Recent publications from the lab

1.   Warchol-Celinska E, Berrandou T,Prejbisz A, Georges A, Dupre D,Januszewicz M, Florczak E, Jozwik-Plebanek K, Dobrowolski P, Smigielski W, Drygas W, Kadziela J, Witkowski A, Kabat M, Szczerbo-Trojanowska M, Pappaccogli M, Persu A, Jeunemaitre X, Januszewicz A, Bouatia-Naji N. Genetic Study of PHACTR1 and Fibromuscular Dysplasia, Meta-Analysis and Effects on Clinical Features of Patients: The ARCADIA-POL Study.
Hypertension. 2020 Jul;76(1):e4-e7. doi: 10.1161/HYPERTENSIONAHA.120.14793.

2.  Georges A, Albuisson J, Berrandou T, Dupré D, Lorthioir A, D'Escamard V, Di Narzo AF, Kadian-Dodov D, Olin JW, Warchol-Celinska E, Prejbisz A, Januszewicz A, Bruneval P, Baranowska AA, Webb TR, Hamby SE, Samani NJ, Adlam D, Fendrikova-Mahlay N, Hazen S, Wang Y, Yang ML, Hunker K, Combaret N, Motreff P, Chédid A, Fiquet B, Plouin PF, Mousseaux E, Azarine A, Amar L, Azizi M, Gornik HL, Ganesh SK, Kovacic JC, JeunemaitreX, Bouatia-Naji N. Rare Loss-of-function Mutations of PTGIR are enriched in Fibromuscular Dysplasia.
Cardiovasc Res. 2020 Jun 12;. doi: 10.1093/cvr/cvaa161

3.  Job S, Georges A, Burnichon N, Buffet A, Amar L, Bertherat J, Bouatia-Naji N, de Reyniès A, Drui D, Lussey-Lepoutre C, Favier J, Gimenez-Roqueplo AP, Castro-Vega LJ. Transcriptome analysis of lncRNAs in pheochromocytomas and paragangliomas. J Clin Endocrinol Metab. 2019Nov 2. pii: dgz168. doi: 10.1210/clinem/dgz168

4.  Georges A, Bouatia-Naji N. Genetics provides a link between cardiovascular diseases predominantly afflicting women]. Med Sci (Paris).2019 Aug-Sep;35(8-9):605-607. doi: 10.1051/medsci/2019119.

5.  Amrani-Midoun A, Kiando SR, Treard C, Jeunemaitre X,Bouatia-Naji N. Genetic association study between T-786C NOS3 polymorphism and essential hypertension in an Algerian population of the Oran city. 
Diabetes Metab Syndr. 2019Mar - Apr;13(2):1317-1320. doi: 10.1016/j.dsx.2019.02.024.

6.   Olin JW, Di Narzo AF, d'Escamard V, Kadian-Dodov D, Cheng H, Georges A,King A, Thomas A, Barwari T, Michelis KC, Bouchareb R, Bander E, Anyanwu A, Stelzer P, Filsoufi F, Florman S, Civelek M, Debette S, Jeunemaitre X, Lm Björkegren J, Mayr M, Bouatia-Naji N, Hao K, Kovacic JC. A Plasma Proteogenomic Signature for Fibromuscular Dysplasia. 
Cardiovasc Res. 2019Aug 19;. doi: 10.1093/cvr/cvz219.

7.   Maas AHEMBouatia-Naji N, Persu A, Adlam D. Spontaneous coronary artery dissections and fibromuscular dysplasia: Current insights on pathophysiology, sex and gender. Int J Cardiol. 2019Jul 1;286:220-225. doi: 10.1016/j.ijcard.2018.11.023. Epub 2018 Nov 9. PubMed PMID: 30448113.

8.  Liu CT, Merino J, Rybin D, DiCorpo D, Benke KS, Bragg-Gresham JL, Canouil M, Corre T, Grallert H, Isaacs A, Kutalik Z, Lahti J, Marullo L, Marzi C, Rasmussen-Torvik LJ, Rocheleau G, Rueedi R, Scapoli C, Verweij N, Vogelzangs N, Willems SM, Yengo L, Bakker SJL, Beilby J, Hui J, Kajantie E, Müller-Nurasyid M, Rathmann W, Balkau B, Bergmann S, Eriksson JG, Florez JC, Froguel P, Harris T, Hung J, James AL, Kavousi M, Miljkovic I, Musk AW, Palmer LJ, Peters A, Roussel R, van der Harst P, van Duijn CM, Vollenweider P, Barroso I, Prokopenko I, Dupuis J, Meigs JB, Bouatia-Naji N. Genome-wide Association Study of Change in Fasting Glucose over time in 13,807 non-diabetic European Ancestry Individuals. 
Sci Rep. 2019Jul 1;9(1):9439. doi: 10.1038/s41598-019-45823-7. PubMed PMID: 31263163; PubMed Central PMCID: PMC6602949.

9.  Toomer KA, Yu M,Fulmer D, Guo L, Moore KS, Moore R, Drayton KD, Glover J, Peterson N, Ramos-Ortiz S, Drohan A, Catching BJ, Stairley R, Wessels A, Lipschutz JH, Delling FN, Jeunemaitre X, Dina C, Collins RL, Brand H, Talkowski ME, Del Monte F, Mukherjee R, Awgulewitsch A, Body S, Hardiman G, Hazard ES, da Silveira WA, Wang B, Leyne M, Durst R, Markwald RR, Le Scouarnec S, Hagege A, Le Tourneau T, Kohl P, Rog-Zielinska EA, Ellinor PT, Levine RA, Milan DJ, Schott JJ, Bouatia-Naji N&, Slaugenhaupt SA&, Norris RA&. Primary cilia defects causing mitral valve prolapse. 
Sci Transl Med. 2019 May 22;11(493). doi: 10.1126/scitranslmed.aax0290. PubMed PMID: 31118289.

10.Yu M, Georges A, Tucker NR, Kyryachenko S, Toomer K, Schott JJ, Delling FN, Fernandez-Friera L, Solis J, Ellinor PT, Levine RA, Slaugenhaupt SA, Hagège AA, Dina C, Jeunemaitre X, Milan DJ, Norris RA, Bouatia-Naji N. Genome-Wide Association Study-Driven Gene-Set Analyses, Genetic, and Functional Follow-Up Suggest GLIS1 as a Susceptibility Gene for Mitral Valve Prolapse. 
Circ Genom Precis Med. 2019 May;12(5):e002497. doi: 10.1161/CIRCGEN.119.002497. 

11.Amrani-Midoun A,Kiando SR, Treard C, Jeunemaitre X, Bouatia-Naji N. Genetic association study between T-786C NOS3 polymorphism and essential hypertension in an Algerian population of the Oran city. 
Diabetes Metab Syndr. 2019 Mar - Apr;13(2):1317-1320. doi: 10.1016/j.dsx.2019.02.024. Epub 2019 Feb 13. 

12.Adlam D, Olson TM, Combaret N, Kovacic JC, Iismaa SE, Al-Hussaini A, O'Byrne MM, Bouajila S, Georges A, Mishra K, Braund PS, d'Escamard V, Huang S, Margaritis M, Nelson CP, de Andrade M, Kadian-Dodov D, Welch CA, Mazurkiewicz S, Jeunemaitre X; DISCO Consortium., Wong CMY, Giannoulatou E, Sweeting M, Muller D, Wood A, McGrath-Cadell L, Fatkin D, Dunwoodie SL, Harvey R, Holloway C, Empana JP, Jouven X; CARDIoGRAMPlusC4D Study Group., Olin JW, Gulati R, Tweet MS, Hayes SN, Samani NJ, Graham RM, Motreff P, Bouatia-Naji N.Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection. 
J Am Coll Cardiol. 2019Jan 8;73(1):58-66. doi: 10.1016/j.jacc.2018.09.085.

13.Maas AHEM, Bouatia-Naji N, Persu A, Adlam D. Spontaneous coronary artery dissections and fibromuscular dysplasia: Current insights on pathophysiology, sex and gender.
Int J Cardiol. 2018 Nov 9. pii: S0167-5273(18)34907-6

14.Touzé E, Southerland AM, Boulanger M, Labeyrie PE, Azizi M, Bouatia-Naji N, Debette S, Gornik HL, Hussain SM, Jeunemaitre X, Joux J, Kirton A, Le Hello C, Majersik JJ, Mocco J, Persu A, Sharma A, Worrall BB, Olin JW, Plouin PF. Fibromuscular Dysplasia and Its Neurologic Manifestations: A Systematic Review. 
JAMA Neurol. 2018 Oct 1. doi: 10.1001/jamaneurol.2018.2848.

15.Jeunemaitre, X Albuisson,J Azizi, M Plouin, PF Bouatia-Naji, N  Arterial fibromuscular dysplasia: nosology, epidemiology and genetics.
Bulletin de l’Academie Nationale de Medecine, 2017. Vol. 201, Issue: 7-9, Pages: 1079-1089.

16.Amrani-Midoun A, Kiando SR, Treard C, Jeunemaitre X, Bouatia-Naji N. The relationship between MTHFR C677T gene polymorphism and essential hypertension in a sample of an Algerian population of Oran city. 
Int J Cardiol. 2016 Dec 15;225:408-411.

17.Castro-Vega LJ, Kiando SR, Burnichon N, Buffet A, Amar L, Simian C, Berdelou A, Galan P, Schlumberger M, Bouatia-Naji N, Favier J, Bressac-de Paillerets B, Gimenez-Roqueplo AP. The MITF, p.E318K Variant, as a Risk Factor for Pheochromocytoma and Paraganglioma. 
J Clin Endocrinol Metab. 2016 Dec;101(12):4764-4768

18.Kiando SR, Tucker NR, Castro-Vega LJ, Katz A, D'Escamard V, Tréard C, Fraher D, Albuisson J, Kadian-Dodov D, Ye Z, Austin E, Yang ML, Hunker K, Barlassina C, Cusi D, Galan P, Empana JP, Jouven X, Gimenez-Roqueplo AP, Bruneval P, Hyun Kim ES, Olin JW, Gornik HL, Azizi M, Plouin PF, Ellinor PT, Kullo IJ, Milan DJ, Ganesh SK, Boutouyrie P, Kovacic JC, Jeunemaitre X, Bouatia-Naji N. PHACTR1 Is a Genetic Susceptibility Locus for Fibromuscular Dysplasia Supporting Its Complex Genetic Pattern of Inheritance.£: Corresponding authors
PLoS Genet. 2016 Oct28;12(10):e1006367.