| 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 | 145 | 2017 |
| 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 | 41 | 2017 |
| 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 | 39 | 2014 |
| 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 | 18 | 2013 |
| 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 | 12 | 2014 |
| 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 | 7 | 2016 |
| 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 | 5 | 2018 |
| 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 | 2 | 2016 |
| 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 | 2 | 2015 |
| 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 | 1 | 2017 |
| 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 |
Tim VanderhasseltUZ Brussel, MD在 uzbrussel.be 的电子邮件经过验证
