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

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

2022

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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

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

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

2019

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Mouse Knockout Models for Pelvic Organ Prolapse: a Systematic Review

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

2022

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A likely HOXC4 predisposition variant for Chiari malformations

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

2023

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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 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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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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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

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

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

2005

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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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No evidence for IL1RAPL1 involvement in selected high-risk autism pedigrees from the AGRE data set

Autism research, 2011-08, Vol.4 (4), p.293-296

2011

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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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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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Diverticulitis Familiality: A Statewide Case-Control Study

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

2023

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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

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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

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Clinical gastroenterology and hepatology, 2023-10

2023

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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

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PD01-05 SIGNIFICANT LINKAGE EVIDENCE FOR INTERSTITIAL CYSTITIS/PAINFUL BLADDER SYNDROME ON CHROMOSOME 3

The Journal of urology, 2017-04, Vol.197 (4), p.e47-e48

2017

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Genetic polymorphisms associated with urinary tract infection in children and adults: a systematic review and meta-analysis

American journal of obstetrics and gynecology, 2023-12

2023

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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

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

Mouse Knockout Models for Pelvic Organ Prolapse: a Systematic Review

A likely HOXC4 predisposition variant for Chiari malformations

Sensitivity and Specificity of Administrative Medical Coding for Pediatric Eosinophilic Esophagitis

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

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

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

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

No evidence for IL1RAPL1 involvement in selected high-risk autism pedigrees from the AGRE data set

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

PD01-05 SIGNIFICANT LINKAGE EVIDENCE FOR INTERSTITIAL CYSTITIS/PAINFUL BLADDER SYNDROME ON CHROMOSOME 3

Genetic polymorphisms associated with urinary tract infection in children and adults: a systematic review and meta-analysis

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