Journal of Genetic Counseling - 2019

139 articles | Last updated: 2025-12-03 14:12:57
Caucasian
2
White
6
European
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Other
5
Article Title Cauc. White Euro. Other Phrases Used
T A T A T A T A
Latinas’ knowledge of and experiences with genetic cancer risk assessment: Barriers and facilitators
Genetic counselors with advanced skills: I. Refining a model of advanced training
How to inform at‐risk relatives? Attitudes of 1379 Dutch patients, relatives, and members of the general population
Genetic counselors with advanced skills: II. A new career trajectory framework
Health professionals’ practice for young people with, or at risk of, Li–Fraumeni syndrome: An Australasian survey
Combining the use of a fetal fraction‐based risk algorithm and probability of an informative redraw in noninvasive prenatal testing for fetal aneuploidy
Knowledge and opinions of the genetic counseling profession of high school students from underrepresented backgrounds
A survey of U. S. state insurance commissioners concerning genetic testing and life insurance: Redux at 27
Further validation of the Genetic Counseling Self‐Efficacy Scale (GCSES): Its relationship with personality characteristics
Genetic health professionals' experiences returning results from diagnostic genomic sequencing to patients
An ethical framework for genetic counseling in the genomic era
Access barriers to genetic services for Spanish‐speaking families in states with rapidly growing migrant populations Hispanics; Spanish-speaking; native Spanish‑speakers
Issue Information
Issue Highlights
Alternative option labeling impacts decision‐making in noninvasive prenatal screening
Genetic counselor and proxy patient perceptions of genetic counselor responses to prenatal patient self‐disclosure requests: Skillfulness is in the eye of the beholder
Genetic testing preferences and intentions in patients with clinically diagnosed familial hypercholesterolemia
Artificial intelligence in genetic services delivery: Utopia or apocalypse?
Demographic differences in the utilization of clinical and direct‐to‐consumer genetic testing
Knowledge and opinions regarding <i>BRCA1</i> and <i>BRCA2</i> genetic testing among primary care physicians
Optimizing efficiency and skill utilization: Analysis of genetic counselors' attitudes regarding delegation in a clinical setting
Trans‐inclusive genetic counseling services: Recommendations from members of the transgender and non‐binary community
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
Translating genomic testing results for pediatric critical care: Opportunities for genetic counselors
Genetic counselors’ attitudes toward and practice related to psychiatric genetic counseling
The personal utility of cfDNA screening: Pregnant patients' experiences with cfDNA screening and views on expanded cfDNA panels
Comparison of pan‐ethnic and ethnic‐based carrier screening panels for individuals of Ashkenazi Jewish descent Ashkenazi Jewish (AJ); also uses terms 'pan-ethnic' and 'ethnic-based'
Knowledge and attitudes of Parkinson’s disease risk in the Gaucher population
Comparing preferences for return of genome sequencing results assessed with rating and ranking items
“I <i>am</i> a Genetic Counselor”: A qualitative exploration of field leaders’ perceptions of the title “genetic counselor”
Genetics professionals’ experiences of facilitating parent/child communication through the genetic clinic
Familial implications of autoimmune disease: Recurrence risks of alopecia areata and associated conditions in first‐degree relatives
Health communication roles in Latino, Pacific Islander, and Caucasian Families: A qualitative investigation Latinos, Pacific Islanders
Issue Information
Issue Highlights
Genetic counselors’ comfort and knowledge of cancer risk assessment for transgender patients
Patients' willingness to reconsider cancer genetic testing after initially declining: Mention it again
Experiencing genetic counseling at the undergraduate level: A course to enrich student horizons
Challenges to informed consent for exome sequencing: A best–worst scaling experiment
Recontacting patients for multigene panel testing in hereditary cancer: Efficacy and insights
Variations in prenatal screening in a US federal healthcare system: Same coverage, different options
Supervision in genetic counselor training in North America: A systematic review
Health professional and at‐risk BRCA young adult perspectives about information needs: What does Gen Y need to know?
Practice variation of genetic counselor engagement in the cystic fibrosis newborn screen‐positive diagnostic resolution process
Patient assessment of chatbots for the scalable delivery of genetic counseling
Defining the role of a genetic counselor within pediatric hematology and oncology comprehensive care teams: Perspectives of the provider team and patients
Yield of whole exome sequencing in undiagnosed patients facing insurance coverage barriers to genetic testing
Attitudes of Israeli parents of children with Down syndrome toward non‐invasive prenatal screening and the scope of prenatal testing
Primary care physicians’ understanding and utilization of pediatric exome sequencing results
Examining genetic counselors’ implicit attitudes toward disability
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
Hypertrophic cardiomyopathy genetic test reports: A qualitative study of patient understanding of uninformative genetic test results
Global celebrities' effect on health awareness among Jordanians: A study using the case of Angelina Jolie Arab population; Jordanians; Jordan; Jordanian
Family communication following a diagnosis of myotonic dystrophy: To tell or not to tell?
Issue Highlights
Issue Information
Assessing the barriers to cardiac care in carriers of Duchenne and Becker muscular dystrophy
Establishing the minimum clinically important difference for the Genetic Counseling Outcome Scale (GCOS‐24)
Insurance coverage does not predict outcomes of genetic testing: The search for meaning in payer decisions for germline cancer tests
Prenatal and preconception genetic counseling for consanguinity: Consanguineous couples' expectations, experiences, and perspectives
Difficulties adapting to Nail‐Patella syndrome: A qualitative study of patients' perspectives
The impact of genetic counseling on patient engagement in a specialty cancer clinic
The current state of genetic counseling assistants in the United States
Development of a motivational interviewing genetic counseling intervention to increase cascade cholesterol screening in families of children with familial hypercholesterolemia
Patient‐centered care and genomic medicine: A qualitative provider study in the military health system
How to inform relatives at risk of hereditary diseases? A mixed‐methods systematic review on patient attitudes
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
Female family members lack understanding of indeterminate negative <i>BRCA1/2</i> test results shared by probands
Genetic testing and eHealth usage among Deaf women
Issue Information
Issue Highlights
Genetic counseling clinical supervision – A call to action
Communication pitfalls in interpreted genetic counseling sessions
Corrigendum
An exploration of novice genetic counselors’ transitional challenges: Commencement is just the beginning
Recontact practices of cancer genetic counselors and an exploration of professional, legal, and ethical duty
Genetic counseling job market in the United States and Canada: An analysis of job advertisements 2014–2016
Developing culturally informed genetic services for the Somali immigrants in Minnesota
Patient perspectives on the process and outcomes of psychiatric genetic counseling: <i>An “Empowering Encounter</i>”
Understanding variants of uncertain significance in the era of multigene panels: Through the eyes of the patient
Evaluation of an automated process for disclosure of negative noninvasive prenatal test results
Men's experiences of recontact about a potential increased risk of prostate cancer due to Lynch Syndrome: “Just another straw on the stack”
Sickle cell carriers' unmet information needs: Beyond knowing trait status African Americans
A toolkit for genetics providers in follow‐up of patients with non‐diagnostic exome sequencing
Issue Information
INTRODUCTION TO EXPLORING THE EXOME SPECIAL ISSUE
Genetic counseling, 2030: An on‐demand service tailored to the needs of a price conscious, genetically literate, and busy world
Rapid clinical exome sequencing in a pediatric ICU: Genetic counselor impacts and challenges
Understanding the present and preparing for the future: Exploring the needs of diagnostic and elective genomic medicine patients
Current genetic counseling practice in the United States following positive non‐invasive prenatal testing for sex chromosome abnormalities
New developmental syndromes: Understanding the family experience
Left ventricular outflow tract obstruction: Uptake of familial cardiac screening and parental knowledge from a single tertiary care center
The relationship between genetic counseling student self‐efficacy and clinical training
Exploring prenatal genetic counselors' perceptions of abortion laws in restrictive states
Impact of the physical environment on patient outcomes of genetic counseling: An exploratory study
Genetics professionals’ attitudes toward prenatal exome sequencing
Prenatal genetic counselors' practices and confidence level when counseling on cancer risk identified on expanded carrier screening
Genetic counseling for consumer‐driven whole exome and whole genome sequencing: A commentary on early experiences
Exploring genetic counselors’ perceptions of usefulness and intentions to use refined risk models in clinical care based on the Technology Acceptance Model (TAM)
Patients' reactions and follow‐up testing decisions related to Tay‐Sachs (<i>HEXA</i>) variants of uncertain significance results
Clinical models of telehealth in genetics: A regional telegenetics landscape
Genetic counselor workforce generational diversity: Millennials to Baby Boomers
Much ado about nothing: A qualitative study of the experiences of an average‐risk population receiving results of exome sequencing
Secondary findings: How did we get here, and where are we going?
Challenges of infertility genetic counseling: Impact on counselors' personal and professional lives
Genetic counseling supervisor strategies: An elaboration of the Reciprocal‐Engagement Model of Supervision
Introduction of cell‐free DNA screening is associated with changes in prenatal genetic counseling indications
Readiness of clinical genetic healthcare professionals to provide genomic medicine: An Australian census
A novel approach to offering additional genomic findings—A protocol to test a two‐step approach in the healthcare system
Perspectives on facilitating whole exome sequencing for international patients at Mayo Clinic
Lexigene®: An online medical genetics translation tool to facilitate communication
Factors complicating the informed consent process for whole exome sequencing in neonatal and pediatic intensive care units
Genetic counselors' perceptions of uncertainty in pretest counseling for genomic sequencing: A qualitative study
Issue Information
2019 National Society of Genetic Counselors Presidential Address
A Heartfelt Thank You to the 2018 <i>Journal of Genetic Counseling</i> Reviewers
Issue Highlights
Cancer genetic counselors' experiences with transgender patients: A qualitative study
Beyond medical actionability: Public perceptions of important actions in response to hypothetical genetic testing results
Talking across generations: Family communication about<i>BRCA1</i>and<i>BRCA2</i>genetic cancer risk
An examination of the factors contributing to the expansion of subspecialty genetic counseling
Cases and evidence for panel testing in cancer genetics: Is site‐specific testing dead?
Developing a genomics rotation: Practical training around variant interpretation for genetic counseling students
Assessing genetic counselors’ experiences with physician aid‐in‐dying and practice implications
Attitudes of clinicians toward cardiac surgery and trisomy 18
Trans‐counseling: A case series of transgender individuals at high risk for <i>BRCA1</i> pathogenic variants
Genetic Literacy of pregnant women and their use of prenatal screening and diagnostic tests in Turkey
Cases from the Undiagnosed Diseases Network: The continued value of counseling skills in a new genomic era
Caregivers' perception of and experience with variants of uncertain significance from whole exome sequencing for children with undiagnosed conditions
The impact of cardiovascular genetic counseling on patient empowerment
Factors affecting breast cancer patients' need for genetic risk information: From information insufficiency to information need
Genetic counseling in pediatric acute care: Reflections on ultra‐rapid genomic diagnoses in neonates
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
Racial and ethnic differences in knowledge and attitudes about genetic testing in the US: Systematic review
Using the diffusion of innovations model to guide participant engagement in the genomics era
Patients' perspectives of variants of uncertain significance and strategies for uncertainty management
Comparison of medical management and genetic counseling options pre‐ and post‐whole exome sequencing for patients with positive and negative results
The impact of health anxiety on perceptions of personal and children’s health in parents with Lynch syndrome
Genetic Counselors' and Genetic Counseling Students' Implicit and Explicit Attitudes toward Homosexuality