Martin Dichgans
Genetic proxies for PCSK9 inhibition associate with lipoprotein(a): Effects on coronary artery disease and ischemic stroke.
De Marchis G, Dittrich T, Malik R, Zietz A, Kriemler L, Ference B, Dichgans M, Georgakis M. Genetic proxies for PCSK9 inhibition associate with lipoprotein(a): Effects on coronary artery disease and ischemic stroke. Atherosclerosis 2022; 361:41-46.
Sep 26, 2022Genetic proxies for PCSK9 inhibition associate with lipoprotein(a): Effects on coronary artery disease and ischemic stroke.
Sep 26, 2022Atherosclerosis 2022; 361:41-46
De Marchis Gian Marco, Dittrich Tolga, Malik Rainer, Zietz Annaelle, Kriemler Lilian, Ference Brian A, Dichgans Martin, Georgakis Marios K
Response to letter by Prof Christian Nolte and colleagues.
Dawson J, Béjot Y, Christensen L, De Marchis G, Dichgans M, Hagberg G, Heldner M, Milionis H, Li L, Pezzella F, Taylor Rowan M, Tiu C, Webb A. Response to letter by Prof Christian Nolte and colleagues. Eur Stroke J 2022; 7:341-342.
Jul 7, 2022Response to letter by Prof Christian Nolte and colleagues.
Jul 7, 2022Eur Stroke J 2022; 7:341-342
Dawson Jesse, Béjot Yannick, Christensen Louisa M, De Marchis Gian Marco, Dichgans Martin, Hagberg Guri, Heldner Mirjam R, Milionis Haralampos, Li Linxin, Pezzella Francesca Romana, Taylor Rowan Martin, Tiu Cristina, Webb Alastair
European Stroke Organisation (ESO) guideline on pharmacological interventions for long-term secondary prevention after ischaemic stroke or transient ischaemic attack.
Dawson J, Béjot Y, Christensen L, De Marchis G, Dichgans M, Hagberg G, Heldner M, Milionis H, Li L, Pezzella F, Taylor Rowan M, Tiu C, Webb A. European Stroke Organisation (ESO) guideline on pharmacological interventions for long-term secondary prevention after ischaemic stroke or transient ischaemic attack. Eur Stroke J 2022; 7:I-II.
Jun 3, 2022European Stroke Organisation (ESO) guideline on pharmacological interventions for long-term secondary prevention after ischaemic stroke or transient ischaemic attack.
Jun 3, 2022Eur Stroke J 2022; 7:I-II
Dawson Jesse, Béjot Yannick, Christensen Louisa M, De Marchis Gian Marco, Dichgans Martin, Hagberg Guri, Heldner Mirjam R, Milionis Haralampos, Li Linxin, Pezzella Francesca Romana, Taylor Rowan Martin, Tiu Cristina, Webb Alastair
Author Correction: Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors.
Ruigrok Y, Sargurupremraj M, Dichgans M, Malik R, Klijn C, Zaroff J, Breen G, Coleman J, Kim H, Ko N, Bown M, Jones G, Martin O, Dauvillier J, Schilling S, Hirsch S, Tatlisumak T, Amouyel P, Debette S, Veldink J, Kamatani Y, Bijlenga P, Redon R, Woo D, Werring D, Broderick J, Lindgren A, von Und Zu Fraunberg M, Jaaskelainen J, Niemelä M, Gaal-Paavola E, Slowik A, Pera J, Worrall B, Rinkel G, Friedrich C, Verschuren W, Zwart J, Chen Z, Millwood I, Liang L, Lin K, Walters R, Matsuda K, Terao C, Akiyama M, Koido M, van Eijk K, Alg V, Hostettler I, Bourcier R, Morel S, van Rheenen W, van der Spek R, Rouleau G, Zhou S, Rannikmäe K, Hveem K, Willer C, Sandvei M, Brumpton B, Johnsen M, Børte S, Winsvold B, Desal H, Eugène F, Shotar E, Gentric J, Naggara O, Dina C, van den Berg L, Houlden H, Sudlow C, Bakker M. Author Correction: Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors. Nat Genet 2021; 53:254.
Feb 1, 2021Author Correction: Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors.
Feb 1, 2021Nat Genet 2021; 53:254
Ruigrok Ynte M, Sargurupremraj Muralidharan, Dichgans Martin, Malik Rainer, Klijn Catharina J M, Zaroff Jonathan G, Breen Gerome, Coleman Jonathan R I, Kim Helen, Ko NeriU, Bown Matthew, Jones Gregory T, Martin Olivier, Dauvillier Jerome, Schilling Sabine, Hirsch Sven, Tatlisumak Turgut, Amouyel Philippe, Debette Stephanie, Veldink Jan H, Kamatani Yoichiro, Bijlenga Philippe, Redon Richard, Woo Daniel, Werring David J, Broderick Joseph P, Lindgren Antti, von Und Zu Fraunberg Mikael, Jaaskelainen Juha E, Niemelä Mika, Gaal-Paavola Emilia I, Slowik Agnieszka, Pera Joanna, Worrall Bradford B, Rinkel Gabriel J E, Friedrich Christoph M, Verschuren W M Monique, Zwart John-Anker, Chen Zhengming, Millwood Iona Y, Liang Liming, Lin Kuang, Walters Robin G, Matsuda Koichi, Terao Chikashi, Akiyama Masato, Koido Masaru, van Eijk Kristel R, Alg Varinder S, Hostettler Isabel, Bourcier Romain, Morel Sandrine, van Rheenen Wouter, van der Spek Rick A A, Rouleau Guy A, Zhou Sirui, Rannikmäe Kristiina, Hveem Kristian, Willer Cristen J, Sandvei Marie Søfteland, Brumpton Ben M, Johnsen Marianne Bakke, Børte Sigrid, Winsvold Bendik S, Desal Hubert, Eugène François, Shotar Eimad, Gentric Jean-Christophe, Naggara Olivier, Dina Christian, van den Berg Leonard H, Houlden Henry, Sudlow Cathie L M, Bakker Mark K
Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors.
Ruigrok Y, Sargurupremraj M, Dichgans M, Malik R, Klijn C, Zaroff J, Breen G, Coleman J, Kim H, Ko N, Bown M, Jones G, Martin O, Dauvillier J, Schilling S, Hirsch S, Tatlisumak T, Amouyel P, Debette S, Veldink J, Kamatani Y, Bijlenga P, Redon R, Woo D, Werring D, Broderick J, Lindgren A, von Und Zu Fraunberg M, Jaaskelainen J, Niemelä M, Gaal-Paavola E, Slowik A, Pera J, Worrall B, Rinkel G, Friedrich C, Verschuren W, Zwart J, Chen Z, Millwood I, Liang L, Lin K, Walters R, Matsuda K, Terao C, Akiyama M, Koido M, van Eijk K, Alg V, Hostettler I, Bourcier R, Morel S, van Rheenen W, van der Spek R, Rouleau G, Zhou S, Rannikmäe K, Hveem K, Willer C, Sandvei M, Brumpton B, Johnsen M, Børte S, Winsvold B, Desal H, Eugène F, Shotar E, Gentric J, Naggara O, Dina C, van den Berg L, Houlden H, Sudlow C, Bakker M. Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors. Nat Genet 2020; 52:1303-1313.
Nov 16, 2020Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors.
Nov 16, 2020Nat Genet 2020; 52:1303-1313
Ruigrok Ynte M, Sargurupremraj Muralidharan, Dichgans Martin, Malik Rainer, Klijn Catharina J M, Zaroff Jonathan G, Breen Gerome, Coleman Jonathan R I, Kim Helen, Ko NeriU, Bown Matthew, Jones Gregory T, Martin Olivier, Dauvillier Jerome, Schilling Sabine, Hirsch Sven, Tatlisumak Turgut, Amouyel Philippe, Debette Stephanie, Veldink Jan H, Kamatani Yoichiro, Bijlenga Philippe, Redon Richard, Woo Daniel, Werring David J, Broderick Joseph P, Lindgren Antti, von Und Zu Fraunberg Mikael, Jaaskelainen Juha E, Niemelä Mika, Gaal-Paavola Emilia I, Slowik Agnieszka, Pera Joanna, Worrall Bradford B, Rinkel Gabriel J E, Friedrich Christoph M, Verschuren W M Monique, Zwart John-Anker, Chen Zhengming, Millwood Iona Y, Liang Liming, Lin Kuang, Walters Robin G, Matsuda Koichi, Terao Chikashi, Akiyama Masato, Koido Masaru, van Eijk Kristel R, Alg Varinder S, Hostettler Isabel, Bourcier Romain, Morel Sandrine, van Rheenen Wouter, van der Spek Rick A A, Rouleau Guy A, Zhou Sirui, Rannikmäe Kristiina, Hveem Kristian, Willer Cristen J, Sandvei Marie Søfteland, Brumpton Ben M, Johnsen Marianne Bakke, Børte Sigrid, Winsvold Bendik S, Desal Hubert, Eugène François, Shotar Eimad, Gentric Jean-Christophe, Naggara Olivier, Dina Christian, van den Berg Leonard H, Houlden Henry, Sudlow Cathie L M, Bakker Mark K