Jozef Gécz

30.5k citations

232 papers · 10.5k indexed · h-index 56

Genetics top 0.1%
- Genetics and Neurodevelopmental Disorders 140
- Genomic variations and chromosomal abnormalities 42
- Genomics and Rare Diseases 35
Molecular Biology top 0.5%
- Ubiquitin and proteasome pathways 26
- RNA modifications and cancer 24
- Epigenetics and DNA Methylation 21
- RNA Research and Splicing 21
- Congenital heart defects research 17
Psychiatry and Mental health top 1%
Developmental 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
Cited by: Genetics Molecular Biology Psychiatry and Mental health
Journals: Nature (3 papers)Nucleic Acids Research (2 papers)Journal of Biological Chemistry (2 papers)
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

The 25 scholars most cited alongside Jozef Gécz, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Jozef Gécz Line = papers co-authored together Jozef Gécz links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	PAK3 pathogenic variant associated with sleep‐related hypermotor epilepsy in a family with parental mosaicism Epilepsia Open ·Antonio Gambardella,Yu‐Chi Liu,Mark F. Bennett,Timothy E. Green,John A. Damiano,Francesco Fortunato,Matthew Coleman,Jacqueline Cherfils,Jean‐Vianney Barnier,Jozef Gécz,Melanie Bahlo,Samuel F. Berkovic,Michael S. Hildebrand	2025	0
2	Epigenomic newborn screening for conditions with intellectual disability and autistic features in Australian newborns 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	2024	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 PLoS Genetics ·Helen M. McRae,Melody Pui-Yee Leong,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	2024	0
4	Mapping combinatorial expression of non-clustered protocadherins in the developing brain identifies novel PCDH19-mediated cell adhesion properties Open Biology ·Stefka Mincheva-Tasheva,Chandran Pfitzner,Raman Kumar,Idha Kurtsdotter,Michaela Scherer,Tarin Ritchie,Jonas Muhr,Jozef Gécz,Paul Q. Thomas	2024	1
5	Genetics of familial adult myoclonus epilepsy: From linkage studies to noncoding repeat expansions Epilepsia ·Mark Corbett,Christel Depienne,Liana Veneziano,Karl Martin Klein,Francesco Brancati,Renzo Guerrini,Federico Zara,Shoji Tsuji,Jozef Gécz	2023	11
6	Transgenic mice with an R342X mutation in Phf6 display clinical features of Börjeson–Forssman–Lehmann Syndrome Human Molecular Genetics ·Raies Ahmed,Shihab Sarwar,Jinghua Hu,Valérie Turcotte- Cardin,Lily R. Qiu,Gerardo Zapata,Lucianne Vandeleur,Keqin Yan,Jason P. Lerch,Mark Corbett,Jozef Gécz,David J. Picketts	2021	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 European Journal of Human Genetics ·Mark F. Bennett,Karen Oliver,Brigid M. Regan,Susannah T. Bellows,Amy Schneider,Haloom Rafehi,Neblina Sikta,Douglas E. Crompton,Matthew Coleman,Michael S. Hildebrand,Mark Corbett,Thessa Kroes,Jozef Gécz,Ingrid E. Scheffer,Samuel F. Berkovic,Melanie Bahlo	2020	22
8	Definition and diagnosis of cerebral palsy in genetic studies: a systematic review Developmental Medicine & Child Neurology ·Ryan Pham,Ben W. Mol,Jozef Gécz,Alastair H. MacLennan,Suzanna C. MacLennan,Mark Corbett,Clare L. van Eyk,Dani L. Webber,Lyle J. Palmer,Jesia G. Berry	2020	28
9	Chromatin-Binding Protein PHF6 Regulates Activity-Dependent Transcriptional Networks to Promote Hunger Response Cell Reports ·Linhua Gan,Jingjing Sun,Shuo Yang,Xiaocui Zhang,Chen Wu,Yiyu Sun,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	2020	6
10	Dysregulations of sonic hedgehog signaling in MED12‐related X‐linked intellectual disability disorders Molecular Genetics & Genomic Medicine ·Siddharth Srivastava,Tejasvi Niranjan,Melanie May,Patrick Tarpey,William Allen,Anna Hackett,Pierre‐Simon Jouk,Lucy Raymond,Slyvain Briault,Cindy Skinner,Annick Toutain,Jozef Gécz,William R. Heath,Roger E. Stevenson,Charles E. Schwartz,Tao Wang	2019	10
11	MED12-related XLID disorders are dose-dependent of immediate early genes (IEGs) expression Human Molecular Genetics ·Lise‐Marie Donnio,Baptiste Bidon,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	2017	17
12	Defects in tRNA Anticodon Loop 2′-O-Methylation Are Implicated in Nonsyndromic X-Linked Intellectual Disability due to Mutations inFTSJ1 Human Mutation ·Michael P. Guy,Marie Shaw,Catherine L. Weiner,Lynne Hobson,Zornitza Stark,Katherine Rose,Vera M. Kalscheuer,Jozef Gécz,Eric M. Phizicky	2015	112
13	FOXP1 mutations cause intellectual disability and a recognizable phenotype American Journal of Medical Genetics Part A ·Anna Le Fevre,Sharelle Taylor,Neva H. Malek,Denise Horn,Christopher W. Carr,Omar Abdul‐Rahman,Sherindan O'Donnell,Trent Burgess,Marie Shaw,Jozef Gécz,Nicole Bain,Kerry Fagan,Matthew F. Hunter	2013	67
14	The UPF3B gene, implicated in intellectual disability, autism, ADHD and childhood onset schizophrenia regulates neural progenitor cell behaviour and neuronal outgrowth Human Molecular Genetics ·Lachlan A. Jolly,Claire C. Homan,R. Jacob,Simon C. Barry,Jozef Gécz	2013	95
15	CCDC22 deficiency in humans blunts activation of proinflammatory NF-κB signaling 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,Agnes Zecha,Hans‐Hilger Ropers,Andreas W. Kuß,Julie McGaughran,Jozef Gécz,Ezra Burstein	2013	77
16	Loss of Usp9x Disrupts Cortical Architecture, Hippocampal Development and TGFβ-Mediated Axonogenesis PLoS ONE ·Shane Stegeman,Lachlan A. Jolly,Susitha Premarathne,Jozef Gécz,Linda J. Richards,Alan Mackay‐Sim,Stephen A. Wood	2013	62
17	Epilepsy and mental retardation limited to females with PCDH19 mutations can present de novo or in single generation families Journal of Medical Genetics ·Kim Hynes,Patrick Tarpey,Leanne M. Dibbens,Marta A. Bayly,Samuel F. Berkovic,Roger Smith,Z. A. Raisi,Samantha J. Turner,Natasha J. Brown,Tarishi Desai,E Haan,G Turner,John Christodoulou,Helen Leonard,Deepak Gill,Michael R. Stratton,Jozef Gécz,Ingrid E. Scheffer	2009	59
18	Oligosaccharyltransferase subunits mutations in non-syndromic mental retardation European Journal of Human Genetics ·Florence Molinari,S. Romano,François Foulquier,Willy Morelle,Pascale de Lonlay,PS Tarpey,J. Teague,Sarah Edkins,PA Futreal,Stratton,M Partington,G. Turner,Gert Matthijs,Jozef Gécz,Arnold Münnich,Laurence Colleaux	2007	4
19	Protein and gene expression analysis of Phf6, the gene mutated in the Börjeson–Forssman–Lehmann Syndrome of intellectual disability and obesity Gene Expression Patterns ·Anne K. Voss,R. Gamble,Caitlin Collin,Cheryl Shoubridge,Mark Corbett,Jozef Gécz,Tim Thomas	2007	37
20	XLMR in MRX families 29, 32, 33 and 38 results from the dup24 mutation in the ARX (Aristaless related homeobox) gene BMC Medical Genetics ·Monica L Stepp,A Lauren Cason,Merran Finnis,Marie Mangelsdorf,Elke Holinski‐Feder,David Macgregor,Andrée MacMillan,Jeanette JA Holden,Jozef Gécz,Roger E. Stevenson,Charles E. Schwartz	2005	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), Genomics and Rare Diseases (35 papers), Ubiquitin and proteasome pathways (26 papers), RNA modifications and cancer (24 papers), Epigenetics and DNA Methylation (21 papers), RNA Research and Splicing (21 papers) and Congenital heart defects research (17 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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