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Wyszukujesz frazę "Debette, Stephanie" wg kryterium: Autor


Autorzy:
Christensen, Hanne
Wardlaw, Joanna
Caso, Valeria
Dippel, Diederik
Diomedi, Marina
Frisullo, Giovanni
Pavlovic, Aleksandra
Ozturk, Serefnur
Audebert, Heinrich
Mikulik, Robert
Béjot, Yannick
Denes, Adam
Wagner, Markus
Toni, Danilo
Tsivgoulis, Georgios
Wilkie, Arlene
Tsiskaridze, Alexander
Kiechl, Stefan
Vivien, Denis
Kõrv, Janika
Urso, Antonella
Christensen, Louisa
Proios, Hariklia
Roaldsen, Melinda Berg
Abilleira, Sonia
Norrving, Bo
Quinn, Terence J.
Molina, Carlos A.
Budincevic, Hrvoje
Tomek, Aleš
Ursillo, Paolo
Zedde, Marialuisa
Kruuse, Christina
Chabriat, Hugues
Casolla, Barbara
Macey, Chris
Charalambous, Marina
Gumbinger, Christoph
Mead, Gillian
Paciaroni, Maurizio
Galofre, Miquel
Hobbs, Richard
Harbison, Joseph
de Leeuw, Frank-Erik
Markus, Hugh Stephan
Flomin, Yuriy
Lang, Wilfried
Lunde, Grethe
Rothwell, Peter
Katan, Mira
Walker, Marion
Bouverie, Juliet
Tuomilehto, Jaakko
Kelly, Peter
Viigimaa, Margus
Steiner, Thorsten
Sacco, Simona
Gdovinová, Zuzana
Santo, Gustavo
Ford, Gary
Drummond, Avril
Forster, Anne
Simonsen, Claus
Stolarz-Skrzypek, Katarzyna
Debette, Stephanie
Ramos, Diana Wong
van Euler, Mia
Dichgans, Martin
Zampolini, Mauro
Persson, Carina U.
Forchammer, Birgitte
Dirnagl, Ulrich
Jurlina, Hrvoje
Michel, Patrik
Santalucia, Paola
Liesz, Arthur
Pezzella, Francesca Romana
Fonseca, Ana Catarina
Jatuzis, Dalius
Ulberg, Teresa
Laatikainen, Tiina
Kidd, Lisa
Sunnerhagen, Katharina S.
Sandset, Else
Webb, Alastair
Lorenzano, Svetlana
Luft, Andreas
Saba, Luca
Vilionskis, Aleksandras
Arsovska, Anita
Biessels, Geert Jan
Dawson, Jesse
Aguiar de Sousa, Diana
Fischer, Urs
Tiu, Cristina
Bartolovic, Jelena
Dostawca treści:
Repozytorium Uniwersytetu Jagiellońskiego
Artykuł
Tytuł:
Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors
Autorzy:
Broderick, Joseph P.
Worrall, Bradford B.
Breen, Gerome
Eugene, François
van Eijk, Kristel R.
Sudlow, Cathie L.M.
Jaaskelainen, Juha E.
Hveem, Kristian
Verschuren, W. M. Monique
Kim, Helen
Zaroff, Jonathan G.
Veldink, Jan H.
von und zu Fraunberg, Mikael
Rinkel, Gabriel J.E.
Gaál-Paavola, Emília I.
Dina, Christian
Bakker, Mark K.
Klijn, Catharina J.M.
Dichgans, Martin
Morel, Sandrine
Study Group, The ICAN
Willer, Cristen J.
Schilling, Sabine
Bijlenga, Philippe
Terao, Chikashi
Jones, Gregory T.
Malik, Rainer
Desal, Hubert
Pera, Joanna
Sandvei, Marie Softeland
Alg, Varinder S.
Hostettler, Isabel C.
Dauvillier, Jérôme
Consortium, International Stroke Genetics
Project Consortium, BioBank Japan
All-In Stroke, HUNT
Matsuda, Koichi
Borte, Sigrid
Hirsch, Sven
Lin, Kuang
Niemela, Mika
Coleman, Jonathan R.I.
Ko, Nerissa U.
Sargurupremraj, Muralidharan
Ruigrok, Ynte M.
Martin, Olivier
Subarachnoid Haemorrhage Study investigator, Genetics and Observational
Amouyel, Philippe
van der Spek, Rick A.A.
Winsvold, Bendik S.
Li, Liming
Zwart, John-Anker
Naggara, Olivier
Tatlisumak, Turgut
Shotar, Eimad
van den Berg, Leonard H.
Słowik, Agnieszka
Bown, Matthew J.
Woo, Daniel
Group, CADISP
Friedrich, Christoph M.
Lindgren, Antti
Akiyama, Masato
Rannikmae, Kristiina
Bourcier, Romain
Chen, Zhengming
Redon, Richard
Rouleau, Guy A.
Gentric, Jean-Christophe
Walters, Robin G.
Brumpton, Ben M.
van Rheenen, Wouter
Werring, David J.
Millwood, Iona Y.
Koido, Masaru
Biobank Collaborative Group, China Kadoorie
Kamatani, Yoichiro
Zhou, Sirui
Johnsen, Marianne Bakke
Debette, Stéphanie
Houlden, Henry
Dostawca treści:
Repozytorium Uniwersytetu Jagiellońskiego
Artykuł
Tytuł:
Contribution of common genetic variants to risk of early-onset ischemic stroke
Autorzy:
Jimenez-Conde, Jordi
Ryan, Kathleen A.
Luke, Sothear
Gieger, Christian
Pera, Joanna
Thijs, Vincent
Smith, Jennifer A.
Mitchell, Braxton D.
Chong, Michael
Rexrode, Kathryn
Cruchaga, Carlos
Torres-Aguila, Nuria P.
Markus, Hugh S.
Heitsch, Laura
Walters, Robin G.
Li, Jiang
Rosand, Jonathan
Jaworek, Thomas
Kamatani, Yoichiro
Meschia, James F.
Holliday, Elizabeth
Mcardle, Patrick F.
Anderson, Christopher D.
Ilinca, Andreea
Bell, Steven
Cushman, Mary
Gaynor, Brady J.
Muller-Nurasyid, Martina
Putaala, Jukka
Cole, John W.
Engstrom, Gunnar
Grittner, Ulrike
Strbian, Daniel
Kardia, Sharon L.R.
Levi, Christopher R.
Hong, Charles C.
O'Donnell, Martin
Pare, Guillaume
Zand, Ramin
Tuladhar, Anil M.
Faul, Jessica D.
Havulinna, Aki S.
Sacco, Ralph L.
Mcdonough, Caitrin W.
Jern, Christina
Boncoraglio, Giorgio B.
Hu, Jie
Rothwell, Peter M.
Metso, Tiina
Lin, Kuang
Giese, Anne-Katrin
Fecteau, Natalie S.
Jackson, Rebecca D.
Johnson, Julie A.
Ribases, Marta
Attia, John
Veldink, Jan H.
de Leeuw, Frank-Erik
Lemmens, Robin
O'Connor, Timothy D.
Danesh, John
Irvin, Marguerite R.
Perry, James A.
Hochberg, Marc C.
Stine, O. Colin
Fernandez-Cadenas, Israel
Tomppo, Liisa
Abedi, Vida
Grewal, Raji P.
Li, Liming
Sanchez-Mora, Cristina
Lange, Leslie
Ross, Owen A.
Chen, Zhengming
Debette, Stephanie
Wassertheil-Smoller, Sylvia
Stanne, Tara M.
Jacob, Mina A.
Smith, Nicholas L.
Dichgans, Martin
Sudlow, Cathie L.M.
Kittner, Steven J.
Rannikmae, Kristiina
Peddareddygari, Leema R.
Lopez, Haley
Peters, Annette
Benavente, Oscar R.
Weir, David R.
Salomaa, Veikko
Enzinger, Chris
Lindgren, Arne G.
Tatlisumak, Turgut
Durda, Jon Peter
Ray, Debashree
Xu, Huichun
Lee, Jin-Moo
Worrall, Bradford B.
Butterworth, Adam
Słowik, Agnieszka
Soderholm, Martin
Woo, Daniel
Carcel-Marquez, Jara
Duggan, David J.
Maguire, Jane
Koido, Masaru
Sharma, Pankaj
Terao, Chikashi
Malik, Rainer
Schmidt, Reinhold
Amouyel, Philippe
Kubo, Michiaki
Rabionet, Raquel
Tregouet, David-Alexandre
Armstrong, Nicole D.
Rundek, Tatjana
Opis:
Background and Objectives:Current genome-wide association studies of ischemic stroke have focused primarily on late-onset disease. As a complement to these studies, we sought to identify the contribution of common genetic variants to risk of early-onset ischemic stroke: Methods: We performed a meta-analysis of genome-wide association studies of early-onset stroke (EOS), ages 18–59 years, using individual-level data or summary statistics in 16,730 cases and 599,237 nonstroke controls obtained across 48 different studies. We further compared effect sizes at associated loci between EOS and late-onset stroke (LOS) and compared polygenic risk scores (PRS) for venous thromboembolism (VTE) between EOS and LOS. Results: We observed genome-wide significant associations of EOS with 2 variants in ABO, a known stroke locus. These variants tag blood subgroups O1 and A1, and the effect sizes of both variants were significantly larger in EOS compared with LOS. The odds ratio (OR) for rs529565, tagging O1, was 0.88 (95% confidence interval [CI]: 0.85–0.91) in EOS vs 0.96 (95% CI: 0.92–1.00) in LOS, and the OR for rs635634, tagging A1, was 1.16 (1.11–1.21) for EOS vs 1.05 (0.99–1.11) in LOS; p-values for interaction = 0.001 and 0.005, respectively. Using PRSs, we observed that greater genetic risk for VTE, another prothrombotic condition, was more strongly associated with EOS compared with LOS (p = 0.008). Discussion: The ABO locus, genetically predicted blood group A, and higher genetic propensity for venous thrombosis are more strongly associated with EOS than with LOS, supporting a stronger role of prothrombotic factors in EOS.
Dostawca treści:
Repozytorium Uniwersytetu Jagiellońskiego
Artykuł
Tytuł:
Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting
Autorzy:
Sharma, Pankaj
Woo, Daniel
Wong, Tien Y.
Beecham, Ashley H.
Cole, John W.
Thijs, Vincent
Griswold, Michael E.
Gudnason, Vilmundur
Montine, Thomas J.
Liewald, David
Maillard, Pauline
McWhirter, Rebekah
Kittner, Steven J.
Launer, Lenore J.
Hernández, Maria del C. Valdés
Aggarwal, Neelum T.
Wardlaw, Joanna M.
Rosand, Jonathan
van der Graaf, Yolanda
Brodaty, Henry
Adams, Hieab H.H.
Rexrode, Kathy
Thomson, Russell
Deary, Ian J.
Romero, Jose R.
Wittfeld, Katharina
Dichgans, Martin
Hofer, Edith
Tzourio, Christophe
Schmidt, Helena
Hopewell, Jemma C.
Schellenberg, Gerard D.
Satizabal, Claudia L.
International Stroke Genetics Consortium,
Rice, Kenneth
Longstreth, W.T.
Asselbergs, Folkert W.
Knopman, David S.
DeStefano, Anita L.
Srikanth, Velandai
Sachdev, Perminder S.
Beekman, Marian
Wright, Clinton B.
Starr, John M.
Armstrong, Nicola J.
Chouraki, Vincent
Jern, Christina
Schofield, Peter R.
van der Lee, Sven J.
Uh, Hae-Won
Saba, Yasaman
Worrall, Bradford B.
Hosten, Norbert
Benavente, Oscar R.
Callisaya, Michele
Schilling, Sabrina
Stott, David J.
van Duijn, Cornelia M.
Kjartansson, Olafur
Yamaguchi, Shuhei
Zhu, Yi-Cheng
Slagboom, Eline
Kaffashian, Sara
Rothwell, Peter M.
Amouyel, Philippe
DeCarli, Charles
Nabika, Toru
Uitterlinden, André G.
Kato, Norihiro
Amin, Najaf
Grewal, Raji P.
Chauhan, Ganesh
Rich, Stephen S.
McArdle, Patrick F.
Johnson, Julie A.
Trompet, Stella
van der Grond, Jeroen
Mitchell, Braxton D.
Gottesman, Rebecca F.
Sargurupremraj, Muralidharan
Phan, Thanh
Mather, Karen A.
Ames, David
Rajan, Kumar B.
Grabe, Hans J.
Jimenez-Conde, Jordi
Pera, Joanna
Meschia, James F.
Sacco, Ralph L.
Blanton, Susan H.
Beva, Steve
Wen, Wei
Kwok, John B.
Psaty, Bruce M.
von Sarnowski, Bettina
Seshadri, Sudha
Ikram, Mohammad K.
Liao, Jiemin
Pulit, Sara L.
de Bakker, Paul I.W.
Windham, B. Gwen
Stroke Genetics Network,
Moran, Chris
Wong, Quenna
Smith, Albert Vernon
Melander, Olle
Luciano, Michelle
Aparicio, Hugo J.
Bastin, Mark E.
Ford, Ian
Traylor, Matthew
Muñoz Maniega, Susana
Vernooij, Meike W.
Jukem, J. Wouter
Fornage, Myriam
Bis, Joshua C.
Thalamuthu, Anbupalam
Levi, Christopher
Geerlings, Mirjam I.
Rotter, Jerome I.
Arnett, Donna K.
Wasssertheil-Smoller, Sylvia
Markus, Hugh S.
Chen, Christopher
Słowik, Agnieszka
Mazoyer, Bernard
Beecham, Gary W.
Evans, Denis A.
Ikram, Mohammad A.
Völker, Uwe
Debette, Stéphanie
Rundek, Tatjana
Malik, Rainer
Hofman, Albert
Lopez, Oscar L.
Teumer, Alexander
Deelen, Joris
Lemmens, Robin
Lee, Jin-Moo
Chong, Elizabeth
De Jager, Philip L.
Schmidt, Reinhold
Cheng, Ching-Yu
Lindgren, Arne
Sudlow, Cathie L.M.
Rutten-Jacob, Loes C.A.
van der Lugt, Aad
Boncoraglio, Giorgio B.
Takeuchi, Fumihiko
Mosley, Thomas H.
METASTROKE,
Wright, Margaret J.
Hilal, Saima
Jian, Xueqiu
Dostawca treści:
Repozytorium Uniwersytetu Jagiellońskiego
Artykuł

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