Sergio Guerrero‐Castillo

Author

Also Known As

Guerrero-Castillo, Sergio, Machteld M. Oud, S. Guerrero‐Castillo, Sergio Guerrero-Castillo, Sergio Guerrero‐Castillo, Sergio Guerrero–Castillo

Publications

2.6K

Citations

H-Index

Concepts

All Affiliations

Radboud University Nijmegen Radboud University Medical Center Radboud Institute for Molecular Life Sciences University Medical Center Universidad Nacional Autónoma de México

About

Sergio Guerrero‐Castillo is an author at Radboud University Nijmegen specializing in medicine, mitochondrial function, and natural sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	19	20	1.6K
2	Natural Sciences	12	13	1.2K
3	Biochemistry	10	10	641
4	Engineering	1	1	64
5	Social Sciences	1	1	19

Sergio Guerrero‐Castillo

Publications

2.3K

Citations

H-Index

Page 1

	Year	Citations
The Assembly Pathway of Mitochondrial Respiratory Chain Complex I Sergio Guerrero‐Castillo, Fabian Baertling, Daniel Kownatzki, Cell Metabolism Assembly PathwayMitochondrial BiogenesisMitochondrial FunctionNatural SciencesMolecular Biology	2016	421
The m -AAA Protease Associated with Neurodegeneration Limits MCU Activity in Mitochondria Tim König, Simon E. Tröder, Kavya Bakka, Molecular Cell Neurodegenerative DiseasesMitophagyMitochondrial FunctionBiochemistryMedicine	2016	206
Evolution and structural organization of the mitochondrial contact site (MICOS) complex and the mitochondrial intermembrane space bridging (MIB) complex Martijn A. Huynen, Mareike Mühlmeister, Katherina Gotthardt, Biochimica et Biophysica Acta (BBA) - Molecular Cell Research	2015	201
A salvage pathway maintains highly functional respiratory complex I Karolina Szczepanowska, Katharina Senft, Juliana Heidler, Nature Communications	2020	114
Mutations in ATP6V1E1 or ATP6V1A Cause Autosomal-Recessive Cutis Laxa Tim Van Damme, Thatjana Gardeitchik, Miski Mohamed, The American Journal of Human Genetics Genetic DisorderGeneticsPathogenesisMolecular GeneticsDisease Gene Identification	2017	113
MR-1S Interacts with PET100 and PET117 in Module-Based Assembly of Human Cytochrome c Oxidase Sara Vidoni, Michael E. Harbour, Sergio Guerrero‐Castillo, Cell Reports Mitochondrial BiogenesisBiochemistryProtein AssemblyProtein FoldingMitochondrial Function	2017	110
Locking loop movement in the ubiquinone pocket of complex I disengages the proton pumps Alfredo Cabrera‐Orefice, Etienne Galemou Yoga, Christophe Wirth, Nature Communications	2018	97
A homozygous missense mutation in ERAL1, encoding a mitochondrial rRNA chaperone, causes Perrault syndrome Iliana A. Chatzispyrou, Mariëlle Alders, Sergio Guerrero‐Castillo, Human Molecular Genetics GeneticsMolecular GeneticsMendelian DisorderMitochondrial BiogenesisPerrault Syndrome	2017	86
Accessory NUMM (NDUFS6) subunit harbors a Zn-binding site and is essential for biogenesis of mitochondrial complex I Katarzyna Kmita, Christophe Wirth, Judith Warnau, Proceedings of the National Academy of Sciences	2015	83
Bi-allelic Mutations in the Mitochondrial Ribosomal Protein MRPS2 Cause Sensorineural Hearing Loss, Hypoglycemia, and Multiple OXPHOS Complex Deficiencies Thatjana Gardeitchik, Miski Mohamed, Benedetta Ruzzenente, The American Journal of Human Genetics Bi-allelic MutationsMitochondrial BiogenesisMitochondrial FunctionGeneticsPhysiology	2018	83

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