Publications

Contribution to Alzheimer’s disease risk of rare variants in TREM2, SORL1, and ABCA7 in 1779 cases and 1273 controls

Bellenguez C, Charbonnier C, Grenier-Boley B, Quenez O, Le Guennec K, Nicolas G, Chauhan G, Wallon D, Rousseau S,
Richard AC, Boland A, Bourque G, Munter HM, Olaso R, Meyer V, Rollin-Sillaire A, Pasquier F, Letenneur L, Redon R,
Dartigues JF, Tzourio C, Frebourg T, Lathrop M, Deleuze JF, Hannequin D, Genin E, Amouyel P, Debette S, Lambert JC,
Campion D; CNR MAJ collaborators.
Neurobiol Aging. 2017 Nov;59:220.e1-220.e9. doi: 10.1016/j.neurobiolaging.2017.07.001. Epub 2017 Jul 14.
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Heritability of the melatonin synthesis variability in autism spectrum disorders

Marion Benabou, Thomas Rolland, Claire S. Leblond, Gaël A. Millot, Guillaume Huguet, Richard Delorme,
Marion Leboyer, Cécile Pagan, Jacques Callebert, Erik Maronde,  and Thomas Bourgeron.
Sci Rep. 2017; 7: 17746.

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Assessing the causal relationship between obesity and venous thromboembolism through a Mendelian Randomization study

Lindström S, Germain M, Crous-Bou M, Smith EN, Morange PE, van Hylckama Vlieg A, de Haan HG, Chasman D, Ridker P, Brody J, de Andrade M, Heit JA, Tang W, DeVivo I, Grodstein F, Smith NL,, Tregouet D, Kabrhel C,; INVENT Consortium.

Hum Genet. 2017 Jul;136(7):897-902. doi: 10.1007/s00439-017-1811-x. Epub 2017 May 20.)

Genome-Wide Association Study Identifies a Novel Genetic Risk Factor for Recurrent Venous Thrombosis

Hugoline G. de Haan, Astrid van Hylckama Vlieg, Marine Germain, Trevor P. Baglin, Jean-François Deleuze, David-Alexandre Trégouët, Frits R. Rosendaal

Circ Genom Precis Med. 2018;11:e001827.

Plasma levels of hsa-miR-152-3p are associated with diabetic nephropathy in patients with type 2 diabetes

Maguelonne Roux, Claire Perret, Eva Feigerlova, Badreddine Mohand Oumoussa, Pierre-Jean Saulnier, Carole Proust, David-Alexandre Trégouët, Samy Hadjadj

Nephrology Dialysis Transplantation, , gfx367, https://doi.org/10.1093/ndt/gfx367.

A novel duplication of PRMD13 causes North Carolina macular dystrophy: overexpression of PRDM13 orthologue in drosophila eye reproduces the human phenotype

Manes G, Joly W, Guignard T, Smirnov V, Berthemy S, Bocquet B, Audo I, Zeitz C, Sahel J, Cazevieille C, Sénéchal A, <u>Deleuze JF</u>, <u>Blanché-Koch H</u>, Boland A, Carroll P, Geneviève D, Zanlonghi X, Arndt C, Hamel CP, Defoort-Dhellemmes S, Meunier I

Hum Mol Genet. 2017 Nov 15;26(22):4367-4374. doi: 10.1093/hmg/ddx322.