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Carl Bruder

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Johanna Sandgren; Teresita Diaz de Ståhl; Robin Andersson; Uwe Menzel; Arkadiusz Piotrowski; Helena Nord; Martin Bäckdahl; Nimrod B Kiss; Michael Brauckhoff; Jan Komorowski; Henning Dralle; Ola Hessman; Catharina Larsson; Göran Akerström; Carl Bruder; Jan P Dumanski; Gunnar Westin
Recurrent genomic alterations in benign and malignant pheochromocytomas and paragangliomas revealed by whole-genome array comparative genomic hybridization analysis.
Anders Enjin; Nadine Bernhardt; Stan T Nakanishi; Anna Vallstedt; Henrik Gezelius; Fatima Memic; Magnus Lind; Tord Hjalt; Warren G Tourtellotte; Carl Bruder; Gregor Eichele; Patrick J Whelan; Klas Kullander
Identification of novel spinal cholinergic genetic subtypes disclose Chodl and Pitx2 as markers for fast motor neurons and partition cells.
Pawandeep Dhami; Peter Saffrey; Alexander W Bruce; Shane C Dillon; Kelly Chiang; Nicolas Bonhoure; Christoph M Koch; Jackie Bye; Keith James; Nicola S Foad; Peter Ellis; Nicholas A Watkins; Willem H Ouwehand; Cordelia Langford; Robert M Andrews; Carl Bruder; David Vetrie
Complex exon-intron marking by histone modifications is not determined solely by nucleosome distribution.

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All Publications

2010: Johanna Sandgren; Teresita Diaz de Ståhl; Robin Andersson; Uwe Menzel; Arkadiusz Piotrowski; Helena Nord; Martin Bäckdahl; Nimrod B Kiss; Michael Brauckhoff; Jan Komorowski; Henning Dralle; Ola Hessman; Catharina Larsson; Göran Akerström; Carl Bruder; Jan P Dumanski; Gunnar Westin
Recurrent genomic alterations in benign and malignant pheochromocytomas and paragangliomas revealed by whole-genome array comparative genomic hybridization analysis.
Endocrine-related cancer 2010;17(3):561-79.
2010: Anders Enjin; Nadine Bernhardt; Stan T Nakanishi; Anna Vallstedt; Henrik Gezelius; Fatima Memic; Magnus Lind; Tord Hjalt; Warren G Tourtellotte; Carl Bruder; Gregor Eichele; Patrick J Whelan; Klas Kullander
Identification of novel spinal cholinergic genetic subtypes disclose Chodl and Pitx2 as markers for fast motor neurons and partition cells.
The Journal of comparative neurology 2010;518(12):2284-304.
2010: Pawandeep Dhami; Peter Saffrey; Alexander W Bruce; Shane C Dillon; Kelly Chiang; Nicolas Bonhoure; Christoph M Koch; Jackie Bye; Keith James; Nicola S Foad; Peter Ellis; Nicholas A Watkins; Willem H Ouwehand; Cordelia Langford; Robert M Andrews; Carl Bruder; David Vetrie
Complex exon-intron marking by histone modifications is not determined solely by nucleosome distribution.
PloS one 2010;5(8):e12339.
2010: Caroline Daelemans; Matthew E Ritchie; Guillaume Smits; Sayeda Abu-Amero; Ian M Sudbery; Matthew S Forrest; Susana Campino; Taane G Clark; Philip Stanier; Dominic Kwiatkowski; Panos Deloukas; Emmanouil T Dermitzakis; Simon Tavaré; Gudrun E Moore; Carl Bruder
High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta.
BMC genetics 2010;11():25.
2009: Alexander W Bruce; Andrés J López-Contreras; Paul Flicek; Thomas A Down; Pawandeep Dhami; Shane C Dillon; Christoph M Koch; Cordelia F Langford; Carl Bruder; Robert M Andrews; David Vetrie
Functional diversity for REST (NRSF) is defined by in vivo binding affinity hierarchies at the DNA sequence level.
Genome research 2009;19(6):994-1005.
2009: Mehdi Motallebipour; Stefan Enroth; Tanel Punga; Adam Ameur; Christoph Koch; Carl Bruder; Jan Komorowski; Johan Ericsson; Claes Wadelius
Novel genes in cell cycle control and lipid metabolism with dynamically regulated binding sites for sterol regulatory element-binding protein 1 and RNA polymerase II in HepG2 cells detected by chromatin immunoprecipitation with microarray detection.
The FEBS journal 2009;276(7):1878-90.
2009: Maria Clara Bonaglia; Roberto Giorda; Silvana Beri; Stefania Bigoni; Alberto Sensi; Anna Baroncini; Antonella Capucci; Cristina De Agostini; Rhian Gwilliam; Panos Deloukas; Carl Bruder; Orsetta Zuffardi
Mosaic 22q13 deletions: evidence for concurrent mosaic segmental isodisomy and gene conversion.
European journal of human genetics : EJHG 2009;17(4):426-33.
2008: Maria Descartes; Judy Franklin; Teresita Diaz de Ståhl; Arkadiusz Piotrowski; Carl Bruder; Jan P Dumanski; Andrew J Carroll; Fady M Mikhail
Distal 22q11.2 microduplication encompassing the BCR gene.
American journal of medical genetics. Part A 2008;146A(23):3075-81.
2008: David Garrick; Marco De Gobbi; Vasiliki Samara; Michelle Rugless; Michelle Holland; Helena Ayyub; Karen Lower; Jacqueline A Sloane-Stanley; Nicki Gray; Christoph Koch; Carl Bruder; Douglas R Higgs
The role of the polycomb complex in silencing alpha-globin gene expression in nonerythroid cells.
Blood 2008;112(9):3889-99.
2008: Arkadiusz Piotrowski; Carl Bruder; Robin Andersson; Teresita Diaz de Ståhl; Uwe Menzel; Johanna Sandgren; Andrzej Poplawski; Desiree von Tell; Chiquito Crasto; Adam Bogdan; Rafal Bartoszewski; Zsuzsa Bebok; Maciej Krzyzanowski; Zbigniew Jankowski; E Christopher Partridge; Jan Komorowski; Jan P Dumanski
Somatic mosaicism for copy number variation in differentiated human tissues.
Human mutation 2008;29(9):1118-24.
2008: Carol A Edwards; Andrew Mungall; Lucy Matthews; Edward Ryder; Dionne J Gray; Andrew J Pask; geoffrey shaw; Jennifer A Marshall Graves; Jane Rogers; Carl Bruder; Marilyn Renfree; Anne C Ferguson-Smith
The evolution of the DLK1-DIO3 imprinted domain in mammals.
PLoS biology 2008;6(6):e135.
2008: Brita Ardesjö; Caisa M Hansson; Carl Bruder; Fredrik Rorsman; Corrado Betterle; Jan P Dumanski; Kämpe Olle; Olov Ekwall
Autoantibodies to glutathione S-transferase theta 1 in patients with primary sclerosing cholangitis and other autoimmune diseases.
Journal of autoimmunity 2008;30(4):273-82.
2008: Robin Andersson; Carl Bruder; Arkadiusz Piotrowski; Uwe Menzel; Helena Nord; Johanna Sandgren; Torgeir R Hvidsten; Teresita Diaz de Ståhl; Jan P Dumanski; Jan Komorowski
A segmental maximum a posteriori approach to genome-wide copy number profiling.
Bioinformatics (Oxford, England) 2008;24(6):751-8.
2008: Carl Bruder; Arkadiusz Piotrowski; Antoinet A C J Gijsbers; Robin Andersson; Stephen Erickson; Teresita Diaz de Ståhl; Uwe Menzel; Johanna Sandgren; Desiree von Tell; Andrzej Poplawski; Michael Crowley; Chiquito Crasto; E Christopher Partridge; Hemant K Tiwari; David Allison; Jan Komorowski; Gert-Jan B van Ommen; Dorret I Boomsma; Nancy L Pedersen; Johan T den Dunnen; Karin Wirdefeldt; Jan P Dumanski
Phenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profiles.
American journal of human genetics 2008;82(3):763-71.
2008: Teresita Díaz de Ståhl; Johanna Sandgren; Arkadiusz Piotrowski; Helena Nord; Robin Andersson; Uwe Menzel; Adam Bogdan; Ann-Charlotte Thuresson; A Poplawski; Desiree von Tell; Caisa M Hansson; Amir I Elshafie; Gehad Elghazali; Stefan Imreh; Magnus Nordenskjöld; Meena Upadhyaya; Jan Komorowski; Carl Bruder; Jan P Dumanski
Profiling of copy number variations (CNVs) in healthy individuals from three ethnic groups using a human genome 32 K BAC-clone-based array.
Human mutation 2008;29(3):398-408.
2008: Charlotte G Cole; Owen T McCann; John E Collins; Karen Oliver; David Willey; Susan M Gribble; Fengtang Yang; Karen McLaren; Jane Rogers; Zemin Ning; David M Beare; Carl Bruder
Finishing the finished human chromosome 22 sequence.
Genome biology 2008;9(5):R78.
2007: Robert P Erickson; Teresita Díaz de Ståhl; Carl Bruder; Jan P Dumanski
A patient with 22q11.2 deletion and Opitz syndrome-like phenotype has the same deletion as velocardiofacial patients.
American journal of medical genetics. Part A 2007;143A(24):3302-8.
2007: Marco De Gobbi; Eduardo Anguita; Jim Hughes; Jacqueline A Sloane-Stanley; Jacqueline A Sharpe; Christoph M Koch; Carl Bruder; Richard J Gibbons; William G Wood; Douglas R Higgs
Tissue-specific histone modification and transcription factor binding in alpha globin gene expression.
Blood 2007;110(13):4503-10.
2007: Fady M Mikhail; Maria Descartes; Arkadiusz Piotrowski; Robin Andersson; Teresita Diaz de Ståhl; Jan Komorowski; Carl Bruder; Jan P Dumanski; Andrew J Carroll
A previously unrecognized microdeletion syndrome on chromosome 22 band q11.2 encompassing the BCR gene.
American journal of medical genetics. Part A 2007;143A(18):2178-84.
2007: Fady M Mikhail; Achara Sathienkijkanchai; Nathaniel H Robin; Sandra Prucka; Julie Sanford Biggerstaff; Jan Komorowski; Robin Andersson; Carl Bruder; Arkadiusz Piotrowski; Teresita Diaz de Ståhl; Jan P Dumanski; Andrew J Carroll
Overlapping phenotype of Wolf-Hirschhorn and Beckwith-Wiedemann syndromes in a girl with der(4)t(4;11)(pter;pter).
American journal of medical genetics. Part A 2007;143A(15):1760-6.
2007: Alvaro Rada-Iglesias; Stefan Enroth; Adam Ameur; Christoph M Koch; Gayle K Clelland; Patricia Respuela-Alonso; Sarah Wilcox; Oliver M Dovey; Peter D Ellis; Cordelia F Langford; Carl Bruder; Jan Komorowski; Claes Wadelius
Butyrate mediates decrease of histone acetylation centered on transcription start sites and down-regulation of associated genes.
Genome research 2007;17(6):708-19.
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: Paola Bignone; K Y Lee; Ying Liu; Gracy Emilion; J Finch; A E R Soosay; F M L Charnock; Stephan Beck; Carl Bruder; Andrew Mungall; Trivadi Ganesan
RPS6KA2, a putative tumour suppressor gene at 6q27 in sporadic epithelial ovarian cancer.
Oncogene 2007;26(5):683-700.
2007: Carol A Edwards; Willem Rens; Oliver Clarke; Andrew Mungall; Timothy Hore; Jennifer A Marshall Graves; Carl Bruder; Anne C Ferguson-Smith; Malcolm A Ferguson-Smith
The evolution of imprinting: chromosomal mapping of orthologues of mammalian imprinted domains in monotreme and marsupial mammals.
BMC evolutionary biology 2007;7():157.
2007: Sergey Nejentsev; Luc J Smink; Deborah Smyth; Rebecca Bailey; Christopher E Lowe; Felicity Payne; Jennifer Masters; Lisa M Taylor; Alex Lam; Oliver Burren; Helen Stevens; Sarah Nutland; Neil M Walker; Anne Smith; Rebecca C J Twells; Bryan J Barratt; Charmain Wright; Lisa French; Yuan Chen; Panos Deloukas; Jane Rogers; Carl Bruder; John A Todd
Sequencing and association analysis of the type 1 diabetes-linked region on chromosome 10p12-q11.
BMC genetics 2007;8():24.
2006: George A Follows; Pawandeep Dhami; Berthold Göttgens; Alexander W Bruce; Peter J Campbell; Shane C Dillon; Aileen M Smith; Christoph Koch; Ian Donaldson; Mike A Scott; Carl Bruder; Mary E Janes; David Vetrie; Anthony R Green
Identifying gene regulatory elements by genomic microarray mapping of DNaseI hypersensitive sites.
Genome research 2006;16(10):1310-9.
2006: Anna González-Neira; Xiayi Ke; Oscar Lao; Francesc Calafell; Arcadi Navarro; David Comas; Howard Cann; Suzannah Bumpstead; Jilur Ghori; Sarah Hunt; Panos Deloukas; Carl Bruder; Lon R Cardon; Jaume Bertranpetit
The portability of tagSNPs across populations: a worldwide survey.
Genome research 2006;16(3):323-30.
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: Kiran K Mantripragada; Ann-Charlotte Thuresson; Arkadiusz Piotrowski; Teresita Díaz de Ståhl; Uwe Menzel; Gintautas Grigelionis; R E Ferner; S Griffiths; L Bolund; Victor Mautner; M Nordling; Eric Legius; David Vetrie; Niklas Dahl; Ludwine MESSIAEN; Meena Upadhyaya; Carl Bruder; Jan P Dumanski
Identification of novel deletion breakpoints bordered by segmental duplications in the NF1 locus using high resolution array-CGH.
Journal of medical genetics 2006;43(1):28-38.
2005: Alvaro Rada-Iglesias; Ola Wallerman; Christoph Koch; Adam Ameur; Stefan Enroth; Gayle K Clelland; Kenneth Wester; Sarah Wilcox; Oliver M Dovey; Peter D Ellis; Vicki L Wraight; Keith James; Rob Andrews; Cordelia Langford; Pawandeep Dhami; Nigel Carter; David Vetrie; Fredrik Pontén; Jan Komorowski; Carl Bruder; Claes Wadelius
Binding sites for metabolic disease related transcription factors inferred at base pair resolution by chromatin immunoprecipitation and genomic microarrays.
Human molecular genetics 2005;14(22):3435-47.
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: Mohammad Bohlooly-Y; Mohammad Bohlooly; Bob Olsson; Carl Bruder; Daniel Lindén; Klara Sjögren; Mikael Bjursell; Emil Egecioglu; Lennart Svensson; Peter Brodin; John C Waterton; Olle G P Isaksson; Frank Sundler; Bo Ahrén; Claes Ohlsson; Jan Oscarsson; Jan Törnell
Growth hormone overexpression in the central nervous system results in hyperphagia-induced obesity associated with insulin resistance and dyslipidemia.
Diabetes 2005;54(1):51-62.
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.
2004: Helena Lindmark; Birgitta Rosengren; Eva Hurt-Camejo; Carl Bruder
Gene expression profiling shows that macrophages derived from mouse embryonic stem cells is an improved in vitro model for studies of vascular disease.
Experimental cell research 2004;300(2):335-44.
2004: Charles Stewart; Roger HORTON; Richard J N Allcock; Jennifer L Ashurst; Alexey Atrazhev; Penny Coggill; Carl Bruder; Simon Forbes; Karen Halls; Joanna M M Howson; Sean Humphray; Sarah Hunt; Andrew Mungall; Kazutoyo Osoegawa; Sophie Palmer; Anne N Roberts; Jane Rogers; Sarah Sims; Yu Wang; Laurens G Wilming; John Elliott; Pieter J de Jong; Stephen Sawcer; John A Todd; John Trowsdale; Stephan Beck
Complete MHC haplotype sequencing for common disease gene mapping.
Genome research 2004;14(6):1176-87.
2004: Aleksandra Trifunovic; Anna Wredenberg; Maria Falkenberg; Johannes N Spelbrink; Anja T Rovio; Carl Bruder; Mohammad Bohlooly-Y; Sebastian Gidlöf; Anders Oldfors; Rolf Wibom; Jan Törnell; Howard T Jacobs; Nils-Göran Larsson
Premature ageing in mice expressing defective mitochondrial DNA polymerase.
Nature 2004;429(6990):417-23.
2004: Joanne E Langan; Charlotte G Cole; Elisabeth J Huckle; Shaun Byrne; Fiona E McRonald; Lynn Rowbottom; Anthony Ellis; Joan M Shaw; Irene M Leigh; David P Kelsell; Carl Bruder; John Field; Janet M Risk
Novel microsatellite markers and single nucleotide polymorphisms refine the tylosis with oesophageal cancer (TOC) minimal region on 17q25 to 42.5 kb: sequencing does not identify the causative gene.
Human genetics 2004;114(6):534-40.
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: John E Collins; Charmain L Wright; Carol A Edwards; Matthew P Davis; James A Grinham; Charlotte G Cole; Melanie E Goward; Begoña Aguado; Meera Mallya; Younes Mokrab; Elizabeth J Huckle; David M Beare; Carl Bruder
A genome annotation-driven approach to cloning the human ORFeome.
Genome biology 2004;5(10):R84.
2003: Caisa M Hansson; Haider Ali; Carl Bruder; Ingegerd Fransson; Sindy Kluge; Björn Andersson; Bruce A Roe; Uwe Menzel; Jan P Dumanski
Strong conservation of the human NF2 locus based on sequence comparison in five species.
Mammalian genome : official journal of the International Mammalian Genome Society 2003;14(8):526-36.
2003: Désirée von Tell; Carl Bruder; Louise V B Anderson; Maria Anvret; Gabrielle Ahlberg
Refined mapping of the Welander distal myopathy region on chromosome 2p13 positions the new candidate region telomeric of the DYSF locus.
Neurogenetics 2003;4(4):173-7.
2003: A R Jeffries; Andrew Mungall; E Dawson; Karen Halls; Cordelia F Langford; Robin M Murray; Carl Bruder; John F Powell
beta-1,3-Glucuronyltransferase-1 gene implicated as a candidate for a schizophrenia-like psychosis through molecular analysis of a balanced translocation.
Molecular psychiatry 2003;8(7):654-63.
2003: Kiran K Mantripragada; Patrick Buckley; Magdalena Benetkiewicz; Cecilia De Bustos; Carina Hirvelä; Caroline Jarbo; Carl Bruder; Helena Wensman; Tiit Mathiesen; Gunnar Nyberg; Laura Papi; V Peter Collins; Koichi Ichimura; Gareth Evans; Jan P Dumanski
High-resolution profiling of an 11 Mb segment of human chromosome 22 in sporadic schwannoma using array-CGH.
International journal of oncology 2003;22(3):615-22.
2003: Carl Bruder; David M Beare; John E Collins
The characteristics of human genes: analysis of human chromosome 22.
Comparative and functional genomics 2003;4(6):635-46.
2003: Irene Szijan; Daniel Rochefort; Carl Bruder; Ezequiel Surace; Gloria Machiavelli; Viviana Dalamon; Javier Cotignola; Verónica Ferreiro; Alvaro Campero; Armando Basso; Jan P Dumanski; Guy A Rouleau
NF2 tumor suppressor gene: a comprehensive and efficient detection of somatic mutations by denaturing HPLC and microarray-CGH.
Neuromolecular medicine 2003;3(1):41-52.
2003: John E Collins; Melanie E Goward; Charlotte G Cole; Luc J Smink; Elizabeth J Huckle; Sarah Knowles; Jacqueline M Bye; David M Beare; Carl Bruder
Reevaluating human gene annotation: a second-generation analysis of chromosome 22.
Genome research 2003;13(1):27-36.
2002: Carl Bruder
Human genome sequences: enigmatic variations.
Mutagenesis 2002;17(6):457-61.
2002: Ying Liu; Phillippa Dodds; Gracy Emilion; Andrew Mungall; Carl Bruder; Stephan Beck; R Spencer Wells; F M L Charnock; Trivadi Ganesan
The human homologue of unc-93 maps to chromosome 6q27 - characterisation and analysis in sporadic epithelial ovarian cancer.
BMC genetics 2002;3():20.
2002: Elisabeth Dawson; Goncalo Abecasis; Suzannah Bumpstead; Yuan Chen; Sarah Hunt; David M Beare; Jagjit Pabial; Thomas Dibling; Emma Tinsley; Susan Kirby; David Carter; Marianna Papaspyridonos; Simon Livingstone; Rocky Ganske; Elin Lõhmussaar; Jana Zernant; Neeme Tõnisson; Maido Remm; Reedik Mägi; Tarmo Puurand; Jaak Vilo; Ants Kurg; Kate Rice; Panos Deloukas; Richard Mott; Andres Metspalu; David R Bentley; Lon R Cardon; Carl Bruder
A first-generation linkage disequilibrium map of human chromosome 22.
Nature 2002;418(6897):544-8.
2002: Ying Liu; Gracy Emilion; Andrew Mungall; Carl Bruder; Stephan Beck; Valerie G Le Meuth-Metzinger; Andrew N Shelling; F M L Charnock; Trivadi Ganesan
Physical and transcript map of the region between D6S264 and D6S149 on chromosome 6q27, the minimal region of allele loss in sporadic epithelial ovarian cancer.
Oncogene 2002;21(3):387-99.
2001: Elisabeth Dawson; Yuan Chen; Sarah Hunt; Luc J Smink; A Hunt; K Rice; S Livingston; Suzannah Bumpstead; R Bruskiewich; P Sham; R Ganske; M Adams; K Kawasaki; N Shimizu; S Minoshima; B Roe; David Bentley; Carl Bruder
A SNP resource for human chromosome 22: extracting dense clusters of SNPs from the genomic sequence.
Genome research 2001;11(1):170-8.
2000: Alison M Dunning; Francine Durocher; Catherine S Healey; M Dawn Teare; Simon McBride; F Carlomagno; Chun-Fang Xu; Elisabeth Dawson; S Rhodes; S Ueda; E Lai; Robert N Luben; E J Van Rensburg; Arto Mannermaa; Vesa Kataja; G Rennart; Carl Bruder; Ian Purvis; Douglas Easton; Bruce A J Ponder
The extent of linkage disequilibrium in four populations with distinct demographic histories.
American journal of human genetics 2000;67(6):1544-54.
2000: Carl Bruder
Genomics - the new rock and roll?
Trends in genetics : TIG 2000;16(10):456-61.
2000: Carl Bruder
The gene guessing game.
Yeast (Chichester, England) 2000;17(3):218-24.
2000: Isabel Tapia-Páez; Kevin P O'Brien; Maria Kost-Alimova; Sigrid Sahlén; Darek Kedra; Carl Bruder; Björn Andersson; Bruce A Roe; P Hu; Stefan Imreh; Elisabeth Blennow; Jan P Dumanski
Fine mapping of the constitutional translocation t(11;22)(q23;q11).
Human genetics 2000;106(5):506-16.
2000: Ilan R Kirsch; Eric Green; Raluca Yonescu; Robert L Strausberg; N Carter; David Bentley; MA Leversha; Carl Bruder; V V Braden; E Hilgenfeld; Gerold Schuler; Alex E Lash; G L Shen; M Martelli; W Michael Kuehl; R D Klausner; Thomas Ried
A systematic, high-resolution linkage of the cytogenetic and physical maps of the human genome.
Nature genetics 2000;24(4):339-40.
2000: M Luijten; Y Wang; B T Smith; Andries Westerveld; Luc J Smink; Carl Bruder; B A Roe; Theo J M Hulsebos
Mechanism of spreading of the highly related neurofibromatosis type 1 (NF1) pseudogenes on chromosomes 2, 14 and 22.
European journal of human genetics : EJHG 2000;8(3):209-14.
2000: Andrew Mungall; Stephan Beck; Howard Cann; Carl Bruder; John Trowsdale; Andreas Ziegler
Report of the Fourth International Chromosome 6 Workshop 1999. 10-12 June 1999. Cambridge, UK. Abstracts.
Cytogenetics and cell genetics 2000;88(3-4):173-96.
1999: Carl Bruder; N Shimizu; B A Roe; S Chissoe; A R Hunt; John E Collins; R Bruskiewich; David M Beare; Michele Clamp; Luc J Smink; R Ainscough; J P Almeida; A Babbage; C Bagguley; J Bailey; K Barlow; Kirsty Bates; O Beasley; Christine P Bird; S Blakey; A M Bridgeman; D Buck; J Burgess; W D Burrill; K P O'Brien
The DNA sequence of human chromosome 22.
Nature 1999;402(6761):489-95.
1999: Carl Bruder; Koichi Ichimura; Elisabeth Blennow; T Ikeuchi; T Yamaguchi; Y Yuasa; V Peter Collins; Jan P Dumanski
Severe phenotype of neurofibromatosis type 2 in a patient with a 7.4-MB constitutional deletion on chromosome 22: possible localization of a neurofibromatosis type 2 modifier gene?
Genes, chromosomes & cancer 1999;25(2):184-90.
1999: Carl Bruder; Koichi Ichimura; Ola Tingby; K Hirakawa; A Komatsuzaki; A Tamura; Y Yuasa; V Peter Collins; Jan P Dumanski
A group of schwannomas with interstitial deletions on 22q located outside the NF2 locus shows no detectable mutations in the NF2 gene.
Human genetics 1999;104(5):418-24.
1999: Carl Bruder; Jan P Dumanski; Darek Kedra
The mouse ortholog of the human SMARCB1 gene encodes two splice forms.
Biochemical and biophysical research communications 1999;257(3):886-90.
1999: RJ Gardner; Andrew Mungall; Carl Bruder; John C K Barber; Julian P H Shield; I Karen Temple; David O Robinson
Localisation of a gene for transient neonatal diabetes mellitus to an 18.72 cR3000 (approximately 5.4 Mb) interval on chromosome 6q.
Journal of medical genetics 1999;36(3):192-6.
1999: M Peyrard; Eyal Seroussi; A C Sandberg-Nordqvist; Ya-Gang Xie; Fei-Yu Han; Ingegerd Fransson; J Collins; Carl Bruder; Maria Kost-Alimova; Stefan Imreh; Jan P Dumanski
The human LARGE gene from 22q12.3-q13.1 is a new, distinct member of the glycosyltransferase gene family.
Proceedings of the National Academy of Sciences of the United States of America 1999;96(2):598-603.
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.
1998: Berge A Minassian; JR Lee; Jo-Anne Herbrick; J Huizenga; S Soder; Andrew Mungall; Carl Bruder; R Gardner; Chung Yan Fong; S Carpenter; Laura B Jardim; P Satishchandra; Eva Andermann; O Carter Snead; I Lopes-Cendes; Lap-Chee Tsui; Antonio V Delgado-Escueta; Guy Rouleau; Stephen W Scherer
Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsy.
Nature genetics 1998;20(2):171-4.
1998: Darek Kedra; HQ Pan; Eyal Seroussi; Ingegerd Fransson; C Guilbaud; J E Collins; Carl Bruder; Elisabeth Blennow; Bruce A Roe; Fredrik Piehl; Jan P Dumanski
Characterization of the human synaptogyrin gene family.
Human genetics 1998;103(2):131-41.
1998: Erik P Sulman; Jan P Dumanski; Peter White; Huaqing Zhao; John M Maris; Tiit Mathiesen; Carl Bruder; Avital Cnaan; Garrett M Brodeur
Identification of a consistent region of allelic loss on 1p32 in meningiomas: correlation with increased morbidity.
Cancer research 1998;58(15):3226-30.
1998: T P Moynihan; Charlotte G Cole; Carl Bruder; L O'Neil; A F Markham; P A Robinson
Fine-mapping, genomic organization, and transcript analysis of the human ubiquitin-conjugating enzyme gene UBE2L3.
Genomics 1998;51(1):124-7.
1997: K M Carlson; Carl Bruder; Magnus Nordenskjöld; Jan P Dumanski
1p and 3p deletions in meningiomas without detectable aberrations of chromosome 22 identified by comparative genomic hybridization.
Genes, chromosomes & cancer 1997;20(4):419-24.
1997: John E Collins; Andrew Mungall; K L Badcock; J M Fay; Carl Bruder
The organization of the gamma-glutamyl transferase genes and other low copy repeats in human chromosome 22q11.
Genome research 1997;7(5):522-31.
1997: A J Theaker; GL Maslen; Carol E Scott; C M Rice; SE Hunt; A King; Andrew Mungall; Carl Bruder; Stephan Beck
The Chromosome 6 database at the Sanger Centre.
DNA sequence : the journal of DNA sequencing and mapping 1997;8(3):167-71.
1997: Andrew Mungall; Sean Humphray; S A Ranby; Carol A Edwards; R W Heathcott; C M Clee; E Holloway; A I Peck; P Harrison; L D Green; A P Butler; Cordelia F Langford; R G William; Elizabeth J Huckle; L Baron; A Smith; MA Leversha; Y H Ramsey; SM Clegg; C M Rice; GL Maslen; SE Hunt; Carol E Scott; CA Soderlund; Carl Bruder
From long range mapping to sequence-ready contigs on human chromosome 6.
DNA sequence : the journal of DNA sequencing and mapping 1997;8(3):151-4.
1997: Stephan Beck; Howard Cann; R Duncan Campbell; Carl Bruder; H Inoko; E C Jazwinska; Jiannis Ragoussis; John Trowsdale; Andreas Ziegler
Third single chromosome 6 workshop: meeting report.
DNA sequence : the journal of DNA sequencing and mapping 1997;8(3):113-29.
1996: Gerold Schuler; Mark S Boguski; E A Stewart; L D Stein; Gabor Gyapay; K Rice; R E White; P Rodriguez-Tomé; A Aggarwal; E Bajorek; S Bentolila; B B Birren; A Butler; A B Castle; N Chiannilkulchai; A Chu; C Clee; S Cowles; Philip Day; T Dibling; N Drouot; Carl Bruder; S Duprat; C East; C Edwards; Jian-Bing Fan; N Fang; C Fizames; C Garrett; L Green; D Hadley; M Harris; P Harrison; S Brady; A Hicks; E Holloway; L Hui; S Hussain; C Louis-Dit-Sully; J Ma; A MacGilvery; C Mader; A Maratukulam; TC Matise; K B McKusick; J Morissette; Andrew Mungall; D Muselet; H C Nusbaum; David C Page; A Peck; S Perkins; M Piercy; F Qin; John Quackenbush; S Ranby; T Reif; Steve Rozen; C Sanders; X She; J Silva; DK Slonim; CA Soderlund; W L Sun; P Tabar; T Thangarajah; N Vega-Czarny; D Vollrath; S Voyticky; T Wilmer; X Wu; Mark D Adams; Charles Auffray; Nicole Walter; R Brandon; AM Dehejia; PN Goodfellow; R Houlgatte; J R Hudson; S E Ide; K R Iorio; W Y Lee; N Seki; T Nagase; K Ishikawa; N Nomura; C Phillips; Mihael H Polymeropoulos; M Sandusky; K Schmitt; R Berry; K Swanson; R Torres; J Craig Venter; James M Sikela; Jacques Beckmann; Jean Weissenbach; Richard Myers; D R Cox; M R James; D Bentley; Panos Deloukas; Eric S Lander; Thomas J Hudson
A gene map of the human genome.
Science (New York, N.Y.) 1996;274(5287):540-6.
1996: Theo J M Hulsebos; EH Bijleveld; P H Riegman; L J Smink; Carl Bruder
Identification and characterization of NF1-related loci on human chromosomes 22, 14 and 2.
Human genetics 1996;98(1):7-11.
1996: UJ Kim; H Shizuya; H L Kang; S S Choi; C L Garrett; L J Smink; Bruce Birren; Julie R Korenberg; Carl Bruder; M I Simon
A bacterial artificial chromosome-based framework contig map of human chromosome 22q.
Proceedings of the National Academy of Sciences of the United States of America 1996;93(13):6297-301.
1996: Darek Kedra; M Peyrard; Ingegerd Fransson; J E Collins; Carl Bruder; B A Roe; Jan P Dumanski
Characterization of a second human clathrin heavy chain polypeptide gene (CLH-22) from chromosome 22q11.
Human molecular genetics 1996;5(5):625-31.
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.
1996: C G Cole; John E Collins; Carl Bruder
YAC library screening. II. Hybridization and PCR-based screening protocols.
Methods in molecular biology (Clifton, N.J.) 1996;54():33-47.
1996: Carl Bruder; G L Maslen
Use of ACEDB as a database for YAC library data management.
Methods in molecular biology (Clifton, N.J.) 1996;54():253-80.
1996: C G Cole; John E Collins; Carl Bruder
YAC library screening. I. Preparation of hybridization filters and PCRpools.
Methods in molecular biology (Clifton, N.J.) 1996;54():23-31.
1996: John E Collins; S Hassock; Carl Bruder
YAC library storage and transport.
Methods in molecular biology (Clifton, N.J.) 1996;54():13-21.
1995: CA Soderlund; Carl Bruder
SAM: a system for iteratively building marker maps.
Computer applications in the biosciences : CABIOS 1995;11(6):645-55.
1995: Theo J M Hulsebos; D J Gilbert; O Delattre; L J Smink; Carl Bruder; Andries Westerveld; Gilles Thomas; N A Jenkins; N G Copeland
Assignment of the beta B1 crystallin gene (CRYBB1) to human chromosome 22 and mouse chromosome 5.
Genomics 1995;29(3):712-8.
1995: D R Bently; Carl Bruder
Mapping human chromosomes.
Current opinion in genetics & development 1995;5(3):328-34.
1994: Galit Rotman; Kinneret Savitsky; Yehiel Ziv; C G Cole; Michael J Higgins; I Bar-Am; Carl Bruder; Anat Bar-Shira; L Vanagaite; S Qin; J Zhang; N J Nowak; Settara C Chandrasekharappa; H Lehrach; Lydia Avivi; T B Shows; Francis S Collins; David R Bentley; Yosef Shiloh
A YAC contig spanning the ataxia-telangiectasia locus (groups A and C) at 11q22-q23.
Genomics 1994;24(2):234-42.
1994: M Peyrard; Ingegerd Fransson; Ya-Gang Xie; Fei-Yu Han; M H Ruttledge; S Swahn; J E Collins; Carl Bruder; V Peter Collins; Jan P Dumanski
Characterization of a new member of the human beta-adaptin gene family from chromosome 22q12, a candidate meningioma gene.
Human molecular genetics 1994;3(8):1393-9.
1993: Ya-Gang Xie; Fei-Yu Han; M Peyrard; M H Ruttledge; Ingegerd Fransson; P DeJong; J Collins; Carl Bruder; Magnus Nordenskjöld; Jan P Dumanski
Cloning of a novel, anonymous gene from a megabase-range YAC and cosmid contig in the neurofibromatosis type 2/meningioma region on human chromosome 22q12.
Human molecular genetics 1993;2(9):1361-8.
1993: Igor Vorechovský; J Holland; Paschalis Sideras; Carl Bruder; Lennart Hammarström; C I Edvard Smith; David R Bentley; David Vetrie
Isolation of cDNA clones mapping around DXS178: a search for human X-linked agammaglobulinaemia gene using yeast artificial chromosomes, cosmids and direct cDNA selection.
Immunodeficiency 1993;4(1-4):221-4.
1992: John E Collins; L A Everett; David R Bentley; Carl Bruder
A panel of human chromosome 22-specific sequence tagged sites.
Genomics 1992;14(4):1098-103.
1992: C G Cole; K Patel; J Shipley; Denise Sheer; Martin Bobrow; David R Bentley; Carl Bruder
Identification of region-specific yeast artificial chromosomes using pools of Alu element-mediated polymerase chain reaction probes labeled via linear amplification.
Genomics 1992;14(4):931-8.
1992: C G Cole; Carl Bruder; A J Coffey; Mark T Ross; S Meier-Ewert; Martin Bobrow; David R Bentley
A random STS strategy for construction of YAC contigs spanning defined chromosomal regions.
Genomics 1992;14(2):256-62.
1992: David R Bentley; C Todd; J Collins; J Holland; Carl Bruder; S Hassock; A Bankier; Francesco Giannelli
The development and application of automated gridding for efficient screening of yeast and bacterial ordered libraries.
Genomics 1992;12(3):534-41.