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Matthew Hodges

Research Profile

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Publications

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Chiuhui Mary Wang; Peter DIxon; S Decordova; Matthew D Hodges; Neil J Sebire; S Ozalp; M Fallahian; A Sensi; F Ashrafi; V Repiska; J Zhao; Y Xiang; P M Savage; Michael J Seckl; Rosemary A Fisher
Identification of 13 novel NLRP7 mutations in 20 families with recurrent hydatidiform mole; missense mutations cluster in the leucine-rich region.
Cheryl Y Gregory-Evans; Mariya Moosajee; Matthew D Hodges; Mackay Donna; Laurence Game; Neil Vargesson; Agnès Bloch-Zupan; Franz Rüschendorf; Lourdes Santos-Pinto; Georges Wackens; Kevin Gregory-Evans
SNP genome scanning localizes oto-dental syndrome to chromosome 11q13 and microdeletions at this locus implicate FGF3 in dental and inner-ear disease and FADD in ocular coloboma.
Beverley Burke; Neil J Sebire; Jill Moss; Matthew D Hodges; Michael J Seckl; Edward S Newlands; Rosemary A Fisher
Evaluation of deletions in 7q11.2 and 8p12-p21 as prognostic indicators of tumour development following molar pregnancy.

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All Publications

2009: Chiuhui Mary Wang; Peter DIxon; S Decordova; Matthew D Hodges; Neil J Sebire; S Ozalp; M Fallahian; A Sensi; F Ashrafi; V Repiska; J Zhao; Y Xiang; P M Savage; Michael J Seckl; Rosemary A Fisher
Identification of 13 novel NLRP7 mutations in 20 families with recurrent hydatidiform mole; missense mutations cluster in the leucine-rich region.
Journal of medical genetics 2009;46(8):569-75.
2007: Cheryl Y Gregory-Evans; Mariya Moosajee; Matthew D Hodges; Mackay Donna; Laurence Game; Neil Vargesson; Agnès Bloch-Zupan; Franz Rüschendorf; Lourdes Santos-Pinto; Georges Wackens; Kevin Gregory-Evans
SNP genome scanning localizes oto-dental syndrome to chromosome 11q13 and microdeletions at this locus implicate FGF3 in dental and inner-ear disease and FADD in ocular coloboma.
Human molecular genetics 2007;16(20):2482-93.
2006: Beverley Burke; Neil J Sebire; Jill Moss; Matthew D Hodges; Michael J Seckl; Edward S Newlands; Rosemary A Fisher
Evaluation of deletions in 7q11.2 and 8p12-p21 as prognostic indicators of tumour development following molar pregnancy.
Gynecologic oncology 2006;103(2):642-8.
2006: Timothy J Aitman; Rong Dong; Timothy J Vyse; Penny J Norsworthy; Michelle D Johnson; Jennifer Smith; Jonathan Mangion; Cheri Roberton-Lowe; Amy J Marshall; Enrico Petretto; Matthew D Hodges; Gurjeet Bhangal; Sheetal G Patel; Kelly Sheehan-Rooney; Mark Duda; Paul R Cook; David J Evans; Jan Domin; Jonathan Flint; Joseph J Boyle; Charles D Pusey; H Terence Cook
Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans.
Nature 2006;439(7078):851-5.
2004: Rosemary A Fisher; Matthew D Hodges; Edward S Newlands
Familial recurrent hydatidiform mole: a review.
The Journal of reproductive medicine 2004;49(8):595-601.
2003: Matthew D Hodges; Helene C Rees; Michael J Seckl; Edward S Newlands; Rosemary A Fisher
Genetic refinement and physical mapping of a biparental complete hydatidiform mole locus on chromosome 19q13.4.
Journal of medical genetics 2003;40(8):e95.
2002: Rosemary A Fisher; Matthew D Hodges; Helene C Rees; Neil J Sebire; Michael J Seckl; Edward S Newlands; David R Genest; Diego H Castrillon
The maternally transcribed gene p57(KIP2) (CDNK1C) is abnormally expressed in both androgenetic and biparental complete hydatidiform moles.
Human molecular genetics 2002;11(26):3267-72.
2002: Matthew D Hodges; Helena Vieira; Kevin Gregory-Evans; Cheryl Y Gregory-Evans
Characterization of the genomic and transcriptional structure of the CRX gene: substantial differences between human and mouse.
Genomics 2002;80(5):531-42.
2001: L C Bibb; James K L Holt; Emma E Tarttelin; Matthew D Hodges; Kevin Gregory-Evans; A Rutherford; Robert J Lucas; Jane C Sowden; Cheryl Y Gregory-Evans
Temporal and spatial expression patterns of the CRX transcription factor and its downstream targets. Critical differences during human and mouse eye development.
Human molecular genetics 2001;10(15):1571-9.