António Jorge dos Santos Pereira de Sequeiros
AuthID: R-000-23K
41
TITLE: Genome-wide association study identifies genetic factors that modify age at onset in Machado-Joseph disease Full Text
AUTHORS: Akçimen, F; Martins, S ; Liao, C; Bourassa, CV; Catoire, H; Nicholson, GA; Riess, O; Raposo, M; França, MC; Vasconcelos, J; Lima, M; Lopes Cendes, I; Saraiva Pereira, ML; Jardim, LB; Sequeiros, J; Dion, PA; Rouleau, GA;
PUBLISHED: 2020, SOURCE: Aging, VOLUME: 12, ISSUE: 6
AUTHORS: Akçimen, F; Martins, S ; Liao, C; Bourassa, CV; Catoire, H; Nicholson, GA; Riess, O; Raposo, M; França, MC; Vasconcelos, J; Lima, M; Lopes Cendes, I; Saraiva Pereira, ML; Jardim, LB; Sequeiros, J; Dion, PA; Rouleau, GA;
PUBLISHED: 2020, SOURCE: Aging, VOLUME: 12, ISSUE: 6
42
TITLE: Management of information within Portuguese families with Huntington disease: a transgenerational process for putting the puzzle together Full Text
AUTHORS: Oliveira, CR; Mendes, A; Sequeiros, J; Sousa, L ;
PUBLISHED: 2020, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 28, ISSUE: 9
AUTHORS: Oliveira, CR; Mendes, A; Sequeiros, J; Sousa, L ;
PUBLISHED: 2020, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 28, ISSUE: 9
43
TITLE: Novel MAG Variant Causes Cerebellar Ataxia with Oculomotor Apraxia: Molecular Basis and Expanded Clinical Phenotype
AUTHORS: Santos, M; Damasio, J; Kun Rodrigues, C; Barbot, C; Sequeiros, J; Bras, J; Alonso, I; Guerreiro, R;
PUBLISHED: 2020, SOURCE: JOURNAL OF CLINICAL MEDICINE, VOLUME: 9, ISSUE: 4
AUTHORS: Santos, M; Damasio, J; Kun Rodrigues, C; Barbot, C; Sequeiros, J; Bras, J; Alonso, I; Guerreiro, R;
PUBLISHED: 2020, SOURCE: JOURNAL OF CLINICAL MEDICINE, VOLUME: 9, ISSUE: 4
44
TITLE: Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment
AUTHORS: Roux, T; Barbier, M; Papin, M; Davoine, CS; Sayah, S; Coarelli, G; Charles, P; Marelli, C; Parodi, L; Tranchant, C; Goizet, C; Klebe, S; Lohmann, E; Van Maldergen, L; van Broeckhoven, C; Coutelier, M; Tesson, C; Stevanin, G; Duyckaerts, C; Brice, A; ...More
PUBLISHED: 2020, SOURCE: Genetics in Medicine, VOLUME: 22, ISSUE: 11
AUTHORS: Roux, T; Barbier, M; Papin, M; Davoine, CS; Sayah, S; Coarelli, G; Charles, P; Marelli, C; Parodi, L; Tranchant, C; Goizet, C; Klebe, S; Lohmann, E; Van Maldergen, L; van Broeckhoven, C; Coutelier, M; Tesson, C; Stevanin, G; Duyckaerts, C; Brice, A; ...More
PUBLISHED: 2020, SOURCE: Genetics in Medicine, VOLUME: 22, ISSUE: 11
45
TITLE: Going Deep into Synaptic Vesicle Machinery Genes and Migraine Susceptibility - A Case-Control Association Study Full Text
AUTHORS: Quintas, M; Neto, JL; Sequeiros, J; Sousa, A; Pereira Monteiro, J; Lemos, C ; Alonso, I;
PUBLISHED: 2020, SOURCE: HEADACHE, VOLUME: 60, ISSUE: 10
AUTHORS: Quintas, M; Neto, JL; Sequeiros, J; Sousa, A; Pereira Monteiro, J; Lemos, C ; Alonso, I;
PUBLISHED: 2020, SOURCE: HEADACHE, VOLUME: 60, ISSUE: 10
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TITLE: Correction: Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment (Genetics in Medicine, (2020), 22, 11, (1851-1862), 10.1038/s41436-020-0899-x)
AUTHORS: Roux, T; Barbier, M; Papin, M; Davoine, CS; Sayah, S; Coarelli, G; Charles, P; Marelli, C; Parodi, L; Tranchant, C; Goizet, C; Klebe, S; Lohmann, E; Van Maldergem, L; van Broeckhoven, C; Coutelier, M; Tesson, C; Stevanin, G; Duyckaerts, C; Brice, A; ...More
PUBLISHED: 2020, SOURCE: Genetics in Medicine, VOLUME: 23, ISSUE: 10
AUTHORS: Roux, T; Barbier, M; Papin, M; Davoine, CS; Sayah, S; Coarelli, G; Charles, P; Marelli, C; Parodi, L; Tranchant, C; Goizet, C; Klebe, S; Lohmann, E; Van Maldergem, L; van Broeckhoven, C; Coutelier, M; Tesson, C; Stevanin, G; Duyckaerts, C; Brice, A; ...More
PUBLISHED: 2020, SOURCE: Genetics in Medicine, VOLUME: 23, ISSUE: 10
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TITLE: Analyzing the Impact of Bariatric Surgery in Kidney Function: a 2-Year Observational Study Full Text
AUTHORS: Daniela S C Magalhaes; Jorge M P Pedro; Pedro E B Souteiro ; Joao Sergio Neves ; Sofia Castro Oliveira; Rita Bettencourt Silva; Maria Manuel Costa ; Ana Varela; Joana Queiros; Paula Freitas ; Davide Carvalho ;
PUBLISHED: 2019, SOURCE: OBESITY SURGERY, VOLUME: 29, ISSUE: 1
AUTHORS: Daniela S C Magalhaes; Jorge M P Pedro; Pedro E B Souteiro ; Joao Sergio Neves ; Sofia Castro Oliveira; Rita Bettencourt Silva; Maria Manuel Costa ; Ana Varela; Joana Queiros; Paula Freitas ; Davide Carvalho ;
PUBLISHED: 2019, SOURCE: OBESITY SURGERY, VOLUME: 29, ISSUE: 1
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TITLE: Comparative Effectiveness of Different Bariatric Procedures in Super Morbid Obesity Full Text
AUTHORS: Rita Bettencourt Silva; Joao Sergio Neves ; Jorge Pedro; Vanessa Guerreiro ; Maria Joao Ferreira ; Daniela Salazar; Pedro Souteiro ; Daniela Magalhaes; Sofia Castro Oliveira; Joana Queiros; Sandra Belo; Ana Varela; Paula Freitas ; Davide Carvalho ;
PUBLISHED: 2019, SOURCE: OBESITY SURGERY, VOLUME: 29, ISSUE: 1
AUTHORS: Rita Bettencourt Silva; Joao Sergio Neves ; Jorge Pedro; Vanessa Guerreiro ; Maria Joao Ferreira ; Daniela Salazar; Pedro Souteiro ; Daniela Magalhaes; Sofia Castro Oliveira; Joana Queiros; Sandra Belo; Ana Varela; Paula Freitas ; Davide Carvalho ;
PUBLISHED: 2019, SOURCE: OBESITY SURGERY, VOLUME: 29, ISSUE: 1
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TITLE: Choosing not to know: accounts of non-engagement with pre-symptomatic testing for Machado-Joseph disease
AUTHORS: Alvaro Mendes ; Milena Paneque ; Angus Clarke; Jorge Sequeiros;
PUBLISHED: 2019, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 27, ISSUE: 3
AUTHORS: Alvaro Mendes ; Milena Paneque ; Angus Clarke; Jorge Sequeiros;
PUBLISHED: 2019, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 27, ISSUE: 3
50
TITLE: Mutational mechanism for DAB1 (ATTTC)(n) insertion in SCA37: ATTTT repeat lengthening and nucleotide substitution Full Text
AUTHORS: Loureiro, JR; Oliveira, CL; Mota, C; Castro, AF; Costa, C; Loureiro, JL; Coutinho, P; Martins, S ; Sequeiros, J; Silveira, I;
PUBLISHED: 2019, SOURCE: HUMAN MUTATION, VOLUME: 40, ISSUE: 4
AUTHORS: Loureiro, JR; Oliveira, CL; Mota, C; Castro, AF; Costa, C; Loureiro, JL; Coutinho, P; Martins, S ; Sequeiros, J; Silveira, I;
PUBLISHED: 2019, SOURCE: HUMAN MUTATION, VOLUME: 40, ISSUE: 4
