O. Beltcheva

发表

An Approach for Object-Oriented Animation Design

M. Gervautz, O. Beltcheva, 2007 .

Selected rapporteur summaries from the XX world congress of psychiatric genetics, Hamburg, Germany, october 14–18, 2012

L. DeLisi, L. Duncan, E. Byrne, 2013, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

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

R. Kaneva, C. Slavov, A. Mitkova, 2016, Turkish journal of medical sciences.

A familial case of severe infantile nephronophthisis explained by oligogenic inheritance.

R. Kaneva, V. Mitev, D. Roussinov, 2017, European journal of medical genetics.

Genetic and Epidemiological Indications for Adiponectin Gene Dysregulation in Gestational Diabetes Mellitus

R. Kaneva, V. Mitev, O. Beltcheva, 2018 .

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

R. Kaneva, V. Mitev, O. Beltcheva, 2014, Archives of Gynecology and Obstetrics.

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

R. Kaneva, E. Nelson, V. Mitev, 2011, Drug and alcohol dependence.

Mutation spectrum in the nephrin gene (NPHS1) in congenital nephrotic syndrome

K. Tryggvason, U. Lenkkeri, O. Beltcheva, 2001, Human mutation.

Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts

Jason D. Robinson, D. Rujescu, S. Cichon, 2015, Behavior Genetics.

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

R. Kaneva, E. Morgunova, V. Mitev, 2010, NDT plus.

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

R. Kaneva, V. Mitev, D. Roussinov, 2016, Renal failure.

Nephrin-mutations in congenital nephrotic syndrome of the Finnish type and cell lineage specific gene regulation

O. Beltcheva, 2005 .

Locus 9p21 and the revolution in cardiovascular genetics - contribution in vascular pathology and evaluation of coronary artery disease risk.

R. Kaneva, V. Mitev, K. Naydenov, 2015 .

Alternatively used promoters and distinct elements direct tissue-specific expression of nephrin.

T. Hökfelt, K. Tryggvason, S. Fetissov, 2003, Journal of the American Society of Nephrology : JASN.

Wolf-Hirschhorn syndrome candidate 1-like 1 epigenetically regulates nephrin gene expression.

R. Kurayama, Y. Nishibori, Y. Akimoto, 2017, American journal of physiology. Renal physiology.

Involvement of GLCCI1 in mouse spermatogenesis

H. Takematsu, K. Nitta, Y. Nishibori, 2022, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Sp1 Specifically Binds to an Evolutionarily Conserved DNA Segment within a Region Necessary for Podocyte-Specific Expression of Nephrin

K. Tryggvason, S. Kontusaari, O. Beltcheva, 2009, Nephron Experimental Nephrology.

Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts

Sarah M. Hartz, Jason D. Robinson, D. Rujescu, 2015, Behavior Genetics.

C283Y mutation and other C‐terminal nucleotide changes in the γ‐sarcoglycan gene in the Bulgarian gypsy population

I. Kremensky, A. Todorova, I. Tournev, 1999, Human mutation.

In situ hybridization detection of miRNA using LNA™ oligonucleotides.

S. C. Doné, O. Beltcheva, 2014, Methods in molecular biology.

Evaluation of the clinical value of the newly identified urine biomarker HIST1H4K for diagnosis and prognosis of prostate cancer in Bulgarian patients.

R. Kaneva, C. Slavov, A. Mitkova, 2013, Journal of B.U.ON. : official journal of the Balkan Union of Oncology.

C283Y mutation and other C‐terminal nucleotide changes in the γ‐sarcoglycan gene in the Bulgarian Gypsy population

I. Kremensky, A. Todorova, I. Tournev, 2000 .

Genome-wide association studies as a contemporary approach to determination of the genetic basis of arterial hypertension - Part Two.

R. Kaneva, V. Mitev, K. Naydenov, 2014 .

Selected rapporteur summaries from the XX world congress of psychiatric genetics, Hamburg, Germany, october 14–18, 2012

L. DeLisi, L. Duncan, Cybele C P Wong, 2013, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

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

R. Kaneva, C. Slavov, A. Mitkova, 2016, Turkish journal of medical sciences.

Rare host variants in ciliary expressed genes contribute to COVID-19 severity in Bulgarian patients

M. Baymakova, K. Mihova, O. Beltcheva, 2024, Scientific reports.

Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts

Sarah M. Hartz, Jason D. Robinson, D. Rujescu, 2015, Behavior Genetics.