In one paragraphArticle in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
2 · The registryThe trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
3 · Its place in the literatureWho cites it
0 citing papers in PubMed, 1 citations in OpenAlex.
No citing paper in PubMed yet.
4 · The recordCorrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
5 · Who and what moneyAuthors and funding
11 authors at 6 institutions in 1 country.
Jianli DuanCenter for Precision Disease Modeling, Department of Medicine, University of Maryland School of Medicine, MD 21201, USA.ORCID 0000-0001-7347-4774 Pei WenCenter for Precision Disease Modeling, Department of Medicine, University of Maryland School of Medicine, MD 21201, USA.ORCID 0000-0001-7065-6396 Yunpo ZhaoCenter for Precision Disease Modeling, Department of Medicine, University of Maryland School of Medicine, MD 21201, USA.ORCID 0000-0002-7942-3406 Joyce van de LeemputCenter for Precision Disease Modeling, Department of Medicine, University of Maryland School of Medicine, MD 21201, USA.ORCID 0000-0003-1903-7295 Jennifer Lai YeeDivision of Nephrology, Department of Pediatric, University of Michigan School of Medicine, Ann Arbor, MI 48105, USA.
Damian FerminDivision of Nephrology, Department of Internal Medicine, University of Michigan School of Medicine, Ann Arbor, MI 48105, USA.
Bradley A WaradyDivision of Pediatric Nephrology, Children's Mercy Kansas City, Kansas City, MO 64108, USA.
Derek K NgDepartment of Epidemiology, Johns Hopkins Bloomberg School of Public Health, MD 21205, USA.
Matthew G SampsonDivision of Nephrology, Department of Pediatrics, Boston Children's Hospital, Boston, MA 02115, USA.ORCID 0000-0001-9560-076X Zhe HanCenter for Precision Disease Modeling, Department of Medicine, University of Maryland School of Medicine, MD 21201, USA.ORCID 0000-0002-5177-7798 University of Maryland, Baltimore · USUniversity of Michigan · USBroad Institute · USChildren's Hospital of Philadelphia · USChildren's Mercy Hospital · USJohns Hopkins University · US
Funding
Chronic Kidney Disease in Children Study (C-Kid)U01DK066174 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI SUSAN L. FURTH · 2003 to 2026
$25.1MCKiD Cardiovascular Testing Travel SupplementU01DK066143 · NIDDK · CHILDREN'S MERCY HOSP (KANSAS CITY, MO) · PI Bradley Alan Warady · 2003 to 2026
$24.2MThe Kidney Disease in Children Data Management and Analysis Center (KIDMAC)U24DK066116 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI Derek K Ng · 2018 to 2026
$12.6MIntegrating large scale genomics and functional studies to accelerate FSGS/NS discoveryRC2DK122397 · NIDDK · BETH ISRAEL DEACONESS MEDICAL CENTER · PI HILDEBRANDT, FRIEDHELM, POLLAK, MARTIN R. · 2020 to 2024
$7.4MWhole Genome Sequencing for Nephrotic Syndrome DiscoveryR01DK119380 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI Dongwon Lee, MATTHEW Gordon SAMPSON · 2019 to 2026
$3.7MModeling Nephrotic Syndrome in Drosophila NephrocytesR01DK098410 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI HAN, ZHE · 2014 to 2022
$3.3MCentral Biochemistry Laboratory of the CKID ConsortiumU24DK082194 · NIDDK · UNIVERSITY OF ROCHESTER · PI SCHWARTZ, GEORGE J · 2018 to 2022
$1.7MNIDDK NIH HHS R01 DK098410NIDDK NIH HHS R01 DK119380NIDDK NIH HHS RC2 DK122397NIDDK NIH HHS U01 DK066143NIDDK NIH HHS U01 DK066174NIDDK NIH HHS U24 DK066116NIDDK NIH HHS U24 DK082194
6 · The paper itselfAbstract
Alport syndrome is a hereditary chronic kidney disease, attributed to rare pathogenic variants in either of three collagen genes (
Indexed as
Alport SyndromeCOL4A5Drosophilaglomerular basement membranenephrocytevariant functional screen
Identifiers
PMID38559272
PMCPMC10979928
OpenAlexW4392725654
What OpenQuestion holds
Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390