Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Andre G. Uitterlinden"'
Autor:
Thorsten Langer, Eva Clemens, Linda Broer, Lara Maier, Andre G. Uitterlinden, Andrica C. H. de Vries, Martine van Grotel, Saskia F.M. Pluijm, Harald Binder, Benjamin Mayer, Annika von dem Knesebeck, Julianne Byrne, Eline van Dulmen-den Broeder, Marco Crocco, Desiree Grabow, Peter Kaatsch, Melanie Kaiser, Claudia Spix, Line Kenborg, Jeanette Falck Winther, Catherine Rechnitzer, Henrik Hasle, Tomas Kepak, Anne-Lotte F. van der Kooi, Leontien C. Kremer, Jarmila Kruseova, Stefan Bielack, Benjamin Sorg, Stefanie Hecker-Nolting, Claudia E. Kuehni, Marc Ansari, Martin Kompis, Heleen van der Pal, Ross Parfitt, Dirk Deuster, Peter Matulat, Amelie Tillmanns, Wim J. E. Tissing, Jörn D. Beck, Susanne Elsner, Antoinette am Zehnhoff-Dinnesen, Marry M. van den Heuvel-Eibrink, Oliver Zolk, PanCareLIFE Consortium Group
Publikováno v:
European Journal of Cancer, 138, 212-224. ELSEVIER SCI LTD
Langer, T, Clemens, E, Broer, L, Maier, L, Uitterlinden, A G, de Vries, A C H, van Grotel, M, Pluijm, S F M, Binder, H, Mayer, B, von dem Knesebeck, A, Byrne, J, van Dulmen-den Broeder, E, Crocco, M, Grabow, D, Kaatsch, P, Kaiser, M, Spix, C, Kenborg, L, Winther, J F, Rechnitzer, C, Hasle, H, Kepak, T, van der Kooi, A L F, Kremer, L C, Kruseova, J, Bielack, S, Sorg, B, Hecker-Nolting, S, Kuehni, C E, Ansari, M, Kompis, M, van der Pal, H, Parfitt, R, Deuster, D, Matulat, P, Tillmanns, A, Tissing, W J E, Beck, J D, Elsner, S, am Zehnhoff-Dinnesen, A, van den Heuvel-Eibrink, M M, Zolk, O & PanCareLIFE Consortium 2020, ' Usefulness of current candidate genetic markers to identify childhood cancer patients at risk for platinum-induced ototoxicity : Results of the European PanCareLIFE cohort study ', European Journal of Cancer, vol. 138, pp. 212-224 . https://doi.org/10.1016/j.ejca.2020.07.019
European Journal of Cancer, 138, 212-224. Elsevier Limited
European Journal of Cancer, 138, 212-224. Elsevier Ltd.
European Journal of Cancer, 138, 212-224. Pergamon
European journal of cancer, Vol. 138 (2020) pp. 212-224
PanCareLIFE Consortium 2020, ' Usefulness of current candidate genetic markers to identify childhood cancer patients at risk for platinum-induced ototoxicity: Results of the European PanCareLIFE cohort study ', European Journal of Cancer, vol. 138, pp. 212-224 . https://doi.org/10.1016/j.ejca.2020.07.019
Langer, T, Clemens, E, Broer, L, Maier, L, Uitterlinden, A G, de Vries, A C H, van Grotel, M, Pluijm, S F M, Binder, H, Mayer, B, von dem Knesebeck, A, Byrne, J, van Dulmen-den Broeder, E, Crocco, M, Grabow, D, Kaatsch, P, Kaiser, M, Spix, C, Kenborg, L, Winther, J F, Rechnitzer, C, Hasle, H, Kepak, T, van der Kooi, A L F, Kremer, L C, Kruseova, J, Bielack, S, Sorg, B, Hecker-Nolting, S, Kuehni, C E, Ansari, M, Kompis, M, van der Pal, H, Parfitt, R, Deuster, D, Matulat, P, Tillmanns, A, Tissing, W J E, Beck, J D, Elsner, S, am Zehnhoff-Dinnesen, A, van den Heuvel-Eibrink, M M, Zolk, O & PanCareLIFE Consortium 2020, ' Usefulness of current candidate genetic markers to identify childhood cancer patients at risk for platinum-induced ototoxicity : Results of the European PanCareLIFE cohort study ', European Journal of Cancer, vol. 138, pp. 212-224 . https://doi.org/10.1016/j.ejca.2020.07.019
European Journal of Cancer, 138, 212-224. Elsevier Limited
European Journal of Cancer, 138, 212-224. Elsevier Ltd.
European Journal of Cancer, 138, 212-224. Pergamon
European journal of cancer, Vol. 138 (2020) pp. 212-224
PanCareLIFE Consortium 2020, ' Usefulness of current candidate genetic markers to identify childhood cancer patients at risk for platinum-induced ototoxicity: Results of the European PanCareLIFE cohort study ', European Journal of Cancer, vol. 138, pp. 212-224 . https://doi.org/10.1016/j.ejca.2020.07.019
Background Irreversible sensorineural hearing loss is a common side effect of platinum treatment with the potential to significantly impair the neurocognitive, social and educational development of childhood cancer survivors. Genetic association stud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74d8f2db88f78dbcfc6e239adea5886a
https://research.rug.nl/en/publications/3dda98e0-06d0-4a16-ad8d-a2a180e05ef0
https://research.rug.nl/en/publications/3dda98e0-06d0-4a16-ad8d-a2a180e05ef0
Autor:
Joop S.E. Laven, Eva Clemens, Thorsten Langer, L. C. M. Kremer, Andre G. Uitterlinden, Oliver Zolk, A. am Zehnhoff-Dinnesen, Carmen L. Wilson, Melissa M. Hudson, Henk Visscher, Jacqueline J. Loonen, Bruce Carleton, E. van Dulmen-den Broeder, L. Broer, Cécile M. Ronckers, S.J.C.M.M. Neggers, S.M.F. Pluijm, A.L.F. van der Kooi, Wim J. E. Tissing, M.M. van den Heuvel-Eibrink
Publikováno v:
Critical Reviews in Oncology/Hematology, 126, 154-167. Elsevier Ireland Ltd
Critical reviews in oncology, hematology
Critical Reviews in Oncology Hematology, 126, 154-167
Critical Reviews in Oncology Hematology, 126, pp. 154-167
Clemens, E, van der Kooi, A L F, Broer, L, van Dulmen-den Broeder, E, Visscher, H, Kremer, L, Tissing, W, Loonen, J, Ronckers, C M, Pluijm, S M F, Neggers, S J C M M, Zolk, O, Langer, T, Zehnhoff-Dinnesen, A A, Wilson, C L, Hudson, M M, Carleton, B, Laven, J S E, Uitterlinden, A G & van den Heuvel-Eibrink, M M 2018, ' The influence of genetic variation on late toxicities in childhood cancer survivors: A review ', Critical Reviews in Oncology/Hematology, vol. 126, pp. 154-167 . https://doi.org/10.1016/j.critrevonc.2018.04.001
Critical reviews in oncology, hematology
Critical Reviews in Oncology Hematology, 126, 154-167
Critical Reviews in Oncology Hematology, 126, pp. 154-167
Clemens, E, van der Kooi, A L F, Broer, L, van Dulmen-den Broeder, E, Visscher, H, Kremer, L, Tissing, W, Loonen, J, Ronckers, C M, Pluijm, S M F, Neggers, S J C M M, Zolk, O, Langer, T, Zehnhoff-Dinnesen, A A, Wilson, C L, Hudson, M M, Carleton, B, Laven, J S E, Uitterlinden, A G & van den Heuvel-Eibrink, M M 2018, ' The influence of genetic variation on late toxicities in childhood cancer survivors: A review ', Critical Reviews in Oncology/Hematology, vol. 126, pp. 154-167 . https://doi.org/10.1016/j.critrevonc.2018.04.001
Contains fulltext : 193305.pdf (Publisher’s version ) (Open Access) INTRODUCTION: The variability in late toxicities among childhood cancer survivors (CCS) is only partially explained by treatment and baseline patient characteristics. Inter-individ
Autor:
Isis Ricaño-Ponce, Daria V. Zhernakova, Patrick Deelen, Oscar Luo, Xingwang Li, Aaron Isaacs, Juha Karjalainen, Jennifer Di Tommaso, Zuzanna Agnieszka Borek, Maria M. Zorro, Javier Gutierrez-Achury, Andre G. Uitterlinden, Albert Hofman, Joyce van Meurs, Mihai G. Netea, Iris H. Jonkers, Sebo Withoff, Cornelia M. van Duijn, Yang Li, Yijun Ruan, Lude Franke, Cisca Wijmenga, Vinod Kumar, Bastiaan T. Heijmans, Peter A.C. 't Hoen, Rick Jansen, Dorret I. Boomsma, René Pool, Jenny van Dongen, Jouke J. Hottenga, Marleen M.J. van Greevenbroek, Coen D.A. Stehouwer, Carla J.H. van der Kallen, Casper G. Schalkwijk, Alexandra Zhernakova, Ettje F. Tigchelaar, P. Eline Slagboom, Marian Beekman, Joris Deelen, Diana van Heemst, Jan H. Veldink, Leonard H. van den Berg, Bert A. Hofman, André G. Uitterlinden, P. Mila Jhamai, Michael Verbiest, H. Eka D. Suchiman, Marijn Verkerk, Ruud van der Breggen, Jeroen van Rooij, Nico Lakenberg, Hailiang Mei, Maarten van Iterson, Michiel van Galen, Jan Bot, Peter van 't Hof, Irene Nooren, Matthijs Moed, Martijn Vermaat, René Luijk, Marc Jan Bonder, Freerk van Dijk, Wibowo Arindrarto, Szymon M. Kielbasa, Morris A. Swertz, Erik W. van Zwet
Publikováno v:
Journal of Autoimmunity, 68, 62-74. Academic Press Inc.
Journal of Autoimmunity, 68, pp. 62-74
Journal of Autoimmunity, 68, 62-74. Elsevier Science
Journal of Autoimmunity, 68, 62-74
Journal of autoimmunity
Journal of Autoimmunity, 68, 62-74. ACADEMIC PRESS LTD-ELSEVIER SCIENCE LTD
Journal of Autoimmunity, 68, 62-74. Academic Press
Ricano-Ponce, I, Zhernakova, D V, Deelen, P, Luo, O, Li, X, Isaacs, A, Karjalainen, J, Di. Tommaso, J, Borek, Z A, Zorro, M M, Gutierrez-Achury, J, Uitterlinden, A G, Hofman, A, van Meurs, J, Boomsma, D I, Pool, R, van Dongen, J, Hottenga, J J, Neteaf, M G, Jonkers, I H, Withoff, S, van Duijn, C M, Li, Y, Ruan, Y, Franke, L, Wijmenga, C & Kumar, V 2016, ' Refined mapping of autoimmune disease associated genetic variants with gene expression suggests an important role for non-coding RNAs ', Journal of Autoimmunity, vol. 68, pp. 62-74 . https://doi.org/10.1016/j.jaut.2016.01.002
Journal of Autoimmunity, 68, pp. 62-74
Journal of Autoimmunity, 68, 62-74. Elsevier Science
Journal of Autoimmunity, 68, 62-74
Journal of autoimmunity
Journal of Autoimmunity, 68, 62-74. ACADEMIC PRESS LTD-ELSEVIER SCIENCE LTD
Journal of Autoimmunity, 68, 62-74. Academic Press
Ricano-Ponce, I, Zhernakova, D V, Deelen, P, Luo, O, Li, X, Isaacs, A, Karjalainen, J, Di. Tommaso, J, Borek, Z A, Zorro, M M, Gutierrez-Achury, J, Uitterlinden, A G, Hofman, A, van Meurs, J, Boomsma, D I, Pool, R, van Dongen, J, Hottenga, J J, Neteaf, M G, Jonkers, I H, Withoff, S, van Duijn, C M, Li, Y, Ruan, Y, Franke, L, Wijmenga, C & Kumar, V 2016, ' Refined mapping of autoimmune disease associated genetic variants with gene expression suggests an important role for non-coding RNAs ', Journal of Autoimmunity, vol. 68, pp. 62-74 . https://doi.org/10.1016/j.jaut.2016.01.002
Contains fulltext : 171367.pdf (Publisher’s version ) (Open Access) Genome-wide association and fine-mapping studies in 14 autoimmune diseases (AID) have implicated more than 250 loci in one or more of these diseases. As more than 90% of AID-associ
Autor:
Dina Vojinovic, Maryam Kavousi, Mohsen Ghanbari, Rutger W. W. Brouwer, Jeroen G. J. van Rooij, Mirjam C. G. N. van den Hout, Robert Kraaij, Wilfred F. J. van Ijcken, Andre G. Uitterlinden, Cornelia M. van Duijn, Najaf Amin
Publikováno v:
Frontiers in Genetics
Frontiers in Genetics, Vol 9 (2018)
Frontiers in Genetics, 9:420. Frontiers Media S.A.
Frontiers in Genetics, Vol 9 (2018)
Frontiers in Genetics, 9:420. Frontiers Media S.A.
Carotid intima-media thickness (cIMT) is an established heritable marker for subclinical atherosclerosis. In this study, we aim to identify rare variants with large effects driving differences in cIMT by performing genome-wide linkage analysis of ind