Journal of Genetic Counseling - 2014

129 articles | Last updated: 2025-12-03 14:12:57
Caucasian
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White
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European
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Other
7
Article Title Cauc. White Euro. Other Phrases Used
T A T A T A T A
Genetic Information‐Seeking Behaviors and Knowledge among Family Members and Patients with Inherited Bone Marrow Failure Syndromes
Parental Communication and Experiences and Knowledge of Adolescent Siblings of Children with 22q11.2 Deletion Syndrome
Erratum to: How Can Psychological Science Inform Research About Genetic Counseling for Clinical Genomic Sequencing?
Reviewing Manuscripts for the Journal of Genetic Counseling: Practical Suggestions
Genetic Counselors and Health Literacy: The Role of Genetic Counselors in Developing a Web‐Based Resource About the Affordable Care Act
The Long and Short of Genetic Counseling Summary Letters: A Case–control Study
Creation of a National, At‐home Model for Ashkenazi Jewish Carrier Screening Ashkenazi Jewish; Jewish
Personalized Medicine Through SNP Testing for Breast Cancer Risk: Clinical Implementation
How Can Psychological Science Inform Research About Genetic Counseling for Clinical Genomic Sequencing?
Public Health Genetic Counselors: Activities, Skills, and Sources of Learning
Testing for Hereditary Breast Cancer: Panel or Targeted Testing? Experience from a Clinical Cancer Genetics Practice
Perceptions of Latinas on the Traditional Prenatal Genetic Counseling Model
2015 NSGC Presidential Address: Gifts of Genetic Counselors: Life's Leadership Lessons
Storage and use of Newborn Screening Blood Specimens for Research: Assessing Public Opinion in Illinois
Reporting Incidental Findings in Clinical Whole Exome Sequencing: Incorporation of the 2013 ACMG Recommendations into Current Practices of Genetic Counseling
Congruence‐Incongruence Patterns in Alpha‐1 Antitrypsin Deficiency Couples’ Genetic Determinist Beliefs and Perceived Control over Genes: Implications for Clinical and Public Health Genomic Communicat
A Genetic Lung Cancer Susceptibility Test may have a Positive Effect on Smoking Cessation
Adults with Chromosome 18 Abnormalities
Congenital Hypothyroidism Long‐Term Follow‐up Project: Navigating the Rough Waters of a Multi‐Center, Multi‐State Public Health Project
Education and Parental Involvement in Decision‐Making About Newborn Screening: Understanding Goals to Clarify Content
Disclosing Genetic Information to Family Members About Inherited Cardiac Arrhythmias: An Obligation or a Choice?
Ethical and Professional Challenges Encountered by Laboratory Genetic Counselors
Health‐Related Quality of Life in Patients with MPS II
Case Report: Concurrent Wilson Disease and Huntington Disease: Lightning Can Strike Twice
Presented Abstracts from the Thirty Third Annual Education Conference of the National Society of Genetic Counselors (New Orleans, LA, September 2014)
Genetics Health Professionals’ Views on Quality of Genetic Counseling Service Provision for Presymptomatic Testing in Late‐Onset Neurological Diseases in Portugal: Core Components, Specific Challenges
Ethical Considerations in Biobanks: How a Public Health Ethics Perspective Sheds New Light on Old Controversies
Genetic Counseling for Indigenous Australians: an Exploratory Study from the Perspective of Genetic Health Professionals
Genetics Professionals’ Opinions of Whole‐Genome Sequencing in the Newborn Period
Genetic Counselors’ and Genetic Counseling Students’ Attitudes Around the Clinical Doctorate and Other Advanced Educational Options for Genetic Counselors: A Report from the Genetic Counseling Advance
Applying Public Health Screening Criteria: How Does Universal Newborn Screening Compare to Universal Tumor Screening for Lynch Syndrome in Adults with Colorectal Cancer?
Non‐Invasive Prenatal Testing: UK Genetic Counselors’ Experiences and Perspectives
Family Communication in a Population at Risk for Hypertrophic Cardiomyopathy
Perceptions and Attitudes About Genetic Counseling Among Residents of a Midwestern Rural Area
Reduced Uptake of Family Screening in Genotype‐Negative Versus Genotype‐Positive Long QT Syndrome
A Qualitative Evaluation of the Psychosocial Impact of Family History Screening in Australian Primary Care
Patient Expectations and Attitudes Towards Specialist Genetic Eye Services
“Is it Going to Hurt?”: The Impact of the Diagnostic Odyssey on Children and Their Families
Public Awareness of Genetic Nondiscrimination Laws in Four States and Perceived Importance of Life Insurance Protections
Genetic Counseling for Fanconi Anemia: Crosslinking Disciplines
Assessment of Parental Understanding of Positive Newborn Screening Results and Carrier Status for Cystic Fibrosis with the use of a Short Educational Video
The Psychological Impact of Predictive Genetic Testing for Huntington′s Disease: A Systematic Review of the Literature
Existing Challenges Associated with Offering Prenatal Genetic Diagnosis in an Arab Society in the Sultanate of Oman
Creation of a Network to Promote Universal Screening for Lynch Syndrome: The Lynch Syndrome Screening Network
Influence of Anchoring on Miscarriage Risk Perception Associated with Amniocentesis
Increasing Participation in Genomic Research and Biobanking Through Community‐Based Capacity Building
Informed Consent Form Challenges for Genetic Research in a Developing Arab Country with High Risk for Genetic Disease
Evaluation of Patient Education Materials: The Example of Circulating cell free DNA Testing for Aneuploidy
American BRCA Outcomes and Utilization of Testing (ABOUT) Study: A Pragmatic Research Model that Incorporates Personalized Medicine/Patient‐Centered Outcomes in a Real World Setting
Using Formative Research to Develop a Counselor Training Program for Newborn Screening in Ghana
To Reflex or Not: Additional BRCA1/2 Testing in Ashkenazi Jewish Individuals Without Founder Mutations Ashkenazi Jewish
“She Came out of mum's Tummy the Wrong way” (Mis) Conceptions Among Siblings of Children with Rare Disorders
“How Should I Tell my Child?” Disclosing the Diagnosis of Sex Chromosome Aneuploidies
Erratum to: The Impact of Supervision Training on Genetic Counselor Supervisory Identity Development
Exploring Barriers to Payer Utilization of Genetic Counselors
The Utilization of Counseling Skills by the Laboratory Genetic Counselor
Interest in Genetic Testing in Ashkenazi Jewish Parkinson's Disease Patients and Their Unaffected Relatives Ashkenazi Jewish (AJ)
BRCA Genetic Counseling Among At‐Risk Latinas in New York City: New Beliefs Shape New Generation
Clinical Utility of Chromosomal Microarray Analysis of DNA from Buccal Cells: Detection of Mosaicism in Three Patients
A Pilot Study of <i>BRCA</i> Mutation Carriers’ Knowledge About the Clinical Impact of Prophylactic‐oophorectomy and Views on Fertility Consultation: A Single‐Center Pilot Study
Use of a Patient‐Entered Family Health History Tool with Decision Support in Primary Care: Impact of Identification of Increased Risk Patients on Genetic Counseling Attendance
Mothers’ Experiences of Genetic Counselling in Johannesburg, South Africa
Understanding the Experience of Myotonic Dystrophy. Mixed Method Study
Parental Decisions Following Prenatal Diagnosis of Chromosomal Abnormalities: Implications for Genetic Counseling Practice in Japan
Genetic Information, Non‐Discrimination, and Privacy Protections in Genetic Counseling Practice
Assessing Deaf Awareness Training: Knowledge and Attitudes of Recent Genetic Counseling Graduates
Commentary on “Conceptualizing Genetic Counseling as Psychotherapy in the era of Genomic Medicine”
“We Don't Know Her History, Her Background”: Adoptive Parents’ Perspectives on Whole Genome Sequencing Results ancestry / "biological family health history and ancestry"
A Survey of Genetic Counselors About the Needs of 18–25 Year Olds from Families with Hereditary Breast and Ovarian Cancer Syndrome
Disparities in Current and Future Childhood and Newborn Carrier Identification
An Assessment of Genetic Counseling Services for Individuals with Multiple Sclerosis
Making the Decision to Participate in Predictive Genetic Testing for Arrhythmogenic Right Ventricular Cardiomyopathy
Promoting Meaning‐Making to Help our Patients Grieve: An Exemplar for Genetic Counselors and Other Health Care Professionals
Genetic Counseling in Direct‐to‐Consumer Exome Sequencing: A Case Report
Information‐Seeking and Sharing Behavior Following Genomic Testing for Diabetes Risk
An Internal Performance Assessment of CancerGene Connect: An Electronic Tool to Streamline, Measure and Improve the Genetic Counseling Process racial and ethnic groups
Conceptualizing Genetic Counseling as Psychotherapy in the Era of Genomic Medicine
The Impact of Supervision Training on Genetic Counselor Supervisory Identity Development
Next Generation Genetic Counseling: Introduction to the Special Issue
Cost Sharing and Hereditary Cancer Risk: Predictors of Willingness‐to‐Pay for Genetic Testing
Attitudes Towards Potentially Carrying the FMR1 Premutation: Before vs After Testing of Non‐Carrier Females with Diminished Ovarian Reserve
Barriers Impacting the Utilization of Supervision Techniques in Genetic Counseling
Client Views and Attitudes to Non‐Invasive Prenatal Diagnosis for Sickle Cell Disease, Thalassaemia and Cystic Fibrosis
It is Time: A Commentary on “An Exploration of Genetic Counselors’ Needs and Experiences with Prenatal Chromosomal Microarray Testing”
Who is at Risk for Compassion Fatigue? An Investigation of Genetic Counselor Demographics, Anxiety, Compassion Satisfaction, and Burnout
Provision of Cardiovascular Genetic Counseling Services: Current Practice and Future Directions
Interdisciplinary Education for Genetic Counselors: Developing the Concept and Assessing the Need in Australasia
Collaboration of Colorado Cancer Genetic Counselors to Integrate Next Generation Sequencing Panels into Clinical Practice
LQTS Parents’ Reflections About Genetic Risk Knowledge and their Need to Know or Not to Know their Children's Carrier Status
The Utilization and Choices of Aneuploidy Screening in a Midwestern Population
Maternal Uniparental Isodisomy Causing Autosomal Recessive GM1 Gangliosidosis: A Clinical Report
Disclosure of Genetic Research Results to Members of a Founder Population Hutterites
Amyotrophic Lateral Sclerosis in a Patient with a Family History of Huntington Disease: Genetic Counseling Challenges
The Evolution of Cancer Risk Assessment in the Era of Next Generation Sequencing
Predictors of Genetic Testing Decisions: A Systematic Review and Critique of the Literature
Demographic and Experiential Correlates of Public Attitudes Towards Cell‐Free Fetal DNA Screening Asian race
Genetic Counselors’ Views and Experiences with the Clinical Integration of Genome Sequencing
Linking Genetic Counseling Content to Short‐Term Outcomes in Individuals at Elevated Breast Cancer Risk
Birth Defects, Causal Attributions, and Ethnicity in the National Birth Defects Prevention Study
Genomic Counseling in the Newborn Period: Experiences and Views of Genetic Counselors
Genetic Counseling Practice in Next Generation Sequencing Research: Implications for the Ethical Oversight of the Informed Consent Process
Motivation to Pursue Genetic Testing in Individuals with a Personal or Family History of Cardiac Events or Sudden Cardiac Death
Genetic Testing of Children for Predisposition to Mood Disorders: Anticipating the Clinical Issues
Evaluation of a Clinical Genetics Service – A Quality Initiative
Cancer Risk Assessment Using Genetic Panel Testing: Considerations for Clinical Application
The Incorporation of Predictive Genomic Testing into Genetic Counseling Programs
Traditional Roles in a Non‐Traditional Setting: Genetic Counseling in Precision Oncology
A Genetic Counseling Intervention to Facilitate Family Communication About Inherited Conditions
Genetic Counseling Graduate Student Debt: Impact on Program, Career and Life Choices
An Exploration of Genetic Counselors’ Needs and Experiences with Prenatal Chromosomal Microarray Testing
An Investigation of Genetic Counselors’ Testing Recommendations: Pedigree Analysis and the Use of Multiplex Breast Cancer Panel Testing
An Assessment of Time Involved in Pre‐test Case Review and Counseling for a Whole Genome Sequencing Clinical Research Program
Psychosocial Stressors of Sickle Cell Disease on Adult Patients in Cameroon
Personalized Genomic Results: Analysis of Informational Needs
Teaching Genomic Counseling: Preparing the Genetic Counseling Workforce for the Genomic Era
NSGC 2014 Presidential Address: Just Own It
Attitudes of Mothers of Children with Down Syndrome Towards Noninvasive Prenatal Testing
Attitudes About Internet Support Groups Among Adolescents and Young Adults with Neurofibromatosis Type 1 and their Parents
Adapting Genetic Counseling Training to the Genomic Era: More an Evolution than a Revolution
Lynch Syndrome Patients’ Views of and Preferences for Return of Results Following Whole Exome Sequencing
Next Generation Sequencing is the Impetus for the Next Generation of Laboratory‐Based Genetic Counselors
The Ophthalmic Experience: Unanticipated Primary Findings in the Era of Next Generation Sequencing
Assessing the Integration of Genomic Medicine in Genetic Counseling Training Programs
Huntington Disease: Who Seeks Presymptomatic Genetic Testing, Why and What are the Outcomes?
The Effect of Genetic Counseling for Adult Offspring of Patients with Type 2 Diabetes on Attitudes Toward Diabetes and its Heredity: A Randomized Controlled Trial
Insufficient Referral for Genetic Counseling in the Management of Hereditary Haemochromatosis in Portugal: A Study of Perceptions of Health Professionals Requesting <i>HFE</i> Genotyping
Balancing Life with an Increased Risk of Cancer: Lived Experiences in Healthy Individuals with Lynch Syndrome
Points to Consider in the Clinical Use of NGS Panels for Mitochondrial Disease: An Analysis of Gene Inclusion and Consent Forms
Preferences Regarding Targeted Education and Risk Assessment in People with a Family History of Major Depressive Disorder