Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 50 Records) |
Query Trace: PLCG2[original query] |
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Examination of the Effect of Rare Variants in TREM2, ABI3, and PLCG2 in LOAD Through Multiple Phenotypes. Journal of Alzheimer's disease : JAD 2020 Sep . Olive Claudia, Ibanez Laura, Farias Fabiana H Geraldo, Wang Fengxian, Budde John P, Norton Joanne B, Gentsch Jen, Morris John C, Li Zeran, Dube Umber, Del-Aguila Jorge, Bergmann Kristy, Bradley Joseph, Benitez Bruno A, Harari Oscar, Fagan Anne, Ances Beau, Cruchaga Carlos, Fernandez Maria Victor |
Novel genetic variants in genes of the Fc gamma receptor-mediated phagocytosis pathway predict non-small cell lung cancer survival. Translational lung cancer research 2020 Jun 9 (3): 575-586. Qian Danwen, Liu Hongliang, Zhao Lingling, Wang Xiaomeng, Luo Sheng, Moorman Patricia G, Patz Edward F, Su Li, Shen Sipeng, Christiani David C, Wei Qing |
Admixture mapping of asthma in southwestern Europeans with North African ancestry influences. American journal of physiology. Lung cellular and molecular physiology 2020 3 318 (5): L965-L975. Guillen-Guio Beatriz, Hernández-Beeftink Tamara, Marcelino-Rodríguez Itahisa, Rodríguez-Pérez Héctor, Lorenzo-Salazar Jose M, Espinilla-Peña Marta, Corrales Almudena, Pino-Yanes Maria, Callero Ariel, Perez-Rodriguez Eva, Villar Jesús, González-Montelongo Rafaela, Flores Carl |
PLCG2 protective variant p.P522R modulates tau pathology and disease progression in patients with mild cognitive impairment. Acta neuropathologica 2020 3 139 (6): 1025-1044. Kleineidam Luca, Chouraki Vincent, Próchnicki Tomasz, van der Lee Sven J, Madrid-Márquez Laura, Wagner-Thelen Holger, Karaca Ilker, Weinhold Leonie, Wolfsgruber Steffen, Boland Anne, Martino Adami Pamela V, Lewczuk Piotr, Popp Julius, Brosseron Frederic, Jansen Iris E, Hulsman Marc, Kornhuber Johannes, Peters Oliver, Berr Claudine, Heun Reinhard, Frölich Lutz, Tzourio Christophe, Dartigues Jean-François, Hüll Michael, Espinosa Ana, Hernández Isabel, de Rojas Itziar, Orellana Adelina, Valero Sergi, Stringa Najada, van Schoor Natasja M, Huisman Martijn, Scheltens Philip, , Rüther Eckart, Deleuze Jean-Francois, Wiltfang Jens, Tarraga Lluis, Schmid Matthias, Scherer Martin, Riedel-Heller Steffi, Heneka Michael T, Amouyel Philippe, Jessen Frank, Boada Merce, Maier Wolfgang, Schneider Anja, González-Pérez Antonio, van der Flier Wiesje M, Wagner Michael, Lambert Jean-Charles, Holstege Henne, Sáez Mª Eugenia, Latz Eicke, Ruiz Agustin, Ramirez Alfre |
Prediction of Outcome in Patients With Chronic Lymphocytic Leukemia Treated With Ibrutinib: Development and Validation of a Four-Factor Prognostic Model. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2020 10 39 (6): 576-585. Ahn Inhye E, Tian Xin, Ipe David, Cheng Mei, Albitar Maher, Tsao L Claire, Zhang Lei, Ma Wanlong, Herman Sarah E M, Gaglione Erika M, Soto Susan, Dean James P, Wiestner Adri |
Protective Variants in Alzheimer's Disease. Current genetic medicine reports 2020 10 7 (1): 1-12. Andrews Shea J, Fulton-Howard Brian, Goate Alis |
Association of ABI3 and PLCG2 missense variants with disease risk and neuropathology in Lewy body disease and progressive supranuclear palsy. Acta neuropathologica communications 2020 Oct 8 (1): 172. Strickland Samantha L, Morel Hélène, Prusinski Christian, Allen Mariet, Patel Tulsi A, Carrasquillo Minerva M, Conway Olivia J, Lincoln Sarah J, Reddy Joseph S, Nguyen Thuy, Malphrus Kimberly G, Soto Alexandra I, Walton Ronald L, Crook Julia E, Murray Melissa E, Boeve Bradley F, Petersen Ronald C, Lucas John A, Ferman Tanis J, Uitti Ryan J, Wszolek Zbigniew K, Ross Owen A, Graff-Radford Neill R, Dickson Dennis W, Ertekin-Taner Nilüf |
Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity. Acta neuropathologica 2020 1 139 (5): 959-962. 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 F M, 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 N M, Alcolea Daniel, Wiendl Heinz, Strickland Samantha L, Pastor Pau, Rodríguez Rodríguez Eloy, , , , , , , Boeve Bradley F, Petersen Ronald C, Ferman Tanis J, van Gerpen Jay A, Reinders Marcel J T, 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 A L, Scheltens Philip, Gasser Thomas, Chinnery Patrick F, Hemmer Bernhard, Huisman Martijn A, Troncoso Juan, Moreno Fermin, Nohr Ellen A, Sørensen Thorkild I A, Heutink Peter, Sánchez-Juan Pascual, Posthuma Danielle, , Clarimón Jordi, Christensen Kaare, Ertekin-Taner Nilüfer, Scholz Sonja W, Ramirez Alfredo, Ruiz Agustín, Slagboom Eline, van der Flier Wiesje M, Holstege Hen |
Novel Alzheimer risk genes determine the microglia response to amyloid-ß but not to TAU pathology. EMBO molecular medicine 2020 Jan e10606. Sierksma Annerieke, Lu Ashley, Mancuso Renzo, Fattorelli Nicola, Thrupp Nicola, Salta Evgenia, Zoco Jesus, Blum David, Buée Luc, De Strooper Bart, Fiers Ma |
Circulating tumor DNA for comprehensive noninvasive monitoring of lymphoma treated with ibrutinib plus nivolumab. Blood advances 2021 9 5 (22): 4674-4685. Bruscaggin Alessio, di Bergamo Lodovico Terzi, Spina Valeria, Hodkinson Brendan, Forestieri Gabriela, Bonfiglio Ferdinando, Condoluci Adalgisa, Wu Wei, Pirosa Maria C, Faderl Martin R, Koch Ricardo, Schaffer Michael, Alvarez John D, Fourneau Nele, Gerber Bernhard, Stussi Georg, Zucca Emanuele, Balasubramanian Sriram, Rossi Davi |
Common variants in Alzheimer's disease and risk stratification by polygenic risk scores.
Nature communications 2021 6 12 (1): 3417. de Rojas Itziar, Moreno-Grau Sonia, Tesi Niccolo, Grenier-Boley Benjamin, Andrade Victor, Jansen Iris E, Pedersen Nancy L, Stringa Najada, Zettergren Anna, Hernández Isabel, Montrreal Laura, Antúnez Carmen, Antonell Anna, Tankard Rick M, Bis Joshua C, 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 C, Lemstra Afina W, Benaque Alba, Pérez-Cordón Alba, Benussi Alberto, Rábano Alberto, Padovani Alessandro, Squassina Alessio, de Mendonça Alexandre, Arias Pastor Alfonso, Kok Almar A L, Meggy Alun, Pastor Ana Belén, Espinosa Ana, Corma-Gómez Anaïs, Martín Montes Angel, Sanabria Ángela, DeStefano Anita L, Schneider Anja, Haapasalo Annakaisa, Kinhult Ståhlbom Anne, Tybjærg-Hansen Anne, Hartmann Annette M, Spottke Annika, Corbatón-Anchuelo Arturo, Rongve Arvid, Borroni Barbara, Arosio Beatrice, Nacmias Benedetta, Nordestgaard Børge G, Kunkle Brian W, Charbonnier Camille, Abdelnour Carla, Masullo Carlo, Martínez Rodríguez Carmen, Muñoz-Fernandez Carmen, Dufouil Carole, Graff Caroline, Ferreira Catarina B, Chillotti Caterina, Reynolds Chandra A, Fenoglio Chiara, Van Broeckhoven Christine, Clark Christopher, Pisanu Claudia, Satizabal Claudia L, 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, Duron Emmanuelle, Boerwinkle Eric, Ferri Evelyn, Tagliavini Fabrizio, Küçükali Fahri, Pasquier Florence, Sanchez-Garcia Florentino, Mangialasche Francesca, Jessen Frank, Nicolas Gaël, Selbæk Geir, Ortega Gemma, Chêne Geneviève, Hadjigeorgiou Georgios, Rossi Giacomina, Spalletta Gianfranco, Giaccone Giorgio, Grande Giulia, Binetti Giuliano, Papenberg Goran, Hampel Harald, Bailly Henri, Zetterberg Henrik, Soininen Hilkka, Karlsson Ida K, Alvarez Ignacio, Appollonio Ildebrando, Giegling Ina, Skoog Ingmar, Saltvedt Ingvild, Rainero Innocenzo, Rosas Allende Irene, Hort Jakub, Diehl-Schmid Janine, Van Dongen Jasper, Vidal Jean-Sebastien, Lehtisalo Jenni, Wiltfang Jens, Thomassen Jesper Qvist, Kornhuber Johannes, Haines Jonathan L, Vogelgsang Jonathan, Pineda Juan A, Fortea Juan, Popp Julius, Deckert Jürgen, Buerger Katharina, Morgan Kevin, Fließbach Klaus, Sleegers Kristel, Molina-Porcel Laura, Kilander Lena, Weinhold Leonie, Farrer Lindsay A, Wang Li-San, Kleineidam Luca, Farotti Lucia, Parnetti Lucilla, Tremolizzo Lucio, Hausner Lucrezia, Benussi Luisa, Froelich Lutz, Ikram M Arfan, Deniz-Naranjo M Candida, Tsolaki Magda, Rosende-Roca Maitée, Löwenmark Malin, Hulsman Marc, Spallazzi Marco, Pericak-Vance Margaret A, Esiri Margaret, Bernal Sánchez-Arjona María, Dalmasso Maria Carolina, Martínez-Larrad María Teresa, Arcaro Marina, Nöthen Markus M, Fernández-Fuertes Marta, Dichgans Martin, Ingelsson Martin, Herrmann Martin J, Scherer Martin, Vyhnalek Martin, Kosmidis Mary H, Yannakoulia Mary, Schmid Matthias, Ewers Michael, Heneka Michael T, Wagner Michael, Scamosci Michela, Kivipelto Miia, Hiltunen Mikko, Zulaica Miren, Alegret Montserrat, Fornage Myriam, Roberto Natalia, van Schoor Natasja M, Seidu Nazib M, Banaj Nerisa, Armstrong Nicola J, Scarmeas Nikolaos, Scherbaum Norbert, Goldhardt Oliver, Hanon Oliver, Peters Oliver, Skrobot Olivia Anna, Quenez Olivier, Lerch Ondrej, Bossù Paola, Caffarra Paolo, Dionigi Rossi Paolo, Sakka Paraskevi, Mecocci Patrizia, Hoffmann Per, Holmans Peter A, Fischer Peter, Riederer Peter, Yang Qiong, Marshall Rachel, Kalaria Rajesh N, Mayeux Richard, Vandenberghe Rik, Cecchetti Roberta, Ghidoni Roberta, Frikke-Schmidt Ruth, Sorbi Sandro, Hägg Sara, Engelborghs Sebastiaan, Helisalmi Seppo, Botne Sando Sigrid, Kern Silke, Archetti Silvana, Boschi Silvia, Fostinelli Silvia, Gil Silvia, Mendoza Silvia, Mead Simon, Ciccone Simona, Djurovic Srdjan, Heilmann-Heimbach Stefanie, Riedel-Heller Steffi, Kuulasmaa Teemu, Del Ser Teodoro, Lebouvier Thibaud, Polak Thomas, Ngandu Tiia, Grimmer Timo, Bessi Valentina, Escott-Price Valentina, Giedraitis Vilmantas, Deramecourt Vincent, Maier Wolfgang, Jian Xueqiu, Pijnenburg Yolande A L, , , , , , Kehoe Patrick Gavin, Garcia-Ribas Guillermo, Sánchez-Juan Pascual, Pastor Pau, Pérez-Tur Jordi, Piñol-Ripoll Gerard, Lopez de Munain Adolfo, García-Alberca Jose María, Bullido María J, Álvarez Victoria, Lleó Alberto, Real Luis M, Mir Pablo, Medina Miguel, Scheltens Philip, Holstege Henne, Marquié Marta, Sáez María Eugenia, Carracedo Ángel, Amouyel Philippe, Schellenberg Gerard D, Williams Julie, Seshadri Sudha, van Duijn Cornelia M, Mather Karen A, Sánchez-Valle Raquel, Serrano-Ríos Manuel, Orellana Adelina, Tárraga Lluís, Blennow Kaj, Huisman Martijn, Andreassen Ole A, Posthuma Danielle, Clarimón Jordi, Boada Mercè, van der Flier Wiesje M, Ramirez Alfredo, Lambert Jean-Charles, van der Lee Sven J, Ruiz Agust |
The impact of rare and low-frequency genetic variants in common variable immunodeficiency (CVID). Scientific reports 2021 Apr 11 (1): 8308. Bisgin Atil, Sonmezler Ozge, Boga Ibrahim, Yilmaz Musta |
PLCG2 rs72824905 Variant Reduces the Risk of Alzheimer's Disease and Multiple Sclerosis. Journal of Alzheimer's disease : JAD 2021 Jan . Chen Fan, Zhang Yan, Wang Longcai, Wang Tao, Han Zhifa, Zhang Haihua, Gao Shan, Hu Yang, Liu Guiy |
Genome-wide association study of liver enzyme elevation in an extended cohort of rheumatoid arthritis patients starting low-dose methotrexate.
Pharmacogenomics 2022 9 23 (15): 813-820. Cavalli Marco, Eriksson Niclas, Sundbaum Johanna Karlsson, Wallenberg Matilda, Kohnke Hugo, Baecklund Eva, Hallberg Pär, Wadelius M |
Identification of variants in genes associated with autoinflammatory disorders in a cohort of patients with psoriatic arthritis. RMD open 2022 9 8 (2): . Atschekzei Faranaz, Dubrowinskaja Natalia, Anim Manfred, Thiele Thea, Witte Torsten, Sogkas Georgi |
Structural Variation Detection and Association Analysis of Whole-Genome-Sequence Data from 16,905 Alzheimer's Diseases Sequencing Project Subjects. medRxiv : the preprint server for health sciences 2023 9 . Hui Wang, Beth A Dombroski, Po-Liang Cheng, Albert Tucci, Ya-Qin Si, John J Farrell, Jung-Ying Tzeng, Yuk Yee Leung, John S Malamon, , Li-San Wang, Badri N Vardarajan, Lindsay A Farrer, Gerard D Schellenberg, Wan-Ping L |
Genetic variants of phospholipase C-?2 alter the phenotype and function of microglia and confer differential risk for Alzheimer's disease. Immunity 2023 9 . Andy P Tsai, Chuanpeng Dong, Peter Bor-Chian Lin, Adrian L Oblak, Gonzalo Viana Di Prisco, Nian Wang, Nicole Hajicek, Adam J Carr, Emma K Lendy, Oliver Hahn, Micaiah Atkins, Aulden G Foltz, Jheel Patel, Guixiang Xu, Miguel Moutinho, John Sondek, Qisheng Zhang, Andrew D Mesecar, Yunlong Liu, Brady K Atwood, Tony Wyss-Coray, Kwangsik Nho, Stephanie J Bissel, Bruce T Lamb, Gary E Landre |
Genetic drivers in the natural history of chronic lymphocytic leukemia development as early as 16 years before diagnosis. Blood 2023 7 . P Martijn Kolijn, Florentin Späth, Mouhamad Khouja, Paul J Hengeveld, Lina Van Der Straten, Nikos Darzentas, Magnus Hultdin, James McKay, Christiane Pott, Roel C H Vermeulen, Anton W Langer |
B-cell receptor pathway mutations are infrequent in patients with chronic lymphocytic leukemia on continuous ibrutinib therapy. Clinical cancer research : an official journal of the American Association for Cancer Research 2023 6 . Jennifer A Woyach, Paolo Ghia, John C Byrd, Inhye E Ahn, Carol Moreno, Susan M O'Brien, Daniel Jones, Leo W K Cheung, Elizabeth Chong, Kevin Kwei, James P Dean, Danelle F James, Adrian Wiestn |
CD49d Expression Identifies a Biologically Distinct Subtype of Chronic Lymphocytic Leukemia with Inferior Progression-Free Survival on BTK Inhibitor Therapy. Clinical cancer research : an official journal of the American Association for Cancer Research 2023 5 OF1-OF10. Anfal Alsadhan, Jonathan Chen, Erika M Gaglione, Chingiz Underbayev, Pamela L Tuma, Xin Tian, Lita A Freeman, Sivasubramanian Baskar, Pia Nierman, Susan Soto, Andy Itsara, Inhye E Ahn, Clare Sun, Elena Bibikova, Tanja Nicole Hartmann, Maissa Mhibik, Adrian Wiestn |
Carriers of the p.P522R variant in PLC?2 have a slightly more responsive immune system. Molecular neurodegeneration 2023 4 18 (1): 25. Annieck M Diks, Cristina Teodosio, Bas de Mooij, Rick J Groenland, Brigitta A E Naber, Inge F de Laat, Sandra A Vloemans, Susan Rohde, Marien I de Jonge, Linda Lorenz, Debbie Horsten, Jacques J M van Dongen, Magdalena A Berkowska, Henne Holste |
Molecular associations of response to the new generation BTK inhibitor zanubrutinib in marginal zone lymphoma. Blood advances 2023 3 . Tatarczuch Maciej, Waltham Mark, Shortt Jake, Polekhina Galina, Hawkes Eliza A, Ho Shir-Jing, Trotman Judith, Brasacchio Daniella, Co Melannie, Li Jessica, Ramakrishnan Vanitha, Dunne Karin, Opat Stephen S, Gregory Gareth |
A rare case of PLCG2-associated antibody deficiency and immune dysregulation associated with a synonymous variant in PLCG2 gene. Rheumatology (Oxford, England) 2023 2 . Wu Na, Wu Di, Shen M |
Clinical and immunological features of an APLAID patient caused by a novel mutation in PLCG2. Frontiers in immunology 2023 2 14 1014150. Peng Qi, Luo Dong, Yang Yi, Zhu Yinghua, Luo Qingming, Chen Huan, Chen Dapeng, Zhou Zhongjun, Lu Xiaom |
Absence of BTK, BCL2, and PLCG2 Mutations in Chronic Lymphocytic Leukemia Relapsing after First-Line Treatment with Fixed-Duration Ibrutinib plus Venetoclax. Clinical cancer research : an official journal of the American Association for Cancer Research 2023 11 OF1-OF8. Nitin Jain, Lisa J Croner, John N Allan, Tanya Siddiqi, Alessandra Tedeschi, Xavier C Badoux, Karl Eckert, Leo W K Cheung, Anwesha Mukherjee, James P Dean, Edith Szafer-Glusman, John F Seymo |
Structural Variation Detection and Association Analysis of Whole-Genome-Sequence Data from 16,905 Alzheimer's Diseases Sequencing Project Subjects. Research square 2023 10 . Wan-Ping Lee, Hui Wang, Beth Dombroski, Po-Liang Cheng, Albert Tucci, Ya-Qin Si, John Farrell, Jung-Ying Tzeng, Yuk Yee Leung, John Malamon, Li-San Wang, Badri Vardarajan, Lindsay Farrer, Gerard Schellenberg, The Alzheimer's Disease Sequencing Project The Alzheimer's D Proje |
Genome-wide Association Study of Methotrexate-Induced Liver Injury in Rheumatoid Arthritis Patients.
Clinical pharmacology and therapeutics 2023 1 . Eektimmerman Frank, Swen Jesse J, den Broeder Alfons A, Hazes Johanna M W, Kurreeman Fina S, Verstappen Suzanne M M, Nair Nisha, Pawlik Andrzej, Nurmohamed Mike T, Dolžan Vita, Böhringer Stefan, Allaart Cornelia F, Guchelaar Henk-J |
BTK and PLCG2 remain unmutated in one third of patients with CLL relapsing on ibrutinib. Blood advances 2023 1 . Bonfiglio Silvia, Sutton Lesley-Ann, Ljungström Viktor, Capasso Antonella, Pandzic Tatjana, Weström Simone, Foroughi-Asl Hassan, Skaftason Aron, Gellerbring Anna, Lyander Anna, Gandini Francesca, Gaidano Gianluca, Trentin Livio, Bonello Lisa, Reda Gianluigi, Bödör Csaba, Stavroyianni Niki, Tam Constantine S, Marasca Roberto, Forconi Francesco, Panayiotidis Panayiotis, Ringshausen Ingo, Jaksic Ozren, Frustaci Anna Maria, Iyengar Sunil, Coscia Marta, Mulligan Stephen P, Ysebaert Loïc, Strugov Vladimir, Pavlovsky Carolina, Walewska Renata, Österborg Anders, Cortese Diego, Ranghetti Pamela, Baliakas Panagiotis, Stamatopoulos Kostas, Scarfò Lydia, Rosenquist Richard, Ghia Pao |
In vivo validation of late-onset Alzheimer's disease genetic risk factors. Alzheimer's & dementia : the journal of the Alzheimer's Association 2024 4 . Michael Sasner, Christoph Preuss, Ravi S Pandey, Asli Uyar, Dylan Garceau, Kevin P Kotredes, Harriet Williams, Adrian L Oblak, Peter Bor-Chian Lin, Bridget Perkins, Disha Soni, Cindy Ingraham, Audrey Lee-Gosselin, Bruce T Lamb, Gareth R Howell, Gregory W Cart |
Cognitively healthy centenarians are genetically protected against Alzheimer's disease. Alzheimer's & dementia : the journal of the Alzheimer's Association 2024 4 . Niccolo' Tesi, Sven van der Lee, Marc Hulsman, Natasja M van Schoor, Martijn Huisman, Yolande Pijnenburg, Wiesje M van der Flier, Marcel Reinders, Henne Holste |
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