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...

Biallelic TRIP13 mutations predispose to Wilms tumor and chromosome missegregation

Nature genetics, 2017-07, Vol.49 (7), p.1148-1151

2017

Volltextzugriff (PDF)

Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14

Nature genetics, 2013-06, Vol.45 (6), p.686-689

2013

Volltextzugriff (PDF)

A genome-wide association study of testicular germ cell tumor

Nature genetics, 2009-07, Vol.41 (7), p.807-810

2009

Volltextzugriff (PDF)

Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer

Nature genetics, 2007-02, Vol.39 (2), p.162-164

2007

Volltextzugriff (PDF)

Mutations in the transcriptional repressor REST predispose to Wilms tumor

Nature genetics, 2015-12, Vol.47 (12), p.1471-1474

2015

Volltextzugriff (PDF)

Accurate clinical detection of exon copy number variants in a targeted NGS panel using DECoN

Wellcome open research, 2016-11, Vol.1, p.20-20

2016

Volltextzugriff (PDF)

The Quality Sequencing Minimum (QSM): providing comprehensive, consistent, transparent next generation sequencing data quality assurance

Wellcome open research, 2018, Vol.3, p.37-37

2018

Volltextzugriff (PDF)

CoverView: a sequence quality evaluation tool for next generation sequencing data

Wellcome open research, 2018, Vol.3, p.36-36

2018

Volltextzugriff (PDF)

The ICR639 CPG NGS validation series: A resource to assess analytical sensitivity of cancer predisposition gene testing

Wellcome open research, 2018, Vol.3, p.68-68

2018

Volltextzugriff (PDF)

A Multicenter Study of Cancer Incidence in CHEK2 1100delC Mutation Carriers

Cancer epidemiology, biomarkers & prevention, 2006-12, Vol.15 (12), p.2542-2545

2006

Volltextzugriff (PDF)

Association analysis identifies 65 new breast cancer risk loci

Nature (London), 2017-11, Vol.551 (7678), p.92-94

2017

Volltextzugriff (PDF)

Whole-exome sequencing reveals the mutational spectrum of testicular germ cell tumours

Nature communications, 2015-01, Vol.6 (1), p.5973-5973, Article 5973

2015

Volltextzugriff (PDF)

Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

Nature genetics, 2017-12, Vol.49 (12), p.1767-1778

2017

Volltextzugriff (PDF)

A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer

Nature genetics, 2018-07, Vol.50 (7), p.968-978

2018

Volltextzugriff (PDF)

Variants near DMRT1 , TERT and ATF7IP are associated with testicular germ cell cancer

Nature genetics, 2010-07, Vol.42 (7), p.604-607

2010

Volltextzugriff (PDF)

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

Nature (London), 2010-04, Vol.464 (7289), p.713-720

2010

Volltextzugriff (PDF)

Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer

Nature (London), 2013-01, Vol.493 (7432), p.406-410

2013

Volltextzugriff (PDF)

Genome-wide association study identifies novel breast cancer susceptibility loci

Nature, 2007-06, Vol.447 (7148), p.1087-1093

2007

Volltextzugriff (PDF)

Predisposition gene identification in common cancers by exome sequencing: insights from familial breast cancer

Breast cancer research and treatment, 2012-07, Vol.134 (1), p.429-433

2012

Volltextzugriff (PDF)

Comparison of 6q25 breast cancer hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC)

PloS one, 2012-08, Vol.7 (8), p.e42380-e42380

2012

Volltextzugriff (PDF)

Predisposition gene identification in common cancers by exome sequencing: insights from familial breast cancer

Breast cancer research and treatment, 2012-07, Vol.134 (1), p.429

2012

Volltextzugriff (PDF)

Mutation and association analysis of GEN1 in breast cancer susceptibility

Breast cancer research and treatment, 2010-11, Vol.124 (1), p.283-288

2010

Volltextzugriff (PDF)

Exploring the link between MORF4L1 and risk of breast cancer

Breast cancer research : BCR, 2011-04, Vol.13 (2), p.R40-R40, Article R40

2011

Volltextzugriff (PDF)

1 – 25 von 28

Suche als RSS-Feed

Aktive Filter

ThemaCancer

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(28)
Mit Volltextzugriff
(20)

Publikationsform

Artikel
(28)

Sprache

Englisch
(28)
Japanisch
(12)

Erscheinungsjahr

n.n

Thema

14 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Biallelic TRIP13 mutations predispose to Wilms tumor and chromosome missegregation

Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14

A genome-wide association study of testicular germ cell tumor

Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer

Mutations in the transcriptional repressor REST predispose to Wilms tumor

Accurate clinical detection of exon copy number variants in a targeted NGS panel using DECoN

The Quality Sequencing Minimum (QSM): providing comprehensive, consistent, transparent next generation sequencing data quality assurance

CoverView: a sequence quality evaluation tool for next generation sequencing data

The ICR639 CPG NGS validation series: A resource to assess analytical sensitivity of cancer predisposition gene testing

A Multicenter Study of Cancer Incidence in CHEK2 1100delC Mutation Carriers

Association analysis identifies 65 new breast cancer risk loci

Whole-exome sequencing reveals the mutational spectrum of testicular germ cell tumours

Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer

Variants near DMRT1 , TERT and ATF7IP are associated with testicular germ cell cancer

One in seven pathogenic variants can be challenging to detect by NGS: an analysis of 450,000 patients with implications for clinical sensitivity and genetic test implementation

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer

Genome-wide association study identifies novel breast cancer susceptibility loci

Predisposition gene identification in common cancers by exome sequencing: insights from familial breast cancer

A genome-wide association study identifies susceptibility loci for Wilms tumor

Comparison of 6q25 breast cancer hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC)

Predisposition gene identification in common cancers by exome sequencing: insights from familial breast cancer

Mutation and association analysis of GEN1 in breast cancer susceptibility

Exploring the link between MORF4L1 and risk of breast cancer

Aktive Filter

Suchergebnisse filtern