Description of stroke mimics after complete neurovascular assessment

Autor: C. Avellaneda-Gómez, A. Rodríguez Campello, E. Giralt Steinhauer, A. Gómez González, M. Serra Martínez, P. de Ceballos Cerrajería, A. Zabalza de Torres, E. Cuadrado-Godia, A. Ois Santiago, J. Jiménez-Conde, J. Roquer

Publikováno v: Neurología (English Edition), Vol 34, Iss 1, Pp 7-13 (2019)

Introduction: A considerable percentage of events initially diagnosed as ischaemic stroke have non-cerebrovascular causes; these are called stroke mimics (SM). Currently available evidence about these events is heterogeneous and comes from studies wi

Externí odkaz: https://doaj.org/article/bde13a64a7dd439399304e230e23df29

Detecting in-hospital stroke: Assessment of results from a training programme for medical personnel

Autor: A. Rodríguez Campello, E. Cuadrado Godia, E. Giralt Steinhauer, E. Rodríguez Fernández, A. Domínguez, G. Romeral, E. Muñoz, J. Roquer

Publikováno v: Neurología (English Edition), Vol 30, Iss 9, Pp 529-535 (2015)

Introduction: In-hospital stroke (IHS) is a frequent event, but its care priority level is not well established in many hospitals. IHS care at our centre has been redefined by implementing a training programme for medical personnel not usually involv

Externí odkaz: https://doaj.org/article/d32d6dd6fde44bc2a7ee907f23101981

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Migraine-associated common genetic variants confer greater risk of posterior vs. anterior circulation ischemic stroke

Autor: P. Frid, H. Xu, B.D. Mitchell, M. Drake, J. Wasselius, B. Gaynor, K. Ryan, A.K. Giese, M. Schirmer, K.L. Donahue, R. Irie, M.J.R.J. Bouts, E.C. McIntosh, S.J.T. Mocking, A.V. Dalca, E. Giralt-Steinhauer, L. Holmegaard, K. Jood, J. Roquer, J.W. Cole, P.F. McArdle, J.P. Broderick, J. Jimenez-Conde, C. Jern, B.M. Kissela, D.O. Kleindorfer, R. Lemmens, J.F. Meschia, J. Rosand, T. Rundek, R.L. Sacco, R. Schmidt, P. Sharma, A. Slowik, V. Thijs, D. Woo, B.B. Worrall, S.J. Kittner, J. Petersson, P. Golland, O. Wu, N.S. Rost, A. Lindgren

OBJECTIVE: To examine potential genetic relationships between migraine and the two distinct phenotypes posterior circulation ischemic stroke (PCiS) and anterior circulation ischemic stroke (ACiS), we generated migraine polygenic risk scores (PRSs) an

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ca438d84e784185271bdb5ecc3b5fec
http://hdl.handle.net/10230/54960

Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation

Autor: Giuseppe Matullo, John R. B. Perry, Meena Kumari, Gemma C Sharp, Tomáš Paus, E. Giralt-Steinhauer, Marta E. Alarcón-Riquelme, Koen F. Dekkers, F. Gagnon, Simonetta Guarrera, Cilla Söderhäll, Rosie M. Walker, Therese Tillin, M. Smarts, Juan E. Castillo-Fernandez, John M. Starr, Jean Shin, Dan Mason, T Esko, Christopher Shaw, Hannah R Elliott, Manon Bernard, David L. Corcoran, Yvonne Awaloff, Ahmad Al Khleifat, Bert Brunekreef, Clara Viberti, John Wright, Gibran Hemani, Kathryn L. Evans, Camilla Schmidt Morgen, Jouke J. Hottenga, Susan M. Ring, Terrie E. Moffitt, Silva Kasela, C. Hale, Idil Yet, Katri Räikkönen, René Luijk, Vanessa Schmoll, Kimberley Burrows, Annelot M. Dekker, D. VanHeemst, Jordana T. Bell, Jordi Jimenez-Conde, Carlotta Sacerdote, Salvatore Panico, Lili Milani, Nabila Kazmi, Torben Hansen, Aleksey Shatunov, J L Min, Richa Gupta, Henning Tiemeier, Grant W. Montgomery, Vincent W. V. Jaddoe, E.J.C. de Geus, Fernando Rivadeneira, Debbie A Lawlor, Carol A. Wang, Toni-Kim Clarke, Susanne Lucae, Nicholas J. Wareham, Jordi Sunyer, Felix R. Day, C. Soriano-Tarraga, Christoph Bock, Juan R. González, D. Aissi, J.B. van Meurs, Ian J. Deary, Ken K. Ong, Louise Arseneault, Eilis Hannon, Bastiaan T. Heijmans, Philip E. Melton, Ashok Kumar, Pierre-Emmanuel Morange, Zdenka Pausova, T.D. Spector, Nicholas G. Martin, J. Mill, Francesc Català-Moll, Alun D. Hughes, Leonard C. Schalkwyk, Giovanni Cugliari, Carlos Ruiz-Arenas, Elena Carnero-Montoro, Marine Germain, Yanni Zeng, Andrew M. McIntosh, Riccardo E. Marioni, Wilfried Karmaus, Ikram, Gonneke Willemsen, Miina Ollikainen, Karen M Ho, Craig E. Pennell, F.I. Rezwan, Darina Czamara, Ramona A. J. Zwamborn, Dorret I. Boomsma, Wendy L. McArdle, J. M. van Dongen, Guillermo Barturen, Matthew Suderman, Richie Poulton, Daniel Lawson, A. Metspalu, David-Alexandre Trégouët, Marian Beekman, Andrew D. Bretherick, Johanna Klughammer, Hongmei Zhang, M.H. van IJzendoorn, Nish Chaturvedi, Jari Lahti, Karen Sugden, Jan H. Veldink, Mariona Bustamante, Avshalom Caspi, Pooja R. Mandaviya, Judith M. Vonk, Tom R. Gaunt, Cheng-Jian Xu, John W. Holloway, Tian Lin, Tom G. Richardson, Caroline L Relton, Naomi R. Wray, Allan F. McRae, George Davey Smith, Erik Melén, Valentina Iotchkova, Ellen A. Nohr, Jaakko Kaprio, Göran Pershagen, Elisabeth B. Binder, A. al Chalabi, T.J. Gorrie-Stone, K. van Eijk, Gerard H. Koppelman, M. Lerro, Alexia Cardona, Sailalitha Bollepalli, P.E. Slagboom, Thorkild I. A. Sørensen, André G. Uitterlinden, Jaume Roquer, Peter M. Visscher, Janine F. Felix, Martin Kerick, Gail Davies, Rae-Chi Huang, Alfredo Iacoangeli, Alison D. Murray

Publikováno v: Nature Genetics
Digital.CSIC. Repositorio Institucional del CSIC
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Nature genetics, 53(9), 1311-1321. Nature Publishing Group
Nature Genetics, 53, 1311-1321. Nature Publishing Group
Nature Genetics, Nature Publishing Group, 2021, 53 (9), pp.1311-1321. ⟨10.1038/s41588-021-00923-x⟩
et al., Min, J L, Hemani, G, Hannon, E, dekkers, K, Castillo-Fernandez, J, Luijk, R, Carnero-Montoro, E, Lawson, D J, Burrows, K, Suderman, M J, Bretherick, A D, Richardson, T G, Klughammer, J, Lochkova, V, Sharp, G C, Al Khleifat, A, Shatunov, A, Lacoangeli, A, Mcardle, W L, Ho, K M, Kumar, A, Soderhall, C, Soriano-Tárraga, C, Giralt-Steinhauer, E, Kazmi, N, Mason, D, McRae, A F, Corcoran, D L, Elliott, H R, Ring, S M, Lawlor, D A, Sørensen, T I A, Davey Smith, G, Gaunt, T R & Relton, C L 2021, ' Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation ', Nature Genetics, vol. 53, no. 9, pp. 1311-1321 . https://doi.org/10.1038/s41588-021-00923-x
Min, J L, Hemani, G, Hannon, E, Dekkers, K F, Castillo-Fernandez, J, Luijk, R, Carnero-Montoro, E, Lawson, D J, Burrows, K, Suderman, M, Bretherick, A D, Richardson, T G, Klughammer, J, Iotchkova, V, Sharp, G, Al Khleifat, A, Shatunov, A, Iacoangeli, A, McArdle, W L, Ho, K M, Kumar, A, Söderhäll, C, Soriano-Tárraga, C, Giralt-Steinhauer, E, Kazmi, N, Mason, D, McRae, A F, Corcoran, D L, Sugden, K, Kasela, S, Cardona, A, Day, F R, Cugliari, G, Viberti, C, Guarrera, S, Lerro, M, Gupta, R, Bollepalli, S, Mandaviya, P, Zeng, Y, Clarke, T K, Walker, R M, Schmoll, V, Czamara, D, Ruiz-Arenas, C, Elliott, H R, Nohr, E A, Sørensen, T I A, Hansen, T, Morgen, C S & BIOS Consortium 2021, ' Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation ', Nature Genetics, vol. 53, no. 9, pp. 1311-1321 . https://doi.org/10.1038/s41588-021-00923-x
Min, J L, van Dongen, J, Hottenga, J J, Willemsen, G, de Geus, E J C, Boomsma, D I, Relton, C L & BIOS Consortium 2021, ' Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation ', Nature genetics, vol. 53, no. 9, pp. 1311-1321 . https://doi.org/10.1038/s41588-021-00923-x
Min, J L, Hemani, G, Hannon, E, Dekkers, K F, Castillo-Fernandez, J, Luijk, R, Carnero-Montoro, E, Lawson, D J, Burrows, K, Suderman, M, Bretherick, A D, Richardson, T G, Klughammer, J, Iotchkova, V, Sharp, G, Al Khleifat, A, Shatunov, A, Iacoangeli, A, McArdle, W L, Ho, K M, Kumar, A, Söderhäll, C, Soriano-Tárraga, C, Giralt-Steinhauer, E, Kazmi, N, Mason, D, McRae, A F, Corcoran, D L, Sugden, K, Kasela, S, Cardona, A, Day, F R, Cugliari, G, Viberti, C, Guarrera, S, Lerro, M, Gupta, R, Bollepalli, S, Mandaviya, P, Zeng, Y, Clarke, T K, Walker, R M, Schmoll, V, Czamara, D, Ruiz-Arenas, C, Rezwan, F I, Marioni, R E, Nohr, E A, Sørensen, T I A, Morgen, C S & BIOS Consortium 2021, ' Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation ', Nature Genetics, vol. 53, no. 9, pp. 1311-1321 . https://doi.org/10.1038/s41588-021-00923-x
Nature Genetics, 53(9), 1311-1321. NATURE PORTFOLIO
Nature Genetics, 2021, 53 (9), pp.1311-1321. ⟨10.1038/s41588-021-00923-x⟩
Nature Genetics, 53(9), 1311-1321. Nature Publishing Group

DNA methylation quantitative trait locus (mQTL) analyses on 32,851 participants identify genetic variants associated with DNA methylation at 420,509 sites in blood, resulting in a database of >270,000 independent mQTLs. Characterizing genetic influen

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9f18b02f6a59803fa5fa39c1daf1e4d
https://pubmed.ncbi.nlm.nih.gov/34493871