UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 81

Sortiert nach

Significant familial clustering of Peyronie's disease in close and distant relatives

Andrology (Oxford), 2022-10, Vol.10 (7), p.1361-1367

2022

Link zum Volltext

Verfügbarkeit prüfen

A rare FGF5 candidate variant (rs112475347) for predisposition to nonsquamous, nonsmall‐cell lung cancer

International journal of cancer, 2023-07, Vol.153 (2), p.364-372

2023

Link zum Volltext

Verfügbarkeit prüfen

Modifiable life style factors and risk for incident endometriosis

Paediatric and perinatal epidemiology, 2019-01, Vol.33 (1), p.19-25

2019

Link zum Volltext

Verfügbarkeit prüfen

Food impactions in Eosinophilic esophagitis and acute exposures to fine particulate pollution

Allergy (Copenhagen), 2019-12, Vol.74 (12), p.2529-2530

2019

Link zum Volltext

Verfügbarkeit prüfen

Population-based familial aggregation of eosinophilic esophagitis suggests a genetic contribution

Journal of allergy and clinical immunology, 2017-10, Vol.140 (4), p.1138-1143

2017

Link zum Volltext

Verfügbarkeit prüfen

Endometriosis diagnosis, staging and typology and adverse pregnancy outcome history

Paediatric and perinatal epidemiology, 2022-11, Vol.36 (6), p.771-781

2022

Link zum Volltext

Verfügbarkeit prüfen

Familiality analysis of provoked vestibulodynia treated by vestibulectomy supports genetic predisposition

American journal of obstetrics and gynecology, 2016-05, Vol.214 (5), p.609.e1-609.e7

2016

Link zum Volltext

Verfügbarkeit prüfen

Mouse Knockout Models for Pelvic Organ Prolapse: a Systematic Review

International Urogynecology Journal, 2022-07, Vol.33 (7), p.1765-1788

2022

Link zum Volltext

Verfügbarkeit prüfen

Phenotyping clinical disorders: lessons learned from pelvic organ prolapse

American journal of obstetrics and gynecology, 2013-05, Vol.208 (5), p.360-365

2013

Link zum Volltext

Verfügbarkeit prüfen

Esophageal Eosinophilia Is Common Among Relatives of Eosinophilic Esophagitis Patients

Clinical gastroenterology and hepatology, 2022-05, Vol.20 (5), p.e957-e963

2022

Link zum Volltext

Verfügbarkeit prüfen

A likely HOXC4 predisposition variant for Chiari malformations

Journal of neurosurgery, 2023-07, Vol.139 (1), p.266

2023

Link zum Volltext

Verfügbarkeit prüfen

Sensitivity and Specificity of Administrative Medical Coding for Pediatric Eosinophilic Esophagitis

Journal of pediatric gastroenterology and nutrition, 2019-08, Vol.69 (2), p.e49-e53

2019

Link zum Volltext

Verfügbarkeit prüfen

Adiposity and Endometriosis Severity and Typology

Journal of minimally invasive gynecology, 2020-11, Vol.27 (7), p.1516-1523

2020

Link zum Volltext

Verfügbarkeit prüfen

Molecular Landscape of Pelvic Organ Prolapse Provides Insights into Disease Etiology

International journal of molecular sciences, 2023-03, Vol.24 (7), p.6087

2023

Link zum Volltext

Verfügbarkeit prüfen

A Rare Variant in MDH2 (rs111879470) Is Associated with Predisposition to Recurrent Breast Cancer in an Extended High-Risk Pedigree

Cancers, 2023-12, Vol.15 (24), p.5851

2023

Link zum Volltext

Verfügbarkeit prüfen

High-Risk Pedigree Study Identifies LRBA (rs62346982) as a Likely Predisposition Variant for Prostate Cancer

Cancers, 2023-03, Vol.15 (7), p.2085

2023

Link zum Volltext

Verfügbarkeit prüfen

Evidence for pelvic organ prolapse predisposition genes on chromosomes 10 and 17

American journal of obstetrics and gynecology, 2015-06, Vol.212 (6), p.771.e1-771.e7

2015

Link zum Volltext

Verfügbarkeit prüfen

Genetic contributions to urgency urinary incontinence in women

The Journal of urology, 2015-06, Vol.193 (6), p.2020

2015

Link zum Volltext

Verfügbarkeit prüfen

PedGenie: an analysis approach for genetic association testing in extended pedigrees and genealogies of arbitrary size

BMC bioinformatics, 2006-04, Vol.7 (1), p.209-209, Article 209

2006

Link zum Volltext

Verfügbarkeit prüfen

PedGenie: meta genetic association testing in mixed family and case-control designs

BMC bioinformatics, 2007-11, Vol.8 (1), p.448-448, Article 448

2007

Link zum Volltext

Verfügbarkeit prüfen

Genome-wide linkage using the Social Responsiveness Scale in Utah autism pedigrees

Molecular autism, 2010-04, Vol.1 (1), p.8-8

2010

Link zum Volltext

Verfügbarkeit prüfen

Heterogeneous association between engrailed-2 and autism in the CPEA network

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2008-03, Vol.147B (2), p.187-193

2008

Link zum Volltext

Verfügbarkeit prüfen

A Role for XRCC4 in Age at Diagnosis and Breast Cancer Risk

Cancer epidemiology, biomarkers & prevention, 2006-07, Vol.15 (7), p.1306-1310

2006

Link zum Volltext

Verfügbarkeit prüfen

Lobular breast cancer: Excess familiality observed in the Utah Population Database

International journal of cancer, 2005-11, Vol.117 (4), p.655-661

2005

Link zum Volltext

Verfügbarkeit prüfen

A unified theory of autism revisited: linkage evidence points to chromosome X using a high-risk subset of AGRE families

Autism research, 2010-04, Vol.3 (2), p.47-52

2010

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 81

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(77)
Mit Volltextzugriff
(70)

Publikationsform

Artikel
(79)
Buchkapitel
(2)

Sprache

Englisch
(81)
Japanisch
(5)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Significant familial clustering of Peyronie's disease in close and distant relatives

A rare FGF5 candidate variant (rs112475347) for predisposition to nonsquamous, nonsmall‐cell lung cancer

Modifiable life style factors and risk for incident endometriosis

Food impactions in Eosinophilic esophagitis and acute exposures to fine particulate pollution

Population-based familial aggregation of eosinophilic esophagitis suggests a genetic contribution

Endometriosis diagnosis, staging and typology and adverse pregnancy outcome history

Familiality analysis of provoked vestibulodynia treated by vestibulectomy supports genetic predisposition

Mouse Knockout Models for Pelvic Organ Prolapse: a Systematic Review

Phenotyping clinical disorders: lessons learned from pelvic organ prolapse

Esophageal Eosinophilia Is Common Among Relatives of Eosinophilic Esophagitis Patients

A likely HOXC4 predisposition variant for Chiari malformations

Sensitivity and Specificity of Administrative Medical Coding for Pediatric Eosinophilic Esophagitis

Adiposity and Endometriosis Severity and Typology

Molecular Landscape of Pelvic Organ Prolapse Provides Insights into Disease Etiology

A Rare Variant in MDH2 (rs111879470) Is Associated with Predisposition to Recurrent Breast Cancer in an Extended High-Risk Pedigree

High-Risk Pedigree Study Identifies LRBA (rs62346982) as a Likely Predisposition Variant for Prostate Cancer

Evidence for pelvic organ prolapse predisposition genes on chromosomes 10 and 17

Genetic contributions to urgency urinary incontinence in women

PedGenie: an analysis approach for genetic association testing in extended pedigrees and genealogies of arbitrary size

PedGenie: meta genetic association testing in mixed family and case-control designs

Genome-wide linkage using the Social Responsiveness Scale in Utah autism pedigrees

Heterogeneous association between engrailed-2 and autism in the CPEA network

A Role for XRCC4 in Age at Diagnosis and Breast Cancer Risk

Lobular breast cancer: Excess familiality observed in the Utah Population Database

A unified theory of autism revisited: linkage evidence points to chromosome X using a high-risk subset of AGRE families

Suchergebnisse filtern