Evidence map›Paper›PMID 33275912›Full record

ArticleAmerican journal of human genetics2020

Response to Hall et al.

Jessica X Chong, Jared C Talbot, Emily M Teets, Samantha Previs, Brit L Martin, Kathryn M Shively, Colby T Marvin, Arthur S Aylsworth, Reem Saadeh-Haddad, Ulrich A Schatz and 22 more

Abstract readLetterComment
PubMed Full text at PMC Publisher
In one paragraph

Article in American journal of human genetics, 2020. 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
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

32 authors.

Jessica X ChongDivision of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, WA 98195, USA; Brotman-Baty Institute, Seattle, WA 98195, USA.
Jared C TalbotDepartment of Molecular Genetics, The Ohio State University, Columbus, OH 43210, USA; Center for Muscle Health and Neuromuscular Disorders, Columbus OH 43210, USA. Electronic address: jared.talbot@maine.edu.
Emily M TeetsDepartment of Molecular Genetics, The Ohio State University, Columbus, OH 43210, USA.
Samantha PrevisDepartment of Molecular Physiology and Biophysics, University of Vermont, Burlington, VT 05405, USA.
Brit L MartinDepartment of Physiology and Cell Biology, The Ohio State University, Columbus, OH 43210, USA.
Kathryn M ShivelyDivision of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, WA 98195, USA.
Colby T MarvinDivision of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, WA 98195, USA.
Arthur S AylsworthDepartments of Pediatrics and Genetics, University of North Carolina, Chapel Hill, NC 27599, USA.
Reem Saadeh-HaddadDivision of Genetics, Department of Pediatrics, Medstar Georgetown University Hospital, Washington, DC 20007, USA.
Ulrich A SchatzHuman Genetics, Medical University, Innsbruck 6020, Austria.
Francesca InzanaGenetic Counseling Service, Department of Pediatrics, Regional Hospital of Bolzano, Bolzano 39100, Italy.
Tawfeg Ben-OmranDivision of Genetic and Genomic Medicine, Sidra Medicine and Hamad Medical Corporation, PO Box 3050, Doha, Qatar.
Fatima AlmusafriDivision of Genetic and Genomic Medicine, Sidra Medicine and Hamad Medical Corporation, PO Box 3050, Doha, Qatar.
Mariam Al-MullaDivision of Genetic and Genomic Medicine, Sidra Medicine and Hamad Medical Corporation, PO Box 3050, Doha, Qatar.
Kati J BuckinghamDivision of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, WA 98195, USA.
Tamar HarelDepartment of Genetics, Hadassah-Hebrew University Medical Center, Jerusalem 91120, Israel.
Hagar Mor-ShakedDepartment of Genetics, Hadassah-Hebrew University Medical Center, Jerusalem 91120, Israel.
Periyasamy RadhakrishnanDepartment of Medical Genetics, Kasturba Medical College, Manipal, Manipal Academy of Higher Education, Manipal 576104, India.
Katta M GirishaDepartment of Medical Genetics, Kasturba Medical College, Manipal, Manipal Academy of Higher Education, Manipal 576104, India.
Shalini S NayakDepartment of Medical Genetics, Kasturba Medical College, Manipal, Manipal Academy of Higher Education, Manipal 576104, India.
Anju ShuklaDepartment of Medical Genetics, Kasturba Medical College, Manipal, Manipal Academy of Higher Education, Manipal 576104, India.
Klaus DieterichDepartment of Medical Genetics, CHU Grenoble Alpes, Génétique Médicale, Grenoble 38700, France; Université Grenoble Alpes, Inserm, U1216, Grenoble Institut des Neurosciences, Grenoble 38706, France.
Julien FaureUniversité Grenoble Alpes, Inserm, U1216, Grenoble Institut des Neurosciences, Grenoble 38706, France; Biochimie Génétique et Moléculaire, CHU Grenoble Alpes, Grenoble 38700, France.
John RenduUniversité Grenoble Alpes, Inserm, U1216, Grenoble Institut des Neurosciences, Grenoble 38706, France; Biochimie Génétique et Moléculaire, CHU Grenoble Alpes, Grenoble 38700, France.
Yline CapriDepartment of Genetics, APHP-Robert DEBRE University Hospital, UF Génétique clinique, Paris 75019, France.
Xenia LatypovaUniversité Grenoble Alpes, Inserm, U1216, Grenoble Institut des Neurosciences, Grenoble 38706, France; Biochimie Génétique et Moléculaire, CHU Grenoble Alpes, Grenoble 38700, France.
Deborah A NickersonBrotman-Baty Institute, Seattle, WA 98195, USA; Department of Genome Sciences, University of Washington, Seattle, WA 98195, USA.
David WarshawDepartment of Molecular Physiology and Biophysics, University of Vermont, Burlington, VT 05405, USA.
Paul M JanssenDepartment of Physiology and Cell Biology, The Ohio State University, Columbus, OH 43210, USA.
University of Washington Center for Mendelian Genomics
Sharon L AmacherDepartment of Molecular Genetics, The Ohio State University, Columbus, OH 43210, USA; Center for Muscle Health and Neuromuscular Disorders, Columbus OH 43210, USA; Dept of Biological Chemistry and Pharmacology, The Ohio State University, Columbus, OH 43210, USA; Center for RNA Biology, The Ohio State University, Columbus, OH 43210, USA.
Michael J BamshadDivision of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, WA 98195, USA; Brotman-Baty Institute, Seattle, WA 98195, USA; Department of Genome Sciences, University of Washington, Seattle, WA 98195, USA; Seattle Children's Hospital, Seattle, WA 98105, USA. Electronic address: mbamshad@uw.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

ArthrogryposisMusculoskeletal AbnormalitiesHumansMutation

Identifiers

PMID33275912
PMCPMC7820630

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.