R. Staneva

发表

Ancient human mitochondrial genomes from Bronze Age Bulgaria: new insights into the genetic history of Thracians

S. Karachanak-Yankova, D. Toncheva, S. Sarno, 2019, Scientific Reports.

ARTICLE; MEDICAL BIOTECHNOLOGY Whole genome methylation analyses of schizophrenia patients before and after treatment

D. Toncheva, V. Milanova, B. Rukova, 2014 .

NGS Nominated CELA 1 , HSPG 2 , and KCNK 5 as Candidate Genes for Predisposition to Balkan Endemic Nephropathy

D. Toncheva, D. Plaseska-Karanfilska, R., 2014 .

NGS Nominated CELA1, HSPG2, and KCNK5 as Candidate Genes for Predisposition to Balkan Endemic Nephropathy

D. Toncheva, D. Plaseska-Karanfilska, P. Dimitrov, 2014, BioMed research international.

Methylation analysis on whole genome level. What did we learn from BEN studies?

D. Toncheva, R. Staneva, 2014, Prilozi.

Endometriosis - Review Of Current Therapeutic Aproaches For Disease Control

D. Toncheva, S. Hadjidekova, O. Antonova, 2019, Annual for Hospital Pharmacy.

Preimplantation genetic testing: method and two case studies of familial three-way complex translocations

D. Toncheva, K. Nikolova, G. Stamenov, 2019, Biotechnology & Biotechnological Equipment.

Changes in the gene expression profile of the bladder cancer cell lines after treatment with Helix lucorum and Rapana venosa hemocyanin.

S. Stevanović, D. Toncheva, L. Yossifova, 2015, Journal of B.U.ON. : official journal of the Balkan Union of Oncology.

Unbalanced human embryos secrete more hyperglycosylated human chorionic gonadotrophin (hCG-H) than balanced ones

F. Scarpellini, R. Ganeva, D. Parvanov, 2020, Journal of Assisted Reproduction and Genetics.

Whole genome methylation array analysis reveals new aspects in Balkan endemic nephropathy etiology

Ruslan Hlushchuk, Valentin Djonov, Momir Polenakovic, 2013, BMC Nephrology.

Rare genetic variants prioritize molecular pathways for semaphorin interactions in Alzheimer’s disease patients

S. Karachanak-Yankova, D. Toncheva, S. Mehrabian, 2021, Biotechnology & Biotechnological Equipment.

Ancient human mitochondrial genomes from Bronze Age Bulgaria: new insights into the genetic history of Thracians

S. Karachanak-Yankova, D. Toncheva, S. Sarno, 2019, Scientific Reports.

Genetic, Genomic and Epigenomic Studies of Balkan Endemic Nephropathy (Ben)

D. Toncheva, P. Dimitrov, M. Polenaković, 2015, Prilozi.

Genome-Wide Methylation Profiling of Schizophrenia

D. Toncheva, V. Milanova, B. Rukova, 2014, Balkan journal of medical genetics : BJMG.

Whole genome methylation analyses of schizophrenia patients before and after treatment

D. Toncheva, V. Milanova, B. Rukova, 2014, Biotechnology, biotechnological equipment.

The Utility of Preimplantation Genetic Test in Couples with History of Infertility and Pregnancy Loss

D. Toncheva, K. Nikolova, G. Stamenov, 2022, Proceedings of the Bulgarian Academy of Sciences.

Detecting EGFR Mutations in Patients with Non-small Cell Lung Cancer

D. Toncheva, D. Nikolova, S. Hadjidekova, 2018, Balkan journal of medical genetics : BJMG.

Benign, Pathogenic and Copy Number Variations of Unknown Clinical Significance in Patients with Congenital Malformations and Developmental Delay

D. Toncheva, S. Hadjidekova, R. Staneva, 2017, Balkan journal of medical genetics : BJMG.

Novel genes and variants associated with longevity in Bulgarian centenarians revealed by whole exome sequencing DNA pools: a pilot study

S. Karachanak-Yankova, D. Toncheva, D. Nesheva, 2020, Journal of Translational Genetics and Genomics.

16p11.2 Duplication Syndrome - a Case Report.

L. Angelova, M. Stoyanova, R. Staneva, 2021, Folia medica.

POOL-SEQ Study of Bulgarian Centenarians Highlights the Relevance for Human Longevity of Gene Expression Pathways

S. Karachanak-Yankova, D. Toncheva, D. Nesheva, 2019 .

Association of a bitter taste receptor mutation with Balkan Endemic Nephropathy (BEN)

D. Toncheva, S. Wooding, S. Atanasova, 2012, BMC Medical Genetics.

MicroRNA Profiling in Patients with Upper Tract Urothelial Carcinoma Associated with Balkan Endemic Nephropathy

D. Toncheva, P. Noveski, K. Popovska-Jankovic, 2016, BioMed research international.

Prioritization of genetic variants predisposing to coronary heart disease in the Bulgarian population using centenarian exomes

S. Karachanak-Yankova, D. Toncheva, D. Nesheva, 2019, Biotechnology & Biotechnological Equipment.

Expression profiling of muscle invasive and non-invasive bladder tumors for biomarkers identification related to drug resistance, sensitivity and tumor progression

C. Slavov, D. Toncheva, D. Nesheva, 2020 .

Clinical impact of copy number variation changes in bladder cancer samples

C. Slavov, D. Toncheva, D. Nesheva, 2021, Experimental and therapeutic medicine.

Detection of pathogenic variants in Alzheimer’s disease related genes in Bulgarian patients by pooled whole-exome sequencing

S. Karachanak-Yankova, D. Toncheva, S. Mehrabian, 2023, Biotechnology & Biotechnological Equipment.

Centenarian Exomes as a Tool for Evaluating the Clinical Relevance of Germline Tumor Suppressor Mutations

S. Karachanak-Yankova, D. Toncheva, D. Nesheva, 2020, Technology in cancer research & treatment.

Prevalence and prognosis of PIK3CA mutations in Bulgarian patients with metastatic breast cancer receiving endocrine therapy in first‐line setting

N. Conev, I. Donev, M. Radanova, 2023, Cancer reports.