Evidence map›Paper›PMID 41468891›Full record

ArticleAmerican journal of human genetics2026

De novo variants in KDM2A cause a syndromic neurodevelopmental disorder.

Eric N Anderson, Stephan Drukewitz, Sukhleen Kour, Anuradha V Chimata, Deepa S Rajan, Senta Schönnagel, Karen L Stals, Deirdre Donnelly, Siobhan O'Sullivan, John F Mantovani and 49 more

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Article in American journal of human genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

59 authors.

Eric N AndersonDepartment of Pediatrics, Children's Hospital of Pittsburgh, University of Pittsburgh Medical Center, Pittsburgh, PA 15224, USA.
Stephan DrukewitzInstitute of Human Genetics, University of Leipzig Medical Center, 04103 Leipzig, Germany.
Sukhleen KourDepartment of Pediatrics, Children's Hospital of Pittsburgh, University of Pittsburgh Medical Center, Pittsburgh, PA 15224, USA.
Anuradha V ChimataDepartment of Biology, University of Dayton, Dayton, OH, USA.
Deepa S RajanDepartment of Pediatrics, Children's Hospital of Pittsburgh, University of Pittsburgh Medical Center, Pittsburgh, PA 15224, USA.
Senta SchönnagelInstitute of Human Genetics, University of Leipzig Medical Center, 04103 Leipzig, Germany.
Karen L StalsRoyal Devon & Exeter NHS Foundation Trust, Exeter Genomics Laboratory, Exeter EX2 5DW, UK.
Deirdre DonnellyNorthern Ireland Regional Genetics Centre, Belfast Health and Social Care Trust/City Hospital, Belfast, Northern Ireland BT9 7AB, UK.
Siobhan O'SullivanNorthern Ireland Regional Genetics Centre, Belfast Health and Social Care Trust/City Hospital, Belfast, Northern Ireland BT9 7AB, UK.
John F MantovaniDivision of Child Neurology, Washington University School of Medicine, Mercy Kids Center for Neurodevelopment & Autism, St. Louis, MO 63110, USA.
Tiong Y TanVictorian Clinical Genetics Services, Murdoch Children's Research Institute, Melbourne, VIC, Australia; Department of Paediatrics, University of Melbourne, Melbourne, VIC, Australia.
Zornitza StarkVictorian Clinical Genetics Services, Murdoch Children's Research Institute, Melbourne, VIC, Australia; Department of Paediatrics, University of Melbourne, Melbourne, VIC, Australia.
Pia ZacherEpilepsy Center Kleinwachau, 01454 Radeberg, Germany.
Nicolas ChatronDepartment of Medical Genetics, University Hospital of Lyon, 69007 Lyon, France.
Pauline MoninDepartment of Medical Genetics, University Hospital of Lyon, 69007 Lyon, France.
Severine DrunatDepartment of Genetics, APHP-Robert DEBRE University Hospital, Sorbonne Paris-Cité University, and INSERM UMR, 1141 Paris, France.
Yoann VialDepartment of Genetics, APHP-Robert DEBRE University Hospital, Sorbonne Paris-Cité University, and INSERM UMR, 1141 Paris, France.
Xenia LatypovaDepartment of Genetics, APHP-Robert DEBRE University Hospital, Sorbonne Paris-Cité University, and INSERM UMR, 1141 Paris, France.
Jonathan LevyDepartment of Genetics, APHP-Robert DEBRE University Hospital, Sorbonne Paris-Cité University, and INSERM UMR, 1141 Paris, France.
Alain VerloesDepartment of Genetics, APHP-Robert DEBRE University Hospital, Sorbonne Paris-Cité University, and INSERM UMR, 1141 Paris, France.
Jennefer N CarterStanford Center for Undiagnosed Diseases, Stanford University, Stanford, CA 94305, USA; Department of Pediatrics, Division of Medical Genetics, Stanford University School of Medicine, Stanford, CA 94305, USA.
Devon E BonnerStanford Center for Undiagnosed Diseases, Stanford University, Stanford, CA 94305, USA; Department of Pediatrics, Division of Medical Genetics, Stanford University School of Medicine, Stanford, CA 94305, USA.
Suma P ShankarDepartments of Pediatrics & Ophthalmology, Genomic Medicine, University of California, Davis Health, Sacramento, CA 95817, USA.
Jonathan A BernsteinStanford Center for Undiagnosed Diseases, Stanford University, Stanford, CA 94305, USA; Department of Pediatrics, Division of Medical Genetics, Stanford University School of Medicine, Stanford, CA 94305, USA.
Julie S CohenDepartment of Neurology and Developmental Medicine, Kennedy Krieger Institute, Baltimore, MD 21205, USA; Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
Anne ComiDepartment of Neurology and Developmental Medicine, Kennedy Krieger Institute, Baltimore, MD 21205, USA; Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
Deanna Alexis CarereGeneDx, LLC, Gaithersburg, MD 20877, USA.
Lisa M DyerGeneDx, LLC, Gaithersburg, MD 20877, USA.
Sureni V MullegamaGeneDx, LLC, Gaithersburg, MD 20877, USA.
Pedro A Sanchez-LaraDepartment of Pediatrics, Cedars-Sinai Medical Center, Los Angeles, CA 90048, USA.
Katheryn GrandDepartment of Pediatrics, Cedars-Sinai Medical Center, Los Angeles, CA 90048, USA.
Hyung-Goo KimDepartment of Neurosurgery, Robert Wood Johnson Medical School, Rutgers University, Piscataway, NJ 08854, USA.
Afif Ben-MahmoudNeurological Disorder Research Center, Qatar Biomedical Research Institute, Qatar Foundation, Hamad Bin Khalifa University, Doha, Qatar.
Sidney M GospeDepartments of Neurology and Pediatrics, University of Washington School of Medicine, Seattle, WA, USA; Department of Pediatrics, Duke University, Durham, NC, USA.
Rebecca S BellesGeisinger Health System, Danville, PA 17821, USA.
Gary BellusGeisinger Health System, Danville, PA 17821, USA.
Klaske D LichtenbeltDepartment of Genetics, Utrecht University Medical Center, 3584 EA Utrecht, the Netherlands.
Renske OegemaDepartment of Genetics, Utrecht University Medical Center, 3584 EA Utrecht, the Netherlands.
Anita RauchInstitute of Medical Genetics, University of Zurich, 8952 Schlieren, Zurich, Switzerland.
Ivan IvanovskiInstitute of Medical Genetics, University of Zurich, 8952 Schlieren, Zurich, Switzerland.
Frederic Tran Mau-ThemLaboratoire de Génomique Médicale - Centre NEOMICS, CHU Dijon Bourgogne, 21000 Dijon, France; INSERM - Université de Bourgogne - UMR1231 GAD, 21000 Dijon, France.
Aurore GardeLaboratoire de Génomique Médicale - Centre NEOMICS, CHU Dijon Bourgogne, 21000 Dijon, France.
Rachel RabinClinical Genetic Services, Department of Pediatrics, NYU School of Medicine, New York, NY 10016, USA.
John PappasClinical Genetic Services, Department of Pediatrics, NYU School of Medicine, New York, NY 10016, USA.
Annette E BleyLeukodystrophy Clinic, University Children's Hospital, University Medical Center, 20246 Hamburg, Germany.
Janna BredowLeukodystrophy Clinic, University Children's Hospital, University Medical Center, 20246 Hamburg, Germany.
Timo WagnerMedizinische Genetik Mainz, Limbach Genetics GmbH, Mainz, Germany.
Eva DeckerMedizinische Genetik Mainz, Limbach Genetics GmbH, Mainz, Germany.
Carsten BergmannMedizinische Genetik Mainz, Limbach Genetics GmbH, Mainz, Germany.
Louis DomenachDepartment of Medical Genetics, MRGM INSERM U1211, Bordeaux University Hospital, University of Bordeaux, Bordeaux, France.
Henri MargotDepartment of Medical Genetics, MRGM INSERM U1211, Bordeaux University Hospital, University of Bordeaux, Bordeaux, France.
Undiagnosed Diseases Network
Johannes R LemkeInstitute of Human Genetics, University of Leipzig Medical Center, 04103 Leipzig, Germany; Center for Rare Diseases, University of Leipzig Medical Center, 04103 Leipzig, Germany.
Rami Abou JamraInstitute of Human Genetics, University of Leipzig Medical Center, 04103 Leipzig, Germany.
Julia HentschelInstitute of Human Genetics, University of Leipzig Medical Center, 04103 Leipzig, Germany.
Heather MeffordCenter for Pediatric Neurological Disease Research, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Amit SinghDepartment of Biology, University of Dayton, Dayton, OH, USA.
Udai Bhan PandeyDepartment of Pediatrics, Children's Hospital of Pittsburgh, University of Pittsburgh Medical Center, Pittsburgh, PA 15224, USA; Children's Neuroscience Institute, Children's Hospital of Pittsburgh, Pittsburgh, PA 15224, USA. Electronic address: udai@pitt.edu.
Konrad PlatzerInstitute of Human Genetics, University of Leipzig Medical Center, 04103 Leipzig, Germany. Electronic address: konrad.platzer@medizin.uni-leipzig.de.

Funding

Sleep and Circadian Dysfunction, Brain and Neurobehavioral Development in AutismP50HD103538 · NICHD · HUGO W. MOSER RES INST KENNEDY KRIEGER · PI S. Ali Fatemi, Bradley L Schlaggar · 2020 to 2026
$9.9M
Genetic Basis of Dorso-Ventral Patterning in the Drosophila EyeR01EY032959 · NEI · UNIVERSITY OF DAYTON · PI KANGO-SINGH, MADHURI, SINGH, AMIT · 2021 to 2025
$2.2M
NEI NIH HHS R01 EY032959NICHD NIH HHS P50 HD103538
6 · The paper itself

Abstract

Germline variants that disrupt components of the epigenetic machinery cause syndromic neurodevelopmental disorders. Using exome and genome sequencing, we identified de novo variants in KDM2A, a lysine demethylase crucial for embryonic development, in 18 individuals with developmental delays and/or intellectual disabilities. The severity ranged from learning disabilities to severe intellectual disability. Other core symptoms included feeding difficulties; growth issues, such as intrauterine growth restriction, short stature, and microcephaly; and recurrent facial features, such as epicanthic folds, upslanted palpebral fissures, thin vermillion of the lips, and low-set ears. Expression of human disease-causing KDM2A variants in a Drosophila melanogaster model led to neural degeneration, motor defects, and reduced lifespan. Interestingly, pathogenic variants in KDM2A affected physiological attributes, including subcellular distribution, expression, and stability in human cells. Genetic epistasis experiments indicated that KDM2A variants act via a dual mechanism-loss of nuclear function for some variants tested and additional cytoplasmic gain-of-function toxicity for c.704C>T (p.Pro235Leu), as eliminating endogenous Drosophila Kdm2 did not produce noticeable neurodevelopmental phenotypes. Data from enzymatic-methylation sequencing support the suggested gene-disease association by showing aberrant methylome profiles in affected individuals' peripheral blood. Combining our genetic, phenotypic, and functional findings, we establish de novo variants in KDM2A as causative for a syndromic neurodevelopmental disorder.

Indexed as

F-Box ProteinsJumonji Domain-Containing Histone DemethylasesNeurodevelopmental DisordersAdolescentAdultAnimalsChildChild, PreschoolDrosophila melanogasterExomeFemaleHumansInfantIntellectual DisabilityMalePhenotypeF-Box ProteinsJumonji Domain-Containing Histone DemethylasesKDM2A protein, humanepigenetic machineryKDM2Aneurodevelopmental disorder

Identifiers

PMID41468891
PMCPMC12824617

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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.