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Lista de obras de Heather Zierhut

A Dominant Mutation in Human RAD51 Reveals Its Function in DNA Interstrand Crosslink Repair Independent of Homologous Recombination

scientific journal article

A Rapid Systematic Review of Outcomes Studies in Genetic Counseling.

artículo científico publicado en 2017

A novel approach to screening for familial hypercholesterolemia in a large public venue

artículo científico publicado en 2016

A report on state-wide implementation of newborn screening for X-linked Adrenoleukodystrophy

scientific article published on 10 May 2019

A roadmap for precision medicine research recruitment: empirical assessment of the public's willingness to participate

artículo científico publicado en 2020

Alternative donor hematopoietic cell transplantation for Fanconi anemia

artículo científico publicado en 2015

Association of rib anomalies and childhood cancers

artículo científico publicado en 2011

Barriers to the identification of familial hypercholesterolemia among primary care providers.

artículo científico publicado en 2018

Beyond medical actionability: Public perceptions of important actions in response to hypothetical genetic testing results

artículo científico publicado en 2019

Canaries in the coal mine: Personal and professional impact of undergoing whole genome sequencing on medical professionals.

artículo científico publicado en 2015

Collaborative Counseling Considerations for Pharmacogenomic Tests

artículo científico publicado en 2017

Defining Our Clinical Practice: The Identification of Genetic Counseling Outcomes Utilizing the Reciprocal Engagement Model.

artículo científico publicado en 2015

Delivery Of Cascade Screening For Hereditary Conditions: A Scoping Review Of The Literature

artículo científico publicado en 2018

Developing culturally informed genetic services for the Somali immigrants in Minnesota

scientific article published on 06 May 2019

Development of FOCUS-GC: Framework for Outcomes of Clinical Communication Services in Genetic Counseling

artículo científico publicado en 2017

Development of a motivational interviewing genetic counseling intervention to increase cascade cholesterol screening in families of children with familial hypercholesterolemia

scientific article published on 05 July 2019

Differences in predicted warfarin dosing requirements between Hmong and East Asians using genotype-based dosing algorithms

artículo científico publicado en 2020

Elaboration of the Reciprocal-Engagement Model of Genetic Counseling Practice: a Qualitative Investigation of Goals and Strategies

artículo científico publicado en 2017

Elucidating Genetic Counseling Outcomes from the Perspective of Genetic Counselors.

artículo científico publicado en 2016

Factors Influencing the Decision-Making Process and Long-Term Interpersonal Outcomes for Parents Who Undergo Preimplantation Genetic Diagnosis for Fanconi Anemia: a Qualitative Investigation

artículo científico publicado en 2016

Family history of cancer and non-malignant diseases and risk of childhood acute lymphoblastic leukemia: a Children's Oncology Group Study

scientific article published on 21 October 2011

Genetic Counselors' Experiences Regarding Communication of Reproductive Risks with Autosomal Recessive Conditions found on Cancer Panels

artículo científico publicado en 2015

Genetic Counselors' Experiences and Interest in Telegenetics and Remote Counseling

artículo científico publicado en 2018

Genetic counseling for Fanconi anemia: crosslinking disciplines.

artículo científico publicado en 2014

Haematopoietic cell transplantation for acute leukaemia and advanced myelodysplastic syndrome in Fanconi anaemia.

artículo científico publicado en 2013

Hmong participants' reactions to return of individual and community pharmacogenetic research results: "A positive light for our community"

artículo científico publicado en 2020

How inclusion of genetic counselors on the research team can benefit translational science

artículo científico publicado en 2011

More than 10 years after the first 'savior siblings': parental experiences surrounding preimplantation genetic diagnosis.

artículo científico publicado en 2013

Navigating the Labyrinth of Pharmacogenetic Testing: A Guide to Test Selection

artículo científico publicado en 2019

Next generation sequencing in endocrine practice

artículo científico publicado en 2015

Pediatric cholesterol screening practices in 9- to 11-year-olds in a large midwestern primary care setting

artículo científico publicado en 2020

Phenotypic variability in patients with Fanconi anemia and biallelic FANCF mutations.

artículo científico publicado en 2016

Potential Clinical Relevance of Differences in Allele Frequencies Found within Very Important Pharmacogenes between Hmong and East Asian Populations

scientific article published on 14 January 2020

Racial and ethnic differences in genetic counseling experiences and outcomes in the United States: A systematic review

artículo científico publicado en 2020

Risk Communication in Families of Children with Familial Hypercholesterolemia: Identifying Motivators and Barriers to Cascade Screening to Improve Diagnosis at a Single Medical Center

scientific article published on 14 August 2018

Seekers, Finders, Settlers, and Stumblers: Identifying the Career Paths of Males in the Genetic Counseling Profession

artículo científico publicado en 2017

Standards for the Reporting of Genetic Counseling Interventions in Research and Other Studies (GCIRS): an NSGC Task Force Report

artículo científico publicado en 2017

Stem cell research and therapy: the position of the National Society of Genetic Counselors.

artículo científico

The role of race and ethnicity in views toward and participation in genetic studies and precision medicine research in the United States: A systematic review of qualitative and quantitative studies

artículo científico publicado en 2019

Waiting for the next Shoe to Drop: The Experience of Parents of Children with Fanconi Anemia

artículo científico publicado el 30 de julio de 2011

Why Is Cancer Genetic Counseling Underutilized by Women Identified as at Risk for Hereditary Breast Cancer? Patient Perceptions of Barriers Following a Referral Letter

artículo científico publicado en 2016