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Nigel Carter

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Qiuju Wang; Yali Xue; Fengtang Yang; Huanming Yang; Weiyan Yang; Yujun Zhang; Yali Zhao; John Burton; Nigel P Carter; Yuan Chen; Ciara Fahey; Tomas Fitzgerald; Dongyi Han; Matthew E Hurles; Qingjie Liu; Quan Long; Bee Ling Ng; Zemin Ning; Michael A Quail; Harold Swerdlow; Daniel J Turner; Chris Tyler-Smith
Genetic basis of Y-linked hearing impairment.
Susan M Gribble; Heidi Hauser; Elizabeth Langley; Sean Maguire; Bee Ling Ng; Elena Prigmore; Michael A Quail; Diana Rajan; Kai Rothkamm; Carol Scott; Olivia Sheppard; Lucy A Stebbings; Philip J Stephens; Victor L J Tybulewicz; Frances K Wiseman; Fengtang Yang; Stephen Clayton; Elizabeth M C Fisher; Tomas Fitzgerald; Beiyuan Fu; Ruby Banerjee; Nigel P Carter
Massively parallel sequencing reveals the complex structure of an irradiated human chromosome on a mouse background in the Tc1 model of Down syndrome.
Érika L Freitas; Marly A S Balarin; Nigel P Carter; Susan M Gribble; Ana Cristina Krepischi-Santos; Elena Prigmore; Carla Rosenberg; Roseane L Silva-Grecco; Milena Simioni; Karoly Szuhai; Arie van Haeringen; Társis P Vieira; Vera Lúcia Gil da Silva Lopes
Maternally inherited partial monosomy 9p (pter → p24.1) and partial trisomy 20p (pter → p12.1) characterized by microarray comparative genomic hybridization.

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All Publications

2013: Qiuju Wang; Yali Xue; Fengtang Yang; Huanming Yang; Weiyan Yang; Yujun Zhang; Yali Zhao; John Burton; Nigel P Carter; Yuan Chen; Ciara Fahey; Tomas Fitzgerald; Dongyi Han; Matthew E Hurles; Qingjie Liu; Quan Long; Bee Ling Ng; Zemin Ning; Michael A Quail; Harold Swerdlow; Daniel J Turner; Chris Tyler-Smith
Genetic basis of Y-linked hearing impairment.
American journal of human genetics 2013;92(2):301-6.
2013: Susan M Gribble; Heidi Hauser; Elizabeth Langley; Sean Maguire; Bee Ling Ng; Elena Prigmore; Michael A Quail; Diana Rajan; Kai Rothkamm; Carol Scott; Olivia Sheppard; Lucy A Stebbings; Philip J Stephens; Victor L J Tybulewicz; Frances K Wiseman; Fengtang Yang; Stephen Clayton; Elizabeth M C Fisher; Tomas Fitzgerald; Beiyuan Fu; Ruby Banerjee; Nigel P Carter
Massively parallel sequencing reveals the complex structure of an irradiated human chromosome on a mouse background in the Tc1 model of Down syndrome.
PloS one 2013;8(4):e60482.
2011: Érika L Freitas; Marly A S Balarin; Nigel P Carter; Susan M Gribble; Ana Cristina Krepischi-Santos; Elena Prigmore; Carla Rosenberg; Roseane L Silva-Grecco; Milena Simioni; Karoly Szuhai; Arie van Haeringen; Társis P Vieira; Vera Lúcia Gil da Silva Lopes
Maternally inherited partial monosomy 9p (pter → p24.1) and partial trisomy 20p (pter → p12.1) characterized by microarray comparative genomic hybridization.
American journal of medical genetics. Part A 2011;155A(11):2754-61.
2011: Dalila Pinto; Aparna Prasad; Elena Prigmore; Diana Rajan; Diane Rigler; Stephen W Scherer; Xinghua Shi; Richard S Smith; Bhooma Thiruvahindrapuram; Tom Fitzgerald; Susan Gribble; Matthew E Hurles; Charles Lee; Anath C Lionel; Jeffrey R MacDonald; Ryan Mills; Kristin Noonan; Ji Hyeon Park; Nigel P Carter; Katayoon Darvishi; Patricia K Donahoe; Lars Feuk
Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants.
Nature biotechnology 2011;29(6):512-20.
2011: Serena Nik-Zainal; Reiner Strick; Mekayla Storer; Ni Huang; Roland Rad; Lionel Willatt; Tomas Fitzgerald; Vicki Martin; Richard Sandford; Nigel P Carter; Andreas R Janecke; Stefan P Renner; Patricia G Oppelt; Peter Oppelt; Christine Schulze; Sara Brucker; Matthew Hurles; Matthias W Beckmann; Pamela L Strissel; Charles Shaw-Smith
High incidence of recurrent copy number variants in patients with isolated and syndromic Müllerian aplasia.
Journal of medical genetics 2011;48(3):197-204.
2010: Bee Ling Ng; Nigel P Carter
Laser excitation power and the flow cytometric resolution of complex karyotypes.
Cytometry. Part A : the journal of the International Society for Analytical Cytology 2010;77(6):585-8.
2010: Hansoo Park; Jong-Il Kim; Young Seok Ju; Omer Gokcumen; Ryan Mills; Sheehyun Kim; Seungbok Lee; Dongwhan Suh; Dongwan Hong; Hyunseok Peter Kang; Yun Joo Yoo; Jong-Yeon Shin; Hyun-Jin Kim; Maryam Yavartanoo; Young Wha Chang; Jung-Sook Ha; Wilson Chong; Ga-Ram Hwang; Katayoon Darvishi; Hyungtae Kim; Song Ju Yang; Kap-Seok Yang; Hyungtae Kim; Matthew E Hurles; Stephen W Scherer; Nigel P Carter; Chris Tyler-Smith; Charles Lee; Jeong-Sun Seo
Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing.
Nature genetics 2010;42(5):400-5.
2010: Gloria W C Tam; Louie van de Lagemaat; Richard Redon; Karen E Strathdee; Mike D R Croning; Mary P Malloy; Walter J Muir; Ben S Pickard; Ian J Deary; Douglas H R Blackwood; Nigel P Carter; Seth G N Grant
Confirmed rare copy number variants implicate novel genes in schizophrenia.
Biochemical Society transactions 2010;38(2):445-51.
2010: Donald F Conrad; Dalila Pinto; Richard Redon; Lars Feuk; Omer Gokcumen; Yujun Zhang; Jan Aerts; T Daniel Andrews; Chris Barnes; Peter Campbell; Tomas Fitzgerald; Min Hu; Chun Hwa Ihm; Kati Kristiansson; Daniel G Macarthur; Jeffrey R MacDonald; Ifejinelo Onyiah; Andy Wing Chun Pang; Sam Robson; Kathy Stirrups; Armand Valsesia; Klaudia Walter; John Wei; Chris Tyler-Smith; Nigel P Carter; Charles Lee; Stephen W Scherer; Matthew E Hurles
Origins and functional impact of copy number variation in the human genome.
Nature 2010;464(7289):704-12.
2009: Gloria W C Tam; Richard Redon; Nigel P Carter; Seth G N Grant
The role of DNA copy number variation in schizophrenia.
Biological psychiatry 2009;66(11):1005-12.
2009: Harinder K Gill; Sian R Parsons; Cosma Spalluto; Angela F Davies; Victoria J Knorz; Clare E G Burlinson; Bee Ling Ng; Nigel P Carter; Caroline Mackie Ogilvie; David I Wilson; Roland Roberts
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: Yali Xue; Qiuju Wang; Quan Long; Bee Ling Ng; Harold Swerdlow; John Burton; Carl Skuce; Ruth Taylor; Zahra Abdellah; Yali Zhao; Daniel G MacArthur; Michael A Quail; Nigel P Carter; Huanming Yang; Chris Tyler-Smith
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: Helen V Firth; Shola M Richards; Anna Bevan; Stephen Clayton; Manuel Corpas; Diana Rajan; Steven Van Vooren; Yves Moreau; Roger M Pettett; Nigel P Carter
DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources.
American journal of human genetics 2009;84(4):524-33.
2009: Susan M Gribble; Bee Ling Ng; Elena Prigmore; Tomas Fitzgerald; Nigel P Carter
Array painting: a protocol for the rapid analysis of aberrant chromosomes using DNA microarrays.
Nature protocols 2009;4(12):1722-36.
2009: Richard Redon; Diane Rigler; Nigel P Carter
Comparative genomic hybridization: DNA preparation for microarray fabrication.
Methods in molecular biology (Clifton, N.J.) 2009;529():259-66.
2009: Richard Redon; Tomas Fitzgerald; Nigel P Carter
Comparative genomic hybridization: DNA labeling, hybridization and detection.
Methods in molecular biology (Clifton, N.J.) 2009;529():267-78.
2009: Richard Redon; Nigel P Carter
Comparative genomic hybridization: microarray design and data interpretation.
Methods in molecular biology (Clifton, N.J.) 2009;529():37-49.
2008: Mai M Abd El-Aziz; Isabel Barragan; Ciara A O'Driscoll; Leo Goodstadt; Elena Prigmore; Salud Borrego; Marcela Mena; Juan I Pieras; Mohamed F El-Ashry; Leen Abu Safieh; Amna Shah; Michael Cheetham; Nigel P Carter; Christina F Chakarova; Chris P Ponting; Shomi S Bhattacharya; Guillermo Antinolo
EYS, encoding an ortholog of Drosophila spacemaker, is mutated in autosomal recessive retinitis pigmentosa.
Nature genetics 2008;40(11):1285-7.
2008: George H Perry; Fengtang Yang; Tomas Marques-Bonet; Carly Murphy; Tomas Fitzgerald; Arthur S Lee; Courtney Hyland; Anne C Stone; Matthew E Hurles; Chris Tyler-Smith; Evan E Eichler; Nigel P Carter; Charles Lee; Richard Redon
Copy number variation and evolution in humans and chimpanzees.
Genome research 2008;18(11):1698-710.
2008: Yali Xue; Donglin Sun; Allan Daly; Fengtang Yang; Xue Zhou; Mengyao Zhao; Ni Huang; Tatiana Zerjal; Charles Lee; Nigel P Carter; Matthew E Hurles; Chris Tyler-Smith
Adaptive evolution of UGT2B17 copy-number variation.
American journal of human genetics 2008;83(3):337-46.
2008: Vardhman K Rakyan; Thomas A Down; Natalie P Thorne; Paul Flicek; Eugene Kulesha; Stefan Gräf; Eleni M Tomazou; Liselotte Bäckdahl; Nathan Johnson; Marlis Herberth; Kevin L Howe; David K Jackson; Marcos M Miretti; Heike Fiegler; John C Marioni; Ewan Birney; Tim Hubbard; Nigel P Carter; Simon Tavaré; Stephan Beck
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: Julia Baptista; Catherine Mercer; Elena Prigmore; Susan M Gribble; Nigel P Carter; Vivienne Maloney; N Simon Thomas; Patricia A Jacobs; John A Crolla
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: Irina Balikova; Kevin Martens; Cindy Melotte; Mustapha Amyere; Steven Van Vooren; Yves Moreau; David Vetrie; Heike Fiegler; Nigel P Carter; Thomas Liehr; Miikka Vikkula; Gert Matthijs; Jean-Pierre Fryns; Ingele Casteels; koenraad devriendt; Joris R Vermeesch
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: Daniel J Turner; Marcos M Miretti; Diana Rajan; Heike Fiegler; Nigel P Carter; Martyn L Blayney; Stephan Beck; Matthew E Hurles
Germline rates of de novo meiotic deletions and duplications causing several genomic disorders.
Nature genetics 2008;40(1):90-5.
2007: Björn Menten; Karen Buysse; Stefan Vermeulen; Valerie Meersschaut; Jo Vandesompele; Bee Ling Ng; Nigel P Carter; Geert R Mortier; Frank Speleman
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: George H Perry; Nathaniel J Dominy; Katrina G Claw; Arthur S Lee; Heike Fiegler; Richard Redon; John Werner; Fernando A Villanea; Joanna L Mountain; Rajeev Misra; Nigel P Carter; Charles Lee; Anne C Stone
Diet and the evolution of human amylase gene copy number variation.
Nature genetics 2007;39(10):1256-60.
2007: Stephen W Scherer; Charles Lee; Ewan Birney; David M Altshuler; Evan E Eichler; Nigel P Carter; Matthew E Hurles; Lars Feuk
Challenges and standards in integrating surveys of structural variation.
Nature genetics 2007;39(7 Suppl):S7-15.
2007: Nigel P Carter
Methods and strategies for analyzing copy number variation using DNA microarrays.
Nature genetics 2007;39(7 Suppl):S16-21.
2007: Christoph M Koch; Robert M Andrews; Paul Flicek; Shane C Dillon; Ulaş Karaöz; Gayle K Clelland; Sarah Wilcox; David M Beare; Joanna C Fowler; Philippe Couttet; Keith D James; Gregory C Lefebvre; Alexander W Bruce; Oliver M Dovey; Peter D Ellis; Pawandeep Dhami; Cordelia F Langford; Zhiping Weng; Ewan Birney; Nigel P Carter; David Vetrie; Carl Bruder
The landscape of histone modifications across 1% of the human genome in five human cell lines.
Genome research 2007;17(6):691-707.
2007: Bee Ling Ng; Fengtang Yang; Nigel P Carter
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: Jeanne Amiel; Marlène Rio; Loïc de Pontual; Richard Redon; valerie malan; Nathalie Boddaert; Perrine Plouin; Nigel P Carter; Stanislas LYONNET; Arnold Munnich; Laurence Colleaux
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: Rebecca E Foster; mahera abdulrahman; Mark Morris; Elena Prigmore; Susan M Gribble; Beeling Ng; Dean Gentle; Steven Ready; Phil M T Weston; Michael S Wiesener; Takeshi Kishida; Masahiro Yao; Val Davison; Jose Luis Barbero; Carol Chu; Nigel P Carter; Farida Latif; Eamonn R Maher
Characterization of a 3;6 translocation associated with renal cell carcinoma.
Genes, chromosomes & cancer 2007;46(4):311-7.
2007: John C Marioni; Natalie P Thorne; Armand Valsesia; Tomas Fitzgerald; Richard Redon; Heike Fiegler; T Daniel Andrews; Barbara E Stranger; Andrew G Lynch; Emmanouil T Dermitzakis; Nigel P Carter; Simon Tavaré; Matthew E Hurles
Breaking the waves: improved detection of copy number variation from microarray-based comparative genomic hybridization.
Genome biology 2007;8(10):R228.
2007: Jennifer L Freeman; Adeola Adeniyi; Ruby Banerjee; Stephanie Dallaire; Sean F Maguire; jianxiang chi; Bee Ling Ng; Cinthya Zepeda; Carol E Scott; Sean Humphray; Jane Rogers; Yi Zhou; Leonard I Zon; Nigel P Carter; Fengtang Yang; Charles Lee
Definition of the zebrafish genome using flow cytometry and cytogenetic mapping.
BMC genomics 2007;8():195.
2007: Heike Fiegler; Richard Redon; Nigel P Carter
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: Heike Fiegler; Jochen B Geigl; Sabine Langer; Diane Rigler; Keith Michael Porter; Kristian Unger; Nigel P Carter; Michael R Speicher
High resolution array-CGH analysis of single cells.
Nucleic acids research 2007;35(3):e15.
2007: Susan M Gribble; Dimitrios Kalaitzopoulos; Deborah C Burford; Elena Prigmore; Rebecca R Selzer; Bee Ling Ng; N S W Matthews; Keith Michael Porter; R Curley; Sarah J Lindsay; J Baptista; Richmond Todd; Nigel P Carter
Ultra-high resolution array painting facilitates breakpoint sequencing.
Journal of medical genetics 2007;44(1):51-8.
2006: Heike Fiegler; Richard Redon; Dan Andrews; Carol Scott; Robert Andrews; Carol Carder; Richard Clark; Oliver M Dovey; Peter Ellis; Lars Feuk; Lisa French; Paul Hunt; Dimitrios Kalaitzopoulos; James R Larkin; Lyndal Montgomery; George H Perry; Bob Plumb; Keith Michael Porter; Rachel E Rigby; Diane Rigler; Armand Valsesia; Cordelia Langford; Sean Humphray; Stephen W Scherer; Charles Lee; Matthew E Hurles; Nigel P Carter
Accurate and reliable high-throughput detection of copy number variation in the human genome.
Genome research 2006;16(12):1566-74.
2006: ML Jacquemont; Damien Sanlaville; Richard Redon; Odile Raoul; Valérie Cormier-Daire; Stanislas LYONNET; Jeanne Amiel; Martine Le Merrer; D Heron; Marie-Christine De Blois; Marguerite Prieur; Michel Vekemans; Nigel P Carter; Arnold Munnich; Laurence Colleaux; Anne Philippe
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: Bee Ling Ng; Nigel P Carter
Factors affecting flow karyotype resolution.
Cytometry. Part A : the journal of the International Society for Analytical Cytology 2006;69(9):1028-36.
2006: Charles Shaw-Smith; Alan Pittman; Lionel Willatt; Howard Martin; Lisa Rickman; Susan M Gribble; Rebecca Curley; Sally Cumming; Carolyn Dunn; Dimitrios Kalaitzopoulos; Keith Michael Porter; Elena Prigmore; Ana Cristina Krepischi-Santos; Monica C Varela; Célia P Koiffmann; Andrew J Lees; Carla Rosenberg; Helen V Firth; Rohan de Silva; Nigel P Carter
Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability.
Nature genetics 2006;38(9):1032-7.
2006: Jennifer L Freeman; George H Perry; Lars Feuk; Richard Redon; Steven A McCarroll; David Altshuler; Hiroyuki Aburatani; Keith W Jones; Chris Tyler-Smith; Matthew E Hurles; Nigel P Carter; Stephen W Scherer; Charles Lee
Copy number variation: new insights in genome diversity.
Genome research 2006;16(8):949-61.
2006: Marjolein Kriek; Karoly Szuhai; Sarina G Kant; Stefan J White; Hans Dauwerse; Heike Fiegler; Nigel P Carter; Jeroen Knijnenburg; Johan T den Dunnen; Hans J Tanke; Martijn H Breuning; Carla Rosenberg
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: Richard Redon; Geneviève Baujat; Damien Sanlaville; Martine Le Merrer; Michel Vekemans; Arnold Munnich; Nigel P Carter; Valérie Cormier-Daire; Laurence Colleaux
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: Michelle Gaasenbeek; Kimberley Howarth; Andrew J Rowan; Patricia A Gorman; Angela Jones; Tracy Chaplin; Ying Liu; David C Bicknell; Eleanor J Davison; Heike Fiegler; Nigel P Carter; Rebecca R Roylance; Ian P M Tomlinson
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: Paul J Mulholland; Heike Fiegler; Chiara Mazzanti; Patricia Gorman; Peter Sasieni; Joanna Adams; Tania A Jones; Jane W Babbage; Radost Vatcheva; Koichi Ichimura; Philip East; Chrysanthos Poullikas; V Peter Collins; Nigel P Carter; Ian P M Tomlinson; Denise Sheer
Genomic profiling identifies discrete deletions associated with translocations in glioblastoma multiforme.
Cell cycle (Georgetown, Tex.) 2006;5(7):783-91.
2006: Lisa Rickman; Heike Fiegler; Charles Shaw-Smith; R Nash; Vincenzo Cirigliano; Gianfranco Voglino; Bee Ling Ng; C Scott; Joanne Whittaker; Matteo Adinolfi; Nigel P Carter; Martin Bobrow
Prenatal detection of unbalanced chromosomal rearrangements by array CGH.
Journal of medical genetics 2006;43(4):353-61.
2006: Christine Fauth; Susan M Gribble; Keith Michael Porter; Montserrat Codina-Pascual; Bee Ling Ng; Jürgen Kraus; Sabine Uhrig; Jürgen Leifheit; Thomas Haaf; Heike Fiegler; Nigel P Carter; Michael R Speicher
Micro-array analyses decipher exceptional complex familial chromosomal rearrangement.
Human genetics 2006;119(1-2):145-53.
2006: Koichi Ichimura; Andrew Mungall; Heike Fiegler; Danita M Pearson; Carl Bruder; Nigel P Carter; V Peter Collins
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: Carla Rosenberg; Jeroen Knijnenburg; Egbert Bakker; Angela M Vianna-Morgante; Willem C R Sloos; P A Otto; Marjolein Kriek; K B M Hansson; Ana Cristina Krepischi-Santos; Heike Fiegler; Nigel P Carter; Emilia K Bijlsma; Arie van Haeringen; Karoly Szuhai; Hans J Tanke
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: Karen J Woodward; Maria Cundall; Karen Sperle; Erik A Sistermans; Mark Ross; Gareth Howell; Susan M Gribble; Deborah C Burford; Nigel P Carter; Donald L Hobson; James Y Garbern; John Kamholz; Hong-Qiang Heng; ME Hodes; Sue Malcolm; Grace M Hobson
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: Eleanor J Davison; Patrick Tarpey; Heike Fiegler; Ian P M Tomlinson; Nigel P Carter
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: Julia Baptista; Elena Prigmore; Susan M Gribble; Patricia A Jacobs; Nigel P Carter; John A Crolla
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: Michael R Speicher; Nigel P Carter
The new cytogenetics: blurring the boundaries with molecular biology.
Nature reviews. Genetics 2005;6(10):782-92.
2005: Lisa Rickman; Heike Fiegler; Nigel P Carter; Martin Bobrow
Prenatal diagnosis by array-CGH.
European journal of medical genetics 2005;48(3):232-40.
2005: Richard Redon; Marlène Rio; Simon G Gregory; R A Cooper; Heike Fiegler; Damien Sanlaville; R Banerjee; C Scott; Philippa Carr; Cordelia Langford; Valérie Cormier-Daire; Arnold Munnich; Nigel P Carter; Laurence Colleaux
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: Angela M Jones; Eleanor J Douglas; Stephanie Halford; Heike Fiegler; Patricia A Gorman; Rebecca R Roylance; Nigel P Carter; Ian P M Tomlinson
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: Katleen De Preter; Jo Vandesompele; Björn Menten; Philippa Carr; Heike Fiegler; Anders Edsjö; Nigel P Carter; Nurten Yigit; Wim Waelput; Nadine Van Roy; Scott Bader; Sven Påhlman; Frank Speleman
Positional and functional mapping of a neuroblastoma differentiation gene on chromosome 11.
BMC genomics 2005;6():97.
2005: Kathryn Woodfine; Nigel P Carter; Carl Bruder; Heike Fiegler
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.
2005: Susan M Gribble; Elena Prigmore; Deborah C Burford; Keith Michael Porter; Bee Ling Ng; Eleanor J Douglas; Heike Fiegler; Philippa Carr; Dimitrios Kalaitzopoulos; SM Clegg; R Sandstrom; I K Temple; Sheila Youings; N Simon Thomas; Nicholas R Dennis; Patricia A Jacobs; John A Crolla; Nigel P Carter
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: Kathryn Woodfine; David M Beare; Koichi Ichimura; Silvana Debernardi; Andrew Mungall; Heike Fiegler; V Peter Collins; Nigel P Carter; Carl Bruder
Replication timing of human chromosome 6.
Cell cycle (Georgetown, Tex.) 2005;4(1):172-6.
2005: Maryou B K Lambros; Heike Fiegler; Angela Jones; Patricia Gorman; Rebecca R Roylance; Nigel P Carter; Ian P M Tomlinson
Analysis of ovarian cancer cell lines using array-based comparative genomic hybridization.
The Journal of pathology 2005;205(1):29-40.
2005: Katrina Prescott; Kathryn Woodfine; Paula Stubbs; Maurice Super; Bronwyn Kerr; Rodger Palmer; Nigel P Carter; Peter J Scambler
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.
2004: Guntram Borck; Richard Redon; Damien Sanlaville; Marlène Rio; Marguerite Prieur; Stanislas LYONNET; Michel Vekemans; Nigel P Carter; Arnold Munnich; Laurence Colleaux; Valérie Cormier-Daire
NIPBL mutations and genetic heterogeneity in Cornelia de Lange syndrome.
Journal of medical genetics 2004;41(12):e128.
2004: Nigel P Carter; David Vetrie
Applications of genomic microarrays to explore human chromosome structure and function.
Human molecular genetics 2004;13 Spec No 2():R297-302.
2004: Nick Gilbert; Shelagh Boyle; Heike Fiegler; Kathryn Woodfine; Nigel P Carter; Wendy A Bickmore
Chromatin architecture of the human genome: gene-rich domains are enriched in open chromatin fibers.
Cell 2004;118(5):555-66.
2004: Guntram Borck; Marlène Rio; Damien Sanlaville; Richard Redon; Florence Molinari; Delphine Bacq; Odile Raoul; Valérie Cormier-Daire; Stanislas LYONNET; Jeanne Amiel; Martine Le Merrer; Marie-Christine De Blois; Marguerite Prieur; Michel Vekemans; Nigel P Carter; Arnold Munnich; Laurence Colleaux
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: Eleanor J Douglas; Heike Fiegler; Andrew Rowan; Stephanie Halford; David C Bicknell; Walter Bodmer; Ian P M Tomlinson; Nigel P Carter
Array comparative genomic hybridization analysis of colorectal cancer cell lines and primary carcinomas.
Cancer research 2004;64(14):4817-25.
2004: Sandra Rodríguez-Perales; Bárbara Meléndez; Susan M Gribble; Laura Valle; Nigel P Carter; Iñigo Santamaría; Lucia Conde; Miguel Urioste; Javier Benítez; Juan C Cigudosa
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: Charles Shaw-Smith; Richard Redon; Lisa Rickman; Marlène Rio; Lionel Willatt; Heike Fiegler; Helen V Firth; Damien Sanlaville; R Winter; Laurence Colleaux; Martin Bobrow; Nigel P Carter
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: Carolyn D Hurst; Heike Fiegler; Philippa Carr; Sarah Williams; Nigel P Carter; Margaret A Knowles
High-resolution analysis of genomic copy number alterations in bladder cancer by microarray-based comparative genomic hybridization.
Oncogene 2004;23(12):2250-63.
2004: Imma Rost; Heike Fiegler; Christine Fauth; Philippa Carr; T Bettecken; Jürgen Kraus; C Meyer; A Enders; A Wirtz; Thomas Meitinger; Nigel P Carter; Michael R Speicher
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: Kathryn Woodfine; Heike Fiegler; David M Beare; John E Collins; Owen T McCann; Bryan D Young; Silvana Debernardi; Richard Mott; Carl Bruder; Nigel P Carter
Replication timing of the human genome.
Human molecular genetics 2004;13(2):191-202.
2004: Heike Fiegler; Nigel P Carter
Genomic array technology.
Methods in cell biology 2004;75():769-85.
2004: Susan M Gribble; Bee Ling Ng; Elena Prigmore; Deborah C Burford; Nigel P Carter
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: Susan M Gribble; Heike Fiegler; Deborah C Burford; Elena Prigmore; Fengtang Yang; Philippa Carr; Bee Ling Ng; T Sun; E S Kamberov; VL Makarov; JP Langmore; Nigel P Carter
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: Fabrizio d'Adda di Fagagna; Philip M Reaper; Lorena Clay-Farrace; Heike Fiegler; Philippa Carr; Thomas von Zglinicki; Gabriele Saretzki; Nigel P Carter; Stephen P Jackson
A DNA damage checkpoint response in telomere-initiated senescence.
Nature 2003;426(6963):194-8.
2003: Heike Fiegler; Susan M Gribble; Deborah C Burford; Philippa Carr; Elena Prigmore; Keith Michael Porter; SM Clegg; John A Crolla; Nicholas R Dennis; P Jacobs; Nigel P Carter
Array painting: a method for the rapid analysis of aberrant chromosomes using DNA microarrays.
Journal of medical genetics 2003;40(9):664-70.
2003: Heike Fiegler; Philippa Carr; Eleanor J Douglas; Deborah C Burford; Sarah Hunt; Carol E Scott; James Smith; David Vetrie; Patricia Gorman; Ian P M Tomlinson; Nigel P Carter
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: Helen F Spriggs; Nigel G Holmes; Matthew G Breen; Panos G Deloukas; Cordelia F Langford; Mark T Ross; Nigel P Carter; Maria E Davis; Catherine E Knights; Angela E Smith; Christine J Farr; Linda C McCarthy; Matthew M Binns
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: Tristan W McMullan; John A Crolla; Simon G Gregory; Nigel P Carter; Rachel A Cooper; Gareth R Howell; David O Robinson
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: Sally H Cross; VH Clark; Martin W Simmen; Wendy A Bickmore; H Maroon; Cordelia F Langford; Nigel P Carter; Adrian P Bird
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: Matthew Breen; R Thomas; Matthew M Binns; Nigel P Carter; Cordelia F Langford
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: AC Heppell-Parton; Elisabeth P Nacheva; Nigel P Carter; J Bergh; D Ogilvie; Pamela Rabbitts
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: AC Heppell-Parton; Elisabeth P Nacheva; Nigel P Carter; Pamela Rabbitts
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: MA Leversha; Carl Bruder; Nigel P Carter
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.
1999: HF Dickens; Nigel G Holmes; EJ Ryder; Matthew Breen; R Thomas; N Suter; J Sampson; Cordelia F Langford; M Ross; Nigel P Carter; Matthew M Binns
Use of cosmid-derived and chromosome-specific canine microsatellites.
The Journal of heredity 1999;90(1):52-4.
1999: Matthew Breen; Cordelia F Langford; Nigel P Carter; Nigel G Holmes; HF Dickens; R Thomas; N Suter; EJ Ryder; M Pope; Matthew M Binns
FISH mapping and identification of canine chromosomes.
The Journal of heredity 1999;90(1):27-30.
1997: Matthew Breen; Cordelia F Langford; Nigel P Carter; P E Fischer; Eliane Marti; C Gerstenberg; WR Allen; Teri L Lear; Matthew M Binns
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: Cordelia F Langford; P E Fischer; Matthew M Binns; Nigel G Holmes; Nigel P Carter
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: Andrew Mungall; C A Edwards; S A Ranby; Sean Humphray; R W Heathcott; C M Clee; C L East; E Holloway; A P Butler; C F Langford; Rhian Gwilliam; K M Rice; G L Maslen; Nigel P Carter; Mark T Ross; Panos Deloukas; David R Bentley; Carl Bruder
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: Albert Schinzel; I Lorda-Sanchez; Franz Binkert; Nigel P Carter; C E Bebb; M A Ferguson-Smith; Urs Eiholzer; M Zachmann; Wendy P Robinson
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: Elisabeth Blennow; K B Nielsen; H Telenius; Nigel P Carter; U Kristoffersson; E Holmberg; C Gillberg; Magnus Nordenskjöld
Fifty probands with extra structurally abnormal chromosomes characterized by fluorescence in situ hybridization.
American journal of medical genetics 1995;55(1):85-94.
1994: A Divane; Nigel P Carter; D H Spathas; Malcolm A Ferguson-Smith
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: Malcolm A Ferguson-Smith; Y L Zheng; Nigel P Carter
Simultaneous immunophenotyping and FISH on fetal cells from maternal blood.
Annals of the New York Academy of Sciences 1994;731():73-9.
1994: Allan J Richards; L al-Imara; Nigel P Carter; J C Lloyd; MA Leversha; F Michael Pope
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: Elisabeth Blennow; H Telenius; D de Vos; Catharina Larsson; P Henriksson; O Johansson; Nigel P Carter; Magnus Nordenskjöld
Tetrasomy 15q: two marker chromosomes with no detectable alpha-satellite DNA.
American journal of human genetics 1994;54(5):877-83.
1994: JV Hunt; M A Bottoms; J Skamarauskas; Nigel P Carter; Malcolm J Mitchinson
Measurement of ceroid accumulation in macrophages by flow cytometry.
Cytometry 1994;15(4):377-82.
1994: Nigel P Carter
Cytogenetic analysis by chromosome painting.
Cytometry 1994;18(1):2-10.
1994: Nigel P Carter
Bivariate chromosome analysis using a commercial flow cytometer.
Methods in molecular biology (Clifton, N.J.) 1994;29():187-204.
1993: Y L Zheng; Nigel P Carter; C M Price; S M Colman; P J Milton; G A Hackett; M F Greaves; Malcolm A Ferguson-Smith
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: D M Bailey; Nigel P Carter; D de Vos; MA Leversha; M T Perryman; Malcolm A Ferguson-Smith
Coincidence painting: a rapid method for cloning region specific DNA sequences.
Nucleic acids research 1993;21(22):5117-23.
1993: Robert A Furlong; D R Goudie; Nigel P Carter; J E Lyall; Nabeel A Affara; Malcolm A Ferguson-Smith
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: D R Goudie; M A Yuille; MA Leversha; Robert A Furlong; Nigel P Carter; M J Lush; Nabeel A Affara; Malcolm A Ferguson-Smith
Multiple self-healing squamous epitheliomata (ESS1) mapped to chromosome 9q22-q31 in families with common ancestry.
Nature genetics 1993;3(2):165-9.
1993: R M Harris; Nigel P Carter; B Griffiths; D Goudie; R M Hampson; J R W Yates; Nabeel A Affara; Malcolm A Ferguson-Smith
Physical mapping within the tuberous sclerosis linkage group in region 9q32-q34.
Genomics 1993;15(2):265-74.
1993: JV Hunt; Keri L H Carpenter; M A Bottoms; Nigel P Carter; C E Marchant; Malcolm J Mitchinson
Flow cytometric measurement of ceroid accumulation in macrophages.
Atherosclerosis 1993;98(2):229-39.
1993: H Telenius; D de Vos; Elisabeth Blennow; L R Willat; Bruce A J Ponder; Nigel P Carter
Chromatid contamination can impair the purity of flow-sorted metaphase chromosomes.
Cytometry 1993;14(1):97-101.
1992: Y L Zheng; Malcolm A Ferguson-Smith; J P Warner; M E Ferguson-Smith; Carole A Sargent; Nigel P Carter
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: H Telenius; Nigel P Carter; C E Bebb; Magnus Nordenskjöld; Bruce A J Ponder; A Tunnacliffe
Degenerate oligonucleotide-primed PCR: general amplification of target DNA by a single degenerate primer.
Genomics 1992;13(3):718-25.
1992: Nigel P Carter; Malcolm A Ferguson-Smith; M T Perryman; H Telenius; A H Pelmear; MA Leversha; M T Glancy; S L Wood; K Cook; H M Dyson
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: A King; R Wheeler; Nigel P Carter; D P Francis; YW Loke
The response of human decidual leukocytes to IL-2.
Cellular immunology 1992;141(2):409-21.
1992: H Telenius; A H Pelmear; A Tunnacliffe; Nigel P Carter; Annemarie Behmel; Malcolm A Ferguson-Smith; Magnus Nordenskjöld; Roswitha Pfragner; Bruce A J Ponder
Cytogenetic analysis by chromosome painting using DOP-PCR amplified flow-sorted chromosomes.
Genes, chromosomes & cancer 1992;4(3):257-63.
1992: S C Dixon; N G Miller; Nigel P Carter; E M Tucker
Bivariate flow cytometry of farm animal chromosomes: a potential tool for gene mapping.
Animal genetics 1992;23(3):203-10.
1992: C F Langford; H Telenius; Nigel P Carter; N G Miller; E M Tucker
Chromosome painting using chromosome-specific probes from flow-sorted pig chromosomes.
Cytogenetics and cell genetics 1992;61(3):221-3.
1991: D M Whitcombe; Nigel P Carter; D G Albertson; S J Smith; Davd A Rhodes; Timothy M Cox
Assignment of the human ferrochelatase gene (FECH) and a locus for protoporphyria to chromosome 18q22.
Genomics 1991;11(4):1152-4.
1991: A King; N Balendran; P Wooding; Nigel P Carter; YW Loke
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: Nigel P Carter; M E Ferguson-Smith; Nabeel A Affara; H Briggs; Malcolm A Ferguson-Smith
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: Keri L H Carpenter; R Y Ball; Nigel P Carter; S E Woods; S L Hartley; S Davies; J H Enright; Malcolm J Mitchinson
Modulation of ceroid accumulation in macrophages in vitro.
Advances in experimental medicine and biology 1989;266():333-43.