Items where Author is "Yang, Min-Lee"

Adlam, David and Berrandou, Takiy-Eddine and Georges, Adrien and Nelson, Christopher P. and Giannoulatou, Eleni and Henry, Joséphine and Ma, Lijiang and Blencowe, Montgomery and Turley, Tamiel N. and Yang, Min-Lee and Chopade, Sandesh and Finan, Chris and Braund, Peter S. and Sadeg-Sayoud, Ines and Iismaa, Siiri E. and Kosel, Matthew L. and Zhou, Xiang and Hamby, Stephen E. and Cheng, Jenny and Liu, Lu and Tarr, Ingrid and Muller, David W. M. and d’Escamard, Valentina and King, Annette and Brunham, Liam R. and Baranowska-Clarke, Ania A. and Debette, Stéphanie and Amouyel, Philippe and Olin, Jeffrey W. and Patil, Snehal and Hesselson, Stephanie E. and Junday, Keerat and Kanoni, Stavroula and Aragam, Krishna G. and Butterworth, Adam S. and Bakker, Mark K. and Ruigrok, Ynte M. and Tweet, Marysia S. and Gulati, Rajiv and Combaret, Nicolas and Kadian-Dodov, Daniella and Kalman, Jonathan M. and Fatkin, Diane and Hingorani, Aroon D. and Saw, Jacqueline and Webb, Tom R. and Hayes, Sharonne N. and Yang, Xia and Ganesh, Santhi K. and Olson, Timothy M. and Kovacic, Jason C. and Graham, Robert M. and Samani, Nilesh J. and Bouatia-Naji, Nabila (2023) Genome-wide association meta-analysis of spontaneous coronary artery dissection identifies risk variants and genes related to artery integrity and tissue-mediated coagulation. Nature Genetics, 55 (6). pp.964-972. ISSN 1061-4036

Georges, Adrien and Yang, Min-Lee and Berrandou, Takiy-Eddine and Bakker, Mark K. and Dikilitas, Ozan and Kiando, Soto Romuald and Ma, Lijiang and Satterfield, Benjamin A. and Sengupta, Sebanti and Yu, Mengyao and Deleuze, Jean-François and Dupré, Delia and Hunker, Kristina L. and Kyryachenko, Sergiy and Liu, Lu and Sayoud-Sadeg, Ines and Amar, Laurence and Brummett, Chad M. and Coleman, Dawn M. and d’Escamard, Valentina and de Leeuw, Peter and Fendrikova-Mahlay, Natalia and Kadian-Dodov, Daniella and Li, Jun Z. and Lorthioir, Aurélien and Pappaccogli, Marco and Prejbisz, Aleksander and Smigielski, Witold and Stanley, James C. and Zawistowski, Matthew and Zhou, Xiang and Zöllner, Sebastian and de Leeuw, Peter and Amouyel, Philippe and De Buyzere, Marc L. and Debette, Stéphanie and Dobrowolski, Piotr and Drygas, Wojciech and Gornik, Heather L. and Olin, Jeffrey W. and Piwonski, Jerzy and Rietzschel, Ernst R. and Ruigrok, Ynte M. and Vikkula, Miikka and Warchol Celinska, Ewa 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 (2021) Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases. Nature Communications, 12 (1). ISSN 2041-1723

Georges, Adrien and Albuisson, Juliette and Berrandou, Takiy and Dupré, Délia and Lorthioir, Aurélien and D’Escamard, Valentina and Di Narzo, Antonio F and Kadian-Dodov, Daniella and Olin, Jeffrey W and Warchol-Celinska, Ewa and Prejbisz, Aleksander and Januszewicz, Andrzej and Bruneval, Patrick and Baranowska, Anna A and Webb, Tom R and Hamby, Stephen E and Samani, Nilesh J and Adlam, David and Fendrikova-Mahlay, Natalia and Hazen, Stanley and Wang, Yu and Yang, Min-Lee and Hunker, Kristina and Combaret, Nicolas and Motreff, Pascal and Chédid, Antoine and Fiquet, Béatrice and Plouin, Pierre-François and Mousseaux, Elie and Azarine, Arshid and Amar, Laurence and Azizi, Michel and Gornik, Heather L and Ganesh, Santhi K and Kovacic, Jason C and Jeunemaitre, Xavier and Bouatia-Naji, Nabila (2021) Rare loss-of-function mutations of PTGIR are enriched in fibromuscular dysplasia. Cardiovascular Research, 117 (4). pp.1154-1165. ISSN 0008-6363