The DNA sequence and analysis of human chromosome 6

I. Dunham | J. L. Ashurst | D. R. Bentley | M. C. Jones | K. L. Howe | R. Durbin | A. Coulson | A. Brown | J. Sulston | T. Andrews | N. Carter | J. Bailey | A. Frankish | S. Searle | M. Kay | C. Steward | T. Hubbard | L. Matthews | S. Whitehead | M. Dunn | P. Heath | D. Grafham | K. Howe | C. Clee | S. Hunt | A. Peck | D. Bentley | J. Mullikin | C. Rice | J. Rogers | M. Ross | C. Bird | J. Burton | M. Griffiths | K. McLay | R. Plumb | S. Sims | R. Ainscough | K. Barlow | J. Davies | M. D. Francis | A. Joy | C. Langford | E. Overton-Larty | A. McMurray | I. Dunham | M. Clamp | P. Dhami | J. Gilbert | D. Leongamornlert | D. Beare | S. Gribble | A. Mungall | S. Beck | L. French | M. Jones | C. Lloyd | S. Milne | J. Wallis | E. Huckle | D. Niblett | K. Oliver | S. Squares | B. Phillimore | G. Bethel | K. Howe | S. Keenan | L. Wilming | C. Scott | M. Wall | A. West | M. Smith | R. Banerjee | M. Leversha | C. Johnson | J. Loveland | J. Ashurst | R. Horton | O. T. McCann | A. Hunt | J. Collins | J. Almeida | A. Babbage | C. Bagguley | K. Bates | O. Beasley | S. Blakey | W. Burrill | C. Carder | G. Clark | S. Clegg | V. Cobley | R. Collier | N. Corby | G. Coville | R. Hall | R. Heathcott | S. Holmes | A. Kimberley | A. King | G. Laird | D. Lloyd | M. Mashreghi-mohammadi | S. McLaren | A. Pearce | S. Phillips | Y. Ramsey | H. Sehra | C. Skuce | D. Willey | T. Wilmer | C. Edwards | S. Ranby | G. Howell | K. Novik | C. Gillson | P. Wray | E. Hart | A. Tracey | S. Palmer | K. Ambrose | R. Ashwell | D. Barker | H. Beasley | S. Bray-Allen | J. Brook | J. Brown | D. Burford | J. Chapman | S. Y. Clark | L. Colman | K. Culley | M. Earthrowl | A. Ellington | K. Evans | L. Faulkner | J. Frankland | P. Garner | J. Garnett | M. Ghori | L. M. Gilby | R. Glithero | M. Grant | C. Griffiths | K. Halls | S. Hammond | J. Harley | P. J. Howden | S. Humphray | M. Humphries | S. Lawlor | J. Lovell | S. Martin | G. Maslen | M. Moore | T. Nickerson | A. Parker | R. Patel | K. Porter | E. Sheridan | S. Smith | L. Spraggon | N. Sycamore | G. Tamlyn-Hall | J. Tester | A. Theaker | D. W. Thomas | A. Thorpe | A. Tromans | B. Tubby | S. S. White | H. Whittaker | A. Wild | J. M. Wood | J. C. Wyatt | L. Young | R. Younger | S. Beck | C. Carder | K. Oliver | A. R. Hunt | R. W. Plumb | J. E. Loveland | T. D. Andrews | S. E. Hunt | C. E. Scott | R. Ainscough | J. P. Almeida | K. D. Ambrose | R. I. S. Ashwell | A. K. Babbage | C. L. Bagguley | J. Bailey | R. Banerjee | D. J. Barker | K. F. Barlow | K. Bates | H. Beasley | O. Beasley | C. P. Bird | S. Bray-Allen | A. J. Brown | J. Y. Brown | W. Burrill | J. Burton | N. P. Carter | J. C. Chapman | C. M. Clee | S. Clegg | R. E. Collier | J. Davies | P. Dhami | M. Dunn | M. E. Earthrowl | L. Faulkner | A. Frankish | L. French | P. Garner | J. Garnett | J. G. R. Gilbert | D. V. Grafham | S. Gribble | C. Griffiths | S. Hammond | J. L. Harley | E. A. Hart | P. D. Heath | E. Huckle | A. A. Joy | M. Kay | A. M. Kimberley | A. King | G. K. Laird | C. Langford | S. Lawlor | D. A. Leongamornlert | M. Leversha | D. M. Lloyd | J. Lovell | S. Martin | M. Mashreghi-Mohammadi | L. Matthews | A. McMurray | S. Milne | T. Nickerson | A. V. Pearce | A. I. Peck | K. M. Porter | B. Phillimore | Y. Ramsey | H. K. Sehra | S. K. Sims | C. D. Skuce | M. Smith | C. A. Steward | N. Sycamore | J. Tester | A. Thorpe | A. Tracey | A. Tromans | M. Wall | J. M. Wallis | A. P. West | S. L. Whitehead | L. Wilming | P. W. Wray | L. Young | A. Coulson | R. Durbin | J. E. Sulston | T. Hubbard | J. Rogers | A. West | G. Bethel | V. Cobley | G. J. Coville | J. Frankland | R. J. Glithero | S. A. Palmer | A. Parker | E. Sheridan | M. T. Ross | D. C. Burford | C. M. Rice | D. M. Beare | S. J. Keenan | M. E. Clamp | J. E. Collins | S. J. McLaren | M. J. F. Moore | B. Tubby | A. J. Mungall | C. A. Edwards | R. Horton | S. Blakey | J. Brook | G. Clark | L. K. Colman | N. R. Corby | K. M. Culley | A. E. Ellington | K. A. Evans | M. J. R. Ghori | C. J. Gillson | M. Grant | M. Griffiths | R. Hall | K. S. Halls | R. Heathcott | S. J. Holmes | G. R. Howell | S. J. Humphray | M. D. Humphries | C. M. Johnson | C. R. Lloyd | G. L. Maslen | K. McLay | J. C. Mullikin | D. Niblett | K. L. Novik | E. K. Overton-Larty | R. Patel | S. Phillips | S. A. Ranby | S. M. Searle | S. Smith | L. Spraggon | S. L. Squares | G. Tamlyn-Hall | A. J. Theaker | H. Whittaker | A. Wild | D. J. Willey | T. E. Wilmer | R. M. Younger | K. Evans | O. McCann | M. Jones | S. Clark | O. Mccann | G. Howell | L. Colman | D. Thomas | S. Searle | J. Brown | D. Barker | M. Jones | J. Brown | S. Smith | J. Wood | M. Francis | A. Brown | P. Heath | S. S. White | J. Wyatt | P. Howden

[1]  Nancy F. Hansen,et al.  Comparative analyses of multi-species sequences from targeted genomic regions , 2003, Nature.

[2]  R. Murray,et al.  β-1,3-Glucuronyltransferase-1 gene implicated as a candidate for a schizophrenia-like psychosis through molecular analysis of a balanced translocation , 2003, Molecular Psychiatry.

[3]  Patrick Gaudray,et al.  Segmental duplications in euchromatic regions of human chromosome 5: a source of evolutionary instability and transcriptional innovation. , 2003, Genome research.

[4]  Margot Albus,et al.  Support for association of schizophrenia with genetic variation in the 6p22.3 gene, dysbindin, in sib-pair families with linkage and in an additional sample of triad families. , 2003, American journal of human genetics.

[5]  Ian Dunham,et al.  Reevaluating human gene annotation: a second-generation analysis of chromosome 22. , 2003, Genome research.

[6]  Patrick Wincker,et al.  The DNA sequence and analysis of human chromosome 14 , 2023, Nature.

[7]  James Robinson,et al.  IMGT/HLA and IMGT/MHC: sequence databases for the study of the major histocompatibility complex , 2003, Nucleic Acids Res..

[8]  D. Haussler,et al.  Human-mouse alignments with BLASTZ. , 2003, Genome research.

[9]  J. Squire,et al.  The role of Alu repeat clusters as mediators of recurrent chromosomal aberrations in tumors , 2002, Genes, chromosomes & cancer.

[10]  M. Carrington,et al.  High-resolution patterns of meiotic recombination across the human major histocompatibility complex. , 2002, American journal of human genetics.

[11]  S Beck,et al.  Epigenomics: genome-wide study of methylation phenomena. , 2002, Current issues in molecular biology.

[12]  M. Adams,et al.  Recent Segmental Duplications in the Human Genome , 2002, Science.

[13]  R. Straub,et al.  Genetic variation in the 6p22.3 gene DTNBP1, the human ortholog of the mouse dysbindin gene, is associated with schizophrenia. , 2002, American journal of human genetics.

[14]  D. Gudbjartsson,et al.  A high-resolution recombination map of the human genome , 2002, Nature Genetics.

[15]  R. Ekong,et al.  Ocular developmental abnormalities and glaucoma associated with interstitial 6p25 duplications and deletions. , 2002, Investigative ophthalmology & visual science.

[16]  Xun Gu,et al.  Age distribution of human gene families shows significant roles of both large- and small-scale duplications in vertebrate evolution , 2002, Nature Genetics.

[17]  J. Trowsdale.  The gentle art of gene arrangement: the meaning of gene clusters , 2002, Genome Biology.

[18]  Michael J. Wilson,et al.  A cluster of ten novel MHC class I related genes on human chromosome 6q24.2-q25.3. , 2002, Genomics.

[19]  Philip Lijnzaad,et al.  The Ensembl genome database project , 2002, Nucleic Acids Res..

[20]  Sue Povey,et al.  Genew: the Human Gene Nomenclature Database , 2002, Nucleic Acids Res..

[21]  A. Syvänen.  Accessing genetic variation: genotyping single nucleotide polymorphisms , 2001, Nature Reviews Genetics.

[22]  S. Eddy.  Non–coding RNA genes and the modern RNA world , 2001, Nature Reviews Genetics.

[23]  A. Jeffreys,et al.  Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex , 2001, Nature Genetics.

[24]  J. Mullikin,et al.  SSAHA: a fast search method for large DNA databases. , 2001, Genome research.

[25]  T. Liesegang.  The physical maps for sequencing human chromosomes 1,6,9,10,13,20 and X. Bentley DR,∗ Deloukas P, Dunham A, et al. Nature 2001;409:942–943. , 2001 .

[26]  David I. Smith,et al.  Cloning and characterization of a senescence inducing and class II tumor suppressor gene in ovarian carcinoma at chromosome region 6q27 , 2001, Oncogene.

[27]  P. Deloukas,et al.  The physical maps for sequencing human chromosomes 1, 6, 9, 10, 13, 20 and X , 2001, Nature.

[28]  M. Daly,et al.  A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms , 2001, Nature.

[29]  P. Deloukas,et al.  Comparison of human genetic and sequence-based physical maps , 2001, Nature.

[30]  The Wellcome Trust Sanger Institute.  The DNA sequence and comparative analysis of human chromosome 20 , 2001 .

[31]  C. Fizames,et al.  Estimate of human gene number provided by genome-wide analysis using Tetraodon nigroviridis DNA sequence , 2000, Nature Genetics.

[32]  J. Ragoussis,et al.  Large-scale chromatin organization of the major histocompatibility complex and other regions of human chromosome 6 and its response to interferon in interphase nuclei. , 2000, Journal of cell science.

[33]  R. Gibbs,et al.  PipMaker--a web server for aligning two genomic DNA sequences. , 2000, Genome research.

[34]  R. White,et al.  Survey and summary: transcription by RNA polymerases I and III. , 2000, Nucleic acids research.

[35]  M. Guyer,et al.  Assessing the quality of the DNA sequence from the Human Genome Project. , 1999, Genome research.

[36]  G. Benson,et al.  Tandem repeats finder: a program to analyze DNA sequences. , 1999, Nucleic acids research.

[37]  S. Scherer,et al.  Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsy , 1998, Nature Genetics.

[38]  J C Murray,et al.  Pediatrics and , 1998 .

[39]  S. Minoshima,et al.  Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism , 1998, Nature.

[40]  C. Soderlund,et al.  From long range mapping to sequence-ready contigs on human chromosome 6. , 1997, DNA Sequence.

[41]  S. Eddy,et al.  tRNAscan-SE: a program for improved detection of transfer RNA genes in genomic sequence. , 1997, Nucleic acids research.

[42]  M. C. Ellis,et al.  A novel MHC class I–like gene is mutated in patients with hereditary haemochromatosis , 1996, Nature Genetics.

[43]  John A Todd,et al.  Genetic Analysis of Autoimmune Disease , 1996, Cell.

[44]  J Ragoussis,et al.  Evidence of a locus for orofacial clefting on human chromosome 6p24 and STS content map of the region. , 1995, Human molecular genetics.

[45]  J. Bonfield,et al.  A new DNA sequence assembly program. , 1995, Nucleic acids research.