ArticleScience (New York, N.Y.)2012
Genetics. Human genetic variation, shared and private.
Article in Science (New York, N.Y.), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.
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
20 citing papers in PubMed.
- An Evolutionary Portrait of the Progenitor SARS-CoV-2 and Its Dominant Offshoots in COVID-19 Pandemic.Molecular biology and evolution · 2021Article
- Admixture Has Shaped Romani Genetic Diversity in Clinically Relevant Variants.Frontiers in genetics · 2021Article
- Proteome-Scale Mapping of Perturbed Proteostasis in Living Cells.Cold Spring Harbor perspectives in biology · 2020Review
- Comprehensive genetic testing of Chinese SNHL patients and variants interpretation using ACMG guidelines and ethnically matched normal controls.European journal of human genetics : EJHG · 2020Article
- The Brazilian Initiative on Precision Medicine (BIPMed): fostering genomic data-sharing of underrepresented populations.NPJ genomic medicine · 2020Article
- Patterns of Genetic Coding Variation in a Native American Population before and after European Contact.American journal of human genetics · 2018Article
- Host and Microbiome Genome-Wide Association Studies: Current State and Challenges.Frontiers in genetics · 2018Review
- Intact piRNA pathway prevents L1 mobilization in male meiosis.Proceedings of the National Academy of Sciences of the United States of America · 2017Article
- Genome-Scale Networks Link Neurodegenerative Disease Genes to α-Synuclein through Specific Molecular Pathways.Cell systems · 2017Article
- Properties of human disease genes and the role of genes linked to Mendelian disorders in complex disease aetiology.Human molecular genetics · 2017Article
- Comprehensive genetic testing with ethnic-specific filtering by allele frequency in a Japanese hearing-loss population.Clinical genetics · 2016Article
- Next-generation Sequencing of RYR1 and CACNA1S in Malignant Hyperthermia and Exertional Heat Illness.Anesthesiology · 2015Article
- Combating neurodegenerative disease with chemical probes and model systems.Nature chemical biology · 2014Review
- Population and genomic lessons from genetic analysis of two Indian populations.Human genetics · 2014Article
- Genetic counselors' views and experiences with the clinical integration of genome sequencing.Journal of genetic counseling · 2014Article
- 8-oxoguanine causes spontaneous de novo germline mutations in mice.Scientific reports · 2014Article
- Clioquinol promotes the degradation of metal-dependent amyloid-β (Aβ) oligomers to restore endocytosis and ameliorate Aβ toxicity.Proceedings of the National Academy of Sciences of the United States of America · 2014Article
- The deleterious mutation load is insensitive to recent population history.Nature genetics · 2014Article
- Population growth inflates the per-individual number of deleterious mutations and reduces their mean effect.Genetics · 2013Article
- Low frequency variants, collapsed based on biological knowledge, uncover complexity of population stratification in 1000 genomes project data.PLoS genetics · 2013Article
Corrections and comments
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Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
PubMed holds no abstract for this paper.
Indexed as
Identifiers
22767915What OpenQuestion holds
Registered trials
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.