Genetic modifiers of sickle cell disease

Cited by (316)

Items 201–300 of 316

1. A microfluidic-informatics assay for quantitative physical occlusion measurement in sickle cell disease
   Xingjian Zhang, Trevor Chan, Judith Carbonella, Xiangyu Gong, Noureen Ahmed, Chang Liu, Israel Demandel, Junqi Zhang, Farzana Pashankar, Michael Mak · 2022 · Lab on a Chip
2. Route Optimization of the Non-covalent Modulator of Hemoglobin PF-07059013 for the Treatment of Sickle Cell Disease, Part I: From Discovery Synthesis to First Kilogram-Scale Manufacture
   Aaron F. Baldwin, Shawn Cabral, Kris N. Jones, Jeffrey T. Kohrt, Chris Limberakis, Yiyang Liu, Javier Magano, Sébastien Monfette, Asaad S. Nematalla, Sami Ovaska et al. · 2023 · Organic Process Research & Development
3. Prevalence of sickle cell anemia in Africa: A protocol for a meta-analysis of existing studies
   Bwambale Jonani, Emmanuel Charles Kasule, Herman Roman Bwire, Otema Ricky, Joel Fredrick Arturo, Matsiko Livingstone, Nassinde Esther, Esther Namirembe, Namale Joanitah, Lillian Nabbanja Naava et al. · 2025 · PLoS ONE
4. Total hip arthroplasty: Concerns and precautions in sickle-cell trait
   Francesco Pisanu, Marco Pes, Gianfilippo Caggiari, Sebastiano Ortu, Maria Luisa Satta, Veronica Amorese, Carlo Doria · 2019 · Journal of Orthopaedics
5. Global prevalence of elevated estimated pulmonary artery systolic pressure in clinically stable children and adults with sickle cell disease: A systematic review and meta-analysis
   Mobin Ghazaiean, Hadi Darvishi‐Khezri, Behnam Najafi, Hossein Karami, Mehrnoush Kosaryan · 2025 · PLoS ONE
6. Role of FOXO3 in regulation of redox homeostasis and promotion of red blood cell longevity in sickle cell disease
   Eluri Pavitra, Meenoo Kumbhakar, Byeongsu Kim, Vivek Sachchelal Gupta, Pragati Gupta, Jeong‐Hwan Lee, Young-Kyu Han, Lakkakula VKS Bhaskar, Ganji Seeta Rama Raju, Yun Suk Huh · 2026 · Cytokine & Growth Factor Reviews
7. Long-Term Complications of Sickle Cell Disease
   Luisanna M. Sánchez, Ajibike Lapite, Alicia Chang, Titilope Fasipe · 2026 · Pediatrics in Review
8. Comments on: “Clinical, hematological and genetic data of a cohort of children with hemoglobin SD”
   Maria Stella Figueiredo · 2016 · Revista Brasileira de Hematologia e Hemoterapia
9. The additional genetic diagnosis of homozygous sickle cell disease in a patient with Waardenburg-Shah syndrome: a case report
   Angela Rankine‐Mullings, Graham Roger Serjeant, Zachary Ramsay, Neil A. Hanchard, Monika Asnani · 2019 · Journal of Medical Case Reports
10. Pattern of Renal Blood Flow and Renovascular Parameters in Adult Patients With Sickle Cell Disease
    Akram Mahmoud Asbeutah, Adekunle D. Adekile, Abdullah Abdulaziz Almajran, Abdul Aziz Asbeutah, Athbi A. Naief, Hassan Al‐Jafar · 2019 · Journal of Ultrasound in Medicine
11. Detection of Haemoglobin S using Multiplex Ligation-Dependent Probe Amplification and Flow-through Hybridization Techniques: Experience in a Tertiary Hospital
    Hafiza Alauddin · 2020 · Medicine & health
12. Basic biochemical and hematological parameters of structural hemoglobin variants in the postpartum women and their respective newborn from Manaus, Amazonas, Brazil
    Roberta da Silva Brito, Lecita Marreira de Lima Barros, Lilian Wallace Moreira, Regina Neves Normando, Thiago de Jesus Bacha, Marilda de Souza Gonçalves, Rajendranath Ramasawmy, Stéfani Ferreira de Oliveira, Keyla Emanulle Ramos da Silva, Nelson Abrahim Fraiji et al. · 2022 · BMC Pregnancy and Childbirth
13. Comparing Hearing Loss in Children with Adults Living with Sickle Cell Disease and Sickle Cell Traits
    TS Ibekwe, Christine Rogers, Lebogang Ramma · 2024 · Nigerian Journal of Clinical Practice
14. The modifiers that cause changes in gene essentiality
    Amandine Batté, Núria Bosch-Guiteras, Carles Pons, Marina Ota, Maykel Lopes, Sushma Sharma, Nicolò Tellini, Claire Paltenghi, Michelle M. Conti, Kwan Ting Kan et al. · 2026 · Cell Systems
15. RETRACTED: Gene frequency reports of sickle cell trait among six human populations of Jammu and Kashmir, India
    Mohd Fareed, Malik Azeem Anwar, Mir Kaisar Ahmad, Mohammad Afzal · 2016 · Gene Reports · Retracted
16. Sickle cell trait in orthopaedic surgery: A real issue or just a bogeyman
    Francesco Pisanu, Gianfilippo Caggiari, Sebastiano Ortu, Maria Luisa Satta, Carlo Doria · 2017 · International Journal of Clinical Rheumatology
17. Hydroxycarbamide decreases the free alpha‐hemoglobin pool in red blood cells of adult patients with sickle cell anemia
    Elisa Domingues‐Hamdi, Corinne Vasseur, Sadaf Pakdaman, Stéphane Moutereau, Anoosha Habibi, Pablo Bartolucci, F. Galactéros, Véronique Baudin‐Creuza · 2020 · American Journal of Hematology
18. Does TGFBR3 Polymorphism Increase the Risk of Silent Cerebral Infarction in Egyptian Children with Sickle Cell Disease?
    Hoda M. A. Hassab, Marwa Hanafi, Ahmed A. ElBeheiry, Mona Hassan, Yasmine El Chazli · 2022 · The Indian Journal of Pediatrics
19. Polymorphism of the Beta Gene in Homozygous Sickle Cell Patients in Senegal and Its Influence on the Main Complications of the Disease
    Dominique Doupa · 2018 · Advances in Biochemistry
20. Sickle Cell Anemia
    Ankit Mangla, Moavia Ehsan, Nikki Agarwal, Smita Maruvada · 2019 · StatPearls
21. Association of polymorphisms in the HBG1‐HBD intergenic region with HbF levels
    Hu Li, Ling Huang, Yuanyuan Han, Tingting Jin, Juan Liu, Minmin Jiang, Xingmei Liu, Yuanyuan Li, Wenping Han, Bangquan An et al. · 2020 · Journal of Clinical Laboratory Analysis
22. Combining microfluidic spleen-like filtering unit with machine learning algorithms to characterize rare hereditary hemolytic anemia
    Valeria Rizzuto, Arianna Mencattini, Begoña Álvarez-González, Davide Di Giuseppe, Eugenio Martinelli, David Benéitez, María del Mar Mañú‐Pereira, Maria Jose Lopez-Martinez, Josep Samitier · 2021 · Research Square
23. Pulmonary Hypertension in Children with Sickle Cell Disease: a Review of the Current Literature
    Jamie K. Harrington, Usha Krishnan · 2019 · Current Pediatrics Reports
24. Markers of Disease Severity Amongst Homozygous Sickle Cell Anaemia Attending Outpatient At Bowen University Teaching Hospital Ogbomoso, Nigeria.
    Kehinde Joyce Olufemi-Aworinde, Tolulase Olutogun, Ademola Toyosi Abolarin, Yetunde Toyin Olasinde, Daniel Adebosu Gbadero · 2020 · International Journal Of Medical Science And Clinical Invention
25. DISTRIBUTION OF SICKLE CELL ALLELE IN ETHNIC SUB-GROUPS OF THARU IN NEPAL
    Manoj Kumar Tharu, Nanda Bahadur Singh · 2023 · EPRA International Journal of Multidisciplinary Research (IJMR)
26. Genetic Modifiers of Sickle Cell Anemia Phenotype in a Cohort of Angolan Children
    Catarina Ginete, Mariana Delgadinho, Brígida Santos, Armandina Miranda, Carina Silva, Paulo Guerreiro, Emile Rugamika Chimusa, Miguel Brito · 2024 · Genes
27. Genetic Variants Associated with the Risk of Stroke in Sickle Cell Anemia: Systematic Review and Meta-Analysis
    Aradhana Kumari, Ganesh Chauhan, Partha Kumar Chaudhuri, Sushma Kumari, Anupa Prasad · 2024 · Hemoglobin
28. Analysis of Haematological Parameters in Sickle Cell Trait and Sickle cell Disease patients of Chhattisgarh
    Sanjana Bhagat · 2024 · Research Journal of Pharmacy and Technology
29. A Novel One‐Sample Mendelian Randomization Approach for Count‐Type Outcomes That Is Robust to Correlated and Uncorrelated Pleiotropic Effects
    Janaka S. S. Liyanage, Jane Silva Hankins, Jeremie Heath Estepp, Deo Kumar Srivastava, Sara R. Rashkin, Clifford M. Takemoto, Yun Li, Yuehua Cui, Motomi Mori, Mitchell J. Weiss et al. · 2024 · Genetic Epidemiology
30. βS haplotypes: Genetic profile and association with biochemical parameters in individuals with Sickle cell anemia in Western Bahia, Brazil
    Ilana Luize Rocha Santana, Raphael Magalhães, Victoria Simões Bernardo, Manoel Ferreira de Magalhães Filho, Pâmela Lourdes Pereira da Silva, Larissa Paola Rodrigues Venâncio · 2025 · Human Gene
31. Splenic sequestration crisis in children with sickle cell disease in the Eastern region of Saudi Arabia
    Abdalla Mohamed Zayed, Sulaiman Almohaimeed, Turki Alotaibi, Hossam Aldosari, Tahani Alotaibi, Basheer Ahmed, Khalid Abdullah, Yasser Awadallah Yasein, Shangrila Joy Ancheta, Zechariah Jebakumar Arulantham et al. · 2025 · BMC Pediatrics
32. Sickle cell disease: suspect, check, diagnose—practical tips for non-SCD experts to suspect and diagnose SCD in low-prevalence European settings
    Giovanni Palazzi, Silvia Benemei, Cristiano Gallucci, Francesco Arcioni, Silverio Perrotta · 2025 · Frontiers in Medicine
33. One-shot Evaluation of Protein Mutability and Epistasis Score Using Structure-Based Model ESM3
    Ngai Hei Ernest Ho, I‐Son Ng, Jo‐Shu Chang · 2025 · Journal of the Taiwan Institute of Chemical Engineers
34. Influence of Alpha Thalassaemia on Hematological and Clinical Presentations in Patients of Sickle Cell-β-Thalassaemia with IVS I-5 (G→C) Mutation ( HBB : C.20A > T/ HBB : C.92 + 5G > C)
    Snehadhini Dehury, Pradeep Kumar Mohanty, Kishalaya Das, Satyabrata Meher, Siris Patel, Sarmila Sahoo · 2025 · Hemoglobin
35. Optimizing the right time to start sickle cell therapies
    Olufunke Y. Martin, Seethal A. Jacob · 2025 · Hematology
36. Epidemiology of vaso-occlusive crisis among sickle cell disease patients in India: A community-based multi-centric study
    Shaily B. Surti, Shubhangi Patel, Yogita Sharma, Deepa Bhat, Parikipandla Sridevi, Jatin Sarmah, Madhusmita Bal, Manoranjan Ranjit‬, Rabindra Kumar Jena, Bontha Veerabahu Babu · 2026 · The Indian Journal of Medical Research
37. Sickle cell disease-associated pulmonary hypertension: an integrated framework linking pathologies, mechanisms, and clinical phenotypes
    Florence Vallelian, Dominik J. Schaer, Benoît Lechartier, Paul W. Buehler, David C. Irwin · 2026 · EBioMedicine
38. Subphenotypes of Sickle Cell Disease: A Guide to Targeting Treatment?
    Martin H. Steinberg · 2026 · American Journal of Hematology
39. Successful Liver Transplantation Case Report from a Deceased Donor with Sickle Cell Anemia
    Lucas Souto Nacif, Estrella Bianca de Mello, Rafael Soares Pinheiro, Fabiana Roberto Lima, Rodrigo Bronze de Martino, Wellington Andraus, Luiz Augusto Carneiro D′Albuquerque · 2018 · Case Reports in Transplantation
40. Sickle Cell Disease
    Daniel A. Dworkis, Martin H. Steinberg · 2014 · Springer eBooks
41. Unraveling DEHP influence on hemoglobin S polymerization in sickle cell disease: Ex vivo, in vitro and in silico analysis
    Rodrigo Abreu Camacho, Aghata Vitoria Machado, Fernanda de Oliveira Mendonça, Lyzes Rosa Teixeira-Alves, Camila Cristina Guimarães-Nobre, Evelyn Mendonça-Reis, Priscila Ferreira da Silva, Thyago R. Cardim-Pires, Leandro Miranda‐Alves, Clemilson Berto Junior · 2024 · Toxicology in Vitro
42. Electrocardiographic Changes and Their Association With Disease Severity in Adults With Sickle Cell Anemia at a Tertiary Care Center: A Cross-Sectional Study
    I G Priyan, Preetam Narayan Wasnik, Pankaj Kumar Kannauje, Pranita Das, Satyajit Singh, Suprava Patel · 2024 · Cureus
43. A Rare Case of Multiple Bone Infarctions and Abnormal Pulmonary Function Tests in a Patient With Compound Heterozygous Hemoglobin S and Type 2 Hereditary Persistence of Fetal Hemoglobin
    Khalid A. Alnaqbi · 2024 · Cureus
44. Case Report: Crosstalk between systemic lupus erythematosus and sickle cell syndromes—two cases from eastern India
    Dhriti Sundar Das · 2024 · Frontiers in Lupus
45. Activation of γ-globin expression by a common variant disrupting IKAROS-binding motif in β-thalassemia
    Hualei Luo, Jueheng Wang, Lang Qin, Xinhua Zhang, Hailiang Liu, Chao Niu, Mengyang Song, Congwen Shao, Peng Xu, Miao Yu et al. · 2024 · Journal of genetics and genomics/Journal of Genetics and Genomics
46. Interplay of co-inherited diseases can turn benign syndromes in a deadly combination: haemoglobinopathy and bilirubin transport disorder.
    T. M. Stolmeijer, A P van der Berg, Jacqueline Koeze, A. S. H. Gouw, Frederik Nanne Croles, Egbert Sieders, Jan G. Zijlstra · 2015 · PubMed
47. Evaluating Microalbuminuria in Children with Sickle Cell Disease: Review of the Literature
    Barbara Speller‐Brown, Claire L. Anderson, Shamir Tuchman, Yunfei Wang, Kirtida Mistry, Brenda Martin, Amy Frantz, Joshua Coons, Deepika S. Darbari · 2018 · The Journal for Nurse Practitioners
48. Health care for people with sickle cell disease in a medium-sized Brazilian city
    Mário Cézar de Oliveira, Rosana Paula Pires, Lúcio Borges de Araújo, João Carlos de Oliveira, Tânia M. Alcântara · 2020 · Open Science Journal
49. A case-control genome-wide association study identifies ge netic modifie rs of fetal hemoglobin in sickle cell disease.
    Li Liu, Alexander Pertsemlidis · 2016 · The Medicine Forum
50. A Versatile and Efficient Novel Approach for Mendelian Randomization Analysis with Application to Assess the Causal Effect of Fetal Hemoglobin on Anemia in Sickle Cell Anemia
    Janaka S. S. Liyanage, Jeremie Heath Estepp, Kumar Srivastava, Sara R. Rashkin, Vivien Sheehan, Jane Silva Hankins, Clifford M. Takemoto, Yun Li, Yuehua Cui, Motomi Mori et al. · 2022 · Mathematics
51. Is Sickle Cell Trait as Benign as it is Usually Assumed
    Carroll N. Flansburg · 2014
52. Haemolysis in sickle cell anaemia: a genotype/phenotype association study
    Andreia Coelho, Alexandra Dias, Anabela Morais, Baltazar Nunes, Emanuel Ferreira, Isabel Picanço, Paula Faustino, João Lavinha · 2014 · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT)
53. PROGRAMA DE PÓS-GRADUAÇÃO EM GENÉTICA
    Jéssika Viviani Okumura · 2013
54. Relationship between adenosine deaminase polymorphism (c.22G > A) and oxidative stress in sickle cell anemia
    Danilo Grünig Humberto da Silva, Edis Belini-Junior, Lidiane S. Torres, Jéssika Viviani Okumura, Willian Marcel Barberino, Renan Garcia de Oliveira, Vanessa Urbinatti Teixeira, Clarisse Lopes de Castro Lobo, Eduardo Alves de Almeida, Cláudia R. Bonini-Domingos · 2016 · Meta Gene
55. Genomics in Toxicology
    David Scoville, Terrance J. Kavanagh · 2017 · Elsevier eBooks
56. An age dependent response to hydroxyurea in pediatric sickle cell anemia patients with alpha thalassemia trait
    Lisa M. Figueiredo, Kerry A. Morrone, Catherine Wei, Karen Ireland, Hillel W. Cohen, Catherine Driscoll, Deepa G. Manwani · 2017 · Blood Cells Molecules and Diseases
57. COMPLICATIONS AND OUTCOMES OF PREGNANCY IN WOMEN WITH SICKLE CELL ANAEMIA- A STUDY CONDUCTED IN A TERTIARY CARE CENTRE IN NORTH KERALA
    Anupama Manjula A, Mary Tresa · 2017 · Journal of Evolution of Medical and Dental Sciences
58. Doença falciforme e atividade laboral
    Rosana Paula Pires · 2019
59. Sickle cell anemia: HBB haplotypes; clinical heterogeneity; iPSC modeling
    Kim Vanuytsel, Martin H. Steinberg, George J. Murphy · 2020 · Elsevier eBooks
60. EXPERIÊNCIAS DE PERDA DENTÁRIA E QUALIDADE DE VIDA EM PACIENTES TRANSPLANTADOS RENAIS HOSPITALIZADOS
    Letícia Brandão Sousa, Danila Lorena Nunes dos Santos, Camila Maria Simas Almondes, Fernanda Ferreira Lopes · 2021
61. Association between hemolysis intensity, genetic markers and clinical evolution in patients with sickle cell disease
    Oladele Simeon Olatunya · 2018
62. Avaliação das variações no número de cópias (CNVs) na susceptibilidade ao acidente vascular cerebral em pacientes com anemia falciforme
    Pedro Rodrigues Sousa da Cruz · 2016
63. Polymorphisms in heme oxygenase-1 and bone morphogenetic protein receptor 1 genes and estimated glomerular filtration rate in brazilian sickle cell anemia patients
    Okeke Chinedu · 2018
64. Chapter 10. Post-Genomics, Cell Reprogramming, and the Obstacle to Biomedicine
    Pierre‐Luc Germain, Giuseppe Testa · 2020 · Hermann eBooks
65. Sickle cell trait in orthopaedic surgery: A real issue or just a bogeyman
    Francesco Pisanu, Gianfilippo Caggiari, Sebastiano Ortu, Maria Luisa Satta, Carlo Doria · 2017 · International Journal of Clinical Rheumatology
66. Sickle cell trait in orthopaedic surgery: A real issue or just a bogeyman
    Francesco Pisanu, Gianfilippo Caggiari, Sebastiano Ortu, Maria Luisa Satta, Carlo Doria · 2017 · International Journal of Clinical Rheumatology
67. Evaluation of anti-inflammatory response in sickle cell anemia patients
    Adekunle Emmanuel Alagbe · 2017
68. Effects of Quantitative Trait Loci (QTLs) of BCL11A and HBS1L-MYB genes on clinical-biological variability of sickle cell disease in a Senegalese pediatric population
    Fatou Guèye Tall, El Hadji Malick Ndour, Moustapha Djité, Oumou K. Barry, Pape Matar Kandji, Papa Madièye Guéye, Aynina Cissé, Philomène Lopez Sall · 2022 · African Journal of Biochemistry Research
69. Are human connectomes heritable?
    Jaewon Chung, Eric Bridgeford, Michael A. Powell, Derek Pisner, Ting Xu, Joshua T Vogelstein · 2023 · bioRxiv (Cold Spring Harbor Laboratory)
70. Association of Vascular Endothelial Growth Factor gene Polymorphism 2578C/A with Vaso-occlusive Crisis in sickle disease
    Marwa Salah Farhan, Mohammed Said ElSheemy, Hams Ahmed Attalla, Wafaa M. Radwan · 2023 · Menoufia Medical Journal
71. Genetic, molecular, and cellular determinations of sex-specific cardiovascular traits
    Felix C. Vaura · 2023 · Elsevier eBooks
72. Genetic variants associated with the risk of stroke in sickle cell disease: a systematic review and meta-analysis
    Aradhana Kumari, Ganesh Chauhan, Partha Kumar Chaudhuri, Anupa Prasad · 2023 · medRxiv
73. Perfil clínico e epidemiológico de pacientes com hemoglobinopatia SC: estudo de coorte prospectivo multicêntrico
    Dahra Teles Soares Cruz · 2023
74. The Impact of the Coinheritance of Alpha Thalassemia and Hemoglobin F Concentration on Sickle Cell Disease
    Hawar Mohammed Saeed, Nasir A.S. Al-Allawi, Adil Abozaid Eissa · 2023 · Pharmacophore
75. Le globule rouge drépanocytaire. Données génétiques et structurelles
    F. Galactéros · 2023 · La Revue de Médecine Interne
76. Prevalence of Asymptomatic Bacteriuria in Children with Sickle Cell Disease
    Ali Nassif, Abdulmoneim Ghanem, Maha Khori, Ahmad Chreitah · 2024 · International Journal of Medical Science
77. Genomics in Toxicology
    David Scoville, Christopher M. Schaupp, Terrance J. Kavanagh · 2024 · Elsevier eBooks
78. CRISPR-CAS9-MEDIATED EX VIVO GENE EDITING FOR INHERITED HEMATOLOGICAL DISORDERS: ADVANCEMENTS, CHALLENGES, AND CLINICAL POTENTIAL
    ATASI RANJAN PANDA, S.R. Das · 2024 · International Journal of Pharmacy and Pharmaceutical Sciences
79. Associations of haematological and inflammatory biomarkers with brain volume in patients with sickle cell anaemia: A cross‐sectional retrospective study
    Naif Ali A. Majrashi, Ali M. Hendi, Turki Dhayihi, Abdullah M. Khamesi, Mohammed Qasem Masmali, Khalid Hakami, Ali S. Alyami, Bandar Alwadani, Wael A. Ageeli, Yahia Madkhali et al. · 2024 · Tropical Medicine & International Health
80. Enfermedad de células falciformes y sistema CRISPR/Cas como herramienta terapéutica. Una revisión narrativa
    Ingrid Chantal Márquez-Vega, Javier Eden Mata-Rosas, Beatriz Hernández-Monjaraz · 2024 · Casos y Revisiones de Salud
81. Identification of Pathogenic Regulatory Variants in Mendelian Diseases
    Zainab Jan, Manoj K Balyan, Nismabi A Nisamudheen, Dinesh Velayutham, Prachi Balyan, Puthen Veettil Jithesh · 2025 · Elsevier eBooks
82. Environmental, Behavioral, Psychological, and Biological Factors Affecting Mental Health in Sickle Cell Disease
    Julia A. O’Brien, Olubusola B. Oluwole, Charles Richard Jonassaint · 2025 · Springer eBooks
83. Development of 3D Intelligent Quantitative Phase Microscope for Sickle Cells Screening
    Sautami Basu, Gyanendra Narayan Singh, Ravinder Agarwal, Vishal Srivastava · 2025 · Journal of Biophotonics
84. Sickle cell health awareness, perspectives and experiences (SHAPE) survey: perspectives on sickle cell disease (SCD) from healthcare providers in India, Malaysia, and Thailand
    Roy Gomez, Annabel Su · 2025 · Orphanet Journal of Rare Diseases
85. Red Blood Cell Extracellular Vesicles as Key Players in Thromboinflammation
    Denis F. Noubouossie, Nigel S. Key · 2025 · Seminars in Thrombosis and Hemostasis
86. Hemolysis and Vaso-Occlusive Crisis in Sickle Cell Disease: A Review
    Amjad Mahmood Qadir, Abdalla Hussein Hama · 2025 · Turkish Journal of Internal Medicine
87. Environmental, Behavioral, Psychological, and Biological Factors Affecting Mental Health in Sickle Cell Disease
    Julia A. O’Brien, Olubusola B. Oluwole, Charles Richard Jonassaint · 2025 · Springer eBooks
88. Development of a Clinical Severity Score for Indian Sickle Cell Anaemia Patients
    Suraj Singh Nongmaithem, AMITABH BISWAS, SWAROOP IYER, Jandhayala Vyshnavi, ARCHANA WATH, Giriraj R. Chandak, Dipty Jain · 2026 · eJHaem
89. Sickle Cell Anemia
    Manu O. Platt, Hannah Song Lee, Liana Hatoum · 2025 · Physiology in health and disease
90. Hydroxycarbamide and Sickle Cell Anemia: Paradoxical Effects Related to Redox Mechanisms of Cellular Adaptation
    Ilana Luize Rocha Santana, Victoria Simões Bernardo, Edis Belini-Junior, Pâmela Lourdes Pereira da Silva, Danilo Grünig Humberto da Silva, Larissa Paola Rodrigues Venâncio · 2025 · ACS Omega
91. Genomics and Oral Health: An Overview
    Ruth M. DeBusk · 2014 · Springer eBooks
92. Additional file 1 of Basic biochemical and hematological parameters of structural hemoglobin variants in the postpartum women and their respective newborn from Manaus, Amazonas, Brazil
    da Silva Brito, Roberta, de Lima Barros, Lecita Marreira, Lilian Wallace Moreira, Regina Neves Normando, de Jesus, Thiago Bacha, Marilda Souza Gonçalves, Rajendranath Ramasawmy, Stéfani Ferreira de Oliveira, Keyla Emanulle Ramos da Silva, Nelson Abrahim Fraiji et al. · 2024 · Figshare
93. Additional file 1 of Global analysis of suppressor mutations that rescue human genetic defects
    Ünlü, Betül, Carles Pons, Uyen Linh Ho, Amandine Batté, Patrick Aloy, van Leeuwen, Jolanda · 2023 · Figshare
94. Additional file 2 of Global analysis of suppressor mutations that rescue human genetic defects
    Ünlü, Betül, Carles Pons, Uyen Linh Ho, Amandine Batté, Patrick Aloy, van Leeuwen, Jolanda · 2024 · Figshare
95. Sickle Cell Disease
    Martin H. Steinberg · 2026 · Springer eBooks
96. Molecular Patterns of Beta-Thalassemia in Taif Province- Saudi Arabia: Determination of Prevalent genotypes and Regions with High Incidence
    Tariq E Elmissbah, Hayaa M. Alhuthali, Mamdouh A. Allahyani, Amal S Alosaimi, Heba M. Elmasry · 2026 · Biomedical & Pharmacology Journal
97. Impact of mechanical and oxidative stress on red blood cell properties in sickle cell disease
    Maria A. Lizarralde-Iragorri · 2018 · theses.fr (ABES)
98. Suivi d’enfants drépanocytaires dépistés en période néonatale : épidémiologie des principales complications et implications méthodologiques
    Julie Sommet · 2021
99. Drépanocytose et polymorphismes génétiques : épidémiologie, prédiction de gravité et stress-oxydant
    Fatou Gueye · 2019 · theses.fr (ABES)
100. Mechanisms and consequences of alterations in vascular function in combined type 2 diabetes and sickle cell trait
     Sarah Chambers Skinner · 2018 · theses.fr (ABES)