LAMA2 Congenital Muscle Dystrophy: A Novel Pathogenic Mutation in Bulgarian Patient

由 Dimova, Ivanka, Kremensky, Ivo
發表在 Case Rep Genet (2018)

Genetic analysis of haemophilia A in Bulgaria

由 Petkova, Rumena, Chakarov, Stoian, Kremensky, Ivo
出版 2004

Association Study between Promoter Polymorphism of TPH1 and Progression of Idiopathic Scoliosis

由 Yablanski, Vasil, Nikolova, Svetla, Vlaev, Evgeni, Savov, Alexey, Kremensky, Ivo
發表在 J Biomark (2016)

Association between Estrogen Receptor Alpha Gene Polymorphisms and Susceptibility to Idiopathic Scoliosis in Bulgarian Patients: A Case-Control Study

由 Nikolova, Svetla, Yablanski, Vasil, Vlaev, Evgeni, Stokov, Luben, Savov, Alexey, Kremensky, Ivo
發表在 Open Access Maced J Med Sci (2015)

Association Study between Idiopathic Scoliosis and Polymorphic Variants of VDR, IGF-1, and AMPD1 Genes

由 Nikolova, Svetla, Yablanski, Vasil, Vlaev, Evgeni, Stokov, Luben, Savov, Alexey Slavkov, Kremensky, Ivo Marinov
發表在 Genet Res Int (2015)

Positive Association between TGFB1 Gene and Susceptibility to Idiopathic Scoliosis in Bulgarian Population

由 Nikolova, Svetla, Dikova, Milka, Dikov, Dobrin, Djerov, Assen, Savov, Alexey, Kremensky, Ivo, Loukanov, Alexandre
發表在 Anal Cell Pathol (Amst) (2018)

Role of the IL-6 Gene in the Etiopathogenesis of Idiopathic Scoliosis

由 Nikolova, Svetla, Dikova, Milka, Dikov, Dobrin, Djerov, Assen, Dzhebir, Gyulnas, Atanasov, Ventseslav, Savov, Alexey, Kremensky, Ivo
發表在 Anal Cell Pathol (Amst) (2015)

In Search of Biomarkers for Idiopathic Scoliosis: Leptin and BMP4 Functional Polymorphisms

由 Nikolova, Svetla, Yablanski, Vasil, Vlaev, Evgeni, Getova, Gergana, Atanasov, Ventseslav, Stokov, Luben, Savov, Alexey Slavkov, Kremensky, Ivo Marinov
發表在 J Biomark (2015)

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

由 Kamenarova, Kunka, Cherninkova, Sylvia, Romero Durán, Margarita, Prescott, DeQuincy, Valdés Sánchez, Maria Lourdes, Mitev, Vanio, Kremensky, Ivo, Kaneva, Radka, Bhattacharya, Shomi S, Tournev, Ivailo, Chakarova, Christina
出版 2013

Novel MLH1 frameshift mutation in an extended hereditary nonpolyposis colorectal cancer family

由 Kadiyska, Tanya Kirilova, Kaneva, Radka Petrova, Nedin, Dimitar Georgiev, Alexandrova, Alexandrina Borisova, Gegova, Antonina Тodorova, Lalchev, Stoyan Ganchev, Christova, Tatyana, Mitev, Vanio Ivanov, Horst, Juergen, Bogdanova, Nadja, Kremensky, Ivo Marinov
出版 2006

Dominant Intermediate Charcot-Marie-Tooth Type C Maps to Chromosome 1p34-p35

由 Jordanova, Albena, Thomas, Florian P., Guergueltcheva, Velina, Tournev, Ivailo, Gondim, Francisco A. A., Ishpekova, Borjana, De Vriendt, Els, Jacobs, An, Litvinenko, Ivan, Ivanova, Neviana, Buzhov, Borjan, De Jonghe, Peter, Kremensky, Ivo, Timmerman, Vincent
出版 2003

Metabolite profile of a mouse model of Charcot–Marie–Tooth type 2D neuropathy: implications for disease mechanisms and interventions

由 Bais, Preeti, Beebe, Kirk, Morelli, Kathryn H., Currie, Meagan E., Norberg, Sara N., Evsikov, Alexei V., Miers, Kathy E., Seburn, Kevin L., Guergueltcheva, Velina, Kremensky, Ivo, Jordanova, Albena, Bult, Carol J., Burgess, Robert W.
發表在 Biol Open (2016)

A Founder Mutation in the GK1 Gene Is Responsible for Galactokinase Deficiency in Roma (Gypsies)

由 Kalaydjieva, Luba, Perez-Lezaun, Anna, Angelicheva, Dora, Onengut, Suna, Dye, Danielle, Bosshard, Nils U., Jordanova, Albena, Savov, Alexei, Yanakiev, Peter, Kremensky, Ivo, Radeva, Brigitta, Hallmayer, Joachim, Markov, Arseni, Nedkova, Vanya, Tournev, Ivailo, Aneva, Lidia, Gitzelmann, Richard
出版 1999

`No evidence of association between 118A>G OPRM1 polymorphism and heroin dependence in a large Bulgarian case-control sample

由 Nikolov, Momchil A., Beltcheva, Olga, Galabova, Antoaneta, Ljubenova, Anna, Jankova, Elena, Gergov, Galin, Russev, Atanas A., Lynskey, Michael T., Nelson, Elliot C., Nesheva, Eleonora, Krasteva, Dorita, Lazarov, Philip, Mitev, Vanio I., Kremensky, Ivo M., Kaneva, Radka P., Todorov, Alexandre A.
出版 2011

Glycyl tRNA Synthetase Mutations in Charcot-Marie-Tooth Disease Type 2D and Distal Spinal Muscular Atrophy Type V

由 Antonellis, Anthony, Ellsworth, Rachel E., Sambuughin, Nyamkhishig, Puls, Imke, Abel, Annette, Lee-Lin, Shih-Queen, Jordanova, Albena, Kremensky, Ivo, Christodoulou, Kyproula, Middleton, Lefkos T., Sivakumar, Kumaraswamy, Ionasescu, Victor, Funalot, Benoit, Vance, Jeffery M., Goldfarb, Lev G., Fischbeck, Kenneth H., Green, Eric D.
出版 2003

The Slavic NBN Founder Mutation: A Role for Reproductive Fitness?

由 Seemanova, Eva, Varon, Raymonda, Vejvalka, Jan, Jarolim, Petr, Seeman, Pavel, Chrzanowska, Krystyna H., Digweed, Martin, Resnick, Igor, Kremensky, Ivo, Saar, Kathrin, Hoffmann, Katrin, Dutrannoy, Véronique, Karbasiyan, Mohsen, Ghani, Mehdi, Barić, Ivo, Tekin, Mustafa, Kovacs, Peter, Krawczak, Michael, Reis, André, Sperling, Karl, Nothnagel, Michael
發表在 PLoS One (2016)

Spectrum and frequencies of BRCA1/2 mutations in Bulgarian high risk breast cancer patients

由 Dodova, Rumyana Ivanova, Mitkova, Atanaska Velichkova, Dacheva, Daniela Rosenova, Hadjo, Lina Basam, Vlahova, Alexandrina Ivanova, - Hadjieva, Margarita Stoyanova Taushanova, Valev, Spartak Stoyanov, Caulevska, Marija Mitko, Popova, Stanislava Dimitrova, Popov, Ivan Emilov, Dikov, Tihomir Iliichev, Sedloev, Theophil Angelov, Ionkov, Atanas Stefanov, Timcheva, Konstanta Velinova, Christova, Svetlana Liubomirova, Kremensky, Ivo Marinov, Mitev, Vanio Ivanov, Kaneva, Radka Petrova
發表在 BMC Cancer (2015)

Erratum to: Spectrum and frequencies of BRCA1/2 mutations in Bulgarian high risk breast cancer patients

由 Dodova, Rumyana Ivanova, Mitkova, Atanaska Velichkova, Dacheva, Daniela Rosenova, Hadjo, Lina Basam, Vlahova, Alexandrina Ivanova, Taushanova – Hadjieva, Margarita Stoyanova, Valev, Spartak Stoyanov, Caulevska, Marija Mitko, Popova, Stanislava Dimitrova, Popov, Ivan Emilov, Dikov, Tihomir Iliichev, Sedloev, Theophil Angelov, Ionkov, Atanas Stefanov, Timcheva, Konstanta Velinova, Christova, Svetlana Liubomirova, Kremensky, Ivo Marinov, Mitev, Vanio Ivanov, Kaneva, Radka Petrova
發表在 BMC Cancer (2017)

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

由 Abou Jamra, Rami , Fuerst, Robert , Kaneva, Radka , Orozco Diaz, Guillermo , Rivas, Fabio , Mayoral, Fermin , Gay, Eudoxia , Sans, Sebastian , González, Maria Jose , Gil, Susana , Cabaleiro, Francisco , del Rio, Francisco , Perez, Fermin , Haro, Jesus , Auburger, Georg , Milanova, Vihra , Kostov, Christian , Chorbov, Vesselin , Stoyanova, Vessela , Nikolova-Hill, Amelia , Onchev, George , Kremensky, Ivo , Jablensky, Assen , Schulze, Thomas G. , Propping, Peter , Rietschel, Marcella , Nöthen, Markus M. , Cichon, Sven , Wienker, Thomas F. , Schumacher, Johannes 
出版 2007

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 Fur...

由 Schumacher, Johannes, Kaneva, Radka, Jamra, Rami Abou, Diaz, Guillermo Orozco, Ohlraun, Stephanie, Milanova, Vihra, Lee, Young-Ae, Rivas, Fabio, Mayoral, Fermin, Fuerst, Robert, Flaquer, Antonia, Windemuth, Christine, Gay, Eudoxia, Sanz, Sebastian, González, Maria José, Gil, Susana, Cabaleiro, Francisco, del Rio, Francisco, Perez, Fermin, Haro, Jesus, Kostov, Christian, Chorbov, Vesselin, Nikolova-Hill, Amelia, Stoyanova, Vessela, Onchev, George, Kremensky, Ivo, Strauch, Konstantin, Schulze, Thomas G., Nürnberg, Peter, Gaebel, Wolfgang, Klimke, Ansgar, Auburger, Georg, Wienker, Thomas F., Kalaydjieva, Luba, Propping, Peter, Cichon, Sven, Jablensky, Assen, Rietschel, Marcella, Nöthen, Markus M.
出版 2005