Matthew Lanktree

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Assistant Professor

McMaster University

Canada

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About

Matthew Lanktree is an Assistant Professor at McMaster University, Canada. His research focuses on kidney diseases, including clonal hematopoiesis, genetic architecture of kidney function, and the implications of familial factors in autosomal dominant polycystic kidney disease. Recent publications highlight investigations into cardiovascular events related to clonal hematopoiesis and the genetic variability associated with renal conditions.

Recent Grants

Grant: Close

Discovery of Inherited Contributors to Diabetic Kidney Disease

Open Date: 2019-07-01

Close Date:

Grant: Close

Assessing the Omnigenic Contribution to Chronic Kidney Disease

Open Date: 2019-07-01

Close Date:

Grant: Close

Improving Polycystic Kidney Disease Prognostication using Imaging, Next Generation Sequencing and Urinary Biomarkers

Open Date: 2017-07-01

Close Date: 2019-06-01

Articles (19)

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2021

Collaborators (3)

Ming Jiang

Research Assistant Professor

Vanderbilt University Medical Center

UNITED STATES

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Xiaoguang Xu

The University of Manchester

UNITED KINGDOM

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Elizabeth Atkinson

Assistant Professor

Baylor College of Medicine

UNITED STATES

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Matthew Lanktree

Research Interests

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About

Recent Grants

Articles (19)

Authors' Reply: Clonal Hematopoiesis of Indeterminate Potential and Cardiovascular Events: Issues to Be Further Explored

Ancestral Variability in the Genetic Architecture of Urine Uromodulin

Genome-wide study investigating effector genes and polygenic prediction for kidney function in persons with ancestry from Africa and the Americas.

Clonal haematopoiesis, ageing and kidney disease

Clonal hematopoiesis of indeterminate potential is associated with acute kidney injury.

How Does ADPKD Severity Differ Between Family Members?

Large Kidney Cysts in HNF1B Nephropathy Mimicking Autosomal Dominant Polycystic Kidney Disease

Incorporating Linear Mixed Models into GWAS of Kidney Function Decline

Kidney Biopsy and Type IV Collagen Gene Sequencing Fail to Explain Hematuria in Loin Pain Hematuria Syndrome

Complex PKD1 Genetics in Early-Onset Cystic Kidney Disease

Basic Research Protocol: Exome Sequencing in Adults With Loin Pain Hematuria Syndrome: A Pilot Study

A novel multi-ancestry proteome-wide Mendelian randomization study implicates extracellular proteins, tubular cells, and fibroblasts in estimated glomerular filtration rate regulation

Proteome-Wide Changes in Blood Biomarkers During Hemodialysis.

Assessing the Risk of Progression to Kidney Failure in Patients With Autosomal Dominant Polycystic Kidney Disease

Decoding Loin Pain Hematuria Syndrome: In-Depth Review of Clinical Characteristics and Family History.

Insights into Autosomal Dominant Polycystic Kidney Disease from Genetic Studies

Patients with Protein-Truncating PKD1 Mutations and Mild ADPKD

Preprint Servers in Kidney Disease Research

The Impact of COVID-19 on Patients With ADPKD

Collaborators (3)

Ming Jiang

Xiaoguang Xu

Elizabeth Atkinson

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