Evidence map›Paper›PMID 34050322›Full record

ArticleEuropean journal of human genetics : EJHG2022

Correction to: First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discovery.

Holger Hengel, Rebecca Buchert, Marc Sturm, Tobias B Haack, Yvonne Schelling, Muhammad Mahajnah, Rajech Sharkia, Abdussalam Azem, Ghassan Balousha, Zaid Ghanem and 9 more

Abstract readPublished Erratum
In one paragraph

Article in European journal of human genetics : EJHG, 2022. 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
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

1 citing paper in PubMed.

  1. Genes · 2024
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors.

Holger HengelDepartment of Neurology and Hertie-Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.ORCID http://orcid.org/0000-0002-9773-2667
Rebecca BuchertInstitute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.ORCID http://orcid.org/0000-0001-7576-3326
Marc SturmInstitute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
Tobias B HaackInstitute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
Yvonne SchellingDepartment of Neurology and Hertie-Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.
Muhammad MahajnahThe Ruth and Bruce Rappaport Faculty of Medicine, Technion, Haifa, Israel.
Rajech SharkiaUnit of Nature Science, Beit-Berl Academic College, Beit-Berl, Israel.
Abdussalam AzemDepartment of Biochemistry and Molecular Biology, Faculty of Life Sciences, Tel-Aviv University, Tel-Aviv, Israel.
Ghassan BaloushaDepartment of Pathology and Histology, Al-Quds University, Eastern Jerusalem, Palestine.
Zaid GhanemPalestine Medical Complex, Ramallah, Palestine.
Mohammed FalanaFaculty of Medicine, Al-Quds University, Eastern Jerusalem, Palestine.ORCID http://orcid.org/0000-0002-5893-8945
Osama BaloushaFaculty of Medicine, Al-Quds University, Eastern Jerusalem, Palestine.
Suhail AyeshMolecular Genetics Laboratory, Al-Makassed Islamic Charitable Hospital, Jerusalem, Israel.
Reinhard KeimerCaritas Baby Hospital Bethlehem, Bethlehem, Palestine.
Werner DeigendeschCaritas Baby Hospital Bethlehem, Bethlehem, Palestine.
Jimmy ZaidanCaritas Baby Hospital Bethlehem, Bethlehem, Palestine.
Hiyam MarzouqaCaritas Baby Hospital Bethlehem, Bethlehem, Palestine.
Peter BauerInstitute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.ORCID http://orcid.org/0000-0001-9414-4555
Ludger SchölsDepartment of Neurology and Hertie-Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany. ludger.schoels@uni-tuebingen.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID34050322
PMCPMC8821631

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.