Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice is a research paper published in Human Molecular Genetics (2020). On theSindex it has a DataRank of 0. It has been cited 26 times.
Scored on demand from live citation data
Linked data & code
DataRank reads this dataset's downstream impact straight off the citation graph — no black box, no proprietary weighting. How is this computed?
FAIR checklist signals are shown for context only and do not affect DataRank scoring.
We only score data papers we can read in full — never from an abstract alone.
Baylor-Hopkins Center for Mendelian Genomics
Grant: UM1 HG006542
National Institutes of Health
Grant: R03HD099516
National Institute of Health, National Institute of Diabetes and Digestive and Kidney Diseases
Grant: R01DK080099
Agence Nationale de la Recherche
Grant: ANR-10-IAHU-01
National Health and Medical Research Council
Grant: ID1042002
National Health and Medical Research Council
Grant: ID1135886
National Health and Medical Research Council
Grant: ID1044543
NICHD NIH HHS
Grant: P50 HD103538
MSD Avenir
NSW Government
FWCI
1.12
Citation Percentile
0.8%
Citation Trend
Fields of Study
MeSH Terms
Keywords
Sustainable Development Goals