List of works - Radka Kaneva

A Large-Scale Analysis of Genetic Variants within Putative miRNA Binding Sites in Prostate Cancer

scientific article

A genetic risk score to guide age-specific, personalized prostate cancer screening

A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer

scientific article published on 14 September 2014

A meta-analysis of genome-wide association studies to identify prostate cancer susceptibility loci associated with aggressive and non-aggressive disease

scientific article

A mutation in an alternative untranslated exon of hexokinase 1 associated with hereditary motor and sensory neuropathy -- Russe (HMSNR).

scientific article

A novel GEFS+ locus on 12p13.33 in a large Roma family

scientific article published on 13 September 2011

A novel locus for autosomal dominant cone-rod dystrophy maps to chromosome 10q.

scientific article published on 29 August 2012

AA9int: SNP interaction pattern search using non-hierarchical additive model set

ANO10 c.1150_1151del is a founder mutation causing autosomal recessive cerebellar ataxia in Roma/Gypsies

scientific article published on 19 October 2011

Acenocoumarol Pharmacogenetic Dosing Algorithms and Their Application in Two Bulgarian Patients with Low Anticoagulant Requirements

scientific article published on 16 September 2015

Alcohol consumption and prostate cancer incidence and progression: A Mendelian randomisation study

scientific article published on 19 September 2016

Assessing the role of insulin-like growth factors and binding proteins in prostate cancer using Mendelian randomization: Genetic variants as instruments for circulating levels

scientific article published on 26 May 2016

Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci

scientific article published on 11 June 2018

Association between estrogen receptor-α gene polymorphisms and dermatomyositis in Bulgarian patients

scientific article published on 6 March 2014

Association of TNF-α polymorphisms with adult dermatomyositis and systemic lupus erythematosus in Bulgarian patients

scientific article published on 22 August 2012

Association of vitamin D receptor gene BsmI B/b and FokI F/f polymorphisms with adult dermatomyositis and systemic lupus erythematosus

scientific article published on 11 March 2016

Atlas of prostate cancer heritability in European and African-American men pinpoints tissue-specific regulation

scientific article published on 7 April 2016

Author Correction: Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci

scholarly article published in Nature Genetics

Author Correction: Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci

scholarly article published in Nature Genetics

Author Correction: Germline variation at 8q24 and prostate cancer risk in men of European ancestry

scientific article published in Nature Communications

Autosomal-recessive congenital cerebellar ataxia is caused by mutations in metabotropic glutamate receptor 1.

scientific article

Bipolar disorder in the Bulgarian Gypsies: genetic heterogeneity in a young founder population

scientific article published in March 2009

Blood lipids and prostate cancer: a Mendelian randomization analysis

scientific article published on 19 March 2016

Clonal dissemination of multilocus sequence type ST15 KPC-2-producing Klebsiella pneumoniae in Bulgaria

scientific article published on 25 August 2015

Combinations of serum prostate-specific antigen and plasma expression levels of let-7c, miR-30c, miR-141, and miR-375 as potential better diagnostic biomarkers for prostate cancer

scientific article

Dominance of multidrug-resistant Denmark(14)-32 (ST230) clone among Streptococcus pneumoniae serotype 19A isolates causing pneumococcal disease in Bulgaria from 1992 to 2013.

scientific article published on 31 July 2014

Exome sequencing in roma families identifies tandem GRM1 mutations in a novel form of congenital cerebellar ataxia

Fine-mapping identifies multiple prostate cancer risk loci at 5p15, one of which associates with TERT expression

scientific article published on 27 March 2013

Fine-mapping identifies multiple prostate cancer risk loci at 5p15, one of which associates with TERT expression.

scientific article

Fine-mapping of prostate cancer susceptibility loci in a large meta-analysis identifies candidate causal variants.

scientific article published on 11 June 2018

Fine-mapping the HOXB region detects common variants tagging a rare coding allele: evidence for synthetic association in prostate cancer

scientific article

Focal epilepsy of probable temporal lobe origin in a Gypsy family showing linkage to a novel locus on 7p21.3

scientific article published in September 2011

Gender-Specific Effect of CYP2C8*3 on the Risk of Essential Hypertension in Bulgarian Patients

scientific article

Gene and pathway level analyses of germline DNA-repair gene variants and prostate cancer susceptibility using the iCOGS-genotyping array

scientific article

Gene and pathway level analyses of germline DNA-repair gene variants and prostate cancer susceptibility using the iCOGS-genotyping array

scientific article published on 13 February 2018

Generation of a human iPSC line from a patient with congenital glaucoma caused by mutation in CYP1B1 gene

scientific article published on 4 January 2018

Genetic association between the phospholipase A2 gene and unipolar affective disorder: a multicentre case???control study

article

Genetically Determined TNF-α Secretion Influences the Development of Dermatomyositis and Systemic Lupus Erythematosus

article

Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types

scientific article published in September 2016

Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies

article

Genomewide scan and fine-mapping linkage studies in four European samples with bipolar affective disorder suggest a new susceptibility locus on chromosome 1p35-p36 and provides further evidence of loci on chromosome 4q31 and 6q24.

scientific article

Germline variation at 8q24 and prostate cancer risk in men of European ancestry

scientific article published in Nature Communications

Height, selected genetic markers and prostate cancer risk: results from the PRACTICAL consortium

scientific article

Height, selected genetic markers and prostate cancer risk: results from the PRACTICAL consortium

article by Artitaya Lophatananon et al published 20 March 2018 in British Journal of Cancer

IDH1/IDH2 but not TP53 mutations predict prognosis in Bulgarian glioblastoma patients

scientific article

Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array

scientific article

Identification of seven new prostate cancer susceptibility loci through a genome-wide association study

scientific article

Investigating the possible causal role of coffee consumption with prostate cancer risk and progression using Mendelian randomization analysis

scientific article published on 14 October 2016

Isolation of Escherichia coli ST131 producing KPC-2 in Bulgaria

scientific article published on 3 January 2017

LTBP2 and CYP1B1 mutations and associated ocular phenotypes in the Roma/Gypsy founder population

scientific article

Lack of association between the 5HT2A receptor polymorphism (T102C) and unipolar affective disorder in a multicentric European study

scientific article published in October 2003

Lack of genetic association between the phospholipase A2 gene and bipolar mood disorder in a European multicentre case-control study.

scientific article published in August 2006

Molecular genetics of retinitis pigmentosa in two Romani (Gypsy) families.

scientific article published on 11 August 2006

Molecular screening for hereditary nonpolyposis colorectal cancer in Bulgaria

scholarly article by Tanya Kadiyska et al published 1 January 2006 in Open Medicine

Multiple novel prostate cancer susceptibility signals identified by fine-mapping of known risk loci among Europeans

scientific article published on 29 May 2015

Novel mutation in Wilms' tumour 1 gene associated with steroid-resistant nephrotic syndrome

scientific article published on 7 October 2010

PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS

scientific article published in December 2016

Partial epilepsy syndrome in a Gypsy family linked to 5q31.3-q32.

scientific article published on 23 March 2009

Polygenic hazard score to guide screening for aggressive prostate cancer: development and validation in large scale cohorts

scientific article published on 10 January 2018

Polymorphisms in androgen metabolism genes AR, CYP1B1, CYP19, and SRD5A2and prostate cancer risk and aggressiveness in Bulgarian patients

scientific article published on 19 April 2016

Polyunsaturated fatty acids and prostate cancer risk: a Mendelian randomisation analysis from the PRACTICAL consortium

scientific article published on 4 August 2016

Positive association of dopamine D2 receptor polymorphism with bipolar affective disorder in a European Multicenter Association Study of affective disorders

scientific article published in March 2002

Positive association of dopamine D2 receptor polymorphism with bipolar affective disorder in a European multicenter association study of affective disorders

scholarly article by Isabelle Massat et al published 14 February 2002 in American Journal of Medical Genetics Part A

Prediction of individual genetic risk to prostate cancer using a polygenic score

scientific article published on 14 July 2015

Prevalence of GBJ2 mutations in patients with severe to profound congenital nonsyndromic sensorineural hearing loss in Bulgarian population.

scientific article published on 29 October 2011

Pubertal development and prostate cancer risk: Mendelian randomization study in a population-based cohort

scientific article published on 4 April 2016

Publisher Correction: Shared heritability and functional enrichment across six solid cancers

scientific article published on 23 September 2019

Reconstructing the population history of European Romani from genome-wide data

scientific article

Role of the promoter polymorphism IL-6 -174G/C in dermatomyositis and systemic lupus erythematosus

scientific article

SNP interaction pattern identifier (SIPI): an intensive search for SNP-SNP interaction patterns

scientific article published on 30 December 2016

Serotonin transporter 5HTTLPR polymorphism and affective disorders: no evidence of association in a large European multicenter study

scientific article

Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study

scientific article

Shared heritability and functional enrichment across six solid cancers

scientific article published in Nature Communications

Shared heritability and functional enrichment across six solid cancers

Steroid-resistant nephrotic syndrome caused by novel WT1 mutation inherited from a mosaic parent

scientific article published in December 2015

The effects of height and BMI on prostate cancer incidence and mortality: a Mendelian randomization study in 20,848 cases and 20,214 controls from the PRACTICAL consortium

scientific article

The first genomewide interaction and locus-heterogeneity linkage scan in bipolar affective disorder: strong evidence of epistatic effects between loci on chromosomes 2q and 6q.

scientific article

The rs266729 single-nucleotide polymorphism in the adiponectin gene shows association with gestational diabetes

scientific article published on 26 September 2013

Three novel SLC2A1 mutations in Bulgarian patients with different forms of genetic generalized epilepsy reflecting the clinical and genetic diversity of GLUT1-deficiency syndrome

scientific article published on 28 November 2017

Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction

scientific article published in January 2021

Validation of an NGS Approach for Diagnostic BRCA1/BRCA2 Mutation Testing

scientific article published on April 2015

Vitamin D and estrogen receptor gene polymorphisms and the risk of colorectal cancer in Bulgaria

scientific article published on 21 June 2006

Whole peripheral blood miR-146a and miR-155 expression levels in Systemic lupus erythematosus patients

scholarly article published in Acta Reumatologica Portuguesa

List of works by Radka Kaneva

A Large-Scale Analysis of Genetic Variants within Putative miRNA Binding Sites in Prostate Cancer

A genetic risk score to guide age-specific, personalized prostate cancer screening

A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer

A meta-analysis of genome-wide association studies to identify prostate cancer susceptibility loci associated with aggressive and non-aggressive disease

A mutation in an alternative untranslated exon of hexokinase 1 associated with hereditary motor and sensory neuropathy -- Russe (HMSNR).

A novel GEFS+ locus on 12p13.33 in a large Roma family

A novel locus for autosomal dominant cone-rod dystrophy maps to chromosome 10q.

AA9int: SNP interaction pattern search using non-hierarchical additive model set

ANO10 c.1150_1151del is a founder mutation causing autosomal recessive cerebellar ataxia in Roma/Gypsies

Acenocoumarol Pharmacogenetic Dosing Algorithms and Their Application in Two Bulgarian Patients with Low Anticoagulant Requirements

Alcohol consumption and prostate cancer incidence and progression: A Mendelian randomisation study

Assessing the role of insulin-like growth factors and binding proteins in prostate cancer using Mendelian randomization: Genetic variants as instruments for circulating levels

Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci

Association between estrogen receptor-α gene polymorphisms and dermatomyositis in Bulgarian patients

Association of TNF-α polymorphisms with adult dermatomyositis and systemic lupus erythematosus in Bulgarian patients

Association of vitamin D receptor gene BsmI B/b and FokI F/f polymorphisms with adult dermatomyositis and systemic lupus erythematosus

Atlas of prostate cancer heritability in European and African-American men pinpoints tissue-specific regulation

Author Correction: Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci

Author Correction: Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci

Author Correction: Germline variation at 8q24 and prostate cancer risk in men of European ancestry

Autosomal-recessive congenital cerebellar ataxia is caused by mutations in metabotropic glutamate receptor 1.

Bipolar disorder in the Bulgarian Gypsies: genetic heterogeneity in a young founder population

Blood lipids and prostate cancer: a Mendelian randomization analysis

Clonal dissemination of multilocus sequence type ST15 KPC-2-producing Klebsiella pneumoniae in Bulgaria

Combinations of serum prostate-specific antigen and plasma expression levels of let-7c, miR-30c, miR-141, and miR-375 as potential better diagnostic biomarkers for prostate cancer

Dominance of multidrug-resistant Denmark(14)-32 (ST230) clone among Streptococcus pneumoniae serotype 19A isolates causing pneumococcal disease in Bulgaria from 1992 to 2013.

Exome sequencing in roma families identifies tandem GRM1 mutations in a novel form of congenital cerebellar ataxia

Fine-mapping identifies multiple prostate cancer risk loci at 5p15, one of which associates with TERT expression

Fine-mapping identifies multiple prostate cancer risk loci at 5p15, one of which associates with TERT expression.

Fine-mapping of prostate cancer susceptibility loci in a large meta-analysis identifies candidate causal variants.

Fine-mapping the HOXB region detects common variants tagging a rare coding allele: evidence for synthetic association in prostate cancer

Focal epilepsy of probable temporal lobe origin in a Gypsy family showing linkage to a novel locus on 7p21.3

Gender-Specific Effect of CYP2C8*3 on the Risk of Essential Hypertension in Bulgarian Patients

Gene and pathway level analyses of germline DNA-repair gene variants and prostate cancer susceptibility using the iCOGS-genotyping array

Gene and pathway level analyses of germline DNA-repair gene variants and prostate cancer susceptibility using the iCOGS-genotyping array

Generation of a human iPSC line from a patient with congenital glaucoma caused by mutation in CYP1B1 gene

Genetic association between the phospholipase A2 gene and unipolar affective disorder: a multicentre case???control study

Genetically Determined TNF-α Secretion Influences the Development of Dermatomyositis and Systemic Lupus Erythematosus

Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types

Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies

Genomewide scan and fine-mapping linkage studies in four European samples with bipolar affective disorder suggest a new susceptibility locus on chromosome 1p35-p36 and provides further evidence of loci on chromosome 4q31 and 6q24.

Germline variation at 8q24 and prostate cancer risk in men of European ancestry

Height, selected genetic markers and prostate cancer risk: results from the PRACTICAL consortium

Height, selected genetic markers and prostate cancer risk: results from the PRACTICAL consortium

IDH1/IDH2 but not TP53 mutations predict prognosis in Bulgarian glioblastoma patients

Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array

Identification of seven new prostate cancer susceptibility loci through a genome-wide association study

Investigating the possible causal role of coffee consumption with prostate cancer risk and progression using Mendelian randomization analysis

Isolation of Escherichia coli ST131 producing KPC-2 in Bulgaria

LTBP2 and CYP1B1 mutations and associated ocular phenotypes in the Roma/Gypsy founder population

Lack of association between the 5HT2A receptor polymorphism (T102C) and unipolar affective disorder in a multicentric European study

Lack of genetic association between the phospholipase A2 gene and bipolar mood disorder in a European multicentre case-control study.

Molecular genetics of retinitis pigmentosa in two Romani (Gypsy) families.

Molecular screening for hereditary nonpolyposis colorectal cancer in Bulgaria

Multiple novel prostate cancer susceptibility signals identified by fine-mapping of known risk loci among Europeans

Novel mutation in Wilms' tumour 1 gene associated with steroid-resistant nephrotic syndrome

PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS

Partial epilepsy syndrome in a Gypsy family linked to 5q31.3-q32.

Polygenic hazard score to guide screening for aggressive prostate cancer: development and validation in large scale cohorts

Polymorphisms in androgen metabolism genes AR, CYP1B1, CYP19, and SRD5A2and prostate cancer risk and aggressiveness in Bulgarian patients

Polyunsaturated fatty acids and prostate cancer risk: a Mendelian randomisation analysis from the PRACTICAL consortium

Positive association of dopamine D2 receptor polymorphism with bipolar affective disorder in a European Multicenter Association Study of affective disorders

Positive association of dopamine D2 receptor polymorphism with bipolar affective disorder in a European multicenter association study of affective disorders

Prediction of individual genetic risk to prostate cancer using a polygenic score

Prevalence of GBJ2 mutations in patients with severe to profound congenital nonsyndromic sensorineural hearing loss in Bulgarian population.

Pubertal development and prostate cancer risk: Mendelian randomization study in a population-based cohort

Publisher Correction: Shared heritability and functional enrichment across six solid cancers

Reconstructing the population history of European Romani from genome-wide data

Role of the promoter polymorphism IL-6 -174G/C in dermatomyositis and systemic lupus erythematosus

SNP interaction pattern identifier (SIPI): an intensive search for SNP-SNP interaction patterns

Serotonin transporter 5HTTLPR polymorphism and affective disorders: no evidence of association in a large European multicenter study

Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study

Shared heritability and functional enrichment across six solid cancers

Shared heritability and functional enrichment across six solid cancers

Steroid-resistant nephrotic syndrome caused by novel WT1 mutation inherited from a mosaic parent

The effects of height and BMI on prostate cancer incidence and mortality: a Mendelian randomization study in 20,848 cases and 20,214 controls from the PRACTICAL consortium

The first genomewide interaction and locus-heterogeneity linkage scan in bipolar affective disorder: strong evidence of epistatic effects between loci on chromosomes 2q and 6q.

The rs266729 single-nucleotide polymorphism in the adiponectin gene shows association with gestational diabetes

Three novel SLC2A1 mutations in Bulgarian patients with different forms of genetic generalized epilepsy reflecting the clinical and genetic diversity of GLUT1-deficiency syndrome