Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Reinders, Marcel JT."'
Autor:
Holstege, Henne, Hulsman, Marc, Charbonnier, Camille, Grenier-Boley, Benjamin, Quenez, Olivier, Grozeva, Detelina, van Rooij, Jeroen GJ, Sims, Rebecca, Ahmad, Shahzad, Amin, Najaf, Norsworthy, Penny J, Dols-Icardo, Oriol, Hummerich, Holger, Kawalia, Amit, Amouyel, Philippe, Beecham, Gary W, Berr, Claudine, Bis, Joshua C, Boland, Anne, Bossù, Paola, Bouwman, Femke, Bras, Jose, Campion, Dominique, Cochran, J Nicholas, Daniele, Antonio, Dartigues, Jean-François, Debette, Stéphanie, Deleuze, Jean-François, Denning, Nicola, DeStefano, Anita L, Farrer, Lindsay A, Fernández, Maria Victoria, Fox, Nick C, Galimberti, Daniela, Genin, Emmanuelle, Gille, Johan JP, Le Guen, Yann, Guerreiro, Rita, Haines, Jonathan L, Holmes, Clive, Ikram, M Arfan, Ikram, M Kamran, Jansen, Iris E, Kraaij, Robert, Lathrop, Marc, Lemstra, Afina W, Lleó, Alberto, Luckcuck, Lauren, Mannens, Marcel MAM, Marshall, Rachel, Martin, Eden R, Masullo, Carlo, Mayeux, Richard, Mecocci, Patrizia, Meggy, Alun, Mol, Merel O, Morgan, Kevin, Myers, Richard M, Nacmias, Benedetta, Naj, Adam C, Napolioni, Valerio, Pasquier, Florence, Pastor, Pau, Pericak-Vance, Margaret A, Raybould, Rachel, Redon, Richard, Reinders, Marcel JT, Richard, Anne-Claire, Riedel-Heller, Steffi G, Rivadeneira, Fernando, Rousseau, Stéphane, Ryan, Natalie S, Saad, Salha, Sanchez-Juan, Pascual, Schellenberg, Gerard D, Scheltens, Philip, Schott, Jonathan M, Seripa, Davide, Seshadri, Sudha, Sie, Daoud, Sistermans, Erik A, Sorbi, Sandro, van Spaendonk, Resie, Spalletta, Gianfranco, Tesi, Niccolo', Tijms, Betty, Uitterlinden, André G, van der Lee, Sven J, Visser, Pieter Jelle, Wagner, Michael, Wallon, David, Wang, Li-San, Zarea, Aline, Clarimon, Jordi, van Swieten, John C, Greicius, Michael D, Yokoyama, Jennifer S, Cruchaga, Carlos, Hardy, John, Ramirez, Alfredo
Publikováno v:
Nature genetics, vol 54, iss 12
Alzheimer's disease (AD), the leading cause of dementia, has an estimated heritability of approximately 70%1. The genetic component of AD has been mainly assessed using genome-wide association studies, which do not capture the risk contributed by rar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::1abd5a69368c55be34fac65f3d72306d
https://escholarship.org/uc/item/3cr7x044
https://escholarship.org/uc/item/3cr7x044
Autor:
Mateus, Pedro, Yu, Jing, Garst, Swier J.F., Harms, Alexander G.J., Cats, Davy, Delgado, Inigo Bermejo, Roshchupkin, Gennady V., Reinders, Marcel JT, Slagboom, Eline, Mei, Haillang, Bron, Esther E
Publikováno v:
Alzheimer's & Dementia: The Journal of the Alzheimer's Association; Dec2023 Supplement 16, Vol. 19, p1-3, 3p
Autor:
Tesi, Niccoló, Van Der Lee, Sven J, Hulsman, Marc, van Schoor, Natasja, Huisman, Martijn, Pijnenburg, Yolande A. L., Flier, Wiesje M., Reinders, Marcel JT, Holstege, Henne
Publikováno v:
Alzheimer's & Dementia: The Journal of the Alzheimer's Association; Dec2023 Supplement 12, Vol. 19, p1-3, 3p
Autor:
Lee, Sven J, Hulsman, Marc, van Spaendonk, Rosalina M.L., Schaar, Jetske, Dijkstra, Janna I.R., van der Flier, Wiesje M., Elting, Mariet, Reinders, Marcel JT, Rojas, Itziar, Haelst, Mieke M., Geus, Christa, Pijnenburg, Yolande A.L., Holstege, Henne
Publikováno v:
Alzheimer's & Dementia: The Journal of the Alzheimer's Association; Dec2023 Supplement 12, Vol. 19, p1-3, 3p
Autor:
Tesi, Niccoló, van der Lee, Sven J., Hulsman, Marc, Jansen, Iris E., Stringa, Najada, van Schoor, Natasja, Huisman, Martijn, Scheltens, Philip, Reinders, Marcel Jt, van der Flier, Wiesje M., Holstege, Henne
Publikováno v:
Alzheimer's & dementia : the journal of the Alzheimer's Association, 17. Elsevier
Tesi, N, van der Lee, S J, Hulsman, M, Jansen, I E, Stringa, N, van Schoor, N, Huisman, M, Scheltens, P, Reinders, M J, van der Flier, W M & Holstege, H 2021, ' Pathway-specific polygenic risk score of AD-associated genetic variants associated with AD risk, resilience against AD, and progression to AD ', Alzheimer's & dementia : the journal of the Alzheimer's Association, vol. 17, pp. e053500 . https://doi.org/10.1002/alz.053500
Tesi, N, van der Lee, S J, Hulsman, M, Jansen, I E, Stringa, N, van Schoor, N, Huisman, M, Scheltens, P, Reinders, M J, van der Flier, W M & Holstege, H 2021, ' Pathway-specific polygenic risk score of AD-associated genetic variants associated with AD risk, resilience against AD, and progression to AD ', Alzheimer's & dementia : the journal of the Alzheimer's Association, vol. 17, pp. e053500 . https://doi.org/10.1002/alz.053500
BACKGROUND: Several collaborative genome-wide-association studies (GWAS) have characterized the genetic landscape of Alzheimer's disease (AD), which now counts >70 single-nucleotide polymorphisms (SNPs) associated with AD-risk. METHOD: We linked thes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::98e036c75e13fbe07d1fab00b01df334
https://research.vumc.nl/en/publications/142eb876-03c5-4923-ad22-b89d93a51d79
https://research.vumc.nl/en/publications/142eb876-03c5-4923-ad22-b89d93a51d79
Autor:
van der Lee, Sven J, Conway, Olivia J, Jansen, Iris, Carrasquillo, Minerva M, Kleineidam, Luca, van den Akker, Erik, Hernández, Isabel, van Eijk, Kristel R, Stringa, Najada, Chen, Jason A, Zettergren, Anna, Andlauer, Till FM, Diez-Fairen, Monica, Simon-Sanchez, Javier, Lleó, Alberto, Zetterberg, Henrik, Nygaard, Marianne, Blauwendraat, Cornelis, Savage, Jeanne E, Mengel-From, Jonas, Moreno-Grau, Sonia, Wagner, Michael, Fortea, Juan, Keogh, Michael J, Blennow, Kaj, Skoog, Ingmar, Friese, Manuel A, Pletnikova, Olga, Zulaica, Miren, Lage, Carmen, de Rojas, Itziar, Riedel-Heller, Steffi, Illán-Gala, Ignacio, Wei, Wei, Jeune, Bernard, Orellana, Adelina, Then Bergh, Florian, Wang, Xue, Hulsman, Marc, Beker, Nina, Tesi, Niccolo, Morris, Christopher M, Indakoetxea, Begoña, Collij, Lyduine E, Scherer, Martin, Morenas-Rodríguez, Estrella, Ironside, James W, van Berckel, Bart NM, Alcolea, Daniel, Wiendl, Heinz, Strickland, Samantha L, Pastor, Pau, Rodríguez Rodríguez, Eloy, DESGESCO (Dementia Genetics Spanish Consortium), EADB (Alzheimer Disease European DNA biobank), IFGC (International FTD-Genomics Consortium), IPDGC (The International Parkinson Disease Genomics Consortium), RiMod-FTD (Risk and Modifying factors in Fronto-Temporal Dementia), Netherlands Brain Bank (NBB), Boeve, Bradley F, Petersen, Ronald C, Ferman, Tanis J, van Gerpen, Jay A, Reinders, Marcel JT, Uitti, Ryan J, Tárraga, Lluís, Maier, Wolfgang, Dols-Icardo, Oriol, Kawalia, Amit, Dalmasso, Maria Carolina, Boada, Mercè, Zettl, Uwe K, van Schoor, Natasja M, Beekman, Marian, Allen, Mariet, Masliah, Eliezer, de Munain, Adolfo López, Pantelyat, Alexander, Wszolek, Zbigniew K, Ross, Owen A, Dickson, Dennis W, Graff-Radford, Neill R, Knopman, David, Rademakers, Rosa, Lemstra, Afina W, Pijnenburg, Yolande AL, Scheltens, Philip, Gasser, Thomas, Chinnery, Patrick F, Hemmer, Bernhard, Huisman, Martijn A, Troncoso, Juan, Moreno, Fermin, Nohr, Ellen A, Sørensen, Thorkild IA, Heutink, Peter, Sánchez-Juan, Pascual, Posthuma, Danielle, GIFT (Genetic Investigation in Frontotemporal Dementia and Alzheimer’s Disease) Study Group, Clarimón, Jordi
Publikováno v:
Acta neuropathologica, vol 139, iss 5
The IPDGC (The International Parkinson Disease Genomics Consortium) and EADB (Alzheimer Disease European DNA biobank) are listed correctly as an author to the article, however, they were incorrectly listed more than once.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::536b60ada64dc674c865651bccb4d7fe
https://escholarship.org/uc/item/6np4j59k
https://escholarship.org/uc/item/6np4j59k
Publikováno v:
BMC Bioinformatics, Vol 10, Iss Suppl 1, p S20 (2009)
Abstract Background Tumors have been hypothesized to be the result of a mixture of oncogenic events, some of which will be reflected in the gene expression of the tumor. Based on this hypothesis a variety of data-driven methods have been employed to
Externí odkaz:
https://doaj.org/article/ba6e821e51514a3ea7f1568922314063
Autor:
van der Lee, Sven J, Conway, Olivia J, Jansen, Iris, Carrasquillo, Minerva M, Kleineidam, Luca, van den Akker, Erik, Hernández, Isabel, van Eijk, Kristel R, Stringa, Najada, Chen, Jason A, Zettergren, Anna, Andlauer, Till FM, Diez-Fairen, Monica, Simon-Sanchez, Javier, Lleó, Alberto, Zetterberg, Henrik, Nygaard, Marianne, Blauwendraat, Cornelis, Savage, Jeanne E, Mengel-From, Jonas, Moreno-Grau, Sonia, Wagner, Michael, Fortea, Juan, Keogh, Michael J, Blennow, Kaj, Skoog, Ingmar, Friese, Manuel A, Pletnikova, Olga, Zulaica, Miren, Lage, Carmen, de Rojas, Itziar, Riedel-Heller, Steffi, Illán-Gala, Ignacio, Wei, Wei, Jeune, Bernard, Orellana, Adelina, Then Bergh, Florian, Wang, Xue, Hulsman, Marc, Beker, Nina, Tesi, Niccolo, Morris, Christopher M, Indakoetxea, Begoña, Collij, Lyduine E, Scherer, Martin, Morenas-Rodríguez, Estrella, Ironside, James W, van Berckel, Bart NM, Alcolea, Daniel, Wiendl, Heinz, Strickland, Samantha L, Pastor, Pau, Rodríguez Rodríguez, Eloy, DESGESCO (Dementia Genetics Spanish Consortium), EADB (Alzheimer Disease European DNA biobank), EADB (Alzheimer Disease European DNA biobank), IFGC (International FTD-Genomics Consortium), IPDGC (The International Parkinson Disease Genomics Consortium), IPDGC (The International Parkinson Disease Genomics Consortium), RiMod-FTD (Risk and Modifying factors in Fronto-Temporal Dementia), Netherlands Brain Bank (NBB), Boeve, Bradley F, Petersen, Ronald C, Ferman, Tanis J, van Gerpen, Jay A, Reinders, Marcel JT, Uitti, Ryan J, Tárraga, Lluís, Maier, Wolfgang, Dols-Icardo, Oriol, Kawalia, Amit, Dalmasso, Maria Carolina, Boada, Mercè, Zettl, Uwe K, van Schoor, Natasja M, Beekman, Marian, Allen, Mariet, Masliah, Eliezer, de Munain, Adolfo López, Pantelyat, Alexander, Wszolek, Zbigniew K, Ross, Owen A, Dickson, Dennis W, Graff-Radford, Neill R, Knopman, David, Rademakers, Rosa, Lemstra, Afina W, Pijnenburg, Yolande AL, Scheltens, Philip, Gasser, Thomas, Chinnery, Patrick F, Hemmer, Bernhard, Huisman, Martijn A, Troncoso, Juan, Moreno, Fermin, Nohr, Ellen A, Sørensen, Thorkild IA, Heutink, Peter, Sánchez-Juan, Pascual, Posthuma, Danielle, GIFT (Genetic Investigation in Frontotemporal Dementia and Alzheimer’s Disease) Study Group, Clarimón, Jordi
Publikováno v:
Acta neuropathologica, vol 138, iss 2
The genetic variant rs72824905-G (minor allele) in the PLCG2 gene was previously associated with a reduced Alzheimer's disease risk (AD). The role of PLCG2 in immune system signaling suggests it may also protect against other neurodegenerative diseas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::188a8e462cd4ec522b2223498c42ecdb
https://escholarship.org/uc/item/4w15z00t
https://escholarship.org/uc/item/4w15z00t
Autor:
Nijkamp Jurgen F, van den Broek Marcel, Datema Erwin, de Kok Stefan, Bosman Lizanne, Luttik Marijke A, Daran-Lapujade Pascale, Vongsangnak Wanwipa, Nielsen Jens, Heijne Wilbert HM, Klaassen Paul, Paddon Chris J, Platt Darren, Kötter Peter, van Ham Roeland C, Reinders Marcel JT, Pronk Jack T, de Ridder Dick, Daran Jean-Marc
Publikováno v:
Microbial Cell Factories, Vol 11, Iss 1, p 36 (2012)
Abstract Saccharomyces cerevisiae CEN.PK 113-7D is widely used for metabolic engineering and systems biology research in industry and academia. We sequenced, assembled, annotated and analyzed its genome. Single-nucleotide variations (SNV), insertions
Externí odkaz:
https://doaj.org/article/ecaf5fd426dc4ccd8a2f5c8bf6b3ac9f
Autor:
Reinders Marcel JT, Holstege Henne, Velds Arno, Klijn Christiaan, de Ronde Jorma J, Jonkers Jos, Wessels Lodewyk FA
Publikováno v:
BMC Research Notes, Vol 3, Iss 1, p 298 (2010)
Abstract Background Most approaches used to find recurrent or differential DNA Copy Number Alterations (CNA) in array Comparative Genomic Hybridization (aCGH) data from groups of tumour samples depend on the discretization of the aCGH data to gain, l
Externí odkaz:
https://doaj.org/article/84a2ae6ea94647b587fadba0cfc246c8