Cholesterol-lowering effect of spreads enriched with microcrystalline plant sterols in hypercholesterolemic subjects von CHRISTIANSEN, L. I, LÄHTEENMÄKI, P. L. A, MANNELIN, M. R, SEPPÄNEN-LAAKSO, T. E, HILTUNEN, R. V. K, YLIRUUSI, J. K

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Features of intracranial hemorrhage in cerebral venous thrombosis von Afifi, K., Bellanger, G., Buyck, P. J., Zuurbier, S. M., Esperon, C. G., Barboza, M. A., Costa, P., Escudero, I., Renard, D., Lemmens, R., Hinteregger, N., Fazekas, F., Conde, J. Jimenez, Giralt-Steinhauer, E., Hiltunen, S., Arauz, A., Pezzini, A., Montaner, J., Putaala, J., Weimar, C., Schlamann, Marc, Gattringer, T., Tatlisumak, T., Coutinho, J. M., Demaerel, P., Thijs, V.

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Loss-of-function variants in ABCA7 confer risk of Alzheimer's disease von Steinberg, Stacy, Stefansson, Hreinn, Jonsson, Thorlakur, Johannsdottir, Hrefna, Ingason, Andres, Helgason, Hannes, Sulem, Patrick, Magnusson, Olafur Th, Gudjonsson, Sigurjon A, Unnsteinsdottir, Unnur, Kong, Augustine, Helisalmi, Seppo, Soininen, Hilkka, Lah, James J, Aarsland, Dag, Fladby, Tormod, Ulstein, Ingun D, Djurovic, Srdjan, Sando, Sigrid B, White, Linda R, Knudsen, Gun-Peggy, Westlye, Lars T, Selbæk, Geir, Giegling, Ina, Hampel, Harald, Hiltunen, Mikko, Levey, Allan I, Andreassen, Ole A, Rujescu, Dan, Jonsson, Palmi V, Bjornsson, Sigurbjorn, Snaedal, Jon, Stefansson, Kari

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Protein kinase C -activating isophthalate derivatives mitigate Alzheimer's disease-related cellular alterations von Sarajärvi, T., Jäntti, M., Paldanius, K.M.A., Natunen, T., Wu, J.C., Mäkinen, P., Tarvainen, I., Tuominen, R.K., Talman, V., Hiltunen, M.

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A genomic mutational constraint map using variation in 76,156 human genomes von Chen, Siwei, Francioli, Laurent C., Goodrich, Julia K., Collins, Ryan L., Kanai, Masahiro, Wang, Qingbo, Alföldi, Jessica, Watts, Nicholas A., Vittal, Christopher, Gauthier, Laura D., Poterba, Timothy, Wilson, Michael W., Tarasova, Yekaterina, Phu, William, Grant, Riley, Yohannes, Mary T., Koenig, Zan, Farjoun, Yossi, Banks, Eric, Donnelly, Stacey, Gabriel, Stacey, Gupta, Namrata, Ferriera, Steven, Tolonen, Charlotte, Novod, Sam, Bergelson, Louis, Roazen, David, Ruano-Rubio, Valentin, Covarrubias, Miguel, Llanwarne, Christopher, Petrillo, Nikelle, Wade, Gordon, Jeandet, Thibault, Munshi, Ruchi, Tibbetts, Kathleen, O’Donnell-Luria, Anne, Solomonson, Matthew, Seed, Cotton, Martin, Alicia R., Talkowski, Michael E., Rehm, Heidi L., Daly, Mark J., Tiao, Grace, Neale, Benjamin M., MacArthur, Daniel G., Karczewski, Konrad J.

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FinnGen provides genetic insights from a well-phenotyped isolated population von Kurki, Mitja I., Karjalainen, Juha, Palta, Priit, Sipilä, Timo P., Donner, Kati M., Reeve, Mary P., Laivuori, Hannele, Kaunisto, Mari A., Loukola, Anu, Lahtela, Elisa, Mattsson, Hannele, Laiho, Päivi, Della Briotta Parolo, Pietro, Lehisto, Arto A., Kanai, Masahiro, Mars, Nina, Heyne, Henrike O., Veerapen, Kumar, Rüeger, Sina, Lemmelä, Susanna, Zhou, Wei, Ruotsalainen, Sanni, Pärn, Kalle, Hiekkalinna, Tero, Koskelainen, Sami, Llorens, Vincent, Gracia-Tabuenca, Javier, Siirtola, Harri, Reis, Kadri, Elnahas, Abdelrahman G., Aalto-Setälä, Katriina, Biswas, Shameek, Dada, Oluwaseun A., Ding, Zhihao, Ehm, Margaret G., Eklund, Kari, Färkkilä, Martti, Finucane, Hilary, Ganna, Andrea, Ghazal, Awaisa, Hakanen, Antti, Hu, Xinli, Hunkapiller, Julie, Jacob, Howard, Jensen, Jan-Nygaard, Joensuu, Heikki, John, Sally, Junttila, Juhani, Kähönen, Mika, Kallio, Lila, Kaprio, Jaakko, Kettunen, Johannes, Kilpeläinen, Elina, Kosma, Veli-Matti, Kuopio, Teijo, Laisk, Triin, Laukkanen, Jari, Liu, Aoxing, Mägi, Reedik, Mäkitie, Antti, Malarstig, Anders, Maranville, Joseph, Niemi, Mari E. K., Niemi, Marianna, Obeidat, Ma´en, Okafo, George, Palomäki, Antti, Palotie, Tuula, Pitkäranta, Anne, Pulford, David, Raghavan, Neha, Rahimov, Fedik, Riley-Gillis, Bridget, Rodosthenous, Rodosthenis, Salminen, Eveliina, Salomaa, Veikko, Schleutker, Johanna, Serpi, Raisa, Shen, Huei-yi, Siegel, Richard, Sul, Jae Hoon, Tachmazidou, Ioanna, Tienari, Pentti, Tukiainen, Taru, Vaura, Felix, Virolainen, Petri, Waring, Jeffrey, Waterworth, Dawn, Yang, Robert, Nelis, Mari, Metspalu, Andres, Milani, Lili, Fox, Caroline, Havulinna, Aki S., Perola, Markus, Jalanko, Anu, Plenge, Robert, Runz, Heiko, Daly, Mark J., Palotie, Aarno

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A structural variation reference for medical and population genetics von Collins, Ryan L., Brand, Harrison, Karczewski, Konrad J., Zhao, Xuefang, Alföldi, Jessica, Francioli, Laurent C., Khera, Amit V., Lowther, Chelsea, Gauthier, Laura D., Wang, Harold, Watts, Nicholas A., Solomonson, Matthew, O’Donnell-Luria, Anne, Baumann, Alexander, Munshi, Ruchi, Walker, Mark, Whelan, Christopher W., Huang, Yongqing, Brookings, Ted, Sharpe, Ted, Stone, Matthew R., Valkanas, Elise, Fu, Jack, Tiao, Grace, Laricchia, Kristen M., Ruano-Rubio, Valentin, Stevens, Christine, Gupta, Namrata, Cusick, Caroline, Margolin, Lauren, Taylor, Kent D., Lin, Henry J., Rich, Stephen S., Post, Wendy S., Chen, Yii-Der Ida, Rotter, Jerome I., Nusbaum, Chad, Philippakis, Anthony, Lander, Eric, Gabriel, Stacey, Neale, Benjamin M., Kathiresan, Sekar, Daly, Mark J., Banks, Eric, MacArthur, Daniel G., Talkowski, Michael E.

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Frequency of Thrombocytopenia and Platelet Factor 4/Heparin Antibodies in Patients With Cerebral Venous Sinus Thrombosis Prior to the COVID-19 Pandemic von Sánchez van Kammen, Mayte, Heldner, Mirjam R, Brodard, Justine, Scutelnic, Adrian, Silvis, Suzanne, Schroeder, Verena, Kremer Hovinga, Johanna A, Middeldorp, Saskia, Levi, Marcel, Hiltunen, Sini, Lindgren, Erik, Mansour, Maryam, Arauz, Antonio, Barboza, Miguel A, Zuurbier, Susanna M, Aguiar de Sousa, Diana, Ferro, Jose M, Fischer, Urs, Field, Thalia S, Jood, Katarina, Tatlisumak, Turgut, Putaala, Jukka, Arnold, Marcel, Coutinho, Jonathan M

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A scoring tool to predict mortality and dependency after cerebral venous thrombosis von Lindgren, Erik, Krzywicka, Katarzyna, de Winter, Maria A., Sánchez Van Kammen, Mayte, Heldner, Mirjam R., Hiltunen, Sini, Aguiar de Sousa, Diana, Mansour, Maryam, Canhão, Patrícia, Ekizoğlu, Esme, Rodrigues, Miguel, Martins Silva, Elisa, Garcia‐Esperon, Carlos, Arnao, Valentina, Aridon, Paolo, Simaan, Naaem Moin, Silvis, Suzanne M., Zuurbier, Susanna M., Scutelnic, Adrian, Sezgin, Mine, Alasheev, Andrey Marisovich, Smolkin, Andrey, Guisado‐Alonso, Daniel, Yesilot, Nilufer, Barboza, Miguel, Ghiasian, Masoud, Leker, Ronen R., Arauz, Antonio, Arnold, Marcel, Putaala, Jukka, Tatlisumak, Turgut, Coutinho, Jonathan M., Jood, Katarina

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Immunogenicity of subcutaneous TNF inhibitors and its clinical significance in real-life setting in patients with spondyloarthritis von Hiltunen, J., Parmanne, P., Sokka, T., Lamberg, T., Isomäki, P., Kaipiainen-Seppänen, O., Peltomaa, R., Uutela, T., Pirilä, L., Taimen, K., Kauppi, M. J., Yli-Kerttula, T., Tuompo, R., Relas, H., Kortelainen, S., Paalanen, K., Asikainen, J., Ekman, P., Santisteban, A., Vidqvist, K.-L., Tadesse, K., Romu, M., Borodina, J., Elfving, P., Valleala, H., Leirisalo-Repo, M., Rantalaiho, V., Kautiainen, H., Jokiranta, T. S., Eklund, K. K.

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Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals von Whiffin, Nicola, Karczewski, Konrad J., Zhang, Xiaolei, Chothani, Sonia, Smith, Miriam J., Evans, D. Gareth, Roberts, Angharad M., Quaife, Nicholas M., Schafer, Sebastian, Rackham, Owen, Alföldi, Jessica, O’Donnell-Luria, Anne H., Francioli, Laurent C., Cook, Stuart A., Barton, Paul J. R., MacArthur, Daniel G., Ware, James S.

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TET2 and CSMD1 genes affect SBP response to hydrochlorothiazide in never-treated essential hypertensives von Chittani, Martina, Zaninello, Roberta, Lanzani, Chiara, Frau, Francesca, Ortu, Maria F, Salvi, Erika, Fresu, Giovanni, Citterio, Lorena, Braga, Daniele, Piras, Daniela A, Carpini, Simona Delli, Velayutham, Dinesh, Simonini, Marco, Argiolas, Giuseppe, Pozzoli, Simona, Troffa, Chiara, Glorioso, Valeria, Kontula, Kimmo K, Hiltunen, Timo P, Donner, Kati M, Turner, Stephen T, Boerwinkle, Eric, Chapman, Arlene B, Padmanabhan, Sandosh, Dominiczak, Anna F, Melander, Olle, Johnson, Julie A, Cooper-Dehoff, Rhonda M, Gong, Yan, Rivera, Natalia V, Condorelli, Gianluigi, Trimarco, Bruno, Manunta, Paolo, Cusi, Daniele, Glorioso, Nicola, Barlassina, Cristina

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Chromosomal Region 11p14.1 is Associated with Pharmacokinetics and Pharmacodynamics of Bisoprolol von Fontana, Vanessa, Turner, Richard Myles, Francis, Ben, Yin, Peng, Pütz, Benno, Hiltunen, Timo P, Ruotsalainen, Sanni, Kontula, Kimmo K, Müller-Myhsok, Bertam, Pirmohamed, Munir

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Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease von Lambert, J-C, Grenier-Boley, B, Harold, D, Zelenika, D, Chouraki, V, Kamatani, Y, Sleegers, K, Ikram, M A, Hiltunen, M, Reitz, C, Mateo, I, Feulner, T, Bullido, M, Galimberti, D, Concari, L, Alvarez, V, Sims, R, Gerrish, A, Chapman, J, Deniz-Naranjo, C, Solfrizzi, V, Sorbi, S, Arosio, B, Spalletta, G, Siciliano, G, Epelbaum, J, Hannequin, D, Dartigues, J-F, Tzourio, C, Berr, C, Schrijvers, E M C, Rogers, R, Tosto, G, Pasquier, F, Bettens, K, Van Cauwenberghe, C, Fratiglioni, L, Graff, C, Delepine, M, Ferri, R, Reynolds, C A, Lannfelt, L, Ingelsson, M, Prince, J A, Chillotti, C, Pilotto, A, Seripa, D, Boland, A, Mancuso, M, Bossù, P, Annoni, G, Nacmias, B, Bosco, P, Panza, F, Sanchez-Garcia, F, Del Zompo, M, Coto, E, Owen, M, O'Donovan, M, Valdivieso, F, Caffara, P, Scarpini, E, Combarros, O, Buée, L, Campion, D, Soininen, H, Breteler, M, Riemenschneider, M, Van Broeckhoven, C, Alpérovitch, A, Lathrop, M, Trégouët, D-A, Williams, J, Amouyel, P

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Genetic associations between modifiable risk factors and Alzheimer disease von Luo, Jiao, Thomassen, Jesper Qvist, Bellenguez, Céline, Grenier-Boley, Benjamin, de Rojas, Itziar, Castillo, Atahualpa, Parveen, Kayenat, Küçükali, Fahri, Nicolas, Aude, Peters, Oliver, Schneider, Anja, Dichgans, Martin, Rujescu, Dan, Scherbaum, Norbert, Jürgen, Deckert, Riedel-Heller, Steffi, Hausner, Lucrezia, Porcel, Laura Molina, Düzel, Emrah, Grimmer, Timo, Wiltfang, Jens, Heilmann-Heimbach, Stefanie, Moebus, Susanne, Tegos, Thomas, Scarmeas, Nikolaos, Clarimon, Jordi, Moreno, Fermin, Pérez-Tur, Jordi, Bullido, María J., Pastor, Pau, Sánchez-Valle, Raquel, Álvarez, Victoria, Boada, Mercè, García-González, Pablo, Puerta, Raquel, Mir, Pablo, Real, Luis M., Piñol-Ripoll, Gerard, García-Alberca, Jose María, Royo, Jose Luís, Rodriguez-Rodriguez, Eloy, Soininen, Hilkka, Kuulasmaa, Teemu, de Mendonça, Alexandre, Mehrabian, Shima, Hort, Jakub, Vyhnalek, Martin, van der Lee, Sven, Graff, Caroline, Papenberg, Goran, Giedraitis, Vilmantas, Boland, Anne, Bacq-Daian, Delphine, Deleuze, Jean-François, Nicolas, Gael, Dufouil, Carole, Pasquier, Florence, Hanon, Olivier, Debette, Stéphanie, Grünblatt, Edna, Popp, Julius, Benussi, Luisa, Galimberti, Daniela, Arosio, Beatrice, Mecocci, Patrizia, Solfrizzi, Vincenzo, Parnetti, Lucilla, Squassina, Alessio, Tremolizzo, Lucio, Borroni, Barbara, Nacmias, Benedetta, Sorbi, Sandro, Caffarra, Paolo, Seripa, Davide, Rainero, Innocenzo, Daniele, Antonio, Masullo, Carlo, Spalletta, Gianfranco, Williams, Julie, Amouyel, Philippe, Jessen, Frank, Kehoe, Patrick, Magda, Tsolaki, Rossi, Giacomina, Sánchez-Juan, Pascual, Sleegers, Kristel, Ingelsson, Martin, Andreassen, Ole A., Hiltunen, Mikko, Van Duijn, Cornelia, Sims, Rebecca, van der Flier, Wiesje, Ruiz, Agustín, Ramirez, Alfredo, Lambert, Jean-Charles, Frikke-Schmidt, Ruth

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Aphasia, Depression, and Non-Verbal Cognitive Impairment in Ischaemic Stroke von Kauhanen, M.-L., Korpelainen, J.T., Hiltunen, P., Määttä, R., Mononen, H., Brusin, E., Sotaniemi, K.A., Myllylä, V.V.

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Correction to: Features of intracranial hemorrhage in cerebral venous thrombosis von Afifi, K., Bellanger, G., Buyck, P. J., Zuurbier, S. M., Garcia-Esperon, C., Barboza, M. A., Costa, P., Escudero, I., Renard, D., Lemmens, R., Hinteregger, N., Fazekas, F., Jimenez-Conde, J., Giralt-Steinhauer, E., Hiltunen, S., Arauz, A., Pezzini, A., Montaner, J., Putaala, J., Weimar, C., Schlamann, Marc, Gattringer, T., Tatlisumak, T., Coutinho, J. M., Demaerel, P., Thijs, V.

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Poststroke depression correlates with cognitive impairment and neurological deficits von KAUHANEN, M.-L, KORPELAINEN, J. T, HILTUNEN, P, BRUSIN, E, MONONEN, H, MÄÄTTÄ, R, NIEMINEN, P, SOTANIEMI, K. A, MYLLYLÄ, V. V

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FinnGen provides genetic insights from a well-phenotyped isolated population (vol 613, pg 508, 2023) von Kurki, MI, Karjalainen, J, Palta, P, Sipila, TP, Kristiansson, K, Donner, KM, Reeve, MP, Laivuori, H, Aavikko, M, Kaunisto, MA

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Elevated hyaluronan concentration without hyaluronidase activation in malignant epithelial ovarian tumors von HILTUNEN, Essi L. J, ANTTILA, Maarit, KOSMA, Veli-Matti, KULTTI, Anne, ROPPONEN, Kirsi, PENTTINEN, Jorma, YLISKOSKI, Merja, KURONEN, Arja T, JUHOLA, Matti, TAMMI, Raija, TAMMI, Markku

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