Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome is a research paper published in Nature Genetics (2006). On theSindex it has a DataRank of 0.976. It has been cited 668 times.
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Base Score Contribution
0.976
From this paper's citation signal
Citation Network Contribution
0
Citation network not refreshed for this result
This paper's DataRank is currently driven only by its base citation score. Citation network data was not refreshed for this result.
Learn more about DataRank methodology →NICHD NIH HHS
Grant: HD043569
National Institutes of Health
Grant: 5R01HD043569-04
SEGMENTAL ANEUSOMY BETWEEN BLOCKS OF DUPLICATED DNA
Wellcome Trust
Grant: unidentified
unidentified
Fields of Study
MeSH Terms
Keywords
Additional file 1 of Characterizing sensitivity and coverage of clinical WGS as a diagnostic test for genetic disorders
Additional file 1 of Characterizing sensitivity and coverage of clinical WGS as a diagnostic test for genetic disorders
Additional file 1 of Sex-specific recombination patterns predict parent of origin for recurrent genomic disorders
Additional file 1 of Sex-specific recombination patterns predict parent of origin for recurrent genomic disorders
Additional file 2 of Sequencing individual genomes with recurrent genomic disorder deletions: an approach to characterize genes for autosomal recessive rare disease traits
Additional file 2 of Sequencing individual genomes with recurrent genomic disorder deletions: an approach to characterize genes for autosomal recessive rare disease traits
Additional file 3 of Sequencing individual genomes with recurrent genomic disorder deletions: an approach to characterize genes for autosomal recessive rare disease traits
Additional file 3 of Sequencing individual genomes with recurrent genomic disorder deletions: an approach to characterize genes for autosomal recessive rare disease traits
Additional file 1 of Sequencing individual genomes with recurrent genomic disorder deletions: an approach to characterize genes for autosomal recessive rare disease traits
Additional file 1 of Sequencing individual genomes with recurrent genomic disorder deletions: an approach to characterize genes for autosomal recessive rare disease traits
Additional file 2 of Characterizing sensitivity and coverage of clinical WGS as a diagnostic test for genetic disorders
Additional file 2 of Characterizing sensitivity and coverage of clinical WGS as a diagnostic test for genetic disorders