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Andrew Donnelly

Research Profile

Anatomy

Disorders

Procedures

Chromosome Mapping

Chemicals & Drugs

Concepts & Ideas

Molecular Sequence Data

Physiology

Genes & Molecular Sequences

Conserved Sequence

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Publications

TOP 3
Vera Kalscheuer; Jiong Tao; Andrew Donnelly; Georgina Hollway; Eberhard Schwinger; Sabine Kübart; Corinna Menzel; Maria Hoeltzenbein; Niels Tommerup; Helen Eyre; Michael Harbord; Eric A Haan; Grant R Sutherland; Hans-Hilger Ropers; Jozef Gécz
Disruption of the serine/threonine kinase 9 gene causes severe X-linked infantile spasms and mental retardation.
Jozef Gécz; S Barnett; J Liu; Georgina Hollway; Andrew Donnelly; Helen Eyre; H S Eshkevari; R Baltazar; Adina Grunn; R Nagaraja; C Gilliam; L Peltonen; Grant R Sutherland; M Baron; John C Mulley
Characterization of the human glutamate receptor subunit 3 gene (GRIA3), a candidate for bipolar disorder and nonspecific X-linked mental retardation.
Andrew Donnelly; Eric A Haan; J Manson; John C Mulley
A novel mutation in exon b (R259C) of the MTM1 gene is associated with a mild myotubular myopathy. Mutation in brief no. 125. Online.

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All Publications

2003: Vera Kalscheuer; Jiong Tao; Andrew Donnelly; Georgina Hollway; Eberhard Schwinger; Sabine Kübart; Corinna Menzel; Maria Hoeltzenbein; Niels Tommerup; Helen Eyre; Michael Harbord; Eric A Haan; Grant R Sutherland; Hans-Hilger Ropers; Jozef Gécz
Disruption of the serine/threonine kinase 9 gene causes severe X-linked infantile spasms and mental retardation.
American journal of human genetics 2003;72(6):1401-11.
1999: Jozef Gécz; S Barnett; J Liu; Georgina Hollway; Andrew Donnelly; Helen Eyre; H S Eshkevari; R Baltazar; Adina Grunn; R Nagaraja; C Gilliam; L Peltonen; Grant R Sutherland; M Baron; John C Mulley
Characterization of the human glutamate receptor subunit 3 gene (GRIA3), a candidate for bipolar disorder and nonspecific X-linked mental retardation.
Genomics 1999;62(3):356-68.
1998: Andrew Donnelly; Eric A Haan; J Manson; John C Mulley
A novel mutation in exon b (R259C) of the MTM1 gene is associated with a mild myotubular myopathy. Mutation in brief no. 125. Online.
Human mutation 1998;11(4):334.

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