About us / Management


Prof. Radka Kaneva, PhD


E-mail: kaneva@mmcbg.org



Education:


2000                PhD in Molecular Biology - Sofia Medical University, Bulgaria

1989                MSc in Molecular Biology, Genetic and Cell Engineering - Biology Faculty, Sofia University St. Kliment Ohridski,

1988                Bachelor in Biotechnology - Biology Faculty, Sofia University St. Kliment Ohridski, Bulgaria




Previous
and Current Employment


2012 -              Associated Professor, Department of Medical Chemistry and Biochemistry, Medical University -Sofia

2010 - 2011   Chief Assistant Professor, Department of Medical Chemistry and Biochemistry, Medical University -Sofia

2009                Senior Assistant Professor, Department of Medical Chemistry and Biochemistry, Medical University -Sofia

2008                Assistant Professor, Department of Chemistry and Biochemistry, Medical University -Sofia

2005 -              Executive manager - Molecular Medicine Center, Medical University – Sofia

1998 - 2008      Molecular Biologist, Laboratory of Molecular Pathology,

University Hospital of Obstetrics and Gynaecology, Sofia

1994 - 1997      Research Associate, Neuroscience and Behaviour Research foundation, Sofia

1992 - 1993     Research Assistant, Laboratory of Molecular Pathology, University Hospital of Obstetrics and Gynaecology, Sofia

1989 - 1991      Graduate Research Assistant, National Centre of Oncology, Medical Academy, Sofia. 
 


Trainings and research fellowships


2003 - 2004       Humboldt Return Fellowship, Alexander von Humboldt Foundation

2001 - 2003     Humboldt PostDoctoral Research Fellow, Institute of Human Genetics, University of Bonn, Germany, Alexander von Humboldt Foundation

1998                French-American School of Neurobehavioural Genetics, University of Northern Colorado, USA

1993 -1994      Visiting Research Fellow, Department of Biochemistry, University of Oxford, UK, Open Society Foundation

1992                Human Genetics Summer Course, Leuven, Belgium



Scientific Awards


2008                Award Panacea of Medical University - Sofia for special contribution to teaching, research and expert activity in the professional biomedical field  



Membership in Professional Societies


International Society of Psychiatric Genetics

European Society of Human Genetics

European Association for Cancer Research

Bulgarian Society of Biochemistry, Biophysics and Molecular Biology

Youth Union Molecular Genetics in Medicine



Teaching Experience


Lecturer in Biochemistry course for medical students, 2008 -

Lecturer in Diagnostics and prevention of inherited disorders. Molecular medicine course for undergraduate medical students

Lecturer in Molecular diagnostics of inherited disorders course in the master program for molecular biology students

Lecturer in course Introduction of Quality Assurance System In Preclinical Disciplines Teaching On Under- And Postgraduate Level Of Bulgarian Medical Universities Funded by the PHARE, TEMPUS

Lecturer in postgraduate course Psychiatric genetics, Department of Psychiatry, Medical University - Sofia

Promoter of 13 master students in Molecular Biology and Genetics

Scientific Consultant of 4 master students in Medical Informatics and Statistics, FMI, Sofia University St. Kl. Ohridski.

Scientific consultant of 5 PhD students in Molecular Biology and Genetics



Expert activities


National Contact Person, Programme IDEAS, 7FP of European Commission



Language proficiency


English, German, Russian



Research interests

Genetics of complex diseases, Neuropsychiatric and behavioral genetics, Oncogenetics, Ophthalmogenetics, Pharmacogenetics and genomics



Participation in Research projects:


Principal Investigator


2009 - 2010    Analysis of polymorphic variants in candidate genes associated with prostate cancer. Project 51/Contract 28/2009 Research Fund of Sofia Medical University,

2008 - 2009    Analysis of large genomic deletions, insertions and rearrangements in MLH1 and MSH2 gene in Bulgarian patients with CRC. Project 40/Contract 15/2008 Research Fund of Sofia Medical University,

2004 - 2008    National programme genomics: Genomics of retinitis pigmentosa, G-3-03/2004-2008, National Science Fund, Ministry of Education and Science

2003 - 2007    National programme genomics: Genomics of affective disorders G-2-03/2003-2007, National Science Fund, Ministry of Education and Science, Coordinator and PI

2004 - 2005    Fine mapping of 4p16 locus linked with a bipolar affective disorder in Bulgarian family, Research Fund of Sofia Medical University, L21/2004-2005

2001 - 2002    Linkage analysis on chromosome 21q22 in patients with Bipolar Affective Disorder in Bulgarian Families, Research Fund of Sofia Medical University 2001-2002

1995 - 1998    Interactions between genetic and psychosocial vulnerability factors in affective disorders, Ministry of Education and Science


Co-Principal Investigator


International


2009 - 2013    Varieties of Impulsivity in Opiate and Stimulant Users, NIDA, USA, R01 DA021421, PI Assist. Prof. J. Vassileva

2007 - 2010    Genetic and phenotype study of partial epilepsies in Gypsies, NHMRC, Australia, ID 458736, PI Prof. L. Kalaydjieva

2006 - 2011    Genetic Epidemiology of Heroin addiction in Bulgaria, NIDA, USA, R01 DA018823, PI Prof. Alexander Todorov, subaward WU-07-50

2005 - 2008    Enhancing the capacity of biomedical research in Bulgaria: Molecular Medicine Centre, FP6-LIFESCIHEALTH LSH-2004-3-3, SSA- Promotion of cooperation with Associated Candidate Countries (ACC)

2005 - 2008    Bipolar Disorder in a genetic isolate, NHMRC, Australia, PI Prof. L. Kalaydjieva

1997 - 2000    European Collaborative Study on Molecular Genetics in Affective Disorders (Genes in Affective Disorders), BIOMED2 program IC20-CT97-0018 European, Coordinator Prof. J.Mendlewicz

1995 - 1996    Morphometric and neural connectivity characteristics of fetal brains at genetic risk for bipolar disorder Stanley Research Foundation Award PI Prof. A. Jablensky

1991 - 1995    EC Concerted Action on Affective Disorders: interactions between genetic and psychosocial vulnerability factors BIOMED1 program of EC, INCO Copernicus, Coordinator Prof. J.Mendlewicz

1991 - 1994    Fetal Brain Development and Schizophrenia NIH Fogarty grant, University of Southern California, PI Prof. V. Mednick

National

2011-2012         Early cognitive disturbances in patients with arterial hypertension., MU-Sofia, Assoc Prof.K. Najdenov

2011-2012         Analysis of the mutations in BRCA1 gene in Bulgarian patients with triple negative breast cancer, MU-Sofia, Assoc Prof. S.Christova

2011-2012         Study of the role of genomic rearrangements, deletions and duplications for the pathology of congenital anomalies of the kidney and urinary tract (CAKUT). MU-Sofia, Assoc Prof. А. Boueva

2011-2012         Association study of candidate genes and phenotypes in bipolar affective disorder MU-Sofia, Prof. V.Milanova

2011-2012         Investigation of mutation in HFE gene in patients with chronic liver disorders with concurrent syndrome of iron overload, MU-Sofia, Prof. L. Vladimirova

2010-2011    Study of the molecular basis of congenital anomalies of the kidney and urinary tract (CAKUT) in Bulgaria. Role of Pax2 for the pathogenesis of CAKUT, MU-Sofia, A/Prof. Bueva

2010-2011    Investigation of the diagnostic specificity of promoter hypermethylation of biomarkers in urine, associated with prostate cancer in Bulgarian patients, MU-Sofia, Prof. Ch. Slavov

2009-2013    National University Complex in Biomedical and Translational Research, infrastructural project, National Science Fund, Ministry of Education and Science, Coordinator, Prof. V. Mitev

2009-2012    Contemporary approaches for unravelling the genetic basis of epilepsy National Science Fund, Ministry of Education and Science,  PI Prof. A. Jordanova

2009-2012    Clinical and molecular markers with predictive value for survival, quality of life and treatment response in high-grade gliomas, National Science Fund, Ministry of Education and Science, PI A/Prof. N. Gabrovsky

2009-2012    Genome-wide screening for CNVs in Mental Retardation, National Science Fund, Ministry of Education and Science, PI Prof. V. Bojinova -Chamova

2009-2012    Study of the genetic variations, associated with increased risk and identification of diagnostics and prognostics markers for prostate cancer, National Science Fund, Ministry of Education and Science, PI Prof. Ch Slavov

2009-2010    Enhancing the capacity of the cores Cell and Tissue Cultures, Microarray and Laser Microdissection in Molecular Medicine Center, MU - Sofia, infrastructural project, 8I-2009, PI Prof. V. Mitev

2009-2010    Genetic, neuropsychological and vascular markers for early detection of Alzheimers Disease, MU - Sofia, PI Prof. L. Trajkov, 4C-2009

2009-2010     Study of candidate genes in linkage region for partial epilepsy, MU – Sofia, PI T. Goranova

2009-2010     Analysis of big deletions, insertions and rearrangements in BRCA1 and BRCA2, MU – Sofia, PI Assist Prof A. Mitkova

2009-2010     Molecular diagnostic of deafness, MU – Sofia, PI Prof. K. Kunev

2009-2010    Squamous cell carcinoma of the larynx and the hypopharynx. Genetic defects associated with carcinogenesis and biological behaviour of the tumor, MU – Sofia, PI A/Prof. I. Chalakov

2009-2010    Familial associative analysis of neurocognitive disorders and DISC1 gene in bipolar affective disorder patients. MU – Sofia, PI Prof. V. Milanova

2009-2010    Study of relationship between polymorphic variants in interleukin 10 (IL10) and the dermatomiositis origin in Bulgaria, MU – Sofia, PI A/Prof. L. Durmishev

2009-2010    Study of the role of hepatocyte nuclear factor 1-beta (HNF1b) for the development of  congenital anomalies of the kidney and urinary tract

2008-2011    Molecular pathways involved in mamary gland cancer, National Science Fund, Ministry of Education and Science, PI Assoc. Prof. E Georgieva

2008-2010    Enhancing the capacity of the Molecular Medicine Center, Medical University-Sofia for functional genomic, proteomic and metabolomic research, D002-118/2008

2008-2009    Study of the role of the polymorphisms in tumor necrosis factor- alfa (TNF-α) for dermatomyositis pathology in Bulgaria, MU – Sofia, PI A/Prof. L. Durmishev

2008-2009    Influence of genetic variants in ABCA4 gene on development of age-related macula degeneration (ARMD) and assessment of the risk for disease on Bulgarian population, MU – Sofia, PI Prof. I. Kremensky

2007-2008    Researching of genetic markers for determinating possibility of development of aerobic and anaerobic quality in sportsman who have active competitive sporting activity, National Sport Academy, PI Assoc.Prof. P. Atanasov

2007-2008    Role of the podocin gene (NPHS2) mutations for the pathology of steroid-resistant nephrotic syndrome and microalbuminuria population risk in Bulgaria, MU – Sofia, PI Assist Prof. O. Beltcheva

2007-2008    Search for mutations in BRCA1 и BRCA2 genes related to breast and prostate cancer, Research Fund of Sofia Medical University, PI Dr.A.Mitkova, contract 27

2007-2008    Investigation of the role of GRM1 gene polymorphisms in the susceptibility to affective disorders and opioide addictions, Research Fund of Sofia Medical University, PI Prof. I. Kremensky, contract 28

2007-2008    Investigation of genetic characteristics, related to aerobic and anaerobic qualities, relevant to sport activities, National Sport Academy, PI, A/Prof. P. Atanasov

2007-2008    Endophenotype characteristics of Bipolar Affective Disorder patients, Research Fund of Sofia Medical University, PI Prof. V. Milanova, contract 45

2006-2008    Establishing a SNP genotyping and Gene Expression Core at Molecular Medicine Center, Medical University, Sofia, DRI-15, 2006, National Science Fund, Ministry of Education and Science, PI Prof.V.Ovcharov

2006-2007    Genetic polymorphisms in XRCC1 and XRCC3 genes related to the early radio-sensitivity reactions in endometrial and cervical cancer. Research Fund of Sofia Medical University, PI Dr A. Savov

2005-2008    Study of the molecular basis of the endometrial cancer in Bulgaria, National Science Fund, Ministry of Education and Science, Bulgaria,, PI Assoc. Prof. N. Doganov

2001-2002    Microsatellite instability analysis in Bulgarian patients with Colorectal Cancer, Research Fund of Sofia Medical University, PI Dr A. Savov

2001-2005    Investigation of the clinical and pathomorphological characteristics of the hereditary and sporadic colorectal cancer, National Science Fund, Ministry of Education and Science, PI Prof. D. Damyanov

1991-1994    Molecular Genetics of endogenous psychosis: Schizophrenia and bipolar affective disorder, Ministry of Education and Science, PI Prof. Jablensky

Consultant


2005-2007      Prevalence of primary aldosteronism in a selected hypertensive population, National Science Fund, Ministry of Education and Science Young Scientists Award, PI Dr. J. Matrozova

2005-2008      Study of the role of genetic polymorphisms of xenobiotic metabolism related enzymes and factors involved in the immune response for the tumor progression and prognosis in colorectal cancer, PI A/Prof. T.Vlaykova, TU-Stara Zagora, VU-L-05/2005, National Science Fund, Ministry of Education and Science



Publications in journals with peer review:


1.     Kote-Jarai Z, Olama AA, Giles GG, Severi G, Schleutker J, Weischer M, Campa D,Riboli E, Key T, Gronberg H, Hunter DJ, Kraft P, Thun MJ, Ingles S, Chanock S, Albanes D, Hayes RB, Neal DE, Hamdy FC, Donovan JL, Pharoah P, Schumacher F, Henderson BE, Stanford JL, Ostrander EA, Sorensen KD, Dörk T, Andriole G, Dickinson JL, Cybulski C, Lubinski J, Spurdle A, Clements JA, Chambers S, Aitken J, Gardiner RA, Thibodeau SN, Schaid D, John EM, Maier C, Vogel W, Cooney KA,Park JY, Cannon-Albright L, Brenner H, Habuchi T, Zhang HW, Lu YJ, Kaneva R, Muir K, Benlloch S, Leongamornlert DA, Saunders EJ, Tymrakiewicz M, Mahmud N, Guy M, O`Brien LT, Wilkinson RA, Hall AL, Sawyer EJ, Dadaev T, Morrison J, Dearnaley DP, Horwich A, Huddart RA, Khoo VS, Parker CC, Van As N, Woodhouse CJ, Thompson A,Christmas T, Ogden C, Cooper CS, Lophatonanon A, Southey MC, Hopper JL, English DR, Wahlfors T, Tammela TL, Klarskov P, Nordestgaard BG, Røder MA, Tybjærg-Hansen A, Bojesen SE, Travis R, Canzian F, Kaaks R, Wiklund F, Aly M, Lindstrom S, Diver WR, Gapstur S, Stern MC, Corral R, Virtamo J, Cox A, Haiman CA, Le Marchand L, Fitzgerald L, Kolb S, Kwon EM, Karyadi DM, Orntoft TF, Borre M, Meyer A, Serth J, Yeager M, Berndt SI, Marthick JR, Patterson B, Wokolorczyk D, Batra J, Lose F, McDonnell SK, Joshi AD, Shahabi A, Rinckleb AE, Ray A, Sellers TA, Lin HY, Stephenson RA, Farnham J, Muller H, Rothenbacher D, Tsuchiya N, Narita S, Cao GW, Slavov C, Mitev V; The UK Genetic Prostate Cancer Study Collaborators/British Association of Urological Surgeons` Section of Oncology; The UK ProtecT Study Collaborators, The Australian Prostate Cancer BioResource; The PRACTICAL Consortium, Easton DF, Eeles RA. Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study. Nat Genet. 2011 Jul 10. doi: 10.1038/ng.882. PubMed PMID: 21743467. IF 2010 (36.377)

2, Azmanov DN, Zhelyazkova S, Radionova M, Morar B, Angelicheva D, Zlatareva D, Kaneva R, Tournev I, Kalaydjieva L, Sander JW. Focal epilepsy of probable temporal lobe origin in a Gypsy family showing linkage to a novel locus on 7p21.3. Epilepsy Res. 2011 Jun 4. PubMed PMID: 21645995. IF 2010 (2.302)

3. Nikolov MA, Beltcheva O, Galabova A, Ljubenova A, Jankova E, Gergov G, Russev AA, Lynskey MT, Nelson EC, Nesheva E, Krasteva D, Lazarov P, Mitev VI, Kremensky IM, Kaneva RP, Todorov AA. No evidence of association between 118A>G OPRM1 polymorphism and heroin dependence in a large Bulgarian case-control sample. Drug Alcohol Depend. 2011 Aug 1;117(1):62-5. Epub 2011 Jan 31. PubMed PMID: 21277709 IF 2010 (3.365)

4. Azmanov DN, Dimitrova S, Florez L, Cherninkova S, Draganov D, Morar B, Saat R, Juan M, Arostegui JI, Ganguly S, Soodyall H, Chakrabarti S, Padh H, López-Nevot MA, Chernodrinska V, Anguelov B, Majumder P, Angelova L, Kaneva R, Mackey DA, Tournev I, Kalaydjieva L. LTBP2 and CYP1B1 mutations and associated ocular phenotypes in the Roma/Gypsy founder population. Eur J Hum Genet. 2011 Mar; 19(3):326-33. Epub 2010 Nov 17. PubMed PMID: 21081970; PubMed Central PMCID: IF 2010 (4.380)

5. Beltcheva O, Boueva A, Morgunova E, Boiadjieva E, Marinova S, Kaneva R and Mitev V. Novel mutation in Wilms tumour 1 gene associated with 6 steroid-resistant nephrotic syndrome, Nephrol Dial Transplant Plus, Volume 4 Issue 1 February 2011: 17-19. IF 2011(3.564)

6. Konstantinova D, Kaneva R, Dimitrov R, Savov A, Ivanov S, Dyankova T, Kremensky I, Mitev V. (2010) Rare mutations in the PIK3CA gene contribute to aggressive endometrial cancer. DNA Cell Biol. 2010 Feb;29(2):65-70. PubMed PMID: 19839777. IF 2009 (2.280)

7. Konstantinova D, Kadiyska T, Sokolova V, Kaneva R, Mirchev M, Savov A, Aleksandrova A, Nedin D, Kostadinov E, Damyanov D, Kremensky I, Mitev V. (2010) CHEK2 I157T and colorectal cancer in Bulgaria. J BUON. 2010 Apr-Jun;15(2):314-7. PubMed PMID: 20658728.

8. Azmanov DN, Dimitrova S, Florez L, Cherninkova S, Draganov D, Morar B, Saat R, Juan M, Arostegui JI, Ganguly S, Soodyall H, Chakrabarti S, Padh H, López-Nevot MA, Chernodrinska V, Anguelov B, Majumder P, Angelova L, Kaneva R, Mackey DA, Tournev I, Kalaydjieva L. (2010) LTBP2 and CYP1B1 mutations and associated ocular phenotypes in the Roma/Gypsy founder population. Eur J Hum Genet. 2010 Nov 17. PubMed PMID: 21081970. IF 2009 ( 3.564)

9. Konstantinova DV, Kadiyska TK, Kaneva RP, Tosheva EG, Guseva VT, Dimitrov BH, Dimitrov RG, Doganov NI, Ivanov SI, Kremensky IM, Mitev VI. (2010) CHEK2 I157T and endometrial cancer. DNA Cell Biol. 2009 Jan;28(1):9-12. PubMed PMID: 18834326. IF 2009 (2.280)

10. Eeles RA, Kote-Jarai Z, Al Olama AA, Giles GG, Guy M, Severi G, Muir K, Hopper JL, Henderson BE, Haiman CA, Schleutker J, Hamdy FC, Neal DE, Donovan JL, Stanford JL, Ostrander EA, Ingles SA, John EM, Thibodeau SN, Schaid D, Park JY, Spurdle A, Clements J, Dickinson JL, Maier C, Vogel W, Dörk T, Rebbeck TR, Cooney KA, Cannon-Albright L, Chappuis PO, Hutter P, Zeegers M, Kaneva R, … Slavov C, Mitkova A, ….. The UK Genetic Prostate Cancer Study Collaborators/British Association of Urological Surgeons Section of Oncology, The UK ProtecT Study Collaborators, The PRACTICAL Consortium, Easton DF (2009) Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. Nat Genet 41(10):1116-21. IF 2009 (34.284)

11. Angelicheva D, Tournev I, Guergueltcheva V, Mihaylova V, Azmanov DN, Morar B, Radionova M, Smith SJ, Zlatareva D, Stevens JM, Kaneva R, Bojinova V, Carter K,Brown M, Jablensky A, Kalaydjieva L, Sander JW. (2009) Partial epilepsy syndrome in a Gypsy family linked to 5q31.3-q32. Epilepsia. 2009 Mar 21.

12. Hantke J, Chandler D, King R, Wanders RJ, Angelicheva D, Tournev I, McNamaraE, Kwa M, Guergueltcheva V, Kaneva R, Baas F, Kalaydjieva L. (2009) A mutation in an alternative untranslated exon of hexokinase 1 associated with Hereditary Motor and Sensory Neuropathy - Russe (HMSNR). Eur J Hum Genet. 2009 Jun 17. IF 2009

13. Kaneva R, Milanova V, Angelicheva D, MacGregor S, Kostov C, Vladimirova R, Aleksiev S, Ivanova M, Stoyanova V, Loh A, Hallmayer J, Kalaydjieva L and Jablensky A. (2008) Bipolar disorder in the Bulgarian Gypsies: genetic heterogeneity in a young founder population, Am J Med Genet, Neuropsych Genet, 2008 Apr 28. IF 2006 ( 4.463)

14. Sivadorai P, Cherninkova S, Bouwer S, Kamenarova K, Angelicheva D, Seeman P, Hollingsworth K, Mihaylova V, Oscar A, Dimitrova G, Kaneva R, Tournev I, Kalaydjieva L (2008) Genetic heterogeneity and minor CYP1B1 involvement in the molecular basis of primary congenital glaucoma in gypsies, Clin Genet. 2008 Jul;74(1):82-7. Epub 2008 Jun 5 IF2006 ( 3.14)

15. Massat I, Lerer B, Souery D, Blackwood D, Muir W, Kaneva R, Nothen MM, Oruc L, Papadimitriou GN, Dikeos D, Serretti A, Bellivier F, Golmard JL, Milanova V, Del-Favero J, Van Broeckhoven C, Mendlewicz J (2007) HTR2C (cys23ser) polymorphism influences early onset in bipolar patients in a large European multicenter association study. Mol Psychiatry. 2007 Sep;12(9):797-8 IF 2006 (11.804)

16. Abou Jamra R, Fuerst R, Kaneva R, Orozco Diaz G, Rivas F, Mayoral F, Gay E, Sans S, Gonzalez MJ, Gil S, Cabaleiro F, Del Rio F, Perez F, Haro J, Auburger G, Milanova V, Kostov C, Chorbov V, Stoyanova V, Nikolova-Hill A, Onchev G, Kremensky I, Jablensky A, Schulze TG, Propping P, Rietschel M, Nothen MM, Cichon S, Wienker TF, Schumacher J (2007) 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. Am J Hum Genet. 2007 Nov;81(5):974-86. IF 2006 (12.629)

17. Konstantinova DV, Kadiyska TK, Kaneva RP, Ivanov SI, Dimitrov RG, Dyankova TV, Meinhardt KP, Gulubova MV, Vlaykova TI, Doganov NI, Mitev VI, Kremensky IM. (2007) Microsatellite instability in Bulgarian patients with endometrial cancer. J BUON. 2007 Jan-Mar;12(1):85-9.

18. Kadiyska T, Yakulov T, Kaneva R, Nedin D, Alexandrova A, Gegova A, Savov A,Mitev V, Kremensky I. (2007)Vitamin D and estrogen receptor gene polymorphisms and the risk of colorectal cancer in Bulgaria. Int J Colorectal Dis. 2007 Apr;22(4):395-400. Epub 2006 Jun 21. IF 2006 (2.006)

19. Kadiyska TK, Kaneva RP, Nedin DG, Alexandrova AB, Gegova AT, Lalchev SG,Christova T, Mitev VI, Horst J, Bogdanova N, Kremensky IM (2006) Novel MLH1 frameshift mutation in an extended hereditary nonpolyposis colorectal cancer family. World J Gastroenterol. 2006 Dec 28;12(48):7848-51.

20. Kadiyska TP, Goranova TE, Dineva GK, Nedin DG, Alexandrova AB, Gegova AT, Kaneva RP, Damyanov DN, Kremensky IM and Mitev VI (2006) Molecular screening for hereditary nonpolyposis colorectal cancer in Bulgaria. Central European Journal of Medicine 2006 June, 1: 2: 128-135

21. Chakarova CF, Cherninkova S, Tournev I, Waseem N, Kaneva R, Jordanova A,Veraitch BK, Gill B, Colclough T, Nakova A, Oscar A, Mihaylova V, Nikolova-Hill A, Wright AF, Black GC, Ramsden S, Kremensky I, Bhattacharya SS.(2006) Molecular genetics of retinitis pigmentosa in two Romani (Gypsy) families.Mol Vis. 2006 Aug 11;12:909-14. IF 2006 (2.377)

22. Dikeos DG, Papadimitriou GN, Souery D, Del-Favero J, Massat I, Blackwood D,Cichon S, Daskalopoulou E, Ivezic S, Kaneva R, Karadima G, Lorenzi C, MilanovaV, Muir W, Nothen M, Oruc L, Rietschel M, Serretti A, Van Broeckhoven C, Soldatos CR, Stefanis CN, Mendlewicz J. (2006) Lack of genetic association between the phospholipase A2 gene and bipolar mood disorder in a European multicentre case-control study. Psychiatr Genet. 2006 Aug; 16(4):169-71. IF 2006 (2.141)

23. Schumacher J, Kaneva R, Jamra RA, Diaz GO, Ohlraun S, Milanova V, Lee YA,Rivas F, Mayoral F, Fuerst R, Flaquer A, Windemuth C, Gay E, Sanz S, Gonzalez MJ, Gil S, Cabaleiro F, del Rio F, Perez F, Haro J, Kostov C, Chorbov V,Nikolova-Hill A, Stoyanova V, Onchev G, Kremensky I, Strauch K, Schulze TG,Nurnberg P, Gaebel W, Klimke A, Auburger G, Wienker TF, Kalaydjieva L, Propping P, Cichon S, Jablensky A, Rietschel M, Nothen MM. (2005) 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.Am J Hum Genet. 2005 Dec;77(6):1102-11. IF 12.649

24. Massat I, Souery D, Del-Favero J, Nothen M, Blackwood D, Muir W, Kaneva R, Serretti A, Lorenzi C, Rietschel M, Milanova V, Papadimitriou GN, Dikeos D, Van Broekhoven C, Mendlewicz J.(2005) Association between COMT (Val158Met) functional polymorphism and early onset in patients with major depressive disorder in a European multicenter genetic association study. Mol Psychiatry. 2005 Jun; 10(6):598-605. IF (9.335),

25. Kaneva R, Chorbov V, Milanova, Kostov C, Nickolov K, Chakarova C, Stoyanova V, Nikolova-Hill A, Krastev S, Onchev G, Kremensky I, Kalaydjieva L, Jablensky A (2004) Linkage analysis in bipolar pedigrees adds support for a susceptibility locus on 21q22. Psychiatr Genet –2004, 2004, Jun;14(2):101-106 IF2004 (2.162),

26. Blairy S, Linotte S, Souery D, Papadimitriou GN, Dikeos D, Lerer B, Kaneva R, Milanova V, Serretti A, Macciardi F, Mendlewicz J. (2004) Social adjustment and self-esteem of bipolar patients: a multicentric study.J Affect Disord. 2004 Apr;79(1-3):97-103. IF 2004 (2.703),

27. Mendlewicz J, Massat I, Souery D, Del-Favero J, Oruc L, Nothen MM, Blackwood D, Muir W, Battersby S, Lerer B, Segman RH, Kaneva R, Serretti A, Lilli R, Lorenzi C, Jakovljevic M, Ivezic S, Rietschel M, Milanova V, Van Broeckhoven C. (2004) Serotonin transporter 5HTTLPR polymorphism and affective disorders: no evidence of association in a large European multicenter study. Eur J Hum Genet. 2004 May;12(5):377-82 IF 2004 (2.741),

28. Papadimitriou GN, Dikeos DG, Souery D, Del-Favero J, Massat I, Avramopoulos D, Blairy S, Cichon S, Ivezic S, Kaneva R, Karadima G, Lilli R, Milanova V, Nothen M, Oruc L, Rietschel M, Serretti A, Van Broeckhoven C, Stefanis CN, Mendlewicz J. (2003) Genetic association between the phospholipase A2 gene and unipolar affectivedisorder: a multicentre case-control study. Psychiatr Genet. 2003 Dec;13(4):211-20. IF 2003 (2.414),

29. Oswald P, Souery D, Massat I, Del-Favero J, Linotte S, Papadimitriou G, Dikeos D, Kaneva R, Milanova V, Oruc L, Ivezic S, Serretti A, Lilli R, Van Broeckhoven C, Mendlewicz J. (2003) Lack of association between the 5HT2A receptor polymorphism (T102C) and unipolar affective disorder in a multicentric European study. Eur Neuropsychopharmacol. 2003 Oct;13(5):365-8. IF2003 (2.437),

30. Kremensky I, Todorova A, Jordanova A, Savov A, Tournev I, Iankova S, Georgieva B, Zaharova B, Kaneva R, Petkova R, Andonova S, Ivanova M, Ivanova N, Rainova R and Kalaydjieva L. (2003) Spectrum of mutations of the most common genetic disorders in Bulgaria J.Q.L.R- E.C. Qua. L., 2003, March – April, 1(2):172-185.,

31. Tzancheva M, Kadiyska T, Gegova AT, Dineva GK, Kaneva RP, Savov A, Marinov M, Kadyan, Penchev P, Nedin S, Alexandrova A, Ilieva J, Damyanov D, Mitev V and Kremensky I. (2003) Microsatelite instability in patients with colorectal cancer: Clinicomorphological Parallels. Annuaire de l Universite de Sofia St.Kliment Ohridski 2003 95:151-158,

32. Kadiyska T., Tzancheva M, Nedin D, Alexandrova A, Marinov M, Kaneva R, Damyanov D, Mitev V and Kremenski I (2003) MLH1 Promotor Hypermethylation in Bulgarian Patients with Colorectal Cancer, BJMG, 2003, 6: 3-8,

33. Massat I, Souery D, Del-Favero J, Van Gestel S, Serretti A, Macciardi F, Smeraldi E, Kaneva R, Adolfsson R, Nylander PO, Blackwood D, Muir W, Papadimitriou GN, Dikeos D, Oruc L, Segman RH, Ivezic S, Aschauer H, Ackenheil M, Fuchshuber S, Dam H, Jakovljevic M, Peltonen L, Hilger C, Hentges F, Staner L, Milanova V, Jazin E, Lerer B, Van Broeckhoven C, Mendlewicz J. (2002): Positive association of dopamine D2 receptor polymorphism with bipolar affective disorder in a European multicenter association study of affective disorders. Am J Med Genet. 2002 Mar 8;114(2):177-85. IF2002 ( 2.378),

34. Massat I, Souery D, Del-Favero J, Oruc L, Noethen MM, Blackwood D, Thomson M, Muir W, Papadimitriou GN, Dikeos DG, Kaneva R, Serretti A, Lilli R, Smeraldi E, Jakovljevic M, Folnegovic V, Rietschel M, Milanova V, Valente F, Van Broeckhoven C, Mendlewicz J. (2002): Excess of allele1 for alpha3 subunit GABA receptor gene (GABRA3) in bipolar patients: a multicentric association study. Mol Psychiatry. 2002;7(2):201-7. IF2002 (5.497),

35. Massat I, Souery D, Del-Favero J, Oruc L, Jakovljevic M, Folnegovic V, Adolfsson R, Kaneva R, Papadimitriou G, Dikeos D, Jazin E, Milanova V, Van Broeckhoven C, Mendlewicz J. (2001): Lack of association between GABRA3 and unipolar affective disorder: a multicentre study. Int J Neuropsychopharmacol. 2001 Sep;4(3):273-8. IF 2001 (2.779),

36. Lerer B, Macciardi F, Segman RH, Adolfsson R, Blackwood D, Blairy S, Del Favero J, Dikeos DG, Kaneva R, Lilli R, Massat I, Milanova V, Muir W, Noethen M, Oruc L, Petrova T, Papadimitriou GN, Rietschel M, Serretti A, Souery D, Van Gestel S, Van Broeckhoven C, Mendlewicz J. (2001): Variability of 5-HT2C receptor cys23ser polymorphism among European populations and vulnerability to affective disorder. Mol Psychiatry. 2001 Sep;6(5):579-85. IF 2001 (6.25),

37. Souery D, Van Gestel S, Massat I, Blairy S, Adolfsson R, Blackwood D, Del-Favero J, Dikeos D, Jakovljevic M, Kaneva R, Lattuada E, Lerer B, Lilli R, Milanova V, Muir W, Nothen M, Oruc L, Papadimitriou G, Propping P, Schulze T, Serretti A, Shapira B, Smeraldi E, Stefanis C, Thomson M, Van Broeckhoven C, Mendlewicz J. (2001): Tryptophan hydroxylase polymorphism and suicidality in unipolar and bipolar affective disorders: a multicenter association study. Biol Psychiatry. Mar 1;49(5):405-9. IF 2001 (5.505),

38. Massat I, Souery D, Lipp O, Blairy S, Papadimitriou G, Dikeos D,Ackenheil M, Fuchshuber S, Hilger C, Kaneva R, Milanova V, Verheyen G, Raeymaekers P, Staner L, Oruc L, Jakovljevic M, Serretti A,Macciardi F, Van Broeckhoven C, Mendlewicz J. (2000): A European multicenter association study of HTR2A receptor polymorphism in bipolar affective disorder. Am J Med Genet. 96(2):136-40 IF2000 (2.479),

39. Serretti A., Macciardi F, Cusin C, Lattuada E, Souery D, Lipp O, Mahieu B, Van Broeckhoven C, Blackwood D, Muir W, Aschauer HN., Heiden AM, Ackenheil M, Fuchshuber S, Raeymaekers P, Verheyen G, Kaneva R, Jablensky A, Papadimitriou GN, Dikeos DG, Stefanis CN, Smeraldi E, Mendlewicz J. (2000): Linkage of mood disorders with D2, D3, and TH genes: a multicenter study. J Affect Disord; 58(1): 51-61 IF2000 (1.938),

40. Kremensky I., Jordanova A., Todorova A., Savov A., Iankova S., Georgieva B., Zaharova B., Kaneva R., Petkova R., Andonova S., Ivanova M., Michaylova E., Ivanova N., Kalaydjieva L. (2000) Mutation profile of the most common genetic disorders in Bulgaria Balkan J Med Genet, 2000,3(4):3-13.,

41. Tzancheva M, Kaneva R, Kumanov P, Williams G, Tyler-Smith C. (1999): Two male patients with ring Y: definition of an interval in Yq contributing to Turner syndrome. J Med Genet; 36(7): 549-53 IF1999 (2.986),

42. Souery D, Lipp O, Rivelli SK, Massat I, Serretti A, Cavallini C, Ackenheil M, Adolfsson R, Aschauer H, Bl