UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 52

Sortiert nach

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

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

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

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

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

A Systematic Genetic Assessment of 1,433 Sequence Variants of Unknown Clinical Significance in the BRCA1 and BRCA2 Breast Cancer–Predisposition Genes

American journal of human genetics, 2007-11, Vol.81 (5), p.873-883

2007

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.2020-2027

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

Genome-wide linkage analyses of two repetitive behavior phenotypes in Utah pedigrees with autism spectrum disorders

Molecular autism, 2010-02, Vol.1 (1), p.3-3, Article 3

2010

Link zum Volltext

Verfügbarkeit prüfen

Primary ovarian insufficiency has strong familiality: results of a multigenerational genealogical study

Fertility and sterility, 2023-01, Vol.119 (1), p.128-134

2023

Link zum Volltext

Verfügbarkeit prüfen

Diverticulitis as a Familial Disease: Evidence from a Population-Based Analysis

Journal of the American College of Surgeons, 2022-11, Vol.235 (5), p.S13-S13

2022

Link zum Volltext

Verfügbarkeit prüfen

The multi-generational familial aggregation of interstitial cystitis, other chronic nociplastic pain disorders, depression, and panic disorder

Psychological medicine, 2023-12, Vol.53 (16), p.7847-7856

2023

Link zum Volltext

Verfügbarkeit prüfen

REPRODUCTIVE POTENTIAL AMONG WOMEN WITH POI IS DIMINISHED, BUT NOT ABSENT, COMPARED TO AGE MATCHED CONTROLS

Fertility and sterility, 2021-09, Vol.116 (3), p.e69-e70

2021

Link zum Volltext

Verfügbarkeit prüfen

Diverticulitis Familiality: A Statewide Case-Control Study

Journal of the American College of Surgeons, 2023-11, Vol.237 (5), p.689-696

2023

Link zum Volltext

Verfügbarkeit prüfen

1219 ACHALASIA IS STRONGLY ASSOCIATED WITH EOSINOPHILIC ESOPHAGITIS AND OTHER ALLERGIC DISORDERS

Gastroenterology (New York, N.Y. 1943), 2023-05, Vol.164 (6), p.S-248-S-248

2023

Link zum Volltext

Verfügbarkeit prüfen

PRIMARY OVARIAN INSUFFICIENCY HAS STRONG HERITABILITY, EVEN AMONG DISTANT RELATIVES; RESULTS OF A MULTIGENERATIONAL GENEALOGICAL OBSERVATIONAL STUDY

Fertility and sterility, 2020-09, Vol.114 (3), p.e15-e15

2020

Link zum Volltext

Verfügbarkeit prüfen

Reply

Clinical gastroenterology and hepatology, 2023-10

2023

Link zum Volltext

Verfügbarkeit prüfen

No evidence of BRCA2 mutations in chromosome 13q-linked Utah high-risk prostate cancer pedigrees

BMC research notes, 2009-05, Vol.2 (1), p.94-94

2009

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 52

Suche als RSS-Feed

Aktive Filter

KollektionIngentaConnect_期刊（NSTL购买）

Nur zeigenGeprüft (Peer-Review)

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Mit Volltextzugriff
(43)

Publikationsform

Artikel
(52)

Sprache

Englisch
(52)
Japanisch
(5)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

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

Menü

Weitere Dienste

Einstellungen

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

Mouse Knockout Models for Pelvic Organ Prolapse: a Systematic Review

Esophageal Eosinophilia Is Common Among Relatives of Eosinophilic Esophagitis Patients

Phenotyping clinical disorders: lessons learned from pelvic organ prolapse

Sensitivity and Specificity of Administrative Medical Coding for Pediatric Eosinophilic Esophagitis

A Systematic Genetic Assessment of 1,433 Sequence Variants of Unknown Clinical Significance in the BRCA1 and BRCA2 Breast Cancer–Predisposition Genes

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

Genome-wide linkage analyses of two repetitive behavior phenotypes in Utah pedigrees with autism spectrum disorders

Primary ovarian insufficiency has strong familiality: results of a multigenerational genealogical study

Diverticulitis as a Familial Disease: Evidence from a Population-Based Analysis

The multi-generational familial aggregation of interstitial cystitis, other chronic nociplastic pain disorders, depression, and panic disorder

REPRODUCTIVE POTENTIAL AMONG WOMEN WITH POI IS DIMINISHED, BUT NOT ABSENT, COMPARED TO AGE MATCHED CONTROLS

Diverticulitis Familiality: A Statewide Case-Control Study

1219 ACHALASIA IS STRONGLY ASSOCIATED WITH EOSINOPHILIC ESOPHAGITIS AND OTHER ALLERGIC DISORDERS

PRIMARY OVARIAN INSUFFICIENCY HAS STRONG HERITABILITY, EVEN AMONG DISTANT RELATIVES; RESULTS OF A MULTIGENERATIONAL GENEALOGICAL OBSERVATIONAL STUDY

Reply

No evidence of BRCA2 mutations in chromosome 13q-linked Utah high-risk prostate cancer pedigrees

Aktive Filter

Suchergebnisse filtern