B. Bereznai

Semmelweis University

Hungary

1144 Citations
15 h-Index

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3 Similar Profiles

Parkinson Disease Medicine & Life Sciences

Mutation Medicine & Life Sciences

Genes Medicine & Life Sciences

Mitochondrial DNA Medicine & Life Sciences

Dystonic Disorders Medicine & Life Sciences

Multiple Sclerosis Medicine & Life Sciences

Dystonia Medicine & Life Sciences

Mitochondrial Diseases Medicine & Life Sciences

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Research Output 1993 2018

1144 Citations
15 h-Index
32 Article

4 Citations (Scopus)

The rs13388259 intergenic polymorphism in the genomic context of the BCYRN1 gene is associated with Parkinson's disease in the hungarian population

Márki, S., Göblös, A., Szlávicz, E., Török, N., Balicza, P., Bereznai, B., Takáts, A., Engelhardt, J., Klivényi, P., Vécsei, L., Molnár, M. J., Nagy, N. & Széll, M., Jan 1 2018, In : Parkinson's Disease. 2018, 9351598.

Research output: Contribution to journal › Article

Parkinson Disease

Long Noncoding RNA

Population

Genes

Penetrance

18 Citations (Scopus)

Rare variants in β-Amyloid precursor protein (APP) and Parkinson's disease

Schulte, E. C., Fukumori, A., Mollenhauer, B., Hor, H., Arzberger, T., Perneczky, R., Kurz, A., Diehl-Schmid, J., Hüll, M., Lichtner, P., Eckstein, G., Zimprich, A., Haubenberger, D., Pirker, W., Brücke, T., Bereznai, B., Molnar, M. J., Lorenzo-Betancor, O., Pastor, P., Peters, A. & 7 others, Gieger, C., Estivill, X., Meitinger, T., Kretzschmar, H. A., Trenkwalder, C., Haass, C. & Winkelmann, J., Oct 22 2015, In : European Journal of Human Genetics. 23, 10, p. 1328-1333 6 p.

Research output: Contribution to journal › Article

Amyloid beta-Protein Precursor

Parkinson Disease

Dementia

Phenotype

Microtubule-Associated Proteins

8 Citations (Scopus)

The coexistence of dynamin 2 mutation and multiple mitochondrial DNA (mtDNA) deletions in the background of severe cardiomyopathy and centronuclear myopathy

Gal, A., Inczedy-Farkas, G., Pal, E., Remenyi, V., Bereznai, B., Gellér, L., Szelid, Z., Merkely, B. & Molnar, M. J., 2015, In : Clinical Neuropathology. 34, 2, p. 89-95 7 p.

Research output: Contribution to journal › Article

Dynamin II

Congenital Structural Myopathies

Cardiomyopathies

Mitochondrial DNA

Mutation