Miguel Fernando Alves Ferreira
AuthID: R-001-S4X
1
TITLE: Integrating functional scoring and regulatory data to predict the effect of non-coding SNPs in a complex neurological disease Full Text
AUTHORS: Felicio, Daniela; Alves Ferreira, Miguel; Santos, Mariana; Quintas, Marlene; Lopes, Alexandra M.; Lemos, Carolina ; Pinto, Nadia ; Martins, Sandra ;
PUBLISHED: 2023, SOURCE: BRIEFINGS IN FUNCTIONAL GENOMICS
AUTHORS: Felicio, Daniela; Alves Ferreira, Miguel; Santos, Mariana; Quintas, Marlene; Lopes, Alexandra M.; Lemos, Carolina ; Pinto, Nadia ; Martins, Sandra ;
PUBLISHED: 2023, SOURCE: BRIEFINGS IN FUNCTIONAL GENOMICS
INDEXED IN: 
WOS
WOS2
TITLE: RAMP1 PROMOTER METHYLATION STATUS IN PORTUGUESE AND SPANISH WOMEN WITH MIGRAINE Full Text
AUTHORS: Carvalho, Estefania; Dias, Andreia; Guerrero, Angel L.; Gomez, Carlos; Sousa, Alda; Lopes, Alexandra M.; Martins, Sandra; Pinto, Nadia ; Lemos, Carolina; Alves Ferreira, Miguel;
PUBLISHED: 2023, SOURCE: 26th Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 102, ISSUE: 13
AUTHORS: Carvalho, Estefania; Dias, Andreia; Guerrero, Angel L.; Gomez, Carlos; Sousa, Alda; Lopes, Alexandra M.; Martins, Sandra; Pinto, Nadia ; Lemos, Carolina; Alves Ferreira, Miguel;
PUBLISHED: 2023, SOURCE: 26th Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 102, ISSUE: 13
INDEXED IN: WOS
WOS3
TITLE: INTEGRATING FUNCTIONAL GENOMIC DATA TO PRIORITIZE CANDIDATE NON-CODING VARIANTS IN MIGRAINE SUSCEPTIBILITY Full Text
AUTHORS: Felicio, Daniela; Martins, Sandra; Santos, Mariana; Lopes, Alexandra M.; Lemos, Carolina ; Pinto, Nadia ; Alves Ferreira, Miguel;
PUBLISHED: 2023, SOURCE: 26th Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 102, ISSUE: 13
AUTHORS: Felicio, Daniela; Martins, Sandra; Santos, Mariana; Lopes, Alexandra M.; Lemos, Carolina ; Pinto, Nadia ; Alves Ferreira, Miguel;
PUBLISHED: 2023, SOURCE: 26th Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 102, ISSUE: 13
INDEXED IN: WOS
WOS4
TITLE: Beyond Val30Met transthyretin (TTR): variants associated with age-at-onset in hereditary ATTRv amyloidosis Full Text
AUTHORS: Alves Ferreira, M; Azevedo, A; Coelho, T; Santos, D; Sequeiros, J ; Alonso, I; Sousa, A; Lemos, C ;
PUBLISHED: 2021, SOURCE: AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS, VOLUME: 28, ISSUE: 2
AUTHORS: Alves Ferreira, M; Azevedo, A; Coelho, T; Santos, D; Sequeiros, J ; Alonso, I; Sousa, A; Lemos, C ;
PUBLISHED: 2021, SOURCE: AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS, VOLUME: 28, ISSUE: 2
5
TITLE: A genetic interaction of NRXN2 with GABRE, SYT1 and CASK in migraine patients: a case-control study Full Text
AUTHORS: Alves Ferreira, M; Quintas, M; Sequeiros, J ; Sousa, A; Pereira Monteiro, J; Alonso, I; Neto, JL; Lemos, C ;
PUBLISHED: 2021, SOURCE: JOURNAL OF HEADACHE AND PAIN, VOLUME: 22, ISSUE: 1
AUTHORS: Alves Ferreira, M; Quintas, M; Sequeiros, J ; Sousa, A; Pereira Monteiro, J; Alonso, I; Neto, JL; Lemos, C ;
PUBLISHED: 2021, SOURCE: JOURNAL OF HEADACHE AND PAIN, VOLUME: 22, ISSUE: 1
6
TITLE: A review of migraine genetics: gathering genomic and transcriptomic factors Full Text
AUTHORS: Dias, A; Mariz, T; Sousa, A; Lemos, C ; Alves Ferreira, M;
PUBLISHED: 2021, SOURCE: HUMAN GENETICS, VOLUME: 141, ISSUE: 1
AUTHORS: Dias, A; Mariz, T; Sousa, A; Lemos, C ; Alves Ferreira, M;
PUBLISHED: 2021, SOURCE: HUMAN GENETICS, VOLUME: 141, ISSUE: 1
7
TITLE: C1QA and C1QC modify age-at-onset in familial amyloid polyneuropathy patients
AUTHORS: Dias, A; Santos, D; Coelho, T; Alves Ferreira, M; Sequeiros, J; Alonso, I; Sousa, A; Lemos, C ;
PUBLISHED: 2019, SOURCE: ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY, VOLUME: 6, ISSUE: 4
AUTHORS: Dias, A; Santos, D; Coelho, T; Alves Ferreira, M; Sequeiros, J; Alonso, I; Sousa, A; Lemos, C ;
PUBLISHED: 2019, SOURCE: ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY, VOLUME: 6, ISSUE: 4
8
TITLE: A Trans-acting Factor May Modify Age at Onset in Familial Amyloid Polyneuropathy ATTRV30M in Portugal Full Text
AUTHORS: Alves Ferreira, M; Coelho, T; Santos, D; Sequeiros, J; Alonso, I; Sousa, A; Lemos, C ;
PUBLISHED: 2018, SOURCE: MOLECULAR NEUROBIOLOGY, VOLUME: 55, ISSUE: 5
AUTHORS: Alves Ferreira, M; Coelho, T; Santos, D; Sequeiros, J; Alonso, I; Sousa, A; Lemos, C ;
PUBLISHED: 2018, SOURCE: MOLECULAR NEUROBIOLOGY, VOLUME: 55, ISSUE: 5
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TITLE: mtDNA copy number associated with age of onset in familial amyloid polyneuropathy
AUTHORS: Santos, D; Santos, MJ; Alves Ferreira, M; Coelho, T; Sequeiros, J; Alonso, I; Oliveira, P ; Sousa, A; Lemos, C ; Grazina, M;
PUBLISHED: 2018, SOURCE: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, VOLUME: 89, ISSUE: 3
AUTHORS: Santos, D; Santos, MJ; Alves Ferreira, M; Coelho, T; Sequeiros, J; Alonso, I; Oliveira, P ; Sousa, A; Lemos, C ; Grazina, M;
PUBLISHED: 2018, SOURCE: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, VOLUME: 89, ISSUE: 3
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TITLE: Proposal of a Portuguese Tool for Quality Assessment of Genetic Counselling: a New Tool for Healthcare Professionals Full Text
AUTHORS: Paneque, M ; Costa, C; Lemos, C ; Alves Ferreira, M; Sequeiros, J; Lemos, MS;
PUBLISHED: 2018, SOURCE: ACTA MEDICA PORTUGUESA, VOLUME: 31, ISSUE: 6
AUTHORS: Paneque, M ; Costa, C; Lemos, C ; Alves Ferreira, M; Sequeiros, J; Lemos, MS;
PUBLISHED: 2018, SOURCE: ACTA MEDICA PORTUGUESA, VOLUME: 31, ISSUE: 6
