Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Pentti, J."'
Autor:
Chia, Ruth, Sabir, Marya S, Bandres-Ciga, Sara, Saez-Atienzar, Sara, Reynolds, Regina H, Gustavsson, Emil, Walton, Ronald L, Ahmed, Sarah, Viollet, Coralie, Ding, Jinhui, Makarious, Mary B, Diez-Fairen, Monica, Portley, Makayla K, Shah, Zalak, Abramzon, Yevgeniya, Hernandez, Dena G, Blauwendraat, Cornelis, Stone, David J, Eicher, John, Parkkinen, Laura, Ansorge, Olaf, Clark, Lorraine, Honig, Lawrence S, Marder, Karen, Lemstra, Afina, St George-Hyslop, Peter, Londos, Elisabet, Morgan, Kevin, Lashley, Tammaryn, Warner, Thomas T, Jaunmuktane, Zane, Galasko, Douglas, Santana, Isabel, Tienari, Pentti J, Myllykangas, Liisa, Oinas, Minna, Cairns, Nigel J, Morris, John C, Halliday, Glenda M, Van Deerlin, Vivianna M, Trojanowski, John Q, Grassano, Maurizio, Calvo, Andrea, Mora, Gabriele, Canosa, Antonio, Floris, Gianluca, Bohannan, Ryan C, Brett, Francesca, Gan-Or, Ziv, Geiger, Joshua T, Moore, Anni, May, Patrick, Krüger, Rejko, Goldstein, David S, Lopez, Grisel, Tayebi, Nahid, Sidransky, Ellen, American Genome Center, Norcliffe-Kaufmann, Lucy, Palma, Jose-Alberto, Kaufmann, Horacio, Shakkottai, Vikram G, Perkins, Matthew, Newell, Kathy L, Gasser, Thomas, Schulte, Claudia, Landi, Francesco, Salvi, Erika, Cusi, Daniele, Masliah, Eliezer, Kim, Ronald C, Caraway, Chad A, Monuki, Edwin S, Brunetti, Maura, Dawson, Ted M, Rosenthal, Liana S, Albert, Marilyn S, Pletnikova, Olga, Troncoso, Juan C, Flanagan, Margaret E, Mao, Qinwen, Bigio, Eileen H, Rodríguez-Rodríguez, Eloy, Infante, Jon, Lage, Carmen, González-Aramburu, Isabel, Sanchez-Juan, Pascual, Ghetti, Bernardino, Keith, Julia, Black, Sandra E, Masellis, Mario, Rogaeva, Ekaterina, Duyckaerts, Charles, Brice, Alexis, Lesage, Suzanne, Xiromerisiou, Georgia, Barrett, Matthew J, Tilley, Bension S, Gentleman, Steve, Logroscino, Giancarlo
Publikováno v:
Nature genetics, vol 53, iss 3
The genetic basis of Lewy body dementia (LBD) is not well understood. Here, we performed whole-genome sequencing in large cohorts of LBD cases and neurologically healthy controls to study the genetic architecture of this understudied form of dementia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::52b7fec594d16d516b448c15f88d94c6
https://escholarship.org/uc/item/7qn6v913
https://escholarship.org/uc/item/7qn6v913
Autor:
Savola, Sara, Kaivola, Karri, Raunio, Anna, Kero, Mia, Mäkelä, Mira, Pärn, Kalle, Palta, Priit, Tanskanen, Maarit, Tuimala, Jarno, Polvikoski, Tuomo, Tienari, Pentti J., Paetau, Anders, Myllykangas, Liisa
Publikováno v:
Neuropathology & Applied Neurobiology; Apr2022, Vol. 48 Issue 3, p1-12, 12p
Autor:
Rostalski, Hannah, Korhonen, Ville, Kuulasmaa, Teemu, Solje, Eino, Krüger, Johanna, Gen, Finn, Kaivola, Karri, Eide, Per Kristian, Lambert, Jean-Charles, Julkunen, Valtteri, Tienari, Pentti J., Remes, Anne M., Leinonen, Ville, Hiltunen, Mikko, Haapasalo, Annakaisa
Publikováno v:
Journal of Alzheimer's Disease; 2021, Vol. 83 Issue 3, p1325-1332, 8p
Akademický článek
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Akademický článek
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Autor:
Pentti J. Tienari, Timo E. Strandberg
Publikováno v:
Alzheimer'sdementia : the journal of the Alzheimer's Association. 15(7)
Autor:
Johan G. Eriksson, Jari Lahti, Pentti J. Tienari, Ville Rantalainen, Katri Räikkönen, Eero Kajantie
Publikováno v:
Neurobiology of Aging
We tested if the ε4 major isoform of the APOE gene and rs405509 and rs440446 promoter and intron-1 polymorphisms predicted risk of any dementia or Alzheimer’s disease with diagnoses derived from the Hospital Discharge and Causes of Death Registers
Autor:
Kaivola, K. (Karri), Kiviharju, A. (Anna), Jansson, L. (Lilja), Rantalainen, V. (Ville), Eriksson, J. G. (Johan G.), Strandberg, T. E. (Timo E.), Laaksovirta, H. (Hannu), Renton, A. E. (Alan E.), Traynor, B. J. (Bryan J.), Myllykangas, L. (Liisa), Tienari, P. J. (Pentti J.)
The hexanucleotide repeat expansion in C9orf72 is a common cause of amyotrophic lateral sclerosis/frontotemporal dementia and also rarely found in other psychiatric and neurodegenerative conditions. Alleles with >30 repeats are often considered an ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2423::4d3821d955d7f2ef55bf7183f660d224
http://urn.fi/urn:nbn:fi-fe202002104962
http://urn.fi/urn:nbn:fi-fe202002104962
Autor:
Anna Kiviharju, Pentti J. Tienari, Johan G. Eriksson, Ville Rantalainen, Timo E. Strandberg, Lilja Jansson, Alan E. Renton, Liisa Myllykangas, Hannu Laaksovirta, Karri Kaivola, Bryan J. Traynor
Publikováno v:
Neurobiol Aging
The hexanucleotide repeat expansion in C9orf72 is a common cause of amyotrophic lateral sclerosis/frontotemporal dementia and also rarely found in other psychiatric and neurodegenerative conditions. Alleles with >30 repeats are often considered an ex
Publikováno v:
Annals of Neurology
Objective To investigate whether midlife atherosclerosis is associated with different dementia subtypes and related underlying pathologies. Methods Participants comprised the cardiovascular cohort of the Swedish prospective population‐based Malmö