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Page 1
Decoding NF1 Intragenic Copy-Number Variations.
Hsiao MC, Piotrowski A, Callens T, Fu C, Wimmer K, Claes KB, Messiaen L. Hsiao MC, et al. Among authors: callens t. Am J Hum Genet. 2015 Aug 6;97(2):238-49. doi: 10.1016/j.ajhg.2015.06.002. Epub 2015 Jul 16. Am J Hum Genet. 2015. PMID: 26189818 Free PMC article.
The development of cutaneous neurofibromas.
Jouhilahti EM, Peltonen S, Callens T, Jokinen E, Heape AM, Messiaen L, Peltonen J. Jouhilahti EM, et al. Among authors: callens t. Am J Pathol. 2011 Feb;178(2):500-5. doi: 10.1016/j.ajpath.2010.10.041. Am J Pathol. 2011. PMID: 21281783 Free PMC article.
Clinical Implications of Rabphillin-3A-Like Gene Alterations in Breast Cancer.
Putcha BD, Jia X, Katkoori VR, Salih C, Shanmugam C, Jadhav T, Bovell LC, Behring MP, Callens T, Messiaen L, Bae S, Grizzle WE, Singh KP, Manne U. Putcha BD, et al. Among authors: callens t. PLoS One. 2015 Jun 12;10(6):e0129216. doi: 10.1371/journal.pone.0129216. eCollection 2015. PLoS One. 2015. PMID: 26070152 Free PMC article.
Analysis of 200 unrelated individuals with a constitutional NF1 deep intronic pathogenic variant reveals that variants flanking the alternatively spliced NF1 exon 31 [23a] cause a classical neurofibromatosis type 1 phenotype while altering predominantly NF1 isoform type II.
Koczkowska M, Chen Y, Xie J, Callens T, Gomes A, Wimmer K, Messiaen LM. Koczkowska M, et al. Among authors: callens t. Hum Genet. 2023 Jul;142(7):849-861. doi: 10.1007/s00439-023-02555-z. Epub 2023 Apr 25. Hum Genet. 2023. PMID: 37186028 Free PMC article.
28 results