D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Medicine D-index 93 Citations 33,746 443 World Ranking 6663 National Ranking 180

Overview

What is he best known for?

The fields of study he is best known for:

  • Internal medicine
  • Gene
  • Mutation

His primary areas of investigation include Internal medicine, Endocrinology, Genetics, Mutation and Blood pressure. His Internal medicine research is multidisciplinary, incorporating elements of Ehlers–Danlos syndrome, Polymorphism and Cardiology. His work in Endocrinology covers topics such as Epithelial sodium channel which are related to areas like Distal convoluted tubule.

His Genetics study combines topics in areas such as Mitral valve and Pathology. His biological study spans a wide range of topics, including Phenotype, Tubulopathy and Genotype. His Blood pressure study combines topics from a wide range of disciplines, such as Case-control study, Genetic epidemiology, Spironolactone, Locus and Hemodynamics.

His most cited work include:

  • Correction: Corrigendum: Dehydrated hereditary stomatocytosis linked to gain-of-function mutations in mechanically activated PIEZO1 ion channels (355 citations)
  • 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. (281 citations)
  • Functional Characterization of a Calcium-Sensing Receptor Mutation in Severe Autosomal Dominant Hypocalcemia with a Bartter-Like Syndrome (268 citations)

What are the main themes of his work throughout his whole career to date?

Xavier Jeunemaitre focuses on Internal medicine, Endocrinology, Genetics, Cardiology and Blood pressure. His Internal medicine research includes elements of Ehlers–Danlos syndrome and Gastroenterology. His research integrates issues of Germline mutation and Genotype in his study of Endocrinology.

The study incorporates disciplines such as Pheochromocytoma and Paraganglioma in addition to Germline mutation. The concepts of his Cardiology study are interwoven with issues in Pulse wave velocity and Fibromuscular dysplasia. Xavier Jeunemaitre has included themes like Mitral valve prolapse and Pathology in his Missense mutation study.

He most often published in these fields:

  • Internal medicine (66.00%)
  • Endocrinology (37.97%)
  • Genetics (23.62%)

What were the highlights of his more recent work (between 2017-2021)?

  • Internal medicine (66.00%)
  • Ehlers–Danlos syndrome (14.79%)
  • Cardiology (19.65%)

In recent papers he was focusing on the following fields of study:

His main research concerns Internal medicine, Ehlers–Danlos syndrome, Cardiology, Fibromuscular dysplasia and Pathology. His Internal medicine study incorporates themes from Gastroenterology and Endocrinology. His Aldosterone and Reabsorption study in the realm of Endocrinology interacts with subjects such as WNK4 and Vascular smooth muscle.

His Ehlers–Danlos syndrome research incorporates elements of Retrospective review, Retrospective cohort study, Natural history and Proband. His research integrates issues of Pulse wave velocity and Arteriovenous fistula in his study of Cardiology. His Pathology research includes themes of ABCC6, Missense mutation, Aneurysm and Mitral valve.

Between 2017 and 2021, his most popular works were:

  • A gain-of-function mutation in the CLCN2 chloride channel gene causes primary aldosteronism (79 citations)
  • A gain-of-function mutation in the CLCN2 chloride channel gene causes primary aldosteronism (79 citations)
  • First International Consensus on the diagnosis and management of fibromuscular dysplasia. (69 citations)

In his most recent research, the most cited papers focused on:

  • Internal medicine
  • Gene
  • Mutation

Xavier Jeunemaitre mainly focuses on Internal medicine, Endocrinology, Mitral valve prolapse, Mitral valve and Fibromuscular dysplasia. His Internal medicine study frequently draws connections between related disciplines such as Cardiology. The various areas that Xavier Jeunemaitre examines in his Endocrinology study include WNK1 and WNK Lysine-Deficient Protein Kinase 1.

His study on Mitral valve prolapse also encompasses disciplines like

  • Genome-wide association study which connect with Myxomatous degeneration, Cilium, Ciliogenesis, Missense mutation and Pathology,
  • Sudden cardiac death, which have a strong connection to Dilated cardiomyopathy and Genetics. Xavier Jeunemaitre has included themes like Dystrophy, Heart valve and Bioinformatics in his Mitral valve study. His Fibromuscular dysplasia course of study focuses on Stenosis and Odds ratio, Gastroenterology, Blood proteins, Biopsy and Disease.

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

Best Publications

Molecular basis of human hypertension: Role of angiotensinogen

Xavier Jeunemaitre;Florent Soubrier;Yuri V. Kotelevtsev;Richard P. Lifton;Richard P. Lifton.
Cell (1992)

2501 Citations

Human hypertension caused by mutations in WNK kinases

Frederick H. Wilson;Sandra Disse-Nicodème;Keith A. Choate;Kazuhiko Ishikawa.
Science (2001)

1521 Citations

Angiotensin II type 1 receptor gene polymorphisms in human essential hypertension.

Alain Bonnardeaux;Eleanor Davies;Xavier Jeunemaitre;Isabelle Fery.
Hypertension (1994)

1164 Citations

The 2017 international classification of the Ehlers-Danlos syndromes

Fransiska Malfait;Clair Francomano;Peter H Byers;John Belmont.
American Journal of Medical Genetics Part C-seminars in Medical Genetics (2017)

1061 Citations

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

Pierre Meneton;Xavier Jeunemaitre;Hugh E. de Wardener;Graham A. Macgregor.
Physiological Reviews (2005)

910 Citations

Genetic Testing in Pheochromocytoma or Functional Paraganglioma

Laurence Amar;Jérôme Bertherat;Eric Baudin;Christiane Ajzenberg.
Journal of Clinical Oncology (2005)

758 Citations

SDHA is a tumor suppressor gene causing paraganglioma

Nelly Burnichon;Jean-Jacques Brière;Rossella Libé;Laure Vescovo.
Human Molecular Genetics (2010)

712 Citations

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

I Inoue;T Nakajima;C S Williams;J Quackenbush.
Journal of Clinical Investigation (1997)

704 Citations

Clinical presentation and penetrance of Pheochromocytoma/ Paraganglioma syndromes.

Diana E. Benn;Anne Paule Gimenez-Roqueplo;Jennifer R. Reilly;Jérôme Bertherat.
The Journal of Clinical Endocrinology and Metabolism (2006)

666 Citations

A molecular variant of angiotensinogen associated with preeclampsia

Ward K;Hata A;Jeunemaitre X;Helin C.
Nature Genetics (1993)

636 Citations

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