Resultados de búsqueda - Dichgans M
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International stroke genetics consortium recommendations for studies of genetics of stroke outcome and recovery
Artículo | por Lindgren, AG; Braun, RG; Majersik, JJ; Clatworthy, P; Mainali, S; Derdeyn, CP; Maguire, J; Jern, C; Rosand, J; Cole, JW; Lee, JM; Khatri, P; Nyquist, P; Debette, S; Wei, LK; Rundek, T; Leifer, D; Thijs, V; Lemmens, R; Heitsch, L; Prasad, K; Conde, JJ; Dichgans, M; Rost, NS; Cramer, SC; Bernhardt, J; Worrall, BB; Fernandez-Cadenas, I; Int Stroke Genetics Consortium | Publicado 2022 | -
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Shared Genetic Contribution to Ischemic Stroke and Alzheimer's Disease
Artículo | por Traylor, M; Adib-Samii, P; Harold, D; Dichgans, M; Williams, J; Lewis, CM; Markus, HS; Clarimón J.; Lleó A. | Publicado 2016 | -
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Increased soluble TREM2 in cerebrospinal fluid is associated with reduced cognitive and clinical decline in Alzheimer's disease
Artículo | por Ewers, M; Franzmeier, N; Suarez-Calvet, M; Morenas-Rodriguez, E; Caballero, MAA; Kleinberger, G; Piccio, L; Cruchaga, C; Deming, Y; Dichgans, M; Trojanowski, JQ; Shaw, LM; Weiner, MW; Haass, C; Alzheimers Dis Neuroimaging Initia | Publicado 2019 | -
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Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis
Artículo | por Hinds, DA; Buil, A; Ziemek, D; Martinez-Perez, A; Malik, R; Folkersen, L; Germain, M; Malarstig, A; Brown, A; Soria, JM; Dichgans, M; Bing, N; Franco-Cereceda, A; Souto, JC; Dermitzakis, ET; Hamsten, A; Worrall, BB; Tung, JY; Sabater-Lleal, M | Publicado 2016 | -
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Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke
Artículo | por Traylor, M; Zhang, CR; Adib-Samii, P; Devan, WJ; Parsons, OE; Lanfranconi, S; Gregory, S; Cloonan, L; Falcone, GJ; Radmanesh, F; Fitzpatrick, K; Kanakis, A; Barrick, TR; Moynihan, B; Lewis, CM; Boncoraglio, GB; Lemmens, R; Thijs, V; Sudlow, C; Wardlaw, J; Rothwell, PM; Meschia, JF; Worrall, BB; Levi, C; Bevan, S; Furie, KL; Dichgans, M; Rosand, J; Markus, HS; Rost, N; Int Stroke Genetics Consortium; Int Stroke Genetics ConsortiumInt Stroke Genetics Consortium | Publicado 2016 | -
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Prognostic relevance of cortical superficial siderosis in cerebral amyloid angiopathy
Artículo | por Wollenweber, FA; Opherk, C; Zedde, M; Catak, C; Malik, R; Duering, M; Konieczny, MJ; Pascarella, R; Samoes, R; Correia, M; Marti-Fabregas, J; Linn, J; Dichgans, M | Publicado 2019 | -
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Machine learning in Alzheimer's disease genetics
Artículo | por Bracher-Smith, M; Melograna, F; Ulm, B; Bellenguez, C; Grenier-Boley, B; Duroux, D; Nevado, AJ; Holmans, P; Tijms, BM; Hulsman, M; de Rojas, I; Campos-Martin, R; van der Lee, S; Castillo, A; Küçükali, F; Peters, O; Schneider, A; Dichgans, M; Rujescu, D; Scherbaum, N; Deckert, J; Riedel-Heller, S; Hausner, L; Molina-Porcel, L; Düzel, E; Grimmer, T; Wiltfang, J; Heilmann-Heimbach, S; Moebus, S; Tegos, T; Scarmeas, N; Dols-Icardo, O; Moreno, F; Pérez-Tur, J; Bullido, MJ; Pastor, P; Sánchez-Valle, R; Alvarez, V; Boada, M; García-González, P; Puerta, R; Mir, P; Real, LM; Piñol-Ripoll, G; García-Alberca, JM; Rodriguez-Rodriguez, E; Soininen, H; Heikkinen, S; de Mendonça, A; Mehrabian, S; Traykov, L; Hort, J; Vyhnalek, M; Sandau, N; Thomassen, JQ; Pijnenburg, YAL; Holstege, H; van Swieten, J; Ramakers, I; Verhey, F; Scheltens, P; Graff, C; Papenberg, G; Giedraitis, V; Williams, J; Amouyel, P; Boland, A; Deleuze, JF; Nicolas, G; Dufouil, C; Pasquier, F; Hanon, O; Debette, S; Grünblatt, E; Popp, J; Ghidoni, R; Galimberti, D; Arosio, B; Mecocci, P; Solfrizzi, V; Parnetti, L; Squassina, A; Tremolizzo, L; Borroni, B; Wagner, M; Nacmias, B; Spallazzi, M; Seripa, D; Rainero, I; Daniele, A; Piras, F; Masullo, C; Rossi, G; Jessen, F; Kehoe, P; Magda, T; Sánchez-Juan, P; Sleegers, K; Ingelsson, M; Hiltunen, M; Sims, R; van der Flier, W; Andreassen, OA; Ruiz, A; Ramirez, A; Frikke-Schmidt, R; Amin, N; Roshchupkin, G; Lambert, JC; Van Steen, K; van Duijn, C; Escott-Price, V | Publicado 2025 | -
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Apolipoprotein(a) Genetic Sequence Variants Associated With Systemic Atherosclerosis and Coronary Atherosclerotic Burden But Not With Venous Thromboembolism
Artículo | por Helgadottir, A; Gretarsdottir, S; Thorleifsson, G; Holm, H; Patel, RS; Gudnason, T; Jones, GT; van Rij, AM; Eapen, DJ; Baas, AF; Tregouet, DA; Morange, PE; Emmerich, J; Lindblad, B; Gottsater, A; Kiemeny, LA; Lindholt, JS; Sakalihasan, N; Ferrell, RE; Carey, DJ; Elmore, JR; Tsao, PS; Grarup, N; Jorgensen, T; Witte, DR; Hansen, T; Pedersen, O; Pola, R; Gaetani, E; Magnadottir, HB; Wijmenga, C; Tromp, G; Ronkainen, A; Ruigrok, YM; Blankensteijn, JD; Mueller, T; Wells, PS; Corral, J; Soria, JM; Souto, JC; Peden, JF; Jalilzadeh, S; Mayosi, BM; Keavney, B; Strawbridge, RJ; Sabater-Lleal, M; Gertow, K; Baldassarre, D; Nyyssonen, K; Rauramaa, R; Smit, AJ; Mannarino, E; Giral, P; Tremoli, E; de Faire, U; Humphries, SE; Hamsten, A; Haraldsdottir, V; Olafsson, I; Magnusson, MK; Samani, NJ; Levey, AI; Markus, HS; Kostulas, K; Dichgans, M; Berger, K; Kuhlenbaumer, G; Ringelstein, EB; Stoll, M; Seedorf, U; Rothwell, PM; Powell, JT; Kuivaniemi, H; Onundarson, PT; Valdimarsson, E; Matthiasson, SE; Gudbjartsson, DF; Thorgeirsson, G; Quyyumi, AA; Watkins, H; Farrall, M; Thorsteinsdottir, U; Stefansson, K | Publicado 2012 | -
9
Contribution of Common Genetic Variants to Risk of Early-Onset Ischemic Stroke
Artículo | por Jaworek, T; Xu, HC; Gaynor, BJ; Cole, JW; Rannikmae, K; Stanne, TM; Tomppo, L; Abedi, V; Amouyel, P; Armstrong, ND; Attia, J; Bell, S; Benavente, OR; Boncoraglio, GB; Butterworth, A; Carcel-Marquez, J; Chen, ZM; Chong, M; Cruchaga, C; Cushman, M; Danesh, J; Debette, S; Duggan, DJ; Durda, JP; Engstrom, G; Enzinger, C; Faul, JD; Fecteau, NS; Fernandez-Cadenas, I; Gieger, C; Giese, AK; Grewal, RP; Grittner, U; Havulinna, AS; Heitsch, L; Hochberg, MC; Holliday, E; Hu, J; Ilinca, A; Irvin, MR; Jackson, RD; Jacob, MA; Rabionet, R; Jimenez-Conde, J; Johnson, JA; Kamatani, Y; Kardia, SLR; Koido, M; Kubo, M; Lange, L; Lee, JM; Lemmens, R; Levi, CR; Li, J; Li, LM; Lin, K; Lopez, H; Luke, S; Maguire, J; McArdle, PF; McDonough, CW; Meschia, JF; Metso, T; Muller-Nurasyid, M; O'Connor, TD; O'Donnell, M; Peddareddygari, LR; Pera, J; Perry, JA; Peters, A; Putaala, J; Ray, D; Rexrode, K; Ribases, M; Rosand, J; Rothwell, PM; Rundek, T; Ryan, KA; Sacco, RL; Salomaa, V; Sanchez-Mora, C; Schmidt, R; Sharma, P; Slowik, A; Smith, JA; Smith, NL; Wassertheil-Smoller, S; Soderholm, M; Stine, OC; Strbian, D; Sudlow, CLM; Tatlisumak, T; Terao, C; Thijs, V; Torres-Aguila, NP; Tregouet, DA; Tuladhar, AM; Veldink, JH; Walters, RG; Weir, DR; Woo, D; Worrall, BB; Hong, CC; Ross, OA; Zand, R; de Leeuw, FE; Lindgren, AG; Pare, G; Anderson, CD; Markus, HS; Jern, C; Malik, R; Dichgans, M; Mitchell, BD; Kittner, SJ | Publicado 2022 | -
10
X-chromosome-wide association study for Alzheimer's disease
Artículo | por Le Borgne, J; Gomez, L; Heikkinen, S; Amin, N; Ahmad, S; Choi, SH; Bis, J; Grenier-Boley, B; Rodriguez, OG; Kleineidam, L; Young, J; Tripathi, KP; Wang, L; Varma, A; Campos-Martin, R; van der Lee, S; Damotte, V; de Rojas, I; Palmal, S; Lipton, R; Reiman, E; McKee, A; De Jager, P; Bush, W; Small, S; Levey, A; Saykin, A; Foroud, T; Albert, M; Hyman, B; Petersen, R; Younkin, S; Sano, M; Wisniewski, T; Vassar, R; Schneider, J; Henderson, V; Roberson, E; DeCarli, C; LaFerla, F; Brewer, J; Swerdlow, R; Van Eldik, L; Hamilton-Nelson, K; Paulson, H; Naj, A; Lopez, O; Chui, H; Crane, P; Grabowski, T; Kukull, W; Asthana, S; Craft, S; Strittmatter, S; Cruchaga, C; Leverenz, J; Goate, A; Kamboh, MI; St George-Hyslop, P; Valladares, O; Kuzma, A; Cantwell, L; Riemenschneider, M; Morris, J; Slifer, S; Dalmasso, C; Castillo, A; Küçükali, F; Peters, O; Schneider, A; Dichgans, M; Rujescu, D; Scherbaum, N; Deckert, J; Riedel-Heller, S; Hausner, L; Molina-Porcel, L; Düzel, E; Grimmer, T; Wiltfang, J; Heilmann-Heimbach, S; Moebus, S; Tegos, T; Scarmeas, N; Dols-Icardo, O; Moreno, F; Pérez-Tur, J; Bullido, MJ; Pastor, P; Sánchez-Valle, R; Alvarez, V; Boada, M; García-González, P; Puerta, R; Mir, P; Real, LM; Piñol-Ripoll, G; García-Alberca, JM; Royo, JL; Rodriguez-Rodriguez, E; Soininen, H; de Mendonça, A; Mehrabian, S; Traykov, L; Hort, J; Vyhnalek, M; Thomassen, JQ; Pijnenburg, YAL; Holstege, H; van Swieten, J; Ramakers, I; Verhey, F; Scheltens, P; Graff, C; Papenberg, G; Giedraitis, V; Boland, A; Deleuze, JF; Nicolas, G; Dufouil, C; Pasquier, F; Hanon, O; Debette, S; Grünblatt, E; Popp, J; Ghidoni, R; Galimberti, D; Arosio, B; Mecocci, P; Solfrizzi, V; Parnetti, L; Squassina, A; Tremolizzo, L; Borroni, B; Nacmias, B; Spallazzi, M; Seripa, D; Rainero, I; Daniele, A; Bossù, P; Masullo, C; Rossi, G; Jessen, F; Fernandez, V; Kehoe, PG; Frikke-Schmidt, R; Tsolaki, M; Sánchez-Juan, P; Sleegers, K; Ingelsson, M; Haines, J; Farrer, L; Mayeux, R; Wang, LS; Sims, R; DeStefano, A; Schellenberg, GD; Seshadri, S; Amouyel, P; Williams, J; van der Flier, W; Ramirez, A; Pericak-Vance, M; Andreassen, OA; Van Duijn, C; Hiltunen, M; Ruiz, A; Dupuis, J; Martin, E; Lambert, JC; Kunkle, B; Bellenguez, C | Publicado 2024 |
Herramientas de búsqueda:
Materias Relacionadas
genetics
genome-wide association study
human
Article
Genome-Wide Association Study
Humans
genetic risk
genetic risk score
ischemic stroke
ABO gene
ALIGATOR
Alzheimer Disease
Alzheimer disease
Alzheimer's disease
Brain Ischemia
Cholesterol metabolism
Cognitive Dysfunction
Data collection
Dementia
Drug Discovery
Endocytosis
Genetic Predisposition to Disease
Immune response
Ischemic Stroke
Neurodegeneration
Pathway analysis
Polymorphism, Single Nucleotide
Stroke
Ubiquitination
Weighted gene co-expression network analysis