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Author Details

Arnaud Gos
Centre Medical Universitaire
1992
22
16
PMIDPaper TitleJournal TitlePublished Year
36866529The Gene Ontology knowledgebase in 2023.Genetics2023
32716361A Coordinated Approach by Public Domain Bioinformatics Resources to Aid the Fight Against Alzheimer's Disease Through Expert Curation of Key Protein Targets.J Alzheimers Dis2020
24848695Genetic variations and diseases in UniProtKB/Swiss-Prot: the ins and outs of expert manual curation.Hum Mutat2014
23161678Gene Ontology annotations and resources.Nucleic Acids Res2013
22123736The UniProt-GO Annotation database in 2011.Nucleic Acids Res2012
18175334Annotating single amino acid polymorphisms in the UniProt/Swiss-Prot knowledgebase.Hum Mutat2008
10598804A testis-specific gene, TPTE, encodes a putative transmembrane tyrosine phosphatase and maps to the pericentromeric region of human chromosomes 21 and 13, and to chromosomes 15, 22, and Y.Hum Genet1999
10393427Assignment of the human dynein heavy chain gene DNAH17L to human chromosome 17p12 by in situ hybridization and radiation hybrid mapping.Cytogenet Cell Genet1999
10049735Isolation and characterization of the mouse Aire gene.Biochem Biophys Res Commun1999
9826911Gene structure and chromosomal localization of the human P2X7 receptor.Recept Channels1998
9032654Fortuitous detection of uniparental isodisomy of chromosome 6.J Med Genet1997
9188657Familial translocation t(Y;15)(q12;p11) and de novo deletion of the Prader-Willi syndrome (PWS) critical region on 15q11-q13.Am J Med Genet1997
9401005Analysis of mutations and chromosomal localisation of the gene encoding RFX5, a novel transcription factor affected in major histocompatibility complex class II deficiency.Hum Mutat1997
8660980The gene for human U2 snRNP auxiliary factor small 35-kDa subunit (U2AF1) maps to the progressive myoclonus epilepsy (EPM1) critical region on chromosome 21q22.3.Genomics1996
8812505Localization of a human homolog of the mouse pericentrin gene (PCNT) to chromosome 21qter.Genomics1996
8660983Mapping of the gene for the p60 subunit of the human chromatin assembly factor (CAF1A) to the Down syndrome region of chromosome 21.Genomics1996
7644464Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.Proc Natl Acad Sci U S A1995
8834001Characterization and chromosomal localization of a human P2X receptor from the urinary bladder.Recept Channels1995
7762575Schizophrenia and chromosomal deletions within 22q11.2.Am J Hum Genet1995
7668265A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombination.Am J Hum Genet1995
7647800Single-minded and Down syndrome?Nat Genet1995
1426044Polarized secretion of urokinase-type plasminogen activator by epithelial cells.Exp Cell Res1992
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Collaborators

Co-authored papers 14
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European Bioinformatics Institute (EMBL-EBI)
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carnegie mellon university
Co-authored papers 4
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University College London, Institute for Cardiovascular Science
Co-authored papers 3
carnegie mellon university
Co-authored papers 3
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Co-authored papers 3
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Co-authored papers 3
carnegie mellon university
Co-authored papers 3
carnegie mellon university - 1 rue Michel Servet CH-1 Geneva 4
Co-authored papers 3
carnegie mellon university
Co-authored papers 3
carnegie mellon university - 1 rue Michel Servet CH-1 Geneva 4
Co-authored papers 3
Centre Medical Universitaire
Co-authored papers 3
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University of Lausanne
Co-authored papers 3
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carnegie mellon university
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European Bioinformatics Institute (EMBL-EBI)
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Co-authored papers 2
California Institute of Technology
Co-authored papers 2
Center for Genetic Medicine, Northwestern University.
Co-authored papers 2