Éva Oláh

1.5k total citations
85 papers, 1.1k citations indexed

About

Éva Oláh is a scholar working on Molecular Biology, Genetics and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Éva Oláh has authored 85 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 21 papers in Genetics and 17 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Éva Oláh's work include Acute Lymphoblastic Leukemia research (10 papers), Acute Myeloid Leukemia Research (9 papers) and Lymphoma Diagnosis and Treatment (9 papers). Éva Oláh is often cited by papers focused on Acute Lymphoblastic Leukemia research (10 papers), Acute Myeloid Leukemia Research (9 papers) and Lymphoma Diagnosis and Treatment (9 papers). Éva Oláh collaborates with scholars based in Hungary, Sweden and Netherlands. Éva Oláh's co-authors include Erzsébet Balogh, László Márkász, György Stuber, Emilie Flaberg, László Székely, Attila Kiss, Staffan Eksborg, Csongor Kiss, Kálmán Rák and Anikó Újfalusi and has published in prestigious journals such as Nature, Scientific Reports and Biochemical and Biophysical Research Communications.

In The Last Decade

Éva Oláh

83 papers receiving 1.0k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Éva Oláh Hungary 19 358 234 187 169 155 85 1.1k
Victoria Bedell United States 16 431 1.2× 181 0.8× 129 0.7× 218 1.3× 108 0.7× 40 1.0k
Daiichiro Hasegawa Japan 18 366 1.0× 252 1.1× 153 0.8× 364 2.2× 233 1.5× 105 1.2k
Noël Philippe France 13 647 1.8× 261 1.1× 165 0.9× 213 1.3× 341 2.2× 17 1.3k
Jasenka Wagner Croatia 23 397 1.1× 246 1.1× 209 1.1× 307 1.8× 472 3.0× 66 1.4k
Judith Margolin United States 18 778 2.2× 285 1.2× 194 1.0× 93 0.6× 223 1.4× 48 1.5k
F. Brok‐Simoni Israel 21 584 1.6× 203 0.9× 141 0.8× 362 2.1× 168 1.1× 70 1.4k
Takafumi Matsumura Japan 25 752 2.1× 270 1.2× 393 2.1× 107 0.6× 175 1.1× 79 1.7k
Miharu Yabe Japan 21 509 1.4× 225 1.0× 134 0.7× 565 3.3× 235 1.5× 84 1.3k
Beryl Crossley United States 13 170 0.5× 240 1.0× 181 1.0× 93 0.6× 41 0.3× 22 796
Miranda R.M. Baert Netherlands 23 694 1.9× 271 1.2× 194 1.0× 269 1.6× 679 4.4× 32 1.7k

Countries citing papers authored by Éva Oláh

Since Specialization
Citations

This map shows the geographic impact of Éva Oláh's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Éva Oláh with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Éva Oláh more than expected).

Fields of papers citing papers by Éva Oláh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Éva Oláh. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Éva Oláh. The network helps show where Éva Oláh may publish in the future.

Co-authorship network of co-authors of Éva Oláh

This figure shows the co-authorship network connecting the top 25 collaborators of Éva Oláh. A scholar is included among the top collaborators of Éva Oláh based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Éva Oláh. Éva Oláh is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Rácz, Gergely, Éva Oláh, Máté Tóth, et al.. (2025). Identification of new reference genes with stable expression patterns for cell cycle experiments in human leukemia cell lines. Scientific Reports. 15(1). 1052–1052. 1 indexed citations
2.
Szakszon, Katalin, et al.. (2019). FBN1 gene mutations in 26 Hungarian patients with suspected Marfan syndrome or related fibrillinopathies. Journal of Biotechnology. 301. 105–111. 3 indexed citations
3.
Buglyó, Gergely, Dániel Beyer, Sándor Bíró, & Éva Oláh. (2018). The Wilms' tumour 1 gene as a factor in non-syndromic hypospadias: evidence and controversy. Pathology. 50(4). 377–381. 1 indexed citations
4.
Mokánszki, Attila, et al.. (2014). Is sperm hyaluronic acid binding ability predictive for clinical success of intracytoplasmic sperm injection: PICSI vs. ICSI?. Systems Biology in Reproductive Medicine. 60(6). 348–354. 37 indexed citations
5.
Szakszon, Katalin, Carmelo Salpietro, Naseebullah Kakar, et al.. (2013). De novo mutations of the gene encoding the histone acetyltransferase KAT6B in two patients with Say‐Barber/Biesecker/Young‐Simpson syndrome. American Journal of Medical Genetics Part A. 161(4). 884–888. 26 indexed citations
6.
Szakszon, Katalin, et al.. (2013). Complete recovery from psychosis upon miglustat treatment in a juvenile Niemann–Pick C patient. European Journal of Paediatric Neurology. 18(1). 75–78. 18 indexed citations
7.
Wolff, Anette S. B., László Maródi, Jaanika Kärner, et al.. (2013). Anti-Cytokine Autoantibodies Preceding Onset of Autoimmune Polyendocrine Syndrome Type I Features in Early Childhood. Journal of Clinical Immunology. 33(8). 1341–1348. 47 indexed citations
8.
Knegt, Alida C., et al.. (2012). Subtelomeric 6.7 Mb trisomy 10p and 5.6 Mb monosomy 21q detected by FISH and array‐CGH in three related patients. American Journal of Medical Genetics Part A. 158A(4). 869–876. 5 indexed citations
9.
Újfalusi, Anikó, et al.. (2011). Jumping translocation of chromosome 1q associated with good clinical outcome in a case of Burkitt leukemia. Cancer Genetics. 204(4). 207–210. 3 indexed citations
10.
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12.
Keresztes, Katalin, Zoltán Beck, Zoltán Szöllősi, et al.. (2006). Association between the Epstein-Barr Virus and Hodgkin’s Lymphoma in the North-Eastern Part of Hungary: Effects on Therapy and Survival. Acta Haematologica. 116(2). 101–107. 12 indexed citations
13.
Melegh, Béla, Judit Bene, Viktória Havasi, et al.. (2004). Phenotypic manifestations of the OCTN2 V295X mutation: Sudden infant death and carnitine‐responsive cardiomyopathy in Roma families. American Journal of Medical Genetics Part A. 131A(2). 121–126. 24 indexed citations
14.
Oláh, Éva, Andreas Gerber, & Johannes H. Wildhaber. (2003). Laryngeal Foreign Body in the Differential Diagnosis of Wheeze in Early Childhood. Pediatric Asthma Allergy & Immunology. 16(2). 101–104. 1 indexed citations
15.
Jakab, Zsuzsanna, István Szegedi, Erzsébet Balogh, Csongor Kiss, & Éva Oláh. (2002). Duchenne muscular dystrophy‐rhabdomyosarcoma, ichthyosis vulgaris/acute monoblastic leukemia: Association of rare genetic disorders and childhood malignant diseases. Medical and Pediatric Oncology. 39(1). 66–68. 15 indexed citations
16.
Benkő, Ilona, Péter Kovács, István Szegedi, et al.. (2001). Effect of myelopoietic and pleiotropic cytokines on colony formation by blast cells of children with acute lymphoblastic leukemia. Naunyn-Schmiedeberg s Archives of Pharmacology. 363(5). 499–508. 9 indexed citations
17.
Beck, Zoltán, Attila Kiss, Ferenc Tóth, et al.. (2000). Alterations ofP53andRBGenes and the Evolution of the Accelerated Phase of Chronic Myeloid Leukemia. Leukemia & lymphoma. 38(5-6). 587–597. 33 indexed citations
18.
Balogh, Erzsébet, et al.. (1994). Translocation 8;21 associated with acute nonlymphocytic leukemia in a down syndrome child. Cancer Genetics and Cytogenetics. 76(1). 72–73. 2 indexed citations
19.
Czeizel, Andrew E., Philippe Kiss, K Méhes, et al.. (1988). A nationwide evaluation of multiple congenital abnormalities in Hungary. Genetic Epidemiology. 5(3). 183–202. 11 indexed citations
20.
Oláh, Éva, et al.. (1962). [Studies on chondrogenesis. VII. The content of tissue hexosamine in regenerating joint surface in different stages of regeneration].. PubMed. 13. 127–38. 2 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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