FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Michael Oldridge

Research Profile

Chemicals & Drugs

Concepts & Ideas

Disorders

Physiology

Genes & Molecular Sequences

Procedures

DNA Mutational Analysis

Anatomy

Fingers

Co-author Network

Publications

TOP 3
Judy Cossins; Tracy Lester; Wei Wei Liu; Susan Maxwell; Michael Oldridge; Stephanie Robb; Katsiaryna Belaya; David Beeson
The spectrum of mutations that underlie the neuromuscular junction synaptopathy in DOK7 congenital myasthenic syndrome.
Michael Bowman; Roel Brekelmans; Caroline Archer; Joanna McParland; Michael Oldridge; Anthony O'Rourke; Anneke Seller; Tracy Lester
Gross deletions in TCOF1 are a cause of Treacher-Collins-Franceschetti syndrome.
David Johnson; Shih-hsin Kan; Michael Oldridge; Richard C Trembath; Philippe Roche; Robert M Esnouf; Henk Giele; Andrew O M Wilkie
Missense mutations in the homeodomain of HOXD13 are associated with brachydactyly types D and E.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Michael Oldridge (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2012: Judy Cossins; Tracy Lester; Wei Wei Liu; Susan Maxwell; Michael Oldridge; Stephanie Robb; Katsiaryna Belaya; David Beeson
The spectrum of mutations that underlie the neuromuscular junction synaptopathy in DOK7 congenital myasthenic syndrome.
Human molecular genetics 2012;21(17):3765-75.
2012: Michael Bowman; Roel Brekelmans; Caroline Archer; Joanna McParland; Michael Oldridge; Anthony O'Rourke; Anneke Seller; Tracy Lester
Gross deletions in TCOF1 are a cause of Treacher-Collins-Franceschetti syndrome.
European journal of human genetics : EJHG 2012;20(7):769-77.
2003: David Johnson; Shih-hsin Kan; Michael Oldridge; Richard C Trembath; Philippe Roche; Robert M Esnouf; Henk Giele; Andrew O M Wilkie
Missense mutations in the homeodomain of HOXD13 are associated with brachydactyly types D and E.
American journal of human genetics 2003;72(4):984-97.
2001: Stephen P Robertson; S Walsh; Michael Oldridge; T Gunn; D Becroft; Andrew O M Wilkie
Linkage of otopalatodigital syndrome type 2 (OPD2) to distal Xq28: evidence for allelism with OPD1.
American journal of human genetics 2001;69(1):223-7.
2001: Andrew O M Wilkie; Michael Oldridge; Z Tang; Robert E Maxson
Craniosynostosis and related limb anomalies.
Novartis Foundation symposium 2001;232():122-33; discussion 133-43.
2000: E M Blair; S Walsh; Michael Oldridge; Steven A Wall; Andrew O M Wilkie
Newly recognised craniosynostosis syndrome that does not map to known disease loci.
American journal of medical genetics 2000;95(1):4-9.
2000: AM Roy; Marion L Carroll; Son V Nguyen; Abdel Halim Salem; Michael Oldridge; Andrew O M Wilkie; Mark A Batzer; Prescott L Deininger
Potential gene conversion and source genes for recently integrated Alu elements.
Genome research 2000;10(10):1485-95.
2000: Georg C Schwabe; Sigrid Tinschert; C Buschow; Peter Meinecke; G Wolff; Gabriele Gillessen-Kaesbach; Michael Oldridge; Andrew O M Wilkie; R Kömec; Stefan Mundlos
Distinct mutations in the receptor tyrosine kinase gene ROR2 cause brachydactyly type B.
American journal of human genetics 2000;67(4):822-31.
2000: Ali R Afzal; A Rajab; CD Fenske; Michael Oldridge; Navaratnam Elanko; E Ternes-Pereira; B Tüysüz; Victoria Murday; Michael A Patton; Andrew O M Wilkie; Steve Jeffery
Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2.
Nature genetics 2000;25(4):419-22.
2000: Rivka L Glaser; W Jiang; Simeon Boyd; A K Tran; Andrea A Zachary; Lionel Van Maldergem; D Johnson; S Walsh; Michael Oldridge; Steven A Wall; Andrew O M Wilkie; Ethylin Jabs
Paternal origin of FGFR2 mutations in sporadic cases of Crouzon syndrome and Pfeiffer syndrome.
American journal of human genetics 2000;66(3):768-77.
2000: Michael Oldridge; A M Fortuna; M Maringa; P Propping; S Mansour; C Pollitt; Thomas M DeChiara; R B Kimble; David M Valenzuela; George D Yancopoulos; Andrew O M Wilkie
Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B.
Nature genetics 2000;24(3):275-8.
1999: Michael Oldridge; I K Temple; H G Santos; Richard J Gibbons; Zehra Mustafa; K E Chapman; John Loughlin; Andrew O M Wilkie
Brachydactyly type B: linkage to chromosome 9q22 and evidence for genetic heterogeneity.
American journal of human genetics 1999;64(2):578-85.
1999: Michael Oldridge; Elaine H Zackai; Donna M McDonald-McGinn; Sachiko Iseki; Gillian M Morriss-Kay; Stephen R F Twigg; David Johnson; Steven A Wall; W Jiang; CHRISTIANE THEDA; Ethylin Jabs; Andrew O M Wilkie
De novo alu-element insertions in FGFR2 identify a distinct pathological basis for Apert syndrome.
American journal of human genetics 1999;64(2):446-61.
1998: David Johnson; Sharon W Horsley; DM Moloney; Michael Oldridge; Stephen R F Twigg; S Walsh; M Barrow; P R Njølstad; Juergen Kunz; G J Ashworth; Steven A Wall; Lyndal Kearney; Andrew O M Wilkie
A comprehensive screen for TWIST mutations in patients with craniosynostosis identifies a new microdeletion syndrome of chromosome band 7p21.1.
American journal of human genetics 1998;63(5):1282-93.
1998: Stephen R F Twigg; H D Burns; Michael Oldridge; John Heath; Andrew O M Wilkie
Conserved use of a non-canonical 5' splice site (/GA) in alternative splicing by fibroblast growth factor receptors 1, 2 and 3.
Human molecular genetics 1998;7(4):685-91.
1997: David Ravine; N K Ragge; D Stephens; Michael Oldridge; Andrew O M Wilkie
Dominant coloboma-microphthalmos syndrome associated with sensorineural hearing loss, hematuria, and cleft lip/palate.
American journal of medical genetics 1997;72(2):227-36.
1997: J Nixon; Michael Oldridge; Andrew O M Wilkie; K Smith
Interstitial deletion of 2q associated with craniosynostosis, ocular coloboma, and limb abnormalities: cytogenetic and molecular investigation.
American journal of medical genetics 1997;70(3):324-7.
1997: DM Moloney; Steven A Wall; G J Ashworth; Michael Oldridge; I A Glass; Clair A Francomano; Maximilian Muenke; Andrew O M Wilkie
Prevalence of Pro250Arg mutation of fibroblast growth factor receptor 3 in coronal craniosynostosis.
Lancet 1997;349(9058):1059-62.
1997: Michael Oldridge; P W Lunt; Elaine H Zackai; Donna M McDonald-McGinn; Maximilian Muenke; DM Moloney; Stephen R F Twigg; John Heath; Timothy Howard; George Hoganson; D M Gagnon; Ethylin Jabs; Andrew O M Wilkie
Genotype-phenotype correlation for nucleotide substitutions in the IgII-IgIII linker of FGFR2.
Human molecular genetics 1997;6(1):137-43.
1996: DM Moloney; SF Slaney; Michael Oldridge; Steven A Wall; P Sahlin; G Stenman; Andrew O M Wilkie
Exclusive paternal origin of new mutations in Apert syndrome.
Nature genetics 1996;13(1):48-53.
1996: SF Slaney; Michael Oldridge; J A Hurst; G M Moriss-Kay; Christine M Hall; Michael Poole; Andrew O M Wilkie
Differential effects of FGFR2 mutations on syndactyly and cleft palate in Apert syndrome.
American journal of human genetics 1996;58(5):923-32.
1995: Michael Oldridge; Andrew O M Wilkie; SF Slaney; Michael Poole; L J Pulleyn; P Rutland; Anthony D Hockley; M J Wake; J H Goldin; Robin M Winter
Mutations in the third immunoglobulin domain of the fibroblast growth factor receptor-2 gene in Crouzon syndrome.
Human molecular genetics 1995;4(6):1077-82.
1995: P Rutland; L J Pulleyn; William Reardon; M Baraitser; R Hayward; B Jones; Sue Malcolm; Robin M Winter; Michael Oldridge; SF Slaney
Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes.
Nature genetics 1995;9(2):173-6.
1995: Andrew O M Wilkie; SF Slaney; Michael Oldridge; Michael Poole; G J Ashworth; Anthony D Hockley; Richard D Hayward; D J David; L J Pulleyn; P Rutland
Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome.
Nature genetics 1995;9(2):165-72.