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Publication

Genetic association analyses highlight biological pathway underlying mitral valve prolapse.

Nat Genet. 2015 Oct

Dina C*, Bouatia-Naji N*, Tucker N, Delling FN, Toomer K, Durst R, Perrocheau M, Fernandez-Friera L, Solis J; PROMESA investigators, Le Tourneau T, Chen MH, Probst V, Bosse Y, Pibarot P, Zelenika D, Lathrop M, Hercberg S, Roussel R, Benjamin EJ, Bonnet F, Lo SH, Dolmatova E, Simonet F, Lecointe S, Kyndt F, Redon R, Le Marec H, Froguel P, Ellinor PT, Vasan RS, Bruneval P, Markwald RR, Norris RA, Milan DJ, Slaugenhaupt SA, Levine RA, Schott JJ, Hagege AA; MVP-France, Jeunemaitre X

 

*: First authors

Read more: Genetic association analyses highlight biological pathway underlying mitral valve prolapse.

4

KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron.

Nat Genet. 2012 Mar


Louis-Dit-Picard H1, Barc J, Trujillano D, Miserey-Lenkei S, Bouatia-Naji N, Pylypenko O, Beaurain G, Bonnefond A, Sand O, Simian C, Vidal-Petiot E, Soukaseum C, Mandet C, Broux F, Chabre O, Delahousse M, Esnault V, Fiquet B, Houillier P, Bagnis CI, Koenig J, Konrad M, Landais P, Mourani C, Niaudet P, Probst V, Thauvin C, Unwin RJ, Soroka SD, Ehret G, Ossowski S, Caulfield M; International Consortium for Blood Pressure (ICBP), Bruneval P, Estivill X, Froguel P, Hadchouel J, Schott JJ, Jeunemaitre X 

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2

Exome sequencing in seven families and gene-based association studies indicate heterogeneity and suggest

possible candidates for Fibromuscular Dysplasia.

J Hypertens. 2015 Sep


Kiando SR, Barlassina C, Cusi D, Galan P, Lathrop M, Plouin PF, Jeunemaitre X, Bouatia-Naji N.

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3

Multiple functional polymorphisms in the G6PC2 gene contribute to the association with higher fasting plasma

glucose levels. 

Diabetologia. 2013


Baerenwald DA1, Bonnefond A, Bouatia-Naji N, Flemming BP, Umunakwe OC, Oeser JK, Pound LD, Conley NL, Cauchi S, Lobbens S, Eury E, Balkau B, Lantieri O; MAGIC Investigators, Dadi PK, Jacobson DA, Froguel P, O'Brien RM.

 

Read more: 3
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