article Open AccessTop 1% cited
DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources
The American Journal of Human Genetics · 2009 · Vol. 84(4) · pp. 524–533
Helen V. Firth✉(University of Cambridge)Shola M. Richards(Wellcome Sanger Institute)A. Paul Bevan(Wellcome Sanger Institute)Stephen Clayton(Wellcome Sanger Institute)Manuel Corpas(Wellcome Sanger Institute)Diana Rajan(Wellcome Sanger Institute)Steven Van Vooren(KU Leuven)Yves Moreau(KU Leuven)Roger Pettett(Wellcome Sanger Institute)Nigel P. Carter(Wellcome Sanger Institute)
Genomic variations and chromosomal abnormalitiesCongenital heart defects researchGenomics and Rare DiseasesDECIPHEREnsemblPhenotypeBiologyComputational biologyGeneticsGenomicsGeneGenome
MeSH terms
AdultChildChild, PreschoolChromosome AberrationsFemaleGenes, DominantHumansMalePhenotypeSyndromeGenome, HumanGene DosageComputational BiologyInternetDatabases, Genetic
Funding
- Wellcome Trust
Citations
2,072
FWCI
27.83
field-weighted impact
References
42
Percentile
100%
vs. same field & year
Citations per year
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References
Familial Adenomatous Polyposis
The American Journal of Gastroenterology · 2006 · 744 citations
Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features
Journal of Medical Genetics · 2004 · 508 citations
Detection of large-scale variation in the human genome
Nature Genetics · 2004 · 2,910 citations
Initial sequencing and analysis of the human genome
Nature · 2001 · 24,452 citations
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DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources
The American Journal of Human Genetics · 2009 · 2,072 citations
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