Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Soto Romuald Kiando"'
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
Autor:
Maëlle Perrocheau, Soto Romuald Kiando, Déwi Vernerey, Christian Dina, Pilar Galan, Albert Hagege, Xavier Jeunemaitre, Nabila Bouatia-Naji
Publikováno v:
Journal of Cardiovascular Development and Disease, Vol 2, Iss 3, Pp 176-189 (2015)
Non-syndromic mitral valve prolapse (MVP) is a common degenerative valvulopathy, predisposing to arrhythmia and sudden death. The etiology of MVP is suspected to be under genetic control, as supported by familial cases and its manifestation in geneti
Externí odkaz:
https://doaj.org/article/879c4807144b406aaa9f772e8fd63b5c
Autor:
Soto Romuald Kiando, Nathan R Tucker, Luis-Jaime Castro-Vega, Alexander Katz, Valentina D'Escamard, Cyrielle Tréard, Daniel Fraher, Juliette Albuisson, Daniella Kadian-Dodov, Zi Ye, Erin Austin, Min-Lee Yang, Kristina Hunker, Cristina Barlassina, Daniele Cusi, Pilar Galan, Jean-Philippe Empana, Xavier Jouven, Anne-Paule Gimenez-Roqueplo, Patrick Bruneval, Esther Soo Hyun Kim, Jeffrey W Olin, Heather L Gornik, Michel Azizi, Pierre-François Plouin, Patrick T Ellinor, Iftikhar J Kullo, David J Milan, Santhi K Ganesh, Pierre Boutouyrie, Jason C Kovacic, Xavier Jeunemaitre, Nabila Bouatia-Naji
Publikováno v:
PLoS Genetics, Vol 12, Iss 10, p e1006367 (2016)
Fibromuscular dysplasia (FMD) is a nonatherosclerotic vascular disease leading to stenosis, dissection and aneurysm affecting mainly the renal and cerebrovascular arteries. FMD is often an underdiagnosed cause of hypertension and stroke, has higher p
Externí odkaz:
https://doaj.org/article/81b279ae7ed0458d82b4b6846aee7c7e
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:
Soto Romuald Kiando, Xavier Jeunemaitre, Nabila Bouatia-Naji, Cyrielle Treard, Asma Amrani-Midoun
Publikováno v:
International Journal of Cardiology. 225:408-411
Background Many studies have investigated the role of 5,10-methylenetetrahydrofolate reductase ( MTHFR ) C677T gene polymorphism in essential hypertension (EH), but with conflicting results. Aim To determine the eventual association between 5,10-meth
Autor:
Soto Romuald Kiando, Cyrielle Treard, Asma Amrani-Midoun, Nabila Bouatia-Naji, Xavier Jeunemaitre
Publikováno v:
Diabetesmetabolic syndrome. 13(2)
Background Essential hypertension is an important risk factor for the development of cardiovascular disease. Important candidate genes such as NOS3 gene have been widely studied and reported to be associated with essential hypertension (HTN) in human
Autor:
Jean-Philippe Haymann, Delphine Vezzosi, Elisabeth Requeda, Agnès Linglart, Guy Lefort, Jean-Claude Souberbielle, Emmanuelle Dubosclard, Bernadette Lucas-Pouliquen, Jean-Marc Kuhn, Françoise Broux, Pascal Houillier, Lamisse Mansour-Hendili, Michel Polak, Sophie Ouzounian, Stéphanie Baron, Xavier Jeunemaitre, Christophe Simian, Sonia Beltran, Caroline Travers, Gérard Maruani, Xavier Debussche, Caroline Silve, Jean-Philippe Bertocchio, Catherine Cormier, Cyrielle Treard, Odile Camard, Celine Eid, Dominique Robier, Marie-Alice Macher, Sylvie Cloarec, Ivan Tack, Véronique Baudouin, Rosa Vargas-Poussou, Soto Romuald Kiando
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 101:2185-2195
Familial hypocalciuric hypercalcemia (FHH) is a genetically heterogeneous condition resembling primary hyperparathyroidism (PHPT) but not curable by surgery; FHH types 1, 2, and 3 are due to loss-of-function mutations of the CASR, GNA11, or AP2S1 gen
Autor:
Nelly Burnichon, Laurence Amar, Pilar Galan, Nabila Bouatia-Naji, Christophe Simian, Luis Jaime Castro-Vega, Soto Romuald Kiando, Martin Schlumberger, Amandine Berdelou, Brigitte Bressac-de Paillerets, Judith Favier, Alexandre Buffet, Anne-Paule Gimenez-Roqueplo
Publikováno v:
Journal of Clinical Endocrinology and Metabolism
Journal of Clinical Endocrinology and Metabolism, Endocrine Society, 2016, 101 (12), pp.4764-4768. ⟨10.1210/jc.2016-2103⟩
Journal of Clinical Endocrinology and Metabolism, Endocrine Society, 2016, 101 (12), pp.4764-4768. 〈10.1210/jc.2016-2103〉
Journal of Clinical Endocrinology and Metabolism, Endocrine Society, 2016, 101 (12), pp.4764-4768. ⟨10.1210/jc.2016-2103⟩
Journal of Clinical Endocrinology and Metabolism, Endocrine Society, 2016, 101 (12), pp.4764-4768. 〈10.1210/jc.2016-2103〉
Context: The microphthalmia-associated transcription factor (MITF) regulates the survival, proliferation, and differentiation of neural crest-derived lineages. Recent studies reported an increased risk of melanomain individuals carrying the rare vari
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e6563455a78db58b62bfbd4cb9cd7a0
https://hal.archives-ouvertes.fr/hal-01607511
https://hal.archives-ouvertes.fr/hal-01607511
Autor:
Nabila Bouatia-Naji, Cyrielle Treard, David J. Milan, Esther Soo Hyun Kim, Patrick T. Ellinor, Iftikhar J. Kullo, Xavier Jeunemaitre, Min-Lee Yang, Daniel Fraher, Nathan R. Tucker, Pilar Galan, Pierre-François Plouin, Jason C. Kovacic, Heather L. Gornik, Erin Austin, Patrick Bruneval, Jeffrey W. Olin, Santhi K. Ganesh, Daniella Kadian-Dodov, Daniele Cusi, Alexander Katz, Xavier Jouven, Michel Azizi, Kristina L. Hunker, Valentina d'Escamard, Pierre Boutouyrie, Zi Ye, Juliette Albuisson, Jean Philippe Empana, Luis Jaime Castro-Vega, Cristina Barlassina, Soto Romuald Kiando, Anne Paule Gimenez-Roqueplo
Publikováno v:
Plos Genetics 10 (12), . (2016)
PLOS genetics (Online) 12 (2016). doi:10.1371/journal.pgen.1006367
info:cnr-pdr/source/autori:Kiando, Soto Romuald; Tucker, Nathan R.; Castro-Vega, Luis-Jaime; Katz, Alexander; D'Escamard, Valentina; Treard, Cyrielle; Fraher, Daniel; Albuisson, Juliette; Kadian-Dodov, Daniella; Ye, Zi; Austin, Erin; Yang, Min-Lee; Hunker, Kristina; Barlassina, Cristina; Cusi, Daniele; Galan, Pilar; Empana, Jean-Philippe; Jouven, Xavier; Gimenez-Roqueplo, Anne-Paule; Bruneval, Patrick; Kim, Esther Soo Hyun; Olin, Jeffrey W.; Gornik, Heather L.; Azizi, Michel; Plouin, Pierre-Francois; Ellinor, Patrick T.; Kullo, Iftikhar J.; Milan, David J.; Ganesh, Santhi K.; Boutouyrie, Pierre; Kovacic, Jason C.; Jeunemaitre, Xavier; Bouatia-Naji, Nabila/titolo:PHACTR1 Is a Genetic Susceptibility Locus for Fibromuscular Dysplasia Supporting Its Complex Genetic Pattern of Inheritance/doi:10.1371%2Fjournal.pgen.1006367/rivista:PLOS genetics (Online)/anno:2016/pagina_da:/pagina_a:/intervallo_pagine:/volume:12
PLoS Genetics
PLoS Genetics, Public Library of Science, 2016, 12 (10), pp.e1006367. ⟨10.1371/journal.pgen.1006367⟩
PLoS Genetics, Vol 12, Iss 10, p e1006367 (2016)
PLoS Genetics, 2016, 12 (10), pp.e1006367. ⟨10.1371/journal.pgen.1006367⟩
PLOS genetics (Online) 12 (2016). doi:10.1371/journal.pgen.1006367
info:cnr-pdr/source/autori:Kiando, Soto Romuald; Tucker, Nathan R.; Castro-Vega, Luis-Jaime; Katz, Alexander; D'Escamard, Valentina; Treard, Cyrielle; Fraher, Daniel; Albuisson, Juliette; Kadian-Dodov, Daniella; Ye, Zi; Austin, Erin; Yang, Min-Lee; Hunker, Kristina; Barlassina, Cristina; Cusi, Daniele; Galan, Pilar; Empana, Jean-Philippe; Jouven, Xavier; Gimenez-Roqueplo, Anne-Paule; Bruneval, Patrick; Kim, Esther Soo Hyun; Olin, Jeffrey W.; Gornik, Heather L.; Azizi, Michel; Plouin, Pierre-Francois; Ellinor, Patrick T.; Kullo, Iftikhar J.; Milan, David J.; Ganesh, Santhi K.; Boutouyrie, Pierre; Kovacic, Jason C.; Jeunemaitre, Xavier; Bouatia-Naji, Nabila/titolo:PHACTR1 Is a Genetic Susceptibility Locus for Fibromuscular Dysplasia Supporting Its Complex Genetic Pattern of Inheritance/doi:10.1371%2Fjournal.pgen.1006367/rivista:PLOS genetics (Online)/anno:2016/pagina_da:/pagina_a:/intervallo_pagine:/volume:12
PLoS Genetics
PLoS Genetics, Public Library of Science, 2016, 12 (10), pp.e1006367. ⟨10.1371/journal.pgen.1006367⟩
PLoS Genetics, Vol 12, Iss 10, p e1006367 (2016)
PLoS Genetics, 2016, 12 (10), pp.e1006367. ⟨10.1371/journal.pgen.1006367⟩
Fibromuscular dysplasia (FMD) is a nonatherosclerotic vascular disease leading to stenosis, dissection and aneurysm affecting mainly the renal and cerebrovascular arteries. FMD is often an underdiagnosed cause of hypertension and stroke, has higher p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6654df71ec772fa18b827fdf5b91564
http://prodinra.inra.fr/record/385276
http://prodinra.inra.fr/record/385276