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Geoffrey Woods

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Jeong Ho Lee; Clare V Logan; Anna Rajab; Carsten Russ; Saghira Malik Sharif; Jennifer L Silhavy; Laszlo Sztriha; Sophie Thomas; Enza Maria Valente; Elizabeth R Waters; C Geoffrey Woods; Maha S Zaki; Masumi Abe; Lihadh Al-Gazali; Tania Attié-Bitach; Christopher P Bennett; Stephanie L Bielas; Francesco Brancati; Erica E Davis; Bill H Diplas; Susan Ferro-Novick; Stacey B Gabriel; Friedhelm Hildebrandt; Kiley J Hill; Miriam Iannicelli; Colin A Johnson; Nicholas Katsanis; Roshan Koul; Ji Eun Lee; Joseph G Gleeson
Evolutionarily assembled cis-regulatory module at a human ciliopathy locus.
Joo-Hee Sir; Alex Sossick; C Geoffrey Woods; Maryam Khurshid; Adeline K Nicholas; Stefanie Reichelt; Alexis R Barr; Ofelia P Carvalho; Clive D'Santos; Fanni Gergely
A primary microcephaly protein complex forms a ring around parental centrioles.
Mehmet Bakircioglu; Ofélia P Carvalho; Maryam Khurshid; James Cox; Beyhan Tuysuz; Tanyeri Barak; Saliha Yilmaz; Okay Caglayan; alp dincer; Adeline K Nicholas; Oliver Quarrell; Kelly Springell; Gulshan Karbani; Saghira Malik; Caroline Gannon; Eamonn Sheridan; Moira Crosier; Steve N Lisgo; Susan Lindsay; Kaya Bilguvar; Fanni Gergely; Murat Gunel; C Geoffrey Woods
The essential role of centrosomal NDE1 in human cerebral cortex neurogenesis.

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2012: Jeong Ho Lee; Clare V Logan; Anna Rajab; Carsten Russ; Saghira Malik Sharif; Jennifer L Silhavy; Laszlo Sztriha; Sophie Thomas; Enza Maria Valente; Elizabeth R Waters; C Geoffrey Woods; Maha S Zaki; Masumi Abe; Lihadh Al-Gazali; Tania Attié-Bitach; Christopher P Bennett; Stephanie L Bielas; Francesco Brancati; Erica E Davis; Bill H Diplas; Susan Ferro-Novick; Stacey B Gabriel; Friedhelm Hildebrandt; Kiley J Hill; Miriam Iannicelli; Colin A Johnson; Nicholas Katsanis; Roshan Koul; Ji Eun Lee; Joseph G Gleeson
Evolutionarily assembled cis-regulatory module at a human ciliopathy locus.
Science (New York, N.Y.) 2012;335(6071):966-9.
2011: Joo-Hee Sir; Alex Sossick; C Geoffrey Woods; Maryam Khurshid; Adeline K Nicholas; Stefanie Reichelt; Alexis R Barr; Ofelia P Carvalho; Clive D'Santos; Fanni Gergely
A primary microcephaly protein complex forms a ring around parental centrioles.
Nature genetics 2011;43(11):1147-53.
2011: Mehmet Bakircioglu; Ofélia P Carvalho; Maryam Khurshid; James Cox; Beyhan Tuysuz; Tanyeri Barak; Saliha Yilmaz; Okay Caglayan; alp dincer; Adeline K Nicholas; Oliver Quarrell; Kelly Springell; Gulshan Karbani; Saghira Malik; Caroline Gannon; Eamonn Sheridan; Moira Crosier; Steve N Lisgo; Susan Lindsay; Kaya Bilguvar; Fanni Gergely; Murat Gunel; C Geoffrey Woods
The essential role of centrosomal NDE1 in human cerebral cortex neurogenesis.
American journal of human genetics 2011;88(5):523-35.
2011: Ofélia P Carvalho; Gemma K Thornton; Joseph Hertecant; Henry Houlden; Adeline K Nicholas; James Cox; Mary Rielly; Lihadh Al-Gazali; C Geoffrey Woods
A novel NGF mutation clarifies the molecular mechanism and extends the phenotypic spectrum of the HSAN5 neuropathy.
Journal of medical genetics 2011;48(2):131-5.
2010: Adeline K Nicholas; Maryam Khurshid; Julie Désir; Ofélia P Carvalho; James Cox; Gemma Thornton; Rizwana Kausar; Muhammad Ansar; Wasim Ahmad; Alain Verloes; Sandrine Passemard; Jean-Paul Misson; Susan Lindsay; Fanni Gergely; William B Dobyns; Emma Roberts; Marc Abramowicz; C Geoffrey Woods
WDR62 is associated with the spindle pole and is mutated in human microcephaly.
Nature genetics 2010;42(11):1010-4.
2010: Frank Reimann; James Cox; Inna Belfer; Luda Diatchenko; Dmitri V Zaykin; Duncan P McHale; Joost P H Drenth; Feng Dai; Jerry Wheeler; Frances Sanders; Linda Wood; Tian-Xia Wu; Jaro Karppinen; Lone Nikolajsen; Minna Männikkö; Mitchell B Max; Carly Kiselycznyk; Minakshi Poddar; Rene H M Te Morsche; Shad Smith; Dustin Gibson; Anthi Kelempisioti; William Maixner; Fiona M Gribble; C Geoffrey Woods
Pain perception is altered by a nucleotide polymorphism in SCN9A.
Proceedings of the National Academy of Sciences of the United States of America 2010;107(11):5148-53.
2010: Julie Higgins; Carol Midgley; Anna-Maria Bergh; Sandra M Bell; Jon M Askham; Emma Roberts; Ruth K Binns; Saghira M Sharif; Christopher Bennett; David M Glover; C Geoffrey Woods; Ewan E Morrison; Jacquelyn Bond
Human ASPM participates in spindle organisation, spindle orientation and cytokinesis.
BMC cell biology 2010;11():85.
2009: Gemma K Thornton; C Geoffrey Woods
Primary microcephaly: do all roads lead to Rome?
Trends in genetics : TIG 2009;25(11):501-10.
2009: A K Nicholas; E A Swanson; James Cox; Gulshan Karbani; S Malik; Kelly Springell; Daniel J Hampshire; M Ahmed; Jacquelyn Bond; D Di Benedetto; M Fichera; Corrado Romano; W B Dobyns; C Geoffrey Woods
The molecular landscape of ASPM mutations in primary microcephaly.
Journal of medical genetics 2009;46(4):249-53.
2009: Esther Meyer; Derek Lim; Shanaz Pasha; Louise Tee; Fatimah Rahman; John R W Yates; C Geoffrey Woods; Wolf Reik; Eamonn R Maher
Germline mutation in NLRP2 (NALP2) in a familial imprinting disorder (Beckwith-Wiedemann Syndrome).
PLoS genetics 2009;5(3):e1000423.
2008: Vincent Cantagrel; Jennifer L Silhavy; Stephanie L Bielas; Dominika Swistun; Sarah E Marsh; Julien Y Bertrand; Sophie Audollent; Tania Attié-Bitach; Kenton R Holden; William B Dobyns; David Traver; Lihadh Al-Gazali; bassam rushdi ali; Tom H Lindner; Tamara Caspary; Edgar Otto; Friedhelm Hildebrandt; Ian A Glass; Clare V Logan; Colin A Johnson; Christopher Bennett; Francesco Brancati; Enza Maria Valente; C Geoffrey Woods; Joseph G Gleeson
Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome.
American journal of human genetics 2008;83(2):170-9.
2006: James Cox; Frank Reimann; Adeline K Nicholas; Gemma Thornton; Emma Roberts; Kelly Springell; Gulshan Karbani; Hussain Jafri; Jovaria Mannan; Yasmin Raashid; Lihadh Al-Gazali; Henan Hamamy; Enza Maria Valente; Shaun Gorman; Richard Williams; Duncan P McHale; John N Wood; Fiona M Gribble; C Geoffrey Woods
An SCN9A channelopathy causes congenital inability to experience pain.
Nature 2006;444(7121):894-8.
2006: Alfredo Ramirez; André Heimbach; Jan Gründemann; Barbara Stiller; Daniel J Hampshire; L Pablo Cid; Ingrid Goebel; Ammar F Mubaidin; Abdul-Latif Wriekat; Jochen Roeper; Amir Al-Din; Axel M Hillmer; Meliha Karsak; Birgit Liss; C Geoffrey Woods; Maria I Behrens; Christian Kubisch
Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase.
Nature genetics 2006;38(10):1184-91.
2006: Simon Holden; James Cox; Ian Kesterton; N S Thomas; C Carr; C Geoffrey Woods
Fanconi anaemia complementation group B presenting as X linked VACTERL with hydrocephalus syndrome.
Journal of medical genetics 2006;43(9):750-4.
2006: James Cox; Andrew P Jackson; Jacquelyn Bond; C Geoffrey Woods
What primary microcephaly can tell us about brain growth.
Trends in molecular medicine 2006;12(8):358-66.
2006: C Geoffrey Woods; Sigmar Stricker; Petra Seemann; Rowena Stern; James Cox; E Sherridan; Emma Roberts; Kelly Springell; Sheila Scott; Gulshan Karbani; S M Sharif; Carmel Toomes; Jacquelyn Bond; D Kumar; Lihadh Al-Gazali; Stefan Mundlos
Mutations in WNT7A cause a range of limb malformations, including Fuhrmann syndrome and Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome.
American journal of human genetics 2006;79(2):402-8.
2006: Neil V Morgan; Shawn K Westaway; Jenny E V Morton; Allison Gregory; Paul Gissen; Scott Sonek; Hakan Cangul; Jason Coryell; Natalie Canham; Nardo Nardocci; Giovanna Zorzi; Shanaz Pasha; Diana Rodriguez; Isabelle Desguerre; Ammar F Mubaidin; Enrico Bertini; Richard C Trembath; Alessandro Simonati; Carolyn Schanen; Colin A Johnson; Barbara Levinson; C Geoffrey Woods; Beth Wilmot; Patricia L Kramer; Jane Gitschier; Eamonn R Maher; Susan J Hayflick
PLA2G6, encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron.
Nature genetics 2006;38(7):752-4.
2006: Rowena Stern; C Geoffrey Woods
Evolutionary Genetics: is brain evolution still continuing in modern humans?
European journal of human genetics : EJHG 2006;14(7):799-800.
2006: C Geoffrey Woods; James Cox; Kelly Springell; Daniel J Hampshire; Moin D Mohamed; Martin McKibbin; Rowena Stern; F Lucy Raymond; Richard Sandford; Saghira Malik Sharif; Gulshan Karbani; Mustaq Ahmed; Jacquelyn Bond; David Clayton; Chris F Inglehearn
Quantification of homozygosity in consanguineous individuals with autosomal recessive disease.
American journal of human genetics 2006;78(5):889-96.
2006: Daniel J Hampshire; Mohammed Ayub; Kelly Springell; Emma Roberts; Hussain Jafri; Yasmin Rashid; Jacquelyn Bond; John H Riley; C Geoffrey Woods
MORM syndrome (mental retardation, truncal obesity, retinal dystrophy and micropenis), a new autosomal recessive disorder, links to 9q34.
European journal of human genetics : EJHG 2006;14(5):543-8.
2006: Josephine L Meade; Erika A de Wynter; Peter Brett; Saghira Malik Sharif; C Geoffrey Woods; Alexander F Markham; Graham P Cook
A family with Papillon-Lefevre syndrome reveals a requirement for cathepsin C in granzyme B activation and NK cell cytolytic activity.
Blood 2006;107(9):3665-8.
2006: Jacquelyn Bond; C Geoffrey Woods
Cytoskeletal genes regulating brain size.
Current opinion in cell biology 2006;18(1):95-101.
2006: K E Chandler; A Del Rio; K Rakshi; Kelly Springell; D K Williams; Neil Stoodley; C Geoffrey Woods; Daniela T Pilz
Leucodysplasia, microcephaly, cerebral malformation (LMC): a novel recessive disorder linked to 2p16.
Brain : a journal of neurology 2006;129(Pt 1):272-7.
2005: J Shen; Wafaa Eyaid; Ganeshwaran H Mochida; F Al-Moayyad; Adria Bodell; C Geoffrey Woods; Christopher Walsh
ASPM mutations identified in patients with primary microcephaly and seizures.
Journal of medical genetics 2005;42(9):725-9.
2005: C Geoffrey Woods; Jacquelyn Bond; Wolfgang Enard
Autosomal recessive primary microcephaly (MCPH): a review of clinical, molecular, and evolutionary findings.
American journal of human genetics 2005;76(5):717-28.
2005: Jacquelyn Bond; Emma Roberts; Kelly Springell; sofia lizarraga; Sophia Lizarraga; Sheila Scott; Julie Higgins; Daniel J Hampshire; Ewan E Morrison; Gabriella F Leal; Elias O Silva; Suzana M R Costa; Diana Baralle; Michela Raponi; Gulshan Karbani; Yasmin Rashid; Hussain Jafri; Christopher Bennett; Peter Corry; Christopher Walsh; C Geoffrey Woods
A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain size.
Nature genetics 2005;37(4):353-5.
2005: Enza Maria Valente; Sarah E Marsh; Marco Castori; Tracy Dixon-Salazar; Enrico Bertini; Lihadh Al-Gazali; Jean Messer; Clara Barbot; C Geoffrey Woods; Eugen Boltshauser; Asma A Al Tawari; Carmelo Damiano Salpietro; Hulya Kayserili; László Sztriha; Moez Gribaa; Michel Koenig; Bruno Dallapiccola; Joseph G Gleeson
Distinguishing the four genetic causes of Jouberts syndrome-related disorders.
Annals of neurology 2005;57(4):513-9.
2005: Jacquelyn Bond; K Flintoff; J Higgins; S Scott; C Bennet; J Parsons; J Mannon; Hussain Jafri; Yasmin Rashid; M Barrow; Richard C Trembath; Geoffrey Woodruff; E Rossa; S Lynch; J Sheilds; Ruth Newbury-Ecob; A Falconer; P Holland; D Cockburn; Gulshan Karbani; S Malik; M Ahmed; Emma Roberts; G Taylor; C Geoffrey Woods
The importance of seeking ALMS1 mutations in infants with dilated cardiomyopathy.
Journal of medical genetics 2005;42(2):e10.
2004: Clare N Lynex; Ian Carr; Jack P Leek; Rajgopal Achuthan; Simon Mitchell; Eamonn R Maher; C Geoffrey Woods; David T Bonthon; Alexander F Markham
Homozygosity for a missense mutation in the 67 kDa isoform of glutamate decarboxylase in a family with autosomal recessive spastic cerebral palsy: parallels with Stiff-Person Syndrome and other movement disorders.
BMC neurology 2004;4(1):20.
2004: Yanick J Crow; R F Massey; J R Innes; Peter W Pairaudeau; C A Rowland Hill; C Geoffrey Woods; Manir Ali; John H Livingston; Pierre Lebon; K Nischall; ME McEntagart; N Hindocha; R M Winter
Congenital glaucoma and brain stem atrophy as features of Aicardi-Goutières syndrome.
American journal of medical genetics. Part A 2004;129A(3):303-7.
2004: C Geoffrey Woods
Neuroscience. Crossing the midline.
Science (New York, N.Y.) 2004;304(5676):1455-6.
2004: Bernard S Chang; Xianhua Piao; C Giannini; G D Cascino; I Scheffer; C Geoffrey Woods; Meral Topcu; K Tezcan; Adria Bodell; R J Leventer; A James Barkovich; P Ellen Grant; Christopher Walsh
Bilateral generalized polymicrogyria (BGP): a distinct syndrome of cortical malformation.
Neurology 2004;62(10):1722-8.
2004: Natalay Kouprina; Adam Pavlicek; Ganeshwaran H Mochida; Greg Solomon; William Gersch; Young-Ho Yoon; Randall V Collura; Maryellen Ruvolo; J Carl Barrett; C Geoffrey Woods; Christopher Walsh; Jerzy Jurka; Vladimir Larionov
Accelerated evolution of the ASPM gene controlling brain size begins prior to human brain expansion.
PLoS biology 2004;2(5):E126.
2004: C Geoffrey Woods
Human microcephaly.
Current opinion in neurobiology 2004;14(1):112-7.
2003: Jacquelyn Bond; Sheila Scott; Daniel J Hampshire; Kelly Springell; Peter Corry; Marc J Abramowicz; Ganeshwaran H Mochida; Raoul Hennekam; Eamonn R Maher; Jean-Pierre Fryns; Abdulrahman Alswaid; Hussain Jafri; Yasmin Rashid; Ammar F Mubaidin; Christopher Walsh; Emma Roberts; C Geoffrey Woods
Protein-truncating mutations in ASPM cause variable reduction in brain size.
American journal of human genetics 2003;73(5):1170-7.
2003: Lesley C Keeler; Sarah E Marsh; Esther P Leeflang; C Geoffrey Woods; László Sztriha; Lihadh Al-Gazali; Gururaj Aithala; Joseph G Gleeson
Linkage analysis in families with Joubert syndrome plus oculo-renal involvement identifies the CORS2 locus on chromosome 11p12-q13.3.
American journal of human genetics 2003;73(3):656-62.
2003: Ammar F Mubaidin; Emma Roberts; Daniel J Hampshire; M Dehyyat; A Shurbaji; M Mubaidien; A Jamil; Amir Al-Din; A Kurdi; C Geoffrey Woods
Karak syndrome: a novel degenerative disorder of the basal ganglia and cerebellum.
Journal of medical genetics 2003;40(7):543-6.
2003: Gabriella F Leal; Emma Roberts; Elias O Silva; S M R Costa; Daniel J Hampshire; C Geoffrey Woods
A novel locus for autosomal recessive primary microcephaly (MCPH6) maps to 13q12.2.
Journal of medical genetics 2003;40(7):540-2.
2003: Yanick J Crow; D N Black; Manir Ali; Jacquelyn Bond; Andrew P Jackson; M Lefson; J Michaud; Emma Roberts; John B P Stephenson; C Geoffrey Woods; Pierre Lebon
Cree encephalitis is allelic with Aicardi-Goutiéres syndrome: implications for the pathogenesis of disorders of interferon alpha metabolism.
Journal of medical genetics 2003;40(3):183-7.
2002: Neil V Morgan; Paul Gissen; Saghira Malik Sharif; Laura Baumber; Joan Sutherland; Deirdre A Kelly; Kingi Aminu; Christopher P Bennett; C Geoffrey Woods; Robert F Mueller; Richard C Trembath; Eamonn R Maher; Colin A Johnson
A novel locus for Meckel-Gruber syndrome, MKS3, maps to chromosome 8q24.
Human genetics 2002;111(4-5):456-61.
2002: Emma Roberts; Daniel J Hampshire; L Pattison; Kelly Springell; Hussain Jafri; Peter Corry; J Mannon; Yasmin Rashid; Yanick J Crow; Jacquelyn Bond; C Geoffrey Woods
Autosomal recessive primary microcephaly: an analysis of locus heterogeneity and phenotypic variation.
Journal of medical genetics 2002;39(10):718-21.
2002: Jacquelyn Bond; Emma Roberts; Ganeshwaran H Mochida; Daniel J Hampshire; Sheila Scott; Jon M Askham; Kelly Springell; Meera Mahadevan; Yanick J Crow; Alexander F Markham; Christopher Walsh; C Geoffrey Woods
ASPM is a major determinant of cerebral cortical size.
Nature genetics 2002;32(2):316-20.
2002: Andrew P Jackson; Helen Eastwood; Sandra M Bell; Jimi Adu; Carmel Toomes; Ian Carr; Emma Roberts; Daniel J Hampshire; Yanick J Crow; Alan J Mighell; Gulshan Karbani; Hussain Jafri; Yasmin Rashid; Robert F Mueller; Alexander F Markham; C Geoffrey Woods
Identification of microcephalin, a protein implicated in determining the size of the human brain.
American journal of human genetics 2002;71(1):136-42.
2002: K B Schwarz; Colin D Ferrie; C Geoffrey Woods
Two siblings with a new Aicardi-Goutières-like syndrome.
Developmental medicine and child neurology 2002;44(6):422-5.
2001: Daniel J Hampshire; Emma Roberts; Yanick J Crow; Jacquelyn Bond; Ammar F Mubaidin; A L Wriekat; Amir Al-Din; C Geoffrey Woods
Kufor-Rakeb syndrome, pallido-pyramidal degeneration with supranuclear upgaze paresis and dementia, maps to 1p36.
Journal of medical genetics 2001;38(10):680-2.
2001: Moin D Mohamed; Martin McKibbin; Hussain Jafri; Y Rasheed; C Geoffrey Woods; Chris F Inglehearn
A new pedigree with recessive mapping to CHED2 locus on 20p13.
The British journal of ophthalmology 2001;85(6):758-9.
2001: John R Ainsworth; Jenny E V Morton; P Good; C Geoffrey Woods; N D George; J P Shield; J Bradbury; M J Henderson; J Chhina
Micro syndrome in Muslim Pakistan children.
Ophthalmology 2001;108(3):491-7.
2000: L Pattison; Yanick J Crow; VJ Deeble; Andrew P Jackson; Hussain Jafri; Yasmin Rashid; Emma Roberts; C Geoffrey Woods
A fifth locus for primary autosomal recessive microcephaly maps to chromosome 1q31.
American journal of human genetics 2000;67(6):1578-80.
2000: Yanick J Crow; Andrew P Jackson; Emma Roberts; Ellen van Beusekom; P Barth; Peter Corry; Colin D Ferrie; Ben C J Hamel; R Jayatunga; Gulshan Karbani; R Kálmánchey; A Kelemen; M King; R Kumar; J Livingstone; R Massey; Robert C McWilliam; A Meager; Christopher Rittey; John B P Stephenson; John Tolmie; A Verrips; Thomas Voit; Hans van Bokhoven; Han G Brunner; C Geoffrey Woods
Aicardi-Goutières syndrome displays genetic heterogeneity with one locus (AGS1) on chromosome 3p21.
American journal of human genetics 2000;67(1):213-21.
2000: Duncan P McHale; Andrew P Jackson; Malcolm Levene; Peter Corry; C Geoffrey Woods; NJ Lench; Robert F Mueller; Alexander F Markham
A gene for ataxic cerebral palsy maps to chromosome 9p12-q12.
European journal of human genetics : EJHG 2000;8(4):267-72.
2000: VJ Deeble; Emma Roberts; A Jackson; NJ Lench; Gulshan Karbani; C Geoffrey Woods
The continuing failure to recognise Alström syndrome and further evidence of genetic homogeneity.
Journal of medical genetics 2000;37(3):219.
2000: LM Moynihan; Andrew P Jackson; Emma Roberts; Gulshan Karbani; I Lewis; Peter Corry; G Turner; Robert F Mueller; NJ Lench; C Geoffrey Woods
A third novel locus for primary autosomal recessive microcephaly maps to chromosome 9q34.
American journal of human genetics 2000;66(2):724-7.
1999: Carmel Toomes; J James; A J Wood; C L Wu; D McCormick; NJ Lench; Chelsee Hewitt; LM Moynihan; Emma Roberts; C Geoffrey Woods; A Markham; M Wong; R Widmer; K A Ghaffar; Michael N Pemberton; I R Hussein; S A Temtamy; R Davies; Andrew P Read; Philip Sloan; Michael J Dixon; Nalin Thakker
Loss-of-function mutations in the cathepsin C gene result in periodontal disease and palmoplantar keratosis.
Nature genetics 1999;23(4):421-4.
1999: Jacopo Celli; Pascal Duijf; Ben C J Hamel; Michael Bamshad; B Kramer; Arie P T Smits; Ruth Newbury-Ecob; Raoul Hennekam; Griet Van Buggenhout; A van Haeringen; C Geoffrey Woods; A J van Essen; R de Waal; G Vriend; D A Haber; A Yang; Frank McKeon; Han G Brunner; Hans van Bokhoven
Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome.
Cell 1999;99(2):143-53.
1999: Emma Roberts; Andrew P Jackson; A C Carradice; VJ Deeble; Jovaria Mannan; Yasmin Rashid; Hussain Jafri; Duncan P McHale; Alexander F Markham; NJ Lench; C Geoffrey Woods
The second locus for autosomal recessive primary microcephaly (MCPH2) maps to chromosome 19q13.1-13.2.
European journal of human genetics : EJHG 1999;7(7):815-20.
1999: MR Nelen; H Kremer; I B Konings; F Schoute; A J van Essen; R Koch; C Geoffrey Woods; J P Fryns; B Hamel; Lies Hoefsloot; E A Peeters; George W Padberg
Novel PTEN mutations in patients with Cowden disease: absence of clear genotype-phenotype correlations.
European journal of human genetics : EJHG 1999;7(3):267-73.
1999: Duncan P McHale; S Mitchell; SE Bundey; LM Moynihan; DA Campbell; C Geoffrey Woods; NJ Lench; Robert F Mueller; Alexander F Markham
A gene for autosomal recessive symmetrical spastic cerebral palsy maps to chromosome 2q24-25.
American journal of human genetics 1999;64(2):526-32.
1998: Andrew P Jackson; Duncan P McHale; DA Campbell; Hussain Jafri; Yasmin Rashid; Jovaria Mannan; Gulshan Karbani; Peter Corry; Malcolm Levene; Robert F Mueller; Alexander F Markham; NJ Lench; C Geoffrey Woods
Primary autosomal recessive microcephaly (MCPH1) maps to chromosome 8p22-pter.
American journal of human genetics 1998;63(2):541-6.
1997: Emma Roberts; VJ Deeble; C Geoffrey Woods; Graham Taylor
Potassium permanganate and tetraethylammonium chloride are a safe and effective substitute for osmium tetroxide in solid-phase fluorescent chemical cleavage of mismatch.
Nucleic acids research 1997;25(16):3377-8.
1997: VJ Deeble; Emma Roberts; M D Robinson; C Geoffrey Woods; Tim BISHOP; Graham Taylor
Comparison of enzyme mismatch cleavage and chemical cleavage of mismatch on a defined set of heteroduplexes.
Genetic testing 1997;1(4):253-9.