Article in Genes, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.
0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 36% 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
8 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.
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
16 authors at 4 institutions in 3 countries.
Noluthando ManyisaDepartment of Medicine, Division of Human Genetics, Faculty of Health Sciences, University of Cape Town, Cape Town 7925, South Africa.
Isabelle SchrauwenCenter for Statistical Genetics, Sergievsky Center and the Department of Neurology, Columbia University Medical Center, New York, NY 10032, USA.ORCID 0000-0001-7310-6082
Leonardo Alves de Souza RiosDepartment of Pathology, Division of Haematology, Faculty of Health Sciences, University of Cape Town, Observatory, Cape Town 7925, South Africa.ORCID 0000-0002-8298-2399
Shaheen MowlaDepartment of Pathology, Division of Haematology, Faculty of Health Sciences, University of Cape Town, Observatory, Cape Town 7925, South Africa.ORCID 0000-0001-6802-0495
Cedrik Tekendo-NgongangMedical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA.ORCID 0000-0002-2709-4807
Kalinka PopelDepartment of Medicine, Division of Human Genetics, Faculty of Health Sciences, University of Cape Town, Cape Town 7925, South Africa.
Kevin EsohDepartment of Medicine, Division of Human Genetics, Faculty of Health Sciences, University of Cape Town, Cape Town 7925, South Africa.ORCID 0000-0002-4024-5681
Thashi BharadwajCenter for Statistical Genetics, Sergievsky Center and the Department of Neurology, Columbia University Medical Center, New York, NY 10032, USA.
Liz M Nouel-SaiedCenter for Statistical Genetics, Sergievsky Center and the Department of Neurology, Columbia University Medical Center, New York, NY 10032, USA.ORCID 0000-0003-0378-7788
Anushree AcharyaCenter for Statistical Genetics, Sergievsky Center and the Department of Neurology, Columbia University Medical Center, New York, NY 10032, USA.
Abdul NasirSynthetic Protein Engineering Lab (SPEL), Department of Molecular Science and Technology, Ajou University, Suwon 443-749, Korea.ORCID 0000-0002-2339-3500
Edmond Wonkam-TingangDepartment of Medicine, Division of Human Genetics, Faculty of Health Sciences, University of Cape Town, Cape Town 7925, South Africa.ORCID 0000-0003-3625-5059
Carmen de KockDepartment of Medicine, Division of Human Genetics, Faculty of Health Sciences, University of Cape Town, Cape Town 7925, South Africa.
Collet DandaraDepartment of Medicine, Division of Human Genetics, Faculty of Health Sciences, University of Cape Town, Cape Town 7925, South Africa.ORCID 0000-0002-5925-4895
Suzanne M LealCenter for Statistical Genetics, Sergievsky Center and the Department of Neurology, Columbia University Medical Center, New York, NY 10032, USA.
Ambroise WonkamDepartment of Medicine, Division of Human Genetics, Faculty of Health Sciences, University of Cape Town, Cape Town 7925, South Africa.ORCID 0000-0003-1420-9051
University of Cape Town · ZAColumbia University Irving Medical Center · USAjou University · KRNational Institutes of Health · US
Funding
Identification of Nonsyndromic Hearing Impairment GenesR01DC003594 · NIDCD · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI SUZANNE M LEAL · 2004 to 2026
$7.7M
Localization of Nonsyndromic Hearing Impairment GenesR01DC011651 · NIDCD · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI LEAL, SUZANNE M · 2011 to 2020
$2.9M
Identification and Functional Evaluation of Autosomal Recessive Nonsyndromic Hearing Impairment Genes in sub-Saharan AfricansR01DC016593 · NIDCD · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI LEAL, SUZANNE M · 2018 to 2022
Hearing impairment (HI) is a sensory disorder with a prevalence of 0.0055 live births in South Africa. DNA samples from a South African family presenting with progressive, autosomal dominant non-syndromic HI were subjected to whole-exome sequencing, and a novel monoallelic variant in
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 Socratic graph.