| Whole-exome sequencing identifies LRIT3 mutations as a cause of autosomal-recessive complete congenital stationary night blindness C Zeitz, SG Jacobson, CP Hamel, K Bujakowska, M Neuillé, E Orhan, ... The American Journal of Human Genetics 92 (1), 67-75, 2013 | 147 | 2013 |
| Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness I Audo, K Bujakowska, E Orhan, CM Poloschek, S Defoort-Dhellemmes, ... The American Journal of Human Genetics 90 (2), 321-330, 2012 | 144 | 2012 |
| KD4v: comprehensible knowledge discovery system for missense variant TD Luu, A Rusu, V Walter, B Linard, L Poidevin, R Ripp, L Moulinier, ... Nucleic acids research 40 (W1), W71-W75, 2012 | 41 | 2012 |
| MSV3d: database of human MisSense Variants mapped to 3D protein structure TD Luu, AM Rusu, V Walter, R Ripp, L Moulinier, J Muller, T Toursel, ... Database 2012, bas018, 2012 | 40 | 2012 |
| The familial dementia gene revisited: a missense mutation revealed by whole-exome sequencing identifies ITM2B as a candidate gene underlying a novel … I Audo, K Bujakowska, E Orhan, S El Shamieh, F Sennlaub, ... Human molecular genetics 23 (2), 491-501, 2014 | 34 | 2014 |
| Knowledge discovery in variant databases using inductive logic programming H Nguyen, TD Luu, O Poch, JD Thompson Bioinformatics and biology insights 7, BBI. S11184, 2013 | 10 | 2013 |
| Extracting knowledge from a mutation database related to human monogenic disease using inductive logic programming T Luu, N Nguyen, A Friedrich, J Muller, L Moulinier, O Poch International Conference on Bioscience, Biochemistry and Bioinformatics, 83-100, 2011 | 7 | 2011 |
| Blueprinting the workflow of medical diagnosis through the lens of machine learning perspective N Duong-Trung, XN Hoang, TBT Tu, KN Minh, VU Tran, TD Luu 2019 International Conference on Advanced Computing and Applications (ACOMP …, 2019 | 3 | 2019 |
| Black Friday sale prediction via extreme gradient boosted trees ND Trung, TD Thien, TD Luu, HX Huynh Proceedings of the 12th National Conference on Basic and Applied Research in …, 2021 | 1 | 2021 |
| Développement d'une infrastructure d'analyse multi-niveaux pour la découverte des relations entre génotype et phénotype dans les maladies génétiques humaines TD Luu Strasbourg, 2012 | 1 | 2012 |
| Region Awareness for Identifying and Extracting Text in the Natural Scene VL Cu, XV Truong, TD Luu, HV Nguyen Proceedings of Sixth International Congress on Information and Communication …, 2022 | | 2022 |
| Ứng dụng giải thuật gom nhóm dữ liệu để nhận diện sự tương đồng giữa các giống lúa LT Đạo, ÂT Tài, VA Pháp, TNM Thư Tạp chí Khoa học Trường Đại học Cần Thơ, 140-144, 2017 | | 2017 |
| HỆ THỐNG GỢI Ý ÁP DỤNG TRONG QUÁ TRÌNH KÊ ĐƠN THUỐC TNM Thư, TQ Lịnh, LT Đạo, ĐMT Tuấn Tạp chí Khoa học Đại học cần Thơ, 179-188, 2015 | | 2015 |
| Christina Zeitz,* Samuel G. Jacobson, 4 Christian P. Hamel, 5 Kinga Bujakowska A Antonio, C Audier, M Letexier, JP Saraiva, TD Luu, F Sennlaub, ... The American Journal of Human Genetics 92, 67-75, 2013 | | 2013 |
| Development of an infrastructure for multi-level analysis to explore the relationship between genotype in human genetic diseases TD LUU Université de Strasbourg, Strasbourg, 2012 | | 2012 |
| http://decrypthon. igbmc. fr/kd4v TD Luu, V Walter, H Nguyen, O Poch | | |
| http://decrypthon. igbmc. fr/msv3d TD Luu, V Walter, H Nguyen, O Poch | | |
| Database tool MSV3d: database of human MisSense variants mapped to 3D protein structure TD Luu, AM Rusu, V Walter, R Ripp, L Moulinier, J Muller, T Toursel, ... | | |
| Human-comprehensible rule generator for identifying deleterious amino acid variants TD Luu, NH Nguyen, A Friedrich, J Muller, L Moulinier, O Poch | | |
Olivier POCHCSTB ICube UMR7357Adresse e-mail validée de unistra.fr
