Current review of genetics of human obesity: from molecular mechanisms to an evolutionary perspective D Albuquerque, E Stice, R Rodríguez-López, L Manco, C Nóbrega Molecular Genetics and Genomics 290 (4), 1191–1221, 2015 | 309 | 2015 |
The contribution of genetics and environment to obesity D Albuquerque, C Nóbrega, L Manco, C Padez British medical bulletin 123 (1), 159-173, 2017 | 299 | 2017 |
The population genomics of archaeological transition in west Iberia: Investigation of ancient substructure using imputation and haplotype-based methods R Martiniano, LM Cassidy, R Ó'Maoldúin, R McLaughlin, NM Silva, ... PLoS genetics 13 (7), e1006852, 2017 | 153 | 2017 |
Association of FTO Polymorphisms with Obesity and Obesity-Related Outcomes in Portuguese Children D Albuquerque, C Nóbrega, L Manco PloS one 8 (1), e54370, 2013 | 81 | 2013 |
A new PKLR gene mutation in the R‐type promoter region affects the gene transcription causing pyruvate kinase deficiency L Manco, ML Ribeiro, V Máximo, H Almeida, A Costa, O Freitas, J Barbot, ... British journal of haematology 110 (4), 993-997, 2000 | 74 | 2000 |
Association study of common polymorphisms in MSRA, TFAP2B, MC4R, NRXN3, PPARGC1A, TMEM18, SEC16B, HOXB5 and OLFM4 genes with obesity-related traits among Portuguese children D Albuquerque, C Nóbrega, R Rodríguez-López, L Manco Journal of human genetics 59 (6), 307-313, 2014 | 57 | 2014 |
DNA methylation age estimation in blood samples of living and deceased individuals using a multiplex SNaPshot assay HC Dias, C Cordeiro, J Pereira, C Pinto, FC Real, E Cunha, L Manco Forensic science international 311, 110267, 2020 | 56 | 2020 |
PK‐LR gene mutations in pyruvate kinase deficient Portuguese patients L Manco, ML Ribeiro, H Almeida, O Freitas, A Abade, G Tamagnini British journal of haematology 105 (3), 591-595, 1999 | 48 | 1999 |
Assessment of obesity and abdominal obesity among Portuguese children. D Albuquerque, C Nobrega, H Samouda, L Manco Acta medica portuguesa 25 (3), 2012 | 45 | 2012 |
Detection of new pathogenic mutations in patients with congenital haemolytic anaemia using next‐generation sequencing R Del Orbe Barreto, B Arrizabalaga, AB De la Hoz, Á García‐Orad, ... International journal of laboratory hematology 38 (6), 629-638, 2016 | 43 | 2016 |
Age estimation based on DNA methylation using blood samples from deceased individuals H Correia Dias, C Cordeiro, F Corte Real, E Cunha, L Manco Journal of forensic sciences 65 (2), 465-470, 2020 | 40 | 2020 |
Pyruvate kinase deficiency in sub-Saharan Africa: identification of a highly frequent missense mutation (G829A; Glu277Lys) and association with malaria P Machado, L Manco, C Gomes, C Mendes, N Fernandes, G Salomé, ... Public Library of Science 7 (10), e47071, 2012 | 36 | 2012 |
Phylogeographic analysis of paternal lineages in NE Portuguese Jewish communities I Nogueiro, L Manco, V Gomes, A Amorim, L Gusmão American Journal of Physical Anthropology: The Official Publication of the …, 2010 | 34 | 2010 |
Influence of physical activity on the association between the FTO variant rs9939609 and adiposity in young adults M Muc, C Padez, L Manco American Journal of Human Biology 27 (5), 734-738, 2015 | 33 | 2015 |
Malaria: looking for selection signatures in the human PKLR gene region P Machado, R Pereira, AM Rocha, L Manco, N Fernandes, J Miranda, ... British journal of haematology 149 (5), 775-784, 2010 | 33 | 2010 |
Analysis of malaria associated genetic traits in Cabo Verde, a melting pot of European and sub Saharan settlers J Alves, P Machado, J Silva, N Gonçalves, L Ribeiro, P Faustino, ... Blood Cells, Molecules, and Diseases 44 (1), 62-68, 2010 | 33 | 2010 |
Polymorphic variations influencing fetal hemoglobin levels: association study in beta-thalassemia carriers and in normal individuals of Portuguese origin C Pereira, L Relvas, C Bento, A Abade, ML Ribeiro, L Manco Blood Cells, Molecules, and Diseases 54 (4), 315-320, 2015 | 30 | 2015 |
Age prediction in living: Forensic epigenetic age estimation based on blood samples HC Dias, E Cunha, FC Real, L Manco Legal Medicine 47, 101763, 2020 | 28 | 2020 |
High prevalence of hemoglobin disorders and glucose-6-phosphate dehydrogenase (G6PD) deficiency in the Republic of Guinea (West Africa) TS Millimono, KM Loua, SL Rath, L Relvas, C Bento, M Diakite, M Jarvis, ... Hemoglobin 36 (1), 25-37, 2012 | 28 | 2012 |
Combined study of ADAMTS13 and complement genes in the diagnosis of thrombotic microangiopathies using next‐generation sequencing T Fidalgo, P Martinho, CS Pinto, AC Oliveira, R Salvado, N Borràs, ... Research and practice in thrombosis and haemostasis 1 (1), 69-80, 2017 | 26 | 2017 |