Matilde Karakachoff - Concepedia

Author

Matilde Karakachoff

Also Known As

Karakachoff, M, Karakachoff, Matilde, M Karakachoff, M. Karakachoff, Mathilde Karakachoff, Matilde KARAKACHOFF, Matilde Karakachoff, Robert Olaso, Stéphanie Chatel, the D.E.S.I.R. Study Group

Publications

Citations

H-Index

Concepts

All Affiliations

Inserm Institut du Thorax Nantes Université Centre Hospitalier Universitaire de Nantes Centre National de la Recherche Scientifique

About

Matilde Karakachoff is an author at Inserm specializing in medicine, hospital medicine, and lung mechanics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	101
2	Cell Biology	1	1	15
3	Critical Care Medicine	1	1	11
4	Emergency Medicine	1	1	11
5	Hospital Medicine	1	1	11

Matilde Karakachoff

Publications

683

Citations

H-Index

Page 1

	Year	Citations
Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndrome Solena Le Scouarnec, Matilde Karakachoff, Jean‐Baptiste Gourraud, Human Molecular Genetics	2015	135
Functionally validated <i>SCN5A</i> variants allow interpretation of pathogenicity and prediction of lethal events in Brugada syndrome Taisuke Ishikawa, Hiroki Kimoto, Hiroyuki Mishima, European Heart Journal	2021	75
New insights into mitral valve dystrophy: a Filamin-A genotype–phenotype and outcome study Thierry Le Tourneau, Solena Le Scouarnec, Caroline Cueff, European Heart Journal	2017	70
Patient-centric synthetic data generation, no reason to risk re-identification in biomedical data analysis Morgan Guillaudeux, Olivia Rousseau, Julien Petot, npj Digital Medicine	2023	66
Hyponatremia is associated with poor outcome in COVID-19 Hugo De Carvalho, Thibault Letellier, Matilde Karakachoff, Journal of Nephrology	2021	59
<i>RRAD</i> mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndrome Nadjet Belbachir, Vincent Portero, Zeina R. Al Sayed, European Heart Journal	2019	51
Rare Coding Variants in ANGPTL6 Are Associated with Familial Forms of Intracranial Aneurysm Romain Bourcier, Solena Le Scouarnec, Stéphanie Bonnaud, The American Journal of Human Genetics Variant InterpretationIntracranial AneurysmVascular MalformationPathologyAngptl6 Are Associated	2018	49
Location of intracranial aneurysms is the main factor associated with rupture in the ICAN population Olivia Rousseau, Matilde Karakachoff, Alban Gaignard, Journal of Neurology Neurosurgery & Psychiatry	2020	38
Evaluation of the Post-COVID-19 Functional Status (PCFS) Scale in a cohort of patients recovering from hypoxemic SARS-CoV-2 pneumonia Naïla Benkalfate, Emmanuel Eschapasse, Thomas Georges, BMJ Open Respiratory Research	2022	30
The genetic history of France Aude Saint Pierre, Joanna Giemza, Isabel Alves, European Journal of Human Genetics MedicineGeneticsEvolutionary BiologyHuman OriginGenetic History	2020	26

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