UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Points to consider for reporting of germline variation in patients undergoing tumor testing: a statement of the American College of Medical Genetics and Genomics (ACMG)

Genetics in medicine, 2020-07, Vol.22 (7), p.1142-1148

2020

Volltextzugriff (PDF)

Reporting genomic secondary findings: ACMG members weigh in

Genetics in medicine, 2015-01, Vol.17 (1), p.27-35

2015

Volltextzugriff (PDF)

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

Genetics in medicine, 2006-02, Vol.8 (2), p.102-108

2006

Volltextzugriff (PDF)

Research priorities for evaluating family history in the prevention of common chronic diseases

American journal of preventive medicine, 2003-02, Vol.24 (2), p.128-135

2003

Volltextzugriff (PDF)

Gnathodiaphyseal dysplasia: report of a family with a novel mutation of the ANO5 gene

Oral surgery, oral medicine, oral pathology and oral radiology, 2016-05, Vol.121 (5), p.e123-e128

2016

Volltextzugriff (PDF)

An electronic family health history tool to identify and manage patients at increased risk for colorectal cancer: protocol for a randomized controlled trial

Trials, 2019-10, Vol.20 (1), p.576-576, Article 576

2019

Volltextzugriff (PDF)

Delivery of genomic medicine for common chronic adult diseases: a systematic review

JAMA : the journal of the American Medical Association, 2008-03, Vol.299 (11), p.1320

2008

Volltextzugriff (PDF)

Health-literate care organizations for precision health

Genetics in medicine, 2024-09, Vol.26 (9), p.101195, Article 101195

2024

Volltextzugriff (PDF)

Securing and Documenting Cancer Family History in the Age of the Electronic Medical Record

Surgical oncology clinics of North America, 2015-10, Vol.24 (4), p.639-652

2015

Volltextzugriff (PDF)

DNA-based screening and population health: a points to consider statement for programs and sponsoring organizations from the American College of Medical Genetics and Genomics (ACMG)

Genetics in medicine, 2021-06, Vol.23 (6), p.989-995

2021

Volltextzugriff (PDF)

Systematic evidence-based review: outcomes from exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability

Genetics in medicine, 2020-06, Vol.22 (6), p.986-1004

2020

Volltextzugriff (PDF)

Genetics professionals are key to the integration of genetic testing within the practice of frontline clinicians

Genetics in medicine, 2023-01, Vol.25 (1), p.103-114

2023

Volltextzugriff (PDF)

Basic vs More Complex Definitions of Family History in the Prediction of Coronary Heart Disease: The Multi-Ethnic Study of Atherosclerosis

Mayo Clinic proceedings, 2018-09, Vol.93 (9), p.1213-1223

2018

Volltextzugriff (PDF)

Laboratory business models and practices: implications for availability and access to germline genetic testing

Genetics in medicine, 2021-09, Vol.23 (9), p.1681-1688

2021

Volltextzugriff (PDF)

Influence of payer coverage and out‐of‐pocket costs on ordering of NGS panel tests for hereditary cancer in diverse settings

Journal of genetic counseling, 2022-02, Vol.31 (1), p.130-139

2022

Volltextzugriff (PDF)

Primary care providers’ responses to unsolicited Lynch syndrome secondary findings of varying clinical significance

Genetics in medicine, 2021-10, Vol.23 (10), p.1977-1983

2021

Volltextzugriff (PDF)

A Cluster Randomized Trial of a Family Health History Platform to Identify and Manage Patients at Increased Risk for Colorectal Cancer

Journal of general internal medicine : JGIM, 2023-05, Vol.38 (6), p.1375-1383

2023

Volltextzugriff (PDF)

The value of genetic testing: beyond clinical utility

Genetics in medicine, 2017-07, Vol.19 (7), p.763-771

2017

Volltextzugriff (PDF)

DNA-based screening and personal health: a points to consider statement for individuals and health-care providers from the American College of Medical Genetics and Genomics (ACMG)

Genetics in medicine, 2021-06, Vol.23 (6), p.979-988

2021

Volltextzugriff (PDF)

A logic model for precision medicine implementation informed by stakeholder views and implementation science

Genetics in medicine, 2019-05, Vol.21 (5), p.1139-1154

2019

Volltextzugriff (PDF)

Factors influencing organizational adoption and implementation of clinical genetic services

Genetics in medicine, 2014-03, Vol.16 (3), p.238-245

2014

Volltextzugriff (PDF)

Developing Family Healthware, a family history screening tool to prevent common chronic diseases

Preventing chronic disease, 2009-01, Vol.6 (1), p.A33

2009

Volltextzugriff (PDF)

Pharmacogenetic testing in the Veterans Health Administration (VHA): policy recommendations from the VHA Clinical Pharmacogenetics Subcommittee

Genetics in medicine, 2019-02, Vol.21 (2), p.382-390

2019

Volltextzugriff (PDF)

Population prevalence of familial cancer and common hereditary cancer syndromes. The 2005 California Health Interview Survey

Genetics in medicine, 2010-11, Vol.12 (11), p.726-735

2010

Volltextzugriff (PDF)

Stakeholders' views on the value of outcomes from clinical genetic and genomic interventions

Genetics in medicine, 2019-06, Vol.21 (6), p.1371-1380

2019

Volltextzugriff (PDF)

1 – 25 von 110

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(102)
Mit Volltextzugriff
(99)

Publikationsform

Artikel
(106)
Buchkapitel
(4)

Sprache

Englisch
(110)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Points to consider for reporting of germline variation in patients undergoing tumor testing: a statement of the American College of Medical Genetics and Genomics (ACMG)

Reporting genomic secondary findings: ACMG members weigh in

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

Research priorities for evaluating family history in the prevention of common chronic diseases

Gnathodiaphyseal dysplasia: report of a family with a novel mutation of the ANO5 gene

An electronic family health history tool to identify and manage patients at increased risk for colorectal cancer: protocol for a randomized controlled trial

Delivery of genomic medicine for common chronic adult diseases: a systematic review

Health-literate care organizations for precision health

Securing and Documenting Cancer Family History in the Age of the Electronic Medical Record

DNA-based screening and population health: a points to consider statement for programs and sponsoring organizations from the American College of Medical Genetics and Genomics (ACMG)

Systematic evidence-based review: outcomes from exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability

Genetics professionals are key to the integration of genetic testing within the practice of frontline clinicians

Basic vs More Complex Definitions of Family History in the Prediction of Coronary Heart Disease: The Multi-Ethnic Study of Atherosclerosis

Laboratory business models and practices: implications for availability and access to germline genetic testing

Influence of payer coverage and out‐of‐pocket costs on ordering of NGS panel tests for hereditary cancer in diverse settings

Primary care providers’ responses to unsolicited Lynch syndrome secondary findings of varying clinical significance

A Cluster Randomized Trial of a Family Health History Platform to Identify and Manage Patients at Increased Risk for Colorectal Cancer

The value of genetic testing: beyond clinical utility

DNA-based screening and personal health: a points to consider statement for individuals and health-care providers from the American College of Medical Genetics and Genomics (ACMG)

A logic model for precision medicine implementation informed by stakeholder views and implementation science

Factors influencing organizational adoption and implementation of clinical genetic services

Developing Family Healthware, a family history screening tool to prevent common chronic diseases

Pharmacogenetic testing in the Veterans Health Administration (VHA): policy recommendations from the VHA Clinical Pharmacogenetics Subcommittee

Population prevalence of familial cancer and common hereditary cancer syndromes. The 2005 California Health Interview Survey

Stakeholders' views on the value of outcomes from clinical genetic and genomic interventions

Suchergebnisse filtern