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Items: 1 to 50 of 85

1.

Age Estimation Based on DNA Methylation Using Blood Samples From Deceased Individuals.

Correia Dias H, Cordeiro C, Corte Real F, Cunha E, Manco L.

J Forensic Sci. 2019 Sep 6. doi: 10.1111/1556-4029.14185. [Epub ahead of print]

PMID:
31490551
2.

Physical activity and the association between the FTO rs9939609 polymorphism and obesity in Portuguese children aged 3 to 11 years.

Manco L, Pinho S, Albuquerque D, Machado-Rodrigues AM, Padez C.

Am J Hum Biol. 2019 Nov;31(6):e23312. doi: 10.1002/ajhb.23312. Epub 2019 Aug 24.

PMID:
31444941
3.

Association study of variants in genes FTO, SLC6A4, DRD2, BDNF and GHRL with binge eating disorder (BED) in Portuguese women.

Palmeira L, Cunha M, Padez C, Alvarez M, Pinto-Gouveia J, Manco L.

Psychiatry Res. 2019 Mar;273:309-311. doi: 10.1016/j.psychres.2019.01.047. Epub 2019 Jan 15.

PMID:
30677719
4.

High AMY1 copy number protects against obesity in Portuguese young adults.

Pinho S, Padez C, Manco L.

Ann Hum Biol. 2018 Aug;45(5):435-439. doi: 10.1080/03014460.2018.1490452. Epub 2018 Sep 10.

PMID:
30200782
5.

Combined study of ADAMTS13 and complement genes in the diagnosis of thrombotic microangiopathies using next-generation sequencing.

Fidalgo T, Martinho P, Pinto CS, Oliveira AC, Salvado R, Borràs N, Coucelo M, Manco L, Maia T, Mendes MJ, Del Orbe Barreto R, Corrales I, Vidal F, Ribeiro ML.

Res Pract Thromb Haemost. 2017 Jun 23;1(1):69-80. doi: 10.1002/rth2.12016. eCollection 2017 Jul.

6.

Venous thromboembolism risk associated with ABO, F11 and FGG loci.

Manco L, Silva C, Fidalgo T, Martinho P, Sarmento AB, Ribeiro ML.

Blood Coagul Fibrinolysis. 2018 Sep;29(6):528-532. doi: 10.1097/MBC.0000000000000753.

PMID:
29995659
7.

The Eastern side of the Westernmost Europeans: Insights from subclades within Y-chromosome haplogroup J-M304.

Manco L, Albuquerque J, Sousa MF, Martiniano R, de Oliveira RC, Marques S, Gomes V, Amorim A, Alvarez L, Prata MJ.

Am J Hum Biol. 2018 Mar;30(2). doi: 10.1002/ajhb.23082. Epub 2017 Nov 29.

PMID:
29193490
8.

The contribution of genetics and environment to obesity.

Albuquerque D, Nóbrega C, Manco L, Padez C.

Br Med Bull. 2017 Sep 1;123(1):159-173. doi: 10.1093/bmb/ldx022.

PMID:
28910990
9.

A generalized parametric response mapping method for analysis of multi-parametric imaging: A feasibility study with application to glioblastoma.

Lausch A, Yeung TP, Chen J, Law E, Wang Y, Urbini B, Donelli F, Manco L, Fainardi E, Lee TY, Wong E.

Med Phys. 2017 Nov;44(11):6074-6084. doi: 10.1002/mp.12562. Epub 2017 Oct 13.

PMID:
28875538
10.

The population genomics of archaeological transition in west Iberia: Investigation of ancient substructure using imputation and haplotype-based methods.

Martiniano R, Cassidy LM, Ó'Maoldúin R, McLaughlin R, Silva NM, Manco L, Fidalgo D, Pereira T, Coelho MJ, Serra M, Burger J, Parreira R, Moran E, Valera AC, Porfirio E, Boaventura R, Silva AM, Bradley DG.

PLoS Genet. 2017 Jul 27;13(7):e1006852. doi: 10.1371/journal.pgen.1006852. eCollection 2017 Jul.

11.

Polymorphisms in the SNRPN gene are associated with obesity susceptibility in a Spanish population.

Albuquerque D, Manco L, González LM, Gervasini G, Benito GM, González JR, Rodríguez-López R.

J Gene Med. 2017 May;19(5). doi: 10.1002/jgm.2956.

PMID:
28387446
12.

Molecular basis of pyruvate kinase deficiency among Tunisians: description of new mutations affecting coding and noncoding regions in the PKLR gene.

Jaouani M, Manco L, Kalai M, Chaouch L, Douzi K, Silva A, Macedo S, Darragi I, Boudriga I, Chaouachi D, Fitouri Z, Van Wijk R, Ribeiro ML, Abbes S.

Int J Lab Hematol. 2017 Apr;39(2):223-231. doi: 10.1111/ijlh.12610. Epub 2017 Jan 30.

PMID:
28133914
13.

Association of 5-HTTLPR genotypes with antisocial behavior in response to childhood environment: A study in young adults of Portuguese origin.

Manco L, Soares A, Wasterlain SN.

Psychiatry Res. 2018 Apr;262:325-327. doi: 10.1016/j.psychres.2017.01.001. Epub 2017 Jan 5. No abstract available.

PMID:
28069247
14.

The lactase -13910C>T polymorphism (rs4988235) is associated with overweight/obesity and obesity-related variables in a population sample of Portuguese young adults.

Manco L, Dias H, Muc M, Padez C.

Eur J Clin Nutr. 2017 Jan;71(1):21-24. doi: 10.1038/ejcn.2016.164. Epub 2016 Aug 31.

PMID:
27577176
15.

Hereditary nonspherocytic hemolytic anemia caused by red cell glucose-6-phosphate isomerase (GPI) deficiency in two Portuguese patients: Clinical features and molecular study.

Manco L, Bento C, Victor BL, Pereira J, Relvas L, Brito RM, Seabra C, Maia TM, Ribeiro ML.

Blood Cells Mol Dis. 2016 Sep;60:18-23. doi: 10.1016/j.bcmd.2016.06.002. Epub 2016 Jun 11.

PMID:
27519939
16.

Detection of new pathogenic mutations in patients with congenital haemolytic anaemia using next-generation sequencing.

Del Orbe Barreto R, Arrizabalaga B, De la Hoz AB, García-Orad Á, Tejada MI, Garcia-Ruiz JC, Fidalgo T, Bento C, Manco L, Ribeiro ML.

Int J Lab Hematol. 2016 Dec;38(6):629-638. doi: 10.1111/ijlh.12551. Epub 2016 Jul 17.

PMID:
27427187
17.

Congenital dyserythropoietic anemia associated to a GATA1 mutation aggravated by pyruvate kinase deficiency.

Pereira J, Bento C, Manco L, Gonzalez A, Vagace J, Ribeiro ML.

Ann Hematol. 2016 Sep;95(9):1551-3. doi: 10.1007/s00277-016-2720-0. Epub 2016 Jun 24. No abstract available.

PMID:
27342114
18.

Association of polymorphisms in 5-HTT (SLC6A4) and MAOA genes with measures of obesity in young adults of Portuguese origin.

Dias H, Muc M, Padez C, Manco L.

Arch Physiol Biochem. 2016;122(1):8-13. doi: 10.3109/13813455.2015.1111390. Epub 2015 Dec 23.

PMID:
26698543
19.

Severe neonatal jaundice due to a de novo glucose-6-phosphate dehydrogenase deficient mutation.

Del Orbe Barreto R, Arrizabalaga B, de la Hoz AB, Aragües P, Garcia-Ruiz JC, Arrieta A, Adán R, Manco L, Macedo-Ribeiro S, Bento C, Ribeiro ML.

Int J Lab Hematol. 2016 Apr;38(2):e27-9. doi: 10.1111/ijlh.12455. Epub 2015 Dec 23. No abstract available.

PMID:
26693676
20.

Intragenic haplotype analysis of common HFE mutations in the Portuguese population.

Toste S, Relvas L, Pinto C, Bento C, Abade A, Ribeiro ML, Manco L.

J Genet. 2015 Jun;94(2):329-33. No abstract available.

21.

Polymorphic variations influencing fetal hemoglobin levels: association study in beta-thalassemia carriers and in normal individuals of Portuguese origin.

Pereira C, Relvas L, Bento C, Abade A, Ribeiro ML, Manco L.

Blood Cells Mol Dis. 2015 Apr;54(4):315-20. doi: 10.1016/j.bcmd.2015.02.001. Epub 2015 Feb 21.

PMID:
25842369
22.

Influence of physical activity on the association between the FTO variant rs9939609 and adiposity in young adults.

Muc M, Padez C, Manco L.

Am J Hum Biol. 2015 Sep-Oct;27(5):734-8. doi: 10.1002/ajhb.22712. Epub 2015 Mar 25.

PMID:
25809737
23.

Triosephosphate isomerase gene promoter variation: -5G/A and -8G/A polymorphisms in clinical malaria groups in two African populations.

Guerra M, Machado P, Manco L, Fernandes N, Miranda J, Arez AP.

Infect Genet Evol. 2015 Jun;32:271-9. doi: 10.1016/j.meegid.2015.03.020. Epub 2015 Mar 20.

PMID:
25801609
24.

Current review of genetics of human obesity: from molecular mechanisms to an evolutionary perspective.

Albuquerque D, Stice E, Rodríguez-López R, Manco L, Nóbrega C.

Mol Genet Genomics. 2015 Aug;290(4):1191-221. doi: 10.1007/s00438-015-1015-9. Epub 2015 Mar 8. Review.

PMID:
25749980
25.

Familial thrombotic risk based on the genetic background of Protein C Deficiency in a Portuguese Study.

Fidalgo T, Martinho P, Salvado R, Manco L, Oliveira AC, Pinto CS, Gonçalves E, Marques D, Sevivas T, Martins N, Ribeiro ML.

Eur J Haematol. 2015 Oct;95(4):294-307. doi: 10.1111/ejh.12488. Epub 2015 Mar 13.

PMID:
25533856
26.

Association study of common polymorphisms in MSRA, TFAP2B, MC4R, NRXN3, PPARGC1A, TMEM18, SEC16B, HOXB5 and OLFM4 genes with obesity-related traits among Portuguese children.

Albuquerque D, Nóbrega C, Rodríguez-López R, Manco L.

J Hum Genet. 2014 Jun;59(6):307-13. doi: 10.1038/jhg.2014.23. Epub 2014 Mar 27.

PMID:
24670271
27.

Novel variants in the MC4R and LEPR genes among severely obese children from the Iberian population.

Albuquerque D, Estévez MN, Víbora PB, Giralt PS, Balsera AM, Cortés PG, López MJ, Luego LM, Gervasini G, Hernández SB, Arroyo-Díez J, Vacas MA, Nóbrega C, Manco L, Rodríguez-López R.

Ann Hum Genet. 2014 May;78(3):195-207. doi: 10.1111/ahg.12058. Epub 2014 Mar 11.

28.

A new recombinant MnSOD prevents the cyclosporine A-induced renal impairment.

Damiano S, Trepiccione F, Ciarcia R, Scanni R, Spagnuolo M, Manco L, Borrelli A, Capasso C, Mancini R, Schiattarella A, Iervolino A, Zacchia E, Bata-Csere A, Florio S, Anastasio P, Pollastro R, Mancini A, Capasso G.

Nephrol Dial Transplant. 2013 Aug;28(8):2066-72. doi: 10.1093/ndt/gft020. Epub 2013 May 15.

PMID:
23677648
29.

Association of FTO polymorphisms with obesity and obesity-related outcomes in Portuguese children.

Albuquerque D, Nóbrega C, Manco L.

PLoS One. 2013;8(1):e54370. doi: 10.1371/journal.pone.0054370. Epub 2013 Jan 14.

30.

Distribution of the - 13910C>T polymorphism in the general population of Portugal and in subjects with gastrointestinal complaints associated with milk consumption.

Manco L, Pires S, Lopes AI, Figueiredo I, Albuquerque D, Alvarez M, Rocha J, Abade A.

Ann Hum Biol. 2013 Mar;40(2):205-8. doi: 10.3109/03014460.2012.754943. Epub 2013 Jan 18.

PMID:
23327608
31.

Y-chromosome diversity in central Portugal reveals signatures of ancient maritime expansions.

Martiniano R, Feitosa Y, Abade A, Manco L.

Anthropol Anz. 2013;70(4):355-67.

PMID:
24620564
32.

The lactase persistence -13910C>T polymorphism shows indication of association with abdominal obesity among Portuguese children.

Albuquerque D, Nóbrega C, Manco L.

Acta Paediatr. 2013 Apr;102(4):e153-7. doi: 10.1111/apa.12134. Epub 2013 Jan 9.

PMID:
23252911
33.

Pyruvate kinase deficiency in sub-Saharan Africa: identification of a highly frequent missense mutation (G829A;Glu277Lys) and association with malaria.

Machado P, Manco L, Gomes C, Mendes C, Fernandes N, Salomé G, Sitoe L, Chibute S, Langa J, Ribeiro L, Miranda J, Cano J, Pinto J, Amorim A, do Rosário VE, Arez AP.

PLoS One. 2012;7(10):e47071. doi: 10.1371/journal.pone.0047071. Epub 2012 Oct 17.

34.

Assessment of obesity and abdominal obesity among Portuguese children.

Albuquerque D, Nóbrega C, Samouda H, Manco L.

Acta Med Port. 2012 May-Jun;25(3):169-73. Epub 2012 Jul 23.

35.

High prevalence of hemoglobin disorders and glucose-6-phosphate dehydrogenase (G6PD) deficiency in the Republic of Guinea (West Africa).

Millimono TS, Loua KM, Rath SL, Relvas L, Bento C, Diakite M, Jarvis M, Daries N, Ribeiro LM, Manco L, Kaeda JS.

Hemoglobin. 2012;36(1):25-37. doi: 10.3109/03630269.2011.600491. Epub 2011 Sep 19.

PMID:
21929367
36.

Chronic hemolytic anemia is associated with a new glucose-6-phosphate dehydrogenase in-frame deletion in an older woman.

Manco L, Pereira J, Relvas L, Rebelo U, Crisóstomo AI, Bento C, Ribeiro ML.

Blood Cells Mol Dis. 2011 Apr 15;46(4):288-93. doi: 10.1016/j.bcmd.2011.02.001. Epub 2011 Mar 11.

PMID:
21397531
37.

SLC40A1 Q248H allele frequencies and associated SLC40A1 haplotypes in three West African population samples.

Albuquerque D, Manco L, Loua KM, Arez AP, Trovoada Mde J, Relvas L, Millimono TS, Rath SL, Lopes D, Nogueira F, Varandas L, Alvarez M, Ribeiro ML.

Ann Hum Biol. 2011 May;38(3):378-81. doi: 10.3109/03014460.2010.541496. Epub 2011 Jan 14.

PMID:
21231898
38.

Triosephosphate isomerase deficiency: a patient with Val231Met mutation.

Serdaroglu G, Aydinok Y, Yilmaz S, Manco L, Ozer E.

Pediatr Neurol. 2011 Feb;44(2):139-42. doi: 10.1016/j.pediatrneurol.2010.08.016.

PMID:
21215915
39.

Malaria: looking for selection signatures in the human PKLR gene region.

Machado P, Pereira R, Rocha AM, Manco L, Fernandes N, Miranda J, Ribeiro L, do Rosário VE, Amorim A, Gusmão L, Arez AP.

Br J Haematol. 2010 Jun;149(5):775-84. doi: 10.1111/j.1365-2141.2010.08165.x. Epub 2010 Apr 4.

PMID:
20377593
40.

Phylogeographic analysis of paternal lineages in NE Portuguese Jewish communities.

Nogueiro I, Manco L, Gomes V, Amorim A, Gusmão L.

Am J Phys Anthropol. 2010 Mar;141(3):373-81. doi: 10.1002/ajpa.21154.

PMID:
19918998
41.

Analysis of malaria associated genetic traits in Cabo Verde, a melting pot of European and sub Saharan settlers.

Alves J, Machado P, Silva J, Gonçalves N, Ribeiro L, Faustino P, do Rosário VE, Manco L, Gusmão L, Amorim A, Arez AP.

Blood Cells Mol Dis. 2010 Jan 15;44(1):62-8. doi: 10.1016/j.bcmd.2009.09.008. Epub 2009 Oct 17.

PMID:
19837619
42.

Chronic haemolytic anaemia because of pyruvate kinase (PK) deficiency in a child heterozygous for haemoglobin S and no clinical features of sickle cell disease.

Manco L, Vagace JM, Relvas L, Rebelo U, Bento C, Villegas A, Letícia Ribeiro M.

Eur J Haematol. 2010 Jan 1;84(1):89-90. doi: 10.1111/j.1600-0609.2009.01353.x. Epub 2009 Sep 16. Review. No abstract available.

PMID:
19758413
43.

Novel human pathological mutations. Gene symbol: PKLR. Disease: pyruvate kinase deficiency.

Manco L, Ribeiro ML.

Hum Genet. 2009 Apr;125(3):343. No abstract available.

PMID:
19320017
44.

Novel human pathological mutations. Gene symbol: PKLR. Disease: pyruvate kinase deficiency.

Manco L, Trovoada MJ, Ribeiro ML.

Hum Genet. 2009 Apr;125(3):340. No abstract available.

PMID:
19309805
45.

Novel human pathological mutations. Gene symbol: PKLR. Disease: pyruvate kinase deficiency.

Manco L, Ribeiro ML.

Hum Genet. 2009 Apr;125(3):340. No abstract available.

PMID:
19309787
46.

Complex inheritance of chronic haemolytic anaemia.

Coutinho R, Bento C, Almeida H, Cunha E, Manco L, Ferreira F, Ribeiro ML.

Br J Haematol. 2009 Feb;144(4):615-6. doi: 10.1111/j.1365-2141.2008.07479.x. Epub 2008 Nov 22. No abstract available.

PMID:
19036089
47.

Gene symbol: PKLR. Disease: Pyruvate kinase deficiency.

Manco L, Relvas L, Rebelo U, Vidán J, Ribeiro ML.

Hum Genet. 2008 Oct;124(3):319. No abstract available.

PMID:
18846674
48.

Analysis of TPI gene promoter variation in three sub-Saharan Africa population samples.

Manco L, Machado P, Lopes D, Nogueira F, Do Rosário VE, Alonso PL, Varandas L, Trovoada Mde J, Amorim A, Arez AP.

Am J Hum Biol. 2009 Jan-Feb;21(1):118-20. doi: 10.1002/ajhb.20819.

PMID:
18792062
49.

G6PD deficient alleles and haplotype analysis of human G6PD locus in São Tomé e Príncipe (West Africa).

Manco L, Botigué LR, Ribeiro ML, Abade A.

Hum Biol. 2007 Dec;79(6):679-86.

PMID:
18494377
50.

Left-sided appendicitis.

Schwartz JH, Manco LG.

J Am Coll Surg. 2008 Mar;206(3):590. doi: 10.1016/j.jamcollsurg.2007.05.019. Epub 2007 Aug 8. No abstract available.

PMID:
18308231

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