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Ibrahim Tanyalcin
Ibrahim Tanyalcin
Verified email at vub.ac.be - Homepage
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Cited by
Year
DEOGEN2: prediction and interactive visualization of single amino acid variant deleteriousness in human proteins
D Raimondi, I Tanyalcin, J Ferté, A Gazzo, G Orlando, T Lenaerts, ...
Nucleic acids research 45 (W1), W201-W206, 2017
1222017
Bi-allelic variants in COL3A1 encoding the ligand to GPR56 are associated with cobblestone-like cortical malformation, white matter changes and cerebellar cysts
L Vandervore, K Stouffs, I Tanyalçin, T Vanderhasselt, F Roelens, ...
Journal of medical genetics 54 (6), 432-440, 2017
382017
Polymicrogyria with dysmorphic basal ganglia? Think tubulin!
D Amrom, I Tanyalcin, H Verhelst, N Deconinck, GJ Brouhard, JC Décarie, ...
Clinical genetics 85 (2), 178-183, 2014
382014
Elaborating the phenotypic spectrum associated with mutations in ARFGEF2: case study and literature review
I Tanyalçin, H Verhelst, DJJ Halley, T Vanderhasselt, L Villard, C Goizet, ...
european journal of paediatric neurology 17 (6), 666-670, 2013
182013
Thin genu of the corpus callosum points to mutation in FOXG1 in a child with acquired microcephaly, trigonocephaly, and intellectual developmental disorder: a case report and …
C De Bruyn, T Vanderhasselt, I Tanyalçin, K Keymolen, KL Van Rompaey, ...
european journal of paediatric neurology 18 (3), 420-426, 2014
122014
I-PV: a CIRCOS module for interactive protein sequence visualization
I Tanyalcin, C Al Assaf, A Gheldof, K Stouffs, W Lissens, AC Jansen
Bioinformatics 32 (3), 447-449, 2016
72016
Lexicon Visualization Library and JavaScript for scientific data visualization
I Tanyalcin, C Al Assaf, J Ferte, F Ancien, T Khan, G Smits, M Rooman, ...
Computing in Science & Engineering 20 (1), 50-65, 2018
52018
Convert your favorite protein modeling program into a mutation predictor:“MODICT”
I Tanyalcin, K Stouffs, D Daneels, C Al Assaf, W Lissens, A Jansen, ...
BMC bioinformatics 17, 1-19, 2016
22016
MPL p. S204P is a recurrent mutation in essential thrombocythemia
CAL Assaf, P Papadopoulos, L Guttierez, S Smits, C Graux, J Emmerechts, ...
Blood 126 (23), 2837, 2015
22015
Indoril: An I-PV Add-On for Visualization of Point Mutations on 3D Cartesian Coordinates
I Tanyalcin, J Ferte, T Khan, CA Assaf
bioRxiv, 148122, 2017
12017
Bi-allelic mutations in COL3A1 encoding the ligand to GPR56 are associated with cobblestone-like cortical malformation, white matter changes and cerebellar cysts
AC Jansen, L Vandervore, I Tanyalçin, T Vanderhasselt, F Roelens, ...
European Journal of Paediatric Neurology 21, e61, 2017
2017
Mutation Analysis of the SCN5A Gene in 122 Brugada Syndrome Probands
D Daneels, U Peeters, P Brugada, ML Bonduelle, A Gazzo, D Raimondi, ...
3rd PhD Day Medical Campus-Research Unlimited, 7-7, 2014
2014
THE RESULTS OF BIOCHEMICAL AND GENETICAL APPROACH TO EXCLUSIVE GALACTOSEMIA CASES IN TURKEY THROUGH SELECTIVE SCREENING
T Tanyalcin, G Kopish, I Tanyalcin, M Baker, G Hoffman, R Laessig, ...
JOURNAL OF INHERITED METABOLIC DISEASE 33, S64-S64, 2010
2010
376 Sweat test results on a suspected cystic fibrosis population with CF mutation analysis and the frequency of borderline results
T Tanyalcin, G Hoffman, I Tanyalcin, P Farrell
Journal of Cystic Fibrosis, S92, 2007
2007
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Articles 1–14