Anthony J Brookes

Anthony J Brookes

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Anthony J Brookes

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GWAS Central: a comprehensive resource for the discovery and comparison of genotype and phenotype data from genome-wide association studies.

Nucleic Acids Res 2019 Oct 15. Epub 2019 Oct 15.

Department of Genetics and Genome Biology, University of Leicester, Leicester LE1 7RH, UK.

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http://dx.doi.org/10.1093/nar/gkz895DOI Listing
October 2019

European Prevention of Alzheimer's Dementia Registry: Recruitment and prescreening approach for a longitudinal cohort and prevention trials.

Alzheimers Dement 2018 06 28;14(6):837-842. Epub 2018 Mar 28.

Department of Neurology and Alzheimer Center, Amsterdam Neuroscience, VU University Medical Center, Amsterdam, The Netherlands; Department of Psychiatry and Neuropsychology, School for Mental Health and Neuroscience, Alzheimer Centre Limburg, Maastricht University, Maastricht, The Netherlands.

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http://dx.doi.org/10.1016/j.jalz.2018.02.010DOI Listing
June 2018

VariantValidator: Accurate validation, mapping, and formatting of sequence variation descriptions.

Hum Mutat 2018 01 17;39(1):61-68. Epub 2017 Oct 17.

Department of Genetics, University of Leicester, Leicester, United Kingdom.

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http://dx.doi.org/10.1002/humu.23348DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5765404PMC
January 2018

Blood and sputum eosinophils in COPD; relationship with bacterial load.

Respir Res 2017 05 8;18(1):88. Epub 2017 May 8.

Division of Infection, Immunity and Respiratory Medicine, School of Biological Sciences, Faculty of Biology, Medicine and Health, Manchester Academic Health Science Centre, The University of Manchester and University Hospital of South Manchester NHS Foundation Trust, Manchester, M23 9QZ, UK.

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http://dx.doi.org/10.1186/s12931-017-0570-5DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5422866PMC
May 2017

Characteristics and longitudinal progression of chronic obstructive pulmonary disease in GOLD B patients.

BMC Pulm Med 2017 02 20;17(1):42. Epub 2017 Feb 20.

Centre for Respiratory Medicine and Allergy, Institute of Inflammation and Repair, Medicines Evaluation Unit, University Hospital of South Manchester Foundation Trust, University of Manchester, Manchester, UK.

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http://dx.doi.org/10.1186/s12890-017-0384-8DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5319137PMC
February 2017

Clinical Interpretation of Variants from Next-Generation Sequencing: The 2016 Scientific Meeting of the Human Genome Variation Society.

Hum Mutat 2016 10 21;37(10):1110-3. Epub 2016 Aug 21.

Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.

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http://dx.doi.org/10.1002/humu.23059DOI Listing
October 2016

Extension to distributed annotation system: Summary and summaryplot commands.

Conf Proc IEEE Eng Med Biol Soc 2015 ;2015:7655-8

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http://dx.doi.org/10.1109/EMBC.2015.7320165DOI Listing
September 2016

Human genotype-phenotype databases: aims, challenges and opportunities.

Nat Rev Genet 2015 Dec 10;16(12):702-15. Epub 2015 Nov 10.

Institute for Medical Genetics and Human Genetics, and the Berlin Brandenburg Center for Regenerative Therapies, Charité Universitätsmedizin Berlin, 13353 Berlin, Germany.

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http://dx.doi.org/10.1038/nrg3932DOI Listing
December 2015

Data Safe Havens in health research and healthcare.

Bioinformatics 2015 Oct 25;31(20):3241-8. Epub 2015 Jun 25.

Public Population Project in Genomics and Society (PG), Montreal, QC H3A 0G1, Canada, Centre of Genomics and Policy, McGill University, Montreal, QC H3A 0G1, Canada.

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http://dx.doi.org/10.1093/bioinformatics/btv279DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4595892PMC
October 2015

Cafe Variome: general-purpose software for making genotype-phenotype data discoverable in restricted or open access contexts.

Hum Mutat 2015 Oct 25;36(10):957-64. Epub 2015 Aug 25.

Department of Genetics, University of Leicester, Leicester, UK.

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http://dx.doi.org/10.1002/humu.22841DOI Listing
October 2015

The BioMart community portal: an innovative alternative to large, centralized data repositories.

Authors:
Damian Smedley Syed Haider Steffen Durinck Luca Pandini Paolo Provero James Allen Olivier Arnaiz Mohammad Hamza Awedh Richard Baldock Giulia Barbiera Philippe Bardou Tim Beck Andrew Blake Merideth Bonierbale Anthony J Brookes Gabriele Bucci Iwan Buetti Sarah Burge Cédric Cabau Joseph W Carlson Claude Chelala Charalambos Chrysostomou Davide Cittaro Olivier Collin Raul Cordova Rosalind J Cutts Erik Dassi Alex Di Genova Anis Djari Anthony Esposito Heather Estrella Eduardo Eyras Julio Fernandez-Banet Simon Forbes Robert C Free Takatomo Fujisawa Emanuela Gadaleta Jose M Garcia-Manteiga David Goodstein Kristian Gray José Afonso Guerra-Assunção Bernard Haggarty Dong-Jin Han Byung Woo Han Todd Harris Jayson Harshbarger Robert K Hastings Richard D Hayes Claire Hoede Shen Hu Zhi-Liang Hu Lucie Hutchins Zhengyan Kan Hideya Kawaji Aminah Keliet Arnaud Kerhornou Sunghoon Kim Rhoda Kinsella Christophe Klopp Lei Kong Daniel Lawson Dejan Lazarevic Ji-Hyun Lee Thomas Letellier Chuan-Yun Li Pietro Lio Chu-Jun Liu Jie Luo Alejandro Maass Jerome Mariette Thomas Maurel Stefania Merella Azza Mostafa Mohamed Francois Moreews Ibounyamine Nabihoudine Nelson Ndegwa Céline Noirot Cristian Perez-Llamas Michael Primig Alessandro Quattrone Hadi Quesneville Davide Rambaldi James Reecy Michela Riba Steven Rosanoff Amna Ali Saddiq Elisa Salas Olivier Sallou Rebecca Shepherd Reinhard Simon Linda Sperling William Spooner Daniel M Staines Delphine Steinbach Kevin Stone Elia Stupka Jon W Teague Abu Z Dayem Ullah Jun Wang Doreen Ware Marie Wong-Erasmus Ken Youens-Clark Amonida Zadissa Shi-Jian Zhang Arek Kasprzyk

Nucleic Acids Res 2015 Jul 20;43(W1):W589-98. Epub 2015 Apr 20.

Center for Translational Genomics and Bioinformatics San Raffaele Scientific Institute, Via Olgettina 58, 20132 Milan, Italy Department of Biological Sciences, Faculty of Science, King Abdulaziz University, Jeddah, Saudi Arabia

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http://dx.doi.org/10.1093/nar/gkv350DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4489294PMC
July 2015

The Human Phenotype Ontology: Semantic Unification of Common and Rare Disease.

Am J Hum Genet 2015 Jul 25;97(1):111-24. Epub 2015 Jun 25.

Institute for Medical and Human Genetics, Charité-Universitätsmedizin Berlin, Augustenburger Platz 1, 13353 Berlin, Germany; Max Planck Institute for Molecular Genetics, Ihnestrasse 63-73, 14195 Berlin, Germany; Berlin Brandenburg Center for Regenerative Therapies, Charité-Universitätsmedizin Berlin, Augustenburger Platz 1, 13353 Berlin, Germany; Institute of Bioinformatics, Department of Mathematics and Computer Science, Freie Universität Berlin, Takustrasse 9, 14195 Berlin, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2015.05.020DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4572507PMC
July 2015

Germline & somatic mosaicism: the 2014 annual scientific meeting of the Human Genome Variation Society.

Hum Mutat 2015 Mar;36(3):390-3

Department of Experimental and Clinical Pharmacology, University of Minnesota, Minneapolis, Minnesota.

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http://dx.doi.org/10.1002/humu.22757DOI Listing
March 2015

GWAS Central: a comprehensive resource for the comparison and interrogation of genome-wide association studies.

Eur J Hum Genet 2014 Jul 4;22(7):949-52. Epub 2013 Dec 4.

Department of Genetics, University of Leicester, Leicester, UK.

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http://dx.doi.org/10.1038/ejhg.2013.274DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4060122PMC
July 2014

HGV2012: leveraging next-generation technology and large datasets to advance disease research.

Hum Mutat 2013 Apr;34(4):657-60

Institute for Human Genetics and Cardiovascular Research Institute, University of California, San Francisco, CA, USA.

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http://doi.wiley.com/10.1002/humu.22270
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http://dx.doi.org/10.1002/humu.22270DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3606662PMC
April 2013

Semantically enabling a genome-wide association study database.

J Biomed Semantics 2012 Dec 17;3(1). Epub 2012 Dec 17.

Department of Genetics, University of Leicester, University Road, Leicester, UK.

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http://dx.doi.org/10.1186/2041-1480-3-9DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3579732PMC
December 2012

Solving bottlenecks in data sharing in the life sciences.

Hum Mutat 2012 Oct 18;33(10):1494-6. Epub 2012 Jun 18.

Department of Genetics, University of Leicester, Leicester, United Kingdom.

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http://dx.doi.org/10.1002/humu.22123DOI Listing
October 2012

Knowledge engineering for health: a new discipline required to bridge the "ICT gap" between research and healthcare.

Hum Mutat 2012 May 4;33(5):797-802. Epub 2012 Apr 4.

Department of Genetics, University of Leicester, Leicester, United Kingdom.

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http://dx.doi.org/10.1002/humu.22066DOI Listing
May 2012

HGV2011: personalized genomic medicine meets the incidentalome.

Hum Mutat 2012 Mar 17;33(3):582-5. Epub 2012 Jan 17.

Department of Statistics, University of California-Berkeley, Berkeley, California, USA.

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http://doi.wiley.com/10.1002/humu.22008
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http://dx.doi.org/10.1002/humu.22008DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3867005PMC
March 2012

Targeted enrichment of genomic DNA regions for next-generation sequencing.

Brief Funct Genomics 2011 Nov 26;10(6):374-86. Epub 2011 Nov 26.

Max Planck Institute for Molecular Genetics, Berlin, Germany.

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http://dx.doi.org/10.1093/bfgp/elr033DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3245553PMC
November 2011

An informatics project and online "Knowledge Centre" supporting modern genotype-to-phenotype research.

Hum Mutat 2011 May 22;32(5):543-50. Epub 2011 Mar 22.

Department of Genetics, University of Leicester, University Road, Leicester, United Kingdom.

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http://dx.doi.org/10.1002/humu.21469DOI Listing
May 2011

The MOLGENIS toolkit: rapid prototyping of biosoftware at the push of a button.

BMC Bioinformatics 2010 Dec 21;11 Suppl 12:S12. Epub 2010 Dec 21.

Genomics Coordination Center, Groningen Bioinformatics Center, University of Groningen & Department of Genetics, University Medical Center Groningen, P.O. Box 30001, 9700 RB Groningen, The Netherlands.

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http://www.biomedcentral.com/content/pdf/1471-2105-11-S12-S1
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http://www.biomedcentral.com/1471-2105/11/S12/S12
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http://dx.doi.org/10.1186/1471-2105-11-S12-S12DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3040526PMC
December 2010

Locus-specific database domain and data content analysis: evolution and content maturation toward clinical use.

Hum Mutat 2010 Oct;31(10):1109-16

Erasmus MC, Faculty of Medicine and Health Sciences, MGC-Department of Cell Biology and Genetics, Rotterdam, The Netherlands.

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http://dx.doi.org/10.1002/humu.21332DOI Listing
October 2010

Genetic structures of copy number variants revealed by genotyping single sperm.

PLoS One 2009 22;4(4):e5236. Epub 2009 Apr 22.

Department of Molecular Genetics, Microbiology, and Immunology/The Cancer Institute of New Jersey, University of Medicine and Dentistry of New Jersey Robert Wood Johnson Medical School, Piscataway, New Jersey, United States of America.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0005236PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2668179PMC
June 2009

HGVbaseG2P: a central genetic association database.

Nucleic Acids Res 2009 Jan 23;37(Database issue):D797-802. Epub 2008 Oct 23.

Department of Genetics, University of Leicester, University Road, Leicester, LE1 7RH, UK.

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http://dx.doi.org/10.1093/nar/gkn748DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2686551PMC
January 2009

Genotype-phenotype databases: challenges and solutions for the post-genomic era.

Nat Rev Genet 2009 Jan;10(1):9-18

Department of Genetics, University of Leicester, University Road, Leicester LE1 7RH, UK.

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http://dx.doi.org/10.1038/nrg2483DOI Listing
January 2009

Defensins and the dynamic genome: what we can learn from structural variation at human chromosome band 8p23.1.

Genome Res 2008 Nov;18(11):1686-97

Department of Genetics, University of Leicester, Leicester LE1 7RH, United Kingdom.

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http://dx.doi.org/10.1101/gr.080945.108DOI Listing
November 2008

SNPs meet CNVs in genome-wide association studies: HGV2007 meeting report.

PLoS Genet 2008 Apr 25;4(4):e1000068. Epub 2008 Apr 25.

Genes and Disease Program, Center for Genomic Regulation (CRG-UPF), Barcelona, Spain.

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http://dx.doi.org/10.1371/journal.pgen.1000068DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2330071PMC
April 2008

Association of ADRB1 and UCP3 gene polymorphisms with insulin sensitivity but not obesity.

Horm Res 2008 4;69(1):31-6. Epub 2007 Dec 4.

Department of Molecular Medicine, National Public Health Institute, University of Helsinki, Biomedicum, Helsinki, Finland.

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http://search.proquest.com/openview/6fb09676703fb7291a2096af
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http://www.karger.com/doi/10.1159/000111793
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http://dx.doi.org/10.1159/000111793DOI Listing
January 2008

MegaPlex PCR: a strategy for multiplex amplification.

Nat Methods 2007 Oct 16;4(10):835-7. Epub 2007 Sep 16.

Department of Genetics, University of Leicester, University Road, Leicester, LE1 7RH, UK.

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http://dx.doi.org/10.1038/nmeth1091DOI Listing
October 2007

Association of arthritis with a gene complex encoding C-type lectin-like receptors.

Arthritis Rheum 2007 Aug;56(8):2620-32

Department of Medicine, Rheumatology Unit, Karolinska Institutet, Karolinska University Hospital, S-17176 Stockholm, Sweden.

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http://dx.doi.org/10.1002/art.22813DOI Listing
August 2007

DNA diagnostics by surface-bound melt-curve reactions.

J Mol Diagn 2007 Feb;9(1):30-41

Department of Genetics, University of Leicester, University Rd., Leicester, LE1 7RH, UK.

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http://dx.doi.org/10.2353/jmoldx.2007.060057DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1867427PMC
February 2007

Seventh international meeting on single nucleotide polymorphism and complex genome analysis: 'ever bigger scans and an increasingly variable genome'.

Hum Genet 2006 May 24;119(4):451-6. Epub 2006 Feb 24.

Genus Cambridge Research Laboratory, University of Cambridge, Department of Pathology, Genus plc, Tennis Court Road, CB2 1QP, Cambridge, UK.

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http://dx.doi.org/10.1007/s00439-006-0151-zDOI Listing
May 2006

Quantitative trait loci in ABCA1 modify cerebrospinal fluid amyloid-beta 1-42 and plasma apolipoprotein levels.

J Hum Genet 2006 22;51(3):171-9. Epub 2005 Dec 22.

Centre for Genomics and Bioinformatics, Karolinska Institute, Berzelius väg 35, 171 77 Stockholm, Sweden.

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http://www.nature.com/doifinder/10.1007/s10038-005-0341-x
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http://dx.doi.org/10.1007/s10038-005-0341-xDOI Listing
April 2006

Rapid melting curve analysis on monolayered beads for high-throughput genotyping of single-nucleotide polymorphisms.

Anal Chem 2006 Apr;78(7):2220-5

Department of Signals, Sensors and Systems, Microsystem Technology, Royal Institute of Technology, 100 44 Stockholm, Sweden.

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http://pubs.acs.org/doi/abs/10.1021/ac051771u
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http://dx.doi.org/10.1021/ac051771uDOI Listing
April 2006

Towards compendia of negative genetic association studies: an example for Alzheimer disease.

Hum Genet 2006 Mar 8;119(1-2):29-37. Epub 2005 Dec 8.

Center for Genomics and Bioinformatics, Karolinska Institute, Berzeliusvag 35, 171 77 Stockholm, Sweden.

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http://dx.doi.org/10.1007/s00439-005-0078-9DOI Listing
March 2006

Longitudinal memory performance during normal aging: twin association models of APOE and other Alzheimer candidate genes.

Behav Genet 2006 Mar 10;36(2):185-94. Epub 2006 Jan 10.

Department of Psychology, University of California--Riverside, 92521, USA.

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http://link.springer.com/10.1007/s10519-005-9027-6
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http://dx.doi.org/10.1007/s10519-005-9027-6DOI Listing
March 2006

Mutation screening of a haplotype block around the insulin degrading enzyme gene and association with Alzheimer's disease.

Am J Med Genet B Neuropsychiatr Genet 2005 Jul;136B(1):69-71

Center for Genomics and Bioinformatics, Karolinska Institute, Stockholm, Sweden.

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http://dx.doi.org/10.1002/ajmg.b.30172DOI Listing
July 2005

Genetic association analysis: lessons from the study of Alzheimers disease.

Mutat Res 2005 Jun;573(1-2):152-9

Department of Genetics, University of Leicester, University Road, Leicester LE1 7RH, UK.

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http://dx.doi.org/10.1016/j.mrfmmm.2004.08.017DOI Listing
June 2005

DNA, diseases and databases: disastrously deficient.

Trends Genet 2005 Jun;21(6):333-8

Erasmus University Medical Center, Faculty of Medicine and Health Sciences, MGC-Department of Cell Biology and Genetics, PO Box 1738, 3000 DR Rotterdam, The Netherlands.

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http://dx.doi.org/10.1016/j.tig.2005.04.004DOI Listing
June 2005

Linkage disequilibrium patterns vary substantially among populations.

Eur J Hum Genet 2005 May;13(5):677-86

Center for Genomics and Bioinformatics, Karolinska Institute, Berzelius väg 35, Stockholm 17177, Sweden.

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http://dx.doi.org/10.1038/sj.ejhg.5201368DOI Listing
May 2005

Haplotype block structures show significant variation among populations.

Genet Epidemiol 2004 Dec;27(4):385-400

Department of Epidemiology and Public Health, Yale University School of Medicine, New Haven, Connecticut 06510, USA.

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http://dx.doi.org/10.1002/gepi.20026DOI Listing
December 2004

Lower rate of genomic variation identified in the trans-membrane domain of monoamine sub-class of Human G-Protein Coupled Receptors: the Human GPCR-DB Database.

BMC Genomics 2004 Dec 4;5:91. Epub 2004 Dec 4.

Center for Genomics and Bioinformatics, Karolinska Institutet, Berzelius väg 35, 17177 Stockholm, Sweden.

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http://dx.doi.org/10.1186/1471-2164-5-91DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC538281PMC
December 2004

Genetic analysis of the RNASEL gene in hereditary, familial, and sporadic prostate cancer.

Clin Cancer Res 2004 Nov;10(21):7150-6

Department of Radiation Sciences, Oncology, and Medical Biosciences, Pathology, University of Umeå, Umeå, Sweden.

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http://dx.doi.org/10.1158/1078-0432.CCR-04-0982DOI Listing
November 2004

Genotyping by dynamic heating of monolayered beads on a microheated surface.

Electrophoresis 2004 Nov;25(21-22):3712-9

Department of Signals, Sensors and Systems, Microsystem Technology, Royal Institute of Technology, Stockholm, Sweden.

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http://dx.doi.org/10.1002/elps.200406065DOI Listing
November 2004

Complex SNP-related sequence variation in segmental genome duplications.

Nat Genet 2004 Aug 11;36(8):861-6. Epub 2004 Jul 11.

Center for Genomics and Bioinformatics, Karolinska Institute, Berzelius väg 35, S-171 77 Stockholm, Sweden.

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http://dx.doi.org/10.1038/ng1401DOI Listing
August 2004

Quantitative trait loci near the insulin-degrading enzyme (IDE) gene contribute to variation in plasma insulin levels.

Diabetes 2004 Aug;53(8):2137-42

Department of Molecular Medicine, Rolf Luft Center for Diabetes Research, Karolinska Hospital, Stockholm, Sweden.

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http://dx.doi.org/10.2337/diabetes.53.8.2137DOI Listing
August 2004

Sequence variation in the proximity of IDE may impact age at onset of both Parkinson disease and Alzheimer disease.

Neurogenetics 2004 Jun 16;5(2):115-9. Epub 2004 Apr 16.

Center for Genomics and Bioinformatics, Karolinska Institute, Stockholm, Sweden.

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http://dx.doi.org/10.1007/s10048-004-0173-4DOI Listing
June 2004

Integrative annotation of 21,037 human genes validated by full-length cDNA clones.

Authors:
Tadashi Imanishi Takeshi Itoh Yutaka Suzuki Claire O'Donovan Satoshi Fukuchi Kanako O Koyanagi Roberto A Barrero Takuro Tamura Yumi Yamaguchi-Kabata Motohiko Tanino Kei Yura Satoru Miyazaki Kazuho Ikeo Keiichi Homma Arek Kasprzyk Tetsuo Nishikawa Mika Hirakawa Jean Thierry-Mieg Danielle Thierry-Mieg Jennifer Ashurst Libin Jia Mitsuteru Nakao Michael A Thomas Nicola Mulder Youla Karavidopoulou Lihua Jin Sangsoo Kim Tomohiro Yasuda Boris Lenhard Eric Eveno Yoshiyuki Suzuki Chisato Yamasaki Jun-ichi Takeda Craig Gough Phillip Hilton Yasuyuki Fujii Hiroaki Sakai Susumu Tanaka Clara Amid Matthew Bellgard Maria de Fatima Bonaldo Hidemasa Bono Susan K Bromberg Anthony J Brookes Elspeth Bruford Piero Carninci Claude Chelala Christine Couillault Sandro J de Souza Marie-Anne Debily Marie-Dominique Devignes Inna Dubchak Toshinori Endo Anne Estreicher Eduardo Eyras Kaoru Fukami-Kobayashi Gopal R Gopinath Esther Graudens Yoonsoo Hahn Michael Han Ze-Guang Han Kousuke Hanada Hideki Hanaoka Erimi Harada Katsuyuki Hashimoto Ursula Hinz Momoki Hirai Teruyoshi Hishiki Ian Hopkinson Sandrine Imbeaud Hidetoshi Inoko Alexander Kanapin Yayoi Kaneko Takeya Kasukawa Janet Kelso Paul Kersey Reiko Kikuno Kouichi Kimura Bernhard Korn Vladimir Kuryshev Izabela Makalowska Takashi Makino Shuhei Mano Regine Mariage-Samson Jun Mashima Hideo Matsuda Hans-Werner Mewes Shinsei Minoshima Keiichi Nagai Hideki Nagasaki Naoki Nagata Rajni Nigam Osamu Ogasawara Osamu Ohara Masafumi Ohtsubo Norihiro Okada Toshihisa Okido Satoshi Oota Motonori Ota Toshio Ota Tetsuji Otsuki Dominique Piatier-Tonneau Annemarie Poustka Shuang-Xi Ren Naruya Saitou Katsunaga Sakai Shigetaka Sakamoto Ryuichi Sakate Ingo Schupp Florence Servant Stephen Sherry Rie Shiba Nobuyoshi Shimizu Mary Shimoyama Andrew J Simpson Bento Soares Charles Steward Makiko Suwa Mami Suzuki Aiko Takahashi Gen Tamiya Hiroshi Tanaka Todd Taylor Joseph D Terwilliger Per Unneberg Vamsi Veeramachaneni Shinya Watanabe Laurens Wilming Norikazu Yasuda Hyang-Sook Yoo Marvin Stodolsky Wojciech Makalowski Mitiko Go Kenta Nakai Toshihisa Takagi Minoru Kanehisa Yoshiyuki Sakaki John Quackenbush Yasushi Okazaki Yoshihide Hayashizaki Winston Hide Ranajit Chakraborty Ken Nishikawa Hideaki Sugawara Yoshio Tateno Zhu Chen Michio Oishi Peter Tonellato Rolf Apweiler Kousaku Okubo Lukas Wagner Stefan Wiemann Robert L Strausberg Takao Isogai Charles Auffray Nobuo Nomura Takashi Gojobori Sumio Sugano

PLoS Biol 2004 Jun 20;2(6):e162. Epub 2004 Apr 20.

Integrated Database Group, Biological Information Research Center, National Institute of Advanced Industrial Science and Technology, Tokyo, Japan.

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http://dx.doi.org/10.1371/journal.pbio.0020162DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC393292PMC
June 2004

Variants of CYP46A1 may interact with age and APOE to influence CSF Abeta42 levels in Alzheimer's disease.

Hum Genet 2004 May 18;114(6):581-7. Epub 2004 Mar 18.

Department of Clinical Neuroscience, Sahlgrenska University Hospital, Göteborg University, Göteborg, Sweden.

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http://dx.doi.org/10.1007/s00439-004-1107-9DOI Listing
May 2004

Common variants of ACE contribute to variable age-at-onset of Alzheimer's disease.

Hum Genet 2004 Apr 17;114(5):478-83. Epub 2004 Feb 17.

Department of Care of the Elderly, The John James Building, Frenchay Hospital, University of Bristol, UK.

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http://dx.doi.org/10.1007/s00439-004-1093-yDOI Listing
April 2004

Genetic variation in CTNNA3 encoding alpha-3 catenin and Alzheimer's disease.

Neurosci Lett 2004 Apr;358(3):220-2

Center for Genomics and Bioinformatics, Karolinska Institute, Berzeliusvag 35, S-171 77 Stockholm, Sweden.

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http://dx.doi.org/10.1016/j.neulet.2004.01.032DOI Listing
April 2004

Single nucleotide polymorphisms in the proximal promoter region of the adiponectin (APM1) gene are associated with type 2 diabetes in Swedish caucasians.

Diabetes 2004 Feb;53 Suppl 1:S31-5

Rolf Luft Center for Diabetes Research, Department of Molecular Medicine, Karolinska Hospital, Stockholm, Sweden.

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http://dx.doi.org/10.2337/diabetes.53.2007.s31DOI Listing
February 2004

Genetic variation in a haplotype block spanning IDE influences Alzheimer disease.

Hum Mutat 2003 Nov;22(5):363-71

Center for Genomics and Bioinformatics, Karolinska Institute, Stockholm, Sweden.

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http://doi.wiley.com/10.1002/humu.10282
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http://dx.doi.org/10.1002/humu.10282DOI Listing
November 2003

Scoring insertion-deletion polymorphisms by dynamic allele-specific hybridization.

Biotechniques 2003 Aug;35(2):292-6, 298

Karolinska Institute, Stockholm, Sweden.

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http://dx.doi.org/10.2144/03352st01DOI Listing
August 2003