| Year |
Citation |
Score |
| 2021 |
van Rheenen W, van der Spek RAA, Bakker MK, van Vugt JJFA, Hop PJ, Zwamborn RAJ, de Klein N, Westra HJ, Bakker OB, Deelen P, Shireby G, Hannon E, Moisse M, Baird D, Restuadi R, ... ... Groen EJN, et al. Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology. Nature Genetics. 53: 1636-1648. PMID 34873335 DOI: 10.1038/s41588-021-00973-1 |
0.419 |
|
| 2018 |
van Rheenen W, Diekstra FP, Harschnitz O, Westeneng HJ, van Eijk KR, Saris CGJ, Groen EJN, van Es MA, Blauw HM, van Vught PWJ, Veldink JH, van den Berg LH. Whole blood transcriptome analysis in amyotrophic lateral sclerosis: A biomarker study. Plos One. 13: e0198874. PMID 29939990 DOI: 10.1371/journal.pone.0198874 |
0.727 |
|
| 2017 |
Bernabò P, Tebaldi T, Groen EJN, Lane FM, Perenthaler E, Mattedi F, Newbery HJ, Zhou H, Zuccotti P, Potrich V, Shorrock HK, Muntoni F, Quattrone A, Gillingwater TH, Viero G. In Vivo Translatome Profiling in Spinal Muscular Atrophy Reveals a Role for SMN Protein in Ribosome Biology. Cell Reports. 21: 953-965. PMID 29069603 DOI: 10.1016/j.celrep.2017.10.010 |
0.308 |
|
| 2016 |
Blokhuis AM, Koppers M, Groen EJ, van den Heuvel DM, Dini Modigliani S, Anink JJ, Fumoto K, van Diggelen F, Snelting A, Sodaar P, Verheijen BM, Demmers JA, Veldink JH, Aronica E, Bozzoni I, et al. Comparative interactomics analysis of different ALS-associated proteins identifies converging molecular pathways. Acta Neuropathologica. 132: 175-96. PMID 27164932 DOI: 10.1007/s00401-016-1575-8 |
0.758 |
|
| 2013 |
Groen EJ, Fumoto K, Blokhuis AM, Engelen-Lee J, Zhou Y, van den Heuvel DM, Koppers M, van Diggelen F, van Heest J, Demmers JA, Kirby J, Shaw PJ, Aronica E, Spliet WG, Veldink JH, et al. ALS-associated mutations in FUS disrupt the axonal distribution and function of SMN. Human Molecular Genetics. 22: 3690-704. PMID 23681068 DOI: 10.1093/hmg/ddt222 |
0.731 |
|
| 2013 |
Blokhuis AM, Groen EJ, Koppers M, van den Berg LH, Pasterkamp RJ. Protein aggregation in amyotrophic lateral sclerosis. Acta Neuropathologica. 125: 777-94. PMID 23673820 DOI: 10.1007/s00401-013-1125-6 |
0.745 |
|
| 2013 |
Saris CGJ, Groen EJN, Koekkoek JAF, Veldink JH, Van Den Berg LH. Meta-analysis of gene expression profiling in amyotrophic lateral sclerosis: A comparison between transgenic mouse models and human patients Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 14: 177-189. PMID 23286751 DOI: 10.3109/21678421.2012.729842 |
0.309 |
|
| 2013 |
Koppers M, Groen EJ, van Vught PW, van Rheenen W, Witteveen E, van Es MA, Pasterkamp RJ, van den Berg LH, Veldink JH. Screening for rare variants in the coding region of ALS-associated genes at 9p21.2 and 19p13.3. Neurobiology of Aging. 34: 1518.e5-7. PMID 23141412 DOI: 10.1016/j.neurobiolaging.2012.09.018 |
0.739 |
|
| 2013 |
Ahmeti KB, Ajroud-Driss S, Al-Chalabi A, Andersen PM, Armstrong J, Birve A, Blauw HM, Brown RH, Bruijn L, Chen W, Chio A, Comeau MC, Cronin S, Diekstra FP, Soraya Gkazi A, ... ... Groen EJ, et al. Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1. Neurobiology of Aging. 34: 357.e7-19. PMID 22959728 DOI: 10.1016/j.neurobiolaging.2012.07.017 |
0.408 |
|
| 2012 |
Diekstra FP, Saris CG, van Rheenen W, Franke L, Jansen RC, van Es MA, van Vught PW, Blauw HM, Groen EJ, Horvath S, Estrada K, Rivadeneira F, Hofman A, Uitterlinden AG, Robberecht W, et al. Mapping of gene expression reveals CYP27A1 as a susceptibility gene for sporadic ALS. Plos One. 7: e35333. PMID 22509407 DOI: 10.1371/Journal.Pone.0035333 |
0.476 |
|
| 2012 |
Groen EJ, van Rheenen W, Koppers M, van Doormaal PT, Vlam L, Diekstra FP, Dooijes D, Pasterkamp RJ, van den Berg LH, Veldink JH. CGG-repeat expansion in FMR1 is not associated with amyotrophic lateral sclerosis. Neurobiology of Aging. 33: 1852.e1-3. PMID 22507827 DOI: 10.1016/j.neurobiolaging.2012.03.007 |
0.735 |
|
| 2012 |
Koppers M, van Blitterswijk MM, Vlam L, Rowicka PA, van Vught PW, Groen EJ, Spliet WG, Engelen-Lee J, Schelhaas HJ, de Visser M, van der Kooi AJ, van der Pol WL, Pasterkamp RJ, Veldink JH, van den Berg LH. VCP mutations in familial and sporadic amyotrophic lateral sclerosis. Neurobiology of Aging. 33: 837.e7-13. PMID 22078486 DOI: 10.1016/j.neurobiolaging.2011.10.006 |
0.744 |
|
| 2011 |
van Es MA, Schelhaas HJ, van Vught PW, Ticozzi N, Andersen PM, Groen EJ, Schulte C, Blauw HM, Koppers M, Diekstra FP, Fumoto K, LeClerc AL, Keagle P, Bloem BR, Scheffer H, et al. Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis. Annals of Neurology. 70: 964-73. PMID 22190368 DOI: 10.1002/Ana.22611 |
0.722 |
|
| 2010 |
Blauw HM, Al-Chalabi A, Andersen PM, van Vught PWJ, Diekstra FP, van Es MA, Saris CGJ, Groen EJN, van Rheenen W, Koppers M, Slot Rvt, Strengman E, Estrada K, Rivadeneira F, Hofman A, et al. A large genome scan for rare CNVs in amyotrophic lateral sclerosis Human Molecular Genetics. 19: 4091-4099. PMID 20685689 DOI: 10.1093/Hmg/Ddq323 |
0.73 |
|
| 2010 |
Groen EJ, van Es MA, van Vught PW, Spliet WG, van Engelen-Lee J, de Visser M, Wokke JH, Schelhaas HJ, Ophoff RA, Fumoto K, Pasterkamp RJ, Dooijes D, Cuppen E, Veldink JH, van den Berg LH. FUS mutations in familial amyotrophic lateral sclerosis in the Netherlands. Archives of Neurology. 67: 224-30. PMID 20142531 DOI: 10.1001/Archneurol.2009.329 |
0.616 |
|
| 2009 |
van Es MA, Veldink JH, Saris CG, Blauw HM, van Vught PW, Birve A, Lemmens R, Schelhaas HJ, Groen EJ, Huisman MH, van der Kooi AJ, de Visser M, Dahlberg C, Estrada K, Rivadeneira F, et al. Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis. Nature Genetics. 41: 1083-7. PMID 19734901 DOI: 10.1038/Ng.442 |
0.597 |
|
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