Lista de obras - Christine Patch - Dominio Público Uruguay

A Delphi study to determine the European core curriculum for Master programmes in genetic counselling

artículo científico publicado en 2013

A Maturity Matrix for Nurse Leaders to Facilitate and Benchmark Progress in Genomic Healthcare Policy, Infrastructure, Education, and Delivery

artículo científico publicado en 2020

A Roadmap for Global Acceleration of Genomics Integration Across Nursing

scientific article published on 17 April 2020

A comparison of a genetic screening strategy and a biochemical strategy for population screening for hemochromatosis

article

A decision analysis model for diagnostic strategies using DNA testing for hereditary haemochromatosis in at risk populations

article

A systematic review of the clinical validity and clinical utility of DNA testing for hereditary haemochromatosis type 1 in at-risk populations.

artículo científico publicado en 2008

A systematic search for uniparental disomy in carriers of chromosome translocations

artículo científico publicado en 1994

Advances in the genetics of schizophrenia: will high-risk copy number variants be useful in clinical genetics or diagnostics?

artículo científico publicado en 2009

Basic cancer genetics

article

Black and Minority Ethnic women's decision-making for risk reduction strategies after BRCA testing: Use of context and knowledge

scientific article published on 12 December 2018

Building the genetic counsellor profession in the United Kingdom: two decades of growth and development

artículo científico publicado en 2013

Chromosomal microarray testing in adults with intellectual disability presenting with comorbid psychiatric disorders.

artículo científico publicado en 2016

Communication about genetic testing with breast and ovarian cancer patients: a scoping review

scientific article published on 20 December 2018

Comparison of genotypic and phenotypic strategies for population screening in hemochromatosis: assessment of anxiety, depression, and perception of health

artículo científico publicado en 2005

Delineating the psychiatric and behavioral phenotype of recurrent 2q13 deletions and duplications.

artículo científico publicado en 2018

Developing a policy for paediatric biobanks: principles for good practice

artículo científico publicado en 2012

Developing an intervention to facilitate family communication about inherited genetic conditions, and training genetic counsellors in its delivery

artículo científico publicado en 2015

Development and mixed-methods evaluation of an online animation for young people about genome sequencing

scientific article published on 02 January 2020

Development of a measure of genome sequencing knowledge for young people: The kids-KOGS

artículo científico publicado en 2019

Diagnostic strategies using DNA testing for hereditary haemochromatosis in at-risk populations: a systematic review and economic evaluation.

scientific article published on April 2009

Direct to consumer genetic tests

artículo científico publicado en 2009

Direct to consumer genetic tests

artículo científico publicado en 2009

Duplication of 10q24 locus: broadening the clinical and radiological spectrum

scientific article published on 08 January 2019

Ethical Challenges Associated with Pathogen and Host Genetics in Infectious Disease

artículo científico publicado en 2022

European recommendations integrating genetic testing into multidisciplinary management of sudden cardiac death

article published in 2019

Factors affecting the clinical use of non‐invasive prenatal testing: a mixed methods systematic review ⬇️

artículo científico publicado el 1 de junio de 2013

Factors affecting the uptake of screening: A randomised controlled non-inferiority trial comparing a genotypic and a phenotypic strategy for screening for haemochromatosis

article

Family communication about cystic fibrosis from the mother's perspective: an exploratory study

scholarly article by Nicola Coates et al published November 2007 in Journal of Research in Nursing

Genetic Counselling in Disorders of Low Penetrance

Genetic Counsellors: A Registration System to Assure Competence in Practice in the United Kingdom

article

Genetic counselling in the era of genomic medicine

artículo científico publicado en 2018

Genetic counselors and Genomic Counseling in the United Kingdom

artículo científico publicado en 2015

Genetic horoscopes: is it all in the genes? Points for regulatory control of direct-to-consumer genetic testing

artículo científico publicado en 2009

Genetic testing and common disorders in a public health framework: how to assess relevance and possibilities. Background Document to the ESHG recommendations on genetic testing and common disorders

artículo científico publicado en 2011

Genetic testing in intellectual disability psychiatry: Opinions and practices of UK child and intellectual disability psychiatrists.

artículo científico publicado en 2017

Haemochromatosis: the need for an agreed case definition

How can the evaluation of genetic tests be enhanced? Lessons learned from the ACCE framework and evaluating genetic tests in the United Kingdom

artículo científico publicado en 2005

Identifying individuals who might benefit from genetic services and information

artículo científico publicado en 2013

Interventions to improve patient access to and utilisation of genetic and genomic counselling services

artículo científico publicado en 2015

Living a normal life in an extraordinary way: A systematic review investigating experiences of families of young people's transition into adulthood when affected by a genetic and chronic childhood condition

artículo científico publicado en 2016

Molecular re-investigation of patients with Huntington's disease in Wessex reveals a family with dentatorubral and pallidoluysian atrophy

artículo científico publicado en 1996

Newborn screening policy in the United Kingdom & the United States: two different communities of practice

artículo científico publicado en 2006

Opening the "black box" of informed consent appointments for genome sequencing: a multisite observational study

artículo científico publicado en 2018

Opportunistic genomic screening. Recommendations of the European Society of Human Genetics

artículo científico publicado en 2020

Parents' motivations, concerns and understanding of genome sequencing: a qualitative interview study

artículo científico publicado en 2020

Participant experiences of genome sequencing for rare diseases in the 100,000 Genomes Project: a mixed methods study

artículo científico publicado en 2022

Penetrance for copy number variants associated with schizophrenia

artículo científico publicado en 2010

Point of View: An evolution from genetic counselling to genomic counselling

artículo científico publicado en 2019

Position statement on opportunistic genomic screening from the Association of Genetic Nurses and Counsellors (UK and Ireland).

artículo científico publicado en 2014

Predictive or not predictive: understanding the mixed messages from the patient's DNA sequence

artículo científico publicado en 2015

Prevalence and Burden of Disease in Hemochromatosis: Estimates Derived from Routine Data

article

Protelomeric sequences are deleted in cases of short arm inverted duplication of chromosome 8

article

Psychosocial aspects of DNA testing for hereditary hemochromatosis in at-risk individuals: a systematic review

artículo científico publicado en 2009

Recommendations for education and training of genetic nurses and counsellors in the United Kingdom.

artículo científico publicado en 1998

Reply to Blendis

Should doctors have a legal duty to warn relatives of their genetic risks?

scientific article published on 26 November 2019

Study of the relationship between Black men, culture and prostate cancer beliefs

article

The 'new genetics' and nursing: what does it have to do with me?

artículo científico publicado en 2000

The new genetics: A research agenda for nurses?

article

The role of genetic counsellors in genomic healthcare in the United Kingdom: a statement by the Association of Genetic Nurses and Counsellors

artículo científico publicado en 2017

Training Genetic Counsellors to Deliver an Innovative Therapeutic Intervention: their Views and Experience of Facilitating Multi-Family Discussion Groups

artículo científico publicado en 2016

Use of antihypertensive medications and mortality of patients with autosomal dominant polycystic kidney disease: a population-based study

artículo científico

Using a community of practice to develop standards of practice and education for genetic counsellors in Europe ⬇️

artículo científico publicado en 2010

Web-based return of BRCA2 research results: one-year genetic counselling experience in Iceland

artículo científico publicado en 2020

Whole-genome sequencing reveals host factors underlying critical COVID-19

artículo científico publicado en 2022

World congress on genetic counselling

artículo científico publicado en 2019

Lista de obras de Christine Patch

A Delphi study to determine the European core curriculum for Master programmes in genetic counselling

A Maturity Matrix for Nurse Leaders to Facilitate and Benchmark Progress in Genomic Healthcare Policy, Infrastructure, Education, and Delivery

A Roadmap for Global Acceleration of Genomics Integration Across Nursing

A comparison of a genetic screening strategy and a biochemical strategy for population screening for hemochromatosis

A decision analysis model for diagnostic strategies using DNA testing for hereditary haemochromatosis in at risk populations

A systematic review of the clinical validity and clinical utility of DNA testing for hereditary haemochromatosis type 1 in at-risk populations.

A systematic search for uniparental disomy in carriers of chromosome translocations

Advances in the genetics of schizophrenia: will high-risk copy number variants be useful in clinical genetics or diagnostics?

Basic cancer genetics

Black and Minority Ethnic women's decision-making for risk reduction strategies after BRCA testing: Use of context and knowledge

Building the genetic counsellor profession in the United Kingdom: two decades of growth and development

Chromosomal microarray testing in adults with intellectual disability presenting with comorbid psychiatric disorders.

Communication about genetic testing with breast and ovarian cancer patients: a scoping review

Comparison of genotypic and phenotypic strategies for population screening in hemochromatosis: assessment of anxiety, depression, and perception of health

Delineating the psychiatric and behavioral phenotype of recurrent 2q13 deletions and duplications.

Developing a policy for paediatric biobanks: principles for good practice

Developing an intervention to facilitate family communication about inherited genetic conditions, and training genetic counsellors in its delivery

Development and mixed-methods evaluation of an online animation for young people about genome sequencing

Development of a measure of genome sequencing knowledge for young people: The kids-KOGS

Diagnostic strategies using DNA testing for hereditary haemochromatosis in at-risk populations: a systematic review and economic evaluation.

Direct to consumer genetic tests

Direct to consumer genetic tests

Duplication of 10q24 locus: broadening the clinical and radiological spectrum

Ethical Challenges Associated with Pathogen and Host Genetics in Infectious Disease

European recommendations integrating genetic testing into multidisciplinary management of sudden cardiac death

Factors affecting the clinical use of non‐invasive prenatal testing: a mixed methods systematic review ⬇️

Factors affecting the uptake of screening: A randomised controlled non-inferiority trial comparing a genotypic and a phenotypic strategy for screening for haemochromatosis

Family communication about cystic fibrosis from the mother's perspective: an exploratory study

Genetic Counselling in Disorders of Low Penetrance

Genetic Counsellors: A Registration System to Assure Competence in Practice in the United Kingdom

Genetic counselling in the era of genomic medicine

Genetic counselors and Genomic Counseling in the United Kingdom

Genetic horoscopes: is it all in the genes? Points for regulatory control of direct-to-consumer genetic testing

Genetic testing and common disorders in a public health framework: how to assess relevance and possibilities. Background Document to the ESHG recommendations on genetic testing and common disorders

Genetic testing in intellectual disability psychiatry: Opinions and practices of UK child and intellectual disability psychiatrists.

Haemochromatosis: the need for an agreed case definition

How can the evaluation of genetic tests be enhanced? Lessons learned from the ACCE framework and evaluating genetic tests in the United Kingdom

Identifying individuals who might benefit from genetic services and information

Interventions to improve patient access to and utilisation of genetic and genomic counselling services

Living a normal life in an extraordinary way: A systematic review investigating experiences of families of young people's transition into adulthood when affected by a genetic and chronic childhood condition

Molecular re-investigation of patients with Huntington's disease in Wessex reveals a family with dentatorubral and pallidoluysian atrophy

Newborn screening policy in the United Kingdom & the United States: two different communities of practice

Opening the "black box" of informed consent appointments for genome sequencing: a multisite observational study

Opportunistic genomic screening. Recommendations of the European Society of Human Genetics

Parents' motivations, concerns and understanding of genome sequencing: a qualitative interview study

Participant experiences of genome sequencing for rare diseases in the 100,000 Genomes Project: a mixed methods study

Penetrance for copy number variants associated with schizophrenia

Point of View: An evolution from genetic counselling to genomic counselling

Position statement on opportunistic genomic screening from the Association of Genetic Nurses and Counsellors (UK and Ireland).

Predictive or not predictive: understanding the mixed messages from the patient's DNA sequence

Prevalence and Burden of Disease in Hemochromatosis: Estimates Derived from Routine Data

Protelomeric sequences are deleted in cases of short arm inverted duplication of chromosome 8

Psychosocial aspects of DNA testing for hereditary hemochromatosis in at-risk individuals: a systematic review

Recommendations for education and training of genetic nurses and counsellors in the United Kingdom.

Reply to Blendis

Should doctors have a legal duty to warn relatives of their genetic risks?

Study of the relationship between Black men, culture and prostate cancer beliefs

The 'new genetics' and nursing: what does it have to do with me?

The new genetics: A research agenda for nurses?

The role of genetic counsellors in genomic healthcare in the United Kingdom: a statement by the Association of Genetic Nurses and Counsellors

Training Genetic Counsellors to Deliver an Innovative Therapeutic Intervention: their Views and Experience of Facilitating Multi-Family Discussion Groups

Use of antihypertensive medications and mortality of patients with autosomal dominant polycystic kidney disease: a population-based study

Using a community of practice to develop standards of practice and education for genetic counsellors in Europe ⬇️

Web-based return of BRCA2 research results: one-year genetic counselling experience in Iceland

Whole-genome sequencing reveals host factors underlying critical COVID-19

World congress on genetic counselling