Jozef Gécz

30.5k citations

232 papers · 10.5k indexed · h-index 56

Molecular Biology top 0.5%
Genetics top 0.1%
Psychiatry and Mental health top 1%
Cognitive Neuroscience top 2%
Cellular and Molecular Neuroscience top 2%

Co-authors: John C. Mulley Cheryl Shoubridge Mark Corbett Alastair H. MacLennan Ági K. Gedeon Ingrid E. Scheffer Grant R. Sutherland Lachlan A. Jolly
Topics: Genetics and Neurodevelopmental Disorders (140 papers)Genomic variations and chromosomal abnormalities (42 papers)Genomics and Rare Diseases (35 papers)
Cited by: Genetics Molecular Biology Psychiatry and Mental health
Journals: Nature Nucleic Acids Research Journal of Biological Chemistry
Partner nations: Australia United States France

In The Last Decade

Jozef Gécz

227 papers receiving 10.4k citations

Peers

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

#	Work	Indexed citations
1	PAK3 pathogenic variant associated with sleep‐related hypermotor epilepsy in a family with parental mosaicism 2025 ·Epilepsia Open ·Antonio Gambardella,Yu‐Chi Liu,Mark F. Bennett,(unknown),John A. Damiano,Francesco Fortunato,Matthew Coleman,Jacqueline Cherfils,Jean‐Vianney Barnier,Jozef Gécz,Melanie Bahlo,Samuel F. Berkovic,Michael S. Hildebrand	0
2	Epigenomic newborn screening for conditions with intellectual disability and autistic features in Australian newborns 2024 ·Epigenomics ·Mohammed Abdullah Alshawsh,Melissa Wake,Jozef Gécz,Mark Corbett,Richard Saffery,James Pitt,Ronda F. Greaves,Katrina Williams,Michael Field,Jeanie L.Y. Cheong,Minh Bui,S. K. Arora,Simon Sadedin,Sebastian Lunke,Meaghan Wall,David J. Amor,David E. Godler	2
3	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 2024 ·PLoS Genetics ·Helen M. McRae,(unknown),Maria Bergamasco,Alexandra L. Garnham,Yifang Hu,Mark Corbett,Lachlan Whitehead,Farrah El-Saafin,Bilal N. Sheikh,Stephen Wilcox,Anthony J. Hannan,Jozef Gécz,Gordon K. Smyth,Tim Thomas,Anne K. Voss	0
4	Mapping combinatorial expression of non-clustered protocadherins in the developing brain identifies novel PCDH19-mediated cell adhesion properties 2024 ·Open Biology ·(unknown),(unknown),Raman Kumar,(unknown),Michaela Scherer,Tarin Ritchie,Jonas Muhr,Jozef Gécz,Paul Q. Thomas	1
5	Genetics of familial adult myoclonus epilepsy: From linkage studies to noncoding repeat expansions 2023 ·Epilepsia ·Mark Corbett,Christel Depienne,Liana Veneziano,Karl Martin Klein,Francesco Brancati,Renzo Guerrini,Federico Zara,Shoji Tsuji,Jozef Gécz	11
6	Transgenic mice with an R342X mutation in Phf6 display clinical features of Börjeson–Forssman–Lehmann Syndrome 2021 ·Human Molecular Genetics ·(unknown),(unknown),Jinghua Hu,(unknown),Lily R. Qiu,Gerardo Zapata,Lucianne Vandeleur,Keqin Yan,Jason P. Lerch,Mark Corbett,Jozef Gécz,David J. Picketts	7
7	Familial adult myoclonic epilepsy type 1 SAMD12 TTTCA repeat expansion arose 17,000 years ago and is present in Sri Lankan and Indian families 2020 ·European Journal of Human Genetics ·Mark F. Bennett,Karen Oliver,Brigid M. Regan,Susannah T. Bellows,Amy Schneider,Haloom Rafehi,(unknown),Douglas E. Crompton,Matthew Coleman,Michael S. Hildebrand,Mark Corbett,Thessa Kroes,Jozef Gécz,Ingrid E. Scheffer,Samuel F. Berkovic,Melanie Bahlo	22
8	Definition and diagnosis of cerebral palsy in genetic studies: a systematic review 2020 ·Developmental Medicine & Child Neurology ·(unknown),Ben W. Mol,Jozef Gécz,Alastair H. MacLennan,(unknown),Mark Corbett,Clare L. van Eyk,Dani L. Webber,Lyle J. Palmer,Jesia G. Berry	28
9	Chromatin-Binding Protein PHF6 Regulates Activity-Dependent Transcriptional Networks to Promote Hunger Response 2020 ·Cell Reports ·(unknown),Jingjing Sun,Shuo Yang,Xiaocui Zhang,Chen Wu,(unknown),Xiaohua Wu,Cheng Cheng,Jing Yuan,Anan Li,Mark Corbett,Mathew P. Dixon,Tim Thomas,Anne K. Voss,Jozef Gécz,Guang-Zhong Wang,Azad Bonni,Qian Li,Ju Huang	6
10	Dysregulations of sonic hedgehog signaling in MED12‐related X‐linked intellectual disability disorders 2019 ·Molecular Genetics & Genomic Medicine ·(unknown),Tejasvi Niranjan,Melanie May,Patrick Tarpey,William Allen,Anna Hackett,Pierre‐Simon Jouk,Lucy Raymond,(unknown),Cindy Skinner,Annick Toutain,Jozef Gécz,William R. Heath,Roger E. Stevenson,Charles E. Schwartz,Tao Wang	10
11	MED12-related XLID disorders are dose-dependent of immediate early genes (IEGs) expression 2017 ·Human Molecular Genetics ·(unknown),(unknown),Satoru Hashimoto,Melanie May,Alexey Epanchintsev,Colm J. Ryan,William Allen,Anna Hackett,Jozef Gécz,Cindy Skinner,Roger E. Stevenson,Arjan P.M. de Brouwer,Charles Coutton,Christine Francannet,Pierre‐Simon Jouk,Charles E. Schwartz,Jean‐Marc Egly	17
12	Defects in tRNA Anticodon Loop 2′-O-Methylation Are Implicated in Nonsyndromic X-Linked Intellectual Disability due to Mutations inFTSJ1 2015 ·Human Mutation ·Michael P. Guy,Marie Shaw,Catherine L. Weiner,Lynne Hobson,Zornitza Stark,Katherine Rose,Vera M. Kalscheuer,Jozef Gécz,Eric M. Phizicky	112
13	FOXP1 mutations cause intellectual disability and a recognizable phenotype 2013 ·American Journal of Medical Genetics Part A ·(unknown),(unknown),(unknown),Denise Horn,Christopher W. Carr,Omar Abdul‐Rahman,(unknown),Trent Burgess,Marie Shaw,Jozef Gécz,(unknown),Kerry Fagan,Matthew F. Hunter	67
14	The UPF3B gene, implicated in intellectual disability, autism, ADHD and childhood onset schizophrenia regulates neural progenitor cell behaviour and neuronal outgrowth 2013 ·Human Molecular Genetics ·Lachlan A. Jolly,Claire C. Homan,R. Jacob,Simon C. Barry,Jozef Gécz	95
15	CCDC22 deficiency in humans blunts activation of proinflammatory NF-κB signaling 2013 ·Journal of Clinical Investigation ·Petro Starokadomskyy,Nathan Gluck,Haiying Li,Baozhi Chen,Mathew Wallis,Gabriel N. Maine,Xicheng Mao,Iram Waris Zaidi,Marco Y. Hein,Fiona J. McDonald,Steffen Lenzner,(unknown),Hans‐Hilger Ropers,Andreas W. Kuß,Julie McGaughran,Jozef Gécz,Ezra Burstein	77
16	Loss of Usp9x Disrupts Cortical Architecture, Hippocampal Development and TGFβ-Mediated Axonogenesis 2013 ·PLoS ONE ·Shane Stegeman,Lachlan A. Jolly,(unknown),Jozef Gécz,Linda J. Richards,Alan Mackay‐Sim,Stephen A. Wood	62
17	Epilepsy and mental retardation limited to females with PCDH19 mutations can present de novo or in single generation families 2009 ·Journal of Medical Genetics ·Kim Hynes,Patrick Tarpey,Leanne M. Dibbens,Marta A. Bayly,Samuel F. Berkovic,Roger Smith,(unknown),Samantha J. Turner,Natasha J. Brown,(unknown),E Haan,G Turner,John Christodoulou,Helen Leonard,Deepak Gill,Michael R. Stratton,Jozef Gécz,Ingrid E. Scheffer	59
18	Oligosaccharyltransferase subunits mutations in non-syndromic mental retardation 2007 ·European Journal of Human Genetics ·Florence Molinari,S. Romano,François Foulquier,Willy Morelle,Pascale de Lonlay,(unknown),J. Teague,Sarah Edkins,PA Futreal,(unknown),(unknown),G. Turner,Gert Matthijs,Jozef Gécz,Arnold Münnich,Laurence Colleaux	4
19	Protein and gene expression analysis of Phf6, the gene mutated in the Börjeson–Forssman–Lehmann Syndrome of intellectual disability and obesity 2007 ·Gene Expression Patterns ·Anne K. Voss,(unknown),Caitlin Collin,Cheryl Shoubridge,Mark Corbett,Jozef Gécz,Tim Thomas	37
20	XLMR in MRX families 29, 32, 33 and 38 results from the dup24 mutation in the ARX (Aristaless related homeobox) gene 2005 ·BMC Medical Genetics ·(unknown),(unknown),Merran Finnis,Marie Mangelsdorf,Elke Holinski‐Feder,(unknown),Andrée MacMillan,(unknown),Jozef Gécz,Roger E. Stevenson,Charles E. Schwartz	23

About Jozef Gécz

Jozef Gécz is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health, having authored 232 papers that have together received 10.5k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (140 papers), Genomic variations and chromosomal abnormalities (42 papers) and Genomics and Rare Diseases (35 papers). The work is most often cited by research in Genetics (5.9k citations), Molecular Biology (6.6k citations) and Psychiatry and Mental health (1.2k citations). Jozef Gécz has collaborated with scholars based in Australia, United States and France. Frequent 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. Their work appears in journals such as Nature, Nucleic Acids Research and Journal of Biological Chemistry.

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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