Jorge Pinto‐Basto

815 total citations
25 papers, 414 citations indexed

About

Jorge Pinto‐Basto is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Jorge Pinto‐Basto has authored 25 papers receiving a total of 414 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 9 papers in Genetics and 6 papers in Cellular and Molecular Neuroscience. Recurrent topics in Jorge Pinto‐Basto's work include Hereditary Neurological Disorders (6 papers), Genetic Neurodegenerative Diseases (5 papers) and Neurological diseases and metabolism (4 papers). Jorge Pinto‐Basto is often cited by papers focused on Hereditary Neurological Disorders (6 papers), Genetic Neurodegenerative Diseases (5 papers) and Neurological diseases and metabolism (4 papers). Jorge Pinto‐Basto collaborates with scholars based in Portugal, Germany and United States. Jorge Pinto‐Basto's co-authors include Jorge Sequeiros, Isabel Alonso, Alda Sousa, Patrı́cia Maciel, Mafalda Barbosa, Clara Barbot, Anabela Ferro, Elı́sio Costa, José Barbot and Gabriela Soares and has published in prestigious journals such as Journal of Bone and Mineral Research, Journal of the Neurological Sciences and Journal of Neuroimmunology.

In The Last Decade

Jorge Pinto‐Basto

25 papers receiving 402 citations

Peers

Countries citing papers authored by Jorge Pinto‐Basto

Since Specialization

Citations

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

Fields of papers citing papers by Jorge Pinto‐Basto

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jorge Pinto‐Basto. 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 Jorge Pinto‐Basto. The network helps show where Jorge Pinto‐Basto may publish in the future.

Co-authorship network of co-authors of Jorge Pinto‐Basto

This figure shows the co-authorship network connecting the top 25 collaborators of Jorge Pinto‐Basto. A scholar is included among the top collaborators of Jorge Pinto‐Basto based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Jorge Pinto‐Basto. Jorge Pinto‐Basto is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	The Liberfarb syndrome, a multisystem disorder affecting eye, ear, bone, and brain development, is caused by a founder pathogenic variant in the PISD gene 2019 ·Genetics in Medicine ·Virginie G. Peter, Mathieu Quinodoz, Jorge Pinto‐Basto, Sérgio B. Sousa, Silvio Alessandro Di Gioia, Gabriela Soares, Gabriela Ferraz Leal, Eduardo Silva, Rosanna Pescini Gobert, Noriko Miyake, Naomichi Matsumoto, Elizabeth C. Engle, Sheila Unger, Frederic Shapiro, Andrea Superti‐Furga, Carlo Rivolta, Belinda Campos‐Xavier	35
2	The first Portuguese family with NEFL-related Charcot-Marie-Tooth type 2 disease. 2019 ·PubMed ·(unknown), Jorge Pinto‐Basto, Luís Negrão	1
3	Bethlem myopathy in a Portuguese patient - case report. 2017 ·PubMed ·Ana Inês Martins, (unknown), Jorge Pinto‐Basto, Luís Negrão	6
4	Whole Gene Deletion of EBF3 Supporting Haploinsufficiency of This Gene as a Mechanism of Neurodevelopmental Disease 2017 ·Frontiers in Genetics ·Fátima Lopes, Gabriela Soares, (unknown), Jorge Pinto‐Basto, Patrı́cia Maciel	14
5	Elevation of gamma-glutamyl transferase in adult: Should we think about progressive familiar intrahepatic cholestasis? 2015 ·Digestive and Liver Disease ·(unknown), (unknown), Ermelinda Santos Silva, Jorge Pinto‐Basto, Helena Miranda	6
6	Charcot-Marie-Tooth 4B2 caused by a novel mutation in the MTMR13/SBF2 gene in two related Portuguese families. 2014 ·PubMed ·Luís Negrão, Luciano Almendra, (unknown), (unknown), (unknown), Jorge Pinto‐Basto	3
7	Autosomal Dominant Spastic Paraplegias 2013 ·JAMA Neurology ·José Leal Loureiro, (unknown), Luís Ruano, (unknown), Ana M. Lopes, (unknown), Leonor Miller‐Fleming, Vítor Tedim Cruz, Mafalda Barbosa, Isabel Silveira, Giovanni Stévanin, Jorge Pinto‐Basto, Jorge Sequeiros, Isabel Alonso, Paula Coutinho	37
8	Alu elements mediate large SPG11 gene rearrangements: further spatacsin mutations 2012 ·Genetics in Medicine ·(unknown), José Leal Loureiro, Jorge Pinto‐Basto, (unknown), Ana M. Lopes, (unknown), (unknown), Ruth Geraldes, Isabel Pavão Martins, Vítor Tedim Cruz, Erik‐Jan Kamsteeg, Han G. Brunner, Paula Coutinho, Jorge Sequeiros, Isabel Alonso	21
9	FXTAS is rare among Portuguese patients with movement disorders: FMR1 premutations may be associated with a wider spectrum of phenotypes 2011 ·Behavioral and Brain Functions ·Ana I. Seixas, José Vale, Paula Jorge, (unknown), Rosário Santos, Isabel Alonso, Ana María Fortuna, Jorge Pinto‐Basto, Paula Coutinho, Russell L. Margolis, Jorge Sequeiros, Isabel Silveira	7
10	[Osteopathia striata with cranial sclerosis]. 2011 ·PubMed ·Mafalda Barbosa, Bram Perdu, (unknown), Filipe Macedo, Wim Van Hul, (unknown), Jorge Pinto‐Basto	7
11	Scope of definitions of genetic testing: evidence from a EuroGentest survey 2010 ·Journal of Community Genetics ·Jorge Pinto‐Basto, (unknown), (unknown), (unknown), (unknown), Jean‐Jacques Cassiman, Helena Kääriäinen, Ulf Kristoffersson, Jörg Schmidtke, Jorge Sequeiros	10
12	Sensory neuronopathy in ataxia with oculomotor apraxia type 2 2010 ·Journal of the Neurological Sciences ·José Gazulla, Isabel Benavente‐Fernández, (unknown), (unknown), Pedro J. Modrego, Isabel Alonso, Jorge Pinto‐Basto	7
13	Clinical and molecular characterization of Diastrophic Dysplasia in the Portuguese population 2010 ·Clinical Genetics ·(unknown), Ana Berta Sousa, Ana Medeira, (unknown), Jorge Saraiva, Jorge Pinto‐Basto, (unknown), Ana María Fortuna, Andrea Superti‐Furga, (unknown), (unknown), Luisa Bonafé	13
14	Large normal and reduced penetrance alleles in Huntington disease: instability in families and frequency at the laboratory, at the clinic and in the population 2010 ·Clinical Genetics ·Jorge Sequeiros, (unknown), (unknown), (unknown), Alda Sousa, Jorge Pinto‐Basto, Isabel Alonso	51
15	Osteopathia striata with cranial sclerosis owing to WTX gene defect 2009 ·Journal of Bone and Mineral Research ·Bram Perdu, Fenna de Freitas, Suzanna G.M. Frints, Meyke Schouten, Connie Schrander‐Stumpel, Mafalda Barbosa, Jorge Pinto‐Basto, (unknown), Marie‐Christine de Vernejoul, Kristin Becker, (unknown), Kathelijn Keymolen, Eric Haan, Ravi Savarirayan, Rainer Koenig, Bernhard Zabel, Filip Vanhoenacker, Wim Van Hul	50
16	Muenke syndrome with osteochondroma 2008 ·American Journal of Medical Genetics Part A ·Mafalda Barbosa, Maria Rosário Almeida, (unknown), Jorge Pinto‐Basto, Heloísa G. dos Santos	6
17	Molecular characterization of Portuguese patients with mucopolysaccharidosis type II shows evidence that the IDS gene is prone to splicing mutations 2006 ·Journal of Inherited Metabolic Disease ·Sandra Alves, (unknown), Maria João Prata, G. Ribeiro, Lurdes Lopes, Helena Ribeiro, Jorge Pinto‐Basto, (unknown), Lúcia Lacerda	31
18	Genotypes at the APOE and SCA2 loci do not predict the course of multiple sclerosis in patients of Portuguese origin 2004 ·Multiple Sclerosis Journal ·Mònica Santos, Maria do Carmo Costa, Maria Edite Rio, María José Sá, Marta Chagas Monteiro, (unknown), (unknown), José Dinis, (unknown), (unknown), (unknown), Isabel Coelho, Teresa Matamá, Jorge Pinto‐Basto, Jorge Sequeiros, Patrı́cia Maciel	23
19	Inherited and acquired risk factors and their combined effects in pediatric stroke 2003 ·Pediatric Neurology ·(unknown), Anabela Ferro, (unknown), Elı́sio Costa, Jorge Pinto‐Basto, Alda Sousa, Jorge Sequeiros, Patrı́cia Maciel, Clara Barbot, José Barbot	58
20	A whole genome screen for association with multiple sclerosis in Portuguese patients 2003 ·Journal of Neuroimmunology ·Mònica Santos, Jorge Pinto‐Basto, M. E. Rio, María José Sá, (unknown), (unknown), José Dinis, (unknown), (unknown), I. Coelho, Stephen Sawcer, Efrosini Setakis, Alastair Compston, Jorge Sequeiros, Patrı́cia Maciel	8

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.

Explore authors with similar magnitude of impact