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...

dbNSFP v3.0: A One-Stop Database of Functional Predictions and Annotations for Human Nonsynonymous and Splice-Site SNVs

Human mutation, 2016-03, Vol.37 (3), p.235-241

2016

Volltextzugriff (PDF)

In silico prediction of splice-altering single nucleotide variants in the human genome

Nucleic acids research, 2014-12, Vol.42 (22), p.13534-13544

2014

Volltextzugriff (PDF)

ACAT: A Fast and Powerful p Value Combination Method for Rare-Variant Analysis in Sequencing Studies

American journal of human genetics, 2019-03, Vol.104 (3), p.410-421

2019

Volltextzugriff (PDF)

The ARIC (Atherosclerosis Risk In Communities) Study: JACC Focus Seminar 3/8

Journal of the American College of Cardiology, 2021-06, Vol.77 (23), p.2939-2959

2021

Volltextzugriff (PDF)

Genetic variation in PNPLA3 confers susceptibility to nonalcoholic fatty liver disease

Nature genetics, 2008-12, Vol.40 (12), p.1461-1465

2008

Volltextzugriff (PDF)

In silico tools for splicing defect prediction: a survey from the viewpoint of end users

Genetics in medicine, 2014-07, Vol.16 (7), p.497-503

2014

Volltextzugriff (PDF)

Genetic Risk, Adherence to a Healthy Lifestyle, and Coronary Disease

The New England journal of medicine, 2016-12, Vol.375 (24), p.2349-2358

2016

Volltextzugriff (PDF)

Rare loss-of-function mutations in ANGPTL family members contribute to plasma triglyceride levels in humans

The Journal of clinical investigation, 2009-01, Vol.119 (1), p.70-79

2009

Volltextzugriff (PDF)

Normal Limits in Relation to Age, Body Size and Gender of Two-Dimensional Echocardiographic Aortic Root Dimensions in Persons ≥15 Years of Age

The American journal of cardiology, 2012-10, Vol.110 (8), p.1189-1194

2012

Volltextzugriff (PDF)

American Heart Association's Life's Simple 7: Lifestyle Recommendations, Polygenic Risk, and Lifetime Risk of Coronary Heart Disease

Circulation (New York, N.Y.), 2022-03, Vol.145 (11), p.808-818

2022

Volltextzugriff (PDF)

A bidirectional Mendelian randomization study supports causal effects of kidney function on blood pressure

Kidney international, 2020-09, Vol.98 (3), p.708-716

2020

Volltextzugriff (PDF)

High-Sensitivity Troponin I and Incident Coronary Events, Stroke, Heart Failure Hospitalization, and Mortality in the ARIC Study

Circulation (New York, N.Y.), 2019-06, Vol.139 (23), p.2642-2653

2019

Volltextzugriff (PDF)

Molecular findings among patients referred for clinical whole-exome sequencing

JAMA : the journal of the American Medical Association, 2014-11, Vol.312 (18), p.1870

2014

Volltextzugriff (PDF)

Atypical angiopoietin-like protein that regulates ANGPTL3

Proceedings of the National Academy of Sciences - PNAS, 2012-11, Vol.109 (48), p.19751-19756

2012

Volltextzugriff (PDF)

Clan Genomics and the Complex Architecture of Human Disease

Cell, 2011-09, Vol.147 (1), p.32-43

2011

Volltextzugriff (PDF)

Identification of a Urate Transporter, ABCG2, with a Common Functional Polymorphism Causing Gout

Proceedings of the National Academy of Sciences - PNAS, 2009-06, Vol.106 (25), p.10338-10342

2009

Volltextzugriff (PDF)

Resolution of Disease Phenotypes Resulting from Multilocus Genomic Variation

The New England journal of medicine, 2017-01, Vol.376 (1), p.21-31

2017

Volltextzugriff (PDF)

Evaluation of mitochondrial DNA copy number estimation techniques

PloS one, 2020-01, Vol.15 (1), p.e0228166

2020

Volltextzugriff (PDF)

Evolution and Functional Impact of Rare Coding Variation from Deep Sequencing of Human Exomes

Science (American Association for the Advancement of Science), 2012-07, Vol.337 (6090), p.64-69

2012

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)

Epigenome-wide association study (EWAS) of BMI, BMI change and waist circumference in African American adults identifies multiple replicated loci

Human molecular genetics, 2015-08, Vol.24 (15), p.4464-4479

2015

Volltextzugriff (PDF)

Epigenome-wide association studies identify DNA methylation associated with kidney function

Nature communications, 2017-11, Vol.8 (1), p.1286-12, Article 1286

2017

Volltextzugriff (PDF)

The Amyloidogenic V122I Transthyretin Variant in Elderly Black Americans

The New England journal of medicine, 2015-01, Vol.372 (1), p.21-29

2015

Volltextzugriff (PDF)

Genome partitioning of genetic variation for complex traits using common SNPs

Nature genetics, 2011-06, Vol.43 (6), p.519-525

2011

Volltextzugriff (PDF)

1 – 25 von 1.765

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(1.709)
Mit Volltextzugriff
(1.489)

Publikationsform

Sprache

Englisch
(1.764)
Japanisch
(1)
Norwegisch
(1)

Erscheinungsjahr

n.n

Thema

Science & Technology
(1.197)
Humans
(1.136)
Life Sciences & Biomedicine
(1.048)
Male
(705)
Female
(704)
Middle Aged
(528)
Genetics & Heredity
(436)
Biological And Medical Sciences
(388)
Risk Factors
(377)
Genome-Wide Association Study
(322)
Polymorphism, Single Nucleotide
(322)
Medical Sciences
(318)
Adult
(309)
Cardiovascular System & Cardiology
(299)
Aged
(295)
Genomes
(285)
Genetics
(255)
Genotype
(240)
Atherosclerosis
(206)
Genetic Predisposition To Disease
(202)

15 weitere anzeigen...

Weniger anzeigen...

Kollektion

EZB-FREE-00999 freely available EZB journals
(1.155)
MEDLINE
(1.153)
Ingenta Connect
(1.098)
Journals@Ovid
(848)
IngentaConnect Journals
(513)
Single Journals
(468)
Access via ScienceDirect (Elsevier)
(331)
Nature
(239)
Access via Wiley Online Library
(187)
Oxford University Press Journals Current
(182)
Nexis Uni
(162)
Oxford Journals 2020 Medicine
(158)
SpringerNature Journals
(116)
EZB-NALI5-00465 Elsevier Archive NL
(115)
Wiley Online Library Full Collection 2018
(91)
EZB-NALI2-00462 Springer Archive NL
(51)
EBSCOhost Psychology and Behavioral Sciences Collection
(40)
ProQuest Dissertations & Theses A&I
(19)
JSTOR Archive Collection A-Z Listing
(18)
Access via Taylor & Francis
(15)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(5)
... seit 90 Tagen
(14)

Menü

Weitere Dienste

Einstellungen

dbNSFP v3.0: A One-Stop Database of Functional Predictions and Annotations for Human Nonsynonymous and Splice-Site SNVs

In silico prediction of splice-altering single nucleotide variants in the human genome

ACAT: A Fast and Powerful p Value Combination Method for Rare-Variant Analysis in Sequencing Studies

The ARIC (Atherosclerosis Risk In Communities) Study: JACC Focus Seminar 3/8

Genetic variation in PNPLA3 confers susceptibility to nonalcoholic fatty liver disease

In silico tools for splicing defect prediction: a survey from the viewpoint of end users

Genetic Risk, Adherence to a Healthy Lifestyle, and Coronary Disease

Rare loss-of-function mutations in ANGPTL family members contribute to plasma triglyceride levels in humans

Normal Limits in Relation to Age, Body Size and Gender of Two-Dimensional Echocardiographic Aortic Root Dimensions in Persons ≥15 Years of Age

American Heart Association's Life's Simple 7: Lifestyle Recommendations, Polygenic Risk, and Lifetime Risk of Coronary Heart Disease

A bidirectional Mendelian randomization study supports causal effects of kidney function on blood pressure

High-Sensitivity Troponin I and Incident Coronary Events, Stroke, Heart Failure Hospitalization, and Mortality in the ARIC Study

Molecular findings among patients referred for clinical whole-exome sequencing

Atypical angiopoietin-like protein that regulates ANGPTL3

Clan Genomics and the Complex Architecture of Human Disease

ANGPTL3 Deficiency and Protection Against Coronary Artery Disease

Identification of a Urate Transporter, ABCG2, with a Common Functional Polymorphism Causing Gout

Resolution of Disease Phenotypes Resulting from Multilocus Genomic Variation

Evaluation of mitochondrial DNA copy number estimation techniques

Evolution and Functional Impact of Rare Coding Variation from Deep Sequencing of Human Exomes

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

Epigenome-wide association study (EWAS) of BMI, BMI change and waist circumference in African American adults identifies multiple replicated loci

Epigenome-wide association studies identify DNA methylation associated with kidney function

The Amyloidogenic V122I Transthyretin Variant in Elderly Black Americans

Genome partitioning of genetic variation for complex traits using common SNPs

Suchergebnisse filtern