Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 732 Records) |
Query Trace: Sickle cell[original query] |
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Evaluation of a prophylactic transfusion program on obstetric outcomes in pregnant women with sickle cell disease: A single centre retrospective cohort study. European journal of obstetrics, gynecology, and reproductive biology 2023 9 290 103-108. O Sobczyk, E Gottardi, M Lefebvre, F Canouï-Poitrine, A Jebali, G De Luna, F Pirenne, D Redel, F Galacteros, E Boutin, P Bartolucci, B Haddad, A Habibi, E Lecarpenti |
Genetic variants and effect modifiers of QT interval prolongation in patients with sickle cell disease. Gene 2023 9 890 147824. Mengna Zhang, William B Hillegass, Xue Yu, Suvankar Majumdar, J Daryl Pollard, Erin Jackson, Jarrod Knudson, Douglas Wolfe, Gregory J Kato, Joseph F Maher, Hao M |
A positive correlation between mutated gene of sickle cell anemia and glucose-6-phosphate dehydrogenase among gond tribes of Chhattisgarh, India. Mutation research 2023 12 828 111849. Ekta Singh, Lohit Raj Shivwanshi, Anil Kum |
HLA haplotype frequencies and diversity in patients with hemoglobinopathies. EJHaem 2023 11 4 (4): 963-969. Graziana M Scigliuolo, Wahid Boukouaci, Barbara Cappelli, Fernanda Volt, Monica M Rivera Franco, Nathalie Dhédin, Regis Peffault de Latour, Christine Devalck, Jean-Hugues Dalle, Martin Castelle, Olivier Hermine, Marie Ouachée Chardin, Xavier Poiré, Bénédicte Brichard, Catherine Paillard, Hanadi Rafii, Chantal Kenzey, Ching-Lien Wu, Jihène Bouassida, Marie Robin, Nicole Raus, Vanderson Rocha, Annalisa Ruggeri, Eliane Gluckman, Ryad Tamouza, |
A-296G variant of THBS1 gene (rs1478605) is associated with a lower frequency of stroke in a Brazilian population with sickle cell anemia. Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2023 11 33 (1): 107474. Jessica M F Oliveira, Gabriela S Arcanjo, Igor F Domingos, Jéssica V G F Batista, Diego A Pereira-Martins, Thais H C Batista, Betânia L D Hatzlhofer, Diego A Falcão, Madi V Diniz, Alexsandro P Silva, Bárbara C V Pires, Ana C Dos Anjos, Fernando F Costa, Aderson S Araujo, Antonio R Lucena-Araujo, Marcos A Bezer |
Silent Cerebral Infarcts in Iraqi Patients with Sickle Cell Disease. Hemoglobin 2023 11 1-4. Noor W Rashid, Nasir Al-Allawi, Hamdy I Tah |
Haptoglobin gene polymorphism and iron profile in sickle cell disease patients with inflammation in Yaounde, Cameroon. Molecular genetics & genomic medicine 2023 11 e2302. Romaric De Manfouo Tuono, Josué Louokdom Simo, Prosper Cabral Biapa Nya, Jean Paul Chedjou, Christian Bernard Kengne Fotsing, Bernard Claude Chetcha, Calvino Fomboh Tah, Claude Tagny Tayou, Wilfried Fon Mbatcham, Constant Anatole Pie |
"SCULP" study: The benefits of skin graft pellets on the pain of sickle cell leg ulcers (SCLU). Journal de medecine vasculaire 2023 11 48 (3-4): 100-104. P Caboche-Salouhi, A Le Seac'h, F Lionnet, A Santin, S Mattioni, F Tamboura, O Steichen, A Barbaud, P Sen |
Impact of Genetic Variations on Thromboembolic Risk in Saudis with Sickle Cell Disease. Genes 2023 10 14 (10): . Mohammad A Alshabeeb, Deemah Alwadaani, Farjah H Al Qahtani, Salah Abohelaika, Mohsen Alzahrani, Abdullah Al Zayed, Hussain H Al Saeed, Hala Al Ajmi, Barrak Alsomaie, Mamoon Rashid, Ann K Da |
Prevalence and Impact of HMOX1 Polymorphism (rs2071746: A?>?T) in Indian Sickle Cell Disease Patients. Journal of laboratory physicians 2023 10 15 (4): 583-589. Hareram Pandey, Kanwaljeet Singh, Ravi Ranjan, Jasmita Dass, Seema Tyagi, Tulika Seth, Renu Saxena, Manoranjan Mahapat |
The German sickle cell disease registry reveals a surprising risk of acute splenic sequestration and an increased transfusion requirement in patients with compound heterozygous sickle cell disease HbS/?-thalassaemia and no or low HbA expression. European journal of haematology 2024 7 . Pierre Allard, Laura Tagliaferri, Vivienn Weru, Holger Cario, Stephan Lobitz, Regine Grosse, Matthias Bleeke, Lena Oevermann, Dani Hakimeh, Andrea Jarisch, Annette Kopp-Schneider, Andreas E Kulozik, Joachim B Kunz, |
Genotyping the BCL11A Single Nucleotide Polymorphism and Associated Levels of Fetal Hemoglobin in Mauritanian Sickle Cell Patients. Frontiers in bioscience (Scholar edition) 2024 6 16 (2): 11. Aminetou Taleb Brahim, Mariem Taleb, Harouna Soumaré, Sidi Mohamed Ghaber, Aminetou Mohamed, Ali Ould Mohamed Salem Boukha |
Relevance of repeated analyses of albuminuria and glomerular filtration rate in African children with sickle cell anaemia. British journal of haematology 2024 6 . Agathe B Nkoy, Floreen M Mumaka, Ange Ngonde, Samuel K Mafumba, Therance T Matoka, Robert Kitenge, Flore M Talu, Blaise Nkolomoni, Léon Tshilolo, Lambertus P van den Heuvel, Pépé M Ekulu, Elena N Levtchenko, Veerle Labarq |
Molecular characterization of HAMP rs10421768 gene and phenotypic expression of hepcidin; a case-control study among sickle cell anaemia patients in Ghana. PloS one 2024 6 19 (6): e0306194. Samuel Kwasi Appiah, Charles Nkansah, Gabriel Abbam, Felix Osei-Boakye, Kofi Mensah, Simon Bannison Bani, Solomon Chemogo, Lydia Sarpong, Takyi Godfred Addae, Daniel Boamah Sefa, Richard Adu Croffien, Larry Adom, Rekhiatu Oboirien Abdul Rauf, Farrid Boadu, Godfred Appiah Amoah, Ejike Felix Chukwur |
Sickle cell trait, APOL1 risk allele status and chronic kidney disease among ART-experienced adults living with HIV in northern Nigeria. International journal of STD & AIDS 2024 6 9564624241262397. Abdurrahman Abdulhamid, Bryan E Shepherd, Usman J Wudil, Chelsea Van Wyk, Faisal S Dankishiya, Nafiu Hussaini, C William Wester, Muktar H Ali |
Clinical and Laboratory Features of Sickle Cell Disease S/D Punjab: Impact of HbF and Hydroxyurea. Mediterranean journal of hematology and infectious diseases 2024 6 16 (1): e2024046. S Alkindi, I B M Al-Busaidi, A V Patha |
Detection of Asymptomatic Sickle Cell Hemoglobin Carriers and Fetal Hemoglobin Regulating Genetic Variants in African Descendants from Oaxaca, Mexico. Anemia 2024 5 2024 4940760. María De Los Ángeles Romero-Tlalolini, Sergio Roberto Aguilar-Ruiz, Rafael Baltiérrez-Hoyos, Jaime Vargas-Arzola, Luis Alberto Hernández-Osorio, Verónica Rocío Vásquez-Garzón, Héctor Ulises Bernardino-Hernández, Honorio Torres-Aguil |
Association of ZBTB38 gene polymorphism (rs724016) with height and fetal hemoglobin in individuals with sickle cell anemia. Molecular genetics and metabolism reports 2024 5 39 101086. Domício Antônio Costa-Júnior, Thaisa N Souza Valente, André Rolim Belisário, Gisele Queiroz Carvalho, Miguel Madeira, Cibele Velloso-Rodrigu |
Systematic Review of Genetic Modifiers Associated with the Development and/or Progression of Nephropathy in Patients with Sickle Cell Disease. International journal of molecular sciences 2024 5 25 (10): . Veerle Labarque, Emmanuel Chide Okocha, |
Distribution of pathogenic variants in the CFTR gene in a representative cohort of people with cystic fibrosis in the Kingdom of Bahrain. Molecular genetics and genomics : MGG 2024 5 299 (1): 52. Osama A Karim Majed, Fatema Osama Majed, Nabeel Jasim Almoamen, Husain Baqer Alsatrawi, Salma Dawood Shehabi, Jana Hrbková, Malgorzata Libik, Milan Mac |
Prevalence of kidney health genetic variants in adults with sickle cell nephropathy. British journal of haematology 2024 5 . Maria Armila Ruiz, Xu Zhang, M Adela Mansilla, Rima S Zahr, Christie P Thomas, Richard J Smith, Victor R Gordeuk, Santosh L Sar |
[Population characterization of mutations for sickle cell anemia and its treatment: One step towards personalized medicine for the disease]. Andes pediatrica : revista Chilena de pediatria 2024 4 95 (1): 41-52. Bernardita Cayupe, Rafael Bar |
Genetic Modifiers of Sickle Cell Anemia Phenotype in a Cohort of Angolan Children. Genes 2024 4 15 (4): . Catarina Ginete, Mariana Delgadinho, Brígida Santos, Armandina Miranda, Carina Silva, Paulo Guerreiro, Emile R Chimusa, Miguel Bri |
Genome-Wide Analysis of Exertional Rhabdomyolysis in Sickle Cell Trait Positive African Americans. Genes 2024 4 15 (4): . Mingqiang Ren, Nyamkhishig Sambuughin, Ognoon Mungunshukh, Daniel Baxter Edgeworth, Daniel Hupalo, Xijun Zhang, Matthew D Wilkerson, Clifton L Dalgard, Francis G O'Connor, Patricia A Deust |
Estimating the serological underrecognition of patients with weak or partial RHD variants. Transfusion 2024 4 . Glenn Ramsey, Christina M Barrite |
Genetic Variants Associated with the Risk of Stroke in Sickle Cell Anemia: Systematic Review and Meta-Analysis. Hemoglobin 2024 4 48 (2): 101-112. Aradhana Kumari, Ganesh Chauhan, Partha Kumar Chaudhuri, Sushma Kumari, Anupa Pras |
Maternal and infant outcomes in women with sickle cell disease: a matched cohort study. Archives of disease in childhood. Fetal and neonatal edition 2024 4 . Oishi Sikdar, Hemant Ambulkar, Allan Jenkinson, Catherine Hedley, Jemma Johns, Ravindra Bhat, Theodore Dassios, Christopher Harris, Anne Greenou |
CETP gene polymorphisms and haplotypes are explanatory variables for HDL cholesterol level in sickle cell disease. Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas 2024 1 57 e12879. N R C Cruz, T N S Valente, F O Ferreira, L R Macedo, A R Belisário, C M da Silva, N S Oliveira, A F F Gomides, C Velloso-Rodrigu |
Association of Normal and Mutated APOL1 G2 Rs60910145 alleles with SCD, Body Mass Index, and Renal Function Biomarkers and Indices. Current research in translational medicine 2024 1 72 (1): 103414. Abazar Mahmoud Ismail, Bakri Mohammed Nour, Adam Dawoud Abakar, Babiker Saad Almugadam, Hisham N Altayb, Rania TagEsir Ahmed, Mubarak Elsaeed Mustafa Elkarsa |
Catechol-O-methyltransferase gene (COMT) is associated with neurocognitive functioning in patients with sickle cell disease. Current research in translational medicine 2024 1 72 (2): 103433. Andrew M Heitzer, Sara R Rashkin, Ana Trpchevska, Jennifer N Longoria, Evadnie Rampersaud, Yunusa Olufadi, Winfred C Wang, Darcy Raches, Brian Potter, Martin H Steinberg, Allison A King, Guolian Kang, Clifford M Takemoto, Jane S Hanki |
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