| Modelling mutational landscapes of human cancers in vitro M Olivier, A Weninger, M Ardin, H Huskova, X Castells, MP Vallée, ... Scientific reports 4 (1), 1-9, 2014 | 80 | 2014 |
| 17q21. 31 duplication causes prominent tau-related dementia with increased MAPT expression K Le Guennec, O Quenez, G Nicolas, D Wallon, S Rousseau, AC Richard, ... Molecular psychiatry 22 (8), 1119-1125, 2017 | 42 | 2017 |
| Meta-analysis of Tourette Syndrome and Attention Deficit Hyperactivity Disorder provides support for a shared genetic basis F Tsetsos, SS Padmanabhuni, J Alexander, I Karagiannidis, M Tsifintaris, ... Frontiers in Neuroscience, 2016 | 27 | 2016 |
| Targeted re-sequencing approach of candidate genes implicates rare potentially functional variants in Tourette syndrome etiology J Alexander, H Potamianou, J Xing, L Deng, I Karagiannidis, F Tsetsos, ... Frontiers in neuroscience 10, 428, 2016 | 18 | 2016 |
| Clinical BRCA1/2 reversion analysis identifies hotspot mutations and predicted neoantigens associated with therapy resistance SJ Pettitt, JR Frankum, M Punta, S Lise, J Alexander, Y Chen, TA Yap, ... Cancer Discovery 10 (10), 1475-1488, 2020 | 15 | 2020 |
| Familial early-onset dementia with complex neuropathologic phenotype and genomic background J Alexander, O Kalev, S Mehrabian, L Traykov, M Raycheva, D Kanakis, ... Neurobiology of aging 42, 199-204, 2016 | 15 | 2016 |
| Low rates of mutation in clinical grade human pluripotent stem cells under different culture conditions O Thompson, F von Meyenn, Z Hewitt, J Alexander, A Wood, ... Nature communications 11 (1), 1-14, 2020 | 13 | 2020 |
| TS-EUROTRAIN: a European-wide investigation and training network on the etiology and pathophysiology of Gilles de la Tourette syndrome NJ Forde, AS Kanaan, J Widomska, SS Padmanabhuni, E Nespoli, ... Frontiers in neuroscience 10, 384, 2016 | 11 | 2016 |
| Variant Ranker: a web-tool to rank genomic data according to functional significance J Alexander, D Mantzaris, M Georgitsi, P Drineas, P Paschou BMC bioinformatics 18 (1), 1-9, 2017 | 10 | 2017 |
| The genetics of Gilles de la Tourette syndrome: a common aetiological basis with comorbid disorders? I Karagiannidis, F Tsetsos, SS Padmanabhuni, J Alexander, M Georgitsi, ... Current Behavioral Neuroscience Reports 3 (3), 218-231, 2016 | 9 | 2016 |
| The Mutational Concordance of Fixed Formalin Paraffin Embedded and Fresh Frozen Gastro-Oesophageal Tumours Using Whole Exome Sequencing IY Chong, N Starling, A Rust, J Alexander, L Aronson, ... Journal of Clinical Medicine 10 (2), 215, 2021 | 1 | 2021 |
| Neuropathology-driven whole-genome sequencing study points to novel candidate genes for healthy brain aging J Alexander, T Ströbel, M Georgitsi, S Hönigschnabl, A Reiner, P Fischer, ... Alzheimer Disease & Associated Disorders 33 (1), 7-14, 2019 | 1 | 2019 |
| Corrigendum: Modelling mutational landscapes of human cancers in vitro M Olivier, A Weninger, M Ardin, H Huskova, X Castells, MP Vallée, ... Scientific reports 7, 2017 | 1 | 2017 |
| Analysis of clinical BRCA1/2 reversions identifies hotspot mutations and predicted neoantigens associated with therapy resistance S Pettitt, J Frankum, M Punta, S Lise, J Alexander, Y Chen, S Haider, ... Cancer Research 80 (16 Supplement), 4072-4072, 2020 | | 2020 |
| Impairment of a distinct cancer-associated fibroblast population limits tumour growth and metastasis U Jungwirth, A van Weverwijk, L Jenkins, J Alexander, D Vicente, Q Gao, ... bioRxiv, 2020 | | 2020 |
| Modelling mutational landscapes of human cancers in vitro (vol 4, 4482, 2017) M Olivier, A Weninger, M Ardin, H Huskova, X Castells, MP Vallee, ... SCIENTIFIC REPORTS 7, 2017 | | 2017 |
| Statistical methodology for the analysis of genomic data J Alexander Δημοκρίτειο Πανεπιστήμιο Θράκης (ΔΠΘ). Σχολή Επιστημών Υγείας. Τμήμα …, 2016 | | 2016 |
Peristera PaschouProfessor, Department of Biological Sciences, Purdue UniversityGeverifieerd e-mailadres voor purdue.edu
