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...

BMI loci and longitudinal BMI from adolescence to young adulthood in an ethnically diverse cohort

International Journal of Obesity, 2017-05, Vol.41 (5), p.759-768

2017

Volltextzugriff (PDF)

Replication of the association between variants in WFS1 and risk of type 2 diabetes in European populations

Diabetologia, 2008-03, Vol.51 (3), p.458-463

2008

Volltextzugriff (PDF)

A mechanism for low penetrance in an ALS family with a novel SOD1 deletion

Neurology, 2009-03, Vol.72 (13), p.1153-1159

2009

Volltextzugriff (PDF)

The interaction between physical activity and obesity gene variants in association with BMI: Does the obesogenic environment matter?

Health & place, 2016-11, Vol.42, p.159-165

2016

Volltextzugriff (PDF)

Variation in the resistin gene is associated with obesity and insulin-related phenotypes in Finnish subjects

Diabetologia, 2004-10, Vol.47 (10), p.1782-1788

2004

Volltextzugriff (PDF)

Moderate to vigorous physical activity interactions with genetic variants and body mass index in a large US ethnically diverse cohort

Pediatric obesity, 2014-04, Vol.9 (2), p.e35-e46

2014

Volltextzugriff (PDF)

Assessment of familial risk in patients with hidradenitis suppurativa

British journal of dermatology (1951), 2021-04, Vol.184 (4), p.753-754

2021

Volltextzugriff (PDF)

Screen time behaviours may interact with obesity genes, independent of physical activity, to influence adolescent BMI in an ethnically diverse cohort

Pediatric obesity, 2013-12, Vol.8 (6), p.e74-e79

2013

Volltextzugriff (PDF)

Estimation of genetic effects on BMI during adolescence in an ethnically diverse cohort: The National Longitudinal Study of Adolescent Health

Nutrition & diabetes, 2012-09, Vol.2 (9), p.e47-e47

2012

Volltextzugriff (PDF)

Metabolic and cardiovascular traits: an abundance of recently identified common genetic variants

Human molecular genetics, 2008-10, Vol.17 (R2), p.R102-R108

2008

Volltextzugriff (PDF)

Multi-ethnic fine-mapping of 14 central adiposity loci

Human molecular genetics, 2014-09, Vol.23 (17), p.4738-4744

2014

Volltextzugriff (PDF)

Replication of LIN28B SNP association with age of menarche in young Filipino women

Pediatric obesity, 2013-10, Vol.8 (5), p.e50-e53

2013

Volltextzugriff (PDF)

Genetic risk score and adiposity interact to influence triglyceride levels in a cohort of Filipino women

Nutrition & diabetes, 2014-06, Vol.4 (6), p.e118-e118

2014

Volltextzugriff (PDF)

High-Throughput Screening for Evidence of Association by Using Mass Spectrometry Genotyping on DNA Pools

Proceedings of the National Academy of Sciences - PNAS, 2002-12, Vol.99 (26), p.16928-16933

2002

Volltextzugriff (PDF)

Mitochondrial polymorphisms and susceptibility to type 2 diabetes-related traits in Finns

Human genetics, 2005-11, Vol.118 (2), p.245-254

2005

Volltextzugriff (PDF)

A Genome-Wide Association Study of IVGTT-Based Measures of First-Phase Insulin Secretion Refines the Underlying Physiology of Type 2 Diabetes Variants

Diabetes (New York, N.Y.), 2017-08, Vol.66 (8), p.2296-2309

2017

Volltextzugriff (PDF)

Genome-Wide Association Study of the Modified Stumvoll Insulin Sensitivity Index Identifies BCL2 and FAM19A2 as Novel Insulin Sensitivity Loci

Diabetes (New York, N.Y.), 2016-10, Vol.65 (10), p.3200-3211

2016

Volltextzugriff (PDF)

Mvwf, a Dominant Modifier of Murine von Willebrand Factor, Results from Altered Lineage-Specific Expression of a Glycosyltransferase

Cell, 1999-01, Vol.96 (1), p.111-120

1999

Volltextzugriff (PDF)

HUGIn: Hi-C Unifying Genomic Interrogator

Bioinformatics (Oxford, England), 2017-12, Vol.33 (23), p.3793-3795

2017

Volltextzugriff (PDF)

Linkage disequilibrium between microsatellite markers extends beyond 1 cM on chromosome 20 in Finns

Genome research, 2001-07, Vol.11 (7), p.1221-1226

2001

Volltextzugriff (PDF)

Replication of the association between variants in WFS1 and risk of type 2 diabetes in European populations

Diabetologia, 2008-03, Vol.51 (3), p.523-523

2008

Volltextzugriff (PDF)

Comparative Mapping of Distal Murine Chromosome 11 and Human 17q21.3 in a Region Containing a Modifying Locus for Murine Plasma von Willebrand Factor Level

Genomics (San Diego, Calif.), 1998-11, Vol.54 (1), p.19-30

1998

Volltextzugriff (PDF)

A common frameshift mutation in von Willebrand factor does not alter mRNA stability but interferes with normal propeptide processing

British journal of haematology, 1996-10, Vol.95 (1), p.184-191

1996

Volltextzugriff (PDF)

A meta-analysis of genome-wide association studies for adiponectin levels in East Asians identifies a novel locus near WDR11-FGFR2

Human molecular genetics, 2014-02, Vol.23 (4), p.1108-1119

2014

Volltextzugriff (PDF)

A Novel Modifier Gene for Plasma Von Willebrand Factor Level Maps to Distal Mouse Chromosome 11

Proceedings of the National Academy of Sciences - PNAS, 1996-12, Vol.93 (26), p.15352-15357

1996

Volltextzugriff (PDF)

1 – 25 von 150

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(148)
Mit Volltextzugriff
(124)

Publikationsform

Artikel
(149)
Tagungsberichte
(1)

Sprache

Englisch
(150)

Erscheinungsjahr

n.n

Thema

Science & Technology
(118)
Humans
(107)
Life Sciences & Biomedicine
(102)
Male
(62)
Genetics & Heredity
(60)
Female
(54)
Genome-Wide Association Study
(54)
Polymorphism, Single Nucleotide
(50)
Genomes
(45)
Diabetes Mellitus, Type 2 - Genetics
(40)
Genetic Predisposition To Disease
(39)
Genetic Aspects
(37)
Diabetes
(36)
Middle Aged
(33)
Body Mass Index
(32)
Medicin Och Hälsovetenskap
(31)
Aged
(30)
Biological And Medical Sciences
(30)
Genetics
(29)
Adult
(26)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Nature Genetics
(19)
Plos Genetics
(19)
Diabetes
(16)
American Journal Of Human Genetics
(14)
Human Molecular Genetics
(11)
Human Molecular Genetics Online/human Molecular Genetics
(8)
Nature Communications
(6)
Blood
(4)
Diabetologia
(4)
Pediatric Obesity
(4)

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

BMI loci and longitudinal BMI from adolescence to young adulthood in an ethnically diverse cohort

Replication of the association between variants in WFS1 and risk of type 2 diabetes in European populations

A mechanism for low penetrance in an ALS family with a novel SOD1 deletion

The interaction between physical activity and obesity gene variants in association with BMI: Does the obesogenic environment matter?

Variation in the resistin gene is associated with obesity and insulin-related phenotypes in Finnish subjects

Moderate to vigorous physical activity interactions with genetic variants and body mass index in a large US ethnically diverse cohort

Assessment of familial risk in patients with hidradenitis suppurativa

Screen time behaviours may interact with obesity genes, independent of physical activity, to influence adolescent BMI in an ethnically diverse cohort

Estimation of genetic effects on BMI during adolescence in an ethnically diverse cohort: The National Longitudinal Study of Adolescent Health

Metabolic and cardiovascular traits: an abundance of recently identified common genetic variants

Multi-ethnic fine-mapping of 14 central adiposity loci

Replication of LIN28B SNP association with age of menarche in young Filipino women

Genetic risk score and adiposity interact to influence triglyceride levels in a cohort of Filipino women

High-Throughput Screening for Evidence of Association by Using Mass Spectrometry Genotyping on DNA Pools

Mitochondrial polymorphisms and susceptibility to type 2 diabetes-related traits in Finns

A Genome-Wide Association Study of IVGTT-Based Measures of First-Phase Insulin Secretion Refines the Underlying Physiology of Type 2 Diabetes Variants

Genome-Wide Association Study of the Modified Stumvoll Insulin Sensitivity Index Identifies BCL2 and FAM19A2 as Novel Insulin Sensitivity Loci

Mvwf, a Dominant Modifier of Murine von Willebrand Factor, Results from Altered Lineage-Specific Expression of a Glycosyltransferase

HUGIn: Hi-C Unifying Genomic Interrogator

Linkage disequilibrium between microsatellite markers extends beyond 1 cM on chromosome 20 in Finns

Replication of the association between variants in WFS1 and risk of type 2 diabetes in European populations

Comparative Mapping of Distal Murine Chromosome 11 and Human 17q21.3 in a Region Containing a Modifying Locus for Murine Plasma von Willebrand Factor Level

A common frameshift mutation in von Willebrand factor does not alter mRNA stability but interferes with normal propeptide processing

A meta-analysis of genome-wide association studies for adiponectin levels in East Asians identifies a novel locus near WDR11-FGFR2

A Novel Modifier Gene for Plasma Von Willebrand Factor Level Maps to Distal Mouse Chromosome 11

Suchergebnisse filtern