Expanding the spectrum of novel candidate genes using trio exome sequencing and identification of monogenic cause in 27.5% of 320 families with steroid-resistant nephrotic syndrome is a research paper published in Genes & Diseases (2024). On theSindex it has a DataRank of 0.208. It has been cited 3 times.
Scored on demand from live citation data
DataRank reads this dataset's downstream impact straight off the citation graph — no black box, no proprietary weighting. How is this computed?
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Base Score Contribution
0.208
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 →National Human Genome Research Institute
Grant: U54 HG006504
Harvard Stem Cell Institute
Grant: DK122766
NIH
Grant: 5R01DK076683\u201313
NIH
Grant: RC2-DK122397
Deutsche Forschungsgemeinschaft
Grant: 403877094
Deutsche Forschungsgemeinschaft
Grant: K08-DK127011
Deutsche Forschungsgemeinschaft
Grant: 442070894
Deutsche Forschungsgemeinschaft
Grant: KO 6579/2-1
NIDDK NIH HHS
Grant: K08 DK125768
NCATS NIH HHS
Grant: UL1 TR001863
National Institutes of Health
Grant: 1K08DK125768-01A1
Delineation of pathogenic mechanisms of NOS1AP and TRIM8 mutations in monogenic SRNS/FSGS.
National Institutes of Health
Grant: 1K08DK127011-01
Discovery and pathogenic characterization of novel monogenic causes of bladder dysfunction.
Canadian Institutes of Health Research
Grant: unidentified
unidentified
National Institutes of Health
Grant: 5T32DK007726-27
Research Training in Pediatric Nephrology
National Institutes of Health
Grant: 3RC2DK122397-04S1
Integrating large scale genomics and functional studies to accelerate FSGS/NS discovery
National Institutes of Health
Grant: 1U54HG006504-01
Yale Center for Mendelian Disorders
National Institutes of Health
Grant: 5K12HD052896-13
Child Health ResearcH Career Development Award (CHRCDA) Program (K12)
National Institutes of Health
Grant: 5R01DK076683-08
Discover and functionally characterize full-penetrance causes of nephrosis/FSGS
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