Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases
(2022)
EUROPEAN JOURNAL OF HUMAN GENETICS.
In European Journal of Human Genetics
30(Supplement 1).
p.46-47
- Author
- Adrien Georges, Min-Lee Yang, Takiy-Eddine Berrandou, Mark Bakker, Ozan Dikilitas, Soto Romuald Kiando, Mengyao Yu, Lu Liu, Sergiy Kyryachenko, Ines Sayoud, Delia Dupre, Aurelien Lorthioir, Laurence Amar, Sebanti Sengupta, Kristina L. Hunker, Benjamin A. Satterfield, Lijiang Ma, Valentina d'Escamard, Daniella Kadian-Dodov, Jean-Francois Deleuze, Chad Brummett, Dawn M. Coleman, Peter de Leeuw, Marco Pappaccogli, Witold Smigielski, Aleksander Prejbisz, Philippe Amouyel, Marc De Buyzere (UGent) , Stephanie Debette, Piotr Dobrowolski, Wojciech Drygas, Heather L. Gornik, Jeffrey W. Olin, Jerzy Piwonski, Ernst Rietzschel (UGent) , Ynte Ruigrok, Miikka Vikkula, Ewa Warchol Celinska, Andrzej Januszewicz, Iftikhar J. Kullo, Michel Azizi, Xavier Jeunemaitre, Alexandre Persu, Jason C. Kovacic, Santhi K. Ganesh and Nabila Bouatia-Naji
- Organization
Citation
Please use this url to cite or link to this publication: http://hdl.handle.net/1854/LU-01GJYY19C6NCRP5QKCZKPMX89Y
- MLA
- Georges, Adrien, et al. “Genetic Investigation of Fibromuscular Dysplasia Identifies Risk Loci and Shared Genetics with Common Cardiovascular Diseases.” EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 30, no. Supplement 1, 2022, pp. 46–47.
- APA
- Georges, A., Yang, M.-L., Berrandou, T.-E., Bakker, M., Dikilitas, O., Kiando, S. R., … Bouatia-Naji, N. (2022). Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases. EUROPEAN JOURNAL OF HUMAN GENETICS, 30(Supplement 1), 46–47.
- Chicago author-date
- Georges, Adrien, Min-Lee Yang, Takiy-Eddine Berrandou, Mark Bakker, Ozan Dikilitas, Soto Romuald Kiando, Mengyao Yu, et al. 2022. “Genetic Investigation of Fibromuscular Dysplasia Identifies Risk Loci and Shared Genetics with Common Cardiovascular Diseases.” In EUROPEAN JOURNAL OF HUMAN GENETICS, 30:46–47.
- Chicago author-date (all authors)
- Georges, Adrien, Min-Lee Yang, Takiy-Eddine Berrandou, Mark Bakker, Ozan Dikilitas, Soto Romuald Kiando, Mengyao Yu, Lu Liu, Sergiy Kyryachenko, Ines Sayoud, Delia Dupre, Aurelien Lorthioir, Laurence Amar, Sebanti Sengupta, Kristina L. Hunker, Benjamin A. Satterfield, Lijiang Ma, Valentina d’Escamard, Daniella Kadian-Dodov, Jean-Francois Deleuze, Chad Brummett, Dawn M. Coleman, Peter de Leeuw, Marco Pappaccogli, Witold Smigielski, Aleksander Prejbisz, Philippe Amouyel, Marc De Buyzere, Stephanie Debette, Piotr Dobrowolski, Wojciech Drygas, Heather L. Gornik, Jeffrey W. Olin, Jerzy Piwonski, Ernst Rietzschel, Ynte Ruigrok, Miikka Vikkula, Ewa Warchol Celinska, Andrzej Januszewicz, Iftikhar J. Kullo, Michel Azizi, Xavier Jeunemaitre, Alexandre Persu, Jason C. Kovacic, Santhi K. Ganesh, and Nabila Bouatia-Naji. 2022. “Genetic Investigation of Fibromuscular Dysplasia Identifies Risk Loci and Shared Genetics with Common Cardiovascular Diseases.” In EUROPEAN JOURNAL OF HUMAN GENETICS, 30:46–47.
- Vancouver
- 1.Georges A, Yang M-L, Berrandou T-E, Bakker M, Dikilitas O, Kiando SR, et al. Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases. In: EUROPEAN JOURNAL OF HUMAN GENETICS. 2022. p. 46–7.
- IEEE
- [1]A. Georges et al., “Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases,” in EUROPEAN JOURNAL OF HUMAN GENETICS, Vienna, Austria, 2022, vol. 30, no. Supplement 1, pp. 46–47.
@inproceedings{01GJYY19C6NCRP5QKCZKPMX89Y,
articleno = {{C10.2}},
author = {{Georges, Adrien and Yang, Min-Lee and Berrandou, Takiy-Eddine and Bakker, Mark and Dikilitas, Ozan and Kiando, Soto Romuald and Yu, Mengyao and Liu, Lu and Kyryachenko, Sergiy and Sayoud, Ines and Dupre, Delia and Lorthioir, Aurelien and Amar, Laurence and Sengupta, Sebanti and Hunker, Kristina L. and Satterfield, Benjamin A. and Ma, Lijiang and d'Escamard, Valentina and Kadian-Dodov, Daniella and Deleuze, Jean-Francois and Brummett, Chad and Coleman, Dawn M. and de Leeuw, Peter and Pappaccogli, Marco and Smigielski, Witold and Prejbisz, Aleksander and Amouyel, Philippe and De Buyzere, Marc and Debette, Stephanie and Dobrowolski, Piotr and Drygas, Wojciech and Gornik, Heather L. and Olin, Jeffrey W. and Piwonski, Jerzy and Rietzschel, Ernst and Ruigrok, Ynte and Vikkula, Miikka and Celinska, Ewa Warchol and Januszewicz, Andrzej and Kullo, Iftikhar J. and Azizi, Michel and Jeunemaitre, Xavier and Persu, Alexandre and Kovacic, Jason C. and Ganesh, Santhi K. and Bouatia-Naji, Nabila}},
booktitle = {{EUROPEAN JOURNAL OF HUMAN GENETICS}},
issn = {{1018-4813}},
language = {{eng}},
location = {{Vienna, Austria}},
number = {{Supplement 1}},
pages = {{C10.2:46--C10.2:47}},
title = {{Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases}},
volume = {{30}},
year = {{2022}},
}