ArticlemedRxiv : the preprint server for health sciences2025
Recessive genomic and phenotypic variation in consanguineous families with cerebral palsy.
Abstract readPreprint
In one paragraph
Article in medRxiv : the preprint server for health sciences, 2025. 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
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
57 authors.
Pritha BisaradDepartments of Child Health, Cellular & Molecular Medicine, Neurology and Program in Genetics, University of Arizona College of Medicine - Phoenix, Phoenix, Arizona, USA.ORCID 0000-0002-2677-9847
Yung-Chun WangDepartment of Genetics, School of Medicine, Washington University, St. Louis, Missouri, USA.ORCID 0000-0002-8775-3472
Peter T SkidmoreDepartments of Child Health, Cellular & Molecular Medicine, Neurology and Program in Genetics, University of Arizona College of Medicine - Phoenix, Phoenix, Arizona, USA.ORCID 0000-0003-1051-5051
Carolina I Galaz-MontoyaDepartments of Child Health, Cellular & Molecular Medicine, Neurology and Program in Genetics, University of Arizona College of Medicine - Phoenix, Phoenix, Arizona, USA.ORCID 0000-0002-9180-8202
Sara A LewisDepartments of Child Health, Cellular & Molecular Medicine, Neurology and Program in Genetics, University of Arizona College of Medicine - Phoenix, Phoenix, Arizona, USA.ORCID 0000-0003-2560-1681
Bader AlhaddadLifera Omics, Riyadh, Saudi Arabia.ORCID 0000-0003-4542-5267
Nahyun KongDepartment of Genetics, School of Medicine, Washington University, St. Louis, Missouri, USA.ORCID 0000-0001-8919-8006
Dominic JulianDepartments of Child Health, Cellular & Molecular Medicine, Neurology and Program in Genetics, University of Arizona College of Medicine - Phoenix, Phoenix, Arizona, USA.ORCID 0000-0001-7352-4997
Helen MageeDepartments of Child Health, Cellular & Molecular Medicine, Neurology and Program in Genetics, University of Arizona College of Medicine - Phoenix, Phoenix, Arizona, USA.
Tyler N KruerDepartments of Child Health, Cellular & Molecular Medicine, Neurology and Program in Genetics, University of Arizona College of Medicine - Phoenix, Phoenix, Arizona, USA.
Yuhan XieDepartment of Biostatistics, Yale School of Public Health, New Haven, Connecticut, USA.ORCID 0000-0002-1738-0885
Wangjie ZhengDepartment of Biostatistics, Yale School of Public Health, New Haven, Connecticut, USA.
Boyang LiDepartment of Biostatistics, Yale School of Public Health, New Haven, Connecticut, USA.ORCID 0000-0003-2808-9986
Fatemeh V RajabpourDepartments of Child Health, Cellular & Molecular Medicine, Neurology and Program in Genetics, University of Arizona College of Medicine - Phoenix, Phoenix, Arizona, USA.
James LiuDepartments of Child Health, Cellular & Molecular Medicine, Neurology and Program in Genetics, University of Arizona College of Medicine - Phoenix, Phoenix, Arizona, USA.
Anjali RevanurDepartments of Child Health, Cellular & Molecular Medicine, Neurology and Program in Genetics, University of Arizona College of Medicine - Phoenix, Phoenix, Arizona, USA.
Khadijah BakurLifera Omics, Riyadh, Saudi Arabia.
Saghar Ghasemi FirouzabadiNikagene Genetic Diagnostic Laboratory, Gorgan, Iran.ORCID 0000-0001-8989-5741
Sarina SharbatkhoriNikagene Genetic Diagnostic Laboratory, Gorgan, Iran.
Abbas TafakhoriIranian Center of Neurological Research, Neuroscience Institute, Tehran University of Medical Sciences, Tehran, Iran.
Ehsan TaghiabadiSkin and Stem Cell Research Center, Tehran University of Medical Sciences, Tehran, Iran.
Ermia NezaminargabadDepartment of Cell Biology, University of Kaiserslautern-Landau, 67663 Kaiserslautern, Germany.ORCID 0009-0006-4134-2121
Shohreh VosooghClinical Research Development Unit (CRDU), Sayad Shirazi Hospital, Golestan University of Medical Sciences, Gorgan, Iran.ORCID 0000-0001-5953-7871
Javad JamshidiNeuroscience Research Australia, Sydney, New South Wales, Australia.ORCID 0000-0002-6607-418X
Serajaddin ArefniaNeonatal and Children's Health Research Center, Golestan University of Medical Sciences, Gorgan, Iran.
Seyed Ahmad HosseiniNeonatal and Children's Health Research Center, Golestan University of Medical Sciences, Gorgan, Iran.
Alireza KhajehmirzaeiDr. Khajehmirzaei Genetic Counseling Clinic, Gorgan, Iran.
Faezeh JamaliDepartment of Medical Genetics and Molecular Medicine, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.ORCID 0009-0000-5815-4924
Azadeh AhmadifardDepartment of Biotechnology, Faculty of Medicine, Lorestan University of Medical Sciences, Khorramabad, Iran.
Hamidreza KhodadadiDepartment of Biotechnology, Faculty of Medicine, Lorestan University of Medical Sciences, Khorramabad, Iran.ORCID 0000-0003-2254-0350
Parvaneh DaneshmandDr. Daneshmand Genetic Diagnostic Laboratory, Amol, Iran.
Saeed BohlegaGenomic Medicine Center of Excellence (GMCoE), King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.ORCID 0000-0002-1046-6571
Sateesh MaddirevulaGenomic Medicine Center of Excellence (GMCoE), King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.ORCID 0000-0003-2999-2229
Seba Saleh NadeefGenomic Medicine Center of Excellence (GMCoE), King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.ORCID 0000-0001-8193-5251
Mais O HashemGenomic Medicine Center of Excellence (GMCoE), King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.
Mustafa A SalihDivision of Pediatric Neurology, Department of Pediatrics, College of Medicine, King Saud University, Riyadh, Saudi Arabia.ORCID 0000-0002-4379-2111
Inaam N MohmedDepartment of Paediatrics and Child Health, Faculty of Medicine, University of Khartoum, Khartoum, Sudan.
Heinrich StichtInstitute of Biochemistry, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.ORCID 0000-0001-5644-045X
Sara Peres MoriasCentre for Predictive and Preventative Genetics (CGPP), Institute of Molecular and Cell Biology (IBMC), Institute for Research and Innovation in Health (i3S), University of Porto, Porto, Portugal.
Joana DamásioCentre for Predictive and Preventative Genetics (CGPP), Institute of Molecular and Cell Biology (IBMC), Institute for Research and Innovation in Health (i3S), University of Porto, Porto, Portugal.ORCID 0000-0002-6539-6398
Mariana SantosCentre for Predictive and Preventative Genetics (CGPP), Institute of Molecular and Cell Biology (IBMC), Institute for Research and Innovation in Health (i3S), University of Porto, Porto, Portugal.ORCID 0000-0002-2343-2215
José Leal LoureiroCentre for Predictive and Preventative Genetics (CGPP), Institute of Molecular and Cell Biology (IBMC), Institute for Research and Innovation in Health (i3S), University of Porto, Porto, Portugal.ORCID 0000-0002-6195-5412
Rita RodriguesNeurology Department, Centro Hospitalar Universitário de Entre Douro e Vouga, Unidade Local de Saúde (ULS) de Entre Douro e Vouga, Santa Maria da Feira, Portugal.ORCID 0000-0003-1954-0309
Giovanni StevaninInstitute for Cognitive and Integrative Neuroscience of Aquitaine (INCIA), UMR5287, Université de Bordeaux, Centre National de la Recherche Scientifique (CNRS), Ecole Pratique des Hautes Etudes (EPHE), Bordeaux, France.ORCID 0000-0001-9368-8657
Mehdi BenkiraneCentre National de la Recherche Scientifique (CNRS), Site Unique de Biologie, Centre Hospitalier Universitaire (CHU) de Montpellier, Montpellier, France.ORCID 0000-0001-6445-6347
Benjamin DauriatDepartment of Medical Genetics, Cytogenetics, and Reproductive Biology, Centre Hospitalier Universitaire (CHU) de Limoges, Limoges, France.
Nicholas HeadExeter Genomics Laboratory, Royal Devon & Exeter NHS Foundation Trust, Exeter, UK.
Júlia BaptistaExeter Genomics Laboratory, Royal Devon & Exeter NHS Foundation Trust, Exeter, UK.ORCID 0000-0003-0915-5028
Saeid ShahhosseiniLaniakea Intelligence Inc., Vancouver, Canada.
Farhan MohammadCollege of Health and Life Sciences, Hamad Bin Khalifa University, Doha, Qatar.ORCID 0000-0002-2465-1508
Hongyu ZhaoDepartment of Biostatistics, Yale School of Public Health, New Haven, Connecticut, USA.ORCID 0000-0003-1195-9607
Sergio Padilla-LopezDepartments of Child Health, Cellular & Molecular Medicine, Neurology and Program in Genetics, University of Arizona College of Medicine - Phoenix, Phoenix, Arizona, USA.ORCID 0009-0009-9354-3402
Fowzan AlkurayaGenomic Medicine Center of Excellence (GMCoE), King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.ORCID 0000-0003-4158-341X
Somayeh BakhtiariDepartments of Child Health, Cellular & Molecular Medicine, Neurology and Program in Genetics, University of Arizona College of Medicine - Phoenix, Phoenix, Arizona, USA.
Michael C KruerDepartments of Child Health, Cellular & Molecular Medicine, Neurology and Program in Genetics, University of Arizona College of Medicine - Phoenix, Phoenix, Arizona, USA.ORCID 0000-0002-1373-7891
Sheng Chih JinDepartment of Genetics, School of Medicine, Washington University, St. Louis, Missouri, USA.ORCID 0000-0002-5777-7262
Hossein DarvishNikagene Genetic Diagnostic Laboratory, Gorgan, Iran.
Funding
Genomic Insights into the Neurobiology of Cerebral PalsyR01NS106298 · NINDS · UNIVERSITY OF ARIZONA · PI KRUER, MICHAEL C · 2019 to 2023
$3.7MGenomic analysis of the Multiplex, Autozygous Populations in Cerebral Palsy (MAP CP) cohort: a focused approach to a complex diseaseR01NS127108 · NINDS · UNIVERSITY OF ARIZONA · PI Michael C Kruer · 2023 to 2026
$2.6MMolecular and cellular characterization of congenital hydrocephalusR01NS131610 · NINDS · WASHINGTON UNIVERSITY · PI Sheng Chih Jin · 2024 to 2026
$1.3MNINDS NIH HHS R01 NS106298NINDS NIH HHS R01 NS127108NINDS NIH HHS R01 NS131610
Abstract
Cerebral palsy (CP) is a neurodevelopmental disorder of motor function, with genetic etiologies, particularly
Identifiers
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.