UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 41

Sortiert nach

Associations Between Cancer Predisposition Testing Panel Genes and Breast Cancer

JAMA oncology, 2017-09, Vol.3 (9), p.1190

2017

Link zum Volltext

Verfügbarkeit prüfen

P396: The need for a longitudinal digital health platform to implement large scale genomic programs

Genetics in Medicine Open, 2023, Vol.1 (1), p.100432, Article 100432

2023

Link zum Volltext

Verfügbarkeit prüfen

Synthesis and electrochemical evaluation of an amorphous titanium dioxide derived from a solid state precursor

Journal of power sources, 2010-04, Vol.195 (7), p.2064-2068

2010

Link zum Volltext

Verfügbarkeit prüfen

Prevalence of Germline Mutations in Polyposis and Colorectal Cancer–Associated Genes in Patients With Multiple Colorectal Polyps

Clinical gastroenterology and hepatology, 2019-09, Vol.17 (10), p.2008-2015.e3

2019

Link zum Volltext

Verfügbarkeit prüfen

Correction to: Pathogenic variants among females with breast cancer and a nonâbreast cancer reveal opportunities for cancer interception

Breast cancer research and treatment, 2023-07, Vol.200 (1), p.73

2023

Link zum Volltext

Verfügbarkeit prüfen

MP34-18 PERFORMANCE OF MULTIGENE PANEL TESTING IN HEREDITARY PROSTATE CANCER

The Journal of urology, 2018-04, Vol.199 (4), p.e444-e445

2018

Link zum Volltext

Verfügbarkeit prüfen

Universal multi-gene panel testing for individuals with pheochromocytomas and paragangliomas

Molecular genetics and metabolism, 2021-04, Vol.132, p.S54-S55

2021

Link zum Volltext

Verfügbarkeit prüfen

eP075 - Multi-gene panel testing results prompt frequent and guideline adherent changes to cancer risk management recommendations based on clinician report

Molecular genetics and metabolism, 2021-04, Vol.132, p.S51-S52

2021

Link zum Volltext

Verfügbarkeit prüfen

Divergent payor medical policy leads to gross disparities in access to hereditary breast and ovarian cancer genetic testing

Molecular genetics and metabolism, 2021-04, Vol.132, p.S54

2021

Link zum Volltext

Verfügbarkeit prüfen

eP080 - Universal multi-gene panel testing for individuals with pheochromocytomas and paragangliomas

Molecular genetics and metabolism, 2021-04, Vol.132, p.S54-S55

2021

Link zum Volltext

Verfügbarkeit prüfen

eP078 - Divergent payor medical policy leads to gross disparities in access to hereditary breast and ovarian cancer genetic testing

Molecular genetics and metabolism, 2021-04, Vol.132, p.S54-S54

2021

Link zum Volltext

Verfügbarkeit prüfen

Multi-gene panel testing results prompt frequent and guideline adherent changes to cancer risk management recommendations based on clinician report

Molecular genetics and metabolism, 2021-04, Vol.132, p.S51-S52

2021

Link zum Volltext

Verfügbarkeit prüfen

Su1777 - Inherited Susceptibility to Biliary Tract and Ampullary Cancers

Gastroenterology (New York, N.Y. 1943), 2017-04, Vol.152 (5), p.S555-S555

2017

Link zum Volltext

Verfügbarkeit prüfen

MP33-15 GENDER DISPARITY: OVERLOOKING HEREDITARY PROSTATE CANCER AND IMPLICATIONS FOR UROLOGY PRACTICE

The Journal of urology, 2017-04, Vol.197 (4), p.e423-e423

2017

Link zum Volltext

Verfügbarkeit prüfen

Pathogenic variants among females with breast cancer and a non-breast cancer reveal opportunities for cancer interception

Breast cancer research and treatment, 2023-07, Vol.200 (1), p.63-72

2023

Link zum Volltext

Verfügbarkeit prüfen

Correction to: Pathogenic variants among females with breast cancer and a non‑breast cancer reveal opportunities for cancer interception

Breast cancer research and treatment, 2023-07, Vol.200 (1), p.73-73

2023

Link zum Volltext

Verfügbarkeit prüfen

1066 - Phenotypic Expression of Cdh1 Germline Mutations Unselected for Hereditary Diffuse Gastric Cancer

Gastroenterology (New York, N.Y. 1943), 2018-05, Vol.154 (6), p.S-204-S-204

2018

Link zum Volltext

Verfügbarkeit prüfen

563: IMPLEMENTATION OF ROUTINE GENETIC SCREENING IN A RURAL GASTROINTESTINAL CLINIC LEADS TO IDENTIFICATION OF INHERITED GASTROINTESTINAL DISORDERS AND OTHER CANCER RISKS IN 20% OF PATIENTS TESTED

Gastroenterology (New York, N.Y. 1943), 2022-05, Vol.162 (7), p.S-135-S-136

2022

Link zum Volltext

Verfügbarkeit prüfen

Case–case analysis addressing ascertainment bias for multigene panel testing implicates BRCA1 and PALB2 in endometrial cancer

Human mutation, 2021-10, Vol.42 (10), p.1265-1278

2021

Link zum Volltext

Verfügbarkeit prüfen

PD30-02 GERMLINE GENETIC ASSOCIATIONS WITH HIGH-RISK PROSTATE CANCER AND AGE AT DIAGNOSIS

The Journal of urology, 2019-04, Vol.201 (Supplement 4)

2019

Link zum Volltext

Verfügbarkeit prüfen

Validation of a prostate cancer polygenic risk score

The Prostate, 2020-11, Vol.80 (15), p.1314-1321

2020

Link zum Volltext

Verfügbarkeit prüfen

The uniform application of protein functional data has an impressive potential to resolve VUS rates in BRCA2

Molecular genetics and metabolism, 2021-04, Vol.132, p.S213-S214

2021

Link zum Volltext

Verfügbarkeit prüfen

OP333 - The uniform application of protein functional data has an impressive potential to resolve VUS rates in BRCA2

Molecular genetics and metabolism, 2021-04, Vol.132, p.S213-S214

2021

Link zum Volltext

Verfügbarkeit prüfen

Inherited Susceptibility to Biliary Tract and Ampullary Cancers

Gastroenterology (New York, N.Y. 1943), 2017-04, Vol.152 (5), p.S555-S555

2017

Link zum Volltext

Verfügbarkeit prüfen

MP39-20 ADVANCES IN THE DIAGNOSIS OF HEREDITARY KIDNEY CANCER: INITIAL RESULTS OF A MULTIGENE PANEL TEST

The Journal of urology, 2017-04, Vol.197 (4), p.e501-e501

2017

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 41

Suche als RSS-Feed

Aktive Filter

KollektionElectronic Journals Library

ThemaMutation

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(38)
Mit Volltextzugriff
(31)

Publikationsform

Sprache

Englisch
(41)
Japanisch
(2)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 7 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Associations Between Cancer Predisposition Testing Panel Genes and Breast Cancer

P396: The need for a longitudinal digital health platform to implement large scale genomic programs

Synthesis and electrochemical evaluation of an amorphous titanium dioxide derived from a solid state precursor

Prevalence of Germline Mutations in Polyposis and Colorectal Cancer–Associated Genes in Patients With Multiple Colorectal Polyps

Correction to: Pathogenic variants among females with breast cancer and a nonâbreast cancer reveal opportunities for cancer interception

MP34-18 PERFORMANCE OF MULTIGENE PANEL TESTING IN HEREDITARY PROSTATE CANCER

Universal multi-gene panel testing for individuals with pheochromocytomas and paragangliomas

eP075 - Multi-gene panel testing results prompt frequent and guideline adherent changes to cancer risk management recommendations based on clinician report

Divergent payor medical policy leads to gross disparities in access to hereditary breast and ovarian cancer genetic testing

eP080 - Universal multi-gene panel testing for individuals with pheochromocytomas and paragangliomas

eP078 - Divergent payor medical policy leads to gross disparities in access to hereditary breast and ovarian cancer genetic testing

Multi-gene panel testing results prompt frequent and guideline adherent changes to cancer risk management recommendations based on clinician report

Su1777 - Inherited Susceptibility to Biliary Tract and Ampullary Cancers

MP33-15 GENDER DISPARITY: OVERLOOKING HEREDITARY PROSTATE CANCER AND IMPLICATIONS FOR UROLOGY PRACTICE

Pathogenic variants among females with breast cancer and a non-breast cancer reveal opportunities for cancer interception

Correction to: Pathogenic variants among females with breast cancer and a non‑breast cancer reveal opportunities for cancer interception

1066 - Phenotypic Expression of Cdh1 Germline Mutations Unselected for Hereditary Diffuse Gastric Cancer

563: IMPLEMENTATION OF ROUTINE GENETIC SCREENING IN A RURAL GASTROINTESTINAL CLINIC LEADS TO IDENTIFICATION OF INHERITED GASTROINTESTINAL DISORDERS AND OTHER CANCER RISKS IN 20% OF PATIENTS TESTED

Case–case analysis addressing ascertainment bias for multigene panel testing implicates BRCA1 and PALB2 in endometrial cancer

PD30-02 GERMLINE GENETIC ASSOCIATIONS WITH HIGH-RISK PROSTATE CANCER AND AGE AT DIAGNOSIS

Validation of a prostate cancer polygenic risk score

The uniform application of protein functional data has an impressive potential to resolve VUS rates in BRCA2

OP333 - The uniform application of protein functional data has an impressive potential to resolve VUS rates in BRCA2

Inherited Susceptibility to Biliary Tract and Ampullary Cancers

MP39-20 ADVANCES IN THE DIAGNOSIS OF HEREDITARY KIDNEY CANCER: INITIAL RESULTS OF A MULTIGENE PANEL TEST

Aktive Filter

Suchergebnisse filtern