ArticleHuman genetics2018
Correction to: Expanding the genetic heterogeneity of intellectual disability.
Abstract readPublished Erratum
In one paragraph
Article in Human genetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
0numbers the graph read from it
0cells of the map it votes in
1citing 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
1 citing paper in PubMed.
- Trauma and posttraumatic stress disorder modulate polygenic predictors of hippocampal and amygdala volume.Translational psychiatry · 2021Article
Corrections and comments
- Erratum for
Authors and funding
43 authors.
Shams AnaziDepartment of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Sateesh MaddirevulaDepartment of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Vincenzo SalpietroDepartment of Molecular Neuroscience, UCL Institute of Neurology, London, UK.
Yasmine T AsiQueen Square Brain Bank for Neurological Disorders, Department of Molecular Neuroscience, UCL Institute of Neurology, University College London, London, UK.
Saud AlsahliDepartment of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Amal AlhashemDepartment of Pediatrics, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
Hanan E ShamseldinDepartment of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Fatema AlZahraniDepartment of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Nisha PatelDepartment of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Niema IbrahimDepartment of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Firdous M AbdulwahabDepartment of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Mais HashemDepartment of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Nadia AlhashmiDepartment of Genetics, College of Medicine, Sultan Qaboos University, Muscat, Sultanate of Oman.
Fathiya Al MurshediDepartment of Genetics, College of Medicine, Sultan Qaboos University, Muscat, Sultanate of Oman.
Adila Al KindyDepartment of Genetics, College of Medicine, Sultan Qaboos University, Muscat, Sultanate of Oman.
Ahmad AlshaerPediatric Neurology, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Ahmed RumayyanKing Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
Saeed Al TalaDepartment of Pediatrics and Genetic Unit, Armed Forces Hospital Khamis Mushayt, Riyadh, Saudi Arabia.
Wesam KurdiDepartment of Obstetrics and Gynecology, King Faisal Specialist Hospital, Riyadh, Saudi Arabia.
Abdulaziz AlsamanDepartment of Pediatric Subspecialties, Children's Hospital, King Fahad Medical City, Riyadh, Saudi Arabia.
Ali AlasmariDepartment of Pediatric Subspecialties, Children's Hospital, King Fahad Medical City, Riyadh, Saudi Arabia.
Selina BanuDepartment of Pediatric Neurology, ICH and SSF Hospital Mirpur, Dhaka, 1216, Bangladesh.
Tipu SultanDepartment of Pediatric Neurology, Institute of Child Health and The Children's Hospital Lahore, 381-D/2, Lahore, Pakistan.
Mohammed M SalehDepartment of Pediatric Subspecialties, Children's Hospital, King Fahad Medical City, Riyadh, Saudi Arabia.
Hisham AlkurayaDepartment of Ophthalmology, Specialized Medical Center Hospital, Riyadh, Saudi Arabia.
Mustafa A SalihDivision of Pediatric Neurology, Department of Pediatrics, King Khalid University Hospital and College of Medicine, King Saud University, Riyadh, Saudi Arabia.
Hesham AldhalaanPediatric Neurology, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Tawfeg Ben-OmranClinical and Metabolic Genetics, Department of Pediatrics, Hamad Medical Corporation, Doha, Qatar.
Fatima Al MusafriClinical and Metabolic Genetics, Department of Pediatrics, Hamad Medical Corporation, Doha, Qatar.
Rehab AliClinical and Metabolic Genetics, Department of Pediatrics, Hamad Medical Corporation, Doha, Qatar.
Jehan SuleimanDivision of Neurology, Department of Pediatrics, Tawam Hospital, Al Ain, United Arab Emirates.
Brahim TabarkiDepartment of Pediatrics, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
Ayman W El-HattabDivision of Clinical Genetics and Metabolic Disorders, Department of Pediatrics, Tawam Hospital, Al-Ain, United Arab Emirates.
Caleb BuppSpectrum Health Genetics, Grand Rapids, MI, USA.
Majid AlfadhelGenetics Division, Department of Pediatrics, King Abdullah International Medical Research Centre, King Saud bin Abdulaziz University for Health Sciences, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
Nada Al TassanDepartment of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Dorota MoniesDepartment of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Stefan T AroldDivision of Biological and Environmental Sciences and Engineering (BESE), Computational Bioscience Research Center (CBRC), King Abdullah University of Science and Technology (KAUST), Thuwal, 23955-6900, Saudi Arabia.
Mohamed AbouelhodaDepartment of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Tammaryn LashleyQueen Square Brain Bank for Neurological Disorders, Department of Molecular Neuroscience, UCL Institute of Neurology, University College London, London, UK.
Henry HouldenDepartment of Molecular Neuroscience, UCL Institute of Neurology, London, UK.
Eissa FaqeihDepartment of Pediatric Subspecialties, Children's Hospital, King Fahad Medical City, Riyadh, Saudi Arabia.
Fowzan S AlkurayaDepartment of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia. falkuraya@kfshrc.edu.sa.ORCID 0000-0003-4158-341X
Funding
No grant is acknowledged in the PubMed record.
Abstract
Variant nomenclature discrepancy was identified in the article.
Identifiers
PMID
29288388What OpenQuestion holds
Textmetadata
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.