ArticleNucleic acids research1998
MITOMAP: a human mitochondrial genome database--1998 update.
Article in Nucleic acids research, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.
What it found
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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
27 citing papers in PubMed.
- Large-scale human genomic resources drive innovations toward forensic intelligent source attribution and precision identification.International journal of legal medicine · 2026Review
- Mitochondrial genetic variation across tissues of the human body.Nucleic acids research · 2026Article
- MitoCommun: a database for decoding mitochondrial communication networks.BMC genomics · 2026Article
- Benchmarking the Effectiveness and Accuracy of Multiple Mitochondrial DNA Variant Callers: Practical Implications for Clinical Application.Frontiers in genetics · 2022Article
- The mining and construction of a knowledge base for gene-disease association in mitochondrial diseases.Scientific reports · 2021Article
- Organ reserve, excess metabolic capacity, and aging.Biogerontology · 2018Review
- Mutation Analysis of the Mitochondrial tRNA Genes in Iranian Coronary Atherosclerosis Patients.Iranian journal of public health · 2017Article
- Fifteen novel mutations in the mitochondrial NADH dehydrogenase subunit 1, 2, 3, 4, 4L, 5 and 6 genes from Iranian patients with Leber's hereditary optic neuropathy (LHON).Molecular biology reports · 2013Article
- Why mitochondria must fuse to maintain their genome integrity.Antioxidants & redox signaling · 2013Review
- Progressive myoclonic epilepsies: review of clinical, molecular and therapeutic aspects.Journal of neurology · 2010Review
- Mitochondrial DNA mutations in oxyphilic and chief cell parathyroid adenomas.BMC endocrine disorders · 2007Article
- Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing loss.Human genetics · 2005Article
- Clinical and molecular characterization of a Chinese patient with auditory neuropathy associated with mitochondrial 12S rRNA T1095C mutation.American journal of medical genetics. Part A · 2005Article
- MITOMAP: a human mitochondrial genome database--2004 update.Nucleic acids research · 2005Article
- Aminoacylation properties of pathology-related human mitochondrial tRNA(Lys) variants.RNA (New York, N.Y.) · 2004Article
- Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family.American journal of human genetics · 2004Article
- MitoP2, an integrated database on mitochondrial proteins in yeast and man.Nucleic acids research · 2004Article
- Techniques and pitfalls in the detection of pathogenic mitochondrial DNA mutations.The Journal of molecular diagnostics : JMD · 2003Review
- A compositional segmentation of the human mitochondrial genome is related to heterogeneities in the guanine mutation rate.Nucleic acids research · 2003Article
- The other, forgotten genome: mitochondrial DNA and mental disorders.Molecular psychiatry · 2001Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
Abstract
We have continued to develop MITOMAP (http://www.gen.emory. edu/MITOMAP ), a comprehensive database for the human mitochondrial DNA (mtDNA). MITOMAP uses the mtDNA sequence as the unifying element for bringing together information on mitochondrial genome structure and function, pathogenic mutations and their clinical characteristics, population associated variation, and gene-gene interactions. Over the past year we have increased the degree of interlinking of MITOMAP information available on the web page, by using our generalized information management system, GENOME. As increasingly larger regions of the human genome are sequenced and characterized, the need for integrating such information is growing. Consequently, MITOMAP and GENOME provide a valuable reference for the mitochondrial biologist, in addition to being a model for the development of comprehensive, information storage and retrieval systems for other components of the human genome. This paper documents the changes to MITOMAP which have been implemented over the past year.
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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.