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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

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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

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Esophageal Eosinophilia Is Common Among Relatives of Eosinophilic Esophagitis Patients

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

2022

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Phenotyping clinical disorders: lessons learned from pelvic organ prolapse

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

2013

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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

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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

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Recurrence of severe diverticulitis is associated with age and birth decade

Journal of gastrointestinal surgery, 2024-04, Vol.28 (4), p.507-512

2024

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Adiposity and Endometriosis Severity and Typology

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

2020

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Molecular Landscape of Pelvic Organ Prolapse Provides Insights into Disease Etiology

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

2023

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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

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

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

2023

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Genetic Contributions to Urgency Urinary Incontinence in Women

The Journal of urology, 2015-06, Vol.193 (6), p.2020-2027

2015

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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

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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

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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

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

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

2010

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

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

2023

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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

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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

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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

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Identification of candidate Parkinson’s disease predisposition genes in high-risk pedigrees (S42.001)

Neurology, 2023-04, Vol.100 (17_supplement_2)

2023

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Characterization of the linkage disequilibrium structure and identification of tagging-SNPs in five DNA repair genes

BMC cancer, 2005-08, Vol.5 (1), p.99-99, Article 99

2005

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RNA SEǪUENCING FROM BIOPSIES PERFORMED DURING FOOD ELIMINATION AND REINTRODUCTION IDENTIFIES SIGNATURES INVOLVED IN EARLY RECURRENCE OF EOE

Gastroenterology (New York, N.Y. 1943), 2024-05, Vol.166 (5), p.458f,458f1,458f2-458f,458f1,458f2

2024

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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

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Clinical gastroenterology and hepatology, 2024-05, Vol.22 (5), p.1145

2024

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

Familiality analysis of provoked vestibulodynia treated by vestibulectomy supports genetic predisposition

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

Recurrence of severe diverticulitis is associated with age and birth decade

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

Genetic Contributions to Urgency Urinary Incontinence in Women

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

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

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

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

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

Identification of candidate Parkinson’s disease predisposition genes in high-risk pedigrees (S42.001)

Characterization of the linkage disequilibrium structure and identification of tagging-SNPs in five DNA repair genes

RNA SEǪUENCING FROM BIOPSIES PERFORMED DURING FOOD ELIMINATION AND REINTRODUCTION IDENTIFIES SIGNATURES INVOLVED IN EARLY RECURRENCE OF EOE

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

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