Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Dina, Vojinovic"'
Autor:
Ashley van der Spek, Sophie C. Warner, Linda Broer, Christopher P. Nelson, Dina Vojinovic, Shahzad Ahmad, Pascal P. Arp, Rutger W. W. Brouwer, Matthew Denniff, Mirjam C. G. N. van den Hout, Jeroen G. J. van Rooij, Robert Kraaij, Wilfred F. J. van IJcken, Nilesh J. Samani, M. Arfan Ikram, André G. Uitterlinden, Veryan Codd, Najaf Amin, Cornelia M. van Duijn
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
Telomeres are important for maintaining genomic stability. Telomere length has been associated with aging, disease, and mortality and is highly heritable (∼82%). In this study, we aimed to identify rare genetic variants associated with telomere len
Externí odkaz:
https://doaj.org/article/c77eae33646043f3bedc794e8a9da48a
Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidate
Autor:
Aniket Mishra, Cécile Duplaà, Dina Vojinovic, Hideaki Suzuki, Muralidharan Sargurupremraj, Nuno R Zilhão, Shuo Li, Traci M Bartz, Xueqiu Jian, Wei Zhao, Edith Hofer, Katharina Wittfeld, Sarah E Harris, Sandra van der Auwera-Palitschka, Michelle Luciano, Joshua C Bis, Hieab H H Adams, Claudia L Satizabal, Rebecca F Gottesman, Piyush G Gampawar, Robin Bülow, Stefan Weiss, Miao Yu, Mark E Bastin, Oscar L Lopez, Meike W Vernooij, Alexa S Beiser, Uwe Völker, Tim Kacprowski, Aicha Soumare, Jennifer A Smith, David S Knopman, Zoe Morris, Yicheng Zhu, Jerome I Rotter, Carole Dufouil, Maria Valdés Hernández, Susana Muñoz Maniega, Mark Lathrop, Erik Boerwinkle, Reinhold Schmidt, Masafumi Ihara, Bernard Mazoyer, Qiong Yang, Anne Joutel, Elizabeth Tournier-Lasserve, Lenore J Launer, Ian J Deary, Thomas H Mosley, Philippe Amouyel, Charles S DeCarli, Bruce M Psaty, Christophe Tzourio, Sharon L R Kardia, Hans J Grabe, Alexander Teumer, Cornelia M van Duijn, Helena Schmidt, Joanna M Wardlaw, M Arfan Ikram, Myriam Fornage, Vilmundur Gudnason, Sudha Seshadri, Paul M Matthews, William T Longstreth, Thierry Couffinhal, Stephanie Debette
Publikováno v:
Brain
Brain, 145(6), 1992-2007. Oxford University Press
Brain : a journal of neurology, vol 145, iss 6
Mishra, A, Duplaà, C, Vojinovic, D, Suzuki, H, Sargurupremraj, M, Zilhão, N R, Li, S, Bartz, T M, Jian, X, Zhao, W, Hofer, E, Wittfeld, K, Harris, S E, van der Auwera-Palitschka, S, Luciano, M, Bis, J C, Adams, H H H, Satizabal, C L, Gottesman, R F, Gampawar, P G, Bülow, R, Weiss, S, Yu, M, Bastin, M E, Lopez, O L, Vernooij, M W, Beiser, A S, Völker, U, Kacprowski, T, Soumare, A, Smith, J A, Knopman, D S, Morris, Z, Zhu, Y, Rotter, J I, Dufouil, C, Valdés Hernández, M, Muñoz Maniega, S, Lathrop, M, Boerwinkle, E, Schmidt, R, Ihara, M, Mazoyer, B, Yang, Q, Joutel, A, Tournier-Lasserve, E, Launer, L J, Deary, I J, Mosley, T H, Amouyel, P, DeCarli, C S, Psaty, B M, Tzourio, C, Kardia, S L R, Grabe, H J, Teumer, A, van Duijn, C M, Schmidt, H, Wardlaw, J M, Ikram, M A, Fornage, M, Gudnason, V, Seshadri, S, Matthews, P M, Longstreth, W T, Couffinhal, T & Debette, S 2022, ' Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidate ', Brain . https://doi.org/10.1093/brain/awab432
Brain 145(6), 1992-2007 (2022). doi:10.1093/brain/awab432
Brain, 145(6), 1992-2007. Oxford University Press
Brain : a journal of neurology, vol 145, iss 6
Mishra, A, Duplaà, C, Vojinovic, D, Suzuki, H, Sargurupremraj, M, Zilhão, N R, Li, S, Bartz, T M, Jian, X, Zhao, W, Hofer, E, Wittfeld, K, Harris, S E, van der Auwera-Palitschka, S, Luciano, M, Bis, J C, Adams, H H H, Satizabal, C L, Gottesman, R F, Gampawar, P G, Bülow, R, Weiss, S, Yu, M, Bastin, M E, Lopez, O L, Vernooij, M W, Beiser, A S, Völker, U, Kacprowski, T, Soumare, A, Smith, J A, Knopman, D S, Morris, Z, Zhu, Y, Rotter, J I, Dufouil, C, Valdés Hernández, M, Muñoz Maniega, S, Lathrop, M, Boerwinkle, E, Schmidt, R, Ihara, M, Mazoyer, B, Yang, Q, Joutel, A, Tournier-Lasserve, E, Launer, L J, Deary, I J, Mosley, T H, Amouyel, P, DeCarli, C S, Psaty, B M, Tzourio, C, Kardia, S L R, Grabe, H J, Teumer, A, van Duijn, C M, Schmidt, H, Wardlaw, J M, Ikram, M A, Fornage, M, Gudnason, V, Seshadri, S, Matthews, P M, Longstreth, W T, Couffinhal, T & Debette, S 2022, ' Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidate ', Brain . https://doi.org/10.1093/brain/awab432
Brain 145(6), 1992-2007 (2022). doi:10.1093/brain/awab432
Cerebral small vessel disease is a leading cause of stroke and a major contributor to cognitive decline and dementia, but our understanding of specific genes underlying the cause of sporadic cerebral small vessel disease is limited. We report a genom
Autor:
Paul M. Thompson, Joshua C. Bis, Julian N. Trollor, Siggi Siggurdsson, Leonie Lampe, Piyush Gampawar, Myriam Fornage, Neda Jahanshad, Dina Vojinovic, Jiyang Jiang, Christophe Tzourio, Helena Schmidt, Shuo Li, Ian J. Deary, Lewis C. Becker, Karen A. Mather, Najaf Amin, Rui Xia, Bernard Mazoyer, Arno Villringer, Albert V. Smith, Henry Brodaty, Jeroen van der Grond, Vilmundur Gudnason, Rainer Malik, Christine Fennema-Notestine, Brian G. Kral, Asta Håberg, Clinton B. Wright, David C. Liewald, Sudha Seshadri, Claudia L. Satizabal, Bruce M. Psaty, Ralph L. Sacco, Reinhold Schmidt, Lisa R. Yanek, Mark Jenkinson, Qiong Yang, Jose R. Romero, Fidel Alfaro-Almagro, Philippe Amouyel, Margaret J. Wright, William T. Longstreth, Muralidharan Sargurupremraj, Mark E. Bastin, John B.J. Kwok, M. Arfan Ikram, David J. Stott, Nicole Dueker, Lukas Pirpamer, Perminder S. Sachdev, Stéphanie Debette, Edith Hofer, Ludovica Griffanti, Alexa S. Beiser, Nicola J. Armstrong, Stephen M. Smith, Lloyd T. Elliott, Wei Wen, J. Wouter Jukema, William S. Kremen, Markus Scholz, Anbupalam Thalamuthu, Peter R. Schofield, Clifford R. Jack, Stella Trompet, Gennady V. Roshchupkin, Matthias L. Schroeter, Joanna M. Wardlaw, Thomas H. Mosley, Michelle Luciano, Lenore J. Launer, Meike W. Vernooij, Maria J. Knol, Pauline Maillard, Charles DeCarli, Jonathan Marchini, Rebecca F. Gottesman, Paul A. Nyquist, Martin Dichgans, Zoe Morris, Cornelia M. van Duijn, David Ames, Veronica A. Witte, Hieab H.H. Adams, Mark A. Logue
Publikováno v:
Stroke, 51(7), 2111-2121. LIPPINCOTT WILLIAMS & WILKINS
Stroke 51(7), 2111-2121 (2020). doi:10.1161/STROKEAHA.119.027544
Stroke
Stroke, American Heart Association, In press, 51 (7), pp.2111-2121. ⟨10.1161/strokeaha.119.027544⟩
Stroke, 51(7), 2111-2121. Lippincott Williams & Wilkins
Stroke, vol 51, iss 7
Armstrong, N J, Mather, K A, Sargurupremraj, M, Knol, M J, Malik, R, Satizabal, C L, Yanek, L R, Wen, W, Gudnason, V G, Dueker, N D, Elliott, L T, Hofer, E, Bis, J, Jahanshad, N, Li, S, Logue, M A, Luciano, M, Scholz, M, Smith, A V, Trompet, S, Vojinovic, D, Xia, R, Alfaro-almagro, F, Ames, D, Amin, N, Amouyel, P, Beiser, A S, Brodaty, H, Deary, I J, Fennema-notestine, C, Gampawar, P G, Gottesman, R, Griffanti, L, Jack, C R, Jenkinson, M, Jiang, J, Kral, B G, Kwok, J B, Lampe, L, C.m. Liewald, D, Maillard, P, Marchini, J, Bastin, M E, Mazoyer, B, Pirpamer, L, Rafael Romero, J, Roshchupkin, G V, Schofield, P R, Schroeter, M L, Stott, D J, Thalamuthu, A, Trollor, J, Tzourio, C, Van Der Grond, J, Vernooij, M W, Witte, V A, Wright, M J, Yang, Q, Morris, Z, Siggurdsson, S, Psaty, B, Villringer, A, Schmidt, H, Haberg, A K, Van Duijn, C M, Jukema, J W, Dichgans, M, Sacco, R L, Wright, C B, Kremen, W S, Becker, L C, Thompson, P M, Mosley, T H, Wardlaw, J M, Ikram, M A, Adams, H H H, Seshadri, S, Sachdev, P S, Smith, S M, Launer, L, Longstreth, W, Decarli, C, Schmidt, R, Fornage, M, Debette, S & Nyquist, P A 2020, ' Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities ', Stroke . https://doi.org/10.1161/STROKEAHA.119.027544
Stroke 51(7), 2111-2121 (2020). doi:10.1161/STROKEAHA.119.027544
Stroke
Stroke, American Heart Association, In press, 51 (7), pp.2111-2121. ⟨10.1161/strokeaha.119.027544⟩
Stroke, 51(7), 2111-2121. Lippincott Williams & Wilkins
Stroke, vol 51, iss 7
Armstrong, N J, Mather, K A, Sargurupremraj, M, Knol, M J, Malik, R, Satizabal, C L, Yanek, L R, Wen, W, Gudnason, V G, Dueker, N D, Elliott, L T, Hofer, E, Bis, J, Jahanshad, N, Li, S, Logue, M A, Luciano, M, Scholz, M, Smith, A V, Trompet, S, Vojinovic, D, Xia, R, Alfaro-almagro, F, Ames, D, Amin, N, Amouyel, P, Beiser, A S, Brodaty, H, Deary, I J, Fennema-notestine, C, Gampawar, P G, Gottesman, R, Griffanti, L, Jack, C R, Jenkinson, M, Jiang, J, Kral, B G, Kwok, J B, Lampe, L, C.m. Liewald, D, Maillard, P, Marchini, J, Bastin, M E, Mazoyer, B, Pirpamer, L, Rafael Romero, J, Roshchupkin, G V, Schofield, P R, Schroeter, M L, Stott, D J, Thalamuthu, A, Trollor, J, Tzourio, C, Van Der Grond, J, Vernooij, M W, Witte, V A, Wright, M J, Yang, Q, Morris, Z, Siggurdsson, S, Psaty, B, Villringer, A, Schmidt, H, Haberg, A K, Van Duijn, C M, Jukema, J W, Dichgans, M, Sacco, R L, Wright, C B, Kremen, W S, Becker, L C, Thompson, P M, Mosley, T H, Wardlaw, J M, Ikram, M A, Adams, H H H, Seshadri, S, Sachdev, P S, Smith, S M, Launer, L, Longstreth, W, Decarli, C, Schmidt, R, Fornage, M, Debette, S & Nyquist, P A 2020, ' Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities ', Stroke . https://doi.org/10.1161/STROKEAHA.119.027544
Background and Purpose: Periventricular white matter hyperintensities (WMH; PVWMH) and deep WMH (DWMH) are regional classifications of WMH and reflect proposed differences in cause. In the first study, to date, we undertook genome-wide association an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b7b7b6d4228442271e5f642b0686e60
https://hdl.handle.net/1887/3184282
https://hdl.handle.net/1887/3184282
Autor:
Yingchang Lu, Denis Rybin, Paul M. Ridker, Tamara B. Harris, Ruth J. F. Loos, Tuomo Rankinen, Patricia A. Peyser, Nora Franceschini, Adolfo Correa, Caroline Hayward, Jerome I. Rotter, Ayse Demirkan, Mohsen Ghanbari, Alison D. Murray, Jonathan Marten, Peitao Wu, Mike A. Nalls, Lawrence F. Bielak, Cornelia M. van Duijn, Salman M. Tajuddin, Yize Li, Michael M. Province, Jingmin Liu, Lynda M. Rose, André G. Uitterlinden, D. C. Rao, Solomon K. Musani, Vilmundur Gudnason, Albert V. Smith, Sharon L.R. Kardia, Raymond Noordam, Susan Redline, Erwin P. Bottinger, Daniel I. Chasman, Lenore J. Launer, Alan B. Zonderman, Renée de Mutsert, Mary F. Feitosa, Ching-Ti Liu, James G. Wilson, Dina Vojinovic, Charles Kooperberg, Josée Dupuis, Najaf Amin, Claude Bouchard, Jose C. Florez, Linda Kao, Dennis O. Mook-Kanamori, Karen Schwander, Blair H. Smith, Michele K. Evans, David S. Siscovick, Jason L. Vassy, James B. Meigs, Sridharan Raghavan, Donna K. Arnett, Trudy Voortman, Jun Liu
Publikováno v:
Wu, P, Rybin, D, Bielak, L F, Feitosa, M F, Franceschini, N, Li, Y, Lu, Y, Marten, J, Musani, S K, Noordam, R, Raghavan, S, Rose, L M, Schwander, K, Smith, A V, Tajuddin, S M, Vojinovic, D, Amin, N, Arnett, D K, Bottinger, E P, Demirkan, A, Florez, J C, Ghanbari, M, Harris, T B, Launer, L J, Liu, J, Liu, J, Mook-Kanamori, D O, Murray, A D, Nalls, M A, Peyser, P A, Uitterlinden, A G, Voortman, T, Bouchard, C, Chasman, D, Correa, A, de Mutsert, R, Evans, M K, Gudnason, V, Hayward, C, Kao, L, Kardia, S L R, Kooperberg, C, Loos, R J F, Province, M M, Rankinen, T, Redline, S, Ridker, P M, Rotter, J I, Siscovick, D, Smith, B H, van Duijn, C, Zonderman, A B, Rao, D C, Wilson, J G, Dupuis, J, Meigs, J B, Liu, C T & Vassy, J L 2020, ' Smoking-by-genotype interaction in type 2 diabetes risk and fasting glucose ', PLoS ONE, vol. 15, no. 5, e0230815 . https://doi.org/10.1371/journal.pone.0230815
PLoS ONE, 15(5). PUBLIC LIBRARY SCIENCE
PLoS One (print), 15(5):e0230815. Public Library of Science
PLoS ONE
PLoS ONE, Vol 15, Iss 5, p e0230815 (2020)
PloS one, vol 15, iss 5
PLoS ONE, 15(5). PUBLIC LIBRARY SCIENCE
PLoS One (print), 15(5):e0230815. Public Library of Science
PLoS ONE
PLoS ONE, Vol 15, Iss 5, p e0230815 (2020)
PloS one, vol 15, iss 5
Publisher's version (útgefin grein)
Smoking is a potentially causal behavioral risk factor for type 2 diabetes (T2D), but not all smokers develop T2D. It is unknown whether genetic factors partially explain this variation. We performed genome-e
Smoking is a potentially causal behavioral risk factor for type 2 diabetes (T2D), but not all smokers develop T2D. It is unknown whether genetic factors partially explain this variation. We performed genome-e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0c1eccf3ca1d1aff1e025d49a3cdcf6
https://ora.ox.ac.uk/objects/uuid:0663cf39-84eb-4f28-b151-5588f22ea9e6
https://ora.ox.ac.uk/objects/uuid:0663cf39-84eb-4f28-b151-5588f22ea9e6
Autor:
Ashley, van der Spek, Sophie C, Warner, Linda, Broer, Christopher P, Nelson, Dina, Vojinovic, Shahzad, Ahmad, Pascal P, Arp, Rutger W W, Brouwer, Matthew, Denniff, Mirjam C G N, van den Hout, Jeroen G J, van Rooij, Robert, Kraaij, Wilfred F J, van IJcken, Nilesh J, Samani, M Arfan, Ikram, André G, Uitterlinden, Veryan, Codd, Najaf, Amin, Cornelia M, van Duijn
Publikováno v:
Frontiers in Genetics
Telomeres are important for maintaining genomic stability. Telomere length has been associated with aging, disease, and mortality and is highly heritable (∼82%). In this study, we aimed to identify rare genetic variants associated with telomere len
Autor:
Nora Franceschini, Lawrence F. Bielak, Anne B. Newman, Maryam Kavousi, Dennis O. Mook-Kanamori, Usman Baber, Shih-Jen Hwang, Lisa R. Yanek, Dermot F. Reilly, Amanda J. Cox, Sharon L.R. Kardia, Gerardo Heiss, Bob D. de Vos, Mika Kähönen, Pradeep Natarajan, Sekar Kathiresan, Mark O. Goodarzi, James G. Wilson, Joanna M. Wardlaw, Thomas H. Mosley, Donald W. Bowden, Dhananjay Vaidya, Nathan O. Stitziel, Michael A. Province, Bruce M. Psaty, Wendy Post, Gina M. Peloso, Jeffrey R. O'Connell, Laura M. Raffield, Stephen Turner, Patricia A. Peyser, Yii-Der Ida Chen, Hayato Tada, Joshua C. Bis, Kari E. North, Renée de Mutsert, Abbas Dehghan, Albert Hofman, Aaron Isaacs, Tamara B. Harris, Udo Hoffmann, Daniel J. Rader, Laura M. Yerges-Armstrong, Jessica van Setten, Kent D. Taylor, Matthijs Oudkerk, Braxton D. Mitchell, Xiuqing Guo, Aad van der Lugt, Harry J. de Koning, Vilmundur Gudnason, Riccardo E. Marioni, Cornelia M. van Duijn, Ingrid B. Borecki, Jerome I. Rotter, Oscar H. Franco, Roxana Mehran, Ivana Išgum, Pim A. de Jong, L. Adrienne Cupples, J. Wouter Jukema, Ruifang Li-Gao, Valentin Fuster, Fernando Rivadeneira, Ulf Schminke, Eric Boerwinkle, Alexander Teumer, Henry Völzke, Frits R. Rosendaal, Stefan Weiss, Leo-Pekka Lyytikäinen, Susan R. Heckbert, Jie Yao, Uwe Völker, James S. Pankow, Ian J. Deary, Stella Trompet, J. Jeffrey Carr, Mary K. Wojczynski, Christopher J. O'Donnell, Albert V. Smith, Mary F. Feitosa, Samantha Sartori, Stephan B. Felix, Ayse Demirkan, Olli T. Raitakari, Diane M. Becker, Terho Lehtimäki, Marcus Dörr, Khanh-Dung H. Nguyen, Brian G. Kral, Min A. Jhun, Rasika A. Mathias, André G. Uitterlinden, Dina Vojinovic, Lewis C. Becker, Najaf Amin, Lenore J. Launer, Joseph M. Massaro, Christina L. Wassel
Publikováno v:
Circulation: Cardiovascular Genetics, 9(6), 511
Circulation. Cardiovascular genetics, 9(6), 511-520. Lippincott Williams and Wilkins
Circulation-cardiovascular genetics, 9(6), 511-520. Lippincott Williams & Wilkins
Natarajan, P, Bis, J C, Bielak, L F, Cox, A J, Dörr, M, Feitosa, M F, Franceschini, N, Guo, X, Hwang, S-J, Isaacs, A, Jhun, M A, Kavousi, M, Li-Gao, R, Lyytikäinen, L-P, Marioni, R E, Schminke, U, Stitziel, N O, Tada, H, van Setten, J, Smith, A V, Vojinovic, D, Yanek, L R, Yao, J, Yerges-Armstrong, L M, Amin, N, Baber, U, Borecki, I B, Carr, J J, Chen, Y-D I, Cupples, L A, de Jong, P A, de Koning, H, de Vos, B D, Demirkan, A, Fuster, V, Franco, O H, Goodarzi, M O, Harris, T B, Heckbert, S R, Heiss, G, Hoffmann, U, Hofman, A, Išgum, I, Jukema, J W, Kähönen, M, Kardia, S L R, Kral, B G, Wardlaw, J M & Deary, I J & Wilson, J G 2016, ' Multiethnic Exome-Wide Association Study of Subclinical Atherosclerosis ', Circulation: Cardiovascular Genetics . https://doi.org/10.1161/CIRCGENETICS.116.001572
Circulation-Cardiovascular genetics, 9(6), 511. Lippincott Williams and Wilkins
Circulation : Cardiovascular Genetics, 9(6), 511-520. LIPPINCOTT WILLIAMS & WILKINS
Circulation-Cardiovascular Genetics, 9(6), 511-520. LIPPINCOTT WILLIAMS & WILKINS
Circulation. Cardiovascular genetics, vol 9, iss 6
Circulation. Cardiovascular genetics, 9(6), 511-520. Lippincott Williams and Wilkins
Circulation-cardiovascular genetics, 9(6), 511-520. Lippincott Williams & Wilkins
Natarajan, P, Bis, J C, Bielak, L F, Cox, A J, Dörr, M, Feitosa, M F, Franceschini, N, Guo, X, Hwang, S-J, Isaacs, A, Jhun, M A, Kavousi, M, Li-Gao, R, Lyytikäinen, L-P, Marioni, R E, Schminke, U, Stitziel, N O, Tada, H, van Setten, J, Smith, A V, Vojinovic, D, Yanek, L R, Yao, J, Yerges-Armstrong, L M, Amin, N, Baber, U, Borecki, I B, Carr, J J, Chen, Y-D I, Cupples, L A, de Jong, P A, de Koning, H, de Vos, B D, Demirkan, A, Fuster, V, Franco, O H, Goodarzi, M O, Harris, T B, Heckbert, S R, Heiss, G, Hoffmann, U, Hofman, A, Išgum, I, Jukema, J W, Kähönen, M, Kardia, S L R, Kral, B G, Wardlaw, J M & Deary, I J & Wilson, J G 2016, ' Multiethnic Exome-Wide Association Study of Subclinical Atherosclerosis ', Circulation: Cardiovascular Genetics . https://doi.org/10.1161/CIRCGENETICS.116.001572
Circulation-Cardiovascular genetics, 9(6), 511. Lippincott Williams and Wilkins
Circulation : Cardiovascular Genetics, 9(6), 511-520. LIPPINCOTT WILLIAMS & WILKINS
Circulation-Cardiovascular Genetics, 9(6), 511-520. LIPPINCOTT WILLIAMS & WILKINS
Circulation. Cardiovascular genetics, vol 9, iss 6
Background— The burden of subclinical atherosclerosis in asymptomatic individuals is heritable and associated with elevated risk of developing clinical coronary heart disease. We sought to identify genetic variants in protein-coding regions associa