Concepedia

Author

Mathieu Anheim

InsermORCID

Also Known As

Alessandro Filla, Anheim, M, Anheim, Mathieu, Christine Tranchant, Ganaëlle Remérand, Gilles Adam, Isabelle Benatru, M Anheim, M. Anheim, Marion Yger

374

Publications

15.8K

Citations

59

H-Index

115

Concepts

All Affiliations

InsermCentre National de la Recherche ScientifiqueSorbonne UniversitéUniversité de StrasbourgInstitut de génétique et de biologie moléculaire et cellulaire
MA

About

Mathieu Anheim is an author at Inserm specializing in medicine, neurology, and neuropathology.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

31

50

6.4K

2

Public Health

4

4

213

3

Engineering

2

2

59

4

Health Sciences

2

2

82

5

Natural Sciences

1

1

127

Mathieu Anheim

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127

Publications

12.2K

Citations

51

H-Index

YearCitations

Neurologic Features in Severe SARS-CoV-2 Infection

Julie Helms, Stéphane Kremer, Hamid Merdji,

New England Journal of Medicine

2020

2.8K

G51D α‐synuclein mutation causes a novel Parkinsonian–pyramidal syndrome

Suzanne Lesage, Mathieu Anheim, Franck Letournel,

Annals of Neurology

2013

708

Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy

Suzanne Lesage, Valérie Drouet, Elisa Majounie,

The American Journal of Human Genetics

2016

427

Delirium and encephalopathy in severe COVID-19: a cohort analysis of ICU patients

Julie Helms, Stéphane Kremer, Hamid Merdji,

Critical Care

2020

366

ADCK3, an Ancestral Kinase, Is Mutated in a Form of Recessive Ataxia Associated with Coenzyme Q10 Deficiency

Clotilde Lagier‐Tourenne, Mériem Tazir, Luís C. López,

The American Journal of Human Genetics

2008

316

Large-scale screening of the Gaucher's disease-related glucocerebrosidase gene in Europeans with Parkinson's disease

Suzanne Lesage, Mathieu Anheim, Christel Condroyer,

Human Molecular Genetics

2010

274

Trial of Lixisenatide in Early Parkinson’s Disease

Wassilios G. Meissner, Philippe Rémy, Caroline Giordana,

New England Journal of Medicine

2024

261

Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration

Giovanni Stévanin, Hamid Azzedine, Paola S. Denora,

Brain

2007

246

Penetrance of Parkinson disease in glucocerebrosidase gene mutation carriers

Mathieu Anheim, Alexis Elbaz, Suzanne Lesage,

Neurology

2012

245

Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients

Mathieu Anheim, B. Monga, Marie‐Céline Fleury,

Brain

2009

242

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