Tolerance to trypanosomatids: a threat, or a key for disease elimination?

Association of Trypanolytic ApoL1 Variants with Kidney Disease in African Americans

Genovese, G., Friedman, D. J., Ross, M. D., Lecordier, L., Uzureau, P., Freedman, B. I., Bowden, D. W., Langefeld, C. D., Oleksyk, T. K., Uscinski Knob, A. L., et al. (2010) · Science · doi:10.1126/science.1193032 · Cited by 2,028 · see citing works

Human African trypanosomiasis

Brun, R., Blum, J., Chappuis, F., & Burri, C. (2010) · The Lancet · doi:10.1016/s0140-6736(09)60829-1 · Cited by 926 · see citing works

LeishVet guidelines for the practical management of canine leishmaniosis

Solano-Gallego, L., Miró, G., Koutinas, A., Cardoso, L., Pennisi, M. G., Ferrer, L., Bourdeau, P., Oliva, G., & Baneth, G. (2011) · Parasites & Vectors · doi:10.1186/1756-3305-4-86 · Cited by 824 · see citing works

Chagas’ Disease

Bern, C. (2015) · New England Journal of Medicine · doi:10.1056/nejmra1410150 · Cited by 781 · see citing works

Canine leishmaniosis – new concepts and insights on an expanding zoonosis: part one

Baneth, G., Koutinas, A. F., Solano‐Gallego, L., Bourdeau, P. J., & Ferrer, L. (2008) · Trends in Parasitology · doi:10.1016/j.pt.2008.04.001 · Cited by 710 · see citing works

The future of Chagas disease control

Schofield, C. J., Jannin, J. G., & Salvatella, R. (2006) · Trends in Parasitology · doi:10.1016/j.pt.2006.09.011 · Cited by 657 · see citing works

The leishmaniases as emerging and reemerging zoonoses

Ashford, R. W. (2000) · International Journal for Parasitology · doi:10.1016/s0020-7519(00)00136-3 · Cited by 583 · see citing works

New Perspectives on a Subclinical Form of Visceral Leishmaniasis

Badaró, R. J. D. S., Jones, T. C., Carvalho, E. M., Pedral-Sampaio, D., Reed, S. G., Barral, A. M. P., Teixeira, R. S., & Johnson, W. D. (1986) · The Journal of Infectious Diseases · doi:10.1093/infdis/154.6.1003 · Cited by 481 · see citing works

Epidemiology of human African trypanosomiasis

Simarro, P. P., Franco, J., Diarra, A., & Jannin, J. G. (2014) · Clinical Epidemiology · doi:10.2147/clep.s39728 · Cited by 413 · see citing works

Chagas disease: what is known and what is needed - A background article

Coura, J. R. (2007) · Memórias do Instituto Oswaldo Cruz · doi:10.1590/s0074-02762007000900018 · Cited by 321 · see citing works

Occurrence ofLeishmania infantumParasitemia in Asymptomatic Blood Donors Living in an Area of Endemicity in Southern France

Fichoux, Y. L., Quaranta, J.-F., Aufeuvre, J.-P., Lelièvre, A., Marty, P., Suffia, I., Rousseau, D., & Kubar, J. (1999) · Journal of Clinical Microbiology · doi:10.1128/jcm.37.6.1953-1957.1999 · Cited by 314 · see citing works

Canine leishmaniosis – new concepts and insights on an expanding zoonosis: part two

Miró, G., Cardoso, L., Pennisi, M. G., Oliva, G., & Baneth, G. (2008) · Trends in Parasitology · doi:10.1016/j.pt.2008.05.003 · Cited by 235 · see citing works

Chagas Disease Cardiomyopathy: Immunopathology and Genetics

Cunha‐Neto, E., & Chevillard, C. (2014) · Mediators of Inflammation · doi:10.1155/2014/683230 · Cited by 210 · see citing works

Chagas disease: what is known and what is needed - A background article

Coura, J. R. (2007) · Memórias do Instituto Oswaldo Cruz · doi:10.1590/s0074-02762007007500001 · Cited by 207 · see citing works

Untreated Human Infections by Trypanosoma brucei gambiense Are Not 100% Fatal

Jamonneau, V., Ilboudo, H., Kaboré, J., Kaba, D., Koffi, M., Solano, P., Garcia, A., Courtin, D., Laveissière, C., Kouakou, L., et al. (2012) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0001691 · Cited by 204 · see citing works

Mapping of quantitative trait loci controlling trypanotolerance in a cross of tolerant West African N'Dama and susceptible East African Boran cattle

Hanotte, O., Ronin, Y. I., Agaba, M. K., Nilsson, P. R., Gelhaus, A., Horstmann, R., Sugimoto, Y., Kemp, S. J., Gibson, J. P., Korol, A. B., et al. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1232392100 · Cited by 196 · see citing works

A whole genome Bayesian scan for adaptive genetic divergence in West African cattle

Gautier, M., Flori, L., Riebler, A., Jaffrézic, F., Laloë, D., Gut, I. G., Moazami‐Goudarzi, K., & Foulley, J. (2009) · BMC Genomics · doi:10.1186/1471-2164-10-550 · Cited by 196 · see citing works

Canine Leishmaniasis: Identification of Asymptomatic Carriers by Polymerase Chain Reaction and Immunoblotting

Berrahal, F., Mary, C., Roze, M., Berenger, A., Escoffier, K., Lamouroux, D., & Dunan, S. (1996) · American Journal of Tropical Medicine and Hygiene · doi:10.4269/ajtmh.1996.55.273 · Cited by 192 · see citing works

A Global Comparative Evaluation of Commercial Immunochromatographic Rapid Diagnostic Tests for Visceral Leishmaniasis

Cunningham, J. A., Hasker, E. C., Das, P. K., Safi, S. E., Goto, H., Mondal, D., Mbuchi, M., Mukhtar, M. M., Rabello, A., Rijal, S., et al. (2012) · Clinical Infectious Diseases · doi:10.1093/cid/cis716 · Cited by 176 · see citing works

On the History of Cattle Genetic Resources

Felius, M., Beerling, M.-L., Buchanan, D., Theunissen, B., Koolmees, P., & Lenstra, J. (2014) · Diversity · doi:10.3390/d6040705 · Cited by 176 · see citing works

Rapid tests for the diagnosis of visceral leishmaniasis in patients with suspected disease

Boelaert, M., Verdonck, K., Menten, J., Sunyoto, T., van Griensven, J., Chappuis, F., & Rijal, S. (2014) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd009135.pub2 · Cited by 169 · see citing works

Infectivity of seropositive dogs, showing different clinical forms of leishmaniasis, to Lutzomyia longipalpis phlebotomine sand flies

Michalsky, É. M., Rocha, M. F., Lima, A. C. V. M. D. R., França-Silva, J. C., Pires, M. Q., de Oliveira, F. S., Pacheco, R. S., dos Santos, S. L., Barata, R. A., Romanha, Á. J., et al. (2007) · Veterinary Parasitology · doi:10.1016/j.vetpar.2007.03.004 · Cited by 169 · see citing works

Genetic susceptibility to leishmanial infections: studies in mice and man

Blackwell, J. M. (1996) · Parasitology · doi:10.1017/s0031182000076678 · Cited by 167 · see citing works

Long-lasting protection against canine visceral leishmaniasis using the LiESAp-MDP vaccine in endemic areas of France: Double-blind randomised efficacy field trial

Lemesre, J.-L., Holzmüller, P., Bras‐Gonçalves, R., Bourdoiseau, G., Hugnet, C., Cavaleyra, M., & Papierok, G. (2007) · Vaccine · doi:10.1016/j.vaccine.2007.02.083 · Cited by 158 · see citing works

Protection against experimental visceral leishmaniasis infection in dogs immunized with purified excreted secreted antigens of Leishmania infantum promastigotes

Lemesre, J.-L., Holzmüller, P., Cavaleyra, M., Bras‐Gonçalves, R., Hottin, G., & Papierok, G. (2004) · Vaccine · doi:10.1016/j.vaccine.2004.11.061 · Cited by 154 · see citing works

Molecular Tools for Diagnosis of Visceral Leishmaniasis: Systematic Review and Meta-Analysis of Diagnostic Test Accuracy

de Ruiter, C. M., van der Veer, C., Leeflang, M., Deborggraeve, S., Lucas, C., & Adams, E. R. (2014) · Journal of Clinical Microbiology · doi:10.1128/jcm.00372-14 · Cited by 149 · see citing works

Detection of Leishmania infantum cryptic infection in asymptomatic blood donors living in an endemic area (Eivissa, Balearic Islands, Spain) by different diagnostic methods

Riera, C., Fisa, R., Udina, M., Gállego, M., & Portús, M. (2003) · Transactions of the Royal Society of Tropical Medicine and Hygiene · doi:10.1016/s0035-9203(03)00015-4 · Cited by 146 · see citing works

The molecular arms race between African trypanosomes and humans

Pays, É., Vanhollebeke, B., Uzureau, P., Lecordier, L., & Pérez-Morga, D. L. (2014) · Nature Reviews Microbiology · doi:10.1038/nrmicro3298 · Cited by 122 · see citing works

Visceral leishmaniasis: elimination with existing interventions

Matlashewski, G., Arana, B. A., Kroeger, A., Battacharya, S., Sundar, S., Das, P. K., Sinha, P. K., Rijal, S., Mondal, D., Zilberstein, D., et al. (2011) · The Lancet Infectious Diseases · doi:10.1016/s1473-3099(10)70320-0 · Cited by 120 · see citing works

Localization of genes controlling resistance to trypanosomiasis in mice

Kemp, S. J., Iraqi, F. A., Darvasi, A., Soller, M., & Teale, A. J. (1997) · Nature Genetics · doi:10.1038/ng0697-194 · Cited by 119 · see citing works

Reducing Human-Tsetse Contact Significantly Enhances the Efficacy of Sleeping Sickness Active Screening Campaigns: A Promising Result in the Context of Elimination

Courtin, F., Camara, M., Rayaissé, J.-B., Kagbadouno, M. S., Dama, E., Camara, O., Traoré, I., Rouamba, J., Peylhard, M., Somda, M. B., et al. (2015) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0003727 · Cited by 115 · see citing works

Navigating parasite webs and parasite flow: Emerging and re-emerging parasitic zoonoses of wildlife origin

Polley, L. (2005) · International Journal for Parasitology · doi:10.1016/j.ijpara.2005.07.003 · Cited by 113 · see citing works

Studies on mediterranean leishmaniasis 2. Asymptomatic cases of visceral leishmaniasis

Pampiglione, S., Manson‐Bahr, P., Giungi, F., Giunti, G., Parenti, A., & Trotti, G. C. (1974) · Transactions of the Royal Society of Tropical Medicine and Hygiene · doi:10.1016/0035-9203(74)90067-4 · Cited by 113 · see citing works

Trypanotolerance, an option for sustainable livestock production in areas at risk from trypanosomosis

D'Ieteren, G. D. M., Authié, É., Wissocq, N. M., & Murray, M. (1998) · Scientific and Technical Review (World Organisation for Animal Health) · doi:10.20506/rst.17.1.1088 · Cited by 112 · see citing works

Common variants in the HLA-DRB1–HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis

Fakiola, M., Strange, A., Cordell, H. J., Miller, E. N., Pirinen, M., Su, Z., Mishra, A., Mehrotra, S., Monteiro, G. R., Band, G., et al. (2013) · Nature Genetics · doi:10.1038/ng.2518 · Cited by 108 · see citing works

Admixture and diversity in West African cattle populations

Freeman, A., Meghen, C., MacHugh, D., Loftus, R., Achukwi, M. D., Bado, A., Sauveroche, B., & Bradley, D. (2004) · Molecular Ecology · doi:10.1111/j.1365-294x.2004.02311.x · Cited by 108 · see citing works

The journey towards elimination of gambiense human African trypanosomiasis: not far, nor easy

Franco, J. R., Simarro, P. P., DIARRA, A., Ruiz-Postigo, J. A., & Jannin, J. G. (2014) · Parasitology · doi:10.1017/s0031182013002102 · Cited by 107 · see citing works

The interplay between environmental and host factors during an outbreak of visceral leishmaniasis in eastern Sudan

Bucheton, B., Kheir, M. M., EL-Safi, S. H., Hammad, A., Mergani, A., Mary, C., Abel, L., & Dessein, A. J. J. (2002) · Microbes and Infection · doi:10.1016/s1286-4579(02)00027-8 · Cited by 107 · see citing works

Genetic Resistance to African Trypanosomiasis

Murray, M., Trail, J. C. M., Davis, C. E. L. B., & Black, S. J. (1984) · The Journal of Infectious Diseases · doi:10.1093/infdis/149.3.311 · Cited by 99 · see citing works

Time to Tap Africa's Livestock Genomes

Hanotte, O., Dessie, T., & Kemp, S. J. (2010) · Science · doi:10.1126/science.1186254 · Cited by 98 · see citing works

Influence of humans and domestic animals on the household prevalence of Trypanosoma cruzi in Triatoma infestans populations in northwest Argentina.

Gürtler, R. E., Cohen, J. E., Cecere, M. C., Lauricella, M. A., Chuit, R., & Segura, E. L. (1998) · American Journal of Tropical Medicine and Hygiene · doi:10.4269/ajtmh.1998.58.748 · Cited by 94 · see citing works

Vaccines for Canine Leishmaniasis

Palatnik, M. (2012) · Frontiers in Immunology · doi:10.3389/fimmu.2012.00069 · Cited by 89 · see citing works

Genetic control of visceral leishmaniasis in a Sudanese population: candidate gene testing indicates a linkage to the NRAMP1 region

Bucheton, B., Abel, L., Kheir, M. M., Mirgani, A., EL-Safi, S. H., Chevillard, C., & Dessein, A. J. J. (2003) · Genes and Immunity · doi:10.1038/sj.gene.6363927 · Cited by 89 · see citing works

Adaptive admixture in the W est A frican bovine hybrid zone: insight from the B orgou population

Flori, L., Thévenon, S., Dayo, G., Sènou, M., Sylla, S., Berthier, D., Moazami‐Goudarzi, K., & Gautier, M. (2014) · Molecular Ecology · doi:10.1111/mec.12816 · Cited by 88 · see citing works

Studies on Trypanosome-resistant cattle. II. The effect of Trypanosomiasis on N'dama, Muturu and Zebu cattle

Roberts, C. J., & Gray, A. R. (1973) · Tropical Animal Health and Production · doi:10.1007/bf02240423 · Cited by 88 · see citing works

Genetic and expression analysis of cattle identifies candidate genes in pathways responding to <i>Trypanosoma congolense</i> infection

Noyes, H., Brass, A., Obara, I., Anderson, S., Archibald, A. L., Bradley, D. G., Fisher, P., Freeman, A., Gibson, J., Gicheru, M., et al. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1013486108 · Cited by 88 · see citing works

Follow‐up of Card Agglutination Trypanosomiasis Test (CATT) positive but apparently aparasitaemic individuals in Côte d'Ivoire: evidence for a complex and heterogeneous population

Garcia, A., Jamonneau, V., Magnus, E., Laveissière, C., Lejon, V., N'Guessan, P., N'Dri, L., Meirvenne, N. V., & Büscher, P. (2000) · Tropical Medicine & International Health · doi:10.1046/j.1365-3156.2000.00623.x · Cited by 87 · see citing works

Trypanotolerance in cattle and prospects for the control of trypanosomiasis by selective breeding

Murray, M., Trail, J. C. M., & D'Ieteren, G. D. (1990) · Scientific and Technical Review (World Organisation for Animal Health) · doi:10.20506/rst.9.2.506 · Cited by 86 · see citing works

Trypanosome Lytic Factor, an Antimicrobial High-Density Lipoprotein, Ameliorates Leishmania Infection

Samanovic, M. I., Molina‐Portela, M. D. P., Chessler, A.-D. C., Burleigh, B. A., & Raper, J. (2009) · PLoS Pathogens · doi:10.1371/journal.ppat.1000276 · Cited by 82 · see citing works

The Indeterminate Phase of Chagas' Disease: Ultrastructural Characterization of Cardiac Changes in the Canine Model

Andrade, Z. A., Andrade, S. G., Sadigursky, M., Wenthold, R. J., Hilbert, S. L., & Ferrans, V. J. (1997) · American Journal of Tropical Medicine and Hygiene · doi:10.4269/ajtmh.1997.57.328 · Cited by 79 · see citing works

Use of the leishmanin skin test and Western blot analysis for epidemiological studies in visceral leishmaniasis areas: experience in a highly endemic focus in Alpes-Maritimes (France)

Marty, P., Lelièvre, A., Quaranta, J.-F., Rahal, A., Gari-Toussaint, M., & Fichoux, Y. L. (1994) · Transactions of the Royal Society of Tropical Medicine and Hygiene · doi:10.1016/0035-9203(94)90214-3 · Cited by 79 · see citing works

Host genetics in African trypanosomiasis

Courtin, D., Berthier, D., Thévenon, S., Dayo, G., Garcia, A., & Bucheton, B. (2008) · Infection Genetics and Evolution · doi:10.1016/j.meegid.2008.02.007 · Cited by 78 · see citing works

Human African Trypanosomiasis Presenting at Least 29 Years after Infection—What Can This Teach Us about the Pathogenesis and Control of This Neglected Tropical Disease?

Sudarshi, D., Lawrence, S., Pickrell, W. O., Eligar, V. S., Walters, R. J. L., Quaderi, S. A., Walker, A., Capewell, P., Clucas, C., Vincent, A. C., et al. (2014) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0003349 · Cited by 78 · see citing works

Susceptibility of N'Dama and Boran cattle to sequential challenges with tsetse‐transmitted clones of Trypanosoma congolense

Paling, R. W., Moloo, S. K., Scott, J., Gettinby, G., McOdimba, F., & Murray, M. (1991) · Parasite Immunology · doi:10.1111/j.1365-3024.1991.tb00295.x · Cited by 78 · see citing works

Human host determinants influencing the outcome of Trypanosoma brucei gambiense infections

Bucheton, B., MacLeod, A., & Jamonneau, V. (2011) · Parasite Immunology · doi:10.1111/j.1365-3024.2011.01287.x · Cited by 76 · see citing works

A Major Susceptibility Locus on Chromosome 22q12 Plays a Critical Role in the Control of Kala-Azar

Bucheton, B., Abel, L., EL-Safi, S. H., Kheir, M. M., Pavek, S., Lemainque, A., & Dessein, A. J. J. (2003) · The American Journal of Human Genetics · doi:10.1086/379084 · Cited by 75 · see citing works

Human and canine leishmaniasis in asymptomatic and symptomatic population in Northwestern Greece

Papadopoulou, C., Kostoula, A., Dimitriou, D., Panagiou, A., Bobojianni, C., & Antoniades, G. (2004) · Journal of Infection · doi:10.1016/j.jinf.2004.05.004 · Cited by 73 · see citing works

Kala-azar in a high transmission focus: an ethnic and geographic dimension.

Ibrahim, M. E., Lambson, B. E., Yousif, A., Deifalla, N. S., Alnaiem, D. A., Ismail, A., Yousif, H., Ghalib, H. W., Khalil, E. A. G., Kadaro, A. Y. E., et al. (1999) · American Journal of Tropical Medicine and Hygiene · doi:10.4269/ajtmh.1999.61.941 · Cited by 69 · see citing works

Strong Association between Serological Status and Probability of Progression to Clinical Visceral Leishmaniasis in Prospective Cohort Studies in India and Nepal

Hasker, E. C., Malaviya, P., Gidwani, K., Picado, A., Ostyn, B., Kansal, S., Singh, R. P., Singh, O. P., Chourasia, A., Singh, A. K., et al. (2014) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0002657 · Cited by 68 · see citing works

Lymphocytes of dogs immunised with purified excreted-secreted antigens of Leishmania infantum co-incubated with Leishmania infected macrophages produce IFN gamma resulting in nitric oxide-mediated amastigote apoptosis

Holzmüller, P., Cavaleyra, M., Moreaux, J., Kovacic, R., Vincendeau, P., Papierok, G.-M., & Lemesre, J.-L. (2005) · Veterinary Immunology and Immunopathology · doi:10.1016/j.vetimm.2005.03.001 · Cited by 67 · see citing works

Is vector control needed to eliminate gambiense human African trypanosomiasis?

Solano, P., Torr, S. J., & Lehane, M. J. (2013) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2013.00033 · Cited by 66 · see citing works

Vaccination with LiESP/QA-21 (CaniLeish®) reduces the intensity of infection in Phlebotomus perniciosus fed on Leishmania infantum infected dogs—A preliminary xenodiagnosis study

Bongiorno, G., Paparcone, R., Manzillo, V. F., Oliva, G., Cuisinier, A., & Gradoni, L. (2013) · Veterinary Parasitology · doi:10.1016/j.vetpar.2013.05.008 · Cited by 64 · see citing works

Genome Wide Association Study (GWAS) of Chagas Cardiomyopathy in Trypanosoma cruzi Seropositive Subjects

Deng, X., Sabino, É. C., Cunha‐Neto, E., Ribeiro, A. L. P., Ianni, B. M., Mady, C., Busch, M. P., Seielstad, M. T., the REDSII Chagas study group from the NHLBI Retrovirus Epidemiology Donor Study-II (REDS-II), & Component, I. (2013) · PLoS ONE · doi:10.1371/journal.pone.0079629 · Cited by 62 · see citing works

Physical Activity, Opportunity for Reinfection, and Sibling History of Heart Disease as Risk Factors for Chagas' Cardiopathy

Zicker, F., Smith, P. G., Netto, J. C. A., de Oliveira, R. C., & Zicker, E. M. S. (1990) · American Journal of Tropical Medicine and Hygiene · doi:10.4269/ajtmh.1990.43.498 · Cited by 61 · see citing works

Genetic susceptibility to Chagas disease cardiomyopathy: involvement of several genes of the innate immunity and chemokine-dependent migration pathways

Frade, A. F., Pissetti, C. W., Ianni, B. M., Saba, B. S., Lin‐Wang, H. T., Nogueira, L., Borges, A. D. M., Buck, P., Dias, F. C., Baron, M., et al. (2013) · BMC Infectious Diseases · doi:10.1186/1471-2334-13-587 · Cited by 59 · see citing works

Research priorities for the control of phlebotomine sand flies

Warburg, A., & Faiman, R. (2011) · Journal of Vector Ecology · doi:10.1111/j.1948-7134.2011.00107.x · Cited by 59 · see citing works

Genetic Susceptibility to Chagas Disease: An Overview about the Infection and about the Association between Disease and the Immune Response Genes

Ayo, C. M., Dalálio, M. M. D. O., Visentainer, J. E. L., Reis, P. G., Sippert, E., Jarduli, L. R., Alves, H. V., & Sell, A. M. (2013) · BioMed Research International · doi:10.1155/2013/284729 · Cited by 58 · see citing works

The protective immune response produced in dogs after primary vaccination with the LiESP/QA-21 vaccine (CaniLeish®) remains effective against an experimental challenge one year later

Martin, V., Vouldoukis, I., Moreno, J., McGahie, D., Gueguen, S., & Cuisinier, A. (2014) · Veterinary Research · doi:10.1186/1297-9716-45-69 · Cited by 58 · see citing works

Detection of selection signatures within candidate regions underlying trypanotolerance in outbred cattle populations

Dayo, G., Thévenon, S., Berthier, D., Moazami‐Goudarzi, K., DENIS, C., Cuny, G., Eggen, A., & Gautier, M. (2009) · Molecular Ecology · doi:10.1111/j.1365-294x.2009.04141.x · Cited by 56 · see citing works

Transcriptional profiling of cattle infected with Trypanosoma congolense highlights gene expression signatures underlying trypanotolerance and trypanosusceptibility

O’Gorman, G. M., Park, S. D. E., Hill, E. W., Meade, K. G., Coussens, P. M., Agaba, M. K., Naessens, J., Kemp, S. J., & MacHugh, D. E. (2009) · BMC Genomics · doi:10.1186/1471-2164-10-207 · Cited by 55 · see citing works

Studies in the epidemiology of East African Leishmaniasis

Southgate, B., & Oriedo, B. V. E. (1962) · Transactions of the Royal Society of Tropical Medicine and Hygiene · doi:10.1016/0035-9203(62)90087-1 · Cited by 55 · see citing works

Canine visceral leishmaniasis in urban and rural areas of Northeast Brazil

Queiroz, P. V. S., Monteiro, G. R., Macedo-Silva, V. P., Rocha, M. A. C., Batista, L. M. M., Queiroz, J. W., Jerônimo, S. M. B., & Ximenes, M. D. F. F. D. M. (2008) · Research in Veterinary Science · doi:10.1016/j.rvsc.2008.07.014 · Cited by 53 · see citing works

A Comparison of Phenotypic Traits Related to Trypanotolerance in Five West African Cattle Breeds Highlights the Value of Shorthorn Taurine Breeds

Berthier, D., Peylhard, M., Dayo, G., Flori, L., Sylla, S., Bolly, S., Sakandé, H., Chantal, I., & Thévenon, S. (2015) · PLoS ONE · doi:10.1371/journal.pone.0126498 · Cited by 49 · see citing works

Diversity of response to Trypanosoma brucei gambiense infections in the Forecariah mangrove focus (Guinea): perspectives for a better control of sleeping sickness

Ilboudo, H., Jamonneau, V., Camara, M., Camara, O., Dama, E., Léno, M., Ff, O., Courtin, F., Sakandé, H., Sanon, R., et al. (2011) · Microbes and Infection · doi:10.1016/j.micinf.2011.05.007 · Cited by 49 · see citing works

Aplicación de un planteamiento global en el uso de marcadores moleculares para incrementar la resistencia a las enfermedades

Gibson, J. P., & Bishop, S. C. (2005) · Scientific and Technical Review (World Organisation for Animal Health) · doi:10.20506/rst.24.1.1573 · Cited by 48 · see citing works

HLA-G 3′ UTR-2 haplotype is associated with Human African trypanosomiasis susceptibility

Courtin, D., Milet, J., Sabbagh, A., Massaro, J. D., Castelli, E. C., Jamonneau, V., Bucheton, B., Sese, C., Favier, B., Rouas‐Freiss, N., et al. (2013) · Infection Genetics and Evolution · doi:10.1016/j.meegid.2013.03.004 · Cited by 48 · see citing works

Effective humoral and cellular immunoprotective responses in Li ESAp-MDP vaccinated protected dogs

Bourdoiseau, G., Hugnet, C., Bras‐Gonçalves, R., Vezilier, F., Petitdidier, E., Papierok, G.-M., & Lemesre, J.-L. (2008) · Veterinary Immunology and Immunopathology · doi:10.1016/j.vetimm.2008.10.309 · Cited by 47 · see citing works

Studies on the Tolerance of N'dama Cattle to Trypanosomiasis

Chandler, R. L. (1958) · Journal of Comparative Pathology and Therapeutics · doi:10.1016/s0368-1742(58)80025-9 · Cited by 45 · see citing works

Interest of tumor necrosis factor-alpha −308 G/A and interleukin-10 −592 C/A polymorphisms in human African trypanosomiasis

Courtin, D., Argiro, L., Jamonneau, V., N'Dri, L., N'Guessan, P., Abel, L., Dessein, A. J. J., Cot, M., Laveissière, C., & Garcia, A. (2005) · Infection Genetics and Evolution · doi:10.1016/j.meegid.2005.03.002 · Cited by 42 · see citing works

Community- and farmer-based management of animal African trypanosomosis in cattle

Bouyer, J., Bouyer, F., Donadeu, M., ROWAN, T. G., & Napier, G. B. (2013) · Trends in Parasitology · doi:10.1016/j.pt.2013.08.003 · Cited by 41 · see citing works

Uniting mathematics and biology for control of visceral leishmaniasis

Rock, K. S., Rutte, E. A. L., de Vlas, S. J., Adams, E. R., Medley, G. F., & Hollingsworth, T. D. (2015) · Trends in Parasitology · doi:10.1016/j.pt.2015.03.007 · Cited by 41 · see citing works

Transmissibility of Trypanosoma brucei during its development in cattle

den Bossche, P. V., Ky-Zerbo, A., Brandt, J., Marcotty, T., Geerts, S., & Deken, R. D. (2005) · Tropical Medicine & International Health · doi:10.1111/j.1365-3156.2005.01467.x · Cited by 40 · see citing works

Association between human African trypanosomiasis and the IL6 gene in a Congolese population

Courtin, D., Milet, J., Jamonneau, V., Sese, C., Kumeso, V. K. B., Bilenge, C. M. M., Bétard, C., & Garcia, A. (2006) · Infection Genetics and Evolution · doi:10.1016/j.meegid.2006.04.001 · Cited by 39 · see citing works

Studies in the epidemiology of East African leishmaniasis. 4. The significance of the positive leishmanin test.

Southgate, B., & Manson‐Bahr, P. (1967) · PubMed · Cited by 38 · see citing works

Kala-azar (Visceral Leishmaniasis) Elimination in Bangladesh: Successes and Challenges

Ahmed, B., Nabi, S. G., Rahman, M., Selim, S., Bashar, A., Rashid, M. M., Lira, F. Y., Choudhury, T. A., & Mondal, D. (2014) · Current Tropical Medicine Reports · doi:10.1007/s40475-014-0027-6 · Cited by 33 · see citing works

Experimental evaluation of xenodiagnosis to detect trypanosomes at low parasitaemia levels in infected hosts

Toukam, C. M. W., Solano, P., Bengaly, Z., Jamonneau, V., & Bucheton, B. (2011) · Parasite · doi:10.1051/parasite/2011184295 · Cited by 33 · see citing works

Human Asymptomatic Infection in Visceral Leishmaniasis: A Seroprevalence Study in an Urban Area of Low Endemicity. Preliminary Results

Barão, S. C., de Camargo-Neves, V. L. F., Resende, M. R., & da Silva, L. J. (2007) · American Journal of Tropical Medicine and Hygiene · doi:10.4269/ajtmh.2007.77.1051 · Cited by 29 · see citing works

Identification of a novel G245R polymorphism in the IL-2 receptor β membrane proximal domain associated with human visceral leishmaniasis

Bucheton, B., Argiro, L., Chevillard, C., Marquet, S., Kheir, M. M., Mergani, A., EL-Safi, S. H., & Dessein, A. J. J. (2006) · Genes and Immunity · doi:10.1038/sj.gene.6364355 · Cited by 28 · see citing works

Serial analysis of gene expression (SAGE) in bovine trypanotolerance: preliminary results

Berthier, D., Quéré, R., Thévenon, S., Belemsaga, D., Piquemal, D., Marti, J., & Maillard, J. (2003) · Genetics Selection Evolution · doi:10.1051/gse:2003015 · Cited by 24 · see citing works

Trypanotolerance : an individual not a breed character

Roelants, G. E., Tamboura, I., & Sidiki, D. B. (1983) · PubMed · doi:10.5169/seals-313120 · Cited by 24 · see citing works

IL2RA Genetic Variants Reduce IL-2–Dependent Responses and Aggravate Human Cutaneous Leishmaniasis

Oliveira, P. R. S., Dessein, H., Romano, A., Cabantous, S., de Brito, M. E. F., Santoro, F., Pitta, M. G. D. R., Pereira, V. R. A., Pontes-de-Carvalho, L. C., Rodrigues, V., et al. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1402047 · Cited by 23 · see citing works

Association studies in QTL regions linked to bovine trypanotolerance in a West African crossbred population

Dayo, G., Gautier, M., Berthier, D., Poivey, J. P., Sidibé, I., Bengaly, Z., Eggen, A., Boichard, D., & Thévenon, S. (2011) · Animal Genetics · doi:10.1111/j.1365-2052.2011.02227.x · Cited by 22 · see citing works

A Comprehensive Genetic Analysis of Candidate Genes Regulating Response to Trypanosoma congolense Infection in Mice

Goodhead, I., Archibald, A. L., Amwayi, P. W., Brass, A., Gibson, J. P., Hall, N., HUGHES, M. A., Limo, M., Iraqi, F. A., Kemp, S. J., et al. (2010) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0000880 · Cited by 14 · see citing works

Study of Bovine Trypanotolerance by Whole Transcriptome Analysis

Berthier, D., Chantal, I., Thévenon, S., Sakandé, H., Maillard, J., Bengaly, Z., Piquemal, D., Marti, J., & Cuny, G. (2008) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1428.062 · Cited by 14 · see citing works

Population parameters for traits defining trypanotolerance in an F2 cross of N’Dama and Boran cattle

van der Waaij, E. H., Hanotte, O., van Arendonk, J. A. M., Kemp, S. J., Kennedy, D., Gibson, J. P., & Teale, A. J. (2003) · Livestock Production Science · doi:10.1016/s0301-6226(03)00078-2 · Cited by 14 · see citing works

Bovine Transcriptome Analysis by SAGE Technology during an Experimental Trypanosoma congolense Infection

Berthier, D., Chantal, I., Thévenon, S., Marti, J., Piquemal, D., & Maillard, J. (2006) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1373.039 · Cited by 13 · see citing works

Epidemiological factors related to the transmission risk of Trypanosoma cruzi in a Quilombola community, State of Mato Grosso do Sul, Brazil

Cominetti, M. C., Andreotti, R., Oshiro, E. T., & Dorval, M. E. M. C. (2011) · Revista da Sociedade Brasileira de Medicina Tropical · doi:10.1590/s0037-86822011000500009 · Cited by 11 · see citing works

High resolution mapping of trypanosomosis resistance loci Tir 2 and Tir 3 using F12 advanced intercross lines with major locus Tir 1 fixed for the susceptible allele

Nganga, J. K., Soller, M., & Iraqi, F. A. (2010) · BMC Genomics · doi:10.1186/1471-2164-11-394 · Cited by 8 · see citing works

Pathological Consequences of Host Response to Parasite

Hontebeyrie, M., Truyens, C., & Brénière, S. F. (2010) · Elsevier eBooks · doi:10.1016/b978-0-12-384876-5.00025-3 · Cited by 1 · see citing works

The skin is a significant but overlooked anatomical reservoir for vector-borne African trypanosomes

Capewell, P., Travaillé, C., Marchesi, F., Johnston, P., Clucas, C., Benson, R. A., Gorman, T.-A., Alvarez, E. C., Crouzols, A., Jouvion, G., et al. (2016) · eLife · doi:10.7554/elife.17716 · Cited by 289 · see citing works

Calpain research for drug discovery: challenges and potential

Ono, Y., Saido, T. C., & Sorimachi, H. (2016) · Nature Reviews Drug Discovery · doi:10.1038/nrd.2016.212 · Cited by 284 · see citing works

Sending a message: extracellular vesicles of pathogenic protozoan parasites

Szempruch, A. J., Dennison, L., Kieft, R., Harrington, J. M., & Hajduk, S. L. (2016) · Nature Reviews Microbiology · doi:10.1038/nrmicro.2016.110 · Cited by 129 · see citing works

Livestock Genomics for Developing Countries – African Examples in Practice

Marshall, K., Gibson, J. P., Mwai, O. A., Mwacharo, J. M., Haile, A., Getachew, T., Mrode, R., & Kemp, S. J. (2019) · Frontiers in Genetics · doi:10.3389/fgene.2019.00297 · Cited by 128 · see citing works

Combatting African Animal Trypanosomiasis (AAT) in livestock: The potential role of trypanotolerance

Yaro, M., Munyard, K. A., Stear, M. J., & Groth, D. M. (2016) · Veterinary Parasitology · doi:10.1016/j.vetpar.2016.05.003 · Cited by 114 · see citing works

African Trypanosomiasis-Associated Anemia: The Contribution of the Interplay between Parasites and the Mononuclear Phagocyte System

Stijlemans, B., BAETSELIER, P. D., Magez, S., Ginderachter, J. A. V., & Trez, C. D. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.00218 · Cited by 101 · see citing works

Extravascular Dermal Trypanosomes in Suspected and Confirmed Cases of gambiense Human African Trypanosomiasis

Camara, M., Soumah, A. M., Ilboudo, H., Travaillé, C., Clucas, C., Cooper, A., Swar, N.-R. K., Camara, O., Sadissou, I. A., Alvarez, E. C., et al. (2020) · Clinical Infectious Diseases · doi:10.1093/cid/ciaa897 · Cited by 72 · see citing works

A multi-breed GWAS for morphometric traits in four Beninese indigenous cattle breeds reveals loci associated with conformation, carcass and adaptive traits

Vanvanhossou, S. F. U., Scheper, C., Dossa, L. H., Yin, T., Brügemann, K., & König, S. (2020) · BMC Genomics · doi:10.1186/s12864-020-07170-0 · Cited by 61 · see citing works

Infections With Extracellular Trypanosomes Require Control by Efficient Innate Immune Mechanisms and Can Result in the Destruction of the Mammalian Humoral Immune System

Magez, S., Torres, J. E. P., Obishakin, E., & Radwanska, M. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00382 · Cited by 40 · see citing works

Identification of Candidate Signature Genes and Key Regulators Associated With Trypanotolerance in the Sheko Breed

Mekonnen, Y. A., Gültas, M., Effa, K., Hanotte, O., & Schmitt, A. O. (2019) · Frontiers in Genetics · doi:10.3389/fgene.2019.01095 · Cited by 37 · see citing works

Assessing Strategies Against Gambiense Sleeping Sickness Through Mathematical Modeling

Rock, K. S., Ndeffo-Mbah, M. L., Castaño, S., Palmer, C., Pandey, A., Atkins, K. E., Ndung’u, J. M., Hollingsworth, T. D., Galvani, A. P., Bever, C. A., et al. (2018) · Clinical Infectious Diseases · doi:10.1093/cid/ciy018 · Cited by 36 · see citing works

Alice in microbes' land: adaptations and counter-adaptations of vector-borne parasitic protozoa and their hosts

Caljon, G., Muylder, G. D., Durnez, L., Jennes, W., Vanaerschot, M., & Dujardin, J. (2016) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuw018 · Cited by 34 · see citing works

Peptide-based vaccine successfully induces protective immunity against canine visceral leishmaniasis

Petitdidier, E., Pagniez, J., Pissarra, J., Holzmüller, P., Papierok, G., Vincendeau, P., Lemesre, J.-L., & Bras‐Gonçalves, R. (2019) · npj Vaccines · doi:10.1038/s41541-019-0144-2 · Cited by 33 · see citing works

Salivarian Trypanosomes Have Adopted Intricate Host-Pathogen Interaction Mechanisms That Ensure Survival in Plain Sight of the Adaptive Immune System

Magez, S., Torres, J. E. P., Oh, S., & Radwanska, M. (2021) · Pathogens · doi:10.3390/pathogens10060679 · Cited by 33 · see citing works

Impact of the Ebola outbreak on Trypanosoma brucei gambiense infection medical activities in coastal Guinea, 2014-2015: A retrospective analysis from the Guinean national Human African Trypanosomiasis control program

Camara, M., Ouattara, E. N., Duvignaud, A., Migliani, R., Camara, O., Léno, M., Solano, P., Bucheton, B., Camara, M., & Malvy, D. J.-M. (2017) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0006060 · Cited by 32 · see citing works

Vector-borne Trypanosoma brucei parasites develop in artificial human skin and persist as skin tissue forms

Reuter, C., Hauf, L., Imdahl, F., Sen, R., Vafadarnejad, E., Fey, P., Finger, T., Jones, N. G., Walles, H., Barquist, L., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-43437-2 · Cited by 31 · see citing works

Free-ranging pigs identified as a multi-reservoir of Trypanosoma brucei and Trypanosoma congolense in the Vavoua area, a historical sleeping sickness focus of Côte d’Ivoire

Traoré, B. M., Koffi, M., N’Djetchi, M. K., Kaba, D., Kaboré, J., Ilboudo, H., Ahouty, B., Koné, M., Coulibaly, B., Konan, T. K., et al. (2021) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0010036 · Cited by 29 · see citing works

Trypanosoma vivax in water buffalo of the Venezuelan Llanos: An unusual outbreak of wasting disease in an endemic area of typically asymptomatic infections

Garcia, H. A., Ramírez, O. J., Rodrigues, C. M. F., Sánchez, R. G., Bethencourt, A., Pérez, G. D. M., Minervino, A. H. H., Rodrigues, A. C., & Teixeira, M. M. G. (2016) · Veterinary Parasitology · doi:10.1016/j.vetpar.2016.10.013 · Cited by 27 · see citing works

Modelling to explore the potential impact of asymptomatic human infections on transmission and dynamics of African sleeping sickness

Aliee, M., Keeling, M. J., & Rock, K. S. (2021) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1009367 · Cited by 21 · see citing works

Identification ofTrypanosoma bruceiAdoMetDC Inhibitors Using a High-Throughput Mass Spectrometry-Based Assay

Volkov, O. A., Cosner, C. C., Brockway, A. J., Kramer, M. L., Booker, M. L., Zhong, S., Ketcherside, A., Wei, S., Longgood, J. C., McCoy, M. K., et al. (2017) · ACS Infectious Diseases · doi:10.1021/acsinfecdis.7b00022 · Cited by 21 · see citing works

Human Leukocyte Antigen-G: A Promising Prognostic Marker of Disease Progression to Improve the Control of Human African Trypanosomiasis

Gineau, L., Courtin, D., Camara, M., Ilboudo, H., Jamonneau, V., Dias, F. C., Tokplonou, L., Milet, J., Mendonça, P. B., Castelli, E. C., et al. (2016) · Clinical Infectious Diseases · doi:10.1093/cid/ciw505 · Cited by 22 · see citing works

Search for Selection Signatures Related to Trypanosomosis Tolerance in African Goats

Serranito, B., Taurisson-Mouret, D., Harkat, S., Laoun, A., Ouchene‐Khelifi, N., Pompanon, F., Benjelloun, B., Cecchi, G., Thévenon, S., Lenstra, J. A., et al. (2021) · Frontiers in Genetics · doi:10.3389/fgene.2021.715732 · Cited by 21 · see citing works

Single nucleotide polymorphisms and copy-number variations in the Trypanosoma brucei repeat (TBR) sequence can be used to enhance amplification and genotyping of Trypanozoon strains

Reet, N. V., Pyana, P. P., Dehou, S., Bebronne, N., Deborggraeve, S., & Büscher, P. (2021) · PLoS ONE · doi:10.1371/journal.pone.0258711 · Cited by 17 · see citing works

Synthesis and evaluation of analogs of 5′-(((Z)-4-amino-2-butenyl)methylamino)-5′-deoxyadenosine (MDL 73811, or AbeAdo) – An inhibitor of S-adenosylmethionine decarboxylase with antitrypanosomal activity

Brockway, A. J., Volkov, O. A., Cosner, C. C., MacMillan, K. S., Wring, S. A., Richardson, T. E., Peel, M. R., Phillips, M. A., & Brabander, J. K. D. (2017) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2017.07.063 · Cited by 15 · see citing works

Blood feeding tsetse flies as hosts and vectors of mammals-pre-adapted African Trypanosoma: current and expected research directions

Geiger, A., Malele, I. I., Abd‐Alla, A. M. M., & Njiokou, F. (2018) · BMC Microbiology · doi:10.1186/s12866-018-1281-x · Cited by 14 · see citing works

Species-Selective Pyrimidineamine Inhibitors of Trypanosoma brucei S-Adenosylmethionine Decarboxylase

Volkov, O. A., Brockway, A. J., Wring, S. A., Peel, M. R., Chen, Z., Phillips, M. A., & Brabander, J. K. D. (2017) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.7b01654 · Cited by 13 · see citing works

Enhancing research integration to improve One Health actions: learning lessons from neglected tropical diseases experiences

Rotureau, B., Waleckx, E., Jamonneau, V., Solano, P., Molia, S., Debré, P., Dellagi, K., & Morand, S. (2022) · BMJ Global Health · doi:10.1136/bmjgh-2022-008881 · Cited by 13 · see citing works

Selection Increases Mitonuclear DNA Discordance but Reconciles Incompatibility in African Cattle

Shi, X., Ma, C., Chen, N., Xu, M., Kambal, S., Cai, Z., Yang, Q., Adeola, A. C., Liu, L.-S., Wang, J., et al. (2025) · Molecular Biology and Evolution · doi:10.1093/molbev/msaf039 · Cited by 12 · see citing works

Goat Science - From Keeping to Precision Production

Kukovics, S. (2023) · IntechOpen eBooks · doi:10.5772/intechopen.104279 · Cited by 11 · see citing works

The implications of herd entrustment practice for the sustainable use of cattle genetic resources in the (agro)-pastoral systems of West Africa: A case study from Benin

Vanvanhossou, S. F. U., Koura, B. I., & Dossa, L. H. (2021) · Pastoralism Research Policy and Practice · doi:10.1186/s13570-020-00189-8 · Cited by 11 · see citing works

Differences in pathogenicity and virulence of Trypanosoma brucei gambiense field isolates in experimentally infected Balb/C mice

Kaboré, J., Camara, O., Koffi, M., Sanou, D., Ilboudo, H., Sakandé, H., Camara, M., Meeûs, T. D., Ravel, S., Bélem, A. M. G., et al. (2018) · Infection Genetics and Evolution · doi:10.1016/j.meegid.2018.05.018 · Cited by 10 · see citing works

Resistencia y resiliencia a las enfermedades en las razas de rumiantes locales: un enfoque en América del Sur

Fíoravantí, M. C. S., Freitas, T. M. S., de Moura, M. I., Costa, G. L., Dias, J. M., Guimarães, L., Carpio, M. M. G., & Landi, V. (2020) · Archivos de Zootecnia · doi:10.21071/az.v69i267.5353 · Cited by 7 · see citing works

Variation in disease phenotype is marked in equine trypanosomiasis

Raftery, A. G., Jallow, S., Coultous, R., Rodgers, J., & Sutton, D. G. M. (2020) · Parasites & Vectors · doi:10.1186/s13071-020-04020-6 · Cited by 6 · see citing works

Let's get fISSical: fastin silicosynchronization as a new tool for cell division cycle analysis

Morriswood, B., & Engstler, M. (2017) · Parasitology · doi:10.1017/s0031182017000038 · Cited by 6 · see citing works

Tripanossomose bovina em um rebanho leiteiro no municipio de Monte Carmelo, Minas Gerais: relato de caso

Ribeiro, L. F., de Souza, A. L., Alves, A. L., Rocha, A. R., Borges, A. V. F., dos Reis, K. B., Silva, L. C. D. S. E., de Oliveira, L. C., Magalhães, L. A., Gonçalves, M. L. D. O., et al. (2019) · PubVet · doi:10.31533/pubvet.v13n10a437.1-5 · Cited by 6 · see citing works

Evolving anti-disease strategies from biochemical pathogenesis of african trypanosomiasis

Igbokwe, I. O. (2018) · Advances in Cytology & Pathology · doi:10.15406/acp.2018.03.00048 · Cited by 5 · see citing works

Functional genomics of trypanotolerant and trypanosusceptible cattle infected with <i>Trypanosoma congolense</i> across multiple time points and tissues

McHugo, G. P., Ward, J. A., Browne, J. A., O’Gorman, G. M., Meade, K. G., Hill, E. W., Hall, T. J., & MacHugh, D. E. (2025) · doi:10.1101/2025.01.31.635858 · Cited by 4 · see citing works

Infection of West African dwarf rams with Trypanosoma brucei brucei and Trypanosoma congolense significantly alter serum electrolytes, redox balance, sperm parameters, and gonadal morphology

Anyogu, D. C., Shoyinka, S. V. O., & Ihedioha, J. I. (2022) · Veterinary Research Communications · doi:10.1007/s11259-022-09921-8 · Cited by 4 · see citing works

Breeding of African sheep reared under low-input/output smallholder production systems for trypanotolerance

Malatji, D. P. (2022) · Veterinary World · doi:10.14202/vetworld.2022.1031-1043 · Cited by 3 · see citing works

Tripanossomose bovina: Revisão

Germano, P. H. V., Silva, A. A., Edler, G. E. C., Lopes, M. C., Modesto, T. C., & dos Reis, J. A. (2018) · PubVet · doi:10.31533/pubvet.v12n8a144.1-6 · Cited by 3 · see citing works

Prevalence of Trypanosomosis in Ruminants in Rivers State and Abia State, Nigeria and the Challenges of Trypanosomosis Control in Goat Production

Akpan, C. A. N. (2023) · IntechOpen eBooks · doi:10.5772/intechopen.1001071 · Cited by 2 · see citing works

HAEMOPARASITIC INFECTIONS AND ASSOCIATED RISK FACTORS AMONG CATTLE SLAUGHTERED AT KATSINA CENTRAL ABATTOIR, KATSINA STATE, NIGERIA

Muhammad, U. Z., Auta, T., & Atalabi, T. E. (2023) · FUDMA Journal of Sciences · doi:10.33003/fjs-2023-0702-2040 · Cited by 2 · see citing works

Upregulation of sialyltransferases ST3Gal1 and ST6Gal1 promotes stabilization of erythrocyte mass and recovery of anemia in Trypanosoma brucei brucei-infected pigs

Atata, J. A., Enam, S. J., Ogbuagu, N. E., Balogun, E. O., Adamu, S., & Esievo, K. A. N. (2022) · Research in Veterinary Science · doi:10.1016/j.rvsc.2022.02.012 · Cited by 2 · see citing works

Individual and combined anti-trypanosomal effects of arteether and diminazene aceturate in the treatment of experimental Trypanosoma brucei brucei infection in rats

Egbe-Nwiyi, T. N., Abalaka, S. E., Sani, N. A., Tenuche, O. Z., & Idoko, I. S. (2020) · Veterinary World · doi:10.14202/vetworld.2020.1858-1862 · Cited by 2 · see citing works

Interleukin 21 is a marker of Human African Trypanosomiasis Infection and a contributor to pathology in micePreprint

Capewell, P., Ilboudo, H., Cooper, A., Kaboré, J. W., Noyes, H. A., Neill, K. O., Camara, M., Jamonneau, V., MacLeod, A., & Bucheton, B. (2024) · medRxiv · doi:10.1101/2024.05.07.24306988 · Cited by 2 · see citing works

Tripanossomose bovina no Brasil

Oliveira, W. J., Barbosa, F. C., & Rosalinski-Moraes, F. (2019) · Revista Acadêmica Ciência Animal · doi:10.7213/1981-4178.2019.17104

Tsetse Flies (Glossinidae)

Benoit, J. B., Attardo, G. M., & Weiss, B. L. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-818731-9.00004-5

Adoption of Genomics and Breeding Strategies to Improve Goat Productivity in Southern Africa

Monau, P. I., Raphaka, K., & Nsoso, S. J. (2022) · Springer eBooks · doi:10.1007/978-3-031-09614-3_21

Prediction of the molecular action of Trypanosoma vivax on bovine reproductive parameters and risk factors associated with trypanosomiasis in northern Minas Gerais, Brazil

de Lima, A. C. N., Bittar, J. F. F., Neto, O. D. S. P., Santos, E. M. S., da Silva, P. E. F., Santos, H. O., de Souza, C. N., dos Santos, F. G., & de Almeida, A. C. (2025) · Veterinary World · doi:10.14202/vetworld.2025.837-850

Additional file 3 of A multi-breed GWAS for morphometric traits in four Beninese indigenous cattle breeds reveals loci associated with conformation, carcass and adaptive traits

Vanvanhossou, S. F. U., Scheper, C., Dossa, L. H., Yin, T., Brügemann, K., & König, S. (2020) · Figshare · doi:10.6084/m9.figshare.13226188

Additional file 8 of Variation in disease phenotype is marked in equine trypanosomiasis

Raftery, A. G., Jallow, S., Coultous, R., Rodgers, J., & Sutton, D. G. M. (2020) · Figshare · doi:10.6084/m9.figshare.12016587

Additional file 1 of Variation in disease phenotype is marked in equine trypanosomiasis

Raftery, A. G., Jallow, S., Coultous, R., Rodgers, J., & Sutton, D. G. M. (2020) · Figshare · doi:10.6084/m9.figshare.12016551

Additional file 4 of A multi-breed GWAS for morphometric traits in four Beninese indigenous cattle breeds reveals loci associated with conformation, carcass and adaptive traits

Vanvanhossou, S. F. U., Scheper, C., Dossa, L. H., Yin, T., Brügemann, K., & König, S. (2020) · Figshare · doi:10.6084/m9.figshare.13226191

Additional file 1 of A multi-breed GWAS for morphometric traits in four Beninese indigenous cattle breeds reveals loci associated with conformation, carcass and adaptive traits

Vanvanhossou, S. F. U., Scheper, C., Dossa, L. H., Yin, T., Brügemann, K., & König, S. (2020) · Figshare · doi:10.6084/m9.figshare.13226182

Additional file 5 of Variation in disease phenotype is marked in equine trypanosomiasis

Raftery, A. G., Jallow, S., Coultous, R., Rodgers, J., & Sutton, D. G. M. (2020) · Figshare · doi:10.6084/m9.figshare.12016572

Additional file 6 of A multi-breed GWAS for morphometric traits in four Beninese indigenous cattle breeds reveals loci associated with conformation, carcass and adaptive traits

Vanvanhossou, S. F. U., Scheper, C., Dossa, L. H., Yin, T., Brügemann, K., & König, S. (2020) · Figshare · doi:10.6084/m9.figshare.13226197

Additional file 5 of A multi-breed GWAS for morphometric traits in four Beninese indigenous cattle breeds reveals loci associated with conformation, carcass and adaptive traits

Vanvanhossou, S. F. U., Scheper, C., Dossa, L. H., Yin, T., Brügemann, K., & König, S. (2020) · Figshare · doi:10.6084/m9.figshare.13226194

Additional file 6 of Variation in disease phenotype is marked in equine trypanosomiasis

Raftery, A. G., Jallow, S., Coultous, R., Rodgers, J., & Sutton, D. G. M. (2020) · Figshare · doi:10.6084/m9.figshare.12016581

Additional file 2 of Variation in disease phenotype is marked in equine trypanosomiasis

Raftery, A. G., Jallow, S., Coultous, R., Rodgers, J., & Sutton, D. G. M. (2020) · Figshare · doi:10.6084/m9.figshare.12016554

Additional file 7 of Variation in disease phenotype is marked in equine trypanosomiasis

Raftery, A. G., Jallow, S., Coultous, R., Rodgers, J., & Sutton, D. G. M. (2020) · Figshare · doi:10.6084/m9.figshare.12016584

Additional file 3 of Variation in disease phenotype is marked in equine trypanosomiasis

Raftery, A. G., Jallow, S., Coultous, R., Rodgers, J., & Sutton, D. G. M. (2020) · Figshare · doi:10.6084/m9.figshare.12016560

Additional file 4 of Variation in disease phenotype is marked in equine trypanosomiasis

Raftery, A. G., Jallow, S., Coultous, R., Rodgers, J., & Sutton, D. G. M. (2020) · Figshare · doi:10.6084/m9.figshare.12016566

Étude des phospholipases du trypanosome africain

Monic, S. (2021) · doi:10.70675/0dec7cdaz18dez40d1zbbccz79acdd29502a

Genomic diversity, population structure and admixture in native cattle breeds of Benin

Zorobouragui, L., Tapsoba, S. A. R., TRAORE, A., Periasamy, K., Pichler, R., Mavunga, T. K., Séidou, A. A., Worogo, H. S. S., Taba, N., Azalou, M., et al. (2026) · World Congress on Genetics Applied to Livestock Production (WCGALP) · doi:10.31274/wcgalp.24000

BindingDB Entry 50000611: Species-Selective Pyrimidineamine Inhibitors of Trypanosoma brucei S-Adenosylmethionine Decarboxylase.

BindingDB (2019) · UC San Diego · doi:10.7270/q22n54r6

Diarrheal diseases

DuPont, H. L., & Hornick, R. B. (1969) · Disease-a-Month · doi:10.1016/s0011-5029(69)80011-8 · Cited by 4 · see citing works

Studies on the Tolerance of N'dama Cattle to Trypanosomiasis

Chandler, R. L. (1958) · Journal of Comparative Pathology and Therapeutics · doi:10.1016/s0368-1742(58)80025-9 · Cited by 45 · see citing works

Human African trypanosomiasis: What are the prospects for control?

Gjini, E. (2017) · Human Parasitic Diseases · doi:10.4137/hpd.s16589 · Cited by 2 · see citing works

How do African game animals control trypanosome infections?

Mulla, A. F., & Rickman, L. R. (1988) · Parasitology Today · doi:10.1016/0169-4758(88)90005-1 · Cited by 51 · see citing works

Host Susceptibility to African Trypanosomiasis: Trypanotolerance

Murray, M., Morrison, W. I., & Whitelaw, D. D. (1982) · Advances in Parasitology/Advances in parasitology · doi:10.1016/s0065-308x(08)60274-2 · Cited by 268 · see citing works