Items where Author is "Ganesh, Santhi K."

Article

Roselli, Carolina and Surakka, Ida and Olesen, Morten S. and Sveinbjornsson, Gardar and Marston, Nicholas A. and Choi, Seung Hoan and Holm, Hilma and Chaffin, Mark and Gudbjartsson, Daniel and Hill, Matthew C. and Aegisdottir, Hildur and Albert, Christine M. and Alonso, Alvaro and Anderson, Christopher D. and Arking, Dan E. and Arnar, David O. and Barnard, John and Benjamin, Emelia J. and Braunwald, Eugene and Brumpton, Ben and Campbell, Archie and Chami, Nathalie and Chasman, Daniel I. and Cho, Kelly and Choi, Eue-Keun and Christophersen, Ingrid E. and Chung, Mina K. and Conen, David and Crijns, Harry J. and Cutler, Michael J. and Czuba, Tomasz and Damrauer, Scott M. and Dichgans, Martin and Dörr, Marcus and Dudink, Elton and Duong, ThuyVy and Erikstrup, Christian and Esko, Tõnu and Fatkin, Diane and Faul, Jessica D. and Ferreira, Manuel and Freitag, Daniel F. and Ganesh, Santhi K. and Gaziano, J. Michael and Geelhoed, Bastiaan and Ghouse, Jonas and Gieger, Christian and Giulianini, Franco and Graham, Sarah E. and Gudnason, Vilmundur and Guo, Xiuqing and Haggerty, Christopher and Hayward, Caroline and Heckbert, Susan R. and Hveem, Kristian and Ito, Kaoru and Johnson, Renee and Jukema, J. Wouter and Jurgens, Sean J. and Kääb, Stefan and Kane, John P. and Kany, Shinwan and Kardia, Sharon L. R. and Kavousi, Maryam and Khurshid, Shaan and Kamanu, Frederick K. and Kirchhof, Paulus and Kleber, Marcus E. and Knight, Stacey and Komuro, Issei and Krieger, Jose E. and Launer, Lenore J. and Li, Dadong and Lin, Honghuang and Lin, Henry J. and Loos, Ruth J. F. and Lotta, Luca and Lubitz, Steven A. and Lunetta, Kathryn L. and Macfarlane, Peter W. and Magnusson, Patrik K. E. and Malik, Rainer and Mantineo, Helene and Marcus, Gregory M. and März, Winfried and McManus, David D. and Melander, Olle and Melloni, Giorgio E. M. and Meyre, Pascal B. and Miyazawa, Kazuo and Mohanty, Sanghamitra and Monfort, Laia M. and Müller-Nurasyid, Martina and Nafissi, Navid A. and Natale, Andrea and Nazarian, Saman and Ostrowski, Sisse R. and Pak, Hui-Nam and Pang, Shichao and Pedersen, Ole B. and Pedersen, Nancy L. and Pereira, Alexandre C. and Pirruccello, James P. and Preuss, Michael and Psaty, Bruce M. and Pullinger, Clive R. and Rader, Daniel J. and Rämö, Joel T. and Ridker, Paul M. and Rienstra, Michiel and Risch, Lorenz and Roden, Dan M. and Rotter, Jerome I. and Sabatine, Marc S. and Schunkert, Heribert and Shah, Svati H. and Shim, Jaemin and Shoemaker, M. Benjamin and Simonson, Bridget and Sinner, Moritz F. and Smit, Roelof A. J. and Smith, Jennifer A. and Smith, Nicholas L. and Smith, J. Gustav and Soliman, Elsayed Z. and Sørensen, Erik and Sotoodehnia, Nona and Strbian, Daniel and Stricker, Bruno H. and Teder-Laving, Maris and Sun, Yan V. and Thériault, Sébastien and Thorolfsdottir, Rosa B. and Thorsteinsdottir, Unnur and Tveit, Arnljot and van der Harst, Pim and van Meurs, Joyce and Wang, Biqi and Weiss, Stefan and Wells, Quinn S. and Weng, Lu-Chen and Wilson, Peter W. and Xiao, Ling and Yang, Pil-Sung and Yao, Jie and Yoneda, Zachary T. and Zeller, Tanja and Zeng, Lingyao and Zhao, Wei and Zhou, Xiang and Zöllner, Sebastian and Ruff, Christian T. and Bundgaard, Henning and Willer, Cristen and Stefansson, Kari and Ellinor, Patrick T. (2025) Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases. Nature Genetics, 57 (3). pp.539-547. ISSN 1061-4036

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