ArticlebioRxiv : the preprint server for biology2025
Long-Read Sequencing of the
Abstract readPreprint
In one paragraph
Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
0numbers the graph read from it
0cells of the map it votes in
1citing 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.
The 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.
Who cites it
1 citing paper in PubMed.
- A Whole-Exome Sequencing-Based Exploration of Chronic Kidney Disease of Unknown Etiology (CKDu) in an Endemic Population in Sri Lanka.International journal of molecular sciences · 2026Article
Corrections and comments
- Updated by
Authors and funding
43 authors.
Alena VrbackáResearch Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.
Anna PřistoupilováResearch Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.
Kendrah O KiddResearch Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.
Václav JanoušekResearch Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.
Martin RadinaResearch Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.
Petr VyleťalResearch Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.
Ibrahim BitarDepartment of Microbiology, Faculty of Medicine and University Hospital Pilsen, Charles University, Pilsen, Czechia.
Viktor StráneckýResearch Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.
Lenka Steiner-MrázováResearch Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.
Helena TrešlováResearch Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.
Jana SovováResearch Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.
Kateřina HodaňováResearch Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.
Hana HartmannováResearch Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.
Dita MušálkováResearch Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.
Klára SvojšováResearch Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.
Tereza KmochováResearch Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.
Veronika BarešováResearch Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.
Abby TaylorWake Forest University School of Medicine, Section on Nephrology, Winston-Salem, North Carolina, USA.
Lauren MartinWake Forest University School of Medicine, Section on Nephrology, Winston-Salem, North Carolina, USA.
Antonio SanchezWake Forest University School of Medicine, Section on Nephrology, Winston-Salem, North Carolina, USA.
Romana RyšaváDepartment of Nephrology, First Faculty of Medicine, Charles University in Prague and General Teaching Hospital in Prague, Prague, Czech Republic.
Innet LajtmanováB. Braun Avitum, Bratislava, Slovakia.
Silvie Rajnochová-BloudíčkováDepartment of Nephrology, Transplant Centre, Institute for Clinical and Experimental Medicine, Videnska 1958, Prague 14021, Czech Republic.
Ondřej ViklickýDepartment of Nephrology, Transplant Centre, Institute for Clinical and Experimental Medicine, Videnska 1958, Prague 14021, Czech Republic.
Gregorius PapagregoriusMolecular Medicine Research Center, biobank.cy Center of Excellence in Biobanking and Biomedical Research, University of Cyprus, Nicosia, Cyprus.
Constantinos DeltasMolecular Medicine Research Center, biobank.cy Center of Excellence in Biobanking and Biomedical Research, University of Cyprus, Nicosia, Cyprus.
Christoforos StavrouEvangelismos Private Hospital, Pafos, Cyprus.
Sofia JorgeDepartment of Nephrology and Renal Transplant, Hospital de Santa Maria, CHULN, EPE, Lisbon, Portugal.
José António LopesDepartment of Nephrology and Renal Transplant, Hospital de Santa Maria, CHULN, EPE, Lisbon, Portugal.
Márcia RodriguesDepartment of Medical Genetics, Hospital de Santa Maria, ULSSM, Lisbon, Portugal.
Elhussein ElhassanDepartment of Nephrology Beaumont Hospital Dublin Ireland.
Michelle ClinceDepartment of Nephrology Beaumont Hospital Dublin Ireland.
Colm RowanDepartment of Nephrology Beaumont Hospital Dublin Ireland.
Peter ConlonDepartment of Nephrology and Renal Transplant, Hospital de Santa Maria, CHULN, EPE, Lisbon, Portugal.
Omri TeltshSchool of Pharmacy and Biomolecular Sciences, Royal College of Surgeons, Dublin, Ireland.
Gianpiero L CavalleriDepartment of Nephrology and Renal Transplant, Hospital de Santa Maria, CHULN, EPE, Lisbon, Portugal.
Brendan BlumenstielBroad Clinical Labs, The Broad Institute, Cambridge, Massachusetts, USA.
Diana ToledoBroad Clinical Labs, The Broad Institute, Cambridge, Massachusetts, USA.
Marina DiStefanoBroad Clinical Labs, The Broad Institute, Cambridge, Massachusetts, USA.
Matthew DeFeliceBroad Clinical Labs, The Broad Institute, Cambridge, Massachusetts, USA.
Martina ŽivnáResearch Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.
Anthony J BleyerResearch Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.
Stanislav KmochResearch Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.
Funding
Wake Forest Clinical and Translational Science AwardUL1TR001420 · NCATS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI ARD, JAMY D, FOLEY, KRISTIE L · 2015 to 2023
$32.3MChronic Kidney Disease (CKD) Biomarkers Consortium Data Coordinating CenterU01DK103225 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI SCHRAUBEN, SARAH JEANNE · 2014 to 2020
$5.5MNCATS NIH HHS UL1 TR001420NIDDK NIH HHS U01 DK103225
Abstract
Background: ADTKD- Methods: We employed Single Molecule, Real-Time (SMRT) sequencing and characterized the genomic sequence of Results: We identified Conclusions: SMRT sequencing outperforms current diagnostic methods for ADTKD-
Indexed as
amplicon sequencingAutosomal Dominant Tubulointerstitial Kidney Diseaseinheritedkidney diseaseMUC1 geneMucin-1 Kidney DiseaseReal-Time (SMRT) sequencingSingle MoleculeVNTR structure
Identifiers
What Socratic holds
Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390
Registered trials
None linked
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.