Lista de obras - Draga Toncheva - Dominio Público Uruguay

A genome-wide association study in 574 schizophrenia trios using DNA pooling

scientific journal article

Analysis of human unfertilized oocytes and pronuclear zygotes--correlation between chromosome/chromatin status and patient-related factors

artículo científico publicado en 2006

Ancient human genomes suggest three ancestral populations for present-day Europeans

artículo científico publicado en 2014

Apoptosis Gene Expression Profile in Early-Stage non Small Cell Lung Cancer

article

Array-Based Comparative Genomic Hybridization Application for Revealing Genomic Micro Imbalances in Congenital Malformations

Association of 20q13.2 copy number changes with the advanced stage of ovarian cancer—tissue microarray analysis

article

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

artículo científico publicado en 2012

Association of cyclinD1 copy number changes with histological type in ovarian tumors

Association study in the 5q31-32 linkage region for schizophrenia using pooled DNA genotyping

artículo científico publicado en 2008

Association study of myo-inositol monophosphatase 2 (IMPA2) polymorphisms with bipolar affective disorder and response to lithium treatment

artículo científico publicado en 2005

Benign and Unknown Copy Number Variations in Bulgarian Patients with Intellectual Disability and Congenital Malformations

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

artículo científico publicado en 2017

Bulgarians vs the other European populations: a mitochondrial DNA perspective

Calorimetric monitoring of the serum proteome in schizophrenia patients

Case-control association study of 59 candidate genes reveals the DRD2 SNP rs6277 (C957T) as the only susceptibility factor for schizophrenia in the Bulgarian population.

artículo científico publicado en 2009

Case-control association study of 65 candidate genes revealed a possible association of a SNP of HTR5A to be a factor susceptible to bipolar disease in Bulgarian population

artículo científico publicado en 2009

Characterization of genomic changes in the cervical pre-cancerous lesions and tumors induced by different types of human papillomaviruses

artículo científico publicado en 2016

Chromosomal disorders and nuclear and cell destruction in cleaving human embryos

artículo científico publicado en 2005

Chromosomal instability in cancer patients

artículo científico publicado en 1998

Chromosome 22q11 deletions, velo-cardio-facial syndrome and early-onset psychosis

article

Coexistence of Copy Number Changes of Different Genes (INK4A, erbB -1, erbB -2, CMYC, CCND1 and ZNF217) in Urothelial Tumors

article

Coexistence of copy number increases of c-Myc, ZNF217, CCND1, ErbB1 and ErbB2 in ovarian cancers

artículo científico publicado en 2009

Comparative (1)H NMR metabolomic urinalysis of people diagnosed with Balkan endemic nephropathy, and healthy subjects, in Romania and Bulgaria: a pilot study

artículo científico publicado en 2011

Comparison of Two Microarray CGH Platforms for Genome-Wide Copy Number Profilings: Oligo-Based Arrays Versus Bacterial Artificial Chromosome Arrays

Comprehensive Genomic Study in Patients with Idiopathic Azoospermia and Oligoasthenoteratozoospermia

Convergent patterns of association between phenylalanine hydroxylase variants and schizophrenia in four independent samples

artículo científico publicado en 2009

Copy Number Changes in 1q21.3 and 1q23.3 have Different Clinical Relevance in Ovarian Tumors

Correlations between c-myc gene copy-number and clinicopathological parameters of ovarian tumours

article

De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia.

artículo científico publicado en 2011

Detection and Genotyping of Human Papillomaviruses in Bulgarian Patients for the Period of 2009–2010

Detection of Genomic Imbalances by Array-Based Comparative Genomic Hybridization in Bulgarian Patients with Autism Spectrum Disorders

scholarly article by Daniela Avdjieva-Tzavella et al published January 2012 in Biotechnology and Biotechnological Equipment

Diagnostic criteria for Balkan endemic nephropathy: proposal by an international panel

artículo científico publicado en 2007

Distinguishing the co-ancestries of haplogroup G Y-chromosomes in the populations of Europe and the Caucasus

artículo científico publicado en 2012

Dopamine transporter gene (DAT1) VNTR polymorphism in major psychiatric disorders: family-based association study in the Bulgarian population

artículo científico publicado en 2002

Epigenetic alterations in patients with type 2 diabetes mellitus

artículo científico publicado en 2015

Etiology of Balkan Endemic Nephropathy and Associated Urothelial Cancer

Etiology of Balkan endemic nephropathy: a multifactorial disease?

artículo científico publicado el 1 de junio de 1998

Expression of chloride intracellular channel protein 1 (CLIC1) and tumor protein D52 (TPD52) as potential biomarkers for colorectal cancer

article published in 2008

Expression profile of the small heat-shock protein alpha-B-crystallin in operated-on non-small-cell lung cancer patients: clinical implication☆☆☆

Fifty years of Balkan endemic nephropathy: challenges of study using epidemiological method

artículo científico publicado en 2009

Fine-mapping reveals novel alternative splicing of the dopamine transporter

artículo científico publicado en 2010

First Study Of 3q Microsatellite Loci in Bulgarian Patients with Balkan Endemic Nephropathy (BEN)

First Study of NAT1 and NAT2 Polymorphisms in Bulgarian Patients with Balkan Endemic Nephropathy (Ben) and Healthy Controls

FoxP3 demethylation is increased in human colorectal cancer and rat cholangiocarcinoma tissue

artículo científico publicado en 2013

Gene expression in peripheral blood of patients with hypertension and patients with type 2 diabetes

article

Gene-specific fluorescence in-situ hybridization analysis on tissue microarray to refine the region of chromosome 20q amplification in melanoma

article

Genetic Predisposition to Balkan Endemic Nephropathy

Genetic characterization of northeastern Italian population isolates in the context of broader European genetic diversity

artículo científico publicado en 2012

Genetic differences between five European populations

artículo científico

Genetic polymorphism of G6PD in a Bulgarian population

artículo científico publicado en 1984

Genetic polymorphisms of cytochrome P450 among patients with Balkan endemic nephropathy (BEN)

artículo científico publicado en 2005

Genetic structure of Europeans: a view from the North-East

artículo científico publicado en 2009

Genetic variation in the seven-pass transmembrane cadherin CELSR1: lack of association with schizophrenia

artículo científico publicado en 2003

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

artículo científico publicado en 2015

Genome-wide association study on bipolar disorder in the Bulgarian population

scientific journal article

Genome-wide methylation profiling of schizophrenia

artículo científico publicado en 2014

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

article

Genotyping of CYP3A5 polymorphisms among Bulgarian patients with sporadic colorectal cancer and controls

artículo científico publicado en 2007

Global diversity, population stratification, and selection of human copy-number variation

artículo científico publicado en 2015

HPV prevalence and type distribution in women with normal or abnormal Pap smear in Bulgaria

artículo científico publicado en 2014

High-throughput tissue microarray analysis of 11q13 gene amplification (CCND1, FGF3, FGF4, EMS1) in urinary bladder cancer

article

High-throughput tissue microarray analysis of erbB-2 gene amplification in urinary bladder cancer. A study of Bulgarian patients

artículo científico publicado en 2003

High-throughput tissue microarray analysis ofCMYC amplificationin urinary bladder cancer

article

In vitro antiproliferative effect of Helix aspersa hemocyanin on multiple malignant cell lines

artículo científico publicado en 2014

Increased C-MYC copy numbers on the background of CDKN2A loss is associated with improved survival in nodular melanoma

scientific article published on 15 September 2006

Influence of detection of pretreatment cytogenetic abnormalities on first complete remission and survival in adult acute lymphoblastic leukemia

artículo científico publicado en 2011

Introduction of the QF-PCR analysis for the purposes of prenatal diagnosis in Bulgaria--estimation of applicability of 6 STR markers on chromosomes 21 and 18.

artículo científico publicado en 2004

MDR1 Haplotypes Modify BEN Disease Risk: A Study in Bulgarian Patients with Balkan Endemic Nephropathy Compared to Healthy Controls

Major psychiatric disorders and the serotonin transporter gene (SLC6A4): family-based association studies

artículo científico publicado en 2002

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

artículo científico publicado en 2016

Mitochondrial DNA mutations in two bulgarian children with autistic spectrum disorders

artículo científico publicado en 2012

NGS nominated CELA1, HSPG2, and KCNK5 as candidate genes for predisposition to Balkan endemic nephropathy

artículo científico publicado en 2014

No association between MDR1 (ABCB1) 2677G>T and 3435C>T polymorphism and sporadic colorectal cancer among Bulgarian patients

artículo científico

Novel Hypomorphic Mutation in FANCD2 Gene Observed in a Fetus with Multiple Congenital Anomalies

artículo científico publicado en 2016

Partial 9P Monosomy and Partial 8Q Trisomy by Adjacent 1 Segregation of Balanced Paternal Translocation Revealed by Molecular Karyotyping

article by Savina Petrova Hadjidekova et al published January 2012 in Biotechnology and Biotechnological Equipment

Physicochemical and biological characterisation of an antisense oligonucleotide targeted against the bcl-2 mRNA complexed with cationic–hydrophilic copolymers

artículo científico publicado en 2000

Prenatal selection and fetal development disturbances occurring in carriers of G6PD deficiency

article

Profile of chromosomal aberrations in different gestational age spontaneous abortions detected by comparative genomic hybridization

artículo científico publicado en 2006

Proteomic Techniques in Colorectal Cancer Research

Rare chromosomal deletions and duplications increase risk of schizophrenia

artículo científico publicado en 2008

Screening of pharmacogenetic variants associated with drug sensitivity in patients with papillary thyroid carcinoma using next generation sequencing

Significance of chromosomal aberrations for the unsuccessful procedures of assisted reproduction

artículo científico publicado en 2000

Spatio-temporal dynamics of pathogenic variants associated with monogenic disorders reconstructed with ancient DNA

artículo científico publicado en 2022

Strong evidence for association between the dystrobrevin binding protein 1 gene (DTNBP1) and schizophrenia in 488 parent-offspring trios from Bulgaria

artículo científico publicado en 2004

Structure–activity relationships of poly(l-lysines): effects of pegylation and molecular shape on physicochemical and biological properties in gene delivery

article

Support for neuregulin 1 as a susceptibility gene for bipolar disorder and schizophrenia

artículo científico publicado en 2008

The Role of Recent Admixture in Forming the Contemporary West Eurasian Genomic Landscape

artículo científico publicado en 2015

The Role of Recent Admixture in Forming the Contemporary West Eurasian Genomic Landscape.

artículo científico publicado en 2015

The Simons Genome Diversity Project: 300 genomes from 142 diverse populations

artículo científico publicado en 2016

The peopling of Europe and the cautionary tale of Y chromosome lineage R-M269

artículo científico publicado en 2012

Tissue Microarray Analysis of C-MYC Oncogene Copy Number Changes in Larynx Carcinoma

article

Tissue Microarray Study of ZNF217 Copy Number Changes in Larynx Carcinoma

Tissue microarray analysis of EGFR and HER2 oncogene copy number alterations in squamous cell carcinoma of the larynx

artículo científico publicado en 2004

Tissue microarray analysis of EGFR and erbB2 copy number changes in ovarian tumors

artículo científico publicado en 2006

Tissue microarray analysis of EGFR gene amplification and gain in Bulgarian patients with colorectal cancer

artículo científico publicado en 2006

Tissue microarray analysis of cyclin D1 gene amplification and gain in colorectal carcinomas

artículo científico publicado en 2004

TruSight Cancer Sequencing Panel reveals pharmacogenetic variants associated with sensitivity to chemotherapy in lung cancer

article by N. Chilingirova et al published 8 December 2015 in Memo – Magazine of European Medical Oncology

Urinary neopterin concentrations in patients with Balkan endemic nephropathy (BEN).

artículo científico publicado en 2003

Urothelial carcinoma associated with Balkan endemic nephropathy. A worldwide disease

artículo científico publicado en 2009

Variants of erythrocyte glucose-6-phosphate dehydrogenase (G6PD) in Bulgarian populations

artículo científico publicado en 1980

Variation in the protocadherin gamma A gene cluster

artículo científico publicado en 2003

Web-Based Software for Storage, Statistical Processing and Analysis of SNP Data in Studies on Complex Disorders

Whole Genome Analysis by Array-Based Comparative Genomic Hybridization in Patients with Congenital Malformations

Whole genome methylation analyses of schizophrenia patients before and after treatment

artículo científico publicado en 2014

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

artículo científico publicado en 2013

Whole genome microarray analysis in non-small cell lung cancer

artículo científico publicado en 2015

Y-chromosome diversity in modern Bulgarians: new clues about their ancestry

artículo científico publicado en 2013

Lista de obras de Draga Toncheva

A genome-wide association study in 574 schizophrenia trios using DNA pooling

Analysis of human unfertilized oocytes and pronuclear zygotes--correlation between chromosome/chromatin status and patient-related factors

Ancient human genomes suggest three ancestral populations for present-day Europeans

Apoptosis Gene Expression Profile in Early-Stage non Small Cell Lung Cancer

Array-Based Comparative Genomic Hybridization Application for Revealing Genomic Micro Imbalances in Congenital Malformations

Association of 20q13.2 copy number changes with the advanced stage of ovarian cancer—tissue microarray analysis

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

Association of cyclinD1 copy number changes with histological type in ovarian tumors

Association study in the 5q31-32 linkage region for schizophrenia using pooled DNA genotyping

Association study of myo-inositol monophosphatase 2 (IMPA2) polymorphisms with bipolar affective disorder and response to lithium treatment

Benign and Unknown Copy Number Variations in Bulgarian Patients with Intellectual Disability and Congenital Malformations

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

Bulgarians vs the other European populations: a mitochondrial DNA perspective

Calorimetric monitoring of the serum proteome in schizophrenia patients

Case-control association study of 59 candidate genes reveals the DRD2 SNP rs6277 (C957T) as the only susceptibility factor for schizophrenia in the Bulgarian population.

Case-control association study of 65 candidate genes revealed a possible association of a SNP of HTR5A to be a factor susceptible to bipolar disease in Bulgarian population

Characterization of genomic changes in the cervical pre-cancerous lesions and tumors induced by different types of human papillomaviruses

Chromosomal disorders and nuclear and cell destruction in cleaving human embryos

Chromosomal instability in cancer patients

Chromosome 22q11 deletions, velo-cardio-facial syndrome and early-onset psychosis

Coexistence of Copy Number Changes of Different Genes (INK4A, erbB -1, erbB -2, CMYC, CCND1 and ZNF217) in Urothelial Tumors

Coexistence of copy number increases of c-Myc, ZNF217, CCND1, ErbB1 and ErbB2 in ovarian cancers

Comparative (1)H NMR metabolomic urinalysis of people diagnosed with Balkan endemic nephropathy, and healthy subjects, in Romania and Bulgaria: a pilot study

Comparison of Two Microarray CGH Platforms for Genome-Wide Copy Number Profilings: Oligo-Based Arrays Versus Bacterial Artificial Chromosome Arrays

Comprehensive Genomic Study in Patients with Idiopathic Azoospermia and Oligoasthenoteratozoospermia

Convergent patterns of association between phenylalanine hydroxylase variants and schizophrenia in four independent samples

Copy Number Changes in 1q21.3 and 1q23.3 have Different Clinical Relevance in Ovarian Tumors

Correlations between c-myc gene copy-number and clinicopathological parameters of ovarian tumours

De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia.

Detection and Genotyping of Human Papillomaviruses in Bulgarian Patients for the Period of 2009–2010

Detection of Genomic Imbalances by Array-Based Comparative Genomic Hybridization in Bulgarian Patients with Autism Spectrum Disorders

Diagnostic criteria for Balkan endemic nephropathy: proposal by an international panel

Distinguishing the co-ancestries of haplogroup G Y-chromosomes in the populations of Europe and the Caucasus

Dopamine transporter gene (DAT1) VNTR polymorphism in major psychiatric disorders: family-based association study in the Bulgarian population

Epigenetic alterations in patients with type 2 diabetes mellitus

Etiology of Balkan Endemic Nephropathy and Associated Urothelial Cancer

Etiology of Balkan endemic nephropathy: a multifactorial disease?

Expression of chloride intracellular channel protein 1 (CLIC1) and tumor protein D52 (TPD52) as potential biomarkers for colorectal cancer

Expression profile of the small heat-shock protein alpha-B-crystallin in operated-on non-small-cell lung cancer patients: clinical implication☆☆☆

Fifty years of Balkan endemic nephropathy: challenges of study using epidemiological method

Fine-mapping reveals novel alternative splicing of the dopamine transporter

First Study Of 3q Microsatellite Loci in Bulgarian Patients with Balkan Endemic Nephropathy (BEN)

First Study of NAT1 and NAT2 Polymorphisms in Bulgarian Patients with Balkan Endemic Nephropathy (Ben) and Healthy Controls

FoxP3 demethylation is increased in human colorectal cancer and rat cholangiocarcinoma tissue

Gene expression in peripheral blood of patients with hypertension and patients with type 2 diabetes

Gene-specific fluorescence in-situ hybridization analysis on tissue microarray to refine the region of chromosome 20q amplification in melanoma

Genetic Predisposition to Balkan Endemic Nephropathy

Genetic characterization of northeastern Italian population isolates in the context of broader European genetic diversity

Genetic differences between five European populations

Genetic polymorphism of G6PD in a Bulgarian population

Genetic polymorphisms of cytochrome P450 among patients with Balkan endemic nephropathy (BEN)

Genetic structure of Europeans: a view from the North-East

Genetic variation in the seven-pass transmembrane cadherin CELSR1: lack of association with schizophrenia

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

Genome-wide association study on bipolar disorder in the Bulgarian population

Genome-wide methylation profiling of schizophrenia

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

Genotyping of CYP3A5 polymorphisms among Bulgarian patients with sporadic colorectal cancer and controls

Global diversity, population stratification, and selection of human copy-number variation

HPV prevalence and type distribution in women with normal or abnormal Pap smear in Bulgaria

High-throughput tissue microarray analysis of 11q13 gene amplification (CCND1, FGF3, FGF4, EMS1) in urinary bladder cancer

High-throughput tissue microarray analysis of erbB-2 gene amplification in urinary bladder cancer. A study of Bulgarian patients

High-throughput tissue microarray analysis ofCMYC amplificationin urinary bladder cancer

In vitro antiproliferative effect of Helix aspersa hemocyanin on multiple malignant cell lines

Increased C-MYC copy numbers on the background of CDKN2A loss is associated with improved survival in nodular melanoma

Influence of detection of pretreatment cytogenetic abnormalities on first complete remission and survival in adult acute lymphoblastic leukemia

Introduction of the QF-PCR analysis for the purposes of prenatal diagnosis in Bulgaria--estimation of applicability of 6 STR markers on chromosomes 21 and 18.

MDR1 Haplotypes Modify BEN Disease Risk: A Study in Bulgarian Patients with Balkan Endemic Nephropathy Compared to Healthy Controls

Major psychiatric disorders and the serotonin transporter gene (SLC6A4): family-based association studies

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

Mitochondrial DNA mutations in two bulgarian children with autistic spectrum disorders

NGS nominated CELA1, HSPG2, and KCNK5 as candidate genes for predisposition to Balkan endemic nephropathy

No association between MDR1 (ABCB1) 2677G>T and 3435C>T polymorphism and sporadic colorectal cancer among Bulgarian patients

Novel Hypomorphic Mutation in FANCD2 Gene Observed in a Fetus with Multiple Congenital Anomalies

Partial 9P Monosomy and Partial 8Q Trisomy by Adjacent 1 Segregation of Balanced Paternal Translocation Revealed by Molecular Karyotyping

Physicochemical and biological characterisation of an antisense oligonucleotide targeted against the bcl-2 mRNA complexed with cationic–hydrophilic copolymers

Prenatal selection and fetal development disturbances occurring in carriers of G6PD deficiency

Profile of chromosomal aberrations in different gestational age spontaneous abortions detected by comparative genomic hybridization

Proteomic Techniques in Colorectal Cancer Research