| Association of genetic vs environmental factors in swedish adoptees with clinically significant tinnitus CR Cederroth, MN PirouziFard, N Trpchevska, E Idrizbegovic, B Canlon, ... JAMA Otolaryngology–Head & Neck Surgery 145 (3), 222-229, 2019 | 15 | 2019 |
| Recommendations on collecting and storing samples for genetic studies in hearing and tinnitus research AJ Szczepek, L Frejo, B Vona, N Trpchevska, CR Cederroth, H Caria, ... Ear and hearing 40 (2), 219, 2019 | 14 | 2019 |
| Sex-specific association of tinnitus with suicide attempts A Lugo, N Trpchevska, X Liu, R Biswas, C Magnusson, S Gallus, ... JAMA Otolaryngology–Head & Neck Surgery 145 (7), 685-687, 2019 | 9 | 2019 |
| Standardised profiling for tinnitus research: The European School for Interdisciplinary Tinnitus Research Screening Questionnaire (ESIT-SQ) E Genitsaridi, M Partyka, S Gallus, JA Lopez-Escamez, M Schecklmann, ... Hearing research 377, 353-359, 2019 | 7 | 2019 |
| A family study of complex chromosome rearrangement involving chromosomes 1, 8, and 11 and its reproductive consequences N Trpchevska, I Dimova, T Arabadji, T Milachich, S Angelova, M Dimitrova, ... Journal of assisted reproduction and genetics 34 (5), 659-669, 2017 | 6 | 2017 |
| A New Buzz for Tinnitus—It’s in the Genes! CR Cederroth, N Trpchevska, B Langguth JAMA Otolaryngology–Head & Neck Surgery 146 (11), 1025-1026, 2020 | 1 | 2020 |
| Sex-Dependent Aggregation of Tinnitus in Swedish Families N Trpchevska, J Bulla, M Prada Hellberg, NK Edvall, A Lazar, G Mehraei, ... Journal of clinical medicine 9 (12), 3812, 2020 | | 2020 |
| The spatial percept of tinnitus is associated with hearing asymmetry: subgroup comparisons E Genitsaridi, T Kypraios, NK Edvall, N Trpchevska, B Canlon, DJ Hoare, ... medRxiv, 2020 | | 2020 |
| Molecular-epidemiologic and epigenetic study of HPV infection in cervical samples of Bulgarian patients M Hristova-Savova, M Koprinarova, S Kovachev, N Trpchevska, I Dimitrov, ... EUROPEAN JOURNAL OF HUMAN GENETICS 26, 1009-1009, 2018 | | 2018 |
| Whole genome study in familial case of Mayer-Rokitansky-Kuster-Hauser syndrome N Trpchevska, V Peicheva, G Stancheva, M Hristova-Savova, M Dimitrova, ... EUROPEAN JOURNAL OF HUMAN GENETICS 26, 831-832, 2018 | | 2018 |
| Chromothripsis and hypodiploidy in abortive materials from malformed fetuses I Dimova, P Chaveeva, J Karagyozova, V Peicheva, G Stancheva, ... EUROPEAN JOURNAL OF HUMAN GENETICS 26, 825-825, 2018 | | 2018 |
| Types and frequency of chromosome aberrations in Bulgarian patients with infertility M Dimitrova, N Trpchevska, M Hristova-Savova, T Timeva, P Andreeva, ... EUROPEAN JOURNAL OF HUMAN GENETICS 26, 825-825, 2018 | | 2018 |
