Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 744 Records) |
| Query Trace: Sickle cell[original query] |
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| Sickle Cell Anemia Screening in Newborns and Analysis of Haplotypes in Patients from Santiago Island, Cape Verde. Anemia 2024 9 2024 1687917. Ariana Freire, Laura Charola-Ramos, Elisa González-Guerra, João Gonçalves, Vanusa Rocha, Vera Afreixo, Enrique Martínez-Carretero, José M Ra |
| A comprehensive analysis of the health effects associated with smoking in the largest population using UK Biobank genotypic and phenotypic data. Heliyon 2024 9 10 (16): e35649. Zixun Lin, Jiayi Xiong, Jiaqi Yang, Yuanfeng Huang, Jinchen Li, Guihu Zhao, Bin |
| Genetic contributions to pain modulation in sickle cell: A focus on single nucleotide polymorphisms. Gene reports 2024 9 36 . Katrina R Hamilton, Lakeya S McGill, Claudia M Campbell, Sophie M Lanzkron, C Patrick Carroll, Alban Latremoliere, Jennifer A Haythornthwaite, Olga A Korczeniews |
| Genetic variants associated with white blood cell count amongst individuals with sickle cell disease. British journal of haematology 2024 9 . Mina Cintho Ozahata, Yuelong Guo, Isabel Gomes, Barbara Malta, André Belisário, Luiz Amorim, Dahra Teles, Miriam Park, Shannon Kelly, Ester C Sabino, Grier P Page, Brian Custer, Carla L Dinardo, |
| Disease severity drives risk of venous thrombotic events in women with sickle cell disease in a single-center retrospective study. Research and practice in thrombosis and haemostasis 2024 8 8 (4): 102471. Jennifer Light, Christina M Abrams, Anton Ilich, Shuai Huang, Hongtu Zhu, Jacquelyn Baskin-Miller, Erica M Sparkenbau |
| Genome editing in K562 cells suggests a functional role for the XmnI Gg polymorphism: a widely used genetic marker in ?-thalassemia and sickle cell disease patients. Cellular and molecular biology (Noisy-le-Grand, France) 2024 8 70 (7): 230-236. Azadeh Ahmadifard, Nahal Maroofi, Maryam Maleki Tehrani, Tahere Dabestani, Masoumeh Sadat Mousavi Maleki, Sepideh Bayrami, Mehdi Ban |
| Identification of genetic variants associated with clinical features of sickle cell disease. Scientific reports 2024 8 14 (1): 20070. Katharine Tsukahara, Xiao Chang, Frank Mentch, Kim Smith-Whitley, Anita Bhandari, Cindy Norris, Joseph T Glessner, Hakon Hakonars |
| Genotyped RHD+ red cells for D-positive patients with sickle cell disease with conventional RHD and unexpected anti-D. Blood 2024 8 . Stella T Chou, Julia Mewha, David F Friedman, VIctoia Lazariu, Shaimaa Makrm, Gorka Ochoa, Sunitha Vege, Connie Marie Westho |
| 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 |
| The endocannabinoid system's genetic polymorphisms in sickle cell anemia patients. Scientific reports 2024 12 14 (1): 31562. Amanda Cristina Meneguetti Berti, Vanessa da Silveira Ramos de Castro, Gabriela Silva Arcanjo, Aderson da Silva Araujo, Antonio Roberto Lucena-Araujo, Marcos André Cavalcanti Bezerra, Lucas Gazarini, Danilo Grünig Humberto da Silva, Edis Belini-Júni |
| Sex-stratified association of variants in the Serotonin 1A receptor gene with acute crisis pain among African American sickle cell disease patients. Experimental hematology 2024 11 104692. Nilanjana Sadhu, Ying He, Yavnika Kashyap, Giokdjen Ilktach, Michael A Wang, Yingwei Yao, Diana J Wilkie, Robert E Molokie, Zaijie Jim Wa |
| Prognostic significance of early acute splenic sequestration in children with severe sickle cell genotypes: A comprehensive longitudinal neonatal cohort study. American journal of hematology 2024 11 . Alizée Soulié, Cécile Arnaud, Serge Pissard, Isabelle Hau, Mickaël Shum, Fouad Madhi, Céline Delestrain, Sandra Biscardi, Sabine Blary, Bassem Khazem, Ekaterina Belozertsteva, Eric Guemas, Ralph Epaud, Annie Kamdem, Corinne Pondar |
| Variants in the ?-globin Locus are Associated with Pneumonia in African American Children. HGG advances 2024 10 100374. Nadine L N Halligan, Sarah C Hanks, Karen Matsuo, Taylor Martins, Sebastian Zöllner, Michael W Quasney, Laura J Scott, Mary K Dahm |
| 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 |
- Page last reviewed:Feb 1, 2024
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