檢索結果 - Piyush Gampawar

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  1. 1
    Telomere length and brain aging: A systematic review and meta-analysis

    Telomere length and brain aging: A systematic review and meta-analysis 由 Piyush Gampawar, Reinhold Schmidt, Helena Schmidt

    出版 2022
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  2. 2
    Epigenetic age acceleration is related to cognitive decline in the elderly: Results of the Austrian Stroke Prevention Study

    Epigenetic age acceleration is related to cognitive decline in the elderly: Results of the Austrian Stroke Prevention Study 由 Piyush Gampawar, Sai Pavan Kumar Veeranki, Katja-Elisabeth Petrovic, Reinhold Schmidt, Helena Schmidt

    出版 2025
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  3. 3
    Comprehensive Genetic Analysis of a Hungarian Amyotrophic Lateral Sclerosis Cohort

    Comprehensive Genetic Analysis of a Hungarian Amyotrophic Lateral Sclerosis Cohort 由 Kornélia Tripolszki, Piyush Gampawar, Helena Schmidt, Zsófia Flóra Nagy, Dóra Nagy, Péter Klivényi, József I. Engelhardt, Márta Széll

    出版 2019
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  4. 4
    Targeted genetic analysis in a large cohort of familial and sporadic cases of aneurysm or dissection of the thoracic aorta

    Targeted genetic analysis in a large cohort of familial and sporadic cases of aneurysm or dissection of the thoracic aorta 由 Ruwan Weerakkody, David Ross, David Parry, Bulat A. Ziganshin, Jana Vandrovcová, Piyush Gampawar, Abdulshakur Abdullah, Jennifer Biggs, Julia Dumfarth, Yousef Ibrahim, Colin Bicknell, Mark Field, John A. Elefteriades, Nick Cheshire, Timothy J. Aitman

    出版 2018
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  5. 5
    Targeted next-generation sequencing makes new molecular diagnoses and expands genotype–phenotype relationship in Ehlers–Danlos syndrome

    Targeted next-generation sequencing makes new molecular diagnoses and expands genotype–phenotype relationship in Ehlers–Danlos syndrome 由 Ruwan Weerakkody, Jana Vandrovcová, Christina Kanonidou, Michael Mueller, Piyush Gampawar, Yousef Ibrahim, Penny J. Norsworthy, Jennifer Biggs, Abdulshakur Abdullah, David Ross, Holly A. Black, David Ferguson, Nicholas Cheshire, Hanadi Kazkaz, Rodney Grahame, Neeti Ghali, Anthony Vandersteen, F M Pope, Timothy J. Aitman

    出版 2016
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  6. 6
    Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities

    Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities 由 Nicola J. Armstrong, Karen A. Mather, Muralidharan Sargurupremraj, Maria J. Knol, Rainer Malik, Claudia L. Satizábal, Lisa R. Yanek, Wei Wen, Vilmundur Guðnason, Nicole Dueker, Lloyd T. Elliott, Edith Hofer, Joshua C. Bis, Neda Jahanshad, Shuo Li, Mark Logue, Michelle Luciano, Markus Scholz, Albert V. Smith, Stella Trompet, Dina Vojinović, Rui Xia, Fidel Alfaro‐Almagro, David Ames, Najaf Amin, Philippe Amouyel, Alexa S. Beiser, Henry Brodaty, Ian J. Deary, Christine Fennema‐Notestine, Piyush Gampawar, Rebecca Gottesman, Ludovica Griffanti, Clifford R. Jack, Mark Jenkinson, Jiyang Jiang, Brian G. Kral, John B. Kwok, Leonie Lampe, David C. Liewald, Pauline Maillard, Jonathan Marchini, Mark E. Bastin, Bernard Mazoyer, Lukas Pirpamer, José R. Romero, Gennady V. Roshchupkin, Peter R. Schofield, Matthias L. Schroeter, David J. Stott, Anbupalam Thalamuthu, Julian N. Trollor, Christophe Tzourio, Jeroen van der Grond, Meike W. Vernooij, A. Veronica Witte, Margaret J. Wright, Qiong Yang, Zoë Morris, Siggi Siggurdsson, Bruce M. Psaty, Arno Villringer, Helena Schmidt, Asta K. Håberg, Cornelia M. van Duijn, J. Wouter Jukema, Martin Dichgans, Ralph L. Sacco, Clinton B. Wright, William S. Kremen, Lewis C. Becker, Paul M. Thompson, Thomas H. Mosley, Joanna M. Wardlaw, M. Arfan Ikram, Hieab H.H. Adams, Sudha Seshadri, Perminder S. Sachdev, Stephen M. Smith, L. J. Launer, W.T. Longstreth, Charles DeCarli, Reinhold Schmidt, Myriam Fornage, Stéphanie Debette, Paul Nyquist

    出版 2020
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  7. 7
    Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease

    Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease 由 Marie‐Gabrielle Duperron, Maria J. Knol, Quentin Le Grand, Tavia E. Evans, Aniket Mishra, Ami Tsuchida, Gennady V. Roshchupkin, Takahiro Konuma, David‐Alexandre Trégouët, José R. Romero, Stefan Frenzel, Michelle Luciano, Edith Hofer, Mathieu Bourgey, Nicole Dueker, Pilar Delgado, Saima Hilal, Rick M. Tankard, Florian Dubost, Jean Shin, Yasaman Saba, Nicola J. Armstrong, Constance Bordes, Mark E. Bastin, Alexa Beiser, Henry Brodaty, Robin Bülow, Caty Carrera, Christopher Chen, Ching‐Yu Cheng, Ian J. Deary, Piyush Gampawar, Jayandra J. Himali, Jiyang Jiang, Takahisa Kawaguchi, Shuo Li, Mélissa Macalli, Pascale Marquis, Zoë Morris, Susana Muñoz Maniega, Susumu Miyamoto, Masakazu Okawa, Matthew Paradise, Pedram Parva, Tatjana Rundek, Muralidharan Sargurupremraj, Sabrina Schilling, Kazuya Setoh, Omar Soukarieh, Yasuharu Tabara, Alexander Teumer, Anbupalam Thalamuthu, Julian N. Trollor, Maria C. Valdés Hernández, Meike W. Vernooij, Uwe Völker, Katharina Wittfeld, Tien Yin Wong, Margaret J. Wright, Junyi Zhang, Wanting Zhao, Yi‐Cheng Zhu, Helena Schmidt, Perminder S. Sachdev, Wei Wen, Kazumichi Yoshida, Anne Joutel, Claudia L. Satizábal, Ralph L. Sacco, Guillaume Bourque, Quentin Le Grand, Mark Lathrop, Tomáš Paus, Israel Fernández‐Cadenas, Qiong Yang, Bernard Mazoyer, Philippe Boutinaud, Yukinori Okada, Hans J. Grabe, Karen A. Mather, Reinhold Schmidt, Marc Joliot, M. Arfan Ikram, Fumihiko Matsuda, Christophe Tzourio, Joanna M. Wardlaw, Sudha Seshadri, Hieab H.H. Adams, Stéphanie Debette

    出版 2023
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  8. 8
    Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies

    Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies 由 Mathias Gorski, Humaira Rasheed, Alexander Teumer, Laurent F. Thomas, Sarah E. Graham, Garðar Sveinbjörnsson, Thomas W. Winkler, Felix Günther, Klaus Stark, Jin Fang Chai, Bamidele O. Tayo, Matthias Wuttke, Yong Li, Adrienne Tin, Tarunveer S. Ahluwalia, Johan Ärnlöv, Bjørn Olav Åsvold, Stephan J. L. Bakker, Bernhard Banas, Nisha Bansal, Mary L. Biggs, Ginevra Biino, Michael Böhnke, Eric Boerwinkle, Erwin P. Böttinger, Hermann Brenner, Ben Brumpton, Robert J. Carroll, Layal Chaker, John Chalmers, Miao-Li Chee, Miao-Ling Chee, Ching‐Yu Cheng, Audrey Y. Chu, Marina Ciullo, Massimiliano Cocca, James P. Cook, Josef Coresh, Daniele Cusi, Martin H. de Borst, Frauke Degenhardt, Kai‐Uwe Eckardt, Karlhans Endlich, Michele K. Evans, Mary F. Feitosa, André Franke, Sandra Freitag‐Wolf, Christian Fuchsberger, Piyush Gampawar, Ron T. Gansevoort, Mohsen Ghanbari, Sahar Ghasemi, Vilmantas Giedraitis, Christian Gieger, Daníel F. Guðbjartsson, Stein Hallan, Pavel Hamet, Asahi Hishida, Kevin Ho, Edith Hofer, Bernd Holleczek, Hilma Hólm, Anselm Hoppmann, Katrin Horn, Nina Hutri‐Kähönen, Kristian Hveem, Shih‐Jen Hwang, M. Arfan Ikram, Navya Shilpa Josyula, Bettina Jung, Mika Kähönen, Irma Karabegović, Chiea Chuen Khor, Wolfgang Köenig, Holly Kramer, Bernhard K. Krämer, Brigitte Kühnel, Johanna Kuusisto, Markku Laakso, Leslie A. Lange, Terho Lehtimäki, Man Li, Wolfgang Lieb, Lars Lind, Cecilia M. Lindgren, Ruth J. F. Loos, Mary Ann Lukas, Leo‐Pekka Lyytikäinen, Anubha Mahajan, Pamela R. Matías‐García, Christa Meisinger, Thomas Meitinger, Olle Melander, Yuri Milaneschi, Pashupati P. Mishra, Nina Mononen, Andrew P. Morris, Josyf C. Mychaleckyj, Girish N. Nadkarni, Mariko Naito

    出版 2022
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  9. 9
    Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline

    Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline 由 Mathias Gorski, Bettina Jung, Yong Li, Pamela R. Matías‐García, Matthias Wuttke, Stefan Coassin, Chris H. L. Thio, Marcus E. Kleber, Thomas W. Winkler, Veronika Wanner, Jin Fang Chai, Audrey Y. Chu, Massimiliano Cocca, Mary F. Feitosa, Sahar Ghasemi, Anselm Hoppmann, Katrin Horn, Man Li, Teresa Nutile, Markus Scholz, Karsten B. Sieber, Alexander Teumer, Adrienne Tin, Judy Wang, Bamidele O. Tayo, Tarunveer S. Ahluwalia, Peter Almgren, Stephan J. L. Bakker, Bernhard Banas, Nisha Bansal, Mary L. Biggs, Eric Boerwinkle, Erwin P. Böttinger, Hermann Brenner, Robert J. Carroll, John Chalmers, Miao-Li Chee, Miao-Ling Chee, Ching‐Yu Cheng, Josef Coresh, Martin H. de Borst, Frauke Degenhardt, Kai‐Uwe Eckardt, Karlhans Endlich, André Franke, Sandra Freitag‐Wolf, Piyush Gampawar, Ron T. Gansevoort, Mohsen Ghanbari, Christian Gieger, Pavel Hamet, Kevin Ho, Edith Hofer, Bernd Holleczek, Valencia Hui Xian Foo, Nina Hutri‐Kähönen, Shih‐Jen Hwang, M. Arfan Ikram, Navya Shilpa Josyula, Mika Kähönen, Chiea Chuen Khor, Wolfgang Köenig, Holly Kramer, Bernhard K. Krämer, Brigitte Kühnel, Leslie A. Lange, Terho Lehtimäki, Wolfgang Lieb, Ruth J. F. Loos, Mary Ann Lukas, Leo‐Pekka Lyytikäinen, Christa Meisinger, Thomas Meitinger, Olle Melander, Yuri Milaneschi, Pashupati P. Mishra, Nina Mononen, Josyf C. Mychaleckyj, Girish N. Nadkarni, Matthias Nauck, Kjell Nikus, Boting Ning, Ilja M. Nolte, Michelle L. O’Donoghue, Marju Orho‐Melander, Sarah A. Pendergrass, Brenda W.J.H. Penninx, Michael Preuß, Bruce M. Psaty, Laura M. Raffield, Olli T. Raitakari, Rainer Rettig, Myriam Rheinberger, Kenneth Rice, Alexander R. Rosenkranz, Peter Rossing, Jerome I. Rotter, Charumathi Sabanayagam, Helena Schmidt, Reinhold Schmidt

    出版 2020
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