| Overcoming artefact: anticipation in 284 Portuguese kindreds with familial amyloid polyneuropathy (FAP) ATTRV30M C Lemos, T Coelho, M Alves-Ferreira, A Martins-da-Silva, J Sequeiros, ... Journal of Neurology, Neurosurgery & Psychiatry 85 (3), 326-330, 2014 | 85 | 2014 |
| Identification of genetic risk factors for maxillary lateral incisor agenesis M Alves-Ferreira, T Pinho, A Sousa, J Sequeiros, C Lemos, I Alonso Journal of Dental Research 93 (5), 452-458, 2014 | 69 | 2014 |
| Variants in RBP4 and AR genes modulate age at onset in familial amyloid polyneuropathy (FAP ATTRV30M) D Santos, T Coelho, M Alves-Ferreira, J Sequeiros, D Mendonça, I Alonso, ... European Journal of Human Genetics 24 (5), 756-760, 2016 | 49 | 2016 |
| Tau/MAPT disease-associated variant A152T alters tau function and toxicity via impaired retrograde axonal transport VJ Butler, DA Salazar, D Soriano-Castell, M Alves-Ferreira, ... Human molecular genetics 28 (9), 1498-1514, 2019 | 35 | 2019 |
| Cellular clearance of circulating transthyretin decreases cell-nonautonomous proteotoxicity in Caenorhabditis elegans K Madhivanan, ER Greiner, M Alves-Ferreira, D Soriano-Castell, ... Proceedings of the National Academy of Sciences 115 (33), E7710-E7719, 2018 | 32 | 2018 |
| A trans-acting factor may modify age at onset in familial amyloid polyneuropathy ATTRV30M in Portugal M Alves-Ferreira, T Coelho, D Santos, J Sequeiros, I Alonso, A Sousa, ... Molecular neurobiology 55, 3676-3683, 2018 | 31 | 2018 |
| mtDNA copy number associated with age of onset in familial amyloid polyneuropathy D Santos, MJ Santos, M Alves-Ferreira, T Coelho, J Sequeiros, I Alonso, ... Journal of Neurology, Neurosurgery & Psychiatry 89 (3), 300-304, 2018 | 26 | 2018 |
| C1QA and C1QC modify age‐at‐onset in familial amyloid polyneuropathy patients A Dias, D Santos, T Coelho, M Alves‐Ferreira, J Sequeiros, I Alonso, ... Annals of Clinical and Translational Neurology 6 (4), 748-754, 2019 | 21 | 2019 |
| Large normal alleles of ATXN2 decrease age at onset in transthyretin familial amyloid polyneuropathy Val30Met patients D Santos, T Coelho, M Alves‐Ferreira, J Sequeiros, D Mendonça, ... Annals of Neurology 85 (2), 251-258, 2019 | 21 | 2019 |
| Genetic overlap between temporomandibular disorders and primary headaches: A systematic review D Cruz, F Monteiro, M Paço, M Vaz-Silva, C Lemos, M Alves-Ferreira, ... Japanese Dental Science Review 58, 69-88, 2022 | 20 | 2022 |
| Familial amyloid polyneuropathy in Portugal: new genes modulating age‐at‐onset D Santos, T Coelho, M Alves‐Ferreira, J Sequeiros, D Mendonça, ... Annals of Clinical and Translational Neurology 4 (2), 98-105, 2017 | 17 | 2017 |
| Beyond Val30Met transthyretin (TTR): variants associated with age-at-onset in hereditary ATTRv amyloidosis M Alves-Ferreira, A Azevedo, T Coelho, D Santos, J Sequeiros, I Alonso, ... Amyloid 28 (2), 100-106, 2021 | 9 | 2021 |
| A review of migraine genetics: gathering genomic and transcriptomic factors A Dias, T Mariz, A Sousa, C Lemos, M Alves-Ferreira Human Genetics, 1-14, 2022 | 8 | 2022 |
| A genetic interaction of NRXN2 with GABRE, SYT1 and CASK in migraine patients: a case-control study M Alves-Ferreira, M Quintas, J Sequeiros, A Sousa, J Pereira-Monteiro, ... The Journal of Headache and Pain 22 (1), 57, 2021 | 6 | 2021 |
| Integrating functional scoring and regulatory data to predict the effect of non-coding SNPs in a complex neurological disease D Felício, M Alves-Ferreira, M Santos, M Quintas, AM Lopes, C Lemos, ... Briefings in Functional Genomics 23 (2), 138-149, 2024 | 3 | 2024 |
| The hidden story behind gender differences in familial amyloid polyneuropathy (FAP) ATTRV30M D Santos, T Coelho, M Alves-Ferreira, J Sequeiros, I Alonso, M Grazina, ... Orphanet Journal of Rare Diseases 10 (1), 1-2, 2015 | 3 | 2015 |
| The role of pain inflexibility and acceptance among headache and temporomandibular disorders patients V Marcelino, M Paço, A Dias, V Almeida, JC Rocha, R Azevedo, ... International Journal of Environmental Research and Public Health 19 (13), 7974, 2022 | 2 | 2022 |
| Functional characterization of a novel PRRT2 variant found in a Portuguese patient with hemiplegic migraine A Dias, M Santos, E Carvalho, D Felício, P Silva, I Alves, T Pinho, A Sousa, ... Clinical Genetics 104 (4), 479-485, 2023 | 1 | 2023 |
| A High Methylation Level of a Novel −284 bp CpG Island in the RAMP1 Gene Promoter Is Potentially Associated with Migraine in Women E Carvalho, A Dias, A Sousa, AM Lopes, S Martins, N Pinto, C Lemos, ... Brain Sciences 12 (5), 526, 2022 | 1 | 2022 |
| Transthyretin-assoziierte familiäre Amyloidpolyneuropathie C Niemietz, C Röcken, M Schilling, J Stypmann, CE Uhlig, HHJ Schmidt DMW-Deutsche Medizinische Wochenschrift 143 (06), 427-430, 2018 | 1 | 2018 |
Alda SousaICBAS, Universidade do Porto在 icbas.up.pt 的电子邮件经过验证
