Human Genome Epidemiology Literature Finder
Heart, Lung, Blood and Sleep Disorders
Records 1 - 30 (of 528 Records) |
Query Trace: Sickle Cell Disease[original query] |
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HLA-F and LILRB1 Genetic Polymorphisms Associated with Alloimmunisation in Sickle Cell Disease. International journal of molecular sciences 2023 9 24 (17): . Emmanuelle Bernit, Estelle Jean, Bastien Marlot, Laurine Laget, Caroline Izard, Isabelle Dettori, Sophie Beley, Isabelle Gautier, Imane Agouti, Coralie Frassati, Pascal Pedini, Christophe Picard, Julien Paganini, Jacques Chiaroni, Julie Di Cristofa |
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 |
An alcohol dehydrogenase 7 gene polymorphism associates with both acute and chronic pain in sickle cell disease. Pharmacogenomics 2023 9 . Yavnika Kashyap, Ying He, Nilanjana Sadhu, Yingwei Yao, Diana J Wilkie, Robert E Molokie, Zaijie Jim Wa |
Evidence that donors with variant RH genotypes are associated with unexpected Rh antibodies. Transfusion 2023 9 . Julie Kirkegaard, Lynsi Rahorst, Anna Burgos, Lejla Music Aplenc, Nazia Tabassum Iqbal, Sunitha Vege, Christine Lomas Francis, Connie M Westho |
Molecular Detection of Hemoglobin O-Arab in the Sudanese Population. International journal of general medicine 2023 8 16 3323-3330. Izzeldin Elbashir, Tagwa Yousif Elsayed Yous |
Pregnancy-related thromboembolism in women with sickle cell disease: An analysis of National Medicaid Data. American journal of hematology 2023 8 . Shreya Agarwal, Joseph R Stanek, Sara K Vesely, Susan E Creary, Robert M Cronin, Andrea H Roe, Sarah H O'Bri |
Clinical significance of mutational variants in beta and alpha genes in patients with hemoglobinopathies from two large Greek centers: a complex interplay between genotype and phenotype. Journal of molecular medicine (Berlin, Germany) 2023 7 . Michael D Diamantidis, Rebecca-Anastasia Karanikola, Chrysoula Polyzoudi, Sophia Delicou, Achilles Manafas, Helen Savera, Aikaterini Xydaki, Angeliki Kotsiafti, Evangelos Tsangalas, Georgia Ikonomou, Eirini Mani, Konstantinos Ntoulas, Evangelos Alexiou, Ioanna Argyrakouli, John Koskinas, Paraskevi Foti |
Detection of Transversions and Transitions in HBG2 Cis-Elements Associated with Sickle Cell Allele in Ghanaians. Biochemical genetics 2023 7 . G K Ababio, I Ekem, J Acquaye, S Y Oppong, A G B Amoah, J Brandful, I K Qua |
Metabolic signatures of cardiorenal dysfunction in plasma from sickle cell patients as a function of therapeutic transfusion and hydroxyurea treatment. Haematologica 2023 7 . Angelo D'Alessandro, S Mehdi Nouraie, Yingze Zhang, Francesca Cendali, Fabia Gamboni, Julie A Reisz, Xu Zhang, Kyle W Bartsch, Matthew D Galbraith, Joaquin M Espinosa, Victor R Gordeuk, Mark T Gladw |
The Role of Hyposthenuria in Enuresis Among Paediatric Patients With Sickle Cell Disease. Sultan Qaboos University medical journal 2023 6 23 (2): 206-211. Jasim N Al-Asadi, Alyaa M Radhi, Dhuha S Jumaa, Meaad K Hass |
MTHFR C677T Polymorphism, Plasma Homocysteine, and PDGF-AA Levels and Transcranial Doppler Velocity in Children with Sickle Cell Disease. Indian pediatrics 2023 6 . Asmaa A Mahmoud, Nahla M S Abd El Hady, Mohammed S Rizk, Ahmed M El-Hawwary, Nagwan Y Sal |
Role of paraoxonase 1 activity and PON1 gene polymorphisms in sickle cell disease. Scientific reports 2023 5 13 (1): 7215. Joelma Figueiredo Menezes, Magda Oliveira Seixas Carvalho, Larissa Carneiro Rocha, Felipe Miranda Dos Santos, Elisângela Vitória Adorno, Cyntia Cajado de Souza, Rayra Pereira Santiago, Caroline Conceição da Guarda, Rodrigo Mota de Oliveira, Camylla Vilas Boas Figueiredo, Suéllen Pinheiro Carvalho, Sètondji Cocou Modeste Alexandre Yahouédéhou, Luciana Magalhães Fiuza, Corynne Stéphanie Ahouefa Adanho, Thassila Nogueira Pitanga, Isa Menezes Lyra, Valma Maria Lopes Nascimento, Alberto Augusto Noronha-Dutra, Marilda Souza Goncalv |
Sickle Cell Hemoglobin Genotypes Affect Malaria Parasite Growth and Correlate with Exosomal miR-451a and let-7i-5p Levels. International journal of molecular sciences 2023 4 24 (8): . Keri Oxendine Harp, Alaijah Bashi, Felix Botchway, Daniel Addo-Gyan, Mark Tetteh-Tsifoanya, Amanda Lamptey, Georgina Djameh, Shareen A Iqbal, Cecilia Lekpor, Saswati Banerjee, Michael D Wilson, Yvonne Dei-Adomakoh, Andrew A Adjei, Jonathan K Stiles, Adel Dri |
RASA3 is a candidate gene in sickle cell disease-associated pulmonary hypertension and pulmonary arterial hypertension. Pulmonary circulation 2023 4 13 (2): e12227. Clare C Prohaska, Xu Zhang, Tae-Hwi L Schwantes-An, Robert S Stearman, Stanley Hooker, Rick A Kittles, Micheala A Aldred, Katie A Lutz, Michael W Pauciulo, William C Nichols, Ankit A Desai, Victor R Gordeuk, Roberto F Macha |
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 |
Estimating the serological underrecognition of patients with weak or partial RHD variants. Transfusion 2024 4 . Glenn Ramsey, Christina M Barrite |
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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- Page last updated:Jun 17, 2024
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