Extended genetic analysis and tumor characteristics in over 4600 women with suspected hereditary breast and ovarian cancer
Öfverholm, Anna, Törngren, Therese, Rosén, Anna, Arver, Brita, Einbeigi, Zakaria, Haraldsson, Karin, Ståhlbom, Anne Kinhult, Kuchinskaya, Ekaterina, Lindblom, Annika, Melin, Beatrice, Paulsson-Karlsson, Ylva, Stenmark-Askmalm, Marie, Tham, Emma, von Wachenfeldt, Anna, Kvist, Anders, Borg, Åke, Ehrencrona, Hans
Published in BMC cancer (10.08.2023)
Published in BMC cancer (10.08.2023)
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Whole-body MRI within a surveillance program for carriers with clinically actionable germline TP53 variants - the Swedish constitutional TP53 study SWEP53
Omran, Meis, Blomqvist, Lennart, Brandberg, Yvonne, Pal, Niklas, Kogner, Per, Ståhlbom, Anne Kinhult, Tham, Emma, Bajalica-Lagercrantz, Svetlana
Published in Hereditary cancer in clinical practice (13.01.2020)
Published in Hereditary cancer in clinical practice (13.01.2020)
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Reduced penetrance of the PSEN1 H163Y autosomal dominant Alzheimer mutation: a 22-year follow-up study
Thordardottir, Steinunn, Rodriguez-Vieitez, Elena, Almkvist, Ove, Ferreira, Daniel, Saint-Aubert, Laure, Kinhult-Ståhlbom, Anne, Thonberg, Håkan, Schöll, Michael, Westman, Eric, Wall, Anders, Eriksdotter, Maria, Zetterberg, Henrik, Blennow, Kaj, Nordberg, Agneta, Graff, Caroline
Published in Alzheimer's research & therapy (10.05.2018)
Published in Alzheimer's research & therapy (10.05.2018)
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Preclinical cerebrospinal fluid and volumetric magnetic resonance imaging biomarkers in Swedish familial Alzheimer's disease
Thordardottir, Steinunn, Ståhlbom, Anne Kinhult, Ferreira, Daniel, Almkvist, Ove, Westman, Eric, Zetterberg, Henrik, Eriksdotter, Maria, Blennow, Kaj, Graff, Caroline
Published in Journal of Alzheimer's disease (01.01.2015)
Published in Journal of Alzheimer's disease (01.01.2015)
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The effects of different familial Alzheimer's disease mutations on APP processing in vivo
Thordardottir, Steinunn, Kinhult Ståhlbom, Anne, Almkvist, Ove, Thonberg, Håkan, Eriksdotter, Maria, Zetterberg, Henrik, Blennow, Kaj, Graff, Caroline
Published in Alzheimer's research & therapy (16.02.2017)
Published in Alzheimer's research & therapy (16.02.2017)
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Prospective blinded surveillance screening of Swedish women with increased hereditary risk of breast cancer
Liljegren, Annelie, von Wachenfeldt, Anna, Azavedo, Edward, Eloranta, Sandra, Grundström, Helene, Ståhlbom, Anne Kinhult, Sundbom, Ann, Sundén, Per, Svane, Gunilla, Ulitzsch, Dieter, Arver, Brita
Published in Breast cancer research and treatment (01.04.2018)
Published in Breast cancer research and treatment (01.04.2018)
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The Effects of Gene Mutations on Default Mode Network in Familial Alzheimer's Disease
Li, Xiaozhen, Westman, Eric, Thordardottir, Steinunn, Ståhlbom, Anne Kinhult, Almkvist, Ove, Blennow, Kaj, Wahlund, Lars-Olof, Graff, Caroline
Published in Journal of Alzheimer's disease (01.01.2017)
Published in Journal of Alzheimer's disease (01.01.2017)
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Predicting Cognitive Decline across Four Decades in Mutation Carriers and Non-carriers in Autosomal-Dominant Alzheimer’s Disease
Almkvist, Ove, Rodriguez-Vieitez, Elena, Thordardottir, Steinunn, Amberla, Kaarina, Axelman, Karin, Basun, Hans, Kinhult-Ståhlbom, Anne, Lilius, Lena, Remes, Anne, Wahlund, Lars-Olof, Viitanen, Matti, Lannfelt, Lars, Graff, Caroline
Published in Journal of the International Neuropsychological Society (01.03.2017)
Published in Journal of the International Neuropsychological Society (01.03.2017)
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Presymptomatic cognitive and neuroanatomical changes in genetic frontotemporal dementia in the Genetic Frontotemporal dementia Initiative (GENFI) study: a cross-sectional analysis
Rohrer, Jonathan D, PhD, Nicholas, Jennifer M, PhD, Cash, David M, PhD, van Swieten, John, Prof, Dopper, Elise, MD, Jiskoot, Lize, MSc, van Minkelen, Rick, PhD, Rombouts, Serge A, Prof, Cardoso, M Jorge, PhD, Clegg, Shona, BSc, Espak, Miklos, PhD, Mead, Simon, PhD, Thomas, David L, PhD, De Vita, Enrico, PhD, Masellis, Mario, MD, Black, Sandra E, Prof, Freedman, Morris, Prof, Keren, Ron, MD, MacIntosh, Bradley J, PhD, Rogaeva, Ekaterina, PhD, Tang-Wai, David, MD, Tartaglia, Maria Carmela, MD, Laforce, Robert, MD, Tagliavini, Fabrizio, MD, Tiraboschi, Pietro, MD, Redaelli, Veronica, MD, Prioni, Sara, MSc, Grisoli, Marina, MD, Borroni, Barbara, MD, Padovani, Alessandro, Prof, Galimberti, Daniela, PhD, Scarpini, Elio, MD, Arighi, Andrea, MD, Fumagalli, Giorgio, MD, Rowe, James B, PhD, Coyle-Gilchrist, Ian, MB, Graff, Caroline, Prof, Fallström, Marie, MSc, Jelic, Vesna, MD, Ståhlbom, Anne Kinhult, PhD, Andersson, Christin, PhD, Thonberg, Håkan, PhD, Lilius, Lena, BSc, Frisoni, Giovanni B, Prof, Binetti, Giuliano, Pievani, Michela, PhD, Bocchetta, Martina, MSc, Benussi, Luisa, PhD, Ghidoni, Roberta, PhD, Finger, Elizabeth, MD, Sorbi, Sandro, Prof, Nacmias, Benedetta, PhD, Lombardi, Gemma, MD, Polito, Cristina, PhD, Warren, Jason D, Prof, Ourselin, Sebastien, Prof, Fox, Nick C, Prof, Rossor, Martin N, Prof
Published in Lancet neurology (01.03.2015)
Published in Lancet neurology (01.03.2015)
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Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores
de Rojas, Itziar, Moreno-Grau, Sonia, Tesi, Niccolo, Grenier-Boley, Benjamin, Andrade, Victor, Jansen, Iris, Pedersen, Nancy, Stringa, Najada, Zettergren, Anna, Hernández, Isabel, Montrreal, Laura, Antúnez, Carmen, Antonell, Anna, Tankard, Rick, Bis, Joshua, Sims, Rebecca, Bellenguez, Céline, Quintela, Inés, González-Perez, Antonio, Calero, Miguel, Franco-Macías, Emilio, Macías, Juan, Blesa, Rafael, Cervera-Carles, Laura, Menéndez-González, Manuel, Frank-García, Ana, Royo, Jose Luís, Moreno, Fermin, Huerto Vilas, Raquel, Baquero, Miquel, Diez-Fairen, Mónica, Lage, Carmen, García-Madrona, Sebastián, García-González, Pablo, Alarcón-Martín, Emilio, Valero, Sergi, Sotolongo-Grau, Oscar, Ullgren, Abbe, Naj, Adam, Lemstra, Afina, Benaque, Alba, Pérez-Cordón, Alba, Benussi, Alberto, Rábano, Alberto, Padovani, Alessandro, Squassina, Alessio, de Mendonça, Alexandre, Arias Pastor, Alfonso, Kok, Almar, Meggy, Alun, Pastor, Ana Belén, Espinosa, Ana, Corma-Gómez, Anaïs, Martín Montes, Angel, Sanabria, Ángela, Destefano, Anita, Schneider, Anja, Haapasalo, Annakaisa, Kinhult Ståhlbom, Anne, Tybjærg-Hansen, Anne, Hartmann, Annette, Spottke, Annika, Corbatón-Anchuelo, Arturo, Rongve, Arvid, Borroni, Barbara, Arosio, Beatrice, Nacmias, Benedetta, Nordestgaard, Børge, Kunkle, Brian, Charbonnier, Camille, Abdelnour, Carla, Masullo, Carlo, Martínez Rodríguez, Carmen, Muñoz-Fernandez, Carmen, Dufouil, Carole, Graff, Caroline, Ferreira, Catarina, Chillotti, Caterina, Reynolds, Chandra, Fenoglio, Chiara, van Broeckhoven, Christine, Clark, Christopher, Pisanu, Claudia, Satizabal, Claudia, Holmes, Clive, Buiza-Rueda, Dolores, Aarsland, Dag, Rujescu, Dan, Alcolea, Daniel, Galimberti, Daniela, Wallon, David, Seripa, Davide, Grünblatt, Edna, Dardiotis, Efthimios, Düzel, Emrah, Scarpini, Elio, Conti, Elisa, Rubino, Elisa, Gelpi, Ellen, Rodriguez-Rodriguez, Eloy
Published in Nature communications (01.12.2021)
Published in Nature communications (01.12.2021)
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GENOTYPE-DEPENDENT LONGITUDINAL TRAJECTORIES OF COGNITIVE DECLINE IN AUTOSOMAL DOMINANT ALZHEIMER’S DISEASE
Almkvist, Ove, Rodriguez-Vieitez, Elena, Thordardottir, Steinunn, Ståhlbom, Anne Kinhult, Viitanen, Matti, Lannfelt, Lars, Graff, Caroline
Published in Alzheimer's & dementia (01.07.2017)
Published in Alzheimer's & dementia (01.07.2017)
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The effects of gene mutations on the cerebrospinal fluid levels of soluble amyloid precursor proteins in familial Alzheimer's disease
Thordardottir, Steinunn, Kinhult-Ståhlbom, Anne, Almkvist, Ove, Jonhagen, Maria Eriksdotter, Zetterberg, Henrik, Blennow, Kaj, Graff, Caroline
Published in Alzheimer's & dementia (01.07.2013)
Published in Alzheimer's & dementia (01.07.2013)
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P1–203: The effects of gene mutations on the cerebrospinal fluid levels of soluble amyloid precursor proteins in familial Alzheimer's disease
Thordardottir, Steinunn, Kinhult‐Ståhlbom, Anne, Almkvist, Ove, Jonhagen, Maria Eriksdotter, Zetterberg, Henrik, Blennow, Kaj, Graff, Caroline
Published in Alzheimer's & dementia (01.07.2013)
Published in Alzheimer's & dementia (01.07.2013)
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A Pan-European Study of the C9orf72 Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability, and Intermediate Repeats
van der Zee, Julie, Dillen, Lubina, Van Langenhove, Tim, Engelborghs, Sebastiaan, Philtjens, Stéphanie, Vandenbulcke, Mathieu, Sleegers, Kristel, Sieben, Anne, Bäumer, Veerle, Borroni, Barbara, Padovani, Alessandro, Archetti, Silvana, Perneczky, Robert, Diehl-Schmid, Janine, de Mendonça, Alexandre, Miltenberger-Miltenyi, Gabriel, Pimentel, José, Graff, Caroline, Chiang, Huei-Hsin, Sanchez-Valle, Raquel, Llado, Albert, Gelpi, Ellen, Santiago, Beatriz, Frisoni, Giovanni, Zanetti, Orazio, Bonvicini, Cristian, vom Hagen, Jennifer Müller, Schöls, Ludger, Heneka, Michael T., Matej, Radoslav, Parobkova, Eva, Kovacs, Gabor G., Ströbel, Thomas, Sarafov, Stayko, Tournev, Ivailo, Jordanova, Albena, Danek, Adrian, Arzberger, Thomas, Testi, Silvia, Salmon, Eric, Santens, Patrick, Cras, Patrick, Vandenberghe, Rik, De Deyn, Peter Paul, Cruts, Marc, Van Broeckhoven, Christine, van der Zee, Julie, Dillen, Lubina, Van Langenhove, Tim, Philtjens, Stéphanie, Sleegers, Kristel, Corsmit, Ellen, Cruts, Marc, Van Broeckhoven, Christine, Engelborghs, Sebastiaan, De Deyn, Peter P., Cras, Patrick, Vandenbulcke, Mathieu, Borroni, Barbara, Padovani, Alessandro, Archetti, Silvana, Maetzler, Walter, Heneka, Michael T., Jessen, Frank, Kurzwelly, Delia, Sachtleben, Carmen, Miltenberger-Miltenyi, Gabriel, Pereira, Sónia, Firmo, Clara, Pimentel, José, Llado, Albert, Antonell, Anna, Gelpi, Ellen, Kinhult Ståhlbom, Anne, Thonberg, Håkan, Nennesmo, Inger, Börjesson-Hanson, Anne, Bagnoli, Silvia, Sorbi, Sandro, Santiago, Beatriz, Helena Ribeiro, Maria, Garret, Carolina, Pires, Paula, Frisoni, Giovanni, Zanetti, Orazio, Bonvicini, Cristian, Sarafov, Stayko, Tournev, Ivailo, Jordanova, Albena, Ströbel, Thomas, Mairer, Wolfgang, Matej, Radoslav, Parobkova, Eva, Danel, Adrian, Arzberger, Thomas, Maria Fabrizi, Gian, Testi, Silvia, Ferrari, Sergio, Cavallaro, Tiziana, Salmon, Eric
Published in Human mutation (01.02.2013)
Published in Human mutation (01.02.2013)
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Author Correction: Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores
de Rojas, Itziar, Tesi, Niccolo, Zettergren, Anna, Montrreal, Laura, Antonell, Anna, Bis, Joshua C., González-Perez, Antonio, Calero, Miguel, Blesa, Rafael, Sotolongo-Grau, Oscar, Benaque, Alba, Benussi, Alberto, de Mendonça, Alexandre, Arias Pastor, Alfonso, Espinosa, Ana, Sanabria, Ángela, DeStefano, Anita L., Schneider, Anja, Haapasalo, Annakaisa, Tybjærg-Hansen, Anne, Hartmann, Annette M., Spottke, Annika, Corbatón-Anchuelo, Arturo, Arosio, Beatrice, Nacmias, Benedetta, Kunkle, Brian W., Charbonnier, Camille, Martínez Rodríguez, Carmen, Reynolds, Chandra A., Fenoglio, Chiara, Van Broeckhoven, Christine, Clark, Christopher, Buiza-Rueda, Dolores, Alcolea, Daniel, Grünblatt, Edna, Dardiotis, Efthimios, Conti, Elisa, Boerwinkle, Eric, Ferri, Evelyn, Pasquier, Florence, Mangialasche, Francesca, Hadjigeorgiou, Georgios, Spalletta, Gianfranco, Soininen, Hilkka, Rainero, Innocenzo, Hort, Jakub, Kornhuber, Johannes, Pineda, Juan A., Fortea, Juan, Popp, Julius, Buerger, Katharina, Molina-Porcel, Laura, Wang, Li-San, Farotti, Lucia, Tsolaki, Magda, Rosende-Roca, Maitée, Hulsman, Marc, Spallazzi, Marco, Bernal Sánchez-Arjona, María, Dalmasso, Maria Carolina, Fernández-Fuertes, Marta, Herrmann, Martin J., Vyhnalek, Martin, Yannakoulia, Mary, Schmid, Matthias, Armstrong, Nicola J., Skrobot, Olivia Anna, Quenez, Olivier, Bossù, Paola, Caffarra, Paolo, Dionigi Rossi, Paolo, Sakka, Paraskevi, Riederer, Peter, Kalaria, Rajesh N., Mayeux, Richard, Vandenberghe, Rik, Sorbi, Sandro, Hägg, Sara, Engelborghs, Sebastiaan, Helisalmi, Seppo, Kern, Silke, Boschi, Silvia, Fostinelli, Silvia, Gil, Silvia, Ciccone, Simona, Djurovic, Srdjan, Riedel-Heller, Steffi, Kuulasmaa, Teemu, del Ser, Teodoro, Ngandu, Tiia, García-Alberca, Jose María, Lleó, Alberto, Real, Luis M., Mir, Pablo, Scheltens, Philip, Holstege, Henne, Amouyel, Philippe, Blennow, Kaj, Andreassen, Ole A., Posthuma, Danielle
Published in Nature communications (09.02.2023)
Published in Nature communications (09.02.2023)
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