Evidence map›Paper›PMID 42826188›Full record

ArticleScience advances2026

The landscape of allele-specific expression in human kidneys.

Ana C Onuchic-Whitford, Junmo Sung, Eric D Sakkas, Michelle T McNulty, Victoria Mezger, Christopher L O'Connor, Anya Greenberg, Jihoon G Yoon, Sowmya Badina, Laura H Mariani and 3 more

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Article in Science advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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 registry

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Ana C Onuchic-WhitfordDivision of Nephrology, Brigham and Women's Hospital, Boston, MA 02115, USA.ORCID 0000-0003-0362-0400
Junmo SungDivision of Nephrology, Brigham and Women's Hospital, Boston, MA 02115, USA.ORCID 0009-0005-6706-6500
Eric D SakkasDivision of Nephrology, Boston Children's Hospital, Boston, MA 02115, USA.ORCID 0000-0001-9283-3306
Michelle T McNultyDivision of Nephrology, Boston Children's Hospital, Boston, MA 02115, USA.ORCID 0000-0002-2080-0940
Victoria MezgerDivision of Nephrology, Boston Children's Hospital, Boston, MA 02115, USA.ORCID 0009-0003-6814-1491
Christopher L O'ConnorDepartment of Medicine, University of Michigan, Ann Arbor, MI 48109, USA.ORCID 0009-0002-1888-728X
Anya GreenbergDivision of Nephrology, Boston Children's Hospital, Boston, MA 02115, USA.ORCID 0000-0003-3616-0666
Jihoon G YoonDivision of Nephrology, Boston Children's Hospital, Boston, MA 02115, USA.ORCID 0000-0002-4401-7803
Sowmya BadinaDivision of Nephrology, Boston Children's Hospital, Boston, MA 02115, USA.ORCID 0009-0004-3004-6760
Laura H MarianiDepartment of Medicine, University of Michigan, Ann Arbor, MI 48109, USA.ORCID 0000-0002-6055-764X
Markus BitzerDepartment of Medicine, University of Michigan, Ann Arbor, MI 48109, USA.
Matthew G SampsonDivision of Nephrology, Boston Children's Hospital, Boston, MA 02115, USA.ORCID 0000-0001-9560-076X
Dongwon LeeDivision of Nephrology, Boston Children's Hospital, Boston, MA 02115, USA.ORCID 0000-0002-1568-2249

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Allele-specific expression (ASE), the preferential expression of one gene copy, is a key mechanism of genomic regulation. However, its role in human kidney disease remains poorly understood. In this study, we generated a high-quality, genome-wide ASE map using paired whole-genome sequencing and RNA sequencing from microdissected glomerular and tubulointerstitial compartments of patients with proteinuric kidney disease. We showed that the majority of common ASE events were deterministic and sequence-mediated. We also found that diseased kidneys exhibited significantly more ASE in glomeruli (GLOM) than tubulointerstitium (TUBE) compared to controls. Unexpectedly, higher ASE in GLOM than TUBE was significantly associated with improved kidney disease outcomes in the disease cohort. Differential gene expression analysis suggested that this was the result of an active, protective transcriptional response, including ribosome and adenosine 5'-triphosphate synthesis up-regulation, rather than pathogenic dysregulation. Our work reveals glomerular ASE as a marker of adaptive transcriptional activity in proteinuric kidney disease.

Indexed as

AllelesGene Expression RegulationKidneyKidney DiseasesFemaleGene Expression ProfilingHumansKidney GlomerulusMale

Identifiers

PMID42826188

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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 OpenQuestion graph.