Draga Toncheva

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 7

Top Topics

Circulating Tumor Cells

Helicobacter Pylori

Mild Cognitive Impairment

Top Venues

Case reports in obstetrics and gynecology

This page only lists publications with an associated author ORCID identifier.

Publications

Sena Karachanak-Yankova, Dimitar Serbezov, Georgi Antov, Mikaela Stancheva, Marta Mihaylova, Savina Hadjidekova, Draga Toncheva, Anastas Dimitrov Pashov, Diyana Belejanska, Yavor Zhelev, Mariya Petrova, Shima Mehrabian, Latchezar Traykov
Rare Pathogenic Variants in Pooled Whole-Exome Sequencing Data Suggest Hyperammonemia as a Possible Cause of Dementia Not Classified as Alzheimer's Disease or Frontotemporal Dementia. Genes 15 (6) (2024)
Sena Karachanak-Yankova, Dimitar Serbezov, Georgi Antov, Mikaela Stancheva, Marta Mihaylova, Savina Hadjidekova, Draga Toncheva, Anastas Dimitrov Pashov, Diyana Belejanska, Yavor Zhelev, Mariya Petrova, Shima Mehrabian, Latchezar Traykov
Rare Pathogenic Variants in Pooled Whole-Exome Sequencing Data Suggest Hyperammonemia as a Possible Cause of Dementia Not Classified as Alzheimer's Disease or Frontotemporal Dementia. Genes 15 (6) (2024)
Draga Toncheva, Maria Marinova, Todor Chobanov, Dimitar Serbezov
Pathogenic Variants Associated with Rare Monogenic Diseases Established in Ancient Neanderthal and Denisovan Genome-Wide Data. Genes 14 (3) (2023)
Draga Toncheva, Maria Marinova, Todor Chobanov, Dimitar Serbezov
Pathogenic Variants Associated with Rare Monogenic Diseases Established in Ancient Neanderthal and Denisovan Genome-Wide Data. Genes 14 (3) (2023)
Draga Toncheva, Maria Marinova, Todor Chobanov, Dimitar Serbezov
Pathogenic Variants Associated with Rare Monogenic Diseases Established in Ancient Neanderthal and Denisovan Genome-Wide Data. Genes 14 (3) (2023)
Draga Toncheva, Maria Marinova, Plamenka Borovska, Dimitar Serbezov
Spatio-temporal dynamics of pathogenic variants associated with monogenic disorders reconstructed with ancient DNA. PloS one 17 (6) (2022)
Radoslava Vazharova, Svetlana Vragaleva, Violeta Dimitrova, Samuil Ivanov, Lubomir Balabanski, Maxim Malinov, Draga Toncheva
Novel Hypomorphic Mutation in FANCD2 Gene Observed in a Fetus with Multiple Congenital Anomalies. Case reports in obstetrics and gynecology 2016 (2016)