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Global distribution of the sickle cell gene and geographical confirmation of the malaria hypothesis
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1001/archinte.1910.00050330050003openalex-snapshot
PECULIAR ELONGATED AND SICKLE-SHAPED RED BLOOD CORPUSCLES IN A CASE OF SEVERE ANEMIA
inferredcites →https://doi.org/10.1002/(sici)1096-8652(199811)59:3<208::aid-ajh5>3.0.co;2-ropenalex-snapshot
Hemoglobins in Togolese Newborns: Hb S, Hb C, Hb Bart's, and α-Globin Gene Status
inferredcites →https://doi.org/10.1002/ajh.2830020104openalex-snapshot
Sickle cell anemia and trait in a population of southern india
inferredcites →https://doi.org/10.1002/ajh.2830060203openalex-snapshot
Sickle cell anemia and trait in Southern India: Further studies
inferredcites →https://doi.org/10.1002/ajh.2830400413openalex-snapshot
Presence of an African β‐globin gene cluster haplotype in normal chromosomes in sicily
inferredcites →https://doi.org/10.1002/ajpa.1330200409openalex-snapshot
The blood and serum groups of selected populations in South India and Ceylon
inferredcites →https://doi.org/10.1002/ajpa.1330300108openalex-snapshot
Distribution of hereditary blood groups among Indians in South America. VII. In Argentina
inferredcites →https://doi.org/10.1002/ajpa.1330420316openalex-snapshot
Genetic distances among the Ho tribe and other groups of Central Indians
inferredcites →https://doi.org/10.1002/ajpa.1330430114openalex-snapshot
Anthropological studies among Libyans. Erythrocyte genetic factors, serum haptoglobin phenotypes and anthropometry
inferredcites →https://doi.org/10.1002/ajpa.1330520404openalex-snapshot
Blood groups and types, hemoglobin variants, and G‐6‐PD deficiency among Abu Dhabians in the United Arab Emirates
inferredcites →https://doi.org/10.1002/ajpa.1330670408openalex-snapshot
A study of some genetic characteristics of the Fur and Baggara tribes of the Sudan
inferredcites →https://doi.org/10.1002/ajpa.1330760306openalex-snapshot
Genetic studies among the sedentes and migrant oraons of eastern India
inferredcites →https://doi.org/10.1007/bf00273124openalex-snapshot
Hemoglobin E: Distribution and population dynamics
inferredcites →https://doi.org/10.1007/bf00274769openalex-snapshot
The distribution and interaction of haemoglobin variants and the ? thalassaemia gene in Liberia
inferredcites →https://doi.org/10.1007/bf00278864openalex-snapshot
Frequency of human Aγ75Thr globin chain in a population from Tunisia
inferredcites →https://doi.org/10.1007/bf00281052openalex-snapshot
Populationsgenetische Untersuchungen �ber die Verteilung von H�moglobin S und Glucose-6-Phosphat-Dehydrogenasemangel im Bodrogk�z (Nordostungarn)
inferredcites →https://doi.org/10.1007/bf00286522openalex-snapshot
Hemoglobins S and C in Upper Volta
inferredcites →https://doi.org/10.1007/bf00394299openalex-snapshot
Red cell glucose-6-phosphate dehydrogenase deficiency and haemoglobin variants among ten endogamous groups of Maharashtra and West Bengal
inferredcites →https://doi.org/10.1007/s00277-002-0471-6openalex-snapshot
Epidemiological profile of hemoglobinopathies in the Mauritanian population
inferredcites →https://doi.org/10.1007/s10682-997-1508-zopenalex-snapshot
Environment change, geographic migration and sickle cell anaemia
inferredcites →https://doi.org/10.1016/0035-9203(50)90055-1openalex-snapshot
A medical survey in a gold coast village
inferredcites →https://doi.org/10.1016/0035-9203(54)90101-7openalex-snapshot
The distribution of the sickle-cell trait in East Africa and elsewhere, and its apparent relationship to the incidence of subtertian malaria
inferredcites →https://doi.org/10.1016/0035-9203(69)90158-8openalex-snapshot
Sickling in Zanzibar Island—its incidence, regional variation, and relationship with splenomegaly rates
inferredcites →https://doi.org/10.1016/0035-9203(70)90197-5openalex-snapshot
A survey of the incidence of sickle cell trait and glucose-6-phosphate dehydrogenase deficiency in Zambia
inferredcites →https://doi.org/10.1016/0035-9203(80)90095-4openalex-snapshot
The immune response to a meningococcal polysaccharide vaccine in an African village
inferredcites →https://doi.org/10.1016/0035-9203(81)90447-8openalex-snapshot
Sickle cell trait and the immune response to meningococcal vaccines
inferredcites →https://doi.org/10.1016/0035-9203(84)90023-3openalex-snapshot
Neonatal screening for sickle cell disease in the Eastern Province of Saudi Arabia
inferredcites →https://doi.org/10.1016/0035-9203(86)90027-1openalex-snapshot
Anaemia of pregnancy in Mozambique
inferredcites →https://doi.org/10.1016/0035-9203(92)90083-oopenalex-snapshot
Morbidity from malaria and immune responses to defined Plasmodium falciparum antigens in children with sickle cell trait in The Gambia
inferredcites →https://doi.org/10.1016/0160-8002(78)90010-2openalex-snapshot
Malarial ecology: A global perspective
inferredcites →https://doi.org/10.1016/j.actatropica.2007.10.003openalex-snapshot
Interethnic differences in carriage of haemoglobin AS and Fcγ receptor IIa (CD32) genotypes in children living in eastern Sudan
inferredcites →https://doi.org/10.1016/j.coi.2009.04.001openalex-snapshot
Genetic control of resistance to human malaria
inferredcites →https://doi.org/10.1016/j.medcli.2009.04.021openalex-snapshot
Incidencia de la anemia de células falciformes en Guinea Ecuatorial
inferredcites →https://doi.org/10.1016/j.mib.2006.06.009openalex-snapshot
Human red blood cell polymorphisms and malaria
inferredcites →https://doi.org/10.1016/j.micinf.2005.12.005openalex-snapshot
Impact of red blood cell polymorphisms on the antibody response to Plasmodium falciparum in Senegal
inferredcites →https://doi.org/10.1016/j.puhe.2007.09.007openalex-snapshot
Thalassaemia screening in a non-prevalent region of a prevalent country (Turkey): is it necessary?
inferredcites →https://doi.org/10.1016/j.puhe.2007.12.005openalex-snapshot
Neonatal screening and clinical care programmes for sickle cell disorders in sub-Saharan Africa: Lessons from pilot studies
inferredcites →https://doi.org/10.1016/j.puhe.2008.01.008openalex-snapshot
Newborn screening for sickle cell disease in a Nigerian hospital
inferredcites →https://doi.org/10.1016/s0009-9120(67)80016-xopenalex-snapshot
Hemoglobin variants in Saskatchewan
inferredcites →https://doi.org/10.1016/s0035-9203(00)90057-9openalex-snapshot
Anaemia in pregnant Ghanaian women: importance of malaria, iron deficiency, and haemoglobinopathies
inferredcites →https://doi.org/10.1016/s0035-9203(03)80010-xopenalex-snapshot
Frequencies of sickle cell trait and glucose-6-phosphate dehydrogenase deficiency differ in highland and nearby lowland malaria-endemic areas of Kenya
inferredcites →https://doi.org/10.1016/s0047-2484(77)80016-xopenalex-snapshot
Genetics, Evolution and Man
inferredcites →https://doi.org/10.1016/s0140-6736(02)08273-9openalex-snapshot
Protective effects of the sickle cell gene against malaria morbidity and mortality
inferredcites →https://doi.org/10.1016/s0140-6736(63)91688-xopenalex-snapshot
THREE INHERITED RED-CELL ABNORMALITIES IN A DISTRICT OF GREECE Thalass�mia, Sickling, and Glucose-6-phosphate-dehydrogenase Deficiency
inferredcites →https://doi.org/10.1016/s0140-6736(66)92137-4openalex-snapshot
SPLENOMEGALY AND SICKLE-CELL TRAIT IN A MALARIA-ENDEMIC VILLAGE
inferredcites →https://doi.org/10.1016/s0140-6736(76)91327-1openalex-snapshot
THALASSÆMIA TRAIT, ABNORMAL HÆMOGLOBINS, AND RAISED FETAL HÆMOGLOBIN IN KARACHI
inferredcites →https://doi.org/10.1016/s0950-3536(05)80071-xopenalex-snapshot
8 The population genetics of the haemoglobinopathies
inferredcites →https://doi.org/10.1016/s0950-3536(98)80069-3openalex-snapshot
1 The population genetics of the haemoglobinopathies
inferredcites →https://doi.org/10.1016/s1473-3099(04)01043-6openalex-snapshot
The global distribution and population at risk of malaria: past, present, and future
inferredcites →https://doi.org/10.1017/cbo9780511542497openalex-snapshot
Human Biology of Afro-Caribbean Populations
inferredcites →https://doi.org/10.1038/171577c0openalex-snapshot
Absence of the Sickle Cell Trait in the Bushmen of South-West Africa
inferredcites →https://doi.org/10.1038/172638a0openalex-snapshot
Absence of the Sickle Cell Trait in Seventy-two Australian Aboriginals
inferredcites →https://doi.org/10.1038/177041b0openalex-snapshot
Absence of Abnormal Hæmoglobins in some Australian Aboriginals
inferredcites →https://doi.org/10.1038/177757a0openalex-snapshot
Abnormal Hæmoglobins in the Kasai Province of the Belgian Congo
inferredcites →https://doi.org/10.1038/190093b0openalex-snapshot
Absence of Abnormal Hæmoglobins in Colombian Tunebo Indians
inferredcites →https://doi.org/10.1038/198492b0openalex-snapshot
Distribution of Sickle-cell Hæmoglobin in Saudi Arabia
inferredcites →https://doi.org/10.1038/321744a0openalex-snapshot
High frequencies of α-thalassaemia are the result of natural selection by malaria
inferredcites →https://doi.org/10.1038/383522a0openalex-snapshot
High incidence of malaria in α-thalassaemic children
inferredcites →https://doi.org/10.1038/nature07632openalex-snapshot
A global network for investigating the genomic epidemiology of malaria
inferredcites →https://doi.org/10.1038/ng.554openalex-snapshot
Genetic variation in human HBB is associated with Plasmodium falciparum transmission
inferredcites →https://doi.org/10.1038/ng1105-1160openalex-snapshot
Malaria-protective traits at odds in Africa?
inferredcites →https://doi.org/10.1038/ng1660openalex-snapshot
Negative epistasis between the malaria-protective effects of α+-thalassemia and the sickle cell trait
inferredcites →https://doi.org/10.1038/nrg2632openalex-snapshot
Spatial patterns of variation due to natural selection in humans
inferredcites →https://doi.org/10.1038/sj.gene.6363703openalex-snapshot
Human genetic factors related to susceptibility to mild malaria in Gabon
inferredcites →https://doi.org/10.1046/j.1365-3156.1997.d01-322.xopenalex-snapshot
Higher resistance to Plasmodium falciparum infection in patients with homozygous sickle cell disease in western Kenya
inferredcites →https://doi.org/10.1046/j.1365-3156.1999.43381.xopenalex-snapshot
Malaria infection and morbidity in infants in relation to genetic polymorphisms in Tanzania
inferredcites →https://doi.org/10.1073/pnas.0910840106openalex-snapshot
Epistatic interactions between genetic disorders of hemoglobin can explain why the sickle-cell gene is uncommon in the Mediterranean
inferredcites →https://doi.org/10.1073/pnas.252649199openalex-snapshot
An Ethiopian pattern of human adaptation to high-altitude hypoxia
inferredcites →https://doi.org/10.1080/00034983.1979.11687243openalex-snapshot
Abnormal haemoglobins in the Sudan savanna of Nigeria
inferredcites →https://doi.org/10.1080/00034983.1980.11687396openalex-snapshot
Anaemia in a rural population in Nigeria (Ilora)
inferredcites →https://doi.org/10.1080/00034983.1984.11811837openalex-snapshot
Anaemia in young Primigravidae in the guinea savanna of Nigeria: sickle-cell trait gives partial protection against malaria
inferredcites →https://doi.org/10.1080/00034983.1986.11812064openalex-snapshot
Cord blood screening for haemoglobinopathies in northern Nigeria
inferredcites →https://doi.org/10.1080/02724936.1986.11748413openalex-snapshot
Haematological values in healthy Nigerian infants
inferredcites →https://doi.org/10.1080/03014467500000671openalex-snapshot
Comparative study of haemoglobin types of two populations of eastern Senegal—Bedik and Niokholonko
inferredcites →https://doi.org/10.1080/03014467600001241openalex-snapshot
Blood polymorphism frequencies in the Sara Majingay of Chad
inferredcites →https://doi.org/10.1080/03014467600001731openalex-snapshot
The blood groups, serum groups, red-cell isoenzymes and haemoglobins of the Sandawe and Nyaturu of Tanzania
inferredcites →https://doi.org/10.1080/03014467700002451openalex-snapshot
Serogenetic studies on the Kavango peoples of South West Africa
inferredcites →https://doi.org/10.1080/03014467900003711openalex-snapshot
The Njinga of Angola: a serogenetic study
inferredcites →https://doi.org/10.1080/03014468700006902openalex-snapshot
The effect of homozygous sickle cell disease on the age at menarche in Nigerian schoolgirls
inferredcites →https://doi.org/10.1080/03014469100001612openalex-snapshot
Population genetics of abnormal haemoglobins in Burkina Faso, West Africa
inferredcites →https://doi.org/10.1080/03630260500310711openalex-snapshot
α-Thalassemia Among Tribal Populations of Eastern India
inferredcites →https://doi.org/10.1080/03630260802341745openalex-snapshot
Carrier Screening and Prenatal Diagnosis of Hemoglobinopathies. A Study of Indigenous and Immigrant Couples in Northern Greece, Over the Last 5 Years
inferredcites →https://doi.org/10.1080/09720073.2008.11891043openalex-snapshot
G6PD Deficiency, Sickle Cell Trait, Haptoglobin and Transferrin Polymorphisms among Koyadoras and Nayakpods of Andhra Pradesh
inferredcites →https://doi.org/10.1080/09720073.2008.11891047openalex-snapshot
Incidence of NESTROFT-Positives and Haemoglobin S among the Jats and Brahmins of Sampla, Haryana
inferredcites →https://doi.org/10.1080/09720073.2008.11891066openalex-snapshot
Glucose-6-Phosphate Dehydrogenase Deficiency and Sickle Cell Hemoglobin among the Warli Tribe of Dadra and Nagar Haveli
inferredcites →https://doi.org/10.1080/09720073.2009.11891083openalex-snapshot
Glucose-6-Phosphate Dehydrogenase Deficiency and Sickle Cell Hemoglobin among the Dhodias of Dadra Nagar Haveli
inferredcites →https://doi.org/10.1086/519221openalex-snapshot
Combining Evidence of Natural Selection with Association Analysis Increases Power to Detect Malaria-Resistance Variants
inferredcites →https://doi.org/10.1086/519390openalex-snapshot
Associations between α+‐Thalassemia andPlasmodium falciparumMalarial Infection in Northeastern Tanzania
inferredcites →https://doi.org/10.1086/589778openalex-snapshot
Factors Determining the Heterogeneity of Malaria Incidence in Children in Kampala, Uganda
inferredcites →https://doi.org/10.1086/592224openalex-snapshot
Sickle Cell Trait Is Associated with a Delayed Onset of Malaria: Implications for Time‐to‐Event Analysis in Clinical Studies of Malaria
inferredcites →https://doi.org/10.1093/hmg/ddm350openalex-snapshot
Haemoglobin S and haemoglobin C: 'quick but costly' versus 'slow but gratis' genetic adaptations to Plasmodium falciparum malaria
inferredcites →https://doi.org/10.1093/oxfordjournals.aje.a114287openalex-snapshot
THE COINCIDENCE OF GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY AND HEMOGLOBIN S GENE IN ÇUXUROVA PROVINCE, TURKEY
inferredcites →https://doi.org/10.1093/oxfordjournals.qjmed.a066790openalex-snapshot
THE NATURAL HISTORY OF HOMOZYGOUS SICKLE-CELL ANAEMIA IN CENTRAL AFRICA
inferredcites →https://doi.org/10.1093/tropej/40.1.12openalex-snapshot
Glucose-6-Phosphate Dehydrogenase Deficiency and the Sickle Cell Gene in Makkah, Saudi Arabia
inferredcites →https://doi.org/10.1093/tropej/41.4.225openalex-snapshot
Glucose-6-phosphate Dehydrogenase Deficiency and Sickle Cell Genes in Bisha
inferredcites →https://doi.org/10.1097/00043426-198507030-00006openalex-snapshot
Incidence, effects, and management of sickle cell disease in Brazil
inferredcites →https://doi.org/10.1097/mph.0b013e318159a570openalex-snapshot
Prevalence of Beta-thalassemia and Sickle Cell Anemia Trait in Premarital Screening in Konya Urban Area, Turkey
inferredcites →https://doi.org/10.1101/sqb.1964.029.01.018openalex-snapshot
Polymorphism and Natural Selection in Human Populations
inferredcites →https://doi.org/10.1111/j.1365-2141.2006.06006.xopenalex-snapshot
Co‐inheritance of α+‐thalassaemia and sickle trait results in specific effects on haematological parameters
inferredcites →https://doi.org/10.1111/j.1447-0756.1996.tb00929.xopenalex-snapshot
Prevalence of Hemoglobin S and β‐Thalassemia in Northern Jordan*
inferredcites →https://doi.org/10.1111/j.1447-0756.1996.tb01050.xopenalex-snapshot
The Prevalence of Hemoglobin S and Glucose‐6‐Phosphate Dehydrogenase Deficiency in Jordanian Newborn
inferredcites →https://doi.org/10.1111/j.1462-5822.2005.00524.xopenalex-snapshot
Erythrocyte variants and the nature of their malaria protective effect
inferredcites →https://doi.org/10.1111/j.1469-1809.1959.tb01478.xopenalex-snapshot
THE HAPTOGLOBINS AND HAEMOGLOBINS OF ALASKAN ESKIMOS AND INDIANS
inferredcites →https://doi.org/10.1111/j.1469-1809.1971.tb00266.xopenalex-snapshot
THE SICKLE‐CELL and HAEMOGLOBIN C GENES IN SOME AFRICAN POPULATIONS
inferredcites →https://doi.org/10.1111/j.1469-1809.1996.tb00426.xopenalex-snapshot
Reproductive Reproductive behaviour and natural selection for the sickle gene in the Baiga Tribe of Central India: The role of social parenting
inferredcites →https://doi.org/10.1111/j.1601-5223.1949.tb03339.xopenalex-snapshot
THE RATE OF MUTATION OF HUMAN GENES
inferredcites →https://doi.org/10.1126/science.129.3343.216openalex-snapshot
Hemoglobin Patterns in American Indians
inferredcites →https://doi.org/10.1126/science.28.706.49openalex-snapshot
Mendelian Proportions in a Mixed Population
inferredcites →https://doi.org/10.1127/anthranz/51/1993/173openalex-snapshot
Sickle cell haemoglobin and glucose-6-phosphate dehydrogenase deficiency among Dhobis of Visakhapatnam, Andhra Pradesh, India
inferredcites →https://doi.org/10.1136/bmj.1.4857.290openalex-snapshot
Protection Afforded by Sickle-cell Trait Against Subtertian Malarial Infection
inferredcites →https://doi.org/10.1136/bmj.1.4857.294openalex-snapshot
Sickle-cell Rates in Kenya and the Southern Sudan
inferredcites →https://doi.org/10.1136/bmj.1.4912.519openalex-snapshot
A Search for Abnormal Haemoglobins in Some Southern Sudanese Peoples
inferredcites →https://doi.org/10.1136/bmj.1.4970.784openalex-snapshot
Sickling and Malaria in the Gold Coast
inferredcites →https://doi.org/10.1136/bmj.1.5021.738openalex-snapshot
A Study of the Survival Rate of Cases of Sickle-cell Anaemia
inferredcites →https://doi.org/10.1136/bmj.1.5448.1476openalex-snapshot
Frequency of Haemoglobin S and Glucose-6-Phosphate Dehydrogenase Deficiency in Southern Tanzania
inferredcites →https://doi.org/10.1136/bmj.2.4934.299openalex-snapshot
Sickling Phenomenon in Northern Greece
inferredcites →https://doi.org/10.1136/bmj.2.4988.333openalex-snapshot
Maintenance of High Sickling Rate in an African Community
inferredcites →https://doi.org/10.1136/jmg.12.1.55openalex-snapshot
Thalassaemia in northern Liberia. A survey in the Mount Nimba area.
inferredcites →https://doi.org/10.1136/jmg.15.6.443openalex-snapshot
Thalassaemia types and their incidence in Sardinia.
inferredcites →https://doi.org/10.1136/jmg.18.4.271openalex-snapshot
Phenotypic and quantitative relationship of red cell acid phosphatase with haemoglobin, haptoglobin, and G6PD phenotypes.
inferredcites →https://doi.org/10.1136/jmg.22.4.291openalex-snapshot
Admission of Hb S heterozygotes to a general hospital is relatively reduced in malarial areas.
inferredcites →https://doi.org/10.1157/13107807openalex-snapshot
Cribado neonatal de hemoglobinopatías. Una visión desde la salud pública
inferredcites →https://doi.org/10.1159/000041066openalex-snapshot
Premarital Screening of Beta-Thalassemia Trait in the Province of Denizli, Turkey
inferredcites →https://doi.org/10.1159/000152050openalex-snapshot
ABO Blood Groups and Sickle-Cell Trait Investigations in Madhya Pradesh Ujjain and Dewas Districts
inferredcites →https://doi.org/10.1159/000152051openalex-snapshot
Sickle-Cell Trait in Koraput District and Other Parts of India
inferredcites →https://doi.org/10.1159/000152167openalex-snapshot
Hemoglobin Types and Gene Flow in Pôrto Alegre, Brazil
inferredcites →https://doi.org/10.1159/000152566openalex-snapshot
Haptoglobin and Abnormal Haemoglobin Types in Sinhalese and Punjabis
inferredcites →https://doi.org/10.1159/000152653openalex-snapshot
Genetic Studies among the Kadar of Kerala
inferredcites →https://doi.org/10.1159/000152659openalex-snapshot
Genetic Markers and Anthropometry in the Populations of the Egyptian Oases of El-Kharga and El-Dakhla
inferredcites →https://doi.org/10.1159/000152707openalex-snapshot
Haemoglobinopathy Survey in an Eti -Turk Village
inferredcites →https://doi.org/10.1159/000152802openalex-snapshot
Population Genetic Studies in Kerala and the Nilgiris (South West India)
inferredcites →https://doi.org/10.1159/000153172openalex-snapshot
Erythrocyte Glutathione Reductase Polymorphism in a Sudanese Population
inferredcites →https://doi.org/10.1159/000153317openalex-snapshot
Genetic Survey of an Isolated Community in Bali, Indonesia
inferredcites →https://doi.org/10.1159/000153318openalex-snapshot
Glucose-6-Phosphate Dehydrogenase and Hemoglobin Variants in Kel Kummer Tuareg and Related Groups
inferredcites →https://doi.org/10.1159/000153609openalex-snapshot
Association of Red Cell Glucose-6-Phosphate Dehydrogenase with Haemoglohinopathies
inferredcites →https://doi.org/10.1159/000207623openalex-snapshot
Hb Bart’s and its Significance in the South African Negro
inferredcites →https://doi.org/10.1159/000226423openalex-snapshot
A Pilot Beta-Thalassaemia Screening Program in the Albanian Population for a Health Planning Program
inferredcites →https://doi.org/10.1179/136485907x154539openalex-snapshot
The distribution of hereditary erythrocytic disorders associated with malaria, in a lowland area of Nepal: a micro-epidemiological study
inferredcites →https://doi.org/10.1179/sre.1970.20.157.340openalex-snapshot
THE INTERNATIONAL YEARBOOK OF CARTOGRAPHY
inferredcites →https://doi.org/10.1182/blood-2005-01-0313openalex-snapshot
Both heterozygous and homozygous α+ thalassemias protect against severe and fatal Plasmodium falciparum malaria on the coast of Kenya
inferredcites →https://doi.org/10.1186/1475-2875-10-378openalex-snapshot
A new world malaria map: Plasmodium falciparum endemicity in 2010
inferredcites →https://doi.org/10.1186/1475-2875-2-18openalex-snapshot
Prevalence of Plasmodium falciparum infection in pregnant women in Gabon
inferredcites →https://doi.org/10.1186/1475-2875-6-17openalex-snapshot
Assembling a global database of malaria parasite prevalence for the Malaria Atlas Project
inferredcites →https://doi.org/10.1186/1475-2875-7-17openalex-snapshot
Multiplicity of Plasmodium falciparum infection in asymptomatic children in Senegal: relation to transmission, age and erythrocyte variants
inferredcites →https://doi.org/10.1201/b17115openalex-snapshot
Hierarchical Modeling and Analysis for Spatial Data
inferredcites →https://doi.org/10.1258/0969141054855300openalex-snapshot
Neonatal screening for sickle cell disorders in Ouagadougou, Burkina Faso: a pilot study
inferredcites →https://doi.org/10.1258/096914106778440626openalex-snapshot
Red blood cell disorders in Rwandese neonates: screening for sickle cell disease and glucose-6-phosphate dehydrogenase deficiency
inferredcites →https://doi.org/10.1258/096914107782066211openalex-snapshot
Neonatal screening for sickle cell disease in Central Africa: a study of 1825 newborns with a new enzyme-linked immunosorbent assay test
inferredcites →https://doi.org/10.1371/annotation/a7ab5bb8-c3bb-4f01-aa34-65cc53af065dopenalex-snapshot
Correction: A World Malaria Map: Plasmodium falciparum Endemicity in 2007
inferredcites →https://doi.org/10.1371/journal.pmed.0020128openalex-snapshot
An Immune Basis for Malaria Protection by the Sickle Cell Trait
inferredcites →https://doi.org/10.1371/journal.pmed.0030172openalex-snapshot
Seasonal Childhood Anaemia in West Africa Is Associated with the Haptoglobin 2-2 Genotype
inferredcites →https://doi.org/10.1371/journal.pmed.1000048openalex-snapshot
A World Malaria Map: Plasmodium falciparum Endemicity in 2007
inferredcites →https://doi.org/10.1371/journal.pntd.0000774openalex-snapshot
The International Limits and Population at Risk of Plasmodium vivax Transmission in 2009
inferredcites →https://doi.org/10.1542/peds.2007-2022uuuopenalex-snapshot
SCREENING NEWBORNS FOR SICKLE CELL DISEASE IN GHANA
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Frecuencia de la hemoglobina S en cinco poblaciones mexicanas y su importancia en la salud pública
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PyMC: Bayesian Stochastic Modelling inPython
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Frequency of haemoglobinopathies and glucose-6-phosphate dehydrogenase deficiency in Basra
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Occurrence of Hemoglobin D Los Angeles in Brahmins of Andhra Pradesh, South India
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Incidence of Hemoglobin S Carriers in Sicily
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Glucose-6-Phosphate Dehydrogenase Deficiency and Sickle Cell Disease in Burkina Faso
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Data on the Abnormal Hemoglobins and Glucose-6-Phosphate Dehydrogenase Deficiency in Human Populations, 1967–1973
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Studies on Plasmodium falciparum Parasitemia and Development of Anemia in Nigerian Infants during their First Year of Life
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Host factors affecting the delay of reappearance of Plasmodium falciparum after radical treatment among a semi-immune population exposed to intense perennial transmission.
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The Effect of α-Thalassemia on Cord Blood Red Cell Indices and Interaction with Sickle Cell Gene
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Anaemia in pregnancy: a survey of pregnant women in Abeokuta, Nigeria.
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The Thalassæmia Syndromes.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Psychosocial Challenges Faced by Caretakers of Patients with Sickle Cell Disease Admitted in a Tertiary Hospital in Eastern Uganda
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Psycho-Social Challenges Faced by Caretakers of Children and Adolescents Aged 0-19 Years with Sickle Cell Disease Admitted in a Tertiary Hospital in Eastern Uganda
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Improving Outcomes for Patients With Sickle Cell Disease in the United States
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Genetic Variation and Sickle Cell Disease Severity
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Antioxidant supplementation for sickle cell disease
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Antioxidant supplementation for sickle cell disease
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Parasitism: Life Cycle and Host Defences against Parasites
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Modifying Our Microbial Environment
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Rapid Diagnostic Tests for the Detection of Sickling Hemoglobin
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Emerging Infectious Diseases
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Framing the research agenda for sickle cell trait: Building on the current understanding of clinical events and their potential implications
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Alteration of lymphocyte phenotype and function in sickle cell anemia: Implications for vaccine responses
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Point‐of‐care screening for sickle cell disease in low‐resource settings: A multi‐center evaluation of HemoTypeSC, a novel rapid test
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Perioperative care of children with sickle cell disease: A systematic review and clinical recommendations
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Randomized control trial of oral arginine therapy for children with sickle cell anemia hospitalized for pain in Nigeria
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Exercise and training in sickle cell disease: Safety, potential benefits, and recommendations
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Arginine Therapy for Pain in Sickle Cell Disease: A Phase‐2 Randomized, Placebo‐Controlled Trial
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Ancestral reconstruction and correlation of the frequencies of the hemoglobin S allele and the D uffy blood group alleles in human populations
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Genomics, the origins of agriculture, and our changing microbe‐scape: Time to revisit some old tales and tell some new ones
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No support for the hereditarian hypothesis of the Black–White achievement gap using polygenic scores and tests for divergent selection
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ACKR1 /Duffy‐null genotype testing for clozapine: A guideline developed by the UK Centre of Excellence in Regulatory Science and Innovation in Pharmacogenomics (CERSI‐PGx)
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Acute chest syndrome in sickle cell disease/HBE patient, A case report
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Innovations in Targeted Anti‐Adhesion Treatment for Sickle Cell Disease
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A novel population of memory‐activated natural killer cells associated with low parasitaemia in Plasmodium falciparum‐exposed sickle‐cell trait children
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Adaptive landscape genetics and malaria across divergent island bird populations
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A Genosensor for Sickle Cell Anemia Trait Determination
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Inferring archaic introgression from hominin genetic data
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Knowledge, Attitude, and Practice of Sickle Cell Disease Among Sickle Cell Disease Patients in Sudurpashchim Province of Nepal: A Cross‐Sectional Study
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Online Biomedical Resources for Malaria‐Related Red Cell Disorders
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FREQMAX provides an alternative approach for determining high‐resolution allele frequency thresholds in carrier screening
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Congolese children with sickle cell trait may exhibit glomerular hyperfiltration: A case control study
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Pharmacological and molecular approaches for the treatment of β‐hemoglobin disorders
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Sickle cell anemia and pregnancy: Profile of hemodynamic changes in sickle cell pregnant women in Kinshasa
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The changing malaria risk patterns in East‐Central Europe and the North Balkans in the last 27 000 years
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A global perspective on sickle cell disease
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Sickle Cell Disease and Hemoglobin S Prevalence in Botswana
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Hydroxyurea for children with sickle cell disease in sub‐Saharan Africa: A summary of the evidence, opportunities, and challenges
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Clinically‐oriented proteomic investigation of sickle cell disease: Opportunities and challenges
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Biomarkers for the central nervous system complications of sickle cell disease: are we there yet?
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Evolutionary psychiatry: foundations, progress and challenges
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Genomics and the Developing World
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Clinical Features of β-Thalassemia and Sickle Cell Disease
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Genetic Basis and Genetic Modifiers of β-Thalassemia and Sickle Cell Disease
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Precision Medicine in Critical Illness: Sepsis and Acute Respiratory Distress Syndrome
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Evaluation of Genetic Kidney Disease in Living Donor Candidates
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Pharmacogenomics: Genetic Polymorphisms
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The Kidney in Sickle Cell Disease
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Blood Rheology: Key Parameters and Impact on Blood Flow
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Sickle Cell Disease: Lessons Learned
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Statistical Analysis of Hematological Parameters for Prediction of Sickle Cell Disease
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A Critical Analysis of Black Immunity Myths and Their Deadly Consequences
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Human Behavior Genetics and Human Evolution
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Sickle Cell Disease in Africa and the Arabian Peninsula: Current Management and Challenges
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Sickle Cell Anemia: History and Epidemiology
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Multiple endokrine Neoplasien
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Comprehensive Management of Sickle Cell Disorders
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Tourniquet use in patients with sickle cell trait (SCT): Mediterranean or African ancestry influences complications, demonstrating a higher prevalence than control patients: matched study of nine hundred and forty SCT versus one thousand, two hundred and sixty three non-SCT patients
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Relative abundance of β-thalassemia-related mutations in southern China correlates with geographical coordinates
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Fifteen years of newborn sickle cell disease screening in Madrid, Spain: an emerging disease in a European country
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Identifying adaptive alleles in the human genome: from selection mapping to functional validation
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Schmerztherapie bei Sichelzellkrankheit
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Mechanisms and tests for geographic clines in genetic polymorphisms
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Selective Heterozygous Advantage of Carriers of с.-23+1G>A Mutation in GJB2 Gene Causing Autosomal Recessive Deafness 1A
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Determination of the Frequency of HBB (c.20 A > T) Gene Mutation in the Nigerian and Zimbabwean Populations in Northern Cyprus
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Using Formative Research to Develop a Counselor Training Program for Newborn Screening in Ghana
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Enhancing the collectivist critique: accounts of the human enhancement debate
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Caught between pity, explicit bias, and discrimination: a qualitative study on the impact of stigma on the quality of life of persons living with sickle cell disease in three African countries
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Testing an Ethnobiological Evolutionary Hypothesis on Plant-Based Remedies to Treat Malaria in Africa
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Material Innovations as Evolutionary Scaffolds: A Niche Construction Perspective on Human Evolution
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Rheumatic Manifestations of Haemoglobinopathies
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Ancestry estimation: Methodological evolution and forensic implications
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Electrophoretic and molecular profile of the hemoglobinopathies in newborns at a reference hospital in Mozambique
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Feasibility of establishing a network of community health workers to support care of people with sickle cell disease in Kumasi, Ghana
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Is sickle cell trait truly benign? A case-control study of physical and mental health outcomes from the sickle cell belt of Eastern India
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Sociodemographic characteristics and healthcare-seeking behaviour of patients with sickle cell disease: a cross-sectional study across five tribal districts in India
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Global research trends and influential contributions in sickle cell disease: a bibliometric analysis of the top 100 cited papers
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Acute exercise shifts inferred immune cell composition and cytotoxic gene programs in pediatric sickle cell anemia
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Red cell polymorphisms and malaria: an evolutionary approach
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Is there still evolution in the human population?
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Comparative valuation of longstanding and novel treatments for sickle cell disease: a multinational MCDA study
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Units and Targets of Natural Selection
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Human Population Genetics/Genomics and Society
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Red Blood Cell Polymorphism and Susceptibility to Plasmodium vivax
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Hepatitis C Infection in Patients With Hemoglobinopathies
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Circulatory, Reticuloendothelial, and Hematopoietic Disorders
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Human genetic diversity in health and disease
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The Management of Pain from Sickle Cell Disease
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Malaria (Plasmodium Species)
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10.1016/b978-1-4557-5414-4.00020-6
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Biomarker of Anopheles exposure in Ghanaian children with hemoglobin S and C
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Whole-Genome-Sequence-Based Haplotypes Reveal Single Origin of the Sickle Allele during the Holocene Wet Phase
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Glaucoma in Black Individuals: How Far Have We Come and Where Do We Go From Here?
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Sickle Cell Disease in Africa
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Physiopathologie de la drépanocytose et perspectives thérapeutiques
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Molecular basis of β thalassemia and potential therapeutic targets
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Development of disease-specific growth curves from Kenyan children with sickle cell anemia
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Neurocognitive functioning of patients with sickle cell disease in low- and middle-income countries
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Tracing the origin of sickle cell disease back to 50 000 years
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Journey of the sickle cell gene
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Sickle cell disease: Clinical presentation and management of a global health challenge
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Point-of-care diagnostic test accuracy in children and adolescents with sickle cell disease: A systematic review and meta-analysis
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Prevalence of Sickle cell disease, Sickle cell trait and HBS-beta-thalassemia in India: A systematic review and Meta-analysis
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Evolutionary race: Malaria evolves to evade sickle cell protection
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History, Advances, and Challenges of Sickle Cell Disease Treatment
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Opportunities to foreground human embeddedness in the Anthropocene biosphere
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Postnatal Prediction of Gestational Age Using Newborn Fetal Hemoglobin Levels
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Combining HbA1c and glycated albumin improves detection of dysglycaemia in mixed-ancestry South Africans
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APOL1 Renal Risk Variants and Sickle Cell Trait Associations With Reduced Kidney Function in a Large Congolese Population-Based Study
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Delivering on the promise of gene editing for cystic fibrosis
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Role of genetic factors and ethnicity on the multiplicity of Plasmodium falciparum infection in children with asymptomatic malaria in Yaoundé, Cameroon
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The Present and Future Global Burden of the Inherited Disorders of Hemoglobin
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Sickle Cell Disease in Sub-Saharan Africa
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Sickle cell disease among children in Africa: An integrative literature review and global recommendations
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Association between sickle cell trait and Plasmodium falciparum infection: evidence for age-specific protection in a cross-sectional study in Guinea-Bissau
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Evolutionary medicine in action: Sickle hemoglobin fuels tumor progression
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Impact of intra-annual runoff nonuniformity on the energy generation of cascaded hydropower plants in Datong River Basin, China
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Delayed Healing of Sickle Cell Ulcers Is due to Impaired Angiogenesis and CXCL12 Secretion in Skin Wounds
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Manifestations en imagerie de la drépanocytose
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Imagerie du syndrome thoracique aigu et d’autres atteintes thoraciques drépanocytaires
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Comparative study of clinical presentation and hematological indices in hospitalized sickle cell patients with severe Plasmodium falciparum malaria
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Prevalence of the Sickle Cell Trait in Gabon: A nationwide study
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Understanding the contrasting spatial haplotype patterns of malaria-protective β-globin polymorphisms
inferred← citeshttps://doi.org/10.1016/j.meegid.2020.104188openalex-snapshot
Joint selection for two malaria resistance mutations in a south-west Colombian population
inferred← citeshttps://doi.org/10.1016/j.meegid.2020.104458openalex-snapshot
Past and current biological factors affecting malaria in the low transmission setting of Botswana: A review
inferred← citeshttps://doi.org/10.1016/j.meegid.2021.104987openalex-snapshot
Asymptomatic malaria infection prevailing risks for human health and malaria elimination
inferred← citeshttps://doi.org/10.1016/j.micinf.2012.01.003openalex-snapshot
Lack of significant influence for FcRIIa-RH131 or hemoglobin AA/AS polymorphisms on immunity and susceptibility to uncomplicated malaria and existence of marked linkage between the two polymorphisms in Daraweesh
inferred← citeshttps://doi.org/10.1016/j.micinf.2012.05.006openalex-snapshot
Abnormal PfEMP1/knob display on Plasmodium falciparum-infected erythrocytes containing hemoglobin variants: fresh insights into malaria pathogenesis and protection
inferred← citeshttps://doi.org/10.1016/j.mjafi.2026.07.008openalex-snapshot
Sickle-cell trait and high-altitude thrombosis in Indian Armed Forces personnel: A prospective multicenter cohort study with point-of-care diagnostic validation
inferred← citeshttps://doi.org/10.1016/j.nefro.2020.10.012openalex-snapshot
Nefropatía falciforme. Manifestaciones clínicas y nuevos mecanismos implicados en el daño renal
inferred← citeshttps://doi.org/10.1016/j.nefroe.2021.10.001openalex-snapshot
Sickle cell nephropathy. Clinical manifestations and new mechanisms involved in kidney injury
inferred← citeshttps://doi.org/10.1016/j.outlook.2025.102353openalex-snapshot
Fractured FRAX: Nurses’ role in reckoning with racism in international osteoporosis fracture risk calculations
inferred← citeshttps://doi.org/10.1016/j.pedn.2022.11.026openalex-snapshot
Psycho-social challenges faced by caretakers of children and adolescents aged 0–19 years with sickle cell disease admitted in a tertiary hospital in Eastern Uganda
inferred← citeshttps://doi.org/10.1016/j.pt.2011.01.003openalex-snapshot
Bayesian geostatistics in health cartography: the perspective of malaria
inferred← citeshttps://doi.org/10.1016/j.pt.2011.02.004openalex-snapshot
Sickle cell disease and malaria morbidity: a tale with two tails
inferred← citeshttps://doi.org/10.1016/j.pt.2016.09.010openalex-snapshot
Might Interspecific Interactions between Pathogens Drive Host Evolution? The Case of Plasmodium Species and Duffy-Negativity in Human Populations
inferred← citeshttps://doi.org/10.1016/j.pt.2021.10.005openalex-snapshot
Falciparum malaria mortality in sub-Saharan Africa in the pretreatment era
inferred← citeshttps://doi.org/10.1016/j.pt.2025.05.007openalex-snapshot
Parasite-resistant variants in African genomes: implications for global genetic medicine
inferred← citeshttps://doi.org/10.1016/j.pt.2026.07.016openalex-snapshot
Metabolite-effector immunity against malaria
inferred← citeshttps://doi.org/10.1016/j.quaint.2020.10.056openalex-snapshot
The potential impacts of climate factors and malaria on the Middle Palaeolithic population patterns of ancient humans
inferred← citeshttps://doi.org/10.1016/j.quaint.2021.02.014openalex-snapshot
The potential persistence of ancient malaria through the Quaternary period in Europe
inferred← citeshttps://doi.org/10.1016/j.quaint.2022.04.003openalex-snapshot
Late Quaternary changes in malaria-free areas in Papua New Guinea and the future perspectives
inferred← citeshttps://doi.org/10.1016/j.semnephrol.2025.151614openalex-snapshot
Acute Kidney Injury in Severe Malaria: A Serious Complication Driven by Hemolysis
inferred← citeshttps://doi.org/10.1016/j.smim.2026.102035openalex-snapshot
The immune system in Latin America and the Caribbean: Insights into diseases and diversity from local perspectives
inferred← citeshttps://doi.org/10.1016/j.socscimed.2025.118723openalex-snapshot
Adults with sickle-cells in a migration-driven rare disease setting: Therapeutic remoteness and graphic medicine in Austria
inferred← citeshttps://doi.org/10.1016/j.tjnut.2023.07.018openalex-snapshot
Biology of Anemia: A Public Health Perspective
inferred← citeshttps://doi.org/10.1016/j.tmrv.2019.06.003openalex-snapshot
Red Blood Cell Alloimmunization in Transfused Patients With Sickle Cell Disease in Sub-Saharan Africa; a Systematic Review and Meta-Analysis
inferred← citeshttps://doi.org/10.1016/j.toxicon.2024.108162openalex-snapshot
Study repair function of mucin-2 on the tight junction protein of uterine epithelial cells under bacterial endotoxins
inferred← citeshttps://doi.org/10.1016/j.tracli.2020.03.008openalex-snapshot
ABO blood group should be considered and reported when red blood cell exchange transfusion is used to treat Plasmodium falciparum Malaria patients
inferred← citeshttps://doi.org/10.1016/j.tracli.2021.01.013openalex-snapshot
Transfusion and sickle cell anemia in Africa
inferred← citeshttps://doi.org/10.1016/j.transci.2017.11.032openalex-snapshot
To prevent or ameliorate severe Plasmodium falciparum malaria, why not evaluate the impact of exchange transfusions of sickle cell trait red blood cells?
inferred← citeshttps://doi.org/10.1016/j.virol.2014.10.004openalex-snapshot
Dengue virus infection of erythroid precursor cells is modulated by both thalassemia trait status and virus adaptation
inferred← citeshttps://doi.org/10.1016/j.xhgg.2024.100374openalex-snapshot
Variants in the β-globin locus are associated with pneumonia in African American children
inferred← citeshttps://doi.org/10.1016/j.xops.2026.101298openalex-snapshot
A Whole-Genome Sequence Genome-Wide Association Study in All of Us Identifies a Novel Glaucoma Risk Locus in African Individuals
inferred← citeshttps://doi.org/10.1016/s0140-6736(12)61229-xopenalex-snapshot
Global epidemiology of sickle haemoglobin in neonates: a contemporary geostatistical model-based map and population estimates
inferred← citeshttps://doi.org/10.1016/s0140-6736(12)61817-0openalex-snapshot
Sickle-cell disorders: limits of descriptive epidemiology
inferred← citeshttps://doi.org/10.1016/s1155-1984(20)83452-9openalex-snapshot
10.1016/s1155-1984(20)83452-9
inferred← citeshttps://doi.org/10.1016/s1155-1984(23)46035-9openalex-snapshot
10.1016/s1155-1984(23)46035-9
inferred← citeshttps://doi.org/10.1016/s2213-2600(15)00543-3openalex-snapshot
A global view of pulmonary hypertension
inferred← citeshttps://doi.org/10.1016/s2214-109x(13)70001-9openalex-snapshot
Global, regional, and national trends in haemoglobin concentration and prevalence of total and severe anaemia in children and pregnant and non-pregnant women for 1995–2011: a systematic analysis of population-representative data
inferred← citeshttps://doi.org/10.1016/s2214-109x(13)70150-5openalex-snapshot
Global migration and the changing distribution of sickle haemoglobin: a quantitative study of temporal trends between 1960 and 2000
inferred← citeshttps://doi.org/10.1016/s2214-109x(15)00288-0openalex-snapshot
Burden of sickle cell trait and disease in the Uganda Sickle Surveillance Study (US3): a cross-sectional study
inferred← citeshttps://doi.org/10.1016/s2214-109x(20)30358-2openalex-snapshot
Burden of non-communicable diseases from infectious causes in 2017: a modelling study
inferred← citeshttps://doi.org/10.1016/s2352-3026(21)00191-5openalex-snapshot
Sickle cell disease in sub-Saharan Africa: transferable strategies for prevention and care
inferred← citeshttps://doi.org/10.1016/s2352-4642(22)00169-9openalex-snapshot
Interplay between sickle cell anaemia and Plasmodium falciparum malaria
inferred← citeshttps://doi.org/10.1016/s2352-4642(26)00048-9openalex-snapshot
Prevalence estimates of sickle cell disease among children and adolescents in sub-Saharan Africa: a systematic review and modelling analysis
inferred← citeshttps://doi.org/10.1017/9781139680295.006openalex-snapshot
Pharmacogenomics and Infectious Diseases in Africa
inferred← citeshttps://doi.org/10.1017/9781316686942.019openalex-snapshot
Early malarial infections and the first epidemiological transition
inferred← citeshttps://doi.org/10.1017/cbo9781139644594.005openalex-snapshot
The Impact of Malaria on African Development over theLongue Durée
inferred← citeshttps://doi.org/10.1017/s0031182015001249openalex-snapshot
Immunity to malaria in an era of declining malaria transmission
inferred← citeshttps://doi.org/10.1017/s1047951120000037openalex-snapshot
Cardiovascular changes in children with sickle cell crisis
inferred← citeshttps://doi.org/10.1017/s1368980021002482openalex-snapshot
Geographical variation and temporal trend in anemia among children aged 6–59 months in low- and middle-income countries during 2000–2018: forecasting the 2030 SDG target
inferred← citeshttps://doi.org/10.1017/ssh.2015.20openalex-snapshot
The Question of Racial Immunity to Yellow Fever in History and Historiography
inferred← citeshttps://doi.org/10.1021/acs.analchem.9b05111openalex-snapshot
Nanofocused Scanning X-ray Fluorescence Microscopy Revealing an Effect of Heterozygous Hemoglobin S and C on Biochemical Activities in Plasmodium falciparum-Infected Erythrocytes
inferred← citeshttps://doi.org/10.1021/acs.jproteome.6c00158openalex-snapshot
Plasma Proteome Signatures in Sickle Cell Anemia and the Effect of Hydroxyurea Treatment
inferred← citeshttps://doi.org/10.1021/jp4025156openalex-snapshot
Mapping Polymerization and Allostery of Hemoglobin S Using Point Mutations
inferred← citeshttps://doi.org/10.1029/2018wr023160openalex-snapshot
A Clustering Preprocessing Framework for the Subannual Calibration of a Hydrological Model Considering Climate‐Land Surface Variations
inferred← citeshttps://doi.org/10.1038/ejhg.2016.181openalex-snapshot
Characterising private and shared signatures of positive selection in 37 Asian populations
inferred← citeshttps://doi.org/10.1038/emi.2017.63openalex-snapshot
Red blood cells release microparticles containing human argonaute 2 and miRNAs to target genes of Plasmodium falciparum
inferred← citeshttps://doi.org/10.1038/gim.2015.143openalex-snapshot
Observed and expected frequencies of structural hemoglobin variants in newborn screening surveys in Africa and the Middle East: deviations from Hardy-Weinberg equilibrium
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