UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 99

Sortiert nach

Associations Between Cancer Predisposition Testing Panel Genes and Breast Cancer

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

2017

Volltextzugriff (PDF)

Differences in TP53 Mutation Carrier Phenotypes Emerge From Panel-Based Testing

JNCI : Journal of the National Cancer Institute, 2018-08, Vol.110 (8), p.863-870

2018

Volltextzugriff (PDF)

Somatic TP53 variants frequently confound germ-line testing results

Genetics in medicine, 2018-08, Vol.20 (8), p.809-816

2018

Volltextzugriff (PDF)

Strong functional data for pathogenicity or neutrality classify BRCA2 DNA-binding-domain variants of uncertain significance

American journal of human genetics, 2021-03, Vol.108 (3), p.458-468

2021

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Genotype–phenotype associations among panel-based TP53+ subjects

Genetics in medicine, 2019-11, Vol.21 (11), p.2478-2484

2019

Volltextzugriff (PDF)

Germline pathogenic variants in cancer risk genes among patients with thyroid cancer and suspected predisposition

Cancer medicine (Malden, MA), 2022-04, Vol.11 (8), p.1745-1752

2022

Volltextzugriff (PDF)

Mutational and splicing landscape in a cohort of 43,000 patients tested for hereditary cancer

Npj genomic medicine, 2022-08, Vol.7 (1), p.49-49, Article 49

2022

Volltextzugriff (PDF)

An integrative model for the comprehensive classification of BRCA1 and BRCA2 variants of uncertain clinical significance

Npj genomic medicine, 2022-06, Vol.7 (1), p.35-35, Article 35

2022

Volltextzugriff (PDF)

False-positive results released by direct-to-consumer genetic tests highlight the importance of clinical confirmation testing for appropriate patient care

Genetics in medicine, 2018-12, Vol.20 (12), p.1515-1521

2018

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Cancer Risks Associated With Germline PALB2 Pathogenic Variants: An International Study of 524 Families

Journal of clinical oncology, 2020-03, Vol.38 (7), p.674-685

2020

Volltextzugriff (PDF)

Abstract P2-09-19: Inequitable access to genetic testing leads to missed screening and prevention opportunities for individuals at risk for hereditary breast and ovarian cancer

Cancer research (Chicago, Ill.), 2022-02, Vol.82 (4_Supplement), p.P2-P2-09-19

2022

Volltextzugriff (PDF)

BAP1 tumor predisposition syndrome: Preliminary data from a laboratory-based multigene panel testing cohort

Journal of clinical oncology, 2017-02, Vol.35 (6_suppl), p.490-490

2017

Volltextzugriff (PDF)

Closing the gap: Trends in inconclusive rates on hereditary cancer testing across racial/ethnic groups

Journal of clinical oncology, 2021-05, Vol.39 (15_suppl), p.10525-10525

2021

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Universal Germline Panel Testing for Individuals With Pheochromocytoma and Paraganglioma Produces High Diagnostic Yield

The journal of clinical endocrinology and metabolism, 2022-04, Vol.107 (5), p.e1917-e1923

2022

Volltextzugriff (PDF)

EPID-16. HEREDITARY BRAIN TUMORS ARE MORE COMMON THAN YOU THINK: GERMLINE MUTATIONS IN BENIGN AND MALIGNANT PRIMARY BRAIN TUMORS

Neuro-oncology (Charlottesville, Va.), 2017-11, Vol.19 (suppl_6), p.vi72-vi72

2017

Volltextzugriff (PDF)

Increased detection of germline cancer susceptibility mutations subsequent to tumor profiling

Journal of clinical oncology, 2018-05, Vol.36 (15_suppl), p.e13613-e13613

2018

Volltextzugriff (PDF)

Abstract P2-09-03: Pathogenic variants among female breast cancer patients with a subsequent cancer demonstrate preventable cancer burden

Cancer research (Chicago, Ill.), 2022-02, Vol.82 (4_Supplement), p.P2-P2-09-03

2022

Volltextzugriff (PDF)

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

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

2018

Volltextzugriff (PDF)

Abstract P6-08-35: Impact of multigene panel testing on medical management: Preliminary pre- and post-test clinician survey results

Cancer research (Chicago, Ill.), 2020-02, Vol.80 (4_Supplement), p.P6-P6-08-35

2020

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

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

2021

Volltextzugriff (PDF)

1 – 25 von 99

Suche als RSS-Feed

Aktive Filter

ThemaGenetics

ThemaMutation

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(98)
Mit Volltextzugriff
(89)

Publikationsform

Artikel
(98)
Berichte
(1)

Sprache

Englisch
(99)
Japanisch
(6)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Associations Between Cancer Predisposition Testing Panel Genes and Breast Cancer

Differences in TP53 Mutation Carrier Phenotypes Emerge From Panel-Based Testing

Somatic TP53 variants frequently confound germ-line testing results

Strong functional data for pathogenicity or neutrality classify BRCA2 DNA-binding-domain variants of uncertain significance

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

Genotype–phenotype associations among panel-based TP53+ subjects

Germline pathogenic variants in cancer risk genes among patients with thyroid cancer and suspected predisposition

Mutational and splicing landscape in a cohort of 43,000 patients tested for hereditary cancer

An integrative model for the comprehensive classification of BRCA1 and BRCA2 variants of uncertain clinical significance

False-positive results released by direct-to-consumer genetic tests highlight the importance of clinical confirmation testing for appropriate patient care

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

Cancer Risks Associated With Germline PALB2 Pathogenic Variants: An International Study of 524 Families

Abstract P2-09-19: Inequitable access to genetic testing leads to missed screening and prevention opportunities for individuals at risk for hereditary breast and ovarian cancer

BAP1 tumor predisposition syndrome: Preliminary data from a laboratory-based multigene panel testing cohort

Closing the gap: Trends in inconclusive rates on hereditary cancer testing across racial/ethnic groups

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

Universal Germline Panel Testing for Individuals With Pheochromocytoma and Paraganglioma Produces High Diagnostic Yield

EPID-16. HEREDITARY BRAIN TUMORS ARE MORE COMMON THAN YOU THINK: GERMLINE MUTATIONS IN BENIGN AND MALIGNANT PRIMARY BRAIN TUMORS

Increased detection of germline cancer susceptibility mutations subsequent to tumor profiling

Abstract P2-09-03: Pathogenic variants among female breast cancer patients with a subsequent cancer demonstrate preventable cancer burden

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

Abstract P6-08-35: Impact of multigene panel testing on medical management: Preliminary pre- and post-test clinician survey results

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

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

Aktive Filter

Suchergebnisse filtern