Evidence map›Paper›PMID 42474752›Full record

ArticleHuman genetics2026

Discovery of a DNA methylation episignature for Weiss-Kruszka syndrome.

Haley McConkey, Liselot van der Laan, Sourav Ghosh, Lotte Kleinendorst, Michael A Levy, Jessica Rzasa, Johanna M van Hagen, Quinten Waisfisz, Heidi L Schulz, Corina Heller and 11 more

Abstract read
In one paragraph

Article in Human genetics, 2026. 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
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

21 authors.

Haley McConkey *Verspeeten Clinical Genome Centre, London Health Science Centre, London, ON, Canada.
Liselot van der Laan *Department of Human Genetics, Amsterdam UMC, Amsterdam, The Netherlands.
Sourav GhoshVerspeeten Clinical Genome Centre, London Health Science Centre, London, ON, Canada.
Lotte KleinendorstDepartment of Human Genetics, Amsterdam UMC, Amsterdam, The Netherlands.
Michael A LevyVerspeeten Clinical Genome Centre, London Health Science Centre, London, ON, Canada.
Jessica RzasaVerspeeten Clinical Genome Centre, London Health Science Centre, London, ON, Canada.
Johanna M van HagenDepartment of Human Genetics, Amsterdam UMC, Amsterdam, The Netherlands.
Quinten WaisfiszDepartment of Human Genetics, Amsterdam UMC, Amsterdam, The Netherlands.
Heidi L SchulzZentrum für Humangenetik Tübingen, Tübingen, Germany.
Corina HellerZentrum für Humangenetik Tübingen, Tübingen, Germany.
Kerstin HuhnZentrum für Humangenetik Tübingen, Tübingen, Germany.
Carolin D ObermaierZentrum für Humangenetik Tübingen, Tübingen, Germany.
Konrad PlatzerInstitute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.
Rami Abou JamraInstitute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.
Nikos MarinakisLaboratory of Medical Genetics, Medical School, National and Kapodistrian University of Athens, "Aghia Sophia" Children's Hospital, Athens, Greece.
Danai VeltraLaboratory of Medical Genetics, Medical School, National and Kapodistrian University of Athens, "Aghia Sophia" Children's Hospital, Athens, Greece.
Konstantina KosmaLaboratory of Genetics, Faculty of Medicine, Democritus University of Thrace, Alexandroupolis, Greece.
Christalena SofocleousLaboratory of Genetics, Faculty of Medicine, Democritus University of Thrace, Alexandroupolis, Greece.
Peter Henneman *Department of Human Genetics, Amsterdam UMC, Amsterdam, The Netherlands.
Bekim Sadikovic *Verspeeten Clinical Genome Centre, London Health Science Centre, London, ON, Canada. bekim.sadikovic@lhsc.on.ca.
Mieke M van Haelst *Department of Human Genetics, Amsterdam UMC, Amsterdam, The Netherlands. m.vanhaelst@amsterdamumc.nl.

Funding

Government of Canada through Genome Canada and the Ontario Genomics Institute OGI-188
6 · The paper itself

Abstract

Weiss-Kruszka syndrome (WSKA; OMIM 618619) is a rare autosomal dominant neurodevelopmental disorder caused by haploinsufficiency of ZNF462, a zinc-finger transcription factor involved in chromatin regulation and early embryonic development. WSKA is characterized by developmental delay, hypotonia, craniofacial dysmorphic features (around 8) and variable congenital anomalies. Genome-wide DNAm profiling was performed on peripheral blood DNA from 9 WSKA cases with (likely) pathogenic ZNF462 variants and matched controls to look for differential methylation. Analysis using the EpiSign™ pipeline identified a robust DNAm pattern, or episignature, specific to WSKA syndrome. Supervised machine-learning classification demonstrated high sensitivity and specificity, with reproducibility confirmed by leave-one-out cross-validation, as well as correctly classifying a validation case with a pathogenic ZNF462 variant. Comparative analysis revealed partial overlap of genome-wide DNA methylation changes between the WSKA episignature and other neurodevelopmental disorders involving chromatin regulators. Functional annotation of differentially methylated probes and regions demonstrated enrichment for pathways related to neurodevelopment, neuron function and cell adhesion. These findings define and validate a distinct DNAm episignature for WSKA, providing a valuable diagnostic biomarker to support variant classification and offering insight into the epigenomic consequences of ZNF462 haploinsufficiency.

Indexed as

DNA MethylationNeurodevelopmental DisordersTranscription FactorsFemaleHaploinsufficiencyHumansTranscription Factors

Identifiers

PMID42474752
PMCPMC13385256

What Socratic holds

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Registered trials

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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 Socratic graph.