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Nigel Carter

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

Research Profile (preview)

Procedures

Devices

Oligonucleotide Array Sequence Analysis

Phenomena

Nucleic Acid Hybridization

Disorders

Genes & Molecular Sequences

Human Genome

Concepts & Ideas

Anatomy

Chemicals & Drugs

Physiology

Phenotype

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Publications

TOP 3
Tam Gloria W C; Redon Richard; Carter Nigel P; Grant Seth G N
The role of DNA copy number variation in schizophrenia.
Gill Harinder K; Parsons Sian R; Spalluto Cosma; Davies Angela F; Knorz Victoria J; Burlinson Clare E G; Ng Bee Ling; Carter Nigel P; Ogilvie Caroline Mackie; Wilson David I; Roberts Roland G
Separation of the PROX1 gene from upstream conserved elements in a complex inversion/translocation patient with hypoplastic left heart.
Xue Yali; Wang Qiuju; Long Quan; Ng Bee Ling; Swerdlow Harold; Burton John; Skuce Carl; Taylor Ruth; Abdellah Zahra; Zhao Yali; Macarthur Daniel G; Quail Michael A; Carter Nigel P; Yang Huanming; Tyler-Smith Chris
Human y chromosome base-substitution mutation rate measured by direct sequencing in a deep-rooting pedigree.

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All Publications

2009: Tam Gloria W C; Redon Richard; Carter Nigel P; Grant Seth G N
The role of DNA copy number variation in schizophrenia.
Biological psychiatry 2009;66(11):1005-12.
2009: Gill Harinder K; Parsons Sian R; Spalluto Cosma; Davies Angela F; Knorz Victoria J; Burlinson Clare E G; Ng Bee Ling; Carter Nigel P; Ogilvie Caroline Mackie; Wilson David I; Roberts Roland G
Separation of the PROX1 gene from upstream conserved elements in a complex inversion/translocation patient with hypoplastic left heart.
European journal of human genetics : EJHG 2009;17(11):1423-31.
2009: Xue Yali; Wang Qiuju; Long Quan; Ng Bee Ling; Swerdlow Harold; Burton John; Skuce Carl; Taylor Ruth; Abdellah Zahra; Zhao Yali; Macarthur Daniel G; Quail Michael A; Carter Nigel P; Yang Huanming; Tyler-Smith Chris
Human y chromosome base-substitution mutation rate measured by direct sequencing in a deep-rooting pedigree.
Current biology : CB 2009;19(17):1453-7.
2009: Firth Helen V; Richards Shola M; Bevan A Paul; Clayton Stephen; Corpas Manuel; Rajan Diana; Van Vooren Steven; Moreau Yves; Pettett Roger M; Carter Nigel P
DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources.
American journal of human genetics 2009;84(4):524-33.
2009: Gribble Susan M; Ng Bee Ling; Prigmore Elena; Fitzgerald Tomas; Carter Nigel P
Array painting: a protocol for the rapid analysis of aberrant chromosomes using DNA microarrays.
Nature protocols 2009;4(12):1722-36.
2009: Redon Richard; Rigler Diane; Carter Nigel P
Comparative genomic hybridization: DNA preparation for microarray fabrication.
Methods in molecular biology (Clifton, N.J.) 2009;529():259-66.
2009: Redon Richard; Fitzgerald Tomas; Carter Nigel P
Comparative genomic hybridization: DNA labeling, hybridization and detection.
Methods in molecular biology (Clifton, N.J.) 2009;529():267-78.
2009: Redon Richard; Carter Nigel P
Comparative genomic hybridization: microarray design and data interpretation.
Methods in molecular biology (Clifton, N.J.) 2009;529():37-49.
2008: Abd El-Aziz Mai M; Barragan Isabel; O'Driscoll Ciara A; Goodstadt Leo; Prigmore Elena; Borrego Salud; Mena Marcela; Pieras Juan I; El-Ashry Mohamed F; Safieh Leen Abu; Shah Amna; Cheetham Michael E; Carter Nigel P; Chakarova Christina; Ponting Chris P; Bhattacharya Shomi S; Antinolo Guillermo
EYS, encoding an ortholog of Drosophila spacemaker, is mutated in autosomal recessive retinitis pigmentosa.
Nature genetics 2008;40(11):1285-7.
2008: Perry George H; Yang Fengtang; Marques-Bonet Tomas; Murphy Carly; Fitzgerald Tomas; Lee Arthur S; Hyland Courtney; Stone Anne C; Hurles Matthew E; Tyler-Smith Chris; Eichler Evan E; Carter Nigel P; Lee Charles; Redon Richard
Copy number variation and evolution in humans and chimpanzees.
Genome research 2008;18(11):1698-710.
2008: Xue Yali; Sun Donglin; Daly Allan; Yang Fengtang; Zhou Xue; Zhao Mengyao; Huang Ni; Zerjal Tatiana; Lee Charles; Carter Nigel P; Hurles Matthew E; Tyler-Smith Chris
Adaptive evolution of UGT2B17 copy-number variation.
American journal of human genetics 2008;83(3):337-46.
2008: Rakyan Vardhman K; Down Thomas A; Thorne Natalie P; Flicek Paul; Kulesha Eugene; Gräf Stefan; Tomazou Eleni M; Bäckdahl Liselotte; Johnson Nathan; Herberth Marlis; Howe Kevin L; Jackson David K; Miretti Marcos M; Fiegler Heike; Marioni John C; Birney Ewan; Hubbard Tim J P; Carter Nigel P; Tavaré Simon; Beck Stephan
An integrated resource for genome-wide identification and analysis of human tissue-specific differentially methylated regions (tDMRs).
Genome research 2008;18(9):1518-29.
2008: Baptista Julia; Mercer Catherine; Prigmore Elena; Gribble Susan M; Carter Nigel P; Maloney Viv; Thomas N Simon; Jacobs Patricia A; Crolla John A
Breakpoint mapping and array CGH in translocations: comparison of a phenotypically normal and an abnormal cohort.
American journal of human genetics 2008;82(4):927-36.
2008: Balikova Irina; Martens Kevin; Melotte Cindy; Amyere Mustapha; Van Vooren Steven; Moreau Yves; Vetrie David; Fiegler Heike; Carter Nigel P; Liehr Thomas; Vikkula Miikka; Matthijs Gert; Fryns Jean-Pierre; Casteels Ingele; Devriendt Koen; Vermeesch Joris Robert
Autosomal-dominant microtia linked to five tandem copies of a copy-number-variable region at chromosome 4p16.
American journal of human genetics 2008;82(1):181-7.
2008: Turner Daniel J; Miretti Marcos; Rajan Diana; Fiegler Heike; Carter Nigel P; Blayney Martyn L; Beck Stephan; Hurles Matthew E
Germline rates of de novo meiotic deletions and duplications causing several genomic disorders.
Nature genetics 2008;40(1):90-5.
2007: Menten Björn; Buysse Karen; Vermeulen Stefan; Meersschaut Valerie; Vandesompele Jo; Ng Bee L; Carter Nigel P; Mortier Geert R; Speleman Frank
Report of a female patient with mental retardation and tall stature due to a chromosomal rearrangement disrupting the OPHN1 gene on Xq12.
European journal of medical genetics 2007;50(6):446-54.
2007: Perry George H; Dominy Nathaniel J; Claw Katrina G; Lee Arthur S; Fiegler Heike; Redon Richard; Werner John; Villanea Fernando A; Mountain Joanna L; Misra Rajeev; Carter Nigel P; Lee Charles; Stone Anne C
Diet and the evolution of human amylase gene copy number variation.
Nature genetics 2007;39(10):1256-60.
2007: Scherer Stephen W; Lee Charles; Birney Ewan; Altshuler David M; Eichler Evan E; Carter Nigel P; Hurles Matthew E; Feuk Lars
Challenges and standards in integrating surveys of structural variation.
Nature genetics 2007;39(7 Suppl):S7-15.
2007: Carter Nigel P
Methods and strategies for analyzing copy number variation using DNA microarrays.
Nature genetics 2007;39(7 Suppl):S16-21.
2007: Koch Christoph M; Andrews Robert M; Flicek Paul; Dillon Shane C; Karaöz Ulas; Clelland Gayle K; Wilcox Sarah; Beare David M; Fowler Joanna C; Couttet Phillippe; James Keith D; Lefebvre Gregory C; Bruce Alexander W; Dovey Oliver M; Ellis Peter D; Dhami Pawandeep; Langford Cordelia F; Weng Zhiping; Birney Ewan; Carter Nigel P; Vetrie David; Dunham Ian
The landscape of histone modifications across 1% of the human genome in five human cell lines.
Genome research 2007;17(6):691-707.
2007: Ng Bee L; Yang Fengtang; Carter Nigel P
Flow analysis and sorting of microchromosomes (<3 Mb).
Cytometry. Part A : the journal of the International Society for Analytical Cytology 2007;71(6):410-3.
2007: Amiel Jeanne; Rio Marlene; de Pontual Loic; Redon Richard; Malan Valerie; Boddaert Nathalie; Plouin Perrine; Carter Nigel P; Lyonnet Stanislas; Munnich Arnold; Colleaux Laurence
Mutations in TCF4, encoding a class I basic helix-loop-helix transcription factor, are responsible for Pitt-Hopkins syndrome, a severe epileptic encephalopathy associated with autonomic dysfunction.
American journal of human genetics 2007;80(5):988-93.
2007: Foster Rebecca E; Abdulrahman Mahera; Morris Mark R; Prigmore Elena; Gribble Susan; Ng Beeling; Gentle Dean; Ready Steven; Weston Phil M T; Wiesener Michael S; Kishida Takeshi; Yao Masahiro; Davison Val; Barbero Jose Luis; Chu Carol; Carter Nigel P; Latif Farida; Maher Eamonn R
Characterization of a 3;6 translocation associated with renal cell carcinoma.
Genes, chromosomes & cancer 2007;46(4):311-7.
2007: Gribble S M; Kalaitzopoulos D; Burford D C; Prigmore E; Selzer R R; Ng B L; Matthews N S W; Porter K M; Curley R; Lindsay S J; Baptista J; Richmond T A; Carter N P
Ultra-high resolution array painting facilitates breakpoint sequencing.
Journal of medical genetics 2007;44(1):51-8.
2007: Marioni John C; Thorne Natalie P; Valsesia Armand; Fitzgerald Tomas; Redon Richard; Fiegler Heike; Andrews T Daniel; Stranger Barbara E; Lynch Andrew G; Dermitzakis Emmanouil T; Carter Nigel P; Tavaré Simon; Hurles Matthew E
Breaking the waves: improved detection of copy number variation from microarray-based comparative genomic hybridization.
Genome biology 2007;8(10):R228.
2007: Freeman Jennifer L; Adeniyi Adeola; Banerjee Ruby; Dallaire Stephanie; Maguire Sean F; Chi Jianxiang; Ng Bee Ling; Zepeda Cinthya; Scott Carol E; Humphray Sean; Rogers Jane; Zhou Yi; Zon Leonard I; Carter Nigel P; Yang Fengtang; Lee Charles
Definition of the zebrafish genome using flow cytometry and cytogenetic mapping.
BMC genomics 2007;8():195.
2007: Fiegler Heike; Redon Richard; Carter Nigel P
Construction and use of spotted large-insert clone DNA microarrays for the detection of genomic copy number changes.
Nature protocols 2007;2(3):577-87.
2007: Fiegler Heike; Geigl Jochen B; Langer Sabine; Rigler Diane; Porter Keith; Unger Kristian; Carter Nigel P; Speicher Michael R
High resolution array-CGH analysis of single cells.
Nucleic acids research 2007;35(3):e15.
2006: Fiegler Heike; Redon Richard; Andrews Dan; Scott Carol; Andrews Robert; Carder Carol; Clark Richard; Dovey Oliver; Ellis Peter; Feuk Lars; French Lisa; Hunt Paul; Kalaitzopoulos Dimitrios; Larkin James; Montgomery Lyndal; Perry George H; Plumb Bob W; Porter Keith; Rigby Rachel E; Rigler Diane; Valsesia Armand; Langford Cordelia; Humphray Sean J; Scherer Stephen W; Lee Charles; Hurles Matthew E; Carter Nigel P
Accurate and reliable high-throughput detection of copy number variation in the human genome.
Genome research 2006;16(12):1566-74.
2006: Jacquemont M-L; Sanlaville D; Redon R; Raoul O; Cormier-Daire V; Lyonnet S; Amiel J; Le Merrer M; Heron D; de Blois M-C; Prieur M; Vekemans M; Carter N P; Munnich A; Colleaux L; Philippe A
Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders.
Journal of medical genetics 2006;43(11):843-9.
2006: Ng Bee Ling; Carter Nigel P
Factors affecting flow karyotype resolution.
Cytometry. Part A : the journal of the International Society for Analytical Cytology 2006;69(9):1028-36.
2006: Shaw-Smith Charles; Pittman Alan M; Willatt Lionel; Martin Howard; Rickman Lisa; Gribble Susan; Curley Rebecca; Cumming Sally; Dunn Carolyn; Kalaitzopoulos Dimitrios; Porter Keith; Prigmore Elena; Krepischi-Santos Ana C V; Varela Monica C; Koiffmann Celia P; Lees Andrew J; Rosenberg Carla; Firth Helen V; de Silva Rohan; Carter Nigel P
Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability.
Nature genetics 2006;38(9):1032-7.
2006: Freeman Jennifer L; Perry George H; Feuk Lars; Redon Richard; McCarroll Steven A; Altshuler David M; Aburatani Hiroyuki; Jones Keith W; Tyler-Smith Chris; Hurles Matthew E; Carter Nigel P; Scherer Stephen W; Lee Charles
Copy number variation: new insights in genome diversity.
Genome research 2006;16(8):949-61.
2006: Kriek Marjolein; Szuhai Karoly; Kant Sarina G; White Stefan J; Dauwerse Hans; Fiegler Heike; Carter Nigel P; Knijnenburg Jeroen; den Dunnen Johan T; Tanke Hans J; Breuning Martijn H; Rosenberg Carla
A complex rearrangement on chromosome 22 affecting both homologues; haplo-insufficiency of the Cat eye syndrome region may have no clinical relevance.
Human genetics 2006;120(1):77-84.
2006: Redon Richard; Baujat Geneviève; Sanlaville Damien; Le Merrer Martine; Vekemans Michel; Munnich Arnold; Carter Nigel P; Cormier-Daire Valérie; Colleaux Laurence
Interstitial 9q22.3 microdeletion: clinical and molecular characterisation of a newly recognised overgrowth syndrome.
European journal of human genetics : EJHG 2006;14(6):759-67.
2006: Gaasenbeek Michelle; Howarth Kimberley; Rowan Andrew J; Gorman Patricia A; Jones Angela; Chaplin Tracy; Liu Ying; Bicknell David; Davison Eleanor J; Fiegler Heike; Carter Nigel P; Roylance Rebecca R; Tomlinson Ian P M
Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex changes and multiple forms of chromosomal instability in colorectal cancers.
Cancer research 2006;66(7):3471-9.
2006: Mulholland Paul J; Fiegler Heike; Mazzanti Chiara; Gorman Patricia; Sasieni Peter; Adams Joanna; Jones Tania A; Babbage Jane W; Vatcheva Radost; Ichimura Koichi; East Philip; Poullikas Chrysanthos; Collins V Peter; Carter Nigel P; Tomlinson Ian P M; Sheer Denise
Genomic profiling identifies discrete deletions associated with translocations in glioblastoma multiforme.
Cell cycle (Georgetown, Tex.) 2006;5(7):783-91.
2006: Rickman L; Fiegler H; Shaw-Smith C; Nash R; Cirigliano V; Voglino G; Ng B L; Scott C; Whittaker J; Adinolfi M; Carter N P; Bobrow M
Prenatal detection of unbalanced chromosomal rearrangements by array CGH.
Journal of medical genetics 2006;43(4):353-61.
2006: Fauth Christine; Gribble Susan M; Porter Keith M; Codina-Pascual Montserrat; Ng Bee Ling; Kraus Jürgen; Uhrig Sabine; Leifheit Jürgen; Haaf Thomas; Fiegler Heike; Carter Nigel P; Speicher Michael R
Micro-array analyses decipher exceptional complex familial chromosomal rearrangement.
Human genetics 2006;119(1-2):145-53.
2006: Ichimura K; Mungall A J; Fiegler H; Pearson D M; Dunham I; Carter N P; Collins V Peter
Small regions of overlapping deletions on 6q26 in human astrocytic tumours identified using chromosome 6 tile path array-CGH.
Oncogene 2006;25(8):1261-71.
2006: Rosenberg C; Knijnenburg J; Bakker E; Vianna-Morgante A M; Sloos W; Otto P A; Kriek M; Hansson K; Krepischi-Santos A C V; Fiegler H; Carter N P; Bijlsma E K; van Haeringen A; Szuhai K; Tanke H J
Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents.
Journal of medical genetics 2006;43(2):180-6.
2005: Woodward Karen J; Cundall Maria; Sperle Karen; Sistermans Erik A; Ross Mark; Howell Gareth; Gribble Susan M; Burford Deborah C; Carter Nigel P; Hobson Donald L; Garbern James Y; Kamholz John; Heng Henry; Hodes M E; Malcolm Sue; Hobson Grace M
Heterogeneous duplications in patients with Pelizaeus-Merzbacher disease suggest a mechanism of coupled homologous and nonhomologous recombination.
American journal of human genetics 2005;77(6):966-87.
2005: Davison Eleanor J; Tarpey Patrick S; Fiegler Heike; Tomlinson Ian P M; Carter Nigel P
Deletion at chromosome band 20p12.1 in colorectal cancer revealed by high resolution array comparative genomic hybridization.
Genes, chromosomes & cancer 2005;44(4):384-91.
2005: Baptista Julia; Prigmore Elena; Gribble Susan M; Jacobs Patricia A; Carter Nigel P; Crolla John A
Molecular cytogenetic analyses of breakpoints in apparently balanced reciprocal translocations carried by phenotypically normal individuals.
European journal of human genetics : EJHG 2005;13(11):1205-12.
2005: Speicher Michael R; Carter Nigel P
The new cytogenetics: blurring the boundaries with molecular biology.
Nature reviews. Genetics 2005;6(10):782-92.
2005: Rickman L; Fiegler H; Carter N P; Bobrow M
Prenatal diagnosis by array-CGH.
European journal of medical genetics 2005;48(3):232-40.
2005: Redon R; Rio M; Gregory S G; Cooper R A; Fiegler H; Sanlaville D; Banerjee R; Scott C; Carr P; Langford C; Cormier-Daire V; Munnich A; Carter N P; Colleaux L
Tiling path resolution mapping of constitutional 1p36 deletions by array-CGH: contiguous gene deletion or "deletion with positional effect" syndrome?
Journal of medical genetics 2005;42(2):166-71.
2005: Gribble S M; Prigmore E; Burford D C; Porter K M; Ng Bee Ling; Douglas E J; Fiegler H; Carr P; Kalaitzopoulos D; Clegg S; Sandstrom R; Temple I K; Youings S A; Thomas N S; Dennis N R; Jacobs P A; Crolla J A; Carter N P
The complex nature of constitutional de novo apparently balanced translocations in patients presenting with abnormal phenotypes.
Journal of medical genetics 2005;42(1):8-16.
2005: Woodfine Kathryn; Beare David M; Ichimura Koichi; Debernardi Silvana; Mungall Andrew J; Fiegler Heike; Collins V Peter; Carter Nigel P; Dunham Ian
Replication timing of human chromosome 6.
Cell cycle (Georgetown, Tex.) 2005;4(1):172-6.
2005: Lambros Maryou B K; Fiegler Heike; Jones Angela; Gorman Patricia; Roylance Rebecca R; Carter Nigel P; Tomlinson Ian P M
Analysis of ovarian cancer cell lines using array-based comparative genomic hybridization.
The Journal of pathology 2005;205(1):29-40.
2005: Prescott Katrina; Woodfine Kathryn; Stubbs Paula; Super Maurice; Kerr Bronwyn; Palmer Rodger; Carter Nigel P; Scambler Peter
A novel 5q11.2 deletion detected by microarray comparative genomic hybridisation in a child referred as a case of suspected 22q11 deletion syndrome.
Human genetics 2005;116(1-2):83-90.
2005: Jones Angela M; Douglas Eleanor J; Halford Sarah Er; Fiegler Heike; Gorman Patricia A; Roylance Rebecca R; Carter Nigel P; Tomlinson Ian P M
Array-CGH analysis of microsatellite-stable, near-diploid bowel cancers and comparison with other types of colorectal carcinoma.
Oncogene 2005;24(1):118-29.
2005: De Preter Katleen; Vandesompele Jo; Menten Björn; Carr Philippa; Fiegler Heike; Edsjö Anders; Carter Nigel P; Yigit Nurten; Waelput Wim; Van Roy Nadine; Bader Scott; Påhlman Sven; Speleman Frank
Positional and functional mapping of a neuroblastoma differentiation gene on chromosome 11.
BMC genomics 2005;6():97.
2005: Woodfine Kathryn; Carter Nigel P; Dunham Ian; Fiegler Heike
Investigating chromosome organization with genomic microarrays.
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 2005;13(3):249-57.
2004: Borck G; Redon R; Sanlaville D; Rio M; Prieur M; Lyonnet S; Vekemans M; Carter N P; Munnich A; Colleaux L; Cormier-Daire V
NIPBL mutations and genetic heterogeneity in Cornelia de Lange syndrome.
Journal of medical genetics 2004;41(12):e128.
2004: Carter Nigel P; Vetrie David
Applications of genomic microarrays to explore human chromosome structure and function.
Human molecular genetics 2004;13 Spec No 2():R297-302.
2004: Gilbert Nick; Boyle Shelagh; Fiegler Heike; Woodfine Kathryn; Carter Nigel P; Bickmore Wendy A
Chromatin architecture of the human genome: gene-rich domains are enriched in open chromatin fibers.
Cell 2004;118(5):555-66.
2004: Borck G; Rio M; Sanlaville D; Redon R; Molinari F; Bacq D; Raoul O; Cormier-Daire V; Lyonnet S; Amiel J; Le Merrer M; de Blois M-C; Prieur M; Vekemans M; Carter N P; Munnich A; Colleaux L
Genome-wide screening using automated fluorescent genotyping to detect cryptic cytogenetic abnormalities in children with idiopathic syndromic mental retardation.
Clinical genetics 2004;66(2):122-7.
2004: Douglas Eleanor J; Fiegler Heike; Rowan Andrew; Halford Sarah; Bicknell David C; Bodmer Walter; Tomlinson Ian P M; Carter Nigel P
Array comparative genomic hybridization analysis of colorectal cancer cell lines and primary carcinomas.
Cancer research 2004;64(14):4817-25.
2004: Rodríguez-Perales Sandra; Meléndez Bárbara; Gribble Susan M; Valle Laura; Carter Nigel P; Santamaría Iñigo; Conde Lucia; Urioste Miguel; Benítez Javier; Cigudosa Juan C
Cloning of a new familial t(3;8) translocation associated with conventional renal cell carcinoma reveals a 5 kb microdeletion and no gene involved in the rearrangement.
Human molecular genetics 2004;13(9):983-90.
2004: Shaw-Smith C; Redon R; Rickman L; Rio M; Willatt L; Fiegler H; Firth H; Sanlaville D; Winter R; Colleaux L; Bobrow M; Carter N P
Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features.
Journal of medical genetics 2004;41(4):241-8.
2004: Rost I; Fiegler H; Fauth C; Carr P; Bettecken T; Kraus J; Meyer C; Enders A; Wirtz A; Meitinger T; Carter N P; Speicher M R
Tetrasomy 21pter-->q21.2 in a male infant without typical Down's syndrome dysmorphic features but moderate mental retardation.
Journal of medical genetics 2004;41(3):e26.
2004: Hurst Carolyn D; Fiegler Heike; Carr Philippa; Williams Sarah; Carter Nigel P; Knowles Margaret A
High-resolution analysis of genomic copy number alterations in bladder cancer by microarray-based comparative genomic hybridization.
Oncogene 2004;23(12):2250-63.
2004: Woodfine Kathryn; Fiegler Heike; Beare David M; Collins John E; McCann Owen T; Young Bryan D; Debernardi Silvana; Mott Richard; Dunham Ian; Carter Nigel P
Replication timing of the human genome.
Human molecular genetics 2004;13(2):191-202.
2004: Fiegler Heike; Carter Nigel P
Genomic array technology.
Methods in cell biology 2004;75():769-85.
2004: Gribble Susan; Ng Bee L; Prigmore Elena; Burford Deborah C; Carter Nigel P
Chromosome paints from single copies of chromosomes.
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 2004;12(2):143-51.
2004: Gribble S M; Fiegler H; Burford D C; Prigmore E; Yang F; Carr P; Ng B L; Sun T; Kamberov E S; Makarov V L; Langmore J P; Carter N P
Applications of combined DNA microarray and chromosome sorting technologies.
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 2004;12(1):35-43.
2003: d'Adda di Fagagna Fabrizio; Reaper Philip M; Clay-Farrace Lorena; Fiegler Heike; Carr Philippa; Von Zglinicki Thomas; Saretzki Gabriele; Carter Nigel P; Jackson Stephen P
A DNA damage checkpoint response in telomere-initiated senescence.
Nature 2003;426(6963):194-8.
2003: Fiegler H; Gribble S M; Burford D C; Carr P; Prigmore E; Porter K M; Clegg S; Crolla J A; Dennis N R; Jacobs P; Carter N P
Array painting: a method for the rapid analysis of aberrant chromosomes using DNA microarrays.
Journal of medical genetics 2003;40(9):664-70.
2003: Fiegler Heike; Carr Philippa; Douglas Eleanor J; Burford Deborah C; Hunt Sarah; Scott Carol E; Smith James; Vetrie David; Gorman Patricia; Tomlinson Ian P M; Carter Nigel P
DNA microarrays for comparative genomic hybridization based on DOP-PCR amplification of BAC and PAC clones.
Genes, chromosomes & cancer 2003;36(4):361-74.
2003: Spriggs Helen F; Holmes Nigel G; Breen Matthew G; Deloukas Panos G; Langford Cordelia F; Ross Mark T; Carter Nigel P; Davis Maria E; Knights Catherine E; Smith Angela E; Farr Christine J; McCarthy Linda C; Binns Matthew M
Construction and integration of radiation-hybrid and cytogenetic maps of dog Chromosome X.
Mammalian genome : official journal of the International Mammalian Genome Society 2003;14(3):214-21.
2002: McMullan Tristan W; Crolla John A; Gregory Simon G; Carter Nigel P; Cooper Rachel A; Howell Gareth R; Robinson David O
A candidate gene for congenital bilateral isolated ptosis identified by molecular analysis of a de novo balanced translocation.
Human genetics 2002;110(3):244-50.
2000: Cross S H; Clark V H; Simmen M W; Bickmore W A; Maroon H; Langford C F; Carter N P; Bird A P
CpG island libraries from human chromosomes 18 and 22: landmarks for novel genes.
Mammalian genome : official journal of the International Mammalian Genome Society 2000;11(5):373-83.
1999: Breen M; Thomas R; Binns M M; Carter N P; Langford C F
Reciprocal chromosome painting reveals detailed regions of conserved synteny between the karyotypes of the domestic dog (Canis familiaris) and human.
Genomics 1999;61(2):145-55.
1999: Heppell-Parton A C; Nacheva E; Carter N P; Bergh J; Ogilvie D; Rabbitts P H
Elucidation of the mechanism of homozygous deletion of 3p12-13 in the U2020 cell line reveals the unexpected involvement of other chromosomes.
Cancer genetics and cytogenetics 1999;111(2):105-10.
1999: Dickens H F; Holmes N G; Ryder E; Breen M; Thomas R; Suter N; Sampson J; Langford C F; Ross M; Carter N P; Binns M M
Use of cosmid-derived and chromosome-specific canine microsatellites.
The Journal of heredity 1999;90(1):52-4.
1999: Breen M; Langford C F; Carter N P; Holmes N G; Dickens H F; Thomas R; Suter N; Ryder E J; Pope M; Binns M M
FISH mapping and identification of canine chromosomes.
The Journal of heredity 1999;90(1):27-30.
1999: Heppell-Parton A C; Nacheva E; Carter N P; Rabbitts P H
A combined approach of conventional and molecular cytogenetics for detailed karyotypic analysis of the small cell lung carcinoma cell line U2020.
Cancer genetics and cytogenetics 1999;108(2):110-9.
1999: Leversha M A; Dunham I; Carter N P
A molecular cytogenetic clone resource for chromosome 22.
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 1999;7(7):571-3.
1997: Breen M; Langford C F; Carter N P; Fischer P E; Marti E; Gerstenberg C; Allen W R; Lear T L; Binns M M
Detection of equine X chromosome abnormalities in equids using a horse X whole chromosome paint probe (WCPP).
Veterinary journal (London, England : 1997) 1997;153(3):235-8.
1996: Langford C F; Fischer P E; Binns M M; Holmes N G; Carter N P
Chromosome-specific paints from a high-resolution flow karyotype of the dog.
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 1996;4(2):115-23.
1996: Mungall A J; Edwards C A; Ranby S A; Humphray S J; Heathcott R W; Clee C M; East C L; Holloway E; Butler A P; Langford C F; Gwilliam R; Rice K M; Maslen G L; Carter N P; Ross M T; Deloukas P; Bentley D R; Dunham I
Physical mapping of chromosome 6: a strategy for the rapid generation of sequence-ready contigs.
DNA sequence : the journal of DNA sequencing and mapping 1996;7(1):47-9.
1995: Schinzel A; Lorda-Sanchez I; Binkert F; Carter N P; Bebb C E; Ferguson-Smith M A; Eiholzer U; Zachmann M; Robinson W P
Kallmann syndrome in a boy with a t(1;10) translocation detected by reverse chromosome painting.
Journal of medical genetics 1995;32(12):957-61.
1995: Blennow E; Nielsen K B; Telenius H; Carter N P; Kristoffersson U; Holmberg E; Gillberg C; Nordenskjöld M
Fifty probands with extra structurally abnormal chromosomes characterized by fluorescence in situ hybridization.
American journal of medical genetics 1995;55(1):85-94.
1994: Divane A; Carter N P; Spathas D H; Ferguson-Smith M A
Rapid prenatal diagnosis of aneuploidy from uncultured amniotic fluid cells using five-colour fluorescence in situ hybridization.
Prenatal diagnosis 1994;14(11):1061-9.
1994: Ferguson-Smith M A; Zheng Y L; Carter N P
Simultaneous immunophenotyping and FISH on fetal cells from maternal blood.
Annals of the New York Academy of Sciences 1994;731():73-9.
1994: Richards A J; al-Imara L; Carter N P; Lloyd J C; Leversha M A; Pope F M
Localization of the gene (LAMA4) to chromosome 6q21 and isolation of a partial cDNA encoding a variant laminin A chain.
Genomics 1994;22(1):237-9.
1994: Blennow E; Telenius H; de Vos D; Larsson C; Henriksson P; Johansson O; Carter N P; Nordenskjöld M
Tetrasomy 15q: two marker chromosomes with no detectable alpha-satellite DNA.
American journal of human genetics 1994;54(5):877-83.
1994: Hunt J V; Bottoms M A; Skamarauskas J; Carter N P; Mitchinson M J
Measurement of ceroid accumulation in macrophages by flow cytometry.
Cytometry 1994;15(4):377-82.
1994: Carter N P
Cytogenetic analysis by chromosome painting.
Cytometry 1994;18(1):2-10.
1994: Carter N P
Bivariate chromosome analysis using a commercial flow cytometer.
Methods in molecular biology (Clifton, N.J.) 1994;29():187-204.
1993: Zheng Y L; Carter N P; Price C M; Colman S M; Milton P J; Hackett G A; Greaves M F; Ferguson-Smith M A
Prenatal diagnosis from maternal blood: simultaneous immunophenotyping and FISH of fetal nucleated erythrocytes isolated by negative magnetic cell sorting.
Journal of medical genetics 1993;30(12):1051-6.
1993: Bailey D M; Carter N P; de Vos D; Leversha M A; Perryman M T; Ferguson-Smith M A
Coincidence painting: a rapid method for cloning region specific DNA sequences.
Nucleic acids research 1993;21(22):5117-23.
1993: Furlong R A; Goudie D R; Carter N P; Lyall J E; Affara N A; Ferguson-Smith M A
Analysis of four microsatellite markers on the long arm of chromosome 9 by meiotic recombination in flow-sorted single sperm.
American journal of human genetics 1993;52(6):1191-9.
1993: Goudie D R; Yuille M A; Leversha M A; Furlong R A; Carter N P; Lush M J; Affara N A; Ferguson-Smith M A
Multiple self-healing squamous epitheliomata (ESS1) mapped to chromosome 9q22-q31 in families with common ancestry.
Nature genetics 1993;3(2):165-9.
1993: Harris R M; Carter N P; Griffiths B; Goudie D; Hampson R M; Yates J R; Affara N A; Ferguson-Smith M A
Physical mapping within the tuberous sclerosis linkage group in region 9q32-q34.
Genomics 1993;15(2):265-74.
1993: Hunt J V; Carpenter K L; Bottoms M A; Carter N P; Marchant C E; Mitchinson M J
Flow cytometric measurement of ceroid accumulation in macrophages.
Atherosclerosis 1993;98(2):229-39.
1993: Telenius H; de Vos D; Blennow E; Willat L R; Ponder B A; Carter N P
Chromatid contamination can impair the purity of flow-sorted metaphase chromosomes.
Cytometry 1993;14(1):97-101.
1992: Zheng Y L; Ferguson-Smith M A; Warner J P; Ferguson-Smith M E; Sargent C A; Carter N P
Analysis of chromosome 21 copy number in uncultured amniocytes by fluorescence in situ hybridization using a cosmid contig.
Prenatal diagnosis 1992;12(11):931-43.
1992: Telenius H; Carter N P; Bebb C E; Nordenskjöld M; Ponder B A; Tunnacliffe A
Degenerate oligonucleotide-primed PCR: general amplification of target DNA by a single degenerate primer.
Genomics 1992;13(3):718-25.
1992: Carter N P; Ferguson-Smith M A; Perryman M T; Telenius H; Pelmear A H; Leversha M A; Glancy M T; Wood S L; Cook K; Dyson H M
Reverse chromosome painting: a method for the rapid analysis of aberrant chromosomes in clinical cytogenetics.
Journal of medical genetics 1992;29(5):299-307.
1992: King A; Wheeler R; Carter N P; Francis D P; Loke Y W
The response of human decidual leukocytes to IL-2.
Cellular immunology 1992;141(2):409-21.
1992: Telenius H; Pelmear A H; Tunnacliffe A; Carter N P; Behmel A; Ferguson-Smith M A; Nordenskjöld M; Pfragner R; Ponder B A
Cytogenetic analysis by chromosome painting using DOP-PCR amplified flow-sorted chromosomes.
Genes, chromosomes & cancer 1992;4(3):257-63.
1992: Dixon S C; Miller N G; Carter N P; Tucker E M
Bivariate flow cytometry of farm animal chromosomes: a potential tool for gene mapping.
Animal genetics 1992;23(3):203-10.
1992: Langford C F; Telenius H; Carter N P; Miller N G; Tucker E M
Chromosome painting using chromosome-specific probes from flow-sorted pig chromosomes.
Cytogenetics and cell genetics 1992;61(3):221-3.
1991: Whitcombe D M; Carter N P; Albertson D G; Smith S J; Rhodes D A; Cox T M
Assignment of the human ferrochelatase gene (FECH) and a locus for protoporphyria to chromosome 18q22.
Genomics 1991;11(4):1152-4.
1991: King A; Balendran N; Wooding P; Carter N P; Loke Y W
CD3- leukocytes present in the human uterus during early placentation: phenotypic and morphologic characterization of the CD56++ population.
Developmental immunology 1991;1(3):169-90.
1990: Carter N P; Ferguson-Smith M E; Affara N A; Briggs H; Ferguson-Smith M A
Study of X chromosome abnormality in XX males using bivariate flow karyotype analysis and flow sorted dot blots.
Cytometry 1990;11(1):202-7.
1989: Carpenter K L; Ball R Y; Carter N P; Woods S E; Hartley S L; Davies S; Enright J H; Mitchinson M J
Modulation of ceroid accumulation in macrophages in vitro.
Advances in experimental medicine and biology 1989;266():333-43.

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