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Bi-allelic PRMT9 loss-of-function variants cause a syndromic form of intellectual disability
Bi-allelic PRMT9 loss-of-function variants cause a syndromic form of intellectual disability
Journal:
American Journal of Human Genetics
Published:
2025-11-18
DOI
:
10.1016/j.ajhg.2025.10.014
Affiliations:
58
Authors:
89
Go to article
Institutions
Authors
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Laboratoire de Génétique Médicale (LGM), France
8.166667
0.09
Ankara Etlik City Hospital, Turkey
5.000000
0.06
AP-HP Pitié-Salpêtrière Hospital, France
4.000000
0.04
University Hospitals of Strasbourg (HUS), France
3.500000
0.04
University of Toronto (U of T), Canada
3.166667
0.04
Karlsruhe Institute of Technology (KIT), Germany
3.000000
0.03
University of Social Welfare and Rehabilitation Sciences, Iran
3.000000
0.03
University of São Paulo (USP), Brazil
3.000000
0.03
University Medical Center Hamburg-Eppendorf (UKE), UHH, Germany
3.000000
0.03
Institute of Genetics and Molecular and Cellular Biology (IGBMC), France
2.500000
0.03
Robert Debré University Hospital, France
2.500000
0.03
Paracelsus Medical University (PMU), Austria
2.500000
0.03
Yokohama City University (YCU), Japan
2.000000
0.02
GeneDx, United States of America (USA)
2.000000
0.02
Telemark Hospital Skien, Norway
2.000000
0.02
The Hospital for Sick Children (SickKids), U of T, Canada
2.000000
0.02
Hamilton Health Sciences (HHS), Canada
2.000000
0.02
Cipher Gene (Beijing) Co., Ltd., China
2.000000
0.02
Institut d’Investigació i Innovació Parc Taulí (I3PT), Spain
2.000000
0.02
Essen University Hospital, Germany
2.000000
0.02
Universitätsklinikum Leipzig, Germany
2.000000
0.02
UPMC Children's Hospital of Pittsburgh (CHP), United States of America (USA)
2.000000
0.02
Medical University of Vienna (MUW), Austria
2.000000
0.02
Ljubljana University Medical Centre (Ljubljana UMC), Slovenia
2.000000
0.02
Boston Children's Hospital (BCH), United States of America (USA)
2.000000
0.02
Leiden University Medical Center (LUMC), Netherlands
2.000000
0.02
Princess Margaret Cancer Centre, U of T, Canada
1.166667
0.01
France Génomique, France
1.000000
0.01
NeuroDiderot, France
1.000000
0.01
Joe DiMaggio Children's Hospital (JDCH), United States of America (USA)
1.000000
0.01
West China Second University Hospital of Sichuan University (WCSUH), SCU, China
1.000000
0.01
University Children's Hospital, North Macedonia
1.000000
0.01
Mendelics Genomic Analysis, Brazil
1.000000
0.01
Anhembi Morumbi University, Brazil
1.000000
0.01
Erasmus University Medical Center (Erasmus MC), Netherlands
1.000000
0.01
Amphia Hospital, Netherlands
1.000000
0.01
Akron Children's Hospital, United States of America (USA)
1.000000
0.01
Groupe Hospitalier du Havre, France
1.000000
0.01
CHI Poissy - Saint-Germain-en-Laye, France
1.000000
0.01
City of Hope Comprehensive Cancer Center, United States of America (USA)
1.000000
0.01
Pasteur Institute, France
0.500000
0.01
Radboudumc Amalia Kinderziekenhuis, Netherlands
0.500000
0.01
University Children’s Hospital Tiršova, Serbia
0.500000
0.01
University of Belgrade, Serbia
0.500000
0.01
Dijon University Hospital, France
0.500000
0.01
Genetics of Development Disorders Team (GAD), France
0.500000
0.01
Heidelberg University (Uni Heidelberg), Germany
0.500000
0.01
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