Ági K. Gedeon

5.0k citations

53 papers · 3.5k indexed · 1 hit paper · h-index 30

Impact in

Genetics top 0.5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
Molecular Biology top 5%
- Mitochondrial Function and Pathology
- Ubiquitin and proteasome pathways
- Congenital heart defects research
- RNA modifications and cancer
- ATP Synthase and ATPases Research

Papers in

Genetics 43
- Genetics and Neurodevelopmental Disorders 33
- Genomic variations and chromosomal abnormalities 11
- Genomics and Rare Diseases 5
- Connective tissue disorders research 5
Molecular Biology 38
- Ubiquitin and proteasome pathways 8
- RNA modifications and cancer 7
- Congenital heart defects research 6

Co-authors: John C. Mulley Daniela Toniolo Patrizia D’Adamo Jozef Gécz Pieter A. Bolhuis Silvia Bione Gillian Turner Elena Maestrini
Journals: Journal of Medical Genetics (7 papers)Nature Genetics (6 papers)The American Journal of Human Genetics (4 papers)Genomics (4 papers)The Medical Journal of Australia (2 papers)
Partner nations: Australia United States Netherlands

In The Last Decade

Ági K. Gedeon

51 papers receiving 3.4k citations

Hit Papers

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A novel X-linked gene, G4.5. is responsible for Barth syndrome 1996 · 565 citations

Peers

Countries citing papers authored by Ági K. Gedeon

Since Specialization

Citations

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

Fields of papers citing papers by Ági K. Gedeon

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ági K. Gedeon. 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 Ági K. Gedeon. The network helps show where Ági K. Gedeon may publish in the future.

Co-authors

The 25 scholars most cited alongside Ági K. Gedeon, 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 Ági K. Gedeon Line = papers co-authored together Ági K. Gedeon links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Direct molecular diagnosis of myotonic dystrophy Clinical Genetics ·洋一川波, Andrew J. Donnelly, Ági K. Gedeon, Roger W. Byard, Eric Haan, Xavier Portell	2008	8
2	Syndromic form of X‐linked mental retardation with marked hypotonia in early life, severe mental handicap, and difficult adult behavior maps to Xp22 American Journal of Medical Genetics Part A ·Gillian Turner, Ági K. Gedeon, Bronwyn Kerr, Rachael E. Bennett, John C. Mulley, M. W. Partington	2002	14
3	Abnormal expression of the KLF8 (ZNF741) gene in a female patient with an X;autosome translocation t(X;21)(p11.2;q22.3) and non-syndromic mental retardation Journal of Medical Genetics ·Anne-Marie Lossi, Yaset Abdi یاسر عبدی, D. Depétris, Jozef Gécz, Ági K. Gedeon, R. Frank Kooy, CE Schwartz, Marie‐Geneviève Mattéi, M. F. Croquette, Laurent Villard	2002	23
4	Gene Structure and Expression Study of the SEDL Gene for Spondyloepiphyseal Dysplasia Tarda Genomics ·Jozef Gécz, Nikki Y. T. Man, Ági K. Gedeon, Timothy C. Cox, Elizabeth Baker, John C. Mulley	2000	38
5	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	1999	145
6	Mutations in GDI1 are responsible for X-linked non-specific mental retardation Nature Genetics ·Patrizia D’Adamo, Andrea Menegon, Cristiana Lo Nigro, Marina Grasso, Massimo Gulisano, Filippo Tamanini, T. Bienvenu, Ági K. Gedeon, Ben A. Oostra, Shih-Kwang Wu, Anurag Tandon, Flavia Valtorta, William E. Balch, Jamel Chelly, Daniela Toniolo	1998	264
7	A novel X-linked gene, G4.5. is responsible for Barth syndrome Nature Genetics ·Silvia Bione, Patrizia D’Adamo, Elena Maestrini, Ági K. Gedeon, Pieter A. Bolhuis, Daniela Toniolo Hit paper breakdown →	1996	565
8	X‐linked mental retardation with dystonic movements of the hands (PRTS): Revisited American Journal of Medical Genetics ·Ági K. Gedeon, M. W. Partington, John C. Mulley	1994	15
9	Regional localisation of a non‐specific X‐linked mental retardation gene (MRX19) to Xp22 American Journal of Medical Genetics ·Andrew J. Donnelly, K.H. Andy Choo, H.M. Kozman, Ági K. Gedeon, David M. Danks, John C. Mulley	1994	26
10	Pericentromeric genes for non‐specific X‐linked mental retardation (MRX) American Journal of Medical Genetics ·Ági K. Gedeon, Bronwyn Kerr, John C. Mulley, Gillian Turner	1994	25
11	Barth syndrome: Clinical features and confirmation of gene localisation to distal Xq28 American Journal of Medical Genetics ·Lesley C. Adès, Ági K. Gedeon, Meredith Wilson, M. C. Latham, M. W. Partington, John C. Mulley, John W. Nelson, Kei Lui, David O. Sillence	1993	104
12	Fragile X syndrome without CCG amplification has an FMR1 deletion Nature Genetics ·Ági K. Gedeon, Emma K. Baker, Harriet L. Robinson, M. W. Partington, Bella Gross, Antonella Manca, Bernhard Korn, Annemarie Poustka, S. Yu, G.R. Sutherland, John C. Mulley	1992	167
13	Localization of non‐specific X‐linked mental retardation genes American Journal of Medical Genetics ·Bronwyn Kerr, Ági K. Gedeon, John C. Mulley, Gillian Turner	1992	39
14	New X‐linked syndrome of mental retardation, gynecomastia, and obesity is linked to DXS255 American Journal of Medical Genetics ·farideh mahdavi, J.C. Mulley, Ági K. Gedeon, Hazel M. Robinson, Gillian Turner	1991	50
15	Addition of MT, D16S10, D16S4, and D16S91 to the linkage map within 16q12.1-q22.1 Genomics ·H.M. Kozman, Ági K. Gedeon, S.A. Whitmore, G K Suthers, David F. Callen, G.R. Sutherland, J.C. Mulley	1991	3
16	Dinucleotide repeat polymorphisms at the DXS294 and DXS300 loci in Xq26 Nucleic Acids Research ·Ági K. Gedeon, Robert I. Richards, John C. Mulley	1991	11
17	Prenatal Diagnosis of Fragile X Syndrome by Direct Detection of the Unstable DNA Sequence New England Journal of Medicine ·Grant R. Sutherland, Ági K. Gedeon, Louise Kornman, Andrew J. Donnelly, Roger W. Byard, John C. Mulley, Eric J. Kremer, Michael Lynch, Melanie Pritchard, Sui Yu, Robert I. Richards	1991	94
18	A linkage group with FRA16B (the fragile site at 16q22.1) Human Genetics ·John C. Mulley, V.J. Hyland, Shoji Tada, K. K. Lee, Ági K. Gedeon, G.R. Sutherland	1989	2
19	Börjeson‐Forssman‐Lehmann syndrome: Clinical manifestations and gene localization to Xq26‐27 American Journal of Medical Genetics ·Gillian Turner, Ági K. Gedeon, John C. Mulley, Grant Sutherland, Luboš Nehyba, HE Renk, Nestene Botha	1989	52
20	Linkage studies with the gene for an X‐linked syndrome of mental retardation, microcephaly and spastic diplegia (MRX2) American Journal of Medical Genetics ·G.R. Sutherland, Ági K. Gedeon, E Haan, Prahallad B S, J.C. Mulley	1988	46

About Ági K. Gedeon

Ági K. Gedeon is a scholar working on Genetics, Molecular Biology, Cognitive Neuroscience, Cell Biology and Cellular and Molecular Neuroscience, having authored 53 papers that have together received 3.5k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (33 papers), Genomic variations and chromosomal abnormalities (11 papers), Ubiquitin and proteasome pathways (8 papers), Autism Spectrum Disorder Research (8 papers), RNA modifications and cancer (7 papers), Congenital heart defects research (6 papers), Genomics and Rare Diseases (5 papers) and Connective tissue disorders research (5 papers). The work is most often cited by research in Genetics (2.0k citations), Molecular Biology (2.5k citations), Clinical Biochemistry (197 citations), Cognitive Neuroscience (512 citations) and Cell Biology (367 citations). Ági K. Gedeon has collaborated with scholars based in Australia, United States and Netherlands. Frequent co-authors include John C. Mulley, Daniela Toniolo, Patrizia D’Adamo, Jozef Gécz, Pieter A. Bolhuis, Silvia Bione, Gillian Turner, Elena Maestrini, Grant R. Sutherland and M. W. Partington. Their work appears in journals such as Journal of Medical Genetics, Nature Genetics, The American Journal of Human Genetics, Genomics and The Medical Journal of Australia.

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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