Agi Gedeon
Agi Gedeon
currently @ UWA
Verified email at uwa.edu.au
TitleCited byYear
A novel X-linked gene, G4. 5. is responsible for Barth syndrome
S Bione, P D'Adamo, E Maestrini, AK Gedeon, PA Bolhuis, D Toniolo
Nature genetics 12 (4), 385-389, 1996
6741996
Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy
P Str°mme, ME Mangelsdorf, MA Shaw, KM Lower, SME Lewis, ...
Nature genetics 30 (4), 441-445, 2002
4272002
Mutations in GDI1 are responsible for X-linked non-specific mental retardation (vol 19, pg 134, 1998)
P D'Adamo, A Menegon, C Lo Nigro, M Grasso, M Gulisano, F Tamanini, ...
NATURE GENETICS 19 (3), 303-303, 1998
368*1998
Mutations in GDI1 are responsible for X-linked non-specific mental retardation
P D'Adamo, A Menegon, CL Nigro, M Grasso, M Gulisano, F Tamanini, ...
Nature genetics 19 (2), 134-139, 1998
3681998
Identification of the gene FMR2, associated with FRAXE mental retardation
J Gecz, AK Gedeon, GR Sutherland, JC Mulley
Nature genetics 13 (1), 105-108, 1996
2911996
The X-linked gene G4. 5 is responsible for different infantile dilated cardiomyopathies
P D'Adamo, L Fassone, A Gedeon, EAM Janssen, S Bione, PA Bolhuis, ...
The American Journal of Human Genetics 61 (4), 862-867, 1997
2621997
Fragile X syndrome without CCG amplification has an FMR1 deletion
AK Gedeon, E Baker, H Robinson, MW Partington, B Gross, A Manca, ...
Nature Genetics 1 (5), 341-344, 1992
2341992
Fragile-X syndrome: unique genetics of the heritable unstable element
S Yu, J Mulley, D Loesch, G Turner, A Donnelly, A Gedeon, D Hillen, ...
American journal of human genetics 50 (5), 968, 1992
2341992
Identification of the gene (SEDL) causing X-linked spondyloepiphyseal dysplasia tarda
┴K Gedeon, A Colley, R Jamieson, EM Thompson, J Rogers, D Sillence, ...
Nature genetics 22 (4), 400-404, 1999
2081999
Mutations in PHF6 are associated with B÷rjeson–Forssman–Lehmann syndrome
KM Lower, G Turner, BA Kerr, KD Mathews, MA Shaw, ┴K Gedeon, ...
Nature genetics 32 (4), 661-665, 2002
1682002
Prenatal diagnosis of fragile X syndrome by direct detection of the unstable DNA sequence
GR Sutherland, A Gedeon, L Kornman, A Donnelly, RW Byard, JC Mulley, ...
New England Journal of Medicine 325 (24), 1720-1722, 1991
1191991
Barth syndrome: clinical features and confirmation of gene localisation to distal Xq28
LC Ades, AK Gedeon, MJ Wilson, M Latham, MW Partington, JC Mulley, ...
American Journal of Medical Genetics Part A 45 (3), 327-334, 1993
1171993
Principal mutation hotspot for central core disease and related myopathies in the C-terminal transmembrane region of the RYR1 gene
MR Davis, E Haan, H Jungbluth, C Sewry, K North, F Muntoni, T Kuntzer, ...
Neuromuscular Disorders 13 (2), 151-157, 2003
1142003
The molecular basis of X-linked spondyloepiphyseal dysplasia tarda
AK Gedeon, GE Tiller, M Le Merrer, S Heuertz, L Tranebjaerg, D Chitayat, ...
The American Journal of Human Genetics 68 (6), 1386-1397, 2001
1092001
FRAXE and mental retardation.
JC Mulley, S Yu, DZ Loesch, DA Hay, A Donnelly, AK Gedeon, ...
Journal of medical genetics 32 (3), 162-169, 1995
951995
Genotype-phenotype relationships in fragile X syndrome: a family study.
DZ Loesch, R Huggins, DA Hay, AK Gedeon, JC Mulley, GR Sutherland
American journal of human genetics 53 (5), 1064, 1993
891993
Letter to the editor: How many X‐linked genes for non‐specific mental retardation (MRX) are there?
AK Gedeon, AJ Donnelly, JC Mulley, B Kerr, G Turner
American Journal of Medical Genetics Part A 64 (1), 158-162, 1996
781996
Erratum: Letter to the Editor: How Many X-Linked Genes for Non-Specific Mental Retardation (MRX) Are There?
AK Gedeon, AJ Donnelly, JC Mulley, B Kerr, G Turner
American Journal of Medical Genetics 66 (1), 118, 1996
78*1996
X chromosome inactivation in carriers of Barth syndrome
KH ěrstavik, RE ěrstavik, AK Naumova, P D'Adamo, A Gedeon, ...
The American Journal of Human Genetics 63 (5), 1457-1463, 1998
721998
Non-specific X linked mental retardation.
B Kerr, G Turner, J Mulley, A Gedeon, M Partington
Journal of medical genetics 28 (6), 378-382, 1991
701991
The system can't perform the operation now. Try again later.
Articles 1–20