Jozef Gécz

30.8k citations
239 papers · 11.4k · h-index 58

Impact in

  • Genetics top 0.1%
    • Genetics and Neurodevelopmental Disorders
    • Genomic variations and chromosomal abnormalities
    • Genomics and Rare Diseases
  • Molecular Biology top 0.5%
    • RNA modifications and cancer
    • RNA Research and Splicing
    • Epigenetics and DNA Methylation
    • Ubiquitin and proteasome pathways

Papers in

  • Genetics 168
    • Genetics and Neurodevelopmental Disorders 140
    • Genomic variations and chromosomal abnormalities 40
    • Genomics and Rare Diseases 33
  • Molecular Biology 141
    • Ubiquitin and proteasome pathways 27
    • RNA modifications and cancer 22
    • RNA Research and Splicing 20
    • Epigenetics and DNA Methylation 18
    • Congenital heart defects research 16
Co-authors
John C. Mulley (17 shared papers)Cheryl Shoubridge (26 shared papers)Alastair H. MacLennan (12 shared papers)Mark Corbett (36 shared papers)Ági K. Gedeon (10 shared papers)Ingrid E. Scheffer (23 shared papers)Grant R. Sutherland (6 shared papers)Lachlan A. Jolly (20 shared papers)
Journals
Human Molecular Genetics (22 papers)European Journal of Human Genetics (19 papers)The American Journal of Human Genetics (18 papers)European Journal of Medical Genetics (7 papers)Genomics (7 papers)
Partner nations
AustraliaUnited StatesFrance

In The Last Decade

Jozef Gécz

232 papers receiving 11.0k citations

Peers

Jozef Gécz
Comparison fields: 5 of 131
  • Genetics 5.9k
  • Molecular Biology 6.6k
  • Psychiatry and Mental health 1.1k
  • Developmental Neuroscience 296
  • Cellular and Molecular Neuroscience 1.0k
Replace Maximilian Muenke with:
Maximilian Muenke United States
Naomichi Matsumoto Japan
André Reis Germany
Gudrun Rappold Germany
Jonathan Sebat United States
Yong‐hui Jiang United States
Hirotomo Saitsu Japan
Antonio Pizzuti Italy
Ben A. Oostra Netherlands
Jacques L. Michaud Canada
Jozef Gécz relative to Maximilian Muenke United States Maximilian Muenke's profile →
Citations per field
00.5×2×3.4×
Maximilian Muenke · 1×
Citations per year

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-authors

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

20 of 20 papers shown

Showing the 20 most-cited of 239 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Duplication of the MECP2 Region Is a Frequent Cause of Severe Mental Retardation and Progressive Neurological Symptoms in Males
The American Journal of Human Genetics ·Hilde Van Esch, Marijke Bauters, Jaakko Ignatius, Mieke Jansen, Martine Raynaud, Karen Hollanders, Dorien Lugtenberg, Thierry Bienvenu, Lars Riff Jensen, Jozef Gécz, Claude Moraine, Peter Marynen, Jean‐Pierre Fryns, Guy Froyen
2005497
2
Mutations of CDKL5 Cause a Severe Neurodevelopmental Disorder with Infantile Spasms and Mental Retardation
The American Journal of Human Genetics ·Linda S. Weaving, John Christodoulou, Sarah Williamson, K. Friend, Olivia L. D. McKenzie, Hayley Archer, Julie Evans, Angus Clarke, Gregory J. Pelka, Patrick Tam, Catherine M. Watson, Hooshang Lahooti, Carolyn Ellaway, Bruce Bennetts, Helen Leonard, Jozef Gécz
2004394
3
Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy
Nature Genetics ·Petter Strømme, Marie Mangelsdorf, Marie Shaw, Karen M. Lower, M. E. Suzanne Lewis, Hélène Bruyèrè, Viggo Lütcherath, Ági K. Gedeon, Robyn H. Wallace, Ingrid E. Scheffer, Gillian Turner, M. W. Partington, Suzanna G.M. Frints, J. P. Fryns, Grant R. Sutherland, John C. Mulley, Jozef Gécz
2002343
4
Mutations in the JARID1C Gene, Which Is Involved in Transcriptional Regulation and Chromatin Remodeling, Cause X-Linked Mental Retardation
The American Journal of Human Genetics ·Lars Riff Jensen, M Amende, Ulf Gurok, Bettina A. Moser, Verena Gimmel, Andreas Tzschach, Andreas Janecke, Gholamali Tariverdian, Jamel Chelly, Jean‐Pierre Fryns, Hilde Van Esch, Tjitske Kleefstra, B Hamel, Claude Moraine, Jozef Gécz, Gillian Turner, Richard Reinhardt, Vera M. Kalscheuer, Hans‐Hilger Ropers, Steffen Lenzner
2005311
5
Cerebral palsy: causes, pathways, and the role of genetic variants
American Journal of Obstetrics and Gynecology ·Alastair H. MacLennan, Suzanna Thompson, Jozef Gécz
2015284
6
Identification of the gene FMR2, associated with FRAXE mental retardation
Nature Genetics ·Jozef Gécz, Ági K. Gedeon, Grant R. Sutherland, John C. Mulley
1996273
7
Mutations in the X-Linked Cyclin-Dependent Kinase–Like 5 (CDKL5/STK9) Gene Are Associated with Severe Neurodevelopmental Retardation
The American Journal of Human Genetics ·Jiong Tao, Hilde Van Esch, M. Hagedorn-Greiwe, Kirsten Hoffmann, Bettina A. Moser, Martine Raynaud, Jürgen Sperner, Jean‐Pierre Fryns, E. Schwinger, Jozef Gécz, Hans‐Hilger Ropers, Vera M. Kalscheuer
2004246
8
Identification of a MicroRNA that Activates Gene Expression by Repressing Nonsense-Mediated RNA Decay
Molecular Cell ·Ivone Bruno, Rachid Karam, Lulu Huang, Anjana Bhardwaj, Chih H. Lou, Eleen Y. Shum, Hye-Won Song, Mark Corbett, Wesley D. Gifford, Jozef Gécz, Samuel L. Pfaff, Miles Wilkinson
2011239
9
Disruption of the Serine/Threonine Kinase 9 Gene Causes Severe X-Linked Infantile Spasms and Mental Retardation
The American Journal of Human Genetics ·Vera M. Kalscheuer, Jiong Tao, Andrew J. Donnelly, Georgina E. Hollway, E. Schwinger, Sabine Kübart, Corinna Menzel, Maria Hoeltzenbein, Niels Tommerup, Helen J. Eyre, Michael Harbord, Eric Haan, Grant R. Sutherland, Hans‐Hilger Ropers, Jozef Gécz
2003233
10
Common genetic variants contribute to risk of rare severe neurodevelopmental disorders
Nature ·Mari Niemi, Hilary C. Martin, Daniel L Rice, Giuseppe Gallone, Scott D. Gordon, Martin Kelemen, Kerrie McAloney, Jeremy F. McRae, Elizabeth J. Radford, Sui Yu, Jozef Gécz, Nicholas G. Martin, Caroline F. Wright, David Fitzpatrick, Helen V. Firth, Matthew E. Hurles, Jeffrey C. Barrett
2018199
11
Mutations in mammalian target of rapamycin regulator DEPDC5 cause focal epilepsy with brain malformations
Annals of Neurology ·Ingrid E. Scheffer, Sarah E. Heron, Brigid M. Regan, Simone Mandelstam, Douglas E. Crompton, Bree Hodgson, Laura Licchetta, Federica Provini, Francesca Bisulli, Lata Vadlamudi, Jozef Gécz, Alan Connelly, Paolo Tinuper, Michael G. Ricos, Samuel F. Berkovic, Leanne M. Dibbens
2014166
12
Infantile spasms, dystonia, and other X-linked phenotypes caused by mutations in Aristaless related homeobox gene, ARX
Brain and Development ·Petter Strømme, Marie Mangelsdorf, Ingrid E. Scheffer, Jozef Gécz
2002161
13
Whole-exome sequencing points to considerable genetic heterogeneity of cerebral palsy
Molecular Psychiatry ·G. McMichael, Matthew N. Bainbridge, Eric Haan, Mark Corbett, Alison Gardner, Suzanna Thompson, Bregje W.M. van Bon, Clare L. van Eyk, J. L. BROADBENT, Chandra A. Reynolds, Michael O’Callaghan, Lam Son Nguyen, David L. Adelson, Remo Russo, Shalini N. Jhangiani, HarshaVardhan Doddapaneni, Donna M. Muzny, Richard A. Gibbs, Jozef Gécz, Alastair H. MacLennan
2015158
14
Identification of the gene (SEDL) causing X-linked spondyloepiphyseal dysplasia tarda
Nature Genetics ·Ági K. Gedeon, Alison Colley, Robyn V. Jamieson, Elizabeth M. Thompson, John Rogers, David Sillence, George E. Tiller, John C. Mulley, Jozef Gécz
1999155
15
The genetic landscape of intellectual disability arising from chromosome X
Trends in Genetics ·Jozef Gécz, Cheryl Shoubridge, Mark Corbett
2009146
16
La FAM fatale: USP9X in development and disease
Cellular and Molecular Life Sciences ·Mariyam Murtaza, Lachlan A. Jolly, Jozef Gécz, Stephen A. Wood
2015144
17
Early onset seizures and Rett-like features associated with mutations in CDKL5
European Journal of Human Genetics ·Julie Evans, Hayley Archer, James Colley, Kirstine Ravn, Jytte Bieber Nielsen, Alison Kerr, Elizabeth Williams, John Christodoulou, Jozef Gécz, Philip Jardine, Michael Wright, Daniela T. Pilz, L. Lazarou, D.N. Cooper, Julian R. Sampson, Rachel Butler, Sharon D. Whatley, Angus Clarke
2005141
18
ARX spectrum disorders: making inroads into the molecular pathology
Human Mutation ·Cheryl Shoubridge, Tod Fullston, Jozef Gécz
2010136
19
The genetic basis of cerebral palsy
Developmental Medicine & Child Neurology ·Michael Fahey, Alastair H. MacLennan, Doris Kretzschmar, Jozef Gécz, Michael C. Kruer
2017126
20
XLMR genes: update 2007
European Journal of Human Genetics ·Pietro Chiurazzi, Charles E. Schwartz, Jozef Gécz, Giovanni Neri
2008125

About Jozef Gécz

Jozef Gécz is a scholar working on Genetics, Molecular Biology, Psychiatry and Mental health, Cellular and Molecular Neuroscience and Cognitive Neuroscience, having authored 239 papers that have together received 11.4k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (140 papers), Genomic variations and chromosomal abnormalities (40 papers), Genomics and Rare Diseases (33 papers), Ubiquitin and proteasome pathways (27 papers), RNA modifications and cancer (22 papers), RNA Research and Splicing (20 papers), Epigenetics and DNA Methylation (18 papers) and Congenital heart defects research (16 papers). The work is most often cited by research in Genetics (5.9k citations), Molecular Biology (6.6k citations), Psychiatry and Mental health (1.1k citations), Developmental Neuroscience (296 citations) and Cellular and Molecular Neuroscience (1.0k citations). Jozef Gécz has collaborated with scholars based in Australia, United States and France. Frequent co-authors include John C. Mulley, Cheryl Shoubridge, Alastair H. MacLennan, Mark Corbett, Ági K. Gedeon, Ingrid E. Scheffer, Grant R. Sutherland, Lachlan A. Jolly, Gillian Turner and M. W. Partington. Their work appears in journals such as Human Molecular Genetics, European Journal of Human Genetics, The American Journal of Human Genetics, European Journal of Medical Genetics and Genomics.

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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