Evidence map›Paper›PMID 24416505›Full record

ArticleClinical case reports2013

Complex cytogenetic rearrangements at the DURS1 locus in syndromic Duane retraction syndrome.

Hagit N Baris, Wai-Man Chan, Caroline Andrews, Doron M Behar, Diana J Donovan, Cynthia C Morton, Judith Ranells, Tuya Pal, Azra H Ligon, Elizabeth C Engle

Open access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Clinical case reports, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 33% of its field
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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 7 institutions in 2 countries.

Hagit N BarisProgram in Genomics, Boston Children's Hospital, Boston, MA 02115 USA ; The Recanati Genetic Institute, Beilinson Hospital, Rabin Medical Center, Petah Tikva, Israel ; Sackler school of Medicine, Tel Aviv University, Israel.
Wai-Man ChanProgram in Genomics, Boston Children's Hospital, Boston, MA 02115 USA ; Department of Medicine (Genetics), Boston Children's Hospital, Boston, MA 02115 USA ; Department of Neurology, Boston Children's Hospital, Boston, MA 02115 USA ; The Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA 02115 USA ; Harvard Medical School, Boston, MA 02115 USA ; Howard Hughes Medical Institute, Chevy Chase, MD 20815 USA.
Caroline AndrewsProgram in Genomics, Boston Children's Hospital, Boston, MA 02115 USA ; Department of Medicine (Genetics), Boston Children's Hospital, Boston, MA 02115 USA ; Department of Neurology, Boston Children's Hospital, Boston, MA 02115 USA ; Department of Ophthalmology, Boston Children's Hospital, Boston, MA 02115 USA ; The Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA 02115 USA ; Harvard Medical School, Boston, MA 02115 USA ; Howard Hughes Medical Institute, Chevy Chase, MD 20815 USA.
Doron M BeharThe Recanati Genetic Institute, Beilinson Hospital, Rabin Medical Center, Petah Tikva, Israel.
Diana J DonovanDepartment of Pathology, Brigham and Women's Hospital, Boston, MA USA.
Cynthia C MortonHarvard Medical School, Boston, MA 02115 USA ; Department of Pathology, Brigham and Women's Hospital, Boston, MA USA.
Judith RanellsDepartment of Pediatrics, University of South Florida, Tampa, FL 33606 USA.
Tuya PalH.Lee Moffitt Cancer Center and Research Institute, Tampa, FL 33612 USA ; The University of South Florida, College of Medicine, Department of Oncologic Sciences, Tampa, FL 33612 USA.
Azra H LigonHarvard Medical School, Boston, MA 02115 USA ; Department of Pathology, Brigham and Women's Hospital, Boston, MA USA.
Elizabeth C EngleProgram in Genomics, Boston Children's Hospital, Boston, MA 02115 USA ; Department of Medicine (Genetics), Boston Children's Hospital, Boston, MA 02115 USA ; Department of Neurology, Boston Children's Hospital, Boston, MA 02115 USA ; Department of Ophthalmology, Boston Children's Hospital, Boston, MA 02115 USA ; FM Kirby Neurobiology Center, Boston Children's Hospital, Boston, MA 02115 USA ; The Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA 02115 USA ; Harvard Medical School, Boston, MA 02115 USA ; Howard Hughes Medical Institute, Chevy Chase, MD 20815 USA.
Harvard University · USUniversity of South Florida · USBoston Children's Hospital · USBrigham and Women's Hospital · USDana-Farber/Boston Children's Cancer and Blood Disorders Center · USHoward Hughes Medical Institute · USRabin Medical Center · IL

Funding

MOLECULAR BASIS OF CONGENITAL STRABISMUSR01EY012498 · NEI · CHILDREN'S HOSPITAL BOSTON · PI ENGLE, ELIZABETH C. · 1999 to 2015
$5.3M
Genetic Etiologies of Horizontal StrabismusR01EY015298 · NEI · CHILDREN'S HOSPITAL BOSTON · PI ENGLE, ELIZABETH C. · 2004 to 2015
$4.9M
Positional Cloning of the Duane Syndrome DURS2 GeneF32EY016306 · NEI · CHILDREN'S HOSPITAL BOSTON · PI BARIS, HAGIT · 2004 to 2005
$95k
NEI NIH HHS F32 EY016306NEI NIH HHS R01 EY012498NEI NIH HHS R01 EY015298
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

8q12 microduplication syndromecopy number variationcytogeneticsDuane retraction syndromeDURS1

Identifiers

PMID24416505
PMCPMC3885256
OpenAlexW2118181611

What 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.