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Dervla M Connaughton

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Western University

Canada

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The Irish Kidney Gene Project - identification and characterisation of novel genetic causes of familial kidney disease

Open Date: 2016-09-01

Close Date: 2020-02-29

Articles (13)

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Collaborators (12)

Neil Boudville

University of Western Australia

AUSTRALIA

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David M. Thal

MONASH UNIVERSITY

AUSTRALIA

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Andrew A. House

Western University

CANADA

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Sisira Sarma

Western University

CANADA

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Pavel Roshanov

Assistant Professor

Western University

CANADA

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Michael Chiu

Western University

CANADA

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Krista L. Lentine

Saint Louis University

UNITED STATES

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Matthew Weir

Associate Professor

Western University

CANADA

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Ngan N. Lam

University of Calgary

CANADA

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Shih-Han Huang

Associate Professor

Western University

CANADA

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John Basmaji

Assistant Professor

Western University

CANADA

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Khaled Lotfy

Assistant Professor

Western University

CANADA

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ApplyKite TwinLearns as you apply

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Dervla M Connaughton

Research Interests

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Recent Grants

Articles (13)

Risk for Scrotal Surgery After Laparoscopic Donor Nephrectomy

Genetic Testing in Adults over 50 Years with Chronic Kidney Disease: Diagnostic Yield and Clinical Implications in a Specialized Kidney Genetics Clinic

The Flow of Living Kidney Donor Candidates Through the Evaluation Process: A Single-Center Experience in Ontario, Canada

Implementation of a Kidney Genetic Service Into the Diagnostic Pathway for Patients With Chronic Kidney Disease in Canada

Utility of Genetic Testing in Adults with CKD

Teaching NeuroImage: Extensive Brainstem and Striatal Involvement in Neuropsychiatric Systemic Lupus Erythematosus.

Vascular calcification in chronic kidney disease associated with pathogenic variants in ABCC6

Reclassification of Genetic Testing Results: A Case Report Demonstrating the Need for Structured Re-Evaluation of Genetic Findings.

Recessive <scp><i>CHRM5</i></scp> variant as a potential cause of neurogenic bladder

Genetic Variants in ARHGEF6 Cause Congenital Anomalies of the Kidneys and Urinary Tract in Humans, Mice, and Frogs

Genotypic analysis of a large cohort of patients with suspected atypical hemolytic uremic syndrome

Maternal health and pregnancy outcomes in autosomal dominant tubulointerstitial kidney disease

Prioritization of Monogenic Congenital Anomalies of the Kidney and Urinary Tract Candidate Genes with Existing Single-Cell Transcriptomics Data of the Human Fetal Kidney

Collaborators (12)

Neil Boudville

David M. Thal

Andrew A. House

Sisira Sarma

Pavel Roshanov

Michael Chiu

Krista L. Lentine

Matthew Weir

Ngan N. Lam

Shih-Han Huang

John Basmaji

Khaled Lotfy

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