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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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Modifiable life style factors and risk for incident endometriosis

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

2019

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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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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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Endometriosis diagnosis, staging and typology and adverse pregnancy outcome history

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

2022

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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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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 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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Adiposity and Endometriosis Severity and Typology

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

2020

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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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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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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

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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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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

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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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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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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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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

A likely HOXC4 predisposition variant for Chiari malformations

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

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

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

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

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

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

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