Lista de obras - Nadeem Qureshi - Dominio Público Uruguay

'Over-the-counter' genetic testing: what does it really mean for primary care?

artículo científico publicado en 2009

030 Primary Care Physicians’ Views On Relevance Of Clinical Guideline Recommendations: Delphi Panel

A randomized controlled trial to assess the psychological impact of a family history screening questionnaire in general practice

artículo científico publicado en 2001

A review of clinical practice guidelines found that they were often based on evidence of uncertain relevance to primary care patients

artículo científico publicado en 2014

Achieving change in primary care--causes of the evidence to practice gap: systematic reviews of reviews.

artículo científico publicado en 2016

Achieving change in primary care--effectiveness of strategies for improving implementation of complex interventions: systematic review of reviews

artículo científico publicado en 2015

Addressing the evidence to practice gap for complex interventions in primary care: a systematic review of reviews protocol

artículo científico publicado en 2014

Assessing family history of heart disease in primary care consultations: a qualitative study

scientific article published on 28 August 2007

Automated Risk Assessment for Stroke in Atrial Fibrillation (AURAS-AF)--an automated software system to promote anticoagulation and reduce stroke risk: study protocol for a cluster randomised controlled trial

artículo científico publicado en 2013

Automated Software System to Promote Anticoagulation and Reduce Stroke Risk: Cluster-Randomized Controlled Trial.

artículo científico

Availability and quality of coronary heart disease family history in primary care medical records: implications for cardiovascular risk assessment

scientific article published on 09 January 2014

Barriers to a software reminder system for risk assessment of stroke in atrial fibrillation: a process evaluation of a cluster randomised trial in general practice

artículo científico publicado en 2018

Benefits of Aldosterone Receptor Antagonism in Chronic Kidney Disease (BARACK D) trial-a multi-centre, prospective, randomised, open, blinded end-point, 36-month study of 2,616 patients within primary care with stage 3b chronic kidney disease [...]

artículo científico publicado en 2014

Beyond beliefs: risk assessment technologies shaping patients' experiences of heart disease prevention.

artículo científico publicado en 2011

Can machine-learning improve cardiovascular risk prediction using routine clinical data?

artículo científico publicado en 2017

Cardiovascular risk assessment and lipid modification: NICE guideline

artículo científico publicado en 2015

Characteristics predicting recommendation for familial breast cancer referral in a cohort of women from primary care

scientific article published on 22 January 2020

Clinical genetics meets primary care

artículo científico publicado en 1993

Clinical utility of cancer family history collection in primary care

artículo científico publicado en 2009

Collecting genetic information in primary care: evaluating a new family history tool

artículo científico publicado en 2005

Collection and use of cancer family history in primary care.

artículo científico publicado en 2007

Communication of carrier status information following universal newborn screening for sickle cell disorders and cystic fibrosis: qualitative study of experience and practice

artículo científico publicado en 2009

Comparison of coronary heart disease genetic assessment with conventional cardiovascular risk assessment in primary care: reflections on a feasibility study

artículo científico publicado en 2015

Consanguinity and genetic morbidity in a British primary care setting: a pilot study with trained linkworkers

artículo científico publicado en 2003

Continuous medical education approaches for clinical genetics: a postal survey of general practitioners

artículo científico publicado en 2002

Controversies in familial hypercholesterolaemia: recommendations of the NICE Guideline Development Group for the identification and management of familial hypercholesterolaemia

artículo científico publicado en 2009

Cost-utility analysis of searching electronic health records and cascade testing to identify and diagnose familial hypercholesterolaemia in England and Wales

article

Dealing with family history of breast cancer: something new, something old.

artículo científico publicado en 2014

Detection of familial hypercholesterolaemia: external validation of the FAMCAT clinical case-finding algorithm to identify patients in primary care

artículo científico publicado en 2019

Does bone mineral density improve the predictive accuracy of fracture risk assessment? A prospective cohort study in Northern Denmark.

artículo científico publicado en 2018

Does the evidence referenced in NICE guidelines reflect a primary care population?

artículo científico publicado en 2011

Early identification of familial hypercholesterolaemia in general practice using patient-specific reminders: focus group with General Practitioners.

artículo científico publicado en 2014

Effect of adding systematic family history enquiry to cardiovascular disease risk assessment in primary care: a matched-pair, cluster randomized trial

artículo científico publicado en 2012

Effectiveness of interventions to identify and manage patients with familial cancer risk in primary care: a systematic review

scientific article published on 06 May 2019

Effectiveness of physical activity and dietary interventions in South Asian populations: a systematic review

artículo científico publicado en 2013

Effectiveness of strategies to facilitate uptake or implementation of complex interventions: A systematic review of reviews

artículo científico publicado en 2015

Engagement barriers and service inequities in the NHS Breast Screening Programme: Views from British-Pakistani women

scientific article published on 02 December 2019

Evolocumab for Treating Primary Hypercholesterolaemia and Mixed Dyslipidaemia: An Evidence Review Group Perspective of a NICE Single Technology Appraisal

artículo científico publicado en 2016

Familial influences on antenatal and newborn haemoglobinopathy screening

article

Family history and improving health

scientific article published on August 2009

Family history in public health practice: a genomic tool for disease prevention and health promotion

artículo científico publicado en 2010

Family history of type 2 diabetes: A population-based screening tool for prevention?

article by Susan Hariri et al published February 2006 in Genetics in Medicine

Feasibility of improving identification of familial hypercholesterolaemia in general practice: intervention development study

artículo científico publicado en 2016

GPs' opinions of their role in prenatal genetic services: a cross-sectional survey

article published in 2005

Genetics Support to Primary Care Practitioners—A Demonstration Project

article

Genomic medicine for underserved minority populations in family medicine

artículo científico publicado en 2005

How does a simple enquiry compare to a detailed family history questionnaire to identify coronary heart disease or diabetic familial risk?

artículo científico publicado en 2011

How genomic information is accessed in clinical practice: an electronic survey of UK general practitioners

scientific article published on 03 March 2020

How should health policy and practice respond to the increased genetic risk associated with close relative marriage? results of a UK Delphi consensus building exercise

scientific article published on 09 July 2019

Identification and management of familial hypercholesterolaemia: what does it mean to primary care?

scientific article published on October 2009

Imparting carrier status results detected by universal newborn screening for sickle cell and cystic fibrosis in England: a qualitative study of current practice and policy challenges

artículo científico publicado en 2007

Improving identification and management of familial hypercholesterolaemia in primary care: Pre- and post-intervention study

artículo científico publicado en 2018

Improving identification of familial hypercholesterolaemia in primary care: derivation and validation of the familial hypercholesterolaemia case ascertainment tool (FAMCAT).

artículo científico publicado en 2014

Improving primary care identification of familial breast cancer risk using proactive invitation and decision support

artículo científico publicado en 2020

Inclusion of diverse populations in genomic research and health services: Genomix workshop report

artículo científico publicado en 2017

Informing children of their newborn screening carrier result for sickle cell or cystic fibrosis: qualitative study of parents' intentions, views and support needs.

artículo científico publicado en 2013

Informing patients of familial diabetes mellitus risk: How do they respond? A cross-sectional survey

artículo científico publicado en 2008

Introducing genetic testing for cardiovascular disease in primary care: a qualitative study

artículo científico publicado en 2014

Leaders, leadership and future primary care clinical research

artículo científico publicado en 2008

Making sense of being at ‘high risk’ of coronary heart disease within primary prevention

artículo científico publicado en 2010

New developments in genetics--knowledge, attitudes and information needs of practice nurses

article

Opportunities and challenges for enhancing preconception health in primary care: qualitative study with women from ethnically diverse communities

artículo científico publicado en 2013

Parents' responses to receiving sickle cell or cystic fibrosis carrier results for their child following newborn screening

artículo científico publicado en 2014

Performance and clinical utility of supervised machine-learning approaches in detecting familial hypercholesterolaemia in primary care

artículo científico publicado en 2020

Personalised medicine in general practice: the example of raised cholesterol

artículo científico publicado en 2018

Perspectives on enhancing physical activity and diet for health promotion among at-risk urban UK South Asian communities: a qualitative study

artículo científico publicado en 2015

Preconception risk assessment for thalassaemia, sickle cell disease, cystic fibrosis and Tay-Sachs disease

artículo científico publicado en 2015

Preconception risk assessment for thalassaemia, sickle cell disease, cystic fibrosis and Tay-Sachs disease.

artículo científico publicado en 2018

Predicting major adverse cardiovascular events for secondary prevention: protocol for a systematic review and meta-analysis of risk prediction models

artículo científico publicado en 2020

Prediction of premature all-cause mortality: A prospective general population cohort study comparing machine-learning and standard epidemiological approaches

artículo científico publicado en 2019

Primary care evidence in clinical guidelines: a mixed methods study of practitioners' views

artículo científico publicado en 2014

Prioritizing health outcomes in a limited world: writing lipid guidelines

artículo científico

Realising the potential of the family history in risk assessment and primary prevention of coronary heart disease in primary care: ADDFAM study protocol

artículo científico publicado en 2009

Realistic genetic competencies achievable by US primary care providers.

artículo científico publicado en 2014

Risk of cardiovascular disease outcomes in primary care subjects with familial hypercholesterolaemia: A cohort study

scientific article published on 24 May 2019

Risks to offspring of consanguineous marriage: we need straight, not crooked thinking

artículo científico publicado en 2011

Screening for Familial Hypercholesterolemia in Children: What Can We Learn From Adult Screening Programs?

artículo científico publicado en 2015

Screening for familial hypercholesterolaemia in primary care: Time for general practice to play its part

Secondary prevention of cardiovascular disease: Time to rethink stratification of disease severity?

artículo científico publicado en 2019

Specialist recommendation for chemoprevention medications in patients at familial risk of breast cancer: a cross-sectional survey in England

artículo científico publicado en 2020

Sub-optimal cholesterol response to initiation of statins and future risk of cardiovascular disease

artículo científico publicado en 2019

Subjective vision and hearing impairment and falls among community-dwelling adults: a prospective study in the Survey of Health, Ageing and Retirement in Europe (SHARE)

scientific article published in 2021

Systematic review: family history in risk assessment for common diseases

artículo científico publicado en 2009

The 'new genetics' and primary care: GPs' views on their role and their educational needs

artículo científico publicado en 1999

The comorbidity burden of type 2 diabetes mellitus: patterns, clusters and predictions from a large English primary care cohort

artículo científico publicado en 2019

The current state of cancer family history collection tools in primary care: a systematic review

artículo científico publicado en 2009

The effects of preconception interventions on improving reproductive health and pregnancy outcomes in primary care: A systematic review

artículo científico publicado en 2015

The genetics liaison nurse role as a means of educating and supporting primary care professionals

artículo científico publicado en 2002

The impact of genetic outreach education and support to primary care on practitioner's confidence and competence in dealing with familial cancers

artículo científico publicado en 2008

The introduction of risk stratified screening into the NHS breast screening Programme: views from British-Pakistani women

artículo científico publicado en 2020

The role of cost-effectiveness analysis in the development of indicators to support incentive-based behaviour in primary care in England

artículo científico publicado en 2016

The value of aspartate aminotransferase and alanine aminotransferase in cardiovascular disease risk assessment

artículo científico publicado en 2015

Timeline: Raising the profile of genetics in primary care

artículo científico publicado en 2004

Using electronic health records to quantify and stratify the severity of type 2 diabetes in primary care in England: rationale and cohort study design

article

Using family history information to promote healthy lifestyles and prevent diseases; a discussion of the evidence

artículo científico publicado en 2010

Using web-based familial risk information for diabetes prevention: a randomized controlled trial

artículo científico publicado en 2013

Venous thromboembolism in adults screened for sickle cell trait: a population-based cohort study with nested case-control analysis

artículo científico publicado en 2017

What hinders minority ethnic access to cancer genetics services and what may help?

artículo científico publicado en 2013

Lista de obras de Nadeem Qureshi

'Over-the-counter' genetic testing: what does it really mean for primary care?

030 Primary Care Physicians’ Views On Relevance Of Clinical Guideline Recommendations: Delphi Panel

A randomized controlled trial to assess the psychological impact of a family history screening questionnaire in general practice

A review of clinical practice guidelines found that they were often based on evidence of uncertain relevance to primary care patients

Achieving change in primary care--causes of the evidence to practice gap: systematic reviews of reviews.

Achieving change in primary care--effectiveness of strategies for improving implementation of complex interventions: systematic review of reviews

Addressing the evidence to practice gap for complex interventions in primary care: a systematic review of reviews protocol

Assessing family history of heart disease in primary care consultations: a qualitative study

Automated Risk Assessment for Stroke in Atrial Fibrillation (AURAS-AF)--an automated software system to promote anticoagulation and reduce stroke risk: study protocol for a cluster randomised controlled trial

Automated Software System to Promote Anticoagulation and Reduce Stroke Risk: Cluster-Randomized Controlled Trial.

Availability and quality of coronary heart disease family history in primary care medical records: implications for cardiovascular risk assessment

Barriers to a software reminder system for risk assessment of stroke in atrial fibrillation: a process evaluation of a cluster randomised trial in general practice

Benefits of Aldosterone Receptor Antagonism in Chronic Kidney Disease (BARACK D) trial-a multi-centre, prospective, randomised, open, blinded end-point, 36-month study of 2,616 patients within primary care with stage 3b chronic kidney disease [...]

Beyond beliefs: risk assessment technologies shaping patients' experiences of heart disease prevention.

Can machine-learning improve cardiovascular risk prediction using routine clinical data?

Cardiovascular risk assessment and lipid modification: NICE guideline

Characteristics predicting recommendation for familial breast cancer referral in a cohort of women from primary care

Clinical genetics meets primary care

Clinical utility of cancer family history collection in primary care

Collecting genetic information in primary care: evaluating a new family history tool

Collection and use of cancer family history in primary care.

Communication of carrier status information following universal newborn screening for sickle cell disorders and cystic fibrosis: qualitative study of experience and practice

Comparison of coronary heart disease genetic assessment with conventional cardiovascular risk assessment in primary care: reflections on a feasibility study

Consanguinity and genetic morbidity in a British primary care setting: a pilot study with trained linkworkers

Continuous medical education approaches for clinical genetics: a postal survey of general practitioners

Controversies in familial hypercholesterolaemia: recommendations of the NICE Guideline Development Group for the identification and management of familial hypercholesterolaemia

Cost-utility analysis of searching electronic health records and cascade testing to identify and diagnose familial hypercholesterolaemia in England and Wales

Dealing with family history of breast cancer: something new, something old.

Detection of familial hypercholesterolaemia: external validation of the FAMCAT clinical case-finding algorithm to identify patients in primary care

Does bone mineral density improve the predictive accuracy of fracture risk assessment? A prospective cohort study in Northern Denmark.

Does the evidence referenced in NICE guidelines reflect a primary care population?

Early identification of familial hypercholesterolaemia in general practice using patient-specific reminders: focus group with General Practitioners.

Effect of adding systematic family history enquiry to cardiovascular disease risk assessment in primary care: a matched-pair, cluster randomized trial

Effectiveness of interventions to identify and manage patients with familial cancer risk in primary care: a systematic review

Effectiveness of physical activity and dietary interventions in South Asian populations: a systematic review

Effectiveness of strategies to facilitate uptake or implementation of complex interventions: A systematic review of reviews

Engagement barriers and service inequities in the NHS Breast Screening Programme: Views from British-Pakistani women

Evolocumab for Treating Primary Hypercholesterolaemia and Mixed Dyslipidaemia: An Evidence Review Group Perspective of a NICE Single Technology Appraisal

Familial influences on antenatal and newborn haemoglobinopathy screening

Family history and improving health

Family history in public health practice: a genomic tool for disease prevention and health promotion

Family history of type 2 diabetes: A population-based screening tool for prevention?

Feasibility of improving identification of familial hypercholesterolaemia in general practice: intervention development study

GPs' opinions of their role in prenatal genetic services: a cross-sectional survey

Genetics Support to Primary Care Practitioners—A Demonstration Project

Genomic medicine for underserved minority populations in family medicine

How does a simple enquiry compare to a detailed family history questionnaire to identify coronary heart disease or diabetic familial risk?

How genomic information is accessed in clinical practice: an electronic survey of UK general practitioners

How should health policy and practice respond to the increased genetic risk associated with close relative marriage? results of a UK Delphi consensus building exercise

Identification and management of familial hypercholesterolaemia: what does it mean to primary care?

Imparting carrier status results detected by universal newborn screening for sickle cell and cystic fibrosis in England: a qualitative study of current practice and policy challenges

Improving identification and management of familial hypercholesterolaemia in primary care: Pre- and post-intervention study

Improving identification of familial hypercholesterolaemia in primary care: derivation and validation of the familial hypercholesterolaemia case ascertainment tool (FAMCAT).

Improving primary care identification of familial breast cancer risk using proactive invitation and decision support

Inclusion of diverse populations in genomic research and health services: Genomix workshop report

Informing children of their newborn screening carrier result for sickle cell or cystic fibrosis: qualitative study of parents' intentions, views and support needs.

Informing patients of familial diabetes mellitus risk: How do they respond? A cross-sectional survey

Introducing genetic testing for cardiovascular disease in primary care: a qualitative study

Leaders, leadership and future primary care clinical research

Making sense of being at ‘high risk’ of coronary heart disease within primary prevention

New developments in genetics--knowledge, attitudes and information needs of practice nurses

Opportunities and challenges for enhancing preconception health in primary care: qualitative study with women from ethnically diverse communities

Parents' responses to receiving sickle cell or cystic fibrosis carrier results for their child following newborn screening

Performance and clinical utility of supervised machine-learning approaches in detecting familial hypercholesterolaemia in primary care

Personalised medicine in general practice: the example of raised cholesterol

Perspectives on enhancing physical activity and diet for health promotion among at-risk urban UK South Asian communities: a qualitative study

Preconception risk assessment for thalassaemia, sickle cell disease, cystic fibrosis and Tay-Sachs disease

Preconception risk assessment for thalassaemia, sickle cell disease, cystic fibrosis and Tay-Sachs disease.

Predicting major adverse cardiovascular events for secondary prevention: protocol for a systematic review and meta-analysis of risk prediction models

Prediction of premature all-cause mortality: A prospective general population cohort study comparing machine-learning and standard epidemiological approaches

Primary care evidence in clinical guidelines: a mixed methods study of practitioners' views

Prioritizing health outcomes in a limited world: writing lipid guidelines

Realising the potential of the family history in risk assessment and primary prevention of coronary heart disease in primary care: ADDFAM study protocol

Realistic genetic competencies achievable by US primary care providers.

Risk of cardiovascular disease outcomes in primary care subjects with familial hypercholesterolaemia: A cohort study

Risks to offspring of consanguineous marriage: we need straight, not crooked thinking

Screening for Familial Hypercholesterolemia in Children: What Can We Learn From Adult Screening Programs?

Screening for familial hypercholesterolaemia in primary care: Time for general practice to play its part

Secondary prevention of cardiovascular disease: Time to rethink stratification of disease severity?