Publication Genetics of leprosy: today and beyond. Fava V, Dallmann-Sauer M, Schurr E. Human genetics. 2019;
Publication CUBN and NEBL common variants in the chromosome 10p13 linkage region are associated with multibacillary leprosy in Vietnam. Grant A, Cobat A, Van Thuc N, et al. Human genetics. 2014;
Publication NOD2 and CCDC122-LACC1 genes are associated with leprosy susceptibility in Brazilians. Sales-Marques C, Salomão H, Fava VM, et al. Human genetics. 2014; 133 (12) : 1525-32.
Publication Genetic variants of complement genes ficolin-2, mannose-binding lectin and complement factor H are associated with leprosy in Han Chinese from Southwest China. Zhang D, Huang X, Wang D, et al. Human genetics. 2013; 132 (6) : 629-40. Download PDF
Publication Linkage disequilibrium pattern and age-at-diagnosis are critical for replicating genetic associations across ethnic groups in leprosy. Alter A, Fava VM, Huong NT, et al. Human genetics. 2013; 132 (1) : 107-16.
Publication Association of variants in BAT1-LTA-TNF-BTNL2 genes within 6p21.3 region show graded risk to leprosy in unrelated cohorts of Indian population. Ali S, Chopra R, Aggarwal S, et al. Springer Berlin / Heidelberg. Human genetics. 2012; 131 (5) : 703-16. Download PDF
Publication Genetic variants of the MRC1 gene and the IFNG gene are associated with leprosy in Han Chinese from Southwest China. Wang D, Feng J, Li Y, et al. Springer Berlin / Heidelberg. Human genetics. 2012; 131 (7) : 1251-60.
Publication IFNG +874 T>A single nucleotide polymorphism is associated with leprosy among Brazilians. Cardoso C C, PEREIRA A C, Brito-de-Souza V N, et al. Human genetics. 2010; 128 (5) : 481-90.
Publication Genetic and functional analysis of common MRC1 exon 7 polymorphisms in leprosy susceptibility. Alter A, Léséleuc L, Van Thuc N, et al. Human genetics. 2010; 127 (3) : 337-48.
Publication Leprosy as a genetic model for susceptibility to common infectious diseases. Alter A, Alcaïs A, Abel L, et al. Human genetics. 2008; 123 (3) : 227-35.
Publication TLR2 Arg677Trp polymorphism in leprosy: revisited. Malhotra D, Relhan V, Reddy B S N, et al. Human genetics. 2005; 116 (5) : 413-5.
Publication IL-10 promoter single nucleotide polymorphisms are significantly associated with resistance to leprosy. Malhotra D, Darvishi K, Sood S, et al. Human genetics. 2005; 118 (2) : 295-300.
Publication Association of polymorphism at COL3A and CTLA4 loci on chromosome 2q31-33 with the clinical phenotype and in-vitro CMI status in healthy and leprosy subjects: a preliminary study. Kaur G, Sachdeva G, Bhutani L K, et al. Human genetics. 1997; 100 (1) : 43-50.
Publication Genetic variations at the T cell receptor gamma locus in circulating peripheral blood mononuclear cells of clinically categorised leprosy patients. Sachdeva G, Kaur G, Bhutani L K, et al. Human genetics. 1997; 100 (1) : 30-4.
Publication Cytogenetic studies in leprosy patients before and after chemotherapy. D'Souza D, Das B C, Thomas I M. Human genetics. 1991; 87 (6) : 665-70.
Publication On the significance of C2, C4, and factor B polymorphisms in disease. Rittner C, Bertrams J. Human genetics. 1981; 56 (3) : 235-47.
Publication The genetic hypothesis for susceptibility to lepromatous leprosy. Smith D G. Human genetics. 1979; 50 (2) : 163-77.
Publication The HLA system and leprosy in Thailand. Greiner J, Schleiermacher E, Smith T, et al. Human genetics. 1978; 42 (2) : 201-13.