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...

Clinical use of current polygenic risk scores may exacerbate health disparities

Nature genetics, 2019-04, Vol.51 (4), p.584-591

2019

Volltextzugriff (PDF)

Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations

American journal of human genetics, 2017-04, Vol.100 (4), p.635-649

2017

Volltextzugriff (PDF)

Multi-trait analysis of genome-wide association summary statistics using MTAG

Nature genetics, 2018-02, Vol.50 (2), p.229-237

2018

Volltextzugriff (PDF)

Predicting Polygenic Risk of Psychiatric Disorders

Biological psychiatry (1969), 2019-07, Vol.86 (2), p.97-109

2019

Volltextzugriff (PDF)

Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights

Nature genetics, 2018-04, Vol.50 (4), p.538-548

2018

Volltextzugriff (PDF)

Phenome-wide heritability analysis of the UK Biobank

PLoS genetics, 2017-04, Vol.13 (4), p.e1006711-e1006711

2017

Volltextzugriff (PDF)

Searching for missing heritability: Designing rare variant association studies

Proceedings of the National Academy of Sciences - PNAS, 2014-01, Vol.111 (4), p.E455-E464

2014

Volltextzugriff (PDF)

Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types

Nature genetics, 2018-04, Vol.50 (4), p.621-629

2018

Volltextzugriff (PDF)

Partitioning heritability by functional annotation using genome-wide association summary statistics

Nature genetics, 2015-11, Vol.47 (11), p.1228-1235

2015

Volltextzugriff (PDF)

Testing for an unusual distribution of rare variants

PLoS genetics, 2011-03, Vol.7 (3), p.e1001322-e1001322

2011

Volltextzugriff (PDF)

Genetic analysis of schizophrenia and bipolar disorder reveals polygenicity but also suggests new directions for molecular interrogation

Current opinion in neurobiology, 2015-02, Vol.30, p.131-138

2015

Volltextzugriff (PDF)

Clonal Hematopoiesis and Blood-Cancer Risk Inferred from Blood DNA Sequence

The New England journal of medicine, 2014-12, Vol.371 (26), p.2477-2487

2014

Volltextzugriff (PDF)

Tractor uses local ancestry to enable the inclusion of admixed individuals in GWAS and to boost power

Nature genetics, 2021-02, Vol.53 (2), p.195-204

2021

Volltextzugriff (PDF)

Polygenic architecture of rare coding variation across 394,783 exomes

Nature (London), 2023-02, Vol.614 (7948), p.492-499

2023

Volltextzugriff (PDF)

Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

Nature genetics, 2016-08, Vol.48 (8), p.856-866

2016

Volltextzugriff (PDF)

Getting genetic ancestry right for science and society

Science (American Association for the Advancement of Science), 2022-04, Vol.376 (6590), p.250-252

2022

Volltextzugriff (PDF)

Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants

Nature neuroscience, 2019-12, Vol.22 (12), p.1961-1965

2019

Volltextzugriff (PDF)

Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population

Nature genetics, 2016-05, Vol.48 (5), p.552-555

2016

Volltextzugriff (PDF)

A framework for the interpretation of de novo mutation in human disease

Nature genetics, 2014-09, Vol.46 (9), p.944-950

2014

Volltextzugriff (PDF)

Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples

Nature genetics, 2017-04, Vol.49 (4), p.504-510

2017

Volltextzugriff (PDF)

Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder

Science (American Association for the Advancement of Science), 2018-12, Vol.362 (6420)

2018

Volltextzugriff (PDF)

Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis

Nature genetics, 2015-12, Vol.47 (12), p.1385-1392

2015

Volltextzugriff (PDF)

Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects

Nature communications, 2018-10, Vol.9 (1), p.4038-8, Article 4038

2018

Volltextzugriff (PDF)

Pervasive sharing of genetic effects in autoimmune disease

PLoS genetics, 2011-08, Vol.7 (8), p.e1002254-e1002254

2011

Volltextzugriff (PDF)

1 – 25 von 450

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(426)
Mit Volltextzugriff
(308)

Publikationsform

Sprache

Englisch
(449)
Japanisch
(115)
Norwegisch
(16)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Nature Genetics
(63)
American Journal Of Medical Genetics. Part B, Neuropsychiatric Genetics
(27)
Nature
(27)
American Journal Of Human Genetics
(25)
Nature Communications
(23)
Plos Genetics
(20)
Nature Neuroscience
(14)
Biological Psychiatry
(13)
Molecular Psychiatry
(13)
Cell Genomics
(11)

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(2)
... seit 90 Tagen
(6)

Menü

Weitere Dienste

Einstellungen

Clinical use of current polygenic risk scores may exacerbate health disparities

Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations

Multi-trait analysis of genome-wide association summary statistics using MTAG

Predicting Polygenic Risk of Psychiatric Disorders

Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights

Phenome-wide heritability analysis of the UK Biobank

Searching for missing heritability: Designing rare variant association studies

Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types

Partitioning heritability by functional annotation using genome-wide association summary statistics

Testing for an unusual distribution of rare variants

Genetic analysis of schizophrenia and bipolar disorder reveals polygenicity but also suggests new directions for molecular interrogation

Clonal Hematopoiesis and Blood-Cancer Risk Inferred from Blood DNA Sequence

Tractor uses local ancestry to enable the inclusion of admixed individuals in GWAS and to boost power

Polygenic architecture of rare coding variation across 394,783 exomes

Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

Getting genetic ancestry right for science and society

Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants

Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population

A framework for the interpretation of de novo mutation in human disease

A genome-wide association study of shared risk across psychiatric disorders implicates gene regulation during fetal neurodevelopment

Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples

Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder

Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis

Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects

Pervasive sharing of genetic effects in autoimmune disease

Suchergebnisse filtern