about
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot projectEmergence of young human genes after a burst of retroposition in primatesEvolutionary comparison provides evidence for pathogenicity of RMRP mutations.A high-resolution anatomical atlas of the transcriptome in the mouse embryoThe GENCODE pseudogene resourceGENCODE: producing a reference annotation for ENCODEEGASP: the human ENCODE Genome Annotation Assessment ProjectEvidence for transcript networks composed of chimeric RNAs in human cellsEvidence for interaction between human PRUNE and nm23-H1 NDPKinasePseudogenes in the ENCODE regions: consensus annotation, analysis of transcription, and evolutionTandem chimerism as a means to increase protein complexity in the human genomeThe genome sequence of taurine cattle: a window to ruminant biology and evolutionSequence and comparative analysis of the chicken genome provide unique perspectives on vertebrate evolutionInitial sequencing and comparative analysis of the mouse genomeMlx, a new Max-like bHLHZip family member: the center stage of a novel transcription factors regulatory pathway?Submicroscopic deletion in patients with Williams-Beuren syndrome influences expression levels of the nonhemizygous flanking genesWBSCR14, a gene mapping to the Williams--Beuren syndrome deleted region, is a new member of the Mlx transcription factor networkThe tripartite motif family identifies cell compartments.The subcellular localization of the ChoRE-binding protein, encoded by the Williams-Beuren syndrome critical region gene 14, is regulated by 14-3-3The Caenorhabditis elegans ortholog of C21orf80, a potential new protein O-fucosyltransferase, is required for normal developmentThe transmembrane serine protease (TMPRSS3) mutated in deafness DFNB8/10 activates the epithelial sodium channel (ENaC) in vitroThe human ROX gene: genomic structure and mutation analysis in human breast tumorsComparative gene finding in chicken indicates that we are closing in on the set of multi-exonic widely expressed human genesGENCODE: the reference human genome annotation for The ENCODE ProjectStructured RNAs in the ENCODE selected regions of the human genomeProminent use of distal 5' transcription start sites and discovery of a large number of additional exons in ENCODE regionsGene finding in the chicken genomeReciprocal Effects on Neurocognitive and Metabolic Phenotypes in Mouse Models of 16p11.2 Deletion and Duplication SyndromesPhenotypic consequences of copy number variation: insights from Smith-Magenis and Potocki-Lupski syndrome mouse modelsNineteen additional unpredicted transcripts from human chromosome 21From PREDs and open reading frames to cDNA isolation: revisiting the human chromosome 21 transcription mapIdentification of additional transcripts in the Williams-Beuren syndrome critical regionChromosome 21: a small land of fascinating disorders with unknown pathophysiologyA novel TMPRSS3 missense mutation in a DFNB8/10 family prevents proteolytic activation of the proteinMolecular cloning and characterization of a novel retinoblastoma-binding proteinChromosome 21 and down syndrome: from genomics to pathophysiologyUsing transcription modules to identify expression clusters perturbed in Williams-Beuren syndromeThe TPTE gene family: cellular expression, subcellular localization and alternative splicingThe implications of alternative splicing in the ENCODE protein complementIdentification and removal of low-complexity sites in allele-specific analysis of ChIP-seq data.
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description
human geneticist from Lausanne, Switzerland
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onderzoeker
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name
Alexandre Reymond
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Alexandre Reymond
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Alexandre Reymond
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Alexandre Reymond
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Alexandre Reymond
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type
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Alexandre Reymond
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Alexandre Reymond
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Alexandre Reymond
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Alexandre Reymond
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Alexandre Reymond
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Alexandre Reymond
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Alexandre Reymond
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Alexandre Reymond
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Alexandre Reymond
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Alexandre Reymond
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P106
P2038
Alexandre_Reymond
P21
P214
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P31
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