Massimo Pandolfo

26.8k citations

207 papers · 10.0k indexed · 2 hit papers · h-index 55

Impact in

Cellular and Molecular Neuroscience top 0.1%
- Genetic Neurodegenerative Diseases
Neurology top 0.5%
- Neurological disorders and treatments
- Parkinson's Disease Mechanisms and Treatments
- Neurological diseases and metabolism

Papers in

Cellular and Molecular Neuroscience 140
- Genetic Neurodegenerative Diseases 130
- Neuroscience and Neuropharmacology Research 14
Neurology 56
- Neurological disorders and treatments 23
- Parkinson's Disease Mechanisms and Treatments 19

Co-authors: Laura Montermini Sarn Jiralerspong Keiichi Ohshima Robert D. Wells Jerry Kaplan Myriam Rai Michael Babcock Annalisa Pastore
Journals: Neurology (21 papers)Human Molecular Genetics (11 papers)Nucleic Acids Research (6 papers)Journal of Neurology (6 papers)Annals of Neurology (6 papers)
Partner nations: Belgium United States Canada

In The Last Decade

Massimo Pandolfo

205 papers receiving 9.8k citations

Hit Papers

align trajectories log scale

Frataxin is Reduced in Friedreich Ataxia Patients and is Associated with Mitochondrial Membranes 1997 · 602 citations

Peers

Countries citing papers authored by Massimo Pandolfo

Since Specialization

Citations

This map shows the geographic impact of Massimo Pandolfo'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 Massimo Pandolfo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Massimo Pandolfo more than expected).

Fields of papers citing papers by Massimo Pandolfo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Massimo Pandolfo. 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 Massimo Pandolfo. The network helps show where Massimo Pandolfo may publish in the future.

Co-authors

The 25 scholars most cited alongside Massimo Pandolfo, 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 Massimo Pandolfo Line = papers co-authored together Massimo Pandolfo links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Friedreich's ataxia—a rare multisystem disease The Lancet Neurology ·Kathrin Reetz, Stella A. Glasmacher, Imis Dogan, Claire Didszun, Miguel Pishnamaz, Kerstin Konrad, Katharina Schuett, Jennifer Farmer, David R. Lynch, Louise A. Corben, Massimo Pandolfo, Jörg B. Schulz, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown)	2025	4
2	Friedreich Ataxia Neurology Genetics ·Massimo Pandolfo	2025	1
3	Test–retest reliability of the Friedreich’s ataxia rating scale Annals of Clinical and Translational Neurology ·Christian Rummey, Theresa A. Zesiewicz, Santiago Perez‐Lloret, Jennifer Farmer, Massimo Pandolfo, David R. Lynch	2020	10
4	Age of onset determines intrinsic functional brain architecture in Friedreich ataxia Annals of Clinical and Translational Neurology ·Gilles Naeije, Vincent Wens, Nicolas Coquelet, Jyothi Vishnu Vardhan Kola, Serge Goldman, Massimo Pandolfo, Xavier De Tiège	2019	19
5	Unveiling a common mechanism of apoptosis in β-cells and neurons in Friedreich's ataxia Human Molecular Genetics ·Mariana Igoillo‐Esteve, Ewa Gurgul-Convey, Amélie Hu, Laila R.B. Santos, Baroj Abdulkarim, Satyan Chintawar, Lorella Marselli, Piero Marchetti, Jean‐Christophe Jonas, Décio L. Eizirik, Massimo Pandolfo, Miriam Cnop	2014	54
6	Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6 Brain ·Kathrin Reetz, Ana Sofia Costa, Shahram Mirzazade, Yosufzai Hk, Hungary Levente, Maria Rakowicz, Romana Bogusławska, Lüdger Schöls, Christoph Linnemann, Caterina Mariotti, Marina Grisoli, Alexandra Dürr, Bart P.C. van de Warrenburg, Dagmar Timmann, Massimo Pandolfo, Peter Bauer, Heike Jacobi, Till‐Karsten Hauser, Thomas Klockgether, Jörg B. Schulz, (unknown)	2013	109
7	Suggestive evidence for a new locus for epilepsy with heterogeneous phenotypes on chromosome 17q Epilepsy Research ·Auli Sirén, Anne Polvi, Christian Cava, Malgorzata Labuda, Buckley Jg, Anna‐Kaisa Anttonen, Maria Kousi, Kari Hirvonen, K. O. J. Simola, Eva Andermann, Asta Laiho, Juhani T. Soini, Dick Minnerly, Reijo Laaksonen, Massimo Pandolfo, Anna‐Elina Lehesjoki	2009	14
8	TARDBP (TDP‐43) sequence analysis in patients with familial and sporadic ALS: identification of two novel mutations European Journal of Neurology ·Roberto Del Bo, Serena Ghezzi, Stefania Corti, Massimo Pandolfo, Michela Ranieri, Domenico Santoro, 成立张, A. Prelle, ΕΥΑΓΓΕΛΟΣ ΒΑΤΣΟΣ, Michelangelo Mancuso, Gianni Sorarú, Chiara Briani, C. Angelini, Gabriele Siciliano, Nereo Bresolin, Giacomo P. Comi	2009	81
9	HDAC Inhibitors Correct Frataxin Deficiency in a Friedreich Ataxia Mouse Model PLoS ONE ·Myriam Rai, Elisabetta Soragni, Bhagyalaxmi Madapur, Ryan Burnett, David Herman, Giovanni Coppola, Daniel H. Geschwind, Joel Gottesfeld, Massimo Pandolfo	2008	172
10	Effects of anti–glutamic acid decarboxylase antibodies associated with neurological diseases Annals of Neurology ·Mario‐Ubaldo Manto, Marie-Aline Laute, Michèle Aguera, Véronique Rogemond, Massimo Pandolfo, Jérôme Honnorat	2007	187
11	Iron and Friedreich ataxia PubMed ·Massimo Pandolfo	2006	38
12	Gene expression profiling in frataxin deficient mice: Microarray evidence for significant expression changes without detectable neurodegeneration Neurobiology of Disease ·Giovanni Coppola, Sang-Hyun Choi, Miguel M. Santos, Carlos J. Miranda, Dmitri Tentler, Eric Wexler, Massimo Pandolfo, Daniel H. Geschwind	2006	40
13	Mild Epilepsy Phenotype in TSC2 Patients with Codon 905 Mutations Epilepsia ·Anna Jansen, Őzgür Sancak, Daniela D’Agostino, AmanPreet Badhwar, Penelope Roberts, G. Gobbi, E. Harre, Denis Melanson, I Vălkov, Madeleine Gans, A M van den Ouweland, Mark Nellist, Massimo Pandolfo, Katherine B. Sims, Elizabeth A. Thiele, Frédérick Andermann, François Dubeau, David J. Kwiatkowski, Dicky Halley, E. Andermann	2005	2
14	Sticky DNA Molecular Cell ·Naoaki Sakamoto, Paul D. Chastain, Paweł Parniewski, Keiichi Ohshima, Massimo Pandolfo, Jack D. Griffith, Robert D. Wells	1999	249
15	Mapping of a Gene Determining Familial Partial Epilepsy with Variable Foci to Chromosome 22q11-q12 The American Journal of Human Genetics ·Lan Xiong, Malgorzata Labuda, Dongsheng Li, Thomas J. Hudson, Richard Desbiens, Albert Costa Roig, Dennis Minano, Pierre Langevin, Suha Mercho, Stephen Barman, Ingrid E. Scheffer, François Dubeau, Samuel F. Berkovic, Frédérick Andermann, Eva Andermann, Massimo Pandolfo	1999	69
16	Molecular genetics and pathogenesis of Friedreich ataxia Neuromuscular Disorders ·Massimo Pandolfo	1998	50
17	Frataxin is Reduced in Friedreich Ataxia Patients and is Associated with Mitochondrial Membranes Human Molecular Genetics ·Victoria Campuzano, Laura Montermini, Yves Lutz, Lidia Cova, C. Hindelang, Sarn Jiralerspong, Yvon Trottier, Stephen J. Kish, Baptiste Faucheux, P Trouillas, François‐Jérôme Authier, Alexandra Dürr, Jean‐Louis Mandel, Angelo L. Vescovi, Massimo Pandolfo, M. Kœnig Hit paper breakdown →	1997	602
18	Mapping of genes predisposing to idiopathic generalized epilepsy Human Molecular Genetics ·Federico Zara, 林振礼, G. Avanzini, Stefano Di Donato, Barbara Castellotti, Pragna I. Patel, Massimo Pandolfo	1995	93
19	Mapping of Friedreich's AtaxiaLocus by Identification ofRecombination Events in PatientsHomozygous by Descent European Journal of Human Genetics ·María Dolores Moltó, Juan J. Vílchez, Massimo Pandolfo, Sakshi Tiwari, R. de Frutos, Félix Prieto, Michel Kœnig, Francesc Palau, Eugènia Monrós, Alexandra Brajnovits, François Rodius, Joaquı́n Cañizares	1994	8
20	Evidence of a genetic marker associated with early onset in Friedreich's ataxia Journal of Neurology ·Sergio Cocozza, A. Antonelli, G Campanella, Francesca Cavalcanti, Giuseppe De Michele, Stefano Di Donato, Alessandro Filla, Antonella Monticelli, Luigi Pianese, Anna Lisa Piccinelli, Antonio Porcellini, S. J. Lowry, S Varrone, Massimo Pandolfo	1993	2

About Massimo Pandolfo

Massimo Pandolfo is a scholar working on Cellular and Molecular Neuroscience, Neurology, Clinical Biochemistry, Molecular Biology and Neurology, having authored 207 papers that have together received 10.0k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (130 papers), Mitochondrial Function and Pathology (109 papers), Neurological disorders and treatments (23 papers), Endoplasmic Reticulum Stress and Disease (22 papers), Parkinson's Disease Mechanisms and Treatments (19 papers), DNA Repair Mechanisms (18 papers), Metabolism and Genetic Disorders (17 papers) and Neuroscience and Neuropharmacology Research (14 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (6.2k citations), Neurology (2.3k citations), Molecular Biology (7.3k citations), Neurology (750 citations) and Clinical Biochemistry (497 citations). Massimo Pandolfo has collaborated with scholars based in Belgium, United States and Canada. Frequent co-authors include Laura Montermini, Sarn Jiralerspong, Keiichi Ohshima, Robert D. Wells, Jerry Kaplan, Myriam Rai, Michael Babcock, Annalisa Pastore, Sandra R. Davis-Kaplan and Robert Oaks. Their work appears in journals such as Neurology, Human Molecular Genetics, Nucleic Acids Research, Journal of Neurology and Annals of Neurology.

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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