UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 66

Sortiert nach

High burden and pervasive positive selection of somatic mutations in normal human skin

Science (American Association for the Advancement of Science), 2015-05, Vol.348 (6237), p.880-886

2015

Volltextzugriff (PDF)

Signatures of mutation and selection in the cancer genome

Nature (London), 2010-02, Vol.463 (7283), p.893-898

2010

Volltextzugriff (PDF)

Patterns of somatic mutation in human cancer genomes

Nature, 2007-03, Vol.446 (7132), p.153-158

2007

Volltextzugriff (PDF)

Somatic mutations of the histone H3K27 demethylase gene UTX in human cancer

Nature genetics, 2009-05, Vol.41 (5), p.521-523

2009

Volltextzugriff (PDF)

Mutation analysis of 24 known cancer genes in the NCI-60 cell line set

Molecular cancer therapeutics, 2006-11, Vol.5 (11), p.2606-2612

2006

Volltextzugriff (PDF)

Mutations in UPF3B , a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation

Nature genetics, 2007-09, Vol.39 (9), p.1127-1133

2007

Volltextzugriff (PDF)

A hypermutation phenotype and somatic MSH6 mutations in recurrent human malignant gliomas after alkylator chemotherapy

Cancer research (Chicago, Ill.), 2006-04, Vol.66 (8), p.3987-3991

2006

Volltextzugriff (PDF)

GLO1-A novel amplified gene in human cancer

Genes chromosomes & cancer, 2010-08, Vol.49 (8), p.711-725

2010

Volltextzugriff (PDF)

The genetic associations of acute anterior uveitis and their overlap with the genetics of ankylosing spondylitis

Genes and immunity, 2016-01, Vol.17 (1), p.46-51

2016

Volltextzugriff (PDF)

Mutations in the Gene Encoding the Sigma 2 Subunit of the Adaptor Protein 1 Complex, AP1S2, Cause X-Linked Mental Retardation

American journal of human genetics, 2006-12, Vol.79 (6), p.1119-1124

2006

Volltextzugriff (PDF)

Recurrent emergence of SARS-CoV-2 spike deletion H69/V70 and its role in the Alpha variant B.1.1.7

Cell reports (Cambridge), 2021-06, Vol.35 (13), p.109292-109292, Article 109292

2021

Volltextzugriff (PDF)

Sequence analysis of the protein kinase gene family in human testicular germ-cell tumors of adolescents and adults

Genes chromosomes & cancer, 2006-01, Vol.45 (1), p.42-46

2006

Volltextzugriff (PDF)

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

Cell, 2018-06, Vol.173 (7), p.1705-1715.e16

2018

Volltextzugriff (PDF)

The zebrafish reference genome sequence and its relationship to the human genome

Nature (London), 2013-04, Vol.496 (7446), p.498-503

2013

Volltextzugriff (PDF)

Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity

Nature genetics, 2012-12, Vol.44 (12), p.1341-1348

2012

Volltextzugriff (PDF)

Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental Disorders

American journal of human genetics, 2018-01, Vol.102 (1), p.175-187

2018

Volltextzugriff (PDF)

Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins

Nature communications, 2014-10, Vol.5 (1), p.5068, Article 5068

2014

Volltextzugriff (PDF)

Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility

Nature genetics, 2011-08, Vol.43 (8), p.761-767

2011

Volltextzugriff (PDF)

Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region

Nature genetics, 2009-12, Vol.41 (12), p.1330-1334

2009

Volltextzugriff (PDF)

Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases

Nature communications, 2018-05, Vol.9 (1), p.1864-11, Article 1864

2018

Volltextzugriff (PDF)

Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data

Scientific reports, 2019-07, Vol.9 (1), p.10351-18, Article 10351

2019

Volltextzugriff (PDF)

A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation

Nature genetics, 2009-05, Vol.41 (5), p.535-543

2009

Volltextzugriff (PDF)

Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease

Human molecular genetics, 2012-11, Vol.21 (22), p.4996-5009

2012

Volltextzugriff (PDF)

Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy

American journal of human genetics, 2019-06, Vol.104 (6), p.1210-1222

2019

Volltextzugriff (PDF)

1 – 25 von 66

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(66)
Mit Volltextzugriff
(59)

Publikationsform

Artikel
(66)

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(59)
Humans
(57)
Life Sciences & Biomedicine
(46)
Genetics & Heredity
(27)
Genome-Wide Association Study
(27)
Male
(27)
Female
(25)
Biological And Medical Sciences
(21)
Medical Sciences
(19)
Polymorphism, Single Nucleotide
(19)
Mutation
(18)
Risk Factors
(18)
Genetic Aspects
(16)
Genetic Predisposition To Disease
(15)
Fundamental And Applied Biological Sciences. Psychology
(14)
Genes
(14)
Genetics
(13)
Genetics Of Eukaryotes. Biological And Molecular Evolution
(13)
Multidisciplinary Sciences
(13)
Science & Technology - Other Topics
(13)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

High burden and pervasive positive selection of somatic mutations in normal human skin

Signatures of mutation and selection in the cancer genome

Patterns of somatic mutation in human cancer genomes

Somatic mutations of the histone H3K27 demethylase gene UTX in human cancer

Mutation analysis of 24 known cancer genes in the NCI-60 cell line set

Mutations in UPF3B , a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation

A hypermutation phenotype and somatic MSH6 mutations in recurrent human malignant gliomas after alkylator chemotherapy

GLO1-A novel amplified gene in human cancer

The genetic associations of acute anterior uveitis and their overlap with the genetics of ankylosing spondylitis

Mutations in the Gene Encoding the Sigma 2 Subunit of the Adaptor Protein 1 Complex, AP1S2, Cause X-Linked Mental Retardation

SARS-CoV-2 evolution during treatment of chronic infection

Recurrent emergence of SARS-CoV-2 spike deletion H69/V70 and its role in the Alpha variant B.1.1.7

Sequence analysis of the protein kinase gene family in human testicular germ-cell tumors of adolescents and adults

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

The zebrafish reference genome sequence and its relationship to the human genome

Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity

Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental Disorders

Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins

Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility

Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region

Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases

Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data

A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation

Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease

Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy

Suchergebnisse filtern