Jozef Gécz

30.5k total citations
232 papers, 10.5k citations indexed

About

Jozef Gécz is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Jozef Gécz has authored 232 papers receiving a total of 10.5k indexed citations (citations by other indexed papers that have themselves been cited), including 169 papers in Genetics, 144 papers in Molecular Biology and 25 papers in Psychiatry and Mental health. Recurrent topics in Jozef Gécz's work include Genetics and Neurodevelopmental Disorders (140 papers), Genomic variations and chromosomal abnormalities (42 papers) and Genomics and Rare Diseases (35 papers). Jozef Gécz is often cited by papers focused on Genetics and Neurodevelopmental Disorders (140 papers), Genomic variations and chromosomal abnormalities (42 papers) and Genomics and Rare Diseases (35 papers). Jozef Gécz collaborates with scholars based in Australia, United States and France. Jozef Gécz's co-authors include John C. Mulley, Cheryl Shoubridge, Mark Corbett, Alastair H. MacLennan, Ági K. Gedeon, Ingrid E. Scheffer, Grant R. Sutherland, Lachlan A. Jolly, Gillian Turner and Lam Son Nguyen and has published in prestigious journals such as Nature, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Jozef Gécz

227 papers receiving 10.4k citations

Peers

Jozef Gécz

GENET

PMH

CMN

Naomichi Matsumoto Japan

Maximilian Muenke United States

André Reis Germany

Gudrun Rappold Germany

Dawna L. Armstrong United States

Hirotomo Saitsu Japan

Antonio Pizzuti Italy

Vania Broccoli Italy

Yong‐hui Jiang United States

Jonathan Sebat United States

Naomichi Matsumoto Japan

Jozef Gécz

6.6k ×1.0

5.0k ×0.8

GENET

746 ×0.6

PMH

321 ×0.3

1.4k ×1.4

CMN

Citations per year, relative to Jozef Gécz Jozef Gécz (= 1×) peers Naomichi Matsumoto

Countries citing papers authored by Jozef Gécz

Since Specialization

Citations

This map shows the geographic impact of Jozef Gécz'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 Jozef Gécz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jozef Gécz more than expected).

Fields of papers citing papers by Jozef Gécz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jozef Gécz. 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 Jozef Gécz. The network helps show where Jozef Gécz may publish in the future.

Co-authorship network of co-authors of Jozef Gécz

This figure shows the co-authorship network connecting the top 25 collaborators of Jozef Gécz. A scholar is included among the top collaborators of Jozef Gécz 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 Jozef Gécz. Jozef Gécz is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Gambardella, Antonio, Yu‐Chi Liu, Mark F. Bennett, et al.. (2025). PAK3 pathogenic variant associated with sleep‐related hypermotor epilepsy in a family with parental mosaicism. Epilepsia Open. 10(2). 593–601.

Alshawsh, Mohammed Abdullah, Melissa Wake, Jozef Gécz, et al.. (2024). Epigenomic newborn screening for conditions with intellectual disability and autistic features in Australian newborns. Epigenomics. 16(18). 1203–1214. 2 indexed citations

McRae, Helen M., Maria Bergamasco, Alexandra L. Garnham, et al.. (2024). Loss of PHF6 causes spontaneous seizures, enlarged brain ventricles and altered transcription in the cortex of a mouse model of the Börjeson–Forssman–Lehmann intellectual disability syndrome. PLoS Genetics. 20(10). e1011428–e1011428.

Kumar, Raman, Michaela Scherer, Tarin Ritchie, et al.. (2024). Mapping combinatorial expression of non-clustered protocadherins in the developing brain identifies novel PCDH19-mediated cell adhesion properties. Open Biology. 14(4). 230383–230383. 1 indexed citations

Corbett, Mark, Christel Depienne, Liana Veneziano, et al.. (2023). Genetics of familial adult myoclonus epilepsy: From linkage studies to noncoding repeat expansions. Epilepsia. 64(S1). S14–S21. 11 indexed citations

Hu, Jinghua, Lily R. Qiu, Gerardo Zapata, et al.. (2021). Transgenic mice with an R342X mutation in Phf6 display clinical features of Börjeson–Forssman–Lehmann Syndrome. Human Molecular Genetics. 30(7). 575–594. 7 indexed citations

Bennett, Mark F., Karen Oliver, Brigid M. Regan, et al.. (2020). Familial adult myoclonic epilepsy type 1 SAMD12 TTTCA repeat expansion arose 17,000 years ago and is present in Sri Lankan and Indian families. European Journal of Human Genetics. 28(7). 973–978. 22 indexed citations

Mol, Ben W., Jozef Gécz, Alastair H. MacLennan, et al.. (2020). Definition and diagnosis of cerebral palsy in genetic studies: a systematic review. Developmental Medicine & Child Neurology. 62(9). 1024–1030. 28 indexed citations

Sun, Jingjing, Shuo Yang, Xiaocui Zhang, et al.. (2020). Chromatin-Binding Protein PHF6 Regulates Activity-Dependent Transcriptional Networks to Promote Hunger Response. Cell Reports. 30(11). 3717–3728.e6. 6 indexed citations

10.

Niranjan, Tejasvi, Melanie May, Patrick Tarpey, et al.. (2019). Dysregulations of sonic hedgehog signaling in MED12‐related X‐linked intellectual disability disorders. Molecular Genetics & Genomic Medicine. 7(4). e00569–e00569. 10 indexed citations

11.

Hashimoto, Satoru, Melanie May, Alexey Epanchintsev, et al.. (2017). MED12-related XLID disorders are dose-dependent of immediate early genes (IEGs) expression. Human Molecular Genetics. 26(11). 2062–2075. 17 indexed citations

12.

Guy, Michael P., Marie Shaw, Catherine L. Weiner, et al.. (2015). Defects in tRNA Anticodon Loop 2′-O-Methylation Are Implicated in Nonsyndromic X-Linked Intellectual Disability due to Mutations inFTSJ1. Human Mutation. 36(12). 1176–1187. 112 indexed citations

13.

Horn, Denise, Christopher W. Carr, Omar Abdul‐Rahman, et al.. (2013). FOXP1 mutations cause intellectual disability and a recognizable phenotype. American Journal of Medical Genetics Part A. 161(12). 3166–3175. 67 indexed citations

14.

Jolly, Lachlan A., Claire C. Homan, R. Jacob, Simon C. Barry, & Jozef Gécz. (2013). The UPF3B gene, implicated in intellectual disability, autism, ADHD and childhood onset schizophrenia regulates neural progenitor cell behaviour and neuronal outgrowth. Human Molecular Genetics. 22(23). 4673–4687. 95 indexed citations

15.

Starokadomskyy, Petro, Nathan Gluck, Haiying Li, et al.. (2013). CCDC22 deficiency in humans blunts activation of proinflammatory NF-κB signaling. Journal of Clinical Investigation. 123(5). 2244–2256. 77 indexed citations

16.

Stegeman, Shane, Lachlan A. Jolly, Jozef Gécz, et al.. (2013). Loss of Usp9x Disrupts Cortical Architecture, Hippocampal Development and TGFβ-Mediated Axonogenesis. PLoS ONE. 8(7). e68287–e68287. 62 indexed citations

17.

Hynes, Kim, Patrick Tarpey, Leanne M. Dibbens, et al.. (2009). Epilepsy and mental retardation limited to females with PCDH19 mutations can present de novo or in single generation families. Journal of Medical Genetics. 47(3). 211–216. 59 indexed citations

18.

Molinari, Florence, S. Romano, François Foulquier, et al.. (2007). Oligosaccharyltransferase subunits mutations in non-syndromic mental retardation. European Journal of Human Genetics. 16. 25. 4 indexed citations

19.

Voss, Anne K., Caitlin Collin, Cheryl Shoubridge, et al.. (2007). Protein and gene expression analysis of Phf6, the gene mutated in the Börjeson–Forssman–Lehmann Syndrome of intellectual disability and obesity. Gene Expression Patterns. 7(8). 858–871. 37 indexed citations

20.

Finnis, Merran, Marie Mangelsdorf, Elke Holinski‐Feder, et al.. (2005). XLMR in MRX families 29, 32, 33 and 38 results from the dup24 mutation in the ARX (Aristaless related homeobox) gene. BMC Medical Genetics. 6(1). 16–16. 23 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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