Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Sergiy Kyryachenko"'
Autor:
Adrien Georges, Min-Lee Yang, Takiy-Eddine Berrandou, Mark K. Bakker, Ozan Dikilitas, Soto Romuald Kiando, Lijiang Ma, Benjamin A. Satterfield, Sebanti Sengupta, Mengyao Yu, Jean-François Deleuze, Delia Dupré, Kristina L. Hunker, Sergiy Kyryachenko, Lu Liu, Ines Sayoud-Sadeg, Laurence Amar, Chad M. Brummett, Dawn M. Coleman, Valentina d’Escamard, Peter de Leeuw, Natalia Fendrikova-Mahlay, Daniella Kadian-Dodov, Jun Z. Li, Aurélien Lorthioir, Marco Pappaccogli, Aleksander Prejbisz, Witold Smigielski, James C. Stanley, Matthew Zawistowski, Xiang Zhou, Sebastian Zöllner, FEIRI investigators, International Stroke Genetics Consortium (ISGC) Intracranial Aneurysm Working Group, MEGASTROKE, Philippe Amouyel, Marc L. De Buyzere, Stéphanie Debette, Piotr Dobrowolski, Wojciech Drygas, Heather L. Gornik, Jeffrey W. Olin, Jerzy Piwonski, Ernst R. Rietzschel, Ynte M. Ruigrok, Miikka Vikkula, Ewa Warchol Celinska, Andrzej Januszewicz, Iftikhar J. Kullo, Michel Azizi, Xavier Jeunemaitre, Alexandre Persu, Jason C. Kovacic, Santhi K. Ganesh, Nabila Bouatia-Naji
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-16 (2021)
Fibromuscular dysplasia is a cardiovascular disease affecting mostly women with a mostly unknown genetic basis. Here the authors have performed a genome-wide association meta-analysis of Fibromuscular dysplasia to identify genetic loci, some of which
Externí odkaz:
https://doaj.org/article/1ca76cab0eb244289d31e35f5458c7b3
Autor:
Adrien Georges, Min-Lee Yang, Takiy-Eddine Berrandou, Mark K. Bakker, Ozan Dikilitas, Soto Romuald Kiando, Lijiang Ma, Benjamin A. Satterfield, Sebanti Sengupta, Mengyao Yu, Jean-François Deleuze, Delia Dupré, Kristina L. Hunker, Sergiy Kyryachenko, Lu Liu, Ines Sayoud-Sadeg, Laurence Amar, Chad M. Brummett, Dawn M. Coleman, Valentina d’Escamard, Peter de Leeuw, Natalia Fendrikova-Mahlay, Daniella Kadian-Dodov, Jun Z. Li, Aurélien Lorthioir, Marco Pappaccogli, Aleksander Prejbisz, Witold Smigielski, James C. Stanley, Matthew Zawistowski, Xiang Zhou, Sebastian Zöllner, FEIRI investigators, International Stroke Genetics Consortium (ISGC) Intracranial Aneurysm Working Group, MEGASTROKE, Philippe Amouyel, Marc L. De Buyzere, Stéphanie Debette, Piotr Dobrowolski, Wojciech Drygas, Heather L. Gornik, Jeffrey W. Olin, Jerzy Piwonski, Ernst R. Rietzschel, Ynte M. Ruigrok, Miikka Vikkula, Ewa Warchol Celinska, Andrzej Januszewicz, Iftikhar J. Kullo, Michel Azizi, ARCADIA Investigators, Xavier Jeunemaitre, Alexandre Persu, Jason C. Kovacic, Santhi K. Ganesh, Nabila Bouatia-Naji
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-1 (2022)
Externí odkaz:
https://doaj.org/article/3dfe61309b2044668fa15fe8a203dd77
Publikováno v:
PLoS ONE, Vol 7, Iss 5, p e37670 (2012)
Mouse incisors grow continuously throughout life with enamel deposition uniquely on the outer, or labial, side of the tooth. Asymmetric enamel deposition is due to the presence of enamel-secreting ameloblasts exclusively within the labial epithelium
Externí odkaz:
https://doaj.org/article/3a08d995cc8f46fab30045efb54c47f3
Autor:
Carolina Roselli, Mengyao Yu, Victor Nauffal, Adrien Georges, Qiong Yang, Katie Love, Lu Chen Weng, Francesca N Delling, Svetlana R Maurya, Maren Schrölkamp, Jacob Tfelt-Hansen, Albert Hagège, Xavier Jeunemaitre, Stéphanie Debette, Philippe Amouyel, Wyliena Guan, Jochen D Muehlschlegel, Simon C Body, Svati Shah, Zainab Samad, Sergiy Kyryachenko, Carol Haynes, Michiel Rienstra, Thierry Le Tourneau, Vincent Probst, Ronan Roussel, Inez J Wijdh-Den Hamer, Joylene E Siland, Kirk U Knowlton, Jean Jacques Schott, Robert A Levine, Emelia J Benjamin, Ramachandran S Vasan, Benjamin D Horne, Joseph B Muhlestein, Giovanni Benfari, Maurice Enriquez-Sarano, Andrea Natale, Sanghamitra Mohanty, Chintan Trivedi, Moore B Shoemaker, Zachary T Yoneda, Quinn S Wells, Michael T Baker, Eric Farber-Eger, Hector I Michelena, Alicia Lundby, Russell A Norris, Susan A Slaugenhaupt, Christian Dina, Steven A Lubitz, Nabila Bouatia-Naji, Patrick T Ellinor, David J Milan
Publikováno v:
Eur Heart J
European Heart Journal, 43(17), 1668-1680. Oxford University Press
European Heart Journal, 43(17), 1668-1680. Oxford University Press
AIMS: Mitral valve prolapse (MVP) is a common valvular heart disease with a prevalence of >2% in the general adult population. Despite this high incidence, there is a limited understanding of the molecular mechanism of this disease, and no medical th
Autor:
Takiy Berrandou, Tony Rubio, Judith Gronwald, Niels Voigt, Adrien Georges, Hassina Baraki, Sergiy Kyryachenko, Mengyao Yu, Ingo Kutschka, Russel Norris, Nabila Bouatia-Naji
Publikováno v:
Circulation. 142
Introduction: Mitral valve prolapse (MVP) is a common valve disease that leads to mitral insufficiency, heart failure, and sudden death. The identification of genetic risk loci provided insight into its genetic architecture, although the causal varia
Autor:
Ozan Dikilitas, Marco Pappaccogli, Peter W. de Leeuw, Witold Smigielski, Valentina d'Escamard, Lijiang Ma, Ernst Rietzschel, Kristina L. Hunker, Lu Liu, Michel Azizi, Matthew Zawistowski, Jeffrey W. Olin, Ynte M. Ruigrok, Min-Lee Yang, Stéphanie Debette, Laurence Amar, Xiang Zhou, Sergiy Kyryachenko, Jun Li, Benjamin A. Satterfield, James C. Stanley, Feiri investigators, Miikka Vikkula, Ewa Warchol Celinska, Mengyao Yu, Dawn M. Coleman, Marc De Buyzere, Nabila Bouatia-Naji, Iftikhar J. Kullo, Megastroke, Aleksander Prejbisz, Andrzej Januszewicz, Piotr Dobrowolski, Wojciech Drygas, Takiy-Eddine Berrandou, Jerzy Piwonski, Sebanti Sengupta, Jason C. Kovacic, Mark K Bakker, Santhi K. Ganesh, Xavier Jeunemaitre, Chad M. Brummett, Jean-François Deleuze, Heather L. Gornik, Sebastian Zoellner, Soto Romuald Kiando, Alexandre Persu, Adrien Georges, Aurélien Lorthioir, Natalia Fendrikova-Mahlay, Daniella Kadian-Dodov, Délia Dupré
Fibromuscular dysplasia (FMD) is an arteriopathy that presents clinically by hypertension and stroke, mostly in early middle-aged women. We report results from the first genome-wide association meta-analysis of FMD including 1962 FMD cases and 7100 c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b59d9eadd9aefc3a3e247d1520eb5b4
https://doi.org/10.1101/2020.09.16.20195701
https://doi.org/10.1101/2020.09.16.20195701
Autor:
Heather L. Gornik, Y. Mengyao, Ozan Dikilitas, Lu Liu, Sergiy Kyryachenko, Adrien Georges, Xavier Jeunemaitre, Takiy-Eddine Berrandou, Stéphanie Debette, Nabila Bouatia-Naji, Aurélien Lorthioir, Jason C. Kovacic, Andrzej Januszewicz, Alexandre Persu, Santhi K. Ganesh, Iftikhar J. Kullo, Min-Lee Yang, M. Azizi, Lijiang Ma, Laurence Amar
Publikováno v:
Archives of Cardiovascular Diseases Supplements. 13:186-187
Introduction Fibromuscular dysplasia (FMD) is a non-atherosclerotic arteriopathy of unknown etiology, affecting mostly middle-aged women. It is characterized by stenotic lesions of the vascular wall in middle-size arteries, sometimes associated with
Autor:
Russell A. Norris, Albert A. Hagège, Nabila Bouatia-Naji, Jean-Jacques Schott, Sergiy Kyryachenko, Xavier Jeunemaitre, Philippe Amouyel, Stéphanie Debette, Thierry Le Tourneau, Mengyao Yu, Christian Dina
Publikováno v:
Circulation-Genomic and Precision Medicine
Circulation-Genomic and Precision Medicine, 2021, 14 (5), pp.CIRCGEN120003148. ⟨10.1161/CIRCGEN.120.003148⟩
Circ Genom Precis Med
Circulation-Genomic and Precision Medicine, 2021, 14 (5), pp.CIRCGEN120003148. ⟨10.1161/CIRCGEN.120.003148⟩
Circ Genom Precis Med
ObjectiveMitral valve prolapse (MVP) is a common cardiac valve disease, which affects 1 in 40 in the general population. Previous GWAS have identified six risk loci for MVP. But these loci explained only partially the genetic risk for MVP. We aim to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9832771b54a64d550694ec1d34f809f
Autor:
Adrien Georges, Russell A. Norris, Takiy Barrandou, Patrick Bruneval, Ingo Kutschka, Mengyao Yu, Niels Voigt, Judith Gronwald, Hassina Baraki, Sergiy Kyryachenko, Tony Rubio, Nabila Bouatia-Naji
RationaleMitral valve prolapse (MVP) is a common valve disease that leads to mitral insufficiency, heart failure and sudden death. The identification of risk loci provided insight into its genetic architecture, although the causal variants and target
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6bdec1e7a7ccf63c2b19f7aa1e49f33d
https://doi.org/10.1101/2020.06.04.20122010
https://doi.org/10.1101/2020.06.04.20122010
Autor:
Adrien Georges, Susan A. Slaugenhaupt, Patrick T. Ellinor, Jean-Jacques Schott, Jorge Solis, David J. Milan, Nabila Bouatia-Naji, Albert Hagège, Katelyn Toomer, Robert A. Levine, Nathan R. Tucker, Russell A. Norris, Xavier Jeunemaitre, Leticia Fernández-Friera, Francesca N. Delling, Sergiy Kyryachenko, Christian Dina, Mengyao Yu
Publikováno v:
Circ Genom Precis Med
Background Mitral valve prolapse (MVP) is a common heart valve disease, the most frequent indication for valve repair or replacement. MVP is characterized by excess extracellular matrix secretion and cellular disorganization, which leads to bulky val