| Latinas’ knowledge of and experiences with genetic cancer risk assessment: Barriers and facilitators |
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| Genetic counselors with advanced skills: I. Refining a model of advanced training |
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| How to inform at‐risk relatives? Attitudes of 1379 Dutch patients, relatives, and members of the general population |
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| Genetic counselors with advanced skills: II. A new career trajectory framework |
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| Health professionals’ practice for young people with, or at risk of, Li–Fraumeni syndrome: An Australasian survey |
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| Combining the use of a fetal fraction‐based risk algorithm and probability of an informative redraw in noninvasive prenatal testing for fetal aneuploidy |
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| Knowledge and opinions of the genetic counseling profession of high school students from underrepresented backgrounds |
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| A survey of U. S. state insurance commissioners concerning genetic testing and life insurance: Redux at 27 |
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| Further validation of the Genetic Counseling Self‐Efficacy Scale (GCSES): Its relationship with personality characteristics |
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| Genetic health professionals' experiences returning results from diagnostic genomic sequencing to patients |
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| An ethical framework for genetic counseling in the genomic era |
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| Access barriers to genetic services for Spanish‐speaking families in states with rapidly growing migrant populations |
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Hispanics; Spanish-speaking; native Spanish‑speakers |
| Issue Information |
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| Issue Highlights |
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| Alternative option labeling impacts decision‐making in noninvasive prenatal screening |
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| Genetic counselor and proxy patient perceptions of genetic counselor responses to prenatal patient self‐disclosure requests: Skillfulness is in the eye of the beholder |
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| Genetic testing preferences and intentions in patients with clinically diagnosed familial hypercholesterolemia |
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| Artificial intelligence in genetic services delivery: Utopia or apocalypse? |
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| Demographic differences in the utilization of clinical and direct‐to‐consumer genetic testing |
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| Knowledge and opinions regarding <i>BRCA1</i> and <i>BRCA2</i> genetic testing among primary care physicians |
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| Optimizing efficiency and skill utilization: Analysis of genetic counselors' attitudes regarding delegation in a clinical setting |
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| Trans‐inclusive genetic counseling services: Recommendations from members of the transgender and non‐binary community |
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| Implementing non‐invasive prenatal testing (NIPT) in the Netherlands: An interview study exploring opinions about and experiences with societal pressure, reimbursement, and an expanding scope |
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| Translating genomic testing results for pediatric critical care: Opportunities for genetic counselors |
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| Genetic counselors’ attitudes toward and practice related to psychiatric genetic counseling |
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| The personal utility of cfDNA screening: Pregnant patients' experiences with cfDNA screening and views on expanded cfDNA panels |
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| Comparison of pan‐ethnic and ethnic‐based carrier screening panels for individuals of Ashkenazi Jewish descent |
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Ashkenazi Jewish (AJ); also uses terms 'pan-ethnic' and 'ethnic-based' |
| Knowledge and attitudes of Parkinson’s disease risk in the Gaucher population |
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| Comparing preferences for return of genome sequencing results assessed with rating and ranking items |
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| “I <i>am</i> a Genetic Counselor”: A qualitative exploration of field leaders’ perceptions of the title “genetic counselor” |
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| Genetics professionals’ experiences of facilitating parent/child communication through the genetic clinic |
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| Familial implications of autoimmune disease: Recurrence risks of alopecia areata and associated conditions in first‐degree relatives |
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| Health communication roles in Latino, Pacific Islander, and Caucasian Families: A qualitative investigation |
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Latinos, Pacific Islanders |
| Issue Information |
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| Issue Highlights |
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| Genetic counselors’ comfort and knowledge of cancer risk assessment for transgender patients |
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| Patients' willingness to reconsider cancer genetic testing after initially declining: Mention it again |
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| Experiencing genetic counseling at the undergraduate level: A course to enrich student horizons |
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| Challenges to informed consent for exome sequencing: A best–worst scaling experiment |
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| Recontacting patients for multigene panel testing in hereditary cancer: Efficacy and insights |
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✓ |
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| Variations in prenatal screening in a US federal healthcare system: Same coverage, different options |
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| Supervision in genetic counselor training in North America: A systematic review |
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| Health professional and at‐risk BRCA young adult perspectives about information needs: What does Gen Y need to know? |
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| Practice variation of genetic counselor engagement in the cystic fibrosis newborn screen‐positive diagnostic resolution process |
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| Patient assessment of chatbots for the scalable delivery of genetic counseling |
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| Defining the role of a genetic counselor within pediatric hematology and oncology comprehensive care teams: Perspectives of the provider team and patients |
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| Yield of whole exome sequencing in undiagnosed patients facing insurance coverage barriers to genetic testing |
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| Attitudes of Israeli parents of children with Down syndrome toward non‐invasive prenatal screening and the scope of prenatal testing |
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| Primary care physicians’ understanding and utilization of pediatric exome sequencing results |
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| Examining genetic counselors’ implicit attitudes toward disability |
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| Lessons learned from testing cardiac channelopathy and cardiomyopathy genes in individuals who died suddenly: A two‐year prospective study in a large medical examiner’s office with an in‐house molecul |
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| Hypertrophic cardiomyopathy genetic test reports: A qualitative study of patient understanding of uninformative genetic test results |
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| Global celebrities' effect on health awareness among Jordanians: A study using the case of Angelina Jolie |
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✓ |
✓ |
Arab population; Jordanians; Jordan; Jordanian |
| Family communication following a diagnosis of myotonic dystrophy: To tell or not to tell? |
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| Issue Highlights |
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| Issue Information |
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| Assessing the barriers to cardiac care in carriers of Duchenne and Becker muscular dystrophy |
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| Establishing the minimum clinically important difference for the Genetic Counseling Outcome Scale (GCOS‐24) |
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| Insurance coverage does not predict outcomes of genetic testing: The search for meaning in payer decisions for germline cancer tests |
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| Prenatal and preconception genetic counseling for consanguinity: Consanguineous couples' expectations, experiences, and perspectives |
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| Difficulties adapting to Nail‐Patella syndrome: A qualitative study of patients' perspectives |
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| The impact of genetic counseling on patient engagement in a specialty cancer clinic |
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| The current state of genetic counseling assistants in the United States |
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| Development of a motivational interviewing genetic counseling intervention to increase cascade cholesterol screening in families of children with familial hypercholesterolemia |
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| Patient‐centered care and genomic medicine: A qualitative provider study in the military health system |
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| How to inform relatives at risk of hereditary diseases? A mixed‐methods systematic review on patient attitudes |
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| A mixed‐methods study of cultural beliefs about dementia and genetic testing among Mexicans and Mexican‐Americans at‐risk for autosomal dominant Alzheimer’s disease |
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| Female family members lack understanding of indeterminate negative <i>BRCA1/2</i> test results shared by probands |
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| Genetic testing and eHealth usage among Deaf women |
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| Issue Information |
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| Issue Highlights |
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| Genetic counseling clinical supervision – A call to action |
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| Communication pitfalls in interpreted genetic counseling sessions |
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| Corrigendum |
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| An exploration of novice genetic counselors’ transitional challenges: Commencement is just the beginning |
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| Recontact practices of cancer genetic counselors and an exploration of professional, legal, and ethical duty |
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| Genetic counseling job market in the United States and Canada: An analysis of job advertisements 2014–2016 |
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| Developing culturally informed genetic services for the Somali immigrants in Minnesota |
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| Patient perspectives on the process and outcomes of psychiatric genetic counseling: <i>An “Empowering Encounter</i>” |
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| Understanding variants of uncertain significance in the era of multigene panels: Through the eyes of the patient |
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| Evaluation of an automated process for disclosure of negative noninvasive prenatal test results |
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| Men's experiences of recontact about a potential increased risk of prostate cancer due to Lynch Syndrome: “Just another straw on the stack” |
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| Sickle cell carriers' unmet information needs: Beyond knowing trait status |
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✓ |
✓ |
African Americans |
| A toolkit for genetics providers in follow‐up of patients with non‐diagnostic exome sequencing |
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| Issue Information |
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| INTRODUCTION TO EXPLORING THE EXOME SPECIAL ISSUE |
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| Genetic counseling, 2030: An on‐demand service tailored to the needs of a price conscious, genetically literate, and busy world |
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| Rapid clinical exome sequencing in a pediatric ICU: Genetic counselor impacts and challenges |
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| Understanding the present and preparing for the future: Exploring the needs of diagnostic and elective genomic medicine patients |
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| Current genetic counseling practice in the United States following positive non‐invasive prenatal testing for sex chromosome abnormalities |
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| New developmental syndromes: Understanding the family experience |
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| Left ventricular outflow tract obstruction: Uptake of familial cardiac screening and parental knowledge from a single tertiary care center |
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| The relationship between genetic counseling student self‐efficacy and clinical training |
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| Exploring prenatal genetic counselors' perceptions of abortion laws in restrictive states |
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| Impact of the physical environment on patient outcomes of genetic counseling: An exploratory study |
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| Genetics professionals’ attitudes toward prenatal exome sequencing |
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| Prenatal genetic counselors' practices and confidence level when counseling on cancer risk identified on expanded carrier screening |
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| Genetic counseling for consumer‐driven whole exome and whole genome sequencing: A commentary on early experiences |
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| Exploring genetic counselors’ perceptions of usefulness and intentions to use refined risk models in clinical care based on the Technology Acceptance Model (TAM) |
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| Patients' reactions and follow‐up testing decisions related to Tay‐Sachs (<i>HEXA</i>) variants of uncertain significance results |
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| Clinical models of telehealth in genetics: A regional telegenetics landscape |
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| Genetic counselor workforce generational diversity: Millennials to Baby Boomers |
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| Much ado about nothing: A qualitative study of the experiences of an average‐risk population receiving results of exome sequencing |
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| Secondary findings: How did we get here, and where are we going? |
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| Challenges of infertility genetic counseling: Impact on counselors' personal and professional lives |
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| Genetic counseling supervisor strategies: An elaboration of the Reciprocal‐Engagement Model of Supervision |
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| Introduction of cell‐free DNA screening is associated with changes in prenatal genetic counseling indications |
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| Readiness of clinical genetic healthcare professionals to provide genomic medicine: An Australian census |
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| A novel approach to offering additional genomic findings—A protocol to test a two‐step approach in the healthcare system |
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| Perspectives on facilitating whole exome sequencing for international patients at Mayo Clinic |
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| Lexigene®: An online medical genetics translation tool to facilitate communication |
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| Factors complicating the informed consent process for whole exome sequencing in neonatal and pediatic intensive care units |
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| Genetic counselors' perceptions of uncertainty in pretest counseling for genomic sequencing: A qualitative study |
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| Issue Information |
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| 2019 National Society of Genetic Counselors Presidential Address |
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| A Heartfelt Thank You to the 2018 <i>Journal of Genetic Counseling</i> Reviewers |
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| Issue Highlights |
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| Cancer genetic counselors' experiences with transgender patients: A qualitative study |
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| Beyond medical actionability: Public perceptions of important actions in response to hypothetical genetic testing results |
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| Talking across generations: Family communication about<i>BRCA1</i>and<i>BRCA2</i>genetic cancer risk |
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| An examination of the factors contributing to the expansion of subspecialty genetic counseling |
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| Cases and evidence for panel testing in cancer genetics: Is site‐specific testing dead? |
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| Developing a genomics rotation: Practical training around variant interpretation for genetic counseling students |
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| Assessing genetic counselors’ experiences with physician aid‐in‐dying and practice implications |
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| Attitudes of clinicians toward cardiac surgery and trisomy 18 |
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| Trans‐counseling: A case series of transgender individuals at high risk for <i>BRCA1</i> pathogenic variants |
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| Genetic Literacy of pregnant women and their use of prenatal screening and diagnostic tests in Turkey |
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| Cases from the Undiagnosed Diseases Network: The continued value of counseling skills in a new genomic era |
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| Caregivers' perception of and experience with variants of uncertain significance from whole exome sequencing for children with undiagnosed conditions |
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| The impact of cardiovascular genetic counseling on patient empowerment |
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| Factors affecting breast cancer patients' need for genetic risk information: From information insufficiency to information need |
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| Genetic counseling in pediatric acute care: Reflections on ultra‐rapid genomic diagnoses in neonates |
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| Evaluation of National Comprehensive Cancer Network guideline‐based Tool for Risk Assessment for breast and ovarian Cancer (N‐TRAC): A patient‐reported survey for genetic high‐risk assessment for brea |
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| Racial and ethnic differences in knowledge and attitudes about genetic testing in the US: Systematic review |
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| Using the diffusion of innovations model to guide participant engagement in the genomics era |
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| Patients' perspectives of variants of uncertain significance and strategies for uncertainty management |
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| Comparison of medical management and genetic counseling options pre‐ and post‐whole exome sequencing for patients with positive and negative results |
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| The impact of health anxiety on perceptions of personal and children’s health in parents with Lynch syndrome |
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| Genetic Counselors' and Genetic Counseling Students' Implicit and Explicit Attitudes toward Homosexuality |
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