List of works - Xavier Jeunemaitre

Molecular basis of human hypertension: role of angiotensinogen

scientific article published on October 2, 1992

Links between dietary salt intake, renal salt handling, blood pressure, and cardiovascular diseases

scientific article

SDHA is a tumor suppressor gene causing paraganglioma

scientific article

Mutations in myosin heavy chain 11 cause a syndrome associating thoracic aortic aneurysm/aortic dissection and patent ductus arteriosus

scientific article

Genetic testing in pheochromocytoma or functional paraganglioma

scientific article published in December 2005

A nucleotide substitution in the promoter of human angiotensinogen is associated with essential hypertension and affects basal transcription in vitro

scientific article published on April 1997

Somatic mutations in ATP1A1 and ATP2B3 lead to aldosterone-producing adenomas and secondary hypertension

scientific article

A molecular variant of angiotensinogen associated with preeclampsia

scientific article

Succinate Dehydrogenase B Gene Mutations Predict Survival in Patients with Malignant Pheochromocytomas or Paragangliomas

article

KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron

scientific article

The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas.

scientific article

The Warburg effect is genetically determined in inherited pheochromocytomas

scientific article

Integrative genomic analysis reveals somatic mutations in pheochromocytoma and paraganglioma

article

The 2017 international classification of the Ehlers-Danlos syndromes

scientific article published on March 2017

Absence of linkage between the angiotensin converting enzyme locus and human essential hypertension

scientific article published in April 1992

Dehydrated hereditary stomatocytosis linked to gain-of-function mutations in mechanically activated PIEZO1 ion channels

scientific article

Functional consequences of a SDHB gene mutation in an apparently sporadic pheochromocytoma

scientific article published in October 2002

Contribution of genetic polymorphism in the renin-angiotensin system to the development of renal complications in insulin-dependent diabetes: Genetique de la Nephropathie Diabetique (GENEDIAB) study group

scientific article published on April 1997

Efficacy and tolerance of spironolactone in essential hypertension

scientific article published in October 1987

Haplotypes of angiotensinogen in essential hypertension

scientific article

Multiple promoters in the WNK1 gene: one controls expression of a kidney-specific kinase-defective isoform

scientific article

Genetic spectrum and clinical correlates of somatic mutations in aldosterone-producing adenoma

scientific article published on 27 May 2014

Association of hypertension with T594M mutation in beta subunit of epithelial sodium channels in black people resident in London

scientific article published in May 1998

Prevalence, clinical, and molecular correlates of KCNJ5 mutations in primary aldosteronism

scientific article published on 23 January 2012

Effect of celiprolol on prevention of cardiovascular events in vascular Ehlers-Danlos syndrome: a prospective randomised, open, blinded-endpoints trial

scientific article

Blood pressure loci identified with a gene-centric array

scientific article

Spectrum of mutations in Gitelman syndrome

scientific article

Genomewide association study using a high-density single nucleotide polymorphism array and case-control design identifies a novel essential hypertension susceptibility locus in the promoter region of endothelial NO synthase

scientific article published on 19 December 2011

WNK1-related Familial Hyperkalemic Hypertension results from an increased expression of L-WNK1 specifically in the distal nephron

scientific article published on 12 August 2013

Phenotype-genotype correlation in antenatal and neonatal variants of Bartter syndrome

scientific article

Decreased ENaC expression compensates the increased NCC activity following inactivation of the kidney-specific isoform of WNK1 and prevents hypertension

scientific article published on October 4, 2010

Change in salt intake affects blood pressure of chimpanzees: implications for human populations

scientific article

Glucocorticoid-suppressible hyperaldosteronism and adrenal tumors occurring in a single French pedigree

scientific article published on November 1, 1995

Paracellin-1 is critical for magnesium and calcium reabsorption in the human thick ascending limb of Henle

scientific article

Mapping of a first locus for autosomal dominant myxomatous mitral-valve prolapse to chromosome 16p11.2-p12.1.

scientific article

Lack of evidence for linkage of the endothelial cell nitric oxide synthase gene to essential hypertension

scientific article published on January 1995

Genetic analysis of the beta subunit of the epithelial Na+ channel in essential hypertension

scientific article

Mutations in DCHS1 cause mitral valve prolapse

scientific journal article

WNK1 regulates vasoconstriction and blood pressure response to α 1-adrenergic stimulation in mice

scientific article

Epithelial to mesenchymal transition is activated in metastatic pheochromocytomas and paragangliomas caused by SDHB gene mutations

scientific article published on 4 April 2012

Molecular Genetics of Human Hypertension: Role of Angiotensinogen*

scientific article published on October 1, 1997

Study of V(1)-vascular vasopressin receptor gene microsatellite polymorphisms in human essential hypertension

scientific article (publication date: April 2000)

A decade (2001-2010) of genetic testing for pheochromocytoma and paraganglioma

scientific article published on 19 April 2012

Seven lessons from two candidate genes in human essential hypertension: angiotensinogen and epithelial sodium channel

scientific article

Aldosterone-Producing Adenoma Formation in the Adrenal Cortex Involves Expression of Stem/Progenitor Cell Markers

article published in 2011

Sib pair linkage analysis of renin gene haplotypes in human essential hypertension

scientific article published on January 1992

Adrenal cortex remodeling and functional zona glomerulosa hyperplasia in primary aldosteronism

scientific article published on 11 October 2010

Familial hyperkalemic hypertension

scientific article

WNK-SPAK-NCC cascade revisited: WNK1 stimulates the activity of the Na-Cl cotransporter via SPAK, an effect antagonized by WNK4.

scientific article published on 11 August 2014

Endothelial function and chronic exposure to air pollution in normal male subjects

scientific article

List of works by Xavier Jeunemaitre

Molecular basis of human hypertension: role of angiotensinogen

Links between dietary salt intake, renal salt handling, blood pressure, and cardiovascular diseases

SDHA is a tumor suppressor gene causing paraganglioma

Mutations in myosin heavy chain 11 cause a syndrome associating thoracic aortic aneurysm/aortic dissection and patent ductus arteriosus

Genetic testing in pheochromocytoma or functional paraganglioma

A nucleotide substitution in the promoter of human angiotensinogen is associated with essential hypertension and affects basal transcription in vitro

Somatic mutations in ATP1A1 and ATP2B3 lead to aldosterone-producing adenomas and secondary hypertension

A molecular variant of angiotensinogen associated with preeclampsia

Succinate Dehydrogenase B Gene Mutations Predict Survival in Patients with Malignant Pheochromocytomas or Paragangliomas

KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron

The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas.

The Warburg effect is genetically determined in inherited pheochromocytomas

Integrative genomic analysis reveals somatic mutations in pheochromocytoma and paraganglioma

The 2017 international classification of the Ehlers-Danlos syndromes

Absence of linkage between the angiotensin converting enzyme locus and human essential hypertension

Dehydrated hereditary stomatocytosis linked to gain-of-function mutations in mechanically activated PIEZO1 ion channels

Functional consequences of a SDHB gene mutation in an apparently sporadic pheochromocytoma

Contribution of genetic polymorphism in the renin-angiotensin system to the development of renal complications in insulin-dependent diabetes: Genetique de la Nephropathie Diabetique (GENEDIAB) study group

Efficacy and tolerance of spironolactone in essential hypertension

Haplotypes of angiotensinogen in essential hypertension

Multiple promoters in the WNK1 gene: one controls expression of a kidney-specific kinase-defective isoform

Genetic spectrum and clinical correlates of somatic mutations in aldosterone-producing adenoma

Association of hypertension with T594M mutation in beta subunit of epithelial sodium channels in black people resident in London

Prevalence, clinical, and molecular correlates of KCNJ5 mutations in primary aldosteronism

Effect of celiprolol on prevention of cardiovascular events in vascular Ehlers-Danlos syndrome: a prospective randomised, open, blinded-endpoints trial

Blood pressure loci identified with a gene-centric array

Spectrum of mutations in Gitelman syndrome

Genomewide association study using a high-density single nucleotide polymorphism array and case-control design identifies a novel essential hypertension susceptibility locus in the promoter region of endothelial NO synthase

WNK1-related Familial Hyperkalemic Hypertension results from an increased expression of L-WNK1 specifically in the distal nephron

Phenotype-genotype correlation in antenatal and neonatal variants of Bartter syndrome

Decreased ENaC expression compensates the increased NCC activity following inactivation of the kidney-specific isoform of WNK1 and prevents hypertension

Change in salt intake affects blood pressure of chimpanzees: implications for human populations

Glucocorticoid-suppressible hyperaldosteronism and adrenal tumors occurring in a single French pedigree

Paracellin-1 is critical for magnesium and calcium reabsorption in the human thick ascending limb of Henle

Mapping of a first locus for autosomal dominant myxomatous mitral-valve prolapse to chromosome 16p11.2-p12.1.

Lack of evidence for linkage of the endothelial cell nitric oxide synthase gene to essential hypertension

Genetic analysis of the beta subunit of the epithelial Na+ channel in essential hypertension

Mutations in DCHS1 cause mitral valve prolapse

WNK1 regulates vasoconstriction and blood pressure response to α 1-adrenergic stimulation in mice

Epithelial to mesenchymal transition is activated in metastatic pheochromocytomas and paragangliomas caused by SDHB gene mutations

Molecular Genetics of Human Hypertension: Role of Angiotensinogen*

Study of V(1)-vascular vasopressin receptor gene microsatellite polymorphisms in human essential hypertension

A decade (2001-2010) of genetic testing for pheochromocytoma and paraganglioma

Seven lessons from two candidate genes in human essential hypertension: angiotensinogen and epithelial sodium channel

Aldosterone-Producing Adenoma Formation in the Adrenal Cortex Involves Expression of Stem/Progenitor Cell Markers

Sib pair linkage analysis of renin gene haplotypes in human essential hypertension

Adrenal cortex remodeling and functional zona glomerulosa hyperplasia in primary aldosteronism

Familial hyperkalemic hypertension

WNK-SPAK-NCC cascade revisited: WNK1 stimulates the activity of the Na-Cl cotransporter via SPAK, an effect antagonized by WNK4.

Endothelial function and chronic exposure to air pollution in normal male subjects