Journal of Genetic Counseling - 2015

115 articles | Last updated: 2025-12-03 14:12:57

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Alone in the Crowd: I Failed the ABGC Certification Exam
Thank You to Reviewers
Lifestyle Risk Factors Among People Who Have Had Cancer Genetic Testing
Impaired Health‐Related Quality of Life in Children and Families Affected by Methylmalonic Acidemia
The Moral Reasoning of Genetic Dilemmas Amongst Jewish Israeli Undergraduate Students with Different Religious Affiliations and Scientific Backgrounds
Obsessive‐Compulsive Disorder: The Process of Parental Adaptation and Implications for Genetic Counseling
Next Generation Sequencing in the Clinic: a Patterns of Care Study in a Retrospective Cohort of Subjects Referred to a Genetic Medicine Clinic for Suspected Lynch Syndrome
Measuring the Effectiveness of a Genetic Counseling Supervision Training Conference
Erratum to: Genetic Counselors’ Experiences Regarding Communication of Reproductive Risks with Autosomal Recessive Conditions found on Cancer Panels
Easing the Burden: Describing the Role of Social, Emotional and Spiritual Support in Research Families with Li‐Fraumeni Syndrome
From Campers to Counselors: a Resource for Prospective Genetic Counseling Students
2020 Vision: Genetic Counselors as Acknowledged Leaders in Integrating Genetics and Genomics into Healthcare
Sex Education and Intellectual Disability: Practices and Insight from Pediatric Genetic Counselors
Communication of Psychiatric Risk in 22q11.2 Deletion Syndrome: A Pilot Project
Impact of Genetic Counseling and Testing on Altruistic Motivations to Test for BRCA1/2: a Longitudinal Study
Experience with genetic counseling: the adolescent perspective
Reproductive Endocrinologists’ Utilization of Genetic Counselors for Oncofertility and Preimplantation Genetic Diagnosis (PGD) Treatment of <i>BRCA1/2</i> Mutation Carriers
From Novice to Seasoned Practitioner: a Qualitative Investigation of Genetic Counselor Professional Development
Erratum to: The Long and Short of Genetic Counseling Letters: A Case–control Study
High Satisfaction and Low Distress in Breast Cancer Patients One Year after <i>BRCA</i>‐Mutation Testing without Prior Face‐to‐Face Genetic Counseling
Survey of the Definition of Fetal Viability and the Availability, Indications, and Decision Making Processes for Post‐Viability Termination of Pregnancy for Fetal Abnormalities and Health Conditions i
Review of Commercially Available Epilepsy Genetic Panels
Development, Experience, and Expression of Meaning in Genetic Counselors’ Lives: an Exploratory Analysis
Cancer Worry, Perceived Risk and Cancer Screening in First‐Degree Relatives of Patients with Familial Gastric Cancer
Presented Abstracts from the Thirty Fourth Annual Education Conference of the National Society of Genetic Counselors (Pittsburgh, PA, October 2015)
Genetic Test Results and Disclosure to Family Members: Qualitative Interviews of Healthcare Professionals’ Perceptions of Ethical and Professional Issues in France
Duchenne Muscular Dystrophy: a Survey of Perspectives on Carrier Testing and Communication Within the Family
Prognostic Factors for Distress After Genetic Testing for Hereditary Cancer
Patient Perceptions of Telephone vs. In‐Person <i>BRCA1/BRCA2</i> Genetic Counseling				✓
Genetic Counseling Milestones: A Framework for Student Competency Evaluation
Genetic Counselors’ Experiences Regarding Communication of Reproductive Risks with Autosomal Recessive Conditions found on Cancer Panels
Communication Between Breast Cancer Patients Who Received Inconclusive Genetic Test Results and Their Daughters and Sisters Years After Testing
Assessment of the Readability of Genetic Counseling Patient Letters
The Quality of Genetic Counseling and Connected Factors as Evaluated by Male BRCA1/2 Mutation Carriers in Finland							✓	✓	Finnish
Predictive Genetic Testing and Alternatives to Face to Face Results Disclosure: A Retrospective Review of Patients Preference for Alternative Modes of BRCA 1 and 2 Results Disclosure in the Republic o
Reproductive Decision‐Making in MMR Mutation Carriers After Results Disclosure: Impact of Psychological Status in Childbearing Options
Patients’ Attitudes Towards Disclosure of Genetic Test Results to Family Members: The Impact of Patients’ Sociodemographic Background and Counseling Experience
Impact of Genetic Counseling in Women with a Family History of Breast Cancer in Italy
Challenges of Pre‐ and Post‐Test Counseling for Orthodox Jewish Individuals in the Premarital Phase
Stories as Gift: Patient Narratives and the Development of Empathy
Genetic Counselors’ Perspectives and Practices Regarding Expanded Carrier Screening after Initial Clinical Availability
A Novel von Hippel Lindau Gene Intronic Variant and Its Reclassification from VUS to Pathogenic: the Impact on a Large Family
Living With Genetic Vulnerability: a Life Course Perspective
Case Report: Direct Access Genetic Testing and A False‐Positive Result For Long QT Syndrome
Counselees’ Expressed Level of Understanding of the Risk Estimate and Surveillance Recommendation are Not Associated with Breast Cancer Surveillance Adherence
Newborn Screening for Lysosomal Storage Disorders: Views of Genetic Healthcare Providers
Reproductive Health CHOICES for Young Adults with Sickle Cell Disease or Trait: Randomized Controlled Trial Outcomes over Two Years
The Life Course Perspective: a Guide for Genetic Counselors							✓	✓	Mexican American caregivers
Genetic Knowledge Among Participants in the Coriell Personalized Medicine Collaborative		✓
Prioritizing Parental Worry Associated with Duchenne Muscular Dystrophy Using Best‐Worst Scaling
Portrait of the Master Genetic Counselor Clinician: A Qualitative Investigation of Expertise in Genetic Counseling
Clinical and Counseling Experiences of Early Adopters of Whole Exome Sequencing
Helping Couples Fulfill the “Highest of Life's Goals”: Mate Selection, Marriage Counselling, and Genetic Counseling in United States
Breast Cancer Risk Perceptions among Relatives of Women with Uninformative Negative <i>BRCA1/2</i> Test Results: The Moderating Effect of the Amount of Shared Information
Review of Spinal Muscular Atrophy (SMA) for Prenatal and Pediatric Genetic Counselors
Exploration of Male Attitudes on Partnerships and Sexuality with Female <i>BRCA1/2</i> Mutation Carriers
Acceptability of, and Information Needs Regarding, Next‐Generation Sequencing in People Tested for Hereditary Cancer: A Qualitative Study
Parents’ Experience with Pediatric Microarray: Transferrable Lessons in the Era of Genomic Counseling
Clients’ Perception of Outcome of Team‐Based Prenatal and Reproductive Genetic Counseling in Serbian Service Using the Perceived Personal Control (PPC) Questionnaire
Genetic Counseling Supervisors’ Self‐Efficacy for Select Clinical Supervision Competencies
Genomic Testing: a Genetic Counselor's Personal Reflection on Three Years of Consenting and Testing
Attitudes Toward Genetic Testing for Celiac Disease
Defining Our Clinical Practice: The Identification of Genetic Counseling Outcomes Utilizing the Reciprocal Engagement Model
Cystic Fibrosis. Edited by Marcus A. Mall and J. Stuart Elborn
Swedish University Students’ Opinion Regarding Information About Soft Markers
Improving Health Education for Women Who Carry an <i>FMR1</i> Premutation
Non‐invasive Prenatal Diagnosis for BRCA Mutations – a Qualitative Pilot Study of Health Professionals’ Views
Comparison of Informed Consent Preferences for Multiplex Genetic Carrier Screening among a Diverse Population
Cultural Concerns when Counseling Orthodox Jewish Couples for Genetic Screening and PGD
An Exploratory Study of Employers’ Attitudes Towards a Clinical Doctorate in Genetic Counseling
“Is It Worth Knowing?” Focus Group Participants’ Perceived Utility of Genomic Preconception Carrier Screening
Reprogenetics, Genetic Tools and Reproductive Risk: Attitudes and Understanding Among Ethnic Groups in Israel
A Comparison of Telephone Genetic Counseling and In‐Person Genetic Counseling from the Genetic Counselor's Perspective
Sickle Cell Trait Screening of Collegiate Athletes: Ethical Reasons for Program Reform
Report on an Investigation into an Entry Level Clinical Doctorate for the Genetic Counseling Profession and a Survey of the Association of Genetic Counseling Program Directors
Perception of Genetic Testing for Deafness and Factors Associated with Interest in Genetic Testing Among Deaf People in a Selected Population in Sub‐Saharan Africa
Experiences of Women Who Underwent Predictive BRCA 1/2 Mutation Testing Before the Age of 30
Subjects At‐Risk for Genetic Diseases in Portugal: Illness Representations
Parents’ Perspectives on Variants of Uncertain Significance from Chromosome Microarray Analysis
Form Follows Function: A Model for Clinical Supervision of Genetic Counseling Students
Attitudes and Knowledge of Maternal‐Fetal Medicine Fellows Regarding Noninvasive Prenatal Testing
Genetics and Personal Insurance: the Perspectives of Canadian Cancer Genetic Counselors
“Suddenly Having two Positive People who are Carriers is a Whole New Thing”‐ Experiences of Couples Both Identified as Carriers of Cystic Fibrosis Through a Population‐Based Carrier Screening Program
Analysis of the Reasons for Non‐Uptake of Predictive Testing for Huntington's Disease in Spain: A Qualitative Study
“Not Tied Up Neatly with a Bow”: Professionals’ Challenging Cases in Informed Consent for Genomic Sequencing
Feasibility of an Assessment Tool for Children's Competence to Consent to Predictive Genetic Testing: a Pilot Study
The Impact of Neurofibromatosis Type 1 on the Health and Wellbeing of Australian Adults
Knowledge, Attitudes, and Practice Regarding Genetic Testing and Genetic Counselors in Jordan: A Population‐Based Survey
Assessing Parental Knowledge About Thalassemia in a Thalassemia Center of Karachi, Pakistan							✓	✓	Urdu speaking, Siraiki, Pathans, Pakistanis; phrases 'ethnic origins' and 'ethnic groups'.
Complexities of Genetic Counseling for ALS: A Case of Two Siblings with Discordant Genetic Test Results
Support Desired by Women Following Termination of Pregnancy for a Fetal Anomaly
Uptake of Genetic Counseling, Knowledge of Bleeding risks and Psychosocial Impact in a South African Cohort of Female Relatives of People with Hemophilia
Randomized Trial of Telegenetics vs. In‐Person Cancer Genetic Counseling: Cost, Patient Satisfaction and Attendance
Psychosocial Responses to being Identified as a Balanced Chromosomal Translocation Carrier: a Qualitative Investigation of Parents in Japan
Introduction to the Special Issue: Public Health Genetics and Genomics
Facilitators and Challenges in Psychosocial Adaptation to Being at Increased Familial Risk of Breast Cancer
Using <i>ApoE</i> Genotyping to Promote Healthy Lifestyles in Finland – Psychological Impacts: Randomized Controlled Trial
Genetic Counseling in Portugal: Education, Practice and a Developing Profession
Psychological Impact of Predictive Genetic Testing in VCP Inclusion Body Myopathy, Paget Disease of Bone and Frontotemporal Dementia
Respecting Autonomous Decision Making Among Filipinos: A Re‐emphasis in Genetic Counseling
Clearing the Air: A Qualitative Investigation of Genetic Counselors’ Experiences of Counselor‐Focused Patient Anger
Bayesian Assessment of Genetic Risk in Families with a Balanced Translocation
Perceptions of Tissue Storage in a Dementia Population Among Spouses and Offspring
Do Attachment Style and Emotion Regulation Strategies Indicate Distress in Predictive Testing?
The Impact on the Family of Four Neurogenetic Syndromes: A Comparative Study of Parental Views
Are Australasian Genetic Counselors Interested in Private Practice at the Primary Care Level of Health Service?
Association of Researcher Characteristics with Views on Return of Incidental Findings from Genomic Research
“Both Sides of the Wheelchair”: The Views of Individuals with, and Parents of Individuals with Friedreich Ataxia Regarding Pre‐symptomatic Testing of Minors
Aligning Policy to Promote Cascade Genetic Screening for Prevention and Early Diagnosis of Heritable Diseases
Reproductive Health Issues for Adults with a Common Genomic Disorder: 22q11.2 Deletion Syndrome
All in the Family: Barriers and Motivators to the Use of Cancer Family History Questionnaires and the Impact on Attendance Rates
Framing recommendations to promote prevention behaviors among people at high risk: A simulation study of responses to melanoma genetic test reporting
Factors Associated with Uptake of Genetics Services for Hypertrophic Cardiomyopathy
Exploring the Genetic Counselor's Role in Facilitating Meaning‐Making: Rare Disease Diagnoses
Erratum to: Existing Challenges Associated with Offering Prenatal Genetic Diagnosis in an Arab Society in the Sultanate of Oman