Author

Albuquerque DM

Hemocentro - UNICAMP - Cited by 1,679 - Hemoglobinopatias - Biologia Molecular

Biography

 Graduated in Biological Sciences from the Universidade Estadual Paulista Julio de Mesquita Filho (1996). Graduate with a focus on molecular biology methods in Virology (HCMV): master's degree in Pharmacology from the University of Campinas (2000) and doctorate in Clinical Medicine at the State University of Campinas (2006). He is currently a biologist responsible for the molecular diagnosis of hemoglobinopathies at the Blood Center of Campinas. It has experience in Molecular Biology, with emphasis on molecular diagnosis of beta thalassemia; Real-time PCR for gene expression and viral load; PCR-RFLP; cloning and DNA sequencing  
Title
Cited by
Year
High levels of proinflammatory cytokines IL-6 and IL-8 are associated with a poor clinical outcome in sickle cell anemia
IF Domingos, DA Pereira-Martins, MJVC Sobreira, RTD Oliveira, ...Annals of Hematology 99, 947-953, 2020202
26
2020
Evaluation of sociodemographic, clinical, and laboratory markers of sickle leg ulcers among young nigerians at a tertiary health institution
OS Olatunya, DM Albuquerque, AD Adekile, FF CostaNigerian Journal of Clinical Practice 21 (7), 882-887, 2018201
19
2018
Deferasirox associated with liver failure and death in a sickle cell anemia patient homozygous for the− 1774delG polymorphism in the Abcc2 gene
CCB Braga, BD Benites, DM de Albuquerque, MC Alvarez, ...Clinical Case Reports 5 (8), 1218, 2017201
13
2017
Influence of alpha thalassemia on clinical and laboratory parameters among nigerian children with sickle cell anemia
OS Olatunya, DM Albuquerque, A Adekile, FF CostaJournal of clinical laboratory analysis 33 (2), e22656, 2019201
12
2019
Angiogenesis‐related genes in endothelial progenitor cells may be involved in sickle cell stroke
MT Ito, SM da Silva Costa, LC Baptista, GQ Carvalho‐Siqueira, ...Journal of the American Heart Association 9 (3), e014143, 2020202
11
2020
Clinical relevance of heterozygosis for aceruloplasminemia
MD Borges, DM de Albuquerque, C Lanaro, FF Costa, KY FertrinAmerican Journal of Medical Genetics Part B: Neuropsychiatric Genetics 180 …, 2019201
11
2019
Influence of UGT1A1 promoter polymorphism, α-thalassemia and βs haplotype in bilirubin levels and cholelithiasis in a large sickle cell anemia cohort
JVGF Batista, GS Arcanjo, THC Batista, MJ Sobreira, RM Santana, ...Annals of Hematology 0, 903-911, 2021202
10
2021
Modulation of fetal hemoglobin in hereditary persistence of fetal hemoglobin deletion type-2, compared to Sicilian δβ-thalassemia, by BCL11A and SOX6-targeting …
TA Fornari, C Lanaro, DM Albuquerque, R Ferreira, FF CostaExperimental Biology and Medicine 242 (3), 267-274, 2017201
10
2017
Uridine diphosphate glucuronosyl transferase 1A (UGT1A1) promoter polymorphism in young patients with sickle cell anaemia: report of the first cohort study from …
OS Olatunya, DM Albuquerque, GO Akanbi, OS Aduayi, AB Taiwo, ...BMC medical genetics 20, 1-8, 20120
9
2019
A chip calorimetry-based method for the real-time investigation of metabolic activity changes in human erythrocytes caused by cell sickling
J Lerchner, POL Volpe, C Lanaro, KY Fertrin, FF Costa, DM Albuquerque, ...Journal of thermal analysis and calorimetry 136, 1-81, 2019201
7
2019
Haptoglobin gene polymorphism in patients with sickle cell anemia: findings from a Nigerian cohort study
OS Olatunya, DM Albuquerque, MNN Santos, TS Kayode, A Adekile, ...The Application of Clinical Genetics, 107-114, 2020202
6
2020
Rare α0-thalassemia deletions detected by MLPA in five unrelated Brazilian patients
NO Mota, EM Kimura, RD Ferreira, GA Pedroso, DM Albuquerque, ...Genetics and Molecular Biology 40, 78-773, 2017201
6
2017
Coinheritance of Hb Bristol-Alesha [β67(E11)Val→Met; HBB: c.202G>A] and the α212 Patchwork Allele in a Brazilian Child with Severe Congenital Hemolytic Anemia
Coinheritance of Hb Bristol-Alesha [β7(E11)Val→Met; HBB: c.202G>A] and the α212 Patchwork Allele in a Brazilian Child with Severe Congenital Hemolytic AnemiaGA Pedroso, EM Kimura, MNN Santos, DM Albuquerque, JLH Ferruzzi, ...Hemoglobin 41 (3), 203-208, 2017201
6
2017
Thalassemia major phenotype caused by HB Zürich‐Albisrieden [α2 59 (E8) Gly> Arg (HBA2: C. 178G> C)] in a Brazilian child
Thalassemia major phenotype caused by HB Zürich‐Albisrieden [α2 9 (E8) Gly> Arg (HBA2: C. 178G> C)] in a Brazilian childGA Pedroso, EM Kimura, MNN Santos, DM Albuquerque, D Malimpensa, ...Pediatric Blood & Cancer 6 (12), e27413, 2018201
5
2018
Endothelial Nitric Oxide Synthase (eNOS) Gene Polymorphisms and Markers of Hemolysis, Inflammation and Endothelial Dysfunction in Brazilian Sickle Cell …
F Chenou, DM Albuquerque, DP Leonardo, IF Domingos, MAC Bezerra, ...Biochemical genetics 58, 580-59, 2020202
4
2020
Polymorphisms in the heme oxygenase-1 and bone morphogenetic protein receptor type 1b genes and estimated glomerular filtration rate in Brazilian sickle cell anemia patients
O Chinedu, WV Tonassé, DM Albuquerque, IF Domingos, AS Araújo, ...Hematology, Transfusion and Cell Therapy 3, 165-170, 2021202
4
2021
A novel α0‐thalassemia deletion in a Brazilian child with Hb H disease [‐‐(Braz)]
NO Mota, EM Kimura, RD Ferreira, DM Albuquerque, DM Ribeiro, ...International journal of laboratory hematology 9 (4), e106-e109, 2017201
3
2017
Association of lymphocyte counts, NLR and PLR with mortality in COVID-19 patients
AE Alagbe, GA Pedroso, BB Oliveira, GAF Maia, E Costa, ...Hematology, Transfusion and Cell Therapy 4, S508-S509, 2021202
3
2021
Lymphocyte ratios progressively worsen in non-survivors of COVID-19
AE Alagbe, GA Pedroso, BB Oliveira, E Costa, GAF Maia, BF Piellusch, ...Blood 138 (Supplement 1), 4196-4196, 010
2
2021
PADI4 gene polymorphism as a risk factor for acute chest syndrome in sickle cell anemia patients
F Chenou, BW Hounkpe, DM Albuquerque, IF Domingos, AS Araujo, ...Blood, The Journal of the American Society of Hematology 130 (Suppl_1), 954-954, 01701
2
2017

Referred From: https://scholar.google.com/citations?user=cP_VW4EAAAAJ&hl=en&oi=ao

Cited by
Citations 1679
h-index 22
i10-index 47
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