of uncertainty following an abnormal fetal anomaly scan: Insights using Han’s taxonomy of uncertainty	18
Genetic counseling, virtual visits, and equity in the era of COVID‐19 and beyond	17
Rapid genome‐wide sequencing in a neonatal intensive care unit: A retrospective qualitative exploration of parental experiences	17
Financial barriers in a county genetics clinic: Problems and solutions	16
A qualitative study of Latinx parents' experiences of clinical exome sequencing	16
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

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	14
Breast cancer polygenic risk scores in the clinical cancer genetic counseling setting: Current practices and impact on patient management	14
Prenatal Genetic Diagnosis of a Sex Chromosome Aneuploidy: Parent Experiences	14
Genetic Counseling for Neurofibromatosis 1, Neurofibromatosis 2, and Schwannomatosis—Practice Resource of the National Society of Genetic Counselors	13
Comprehension and personal value of negative non‐diagnostic genetic panel testing	13
Influence of payer coverage and out‐of‐pocket costs on ordering of NGS panel tests for hereditary cancer in diverse settings	13
Impact of variant reclassification in the clinical setting of cardiovascular genetics	13
Genetic counseling following direct‐to consumer genetic testing: Consumer perspectives	13
A systematic review and meta‐analysis of telephone vs in‐person genetic counseling in BRCA1/BRCA2 genetic testing	12
A narrative literature review: Growing the workforce through increased fieldwork capacity in genetic counseling training programs	12
Do research participants share genomic screening results with family members?	12
Genetic counselor experiences with telehealth before and after COVID‐19	12
Geographical analysis of the distribution of certified genetic counselors in the United States	12
Influence of lived experience on risk perception among women who received a breast cancer polygenic risk score: ‘Another piece of the pie’	12
Transgender patients’ perspectives on their cancer genetic counseling experiences	11
Considerations for the use of qualitative methodologies in genetic counseling research	11
Genetic counseling student demographics: an empirical comparison of two cohorts	11
A pilot randomized trial of an educational intervention to increase genetic counseling and genetic testing among Latina breast cancer survivors	11
A road map for the future: An exploration of attitudes, perceptions, and beliefs among African Americans to tailor health promotion of cancer‐related genetic counseling and testing	11
A review and definition of ‘usual care’ in genetic counseling trials to standardize use in research	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
Contributors to and consequences of burnout among clinical genetic counselors in the United States	10
Implementing innovative service delivery models in genetic counseling: a qualitative analysis of facilitators and barriers	10
Exploring experiences and expectations of prenatal health care and genetic counseling/testing in immigrant Latinas	10
Enhancing inclusion of diverse populations in genomics: A competence framework	10
Pharmacogenomic education among genetic counseling training programs in North America	10
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’	10
Understanding access to genomics in an ethnically diverse south Florida population: A comparison of demographics in odyssey and rapid whole genome sequencing programs	10
After genomic testing results: Parents’ long‐term views	10
Characterizing standardized patients and genetic counseling graduate education	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
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
Advancing the genetic counseling profession through research: Identification of priorities by the National Society of Genetic Counselors research task force	9
Preconception expanded carrier screening: Impact of information presented by text or video on genetic knowledge and attitudes	9
Genetic counseling for congenital heart disease – Practice resource of the National Society of Genetic Counselors	9
State of recent literature on communication about cancer genetic testing among Latinx populations	9
Social support networks of adults with sickle cell disease	9
The Canadian genetic counseling workforce: Perspectives from employers and recent graduates	9
Genetic counseling for patients with positive genomic screening results: Considerations for when the genetic test comes first	9
Expanded carrier screening in the United States: A systematic evidence review exploring client and provider experiences	9
Reflections of parents of children with 22q11.2 Deletion Syndrome on the experience of receiving psychiatric genetic counseling: ‘Awareness to Act’	9
Telehealth genetic services during the COVID‐19 Pandemic: Implementation and patient experiences across multiple specialties in Nebraska	8
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	8
An evidence‐based practice guideline of the National Society of Genetic Counselors for telehealth genetic counseling	8
Family communication of genetic test results among women with inherited breast cancer genes	8
Adapting genetic counseling operations amidst the COVID‐19 pandemic	8
Pursuing genetic testing for children with autism spectrum disorders: What do parents think?	8
Genetic counselors and legal recognition: A made‐for‐Canada approach	8

Pregnant Hispanic women's views and knowledge of prenatal genetic testing	8
The current landscape of genetic test stewardship: A multi‐center prospective study	8
COVID‐19 vaccine hesitancy and acceptance among pregnant people contacting a teratogen information service	8
A report of the AGCPD task force to evaluate associations between select admissions requirements, demographics, and performance on ABGC certification examination	8
Experiences and lessons learned by genetic counselors in returning secondary genetic findings to patients	8
A family systems approach to genetic counseling: Development of narrative interventions	8
Improving gender‐affirming care in genetic counseling: Using educational tools that amplify transgender and/or gender non‐binary community voices	7
Australian healthcare professionals' perspectives on the ethical and practical issues associated with genomic newborn screening	7
Examining clinical training through a bicultural lens: Experiences of genetic counseling students who identify with a racial or ethnic minority group	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
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
How do geneticists and prospective parents interpret and negotiate an uncertain prenatal genetic result? An analysis of clinical interactions	7
COVID contingencies: Early epicenter experiences of different genetics clinics at a New York City institution inform emergency adaptation strategies	7
Expanded carrier screening for reproductive risk assessment: An evidence‐based practice guideline from the National Society of Genetic Counselors	7
Family planning in carriers of BRCA1 and BRCA2 pathogenic variants	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
Diagnostic uncertainties, ethical tensions, and accounts of role responsibilities in genetic counseling communication	7
Changes in genetic variant results over time in pediatric cardiomyopathy and electrophysiology	7
Genetic counselors’ perspectives on population‐based screening for BRCA‐related hereditary breast and ovarian cancer and Lynch syndrome	7
Clinical genetic counseling and translation considerations for polygenic scores in personalized risk assessments: A Practice Resource from the National Society of Genetic Counselors	7
The long‐term impact of receiving incidental findings on parents undergoing genome‐wide sequencing	6
Social media usage in family communication about genetic information: ‘I no longer speak with my sister but she needed to know’	6
Experiences of reproductive genetic counselors with abortion regulations in Ohio	6
Large‐scale group genetic counseling: Evaluation of a novel service delivery model in a Canadian hereditary cancer clinic	6
Integrating genetic assistants into the workforce: An 18‐year productivity analysis and development of a staff mix planning tool	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
Adaptation and validation of the Genetic Counseling Outcome Scale for autism spectrum disorders and related conditions	6
Predictive testing for neurodegenerative diseases in the age of next‐generation sequencing	6
The impact of a cascade testing video on recipients’ knowledge, cognitive message processing, and affective reactions: A formative evaluation	6
Prenatal genetic counselors' perceptions of the impact of abortion legislation on counseling and access in the United States	6
40 years and beyond for the National Society of Genetic Counselors: Reflections on genetic counseling practice	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
The COVID‐19 pandemic and reproductive genetic counseling: Changes in access and service delivery at an academic medical center in the United States	6
Effects of monitoring versus blunting on the public’s preferences for information in a hypothetical cancer diagnosis scenario	6
Assessing clinical education tools for expanded carrier screening	6
Motivational interviewing for genetic counseling: A unified framework for persuasive and equipoise conversations	6
Application of motivational interviewing strategies with the extended parallel process model to improve risk communication for parents of children with familial hypercholesterolemia	6
Communication about positive BRCA1 and BRCA2 genetic test results and uptake of testing in relatives in a diverse Asian setting	6
Content analysis of Journal of Genetic Counseling research articles: A multi‐year perspective	6
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
Diversity training experiences and factors associated with implicit racial bias among recent genetic counselor graduates of accredited programs in the United States and Canada	5
Clinical genetic counselor experience in the adoption of telehealth in the United States and Canada during the COVID‐19 pandemic	5
The uptake and utility of genetic testing and genetic counseling for hypertrophic cardiomyopathy—A systematic review and meta‐analysis	5
DNA testing information on YouTube: Inadequate advice can mislead and harm the public	5
Utilization of genetic testing: Analysis of 4,499 prior authorization requests for molecular genetic tests at four US regional health plans	5
Reasons affecting the uptake of reproductive genetic carrier screening among nonpregnant reproductive‐aged women in Flanders (Belgium)	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
Process evaluation of a culturally targeted video for Latinas at risk of hereditary breast and ovarian cancer	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
Genetic counseling and diagnostic genetic testing for familial amyotrophic lateral sclerosis and/or frontotemporal dementia: A qualitative study of client experiences	5
Characterization of variant reclassification and patient re‐contact in a cancer genetics clinic	5
‘Steep learning curves’ to ‘Smooth Sailing’: A reappraisal of telegenetics amidst the COVID‐19 pandemic	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 adolescents and their parents after receiving adolescents’ genomic screening results	5
Genome sequencing among children with medical complexity: What constitutes value from parents’ perspective?	5
Genetic counseling in the time of COVID‐19: The Philippine experience with telegenetics	5
Professional regulation for Australasian genetic counselors	5
Informing models of cancer genetics care in the era of multigene panel testing with patient‐led recommendations	5
Courtesy stigma of parents of children with Down syndrome: Adaptation process and transcendent stage	5
Conscience clauses in genetic counseling: Awareness and attitudes	5
Revising the FOCUS framework through a qualitative study assessing self‐reported counseling skills of genetic counselors	4
Between responsibility and desire: Accounts of reproductive decisions from those at risk for or affected by late‐onset neurological diseases	4
	4
The incidence and carrier frequency of Tay‐Sachs disease in the French‐Canadian population of Quebec based on retrospective data from 24 years, 1992–2015	4
Stagnation in quality of next‐generation sequencing assays for the diagnosis of hereditary hematopoietic malignancies	4
Understanding patients' views and willingness toward the use of telehealth in a cancer genetics service in Asia	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
Introduction: The state of minority and health disparities in research and practice in genetic counseling and genomic medicine	4
Adapting to the challenges of the global pandemic on genetic counselor education: Evaluating students’ satisfaction with virtual clinical experiences	4
Exploring empathy in genetic counseling students and new genetic counselors	4

Adaptation of the working alliance inventory for the assessment of the therapeutic alliance in genetic counseling	4
Ethical and moral perspectives of individuals who considered/used preimplantation (embryo) genetic testing	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
Implicit and explicit racial prejudice and stereotyping toward Black (vs. White) Americans: The prevalence and variation among genetic counselors in North America	4
Genetic counseling for advanced paternal age: A survey of genetic counselors' current practice	4
The genetic counseling profession in Austria: Stakeholders’ perspectives	4
Opinions of adults affected with later‐onset lysosomal storage diseases regarding newborn screening: A qualitative study	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
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
Polygenic risk in familial breast cancer: Changing the dynamics of communicating genetic risk	4
Exploring how mothers of a child with a genetic disorder experience their couple relationship in a low socio‐economic setting	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 student rotations in industry: How COVID‐19 magnified the urgency for virtual learning options in diverse training settings	4
Strength of the genetic counselor: patient relationship is associated with extent of increased empowerment in patients with arrhythmogenic cardiomyopathy	4
The experiences of families receiving a diagnosis of 22q11.2 deletion syndrome in Ireland	4
Disclosure and comfort during genetic counseling sessions with LGBTQ+ patients: An updated assessment	4
Sudden shift to remote genetic counseling during the COVID‐19 pandemic: Experiences of genetics professionals in Italy	4
Family genetic result communication in rare and undiagnosed disease communities: Understanding the practice	4
Genetic counseling for fetal sex prediction by NIPT: Challenges and opportunities	4
The evolution of genetic counseling graduate education in New York City during the COVID‐19 pandemic: In the eye of the storm	4
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”	4
Challenges and opportunities in the establishment of a hereditary breast cancer clinic at an academic medical center in a low‐middle income country	3
Need for additional training to be a laboratory genetic counselor—A qualitative exploration	3
Patterns of germline and somatic testing after universal tumor screening for Lynch syndrome: A clinical practice survey of active members of the Collaborative Group of the Americas on Inherited Gastro	3
Changes to the genetic counseling workforce as a result of the COVID‐19 pandemic	3
Characterization of genetic counselor practices in inpatient care settings	3
Examining career shadowing in genetic counseling: Perspectives of shadowees, program directors, and genetic counselors	3
Helping young children understand inherited cancer predisposition syndromes using bibliotherapy	3
Eliciting culturally and medically informative family health histories from Marshallese patients living in the United States	3
Unraveling non‐participation in genomic research: A complex interplay of barriers, facilitators, and sociocultural factors	3
Medical interpreter‐mediated genetic counseling for Spanish preferring adults at risk for a hereditary cancer syndrome	3
Pre‐genetics clinic resource evaluation for adults with intellectual disability: The pre‐genetics clinic aid	3
No longer “non‐traditional”: Genetic counselors' perceptions towards laboratory and industry roles	3
Latinx attitudes, barriers, and experiences with genetic counseling and testing: A systematic review	3
Pursuing germline genome sequencing to reduce illness uncertainty may involve additional uncertainties for cancer patients: A mixed‐methods study	3
Building a foundation in self‐awareness: Genetic counseling students’ experiences with self‐care, reflection, and mindfulness	3
Understanding and perception of direct‐to‐consumer genetic testing in Hong Kong	3
Trends in coverage and reimbursement for reproductive genetic counseling in New Jersey by multiple payers from 2010 to 2018	3
Barriers in applying to genetic counseling Master's degree programs: Perceptions of prospective applicants when compared with Canadian admissions committee members	3
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	3
Barriers to family history knowledge and family communication among LGBTQ+ individuals in the context of hereditary cancer risk assessment	3
Knowledge and attitudes about genetic counseling in patients at a major hospital in Addis Ababa, Ethiopia	3
Clinical application of a scale to assess genomic healthcare empowerment (GEmS): Process and illustrative case examples	3
A descriptive investigation of clinical practice models used by cardiovascular genetic counselors in North America	3
Assessing genetic counselor communication in response to virtual, asynchronous simulated video prompts	3
Attitudes toward offering genetic counseling for psychiatric conditions among genetics healthcare practitioners in the United Kingdom: A qualitative study	3
Management of amended variant classification laboratory reports by genetic counselors in the United States and Canada: An exploratory study	3
Elective genomic testing: Practice resource of the National Society of Genetic Counselors	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
Examining the effect of patient personality types and coping styles on outcomes of genetic counseling	3
Views of Israeli healthcare professionals regarding communication of genetic variants of uncertain significance to patients	3
Clinical geneticists' views on and experiences with unsolicited findings in next‐generation sequencing: “A great technology creating new dilemmas”	3
Experiences of United States genetic counseling supervisors regarding race/ethnicity in supervision: A qualitative investigation	3
Critical components of genomic medicine practice for non‐genetics healthcare professionals: Genetic counselors' perspectives and implications for medical education	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
Adding a genetic counseling assistant improves efficiency of hereditary cancer genetic counseling without impacting patient experience	3
The goldilocks conundrum: Disclosing discrimination risks in informed consent	3
Ethical concerns surrounding sex prediction using noninvasive prenatal screening from pediatric endocrinologists' perspective	3
Cancer genetic counseling for childhood cancer predisposition is associated with improved levels of knowledge and high satisfaction in parents	3
Evolving approaches to prenatal genetic counseling for Spinal Muscular Atrophy in the new treatment era	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
Prognostic imagination: Genetic counseling amidst therapeutic innovation and evolving futures	3
Cascade testing for inherited arrhythmia conditions: Experiences and attitudes of family communication approaches for a Canadian cohort	3
Genetic counseling clinical documentation: Practice Resource of the National Society of Genetic Counselors	3
The role of psychosocial factors in Black women's self‐efficacy in receiving genetic counseling and testing	3
Outcomes of psychiatric genetic counseling in relation to time since diagnosis and symptom onset	3
Preparing the genetic counseling workforce for the future in Australasia	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
Evaluation of barriers to referral for cancer predisposition syndromes in pediatric oncology patients in the United States	3
Preferences of Italian patients for return of secondary findings from clinical genome/exome sequencing	3
Implementing genomics in the neonatal period: An assessment of parental decision making and anxiety	3
Use of telephone intake for family history taking at a cancer genetics service in Asia	3
A qualitative study of LGBTQIA+ genetic counselors' experiences while applying to graduate school	2
How are uncertain prenatal genetic results perceived and managed two years after they were received? A qualitative interview study	2
What knowledge is required for an informed choice related to non‐invasive prenatal screening?	2
Open communication of Duchenne muscular dystrophy facilitates disclosure process by parents to unaffected siblings	2
International genetic counseling: What do genetic counselors actually do?	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
Assessing the acceptability, feasibility, and usefulness of a psychosocial screening tool to patients and clinicians in a clinical genetics service in Australia	2
Advocating for equitable management of hereditary cancer syndromes	2
Prenatal patient perceptions of receiving difficult news over the telephone	2
Factors that influence genetic counselors' participation in research	2
An internship in psychiatric genetic counseling: Impact on genetic counseling graduates' practice and career choices	2
Explanatory models for the cause of Fragile X Syndrome in rural Cameroon	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
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
Attitudes and beliefs regardingrace‐targetedgenetic testing of Black people: A systematic review	2
Public perceived knowledge of, attitude toward, and use of genetic testing in urban China	2
Moral distress in genetic counseling: A study of North American genetic counselors	2