FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Judy Fantes

Research Profile

Procedures

Anatomy

Concepts & Ideas

Molecular Sequence Data

Chemicals & Drugs

Living Beings

Mouse

Disorders

Devices

Yeast Artificial Chromosomes

Co-author Network

Publications

TOP 3
Laura A Lettice; Harris Morrison; Elizabeth Sweeney; Shanmugasundaram Venkataraman; Sarah Daniels; Paul S Devenney; Judy A Fantes; Philippe Gautier; Robert E Hill; David R FitzPatrick
Enhancer-adoption as a mechanism of human developmental disease.
Louise Harewood; Monica Liu; Jean Keeling; Alan Howatson; Margo Whiteford; Peter Branney; Margaret Evans; Judy A Fantes; David R FitzPatrick
Bilateral renal agenesis/hypoplasia/dysplasia (BRAHD): postmortem analysis of 45 cases with breakpoint mapping of two de novo translocations.
Jannine Clapp; Laura M Mitchell; Daniel J Bolland; Judy A Fantes; Anne E Corcoran; Paul J Scotting; John A L Armour; Jane E Hewitt
Evolutionary conservation of a coding function for D4Z4, the tandem DNA repeat mutated in facioscapulohumeral muscular dystrophy.

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 Judy Fantes (preview)

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

Flash Player Required

All Publications

2011: Laura A Lettice; Harris Morrison; Elizabeth Sweeney; Shanmugasundaram Venkataraman; Sarah Daniels; Paul S Devenney; Judy A Fantes; Philippe Gautier; Robert E Hill; David R FitzPatrick
Enhancer-adoption as a mechanism of human developmental disease.
Human mutation 2011;32(12):1492-9.
2010: Louise Harewood; Monica Liu; Jean Keeling; Alan Howatson; Margo Whiteford; Peter Branney; Margaret Evans; Judy A Fantes; David R FitzPatrick
Bilateral renal agenesis/hypoplasia/dysplasia (BRAHD): postmortem analysis of 45 cases with breakpoint mapping of two de novo translocations.
PloS one 2010;5(8):e12375.
2007: Jannine Clapp; Laura M Mitchell; Daniel J Bolland; Judy A Fantes; Anne E Corcoran; Paul J Scotting; John A L Armour; Jane E Hewitt
Evolutionary conservation of a coding function for D4Z4, the tandem DNA repeat mutated in facioscapulohumeral muscular dystrophy.
American journal of human genetics 2007;81(2):264-79.
2006: Konstantina Plastira; Eddy Maher; Judy A Fantes; Jacqueline Ramsay; Roxani Angelopoulou
Using BAC clones to characterize unbalanced chromosome abnormalities in interphase cells.
European journal of medical genetics 2006;49(3):235-46.
2006: Kathleen A Williamson; Ann M Hever; Joe Rainger; R. Curtis Rogers; Alex Magee; Zdenek Fiedler; Wee Teik Keng; Freddie H Sharkey; Niolette I McGill; Clare J Hill; Adele Schneider; Mario Messina; Peter D Turnpenny; Judy A Fantes; Veronica van Heyningen; David R FitzPatrick
Mutations in SOX2 cause anophthalmia-esophageal-genital (AEG) syndrome.
Human molecular genetics 2006;15(9):1413-22.
2003: David R FitzPatrick; Ian Carr; Lorna McLaren; Jack P Leek; Patrick J Wightman; Kathy Williamson; Philippe Gautier; Niolette I McGill; Caroline Hayward; Helen Firth; Alexander F Markham; Judy A Fantes; David T Bonthron
Identification of SATB2 as the cleft palate gene on 2q32-q33.
Human molecular genetics 2003;12(19):2491-501.
2003: Judy A Fantes; Nicola K Ragge; Sally-Ann Lynch; Niolette I McGill; J R O Collin; Patricia N Howard-Peebles; Caroline Hayward; Anthony J Vivian; Kathy Williamson; Veronica van Heyningen; David R FitzPatrick
Mutations in SOX2 cause anophthalmia.
Nature genetics 2003;33(4):461-3.
2002: Sixto Garcia-Miñaur; Judy A Fantes; R S Murray; M E M Porteous; L Strain; J E Burns; J Stephen; JP Warner
A novel atypical 22q11.2 distal deletion in father and son.
Journal of medical genetics 2002;39(10):E62.
2001: Kathryn L Evans; Stéphanie Le Hellard; stewart morris; D Lawson; Claire Whitton; Colin Semple; Judy A Fantes; Helen S Torrance; M Pat Malloy; John Maule; Sean Humphray; Mark T Ross; David R Bentley; Walter J Muir; D H R Blackwood; David J Porteous
A 6.9-Mb high-resolution BAC/PAC contig of human 4p15.3-p16.1, a candidate region for bipolar affective disorder.
Genomics 2001;71(3):315-23.
1997: Cora M Aalfs; Judy A Fantes; L J Wenniger-Prick; Sigrid Sluijter; Raoul Hennekam; Veronica van Heyningen; Jan M N Hoovers
Tandem duplication of 11p12-p13 in a child with borderline development delay and eye abnormalities: dose effect of the PAX6 gene product?
American journal of medical genetics 1997;73(3):267-71.
1997: J Kent; M Lee; Andreas Schedl; Shelagh Boyle; Judy A Fantes; M Powell; N Rushmere; C Abbott; Veronica van Heyningen; Wendy A Bickmore
The reticulocalbin gene maps to the WAGR region in human and to the Small eye Harwell deletion in mouse.
Genomics 1997;42(2):260-7.
1997: John A Crolla; J E Cawdery; C A Oley; I D Young; Joe Gray; Judy A Fantes; Veronica van Heyningen
A FISH approach to defining the extent and possible clinical significance of deletions at the WAGR locus.
Journal of medical genetics 1997;34(3):207-12.
1997: Bruce E Hayward; JP Warner; N Dunlop; Judy A Fantes; S Intody; Jack P Leek; Alexander F Markham; David T Bonthron
Molecular genetics of the human glucokinase regulator-fructokinase (GCKR-KHK) region of chromosome 2p23.
Biochemical Society transactions 1997;25(1):140-5.
1996: M Mackay; Judy A Fantes; S Scherer; Shelagh Boyle; K West; L C Tsui; E Belloni; Eve M Lutz; Veronica van Heyningen; Anthony J Harmar
Chromosomal localization in mouse and human of the vasoactive intestinal peptide receptor type 2 gene: a possible contributor to the holoprosencephaly 3 phenotype.
Genomics 1996;37(3):345-53.
1996: Bruce E Hayward; Judy A Fantes; JP Warner; S Intody; Jack P Leek; Alexander F Markham; David T Bonthron
Co-localization of the ketohexokinase and glucokinase regulator genes to a 500-kb region of chromosome 2p23.
Mammalian genome : official journal of the International Mammalian Genome Society 1996;7(6):454-8.
1995: Judy A Fantes; D K Green; W Hill; M H Stark; J M Gordon; J Piper
Application of automation to the detection of radiation damage using FISH technology.
International journal of radiation biology 1995;68(3):263-76.
1995: Judy A Fantes; B Redeker; M Breen; Shelagh Boyle; J Brown; J Fletcher; S Jones; Wendy A Bickmore; Y Fukushima; marcel mannens
Aniridia-associated cytogenetic rearrangements suggest that a position effect may cause the mutant phenotype.
Human molecular genetics 1995;4(3):415-22.
1995: Judy A Fantes; K Oghene; Shelagh Boyle; S Danes; J M Fletcher; E A Bruford; K Williamson; Anne Seawright; Andreas Schedl; Isabel M Hanson
A high-resolution integrated physical, cytogenetic, and genetic map of human chromosome 11: distal p13 to proximal p15.1.
Genomics 1995;25(2):447-61.
1995: Walter J Muir; C M Gosden; Anthony J Brookes; Judy A Fantes; K L Evans; S M Maguire; B Stevenson; Shelagh Boyle; D H Blackwood; D M St Clair
Direct microdissection and microcloning of a translocation breakpoint region, t(1;11)(q42.2;q21), associated with schizophrenia.
Cytogenetics and cell genetics 1995;70(1-2):35-40.
1995: S du Manoir; Olli Kallioniemi; Peter Lichter; J Piper; P A Benedetti; Andrew D Carothers; Judy A Fantes; JM García-Sagredo; Tommy Gerdes; Michel Giollant
Hardware and software requirements for quantitative analysis of comparative genomic hybridization.
Cytometry 1995;19(1):4-9.
1994: J Prosser; A Condie; M Wright; J M Horn; Judy A Fantes; A H Wyllie; M G Dunlop
APC mutation analysis by chemical cleavage of mismatch and a protein truncation assay in familial adenomatous polyposis.
British journal of cancer 1994;70(5):841-6.
1994: M Gaudoin; D Rutovitz; J Piper; P Eason; H Finlayson; A E Hill; Judy A Fantes; Paul Perry; I Poole; J B Scrimgeour
Rapid on-slide location and analysis of enriched fetal nucleated cells from maternal blood.
Annals of the New York Academy of Sciences 1994;731():136-7.
1994: G C Sellar; S A Jordan; Wendy A Bickmore; Judy A Fantes; Veronica van Heyningen; Alexander S Whitehead
The human serum amyloid A protein (SAA) superfamily gene cluster: mapping to chromosome 11p15.1 by physical and genetic linkage analysis.
Genomics 1994;19(2):221-7.
1994: Judy A Fantes; D K Green; A Sharkey
Chromosome sorting by flow cytometry. Production of DNA libraries and gene mapping.
Methods in molecular biology (Clifton, N.J.) 1994;29():205-19.
1993: David T Bonthron; S J Smith; Judy A Fantes; C M Gosden
De novo microdeletion on an inherited Robertsonian translocation chromosome: a cause for dysmorphism in the apparently balanced translocation carrier.
American journal of human genetics 1993;53(3):629-37.
1993: K L Evans; Judy A Fantes; C Simpson; Benoît Arveiler; Walter Muir; J Fletcher; Veronica van Heyningen; K P Steel; K A Brown; S D Brown
Human olfactory marker protein maps close to tyrosinase and is a candidate gene for Usher syndrome type I.
Human molecular genetics 1993;2(2):115-8.
1992: Judy A Fantes; Wendy A Bickmore; J M Fletcher; F Ballesta; Isabel M Hanson; Veronica van Heyningen
Submicroscopic deletions at the WAGR locus, revealed by nonradioactive in situ hybridization.
American journal of human genetics 1992;51(6):1286-94.
1992: Niolette I McGill; Judy A Fantes; Howard J Cooke
Lambda CM8, a human sequence with putative centromeric function, does not map to the centromere but is present in one to two copies at 9qter.
Human molecular genetics 1992;1(9):749-51.
1992: A M Sharkey; L McLaren; M Carroll; Judy A Fantes; D Green; D Wilson; P J Scambler; H J Evans
Isolation of anonymous DNA markers for human chromosome 22q11 from a flow-sorted library, and mapping using hybrids from patients with DiGeorge syndrome.
Human genetics 1992;89(1):73-8.
1991: C Farr; Judy A Fantes; P Goodfellow; Howard J Cooke
Functional reintroduction of human telomeres into mammalian cells.
Proceedings of the National Academy of Sciences of the United States of America 1991;88(16):7006-10.
1991: JR Gosden; D Hanratty; J Starling; Judy A Fantes; A Mitchell; David J Porteous
Oligonucleotide-primed in situ DNA synthesis (PRINS): a method for chromosome mapping, banding, and investigation of sequence organization.
Cytogenetics and cell genetics 1991;57(2-3):100-4.
1990: S Cross; J Lindsey; Judy A Fantes; S McKay; Niolette I McGill; Howard J Cooke
The structure of a subterminal repeated sequence present on many human chromosomes.
Nucleic acids research 1990;18(22):6649-57.
1990: J Piper; Judy A Fantes; JR Gosden; L A Ji
Automatic detection of fragile X chromosomes using an X centromere probe.
Cytometry 1990;11(1):73-9.
1989: Judy A Fantes; D K Green; P Malloy; A T Sumner
Flow cytometry measurements of human chromosome kinetochore labeling.
Cytometry 1989;10(2):134-42.
1989: D Saltman; F M Ross; Judy A Fantes; Robin C Allshire; G E Turner; H J Evans
Telomeric associations in a lymphoblastoid cell line from a patient with B-cell follicular lymphoma.
Cytogenetics and cell genetics 1989;50(4):230-3.
1988: Judy A Fantes; JR Gosden; J Piper
Use of an alphoid satellite sequence to locate the X chromosome automatically, with particular reference to identification of the fragile X.
Cytogenetics and cell genetics 1988;48(3):142-7.
1988: Anne Seawright; J M Fletcher; Judy A Fantes; H Morrison; David J Porteous; S S Li; Nicholas D Hastie; Veronica van Heyningen
Analysis of WAGR deletions and related translocations with gene-specific DNA probes, using FACS-selected cell hybrids.
Somatic cell and molecular genetics 1988;14(1):21-30.
1986: D J Porteous; J E Morten; G Cranston; J M Fletcher; A Mitchell; Veronica van Heyningen; Judy A Fantes; P A Boyd; Nicholas D Hastie
Molecular and physical arrangements of human DNA in HRAS1-selected, chromosome-mediated transfectants.
Molecular and cellular biology 1986;6(6):2223-32.
1985: Veronica van Heyningen; P A Boyd; Anne Seawright; J M Fletcher; Judy A Fantes; K E Buckton; G Spowart; David J Porteous; R E Hill; M S Newton
Molecular analysis of chromosome 11 deletions in aniridia-Wilms tumor syndrome.
Proceedings of the National Academy of Sciences of the United States of America 1985;82(24):8592-6.
1984: D K Green; Judy A Fantes; K E Buckton; J K Elder; P Malloy; Andrew D Carothers; H J Evans
Karyotyping and identification of human chromosome polymorphisms by single fluorochrome flow cytometry.
Human genetics 1984;66(2-3):143-6.
1983: Judy A Fantes; D K Green; Howard J Cooke
Purifying human Y chromosomes by flow cytometry and sorting.
Cytometry 1983;4(1):88-91.
1983: Judy A Fantes; D K Green; J K Elder; P Malloy; H J Evans
Detecting radiation damage to human chromosomes by flow cytometry.
Mutation research 1983;119(2):161-8.