2026 Susan Treves: Biology and Biochemistry Researcher – H-Index, Publications & Awards

Discipline name	D-Index	World Ranking	Current World Ranking	National Ranking	Current National Ranking	Publications	Citations
Biology and Biochemistry	51	17306	15885	324	285	202	8010

Overview

Susan Treves is affiliated with the University Hospital of Basel in Switzerland. Their research contributions span multiple areas within biochemistry, genetics, and molecular biology, with a significant focus on medicine.

The main fields of study for their publications include:

Biochemistry, Genetics and Molecular Biology
Medicine

Within these broader fields, the subfields addressed in their work cover:

Molecular Biology
Cardiology and Cardiovascular Medicine
Genetics
Cell Biology
Cellular and Molecular Neuroscience

Their research focuses on key topics such as:

Muscle Physiology and Disorders
Ion channel regulation and function
Cardiomyopathy and Myosin Studies
Cardiovascular Effects of Exercise
Genetic Neurodegenerative Diseases
Muscle and Compartmental Disorders
Neurogenetic and Muscular Disorders Research

Susan Treves has contributed to several scientific papers. Recent publications include:

Rapid subcellular calcium responses and dynamics by calcium sensor G-CatchER+, 2021, iScience
Quantitative proteomic analysis of skeletal muscles from wild-type and transgenic mice carrying recessive Ryr1 mutations linked to congenital myopathies, 2023, eLife
RYR1-Related Rhabdomyolysis: A Spectrum of Hypermetabolic States Due to Ryanodine Receptor Dysfunction, 2021, Current Pharmaceutical Design
Pre-operative exercise and pyrexia as modifying factors in malignant hyperthermia (MH), 2022, Neuromuscular Disorders
Neuromuscular symptoms in patients with RYR1-related malignant hyperthermia and rhabdomyolysis, 2022, Brain Communications

Frequent publication venues for their work are:

Neuromuscular Disorders
bioRxiv (Cold Spring Harbor Laboratory)
eLife
Brain Communications
Human Molecular Genetics

Susan Treves collaborates regularly with a number of researchers, including:

Francesco Zorzato
Heinz Jungbluth
Alexis Ruiz
Nicol C. Voermans
Sofia Benucci

Best Publications

RYR1 mutations are a common cause of congenital myopathies with central nuclei

J M Wilmshurst;S Lillis;H Zhou;K Pillay

282
Citations
Congenital myopathies: disorders of excitation–contraction coupling and muscle contraction

Heinz Jungbluth;Heinz Jungbluth;Heinz Jungbluth;Susan Treves;Susan Treves;Francesco Zorzato;Francesco Zorzato;Anna Sarkozy

231
Citations
Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies

Haiyan Zhou;Heinz Jungbluth;Caroline A. Sewry;Lucy Feng

197
Citations
Mutations in RYR1 are a common cause of exertional myalgia and rhabdomyolysis

N. Dlamini;N.C. Voermans;S. Lillis;K. Stewart

196
Citations
Identification of four novel mutations in the C-terminal membrane spanning domain of the ryanodine receptor 1: association with central core disease and alteration of calcium homeostasis

Nikola Tilgen;Francesco Zorzato;Birgit Halliger-Keller;Francesco Muntoni

196
Citations
Congenital muscle disorders with cores: the ryanodine receptor calcium channel paradigm.

Susan Treves;Heinz Jungbluth;Francesco Muntoni;Francesco Zorzato;Francesco Zorzato

172
Citations
Ryanodine receptor 1 mutations, dysregulation of calcium homeostasis and neuromuscular disorders.

Susan Treves;Ayuk A. Anderson;Sylvie Ducreux;Alexandra Divet

163
Citations
Activation of endoplasmic reticulum stress response by hepatitis viruses up‐regulates protein phosphatase 2A

Verena Christen;Susan Treves;Francois H. T. Duong;Markus H. Heim

160
Citations
Chlorocresol: an activator of ryanodine receptor-mediated Ca2+ release.

Francesco Zorzato;Erica Scutari;Vincenzo Tegazzin;Emilio Clementi

160
Citations
Apoptosis Is Dependent on Intracellular Zinc and Independent of Intracellular Calcium in Lymphocytes

Susan Treves;Pier Luigi Trentini;Monica Ascanelli;Gianna Bucci

146
Citations
Interaction of S100A1 with the Ca2+ release channel (ryanodine receptor) of skeletal muscle.

Susan Treves;Erica Scutari;Mylène Robert;Séverine Groh

145
Citations
Ectosomes Released by Polymorphonuclear Neutrophils Induce a MerTK-dependent Anti-inflammatory Pathway in Macrophages

Ceylan Eken;Perrine J. Martin;Salima Sadallah;Susan Treves

144
Citations
Junctate is a key element in calcium entry induced by activation of InsP3 receptors and/or calcium store depletion

Susan Treves;Clara Franzini-Armstrong;Luca Moccagatta;Christophe Arnoult

140
Citations
Calreticulin is a candidate for a calsequestrin-like function in Ca2+-storage compartments (calciosomes) of liver and brain

S Treves;M De Mattei;M Landfredi;A Villa

136
Citations
RYR1-related myopathies: a wide spectrum of phenotypes throughout life.

M. Snoeck;B.G.M. van Engelen;B. Kusters;B. Kusters;M.M. Lammens;M.M. Lammens

136
Citations
Effect of Ryanodine Receptor Mutations on Interleukin-6 Release and Intracellular Calcium Homeostasis in Human Myotubes from Malignant Hyperthermia-susceptible Individuals and Patients Affected by Central Core Disease *

Sylvie Ducreux;Francesco Zorzato;Clemens Müller;Caroline Sewry

133
Citations
Centronuclear myopathy due to a de novo dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene

Heinz Jungbluth;Haiyan Zhou;Caroline A. Sewry;Caroline A. Sewry;Stephanie Robb

132
Citations
Molecular cloning, expression, functional characterization, chromosomal localization, and gene structure of junctate, a novel integral calcium binding protein of sarco(endo)plasmic reticulum membrane.

Susan Treves;Giordana Feriotto;Luca Moccagatta;Roberto Gambari

127
Citations
Intracellular calcium homeostasis in human primary muscle cells from malignant hyperthermia-susceptible and normal individuals. Effect Of overexpression of recombinant wild-type and Arg163Cys mutated ryanodine receptors.

K Censier;A Urwyler;F Zorzato;S Treves

126
Citations
Characterization of recessive RYR1 mutations in core myopathies

Haiyan Zhou;Naohiro Yamaguchi;Le Xu;Ying Wang

118
Citations