M. Girós

1.5k citations

40 papers · 749 indexed · h-index 16

Impact in

Clinical Biochemistry top 2%
- Metabolism and Genetic Disorders
Physiology top 10%
- Adipose Tissue and Metabolism
- Lysosomal Storage Disorders Research

Papers in ⓘ

Molecular Biology 28
- Peroxisome Proliferator-Activated Receptors 21
Clinical Biochemistry 13
- Metabolism and Genetic Disorders 13

Co-authors: Teresa Pàmpols (14 shared papers)Montserrat Ruíz (9 shared papers)Carme Camps (3 shared papers)Aurora Pujol (3 shared papers)Isidró Ferrer (3 shared papers)Jean‐Louis Mandel (2 shared papers)C. Hindelang (1 shared paper)Noëlle Callizot (1 shared paper)
Journals: Journal of Inherited Metabolic Disease (8 papers)Advances in experimental medicine and biology (2 papers)Human Molecular Genetics (2 papers)Acta Neuropathologica (2 papers)Human Mutation (2 papers)
Partner nations: Spain Belgium United Kingdom

In The Last Decade

M. Girós

36 papers receiving 736 citations

Peers

Countries citing papers authored by M. Girós

Since Specialization

Citations

This map shows the geographic impact of M. Girós's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by M. Girós with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M. Girós more than expected).

Fields of papers citing papers by M. Girós

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M. Girós. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by M. Girós. The network helps show where M. Girós may publish in the future.

Co-authors

The 25 scholars most cited alongside M. Girós, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with M. Girós Line = papers co-authored together M. Girós links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 40 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Functional overlap between ABCD1 (ALD) and ABCD2 (ALDR) transporters: a therapeutic target for X-adrenoleukodystrophy Human Molecular Genetics ·Aurora Pujol, Isidró Ferrer, Carme Camps, Elisabeth Metzger, C. Hindelang, Noëlle Callizot, Montserrat Ruíz, Teresa Pàmpols, M. Girós, Jean‐Louis Mandel	2004	158
2	A key role for the peroxisomalABCD2transporter in fatty acid homeostasis American Journal of Physiology-Endocrinology and Metabolism ·Stéphane Fourcade, Montserrat Ruíz, Carme Camps, Agatha Schlüter, Sander M. Houten, P. A. W. Mooyer, Teresa Pàmpols, G. Dacremont, Ronald J. A. Wanders, M. Girós, Aurora Pujol	2008	86
3	Cholestane-3β,5α,6β-triol: high levels in Niemann-Pick type C, cerebrotendinous xanthomatosis, and lysosomal acid lipase deficiency Journal of Lipid Research ·Sonia Pajares, Ángela Arias, Judit García‐Villoria, Judit Macías‐Vidal, Emilio Ros, Javier de las Heras, M. Girós, María Josep Coll, Antònia Ribes	2015	52
4	Evaluation of the Preventive Effect of Glyceryl Trioleate-Trierucate (“Lorenzo’s Oil”) Therapy in X-Linked Adrenoleukodystrophy: Results of Two Concurrent Trials Advances in experimental medicine and biology ·Hugo W. Moser, Gerald V. Raymond, Wolfgang Köehler, Piotr Sokolowski, F. Hanefeld, Georg Christoph Korenke, A. J. Green, Daniel J. Loes, D. H. Hunneman, Richard O. Jones, Shou‐En Lu, Graziella Uziel, M. Girós, Frank Roels	2003	42
5	Neuronopathic juvenile glucosylceramidosis due to sap -C deficiency: clinical course, neuropathology and brain lipid composition in this Gaucher disease variant Acta Neuropathologica ·Teresa Pàmpols, M. Pineda, M. Girós, Isidró Ferrer, V. Cusí, Amparo Chabás, Francesc Sanmartí, M. T. Vanier, H. Christomanou	1999	38
6	Autophagy induction halts axonal degeneration in a mouse model of X-adrenoleukodystrophy Acta Neuropathologica ·Nathalie Launay, Carmen Aguado, Stéphane Fourcade, Montserrat Ruíz, Laia Grau, Jordi Riera, Cristina Guilera, M. Girós, Isidró Ferrer, Erwin Knecht, Aurora Pujol	2014	38
7	X‐linked adrenoleukodystrophy in Spain. Identification of 26 novel mutations in the ABCD1 gene in 80 patients. Improvement of genetic counseling in 162 relative females Clinical Genetics ·MJ Coll, Núria Palau, Carme Camps, Montserrat Ruíz, Teresa Pàmpols, M. Girós	2005	28
8	A Population-Based Study on Congenital Disorders of Protein N- and Combined with O-Glycosylation Experience in Clinical and Genetic Diagnosis The Journal of Pediatrics ·Celia Pérez‐Cerdá, M. Girós, Mercedes Serrano, María Jesús Ecay, Laura Gort, Belén Pérez‐Dueñas, Celia Medrano, Alfredo García‐Alix, Rafael Artuch, Paz Briones, Belén Pérez	2017	26
9	Identification of a new frameshift mutation (1801delAG) in the ALD gene Human Molecular Genetics ·Anna Barceló, M. Girós, Claude‐Olivier Sarde, A Martínez-Bermejo, Jean‐Louis Mandel, Teresa Pàmpols, Xavier Estivill	1994	23
10	The proteasome inhibitor bortezomib reduced cholesterol accumulation in fibroblasts from Niemann–Pick type C patients carrying missense mutations FEBS Journal ·Judit Macías‐Vidal, M. Girós, Martina Guerrero‐Hernández, Pere Gascón, Joan Serratosa, Oriol Bachs, María Josep Coll	2014	22
11	Second spontaneous pregnancy in a galactosaemic woman homozygous for the Q188R mutation Journal of Inherited Metabolic Disease ·P. Briones, M. Girós, Victoria Marinella Rivera Martínez	2001	20
12	Lysine Restriction and Pyridoxal Phosphate Administration in a NADK2 Patient PEDIATRICS ·Frederic Tort, Olatz Ugarteburu, María Ángeles Torres, Judit García‐Villoria, M. Girós, Ángeles Ruiz, Antònia Ribes	2016	18
13	Immunolocalization of a 43 kDa peroxisomal membrane protein in the liver of patients with generalized peroxisomal disorders. PubMed ·Marc Espeel, Frank Roels, M. Girós, Hanna Mandel, Amanda Peltier, F Poggi, Bwee Tien Poll‐The, Jan Smeıtınk, Lionel Van Maldergem, María José Santos	1995	18
14	Mutational spectrum of classical galactosaemia in Spain and Portugal Journal of Inherited Metabolic Disease ·Laura Gort, Ma Dolores Boleda, Linda Tyfield, Laura Vilarinho, Isabel Rivera, Maria Luı́s Cardoso, M. Santos‐Leite, M. Girós, P. Briones	2006	18
15	The role of the abnormalities in the distal pathway of cholesterol biosynthesis in the Conradi–Hünermann–Happle syndrome Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids ·Javier Cañueto, M. Girós, Rogelio González‐Sarmiento	2013	15
16	Usefulness of cholestanol levels in the diagnosis and follow-up of patients with cerebrotendinous xanthomatosis SHILAP Revista de lepidopterología ·B. Pilo de la Fuente, M.J. Sobrido, M. Girós, Lucila Paulina Rosas Pozo, M. Lustres, Francisco Javier Barrero, Jesús Macarrón, Muñoz Díaz, Adriano Jiménez‐Escrig	2011	15
17	Diagnosis and Follow-Up of a Case of Peroxisomal Disorder With Peroxisomal Mosaicism Journal of Child Neurology ·Mercédes Pineda, M. Girós, Frank Roels, Marc Espeel, Montserrat Ruíz, Ann B. Moser, Hugo W. Moser, Ronald J. A. Wanders, Carlos Pavía, Juan Conill, Asunción Aracil, Luis Amat, Teresa Pàmpols	1999	15
18	Lowβ‐glucuronidase activity in a healthy member of a family with mucopolysaccharidosis VII Journal of Inherited Metabolic Disease ·Amparo Chabás, M. Girós, Ana Guardiola	1991	15
19	Long Survival in a Case of Peroxisomal Biogenesis Disorder with Peroxisome Mosaicism in the Liver Annals of the New York Academy of Sciences ·M. Girós, Frank Roels, J M Prats, Montserrat Ruíz, Antònia Ribes, Marc Espeel, Ronald J. A. Wanders, R. B. H. Schutgens, Teresa Pàmpols	1996	14
20	Peroxisome Mosaics in the Liver of Patients and the Regulation of Peroxisome Expression in Rat Hepatocyte Cultures^a Annals of the New York Academy of Sciences ·Frank Roels, Tom Tytgat, Sonja Beken, M. Girós, Marc Espeel, B. De Prest, Ingrid Kerckaert, Teresa Pàmpols, Vera Rogiers	1996	13

About M. Girós

M. Girós is a scholar working on Molecular Biology, Clinical Biochemistry, Physiology, Surgery and Biochemistry, having authored 40 papers that have together received 749 indexed citations. Recurring topics across this work include Peroxisome Proliferator-Activated Receptors (21 papers), Metabolism and Genetic Disorders (13 papers), Adipose Tissue and Metabolism (8 papers), Cholesterol and Lipid Metabolism (6 papers), Lysosomal Storage Disorders Research (5 papers), Pancreatic function and diabetes (3 papers), Fatty Acid Research and Health (3 papers) and Lipid metabolism and biosynthesis (3 papers). The work is most often cited by research in Clinical Biochemistry (215 citations), Physiology (48 citations), Physiology (267 citations), Biochemistry (74 citations) and Molecular Biology (556 citations). M. Girós has collaborated with scholars based in Spain, Belgium and United Kingdom. Frequent co-authors include Teresa Pàmpols, Montserrat Ruíz, Carme Camps, Aurora Pujol, Isidró Ferrer, Jean‐Louis Mandel, C. Hindelang, Noëlle Callizot, Stéphane Fourcade and Ronald J. A. Wanders. Their work appears in journals such as Journal of Inherited Metabolic Disease, Advances in experimental medicine and biology, Human Molecular Genetics, Acta Neuropathologica and Human Mutation.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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