K. Watschinger, M. A. Keller, and G. Golderer, Biochemical characterization of AGMO variants implicated in relapses in visceral leishmaniasis, J Infect Dis, vol.217, pp.1846-1853, 2018.

S. Marquet, B. Bucheton, and C. Reymond, Exome sequencing identifies two variants of the alkylglycerol monooxygenase gene as a cause of relapses in visceral leishmaniasis in children, in Sudan, J Infect Dis, vol.216, pp.22-30, 2017.
URL : https://hal.archives-ouvertes.fr/hal-01741722

L. Heinz, G. J. Kim, and S. Marrakchi, Mutations in SULT2B1 cause autosomal-recessive congenital ichthyosis in humans, Am J Hum Genet, vol.100, pp.926-965, 2017.

S. Tang, X. Wang, and W. Li, Biallelic mutations in CFAP43 and CFAP44 cause male infertility with multiple morphological abnormalities of the sperm flagella, Am J Hum Genet, vol.100, pp.854-64, 2017.

M. Srour, N. Shimokawa, and F. F. Hamdan, Dysfunction of the cerebral glucose transporter SLC45A1 in individuals with intellectual disability and epilepsy, Am J Hum Genet, vol.100, pp.824-854, 2017.