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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1992 2
1993 2
1994 1
1995 2
1996 4
1998 1
2001 5
2002 3
2003 1
2004 3
2005 2
2006 3
2007 6
2008 3
2009 2
2010 2
2011 1
2012 1
2013 1
2014 1
2015 1
2016 1
2017 2
2018 1
2022 2
2023 1
2024 0

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48 results

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Page 1
Understanding familial and non-familial renal cell cancer.
Bodmer D, van den Hurk W, van Groningen JJ, Eleveld MJ, Martens GJ, Weterman MA, van Kessel AG. Bodmer D, et al. Among authors: weterman ma. Hum Mol Genet. 2002 Oct 1;11(20):2489-98. doi: 10.1093/hmg/11.20.2489. Hum Mol Genet. 2002. PMID: 12351585 Review.
Deregulated expression of EZH2 in congenital brainstem disconnection.
Barth PG, Aronica E, Fox S, Fluiter K, Weterman MAJ, Poretti A, Miller DC, Boltshauser E, Harding B, Santi M, Baas F. Barth PG, et al. Among authors: weterman maj. Neuropathol Appl Neurobiol. 2017 Jun;43(4):358-365. doi: 10.1111/nan.12368. Neuropathol Appl Neurobiol. 2017. PMID: 27886392 No abstract available.
Pathogenic variants in three families with distal muscle involvement.
Weterman MAJ, Bronk M, Jongejan A, Hoogendijk JE, Krudde J, Karjosukarso D, Goebel HH, Aronica E, Jöbsis GJ, van Ruissen F, van Spaendonck-Zwarts KY, de Visser M, Baas F. Weterman MAJ, et al. Neuromuscul Disord. 2023 Jan;33(1):58-64. doi: 10.1016/j.nmd.2022.11.007. Epub 2022 Nov 29. Neuromuscul Disord. 2023. PMID: 36539320 Free article.
Molecular markers of melanocytic tumor progression.
Weterman MA, van Muijen GN, Bloemers HP, Ruiter DJ. Weterman MA, et al. Lab Invest. 1994 May;70(5):593-608. Lab Invest. 1994. PMID: 8196357 Review. No abstract available.
Phenotype of Charcot-Marie-Tooth disease Type 2.
Bienfait HM, Baas F, Koelman JH, de Haan RJ, van Engelen BG, Gabreëls-Festen AA, Ongerboer de Visser BW, Meggouh F, Weterman MA, De Jonghe P, Timmerman V, de Visser M. Bienfait HM, et al. Among authors: weterman ma. Neurology. 2007 May 15;68(20):1658-67. doi: 10.1212/01.wnl.0000263479.97552.94. Neurology. 2007. PMID: 17502546
tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia.
Budde BS, Namavar Y, Barth PG, Poll-The BT, Nürnberg G, Becker C, van Ruissen F, Weterman MA, Fluiter K, te Beek ET, Aronica E, van der Knaap MS, Höhne W, Toliat MR, Crow YJ, Steinling M, Voit T, Roelenso F, Brussel W, Brockmann K, Kyllerman M, Boltshauser E, Hammersen G, Willemsen M, Basel-Vanagaite L, Krägeloh-Mann I, de Vries LS, Sztriha L, Muntoni F, Ferrie CD, Battini R, Hennekam RC, Grillo E, Beemer FA, Stoets LM, Wollnik B, Nürnberg P, Baas F. Budde BS, et al. Among authors: weterman ma. Nat Genet. 2008 Sep;40(9):1113-8. doi: 10.1038/ng.204. Nat Genet. 2008. PMID: 18711368
Hypermorphic and hypomorphic AARS alleles in patients with CMT2N expand clinical and molecular heterogeneities.
Weterman MAJ, Kuo M, Kenter SB, Gordillo S, Karjosukarso DW, Takase R, Bronk M, Oprescu S, van Ruissen F, Witteveen RJW, Bienfait HME, Breuning M, Verhamme C, Hou YM, de Visser M, Antonellis A, Baas F. Weterman MAJ, et al. Hum Mol Genet. 2018 Dec 1;27(23):4036-4050. doi: 10.1093/hmg/ddy290. Hum Mol Genet. 2018. PMID: 30124830 Free PMC article.
A LRSAM1 mutation links Charcot-Marie-Tooth type 2 to Parkinson's disease.
Aerts MB, Weterman MA, Quadri M, Schelhaas HJ, Bloem BR, Esselink RA, Baas F, Bonifati V, van de Warrenburg BP. Aerts MB, et al. Among authors: weterman ma. Ann Clin Transl Neurol. 2015 Dec 22;3(2):146-9. doi: 10.1002/acn3.281. eCollection 2016 Feb. Ann Clin Transl Neurol. 2015. PMID: 26900582 Free PMC article.
CLP1 founder mutation links tRNA splicing and maturation to cerebellar development and neurodegeneration.
Schaffer AE, Eggens VR, Caglayan AO, Reuter MS, Scott E, Coufal NG, Silhavy JL, Xue Y, Kayserili H, Yasuno K, Rosti RO, Abdellateef M, Caglar C, Kasher PR, Cazemier JL, Weterman MA, Cantagrel V, Cai N, Zweier C, Altunoglu U, Satkin NB, Aktar F, Tuysuz B, Yalcinkaya C, Caksen H, Bilguvar K, Fu XD, Trotta CR, Gabriel S, Reis A, Gunel M, Baas F, Gleeson JG. Schaffer AE, et al. Among authors: weterman ma. Cell. 2014 Apr 24;157(3):651-63. doi: 10.1016/j.cell.2014.03.049. Cell. 2014. PMID: 24766810 Free PMC article.
48 results