John V. Raelson

Montreal, QC, Canada

Last Updated: 09/26/2026

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Found 16 publications

Bi-allelic variants in MYH3 cause recessively-inherited arthrogryposis.

Bi-allelic variants in MYH3 cause recessively-inherited arthrogryposis.

Journal: Clinical genetics

Published: July 04, 2023

A Variant in the Nicotinic Acetylcholine Receptor Alpha 3 Subunit Gene Is Associated With Hypertension Risks in Hypogonadic Patients.

A Variant in the Nicotinic Acetylcholine Receptor Alpha 3 Subunit Gene Is Associated With Hypertension Risks in Hypogonadic Patients.

Journal: Frontiers in genetics

Published: March 02, 2020

EPHA4 regulates vascular smooth muscle cell contractility and is a sex-specific hypertension risk gene in individuals with type 2 diabetes.

EPHA4 regulates vascular smooth muscle cell contractility and is a sex-specific hypertension risk gene in individuals with type 2 diabetes.

Journal: Journal of hypertension

Published: March 01, 2019

Analysis of the association of EPHB6, EFNB1 and EFNB3 variants with hypertension risks in males with hypogonadism.

Analysis of the association of EPHB6, EFNB1 and EFNB3 variants with hypertension risks in males with hypogonadism.

Journal: Scientific reports

Published: August 21, 2017

PROX1 gene CC genotype as a major determinant of early onset of type 2 diabetes in slavic study participants from Action in Diabetes and Vascular Disease: Preterax and Diamicron MR Controlled Evaluation study.

PROX1 gene CC genotype as a major determinant of early onset of type 2 diabetes in slavic study participants from Action in Diabetes and Vascular Disease: Preterax and Diamicron MR Controlled Evaluation study.

Journal: Journal of hypertension

Published: January 07, 2017

The role of GRIP1 and ephrin B3 in blood pressure control and vascular smooth muscle cell contractility.

The role of GRIP1 and ephrin B3 in blood pressure control and vascular smooth muscle cell contractility.

Journal: Scientific reports

Published: June 24, 2016

Evidence from single nucleotide polymorphism analyses of ADVANCE study demonstrates EFNB3 as a hypertension risk gene.

Evidence from single nucleotide polymorphism analyses of ADVANCE study demonstrates EFNB3 as a hypertension risk gene.

Journal: Scientific reports

Published: June 10, 2016

Validating genetic markers of response to recombinant human growth hormone in children with growth hormone deficiency and Turner syndrome: the PREDICT validation study.

Validating genetic markers of response to recombinant human growth hormone in children with growth hormone deficiency and Turner syndrome: the PREDICT validation study.

Journal: European journal of endocrinology

Published: April 20, 2016

Reduced blood pressure after smooth muscle EFNB2 deletion and the potential association of EFNB2 mutation with human hypertension risk.

Reduced blood pressure after smooth muscle EFNB2 deletion and the potential association of EFNB2 mutation with human hypertension risk.

Journal: European journal of human genetics : EJHG

Published: November 27, 2015

TGFBI (βIG-H3) is a diabetes-risk gene based on mouse and human genetic studies.

TGFBI (βIG-H3) is a diabetes-risk gene based on mouse and human genetic studies.

Journal: Human molecular genetics

Published: April 15, 2014

A pharmacogenomic approach to the treatment of children with GH deficiency or Turner syndrome.

A pharmacogenomic approach to the treatment of children with GH deficiency or Turner syndrome.

Journal: European journal of endocrinology

Published: June 14, 2013

Monoallelic chromatin conformation flanking long-range silenced domains in cancer-derived and normal cells.

Monoallelic chromatin conformation flanking long-range silenced domains in cancer-derived and normal cells.

Journal: PloS one

Published: February 15, 2013

Showing 1-12 of 16

Last Updated: 09/26/2026