Evidence map›Paper›PMID 38282074›Full record

ArticleEuropean journal of human genetics : EJHG2024

A new blood DNA methylation signature for Koolen-de Vries syndrome: Classification of missense KANSL1 variants and comparison to fibroblast cells.

Zain Awamleh, Sanaa Choufani, Wendy Wu, Dmitrijs Rots, Alexander J M Dingemans, Nael Nadif Kasri, Susana Boronat, Salvador Ibañez-Mico, Laura Cuesta Herraiz, Irene Ferrer and 7 more

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in European journal of human genetics : EJHG, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.6field-weighted citation impact, top 11% of its field
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

7 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Looking back at 2024 in the European Journal of Human Genetics.European journal of human genetics : EJHG · 2025
    Article
  7. Solving medical mysteries with genomics.European journal of human genetics : EJHG · 2024
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 10 institutions in 4 countries.

Zain AwamlehGenetics and Genome Biology Program, Research Institute, the Hospital for Sick Children, Toronto, ON, M5G 1×8, Canada.
Sanaa ChoufaniGenetics and Genome Biology Program, Research Institute, the Hospital for Sick Children, Toronto, ON, M5G 1×8, Canada.
Wendy WuGenetics and Genome Biology Program, Research Institute, the Hospital for Sick Children, Toronto, ON, M5G 1×8, Canada.
Dmitrijs RotsDepartment of Human Genetics, Radboud university medical center, Donders Institute for Brain, Cognition, and Behavior, Nijmegen, The Netherlands.
Alexander J M DingemansDepartment of Human Genetics, Radboud university medical center, Donders Institute for Brain, Cognition, and Behavior, Nijmegen, The Netherlands.
Nael Nadif KasriDepartment of Human Genetics, Radboud university medical center, Donders Institute for Brain, Cognition, and Behavior, Nijmegen, The Netherlands.ORCID 0000-0002-7448-9289
Susana BoronatDepartment of Pediatrics, Hospital del Santa Creu y Sant Pau, Barcelona, Spain.
Salvador Ibañez-MicoDepartment of Pediatric Neurology, Hospital Virgen de la Arrixaca, Murcia, Madrid, Spain.ORCID 0000-0003-4582-6511
Laura Cuesta HerraizDepartment of Pediatric Neurology, Hospital de Manises, Valencia, Spain.
Irene FerrerDepartment of Genetics, Consorcio Hospital General de Valencia, Valencia, Spain.
Antonio Martínez CarrascalDepartment of Pediatrics, Hospital de Requena, Valencia, Spain.
Luis A Pérez-JuradoGenetics Unit, Universitat Pompeu Fabra, Hospital del Mar Research Institute (IMIM) and CIBERER, Barcelona, Spain.ORCID 0000-0002-1988-3005
Gemma Aznar LainGenetics Unit, Universitat Pompeu Fabra, Hospital del Mar Research Institute (IMIM) and CIBERER, Barcelona, Spain.ORCID 0000-0002-6468-1939
Juan Dario Ortigoza-EscobarMovement Disorders Unit, Institut de Recerca Sant Joan de Déu, CIBERER-ISCIII and European Reference Network for Rare Neurological Diseases (ERN-RND), Barcelona, Spain.
Bert B A de VriesDepartment of Human Genetics, Radboud university medical center, Donders Institute for Brain, Cognition, and Behavior, Nijmegen, The Netherlands.ORCID 0000-0002-0000-2917
David A KoolenDepartment of Human Genetics, Radboud university medical center, Donders Institute for Brain, Cognition, and Behavior, Nijmegen, The Netherlands. david.koolen@radboudumc.nl.ORCID 0000-0002-2152-4626
Rosanna WeksbergGenetics and Genome Biology Program, Research Institute, the Hospital for Sick Children, Toronto, ON, M5G 1×8, Canada. rweksb@sickkids.ca.ORCID 0000-0002-6501-4150
Radboud University Nijmegen · NLHospital for Sick Children · CAUniversitat Pompeu Fabra · ESHospital Arnau de Vilanova · ESHospital de Manises · ESHospital de Sant Pau · ESHospital General Universitario De Valencia · ESHospital Universitario Virgen de la Arrixaca · ESInstituto de Salud Carlos III · ESUniversity of Toronto · CA

Funding

Gouvernement du Canada | Canadian Institutes of Health Research (Instituts de Recherche en Santé du Canada) PJT-178315
6 · The paper itself

Abstract

Pathogenic variants in KANSL1 and 17q21.31 microdeletions are causative of Koolen-de Vries syndrome (KdVS), a neurodevelopmental syndrome with characteristic facial dysmorphia. Our previous work has shown that syndromic conditions caused by pathogenic variants in epigenetic regulatory genes have identifiable patterns of DNA methylation (DNAm) change: DNAm signatures or episignatures. Given the role of KANSL1 in histone acetylation, we tested whether variants underlying KdVS are associated with a DNAm signature. We profiled whole-blood DNAm for 13 individuals with KANSL1 variants, four individuals with 17q21.31 microdeletions, and 21 typically developing individuals, using Illumina's Infinium EPIC array. In this study, we identified a robust DNAm signature of 456 significant CpG sites in 8 individuals with KdVS, a pattern independently validated in an additional 7 individuals with KdVS. We also demonstrate the diagnostic utility of the signature and classify two KANSL1 VUS as well as four variants in individuals with atypical clinical presentation. Lastly, we investigated tissue-specific DNAm changes in fibroblast cells from individuals with KdVS. Collectively, our findings contribute to the understanding of the epigenetic landscape related to KdVS and aid in the diagnosis and classification of variants in this structurally complex genomic region.

Indexed as

Abnormalities, MultipleChromosome DeletionIntellectual DisabilityChromosomes, Human, Pair 17DNA MethylationGenes, RegulatorHumansNuclear ProteinsNSL1 protein, humanNuclear Proteins

Identifiers

PMID38282074
PMCPMC10923882
OpenAlexW4391313179

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.