Céline Besse

Germline CYBB mutations that selectively affect macrophages in kindreds with X-linked predisposition to tuberculous mycobacterial disease

Jacinta Bustamante, Andrés A. Arias, Guillaume Vogt et al. · Nature Immunology · 2011 · 280 citations · Full text

Medical Microbiology, Pulmonary Tuberculosis, Tuberculosis Prevention +9

Human adenylate kinase 2 deficiency causes a profound hematopoietic defect associated with sensorineural deafness

Chantal Lagresle‐Peyrou, Emmanuelle Six, Capucine Pïcard et al. · Nature Genetics · 2008 · 234 citations · Full text

Health Sciences, Profound Hematopoietic Defect, Physiology +7

Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility

Jennifer Wessel, Audrey Y. Chu, Sara M. Willems et al. · Nature Communications · 2015 · 196 citations · Full text

Genome-wide Association Study, Metabolic Syndrome, Genetic Determinant +12

Evidence of Austronesian Genetic Lineages in East Africa and South Arabia: Complex Dispersal from Madagascar and Southeast Asia

Nicolas Brucato, Verónica Fernandes, Pradiptajati Kusuma et al. · Genome Biology and Evolution · 2019 · 120 citations · Full text

Genetics, East Africa, Phylogenetics +16

Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease

Isabelle Le Ber, A. Camuzat, E. Berger et al. · Neurology · 2009 · 95 citations