Jorge Sequeiros

9.7k citations

209 papers · 5.0k indexed · h-index 39

Impact in

Cellular and Molecular Neuroscience top 0.5%
- Genetic Neurodegenerative Diseases
Neurology top 1%
- Neurological disorders and treatments
- Parkinson's Disease Mechanisms and Treatments
- Neurological diseases and metabolism

Papers in ⓘ

Molecular Biology 123
- Mitochondrial Function and Pathology 78
- DNA Repair Mechanisms 36
- Amyloidosis: Diagnosis, Treatment, Outcomes 19
Cellular and Molecular Neuroscience 111
- Genetic Neurodegenerative Diseases 108

Co-authors: Paula Coutinho (39 shared papers)Isabel Silveira (34 shared papers)Alda Sousa (33 shared papers)José Barros (29 shared papers)Isabel Alonso (49 shared papers)Teresa Coelho (15 shared papers)Patrı́cia Maciel (28 shared papers)Laura Bannach Jardim (21 shared papers)
Journals: European Journal of Human Genetics (20 papers)Clinical Genetics (10 papers)Public Health Genomics (4 papers)The Cerebellum (4 papers)Acta Neurologica Scandinavica (4 papers)
Partner nations: Portugal France United Kingdom

In The Last Decade

Jorge Sequeiros

204 papers receiving 4.9k citations

Peers

Countries citing papers authored by Jorge Sequeiros

Since Specialization

Citations

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

Fields of papers citing papers by Jorge Sequeiros

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Jorge Sequeiros, 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 Jorge Sequeiros Line = papers co-authored together Jorge Sequeiros 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 209 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	The gene mutated in ataxia-ocular apraxia 1 encodes the new HIT/Zn-finger protein aprataxin Nature Genetics ·Maria-Céu Moreira, Clara Barbot, Nobutada Tachi, Naoki Kozuka, Eiji Uchida, Toby J. Gibson, Pedro Mendonça, Maria Manuela Ribeiro Costa, José Barros, Takayuki Yanagisawa, Masao Watanabe, Yoshio Ikeda, Masashi Aoki, Tetsuya Nagata, Paula Coutinho, Jorge Sequeiros, Michel Kœnig	2001	323
2	Genetic epidemiology of familial amyloidotic polyneuropathy (FAP)‐type I in Póvoa do Varzim and Vila do Conde (north of Portugal) American Journal of Medical Genetics ·Alda Sousa, Teresa Coelho, José Barros, Jorge Sequeiros	1995	192
3	Epidemiology and clinical aspects of Machado-Joseph disease. PubMed ·Jorge Sequeiros, Paula Coutinho	1993	160
4	Frataxin knockin mouse FEBS Letters ·Carlos J. Miranda, Miguel M. Santos, Keiichi Ohshima, Julie Smith, Liangtao Li, Michaeline Bunting, Mireille Cossée, Michael L. Koenig, Jorge Sequeiros, Jerry Kaplan, Massimo Pandolfo	2002	130
5	The interface between assisted reproductive technologies and genetics: technical, social, ethical and legal issues European Journal of Human Genetics ·(unknown), Sirpa Soini, Dolores Ibarreta, Violetta Anastasiadou, Ségolène Aymé, Suzanne Braga, Martina C. Cornel, Domenico Coviello, Gerry Evers‐Kiebooms, Joep Geraedts, Luca Gianaroli, Joyce Harper, György Kosztolányi, Kersti Lundin, Emilio Rodrigues-Cerezo, Karen Sermon, Jorge Sequeiros, Lisbeth Tranebjærg, Helena Kääriäinen	2006	112
6	Neurologic Findings in Machado-Joseph Disease Archives of Neurology ·Laura Bannach Jardim, Maria Luiza Saraiva Pereira, Isabel Silveira, Anabela Ferro, Jorge Sequeiros, Roberto Giugliani	2001	109
7	Hereditary Ataxia and Spastic Paraplegia in Portugal JAMA Neurology ·Paula Coutinho, Luís Ruano, José Leal Loureiro, Vítor Tedim Cruz, José Barros, Assunção Tuna, Clara Barbot, João Tiago Guimarães, Isabel Alonso, Isabel Silveira, Jorge Sequeiros, José Marques Neves, Pedro Serrano, Carolina Silva	2013	96
8	Mutations in PNKP Cause Recessive Ataxia with Oculomotor Apraxia Type 4 The American Journal of Human Genetics ·José Brás, Isabel Alonso, Clara Barbot, Maria Manuela Costa, Lee Darwent, Tatiana Orme, Jorge Sequeiros, John Hardy, Paula Coutinho, Rita Guerreiro	2015	93
9	Ataxia Rating Scales—Psychometric Profiles, Natural History and Their Application in Clinical Trials The Cerebellum ·(unknown), Jonas Alex Morales Saute, Karina Carvalho Donis, Carmen Serrano, David Genı́s, Luis Torres Ramírez, Pilar Mazzetti, Luis Velázquez‐Pérez, Pilar Latorre, Jorge Sequeiros, Antoni Matilla‐Dueñas, Laura Bannach Jardim	2011	92
10	First Mutation in the Voltage-Gated Na_v1.1 Subunit Gene SCN1A with Co-Occurring Familial Hemiplegic Migraine and Epilepsy Cephalalgia ·M‐J Castro, AH Stam, Carolina Lemos, Boukje de Vries, KRJ Vanmolkot, José Barros, GM Terwindt, R.R. Frants, Jorge Sequeiros, Michel D. Ferrari, José Pereira‐Monteiro, AMJM van den Maagdenberg	2008	74
11	How communication of genetic information within the family is addressed in genetic counselling: a systematic review of research evidence European Journal of Human Genetics ·Álvaro Mendes, Milena Paneque, Liliana Sousa, Angus Clarke, Jorge Sequeiros	2015	70
12	A survey of spinocerebellar ataxia in South Brazil - 66 new cases with Machado-Joseph disease, SCA7, SCA8, or unidentified disease-causing mutations Journal of Neurology ·Laura Bannach Jardim, Isabel Silveira, Maria Luzia Pereira, Anabela Ferro, Isabel Alonso, Maria do Céu Moreira, Pedro Mendonça, Fátima Ferreirinha, Jorge Sequeiros, Roberto Giugliani	2001	70
13	Recessive Ataxia With Ocular Apraxia Archives of Neurology ·Clara Barbot, Paula Coutinho, Rui Chorão, Carla Ferreira, José Barros, Isabel Fineza, Karin Ziliotto Dias, José Paulo Monteiro, António Guimarães, Pedro Mendonça, Maria do Céu Moreira, Jorge Sequeiros	2001	68
14	Movement disorders in Rett syndrome: An analysis of 60 patients with detected MECP2 mutation and correlation with mutation type Movement Disorders ·Teresa Temudo, Elisabete Ramos, Karin Ziliotto Dias, Clara Barbot, José Pedro Vieira, Ana Moreira, Eulália Calado, Inês Carrilho, Guiomar Oliveira, A Levy, Maria José Fonseca, Alexandra Cabral, Pedro Cabral, João Monteiro, Luís Borges, Roseli Gomes, Miguel M. Santos, Jorge Sequeiros, Patrı́cia Maciel	2008	66
15	Consensus and controversies in best practices for molecular genetic testing of spinocerebellar ataxias European Journal of Human Genetics ·Jorge Sequeiros, Sara Seneca, Joanne Martindale	2010	64
16	‘Costa da Morte’ ataxia is spinocerebellar ataxia 36: clinical and genetic characterization Brain ·María García-Murias, Beatriz Quintáns, Manuel Arias, Ana I. Seixas, Pilar Cacheiro, Rosa Tarrı́o, Julio Pardo, María Jesús Rosado Millán, Susana Arias‐Rivas, Patricia Blanco, D Dapena, Ramón Moreira, Francisco Rodrı́guez-Trelles, Jorge Sequeiros, Ãngel Carracedo, Isabel Silveira, María Jesús Sobrido	2012	64
17	Phenotypes of Spinocerebellar Ataxia Type 6 and Familial Hemiplegic Migraine Caused by a Unique CACNA1A Missense Mutation in Patients From a Large Family Archives of Neurology ·Isabel Alonso, José Barros, Assunção Tuna, João Coelho, Jorge Sequeiros, Isabel Silveira, Paula Coutinho	2003	62
18	What is ideal genetic counselling? A survey of current international guidelines European Journal of Human Genetics ·Elina Rantanen, Marja Hietala, Ulf Kristoffersson, Irmgard Nippert, Jörg Schmidtke, Jorge Sequeiros, Helena Kääriäinen	2008	62
19	High Germinal Instability of the (CTG)n at the SCA8 Locus of Both Expanded and Normal Alleles The American Journal of Human Genetics ·Isabel Silveira, Isabel Alonso, Laura Guimarães, Pedro Mendonça, Célia Santos, Patrı́cia Maciel, Joao Matos, M. Costa, Clara Barbot, Assunção Tuna, José Barros, Laura Bannach Jardim, Paula Coutinho, Jorge Sequeiros	2000	61
20	Functional genomics and biochemical characterization of the C. elegans orthologue of the Machado‐Joseph disease protein ataxin‐3 The FASEB Journal ·Ana João Rodrigues, Giovanni Coppola, Cláudia Sofia Santos, Maria do Carmo Costa, Michael Ailion, Jorge Sequeiros, Daniel H. Geschwind, Patrícia Mariel	2007	60

About Jorge Sequeiros

Jorge Sequeiros is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Genetics, Neurology and Psychiatry and Mental health, having authored 209 papers that have together received 5.0k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (108 papers), Mitochondrial Function and Pathology (78 papers), DNA Repair Mechanisms (36 papers), BRCA gene mutations in cancer (29 papers), Parkinson's Disease Mechanisms and Treatments (24 papers), Amyloidosis: Diagnosis, Treatment, Outcomes (19 papers), Migraine and Headache Studies (18 papers) and Genomics and Rare Diseases (17 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (2.6k citations), Neurology (1.1k citations), Neurology (450 citations), Molecular Biology (3.3k citations) and Genetics (1.0k citations). Jorge Sequeiros has collaborated with scholars based in Portugal, France and United Kingdom. Frequent co-authors include Paula Coutinho, Isabel Silveira, Alda Sousa, José Barros, Isabel Alonso, Teresa Coelho, Patrı́cia Maciel, Laura Bannach Jardim, Carolina Lemos and Milena Paneque. Their work appears in journals such as European Journal of Human Genetics, Clinical Genetics, Public Health Genomics, The Cerebellum and Acta Neurologica Scandinavica.

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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