ArticleAmerican journal of human genetics1995
Computer programs for multilocus haplotyping of general pedigrees.
Article in American journal of human genetics, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 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
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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
78 citing papers in PubMed.
- Article
- Comprehensive genomic analyses associate UGT8 variants with musical ability in a Mongolian population.Journal of medical genetics · 2012Article
- TGFB2 mutations cause familial thoracic aortic aneurysms and dissections associated with mild systemic features of Marfan syndrome.Nature genetics · 2012Article
- Novel mutation and three other sequence variants segregating with phenotype at keratoconus 13q32 susceptibility locus.European journal of human genetics : EJHG · 2012Article
- Sex-specific effect of the TP53 PIN3 polymorphism on cancer risk in a cohort study of TP53 germline mutation carriers.Human genetics · 2011Article
- Imputation of missing genotypes from sparse to high density using long-range phasing.Genetics · 2011Article
- Sequence variants in COL4A1 and COL4A2 genes in Ecuadorian families with keratoconus.Molecular vision · 2011Article
- Autosomal dominant progressive sensorineural hearing loss due to a novel mutation in the KCNQ4 gene.Archives of otolaryngology--head & neck surgery · 2011Article
- BDNF contributes to the genetic variance of milk fat yield in german holstein cattle.Frontiers in genetics · 2011Article
- Identification of novel suggestive loci for high-grade myopia in Polish families.Molecular vision · 2011Article
- Novel autosomal recessive nonsyndromic hearing impairment locus DFNB90 maps to 7p22.1-p15.3.Human heredity · 2011Article
- Identification of missense mutation (I12T) in the BSND gene and bioinformatics analysis.Journal of biomedicine & biotechnology · 2011Article
- Article
- Ordered subset analysis identifies loci influencing lung cancer risk on chromosomes 6q and 12q.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2010Article
- A fourth locus for autosomal dominant hypercholesterolemia maps at 16q22.1.European journal of human genetics : EJHG · 2010Article
- Genetic mapping of a novel hypotrichosis locus to chromosome 7p21.3-p22.3 in a Pakistani family and screening of the candidate genes.Human genetics · 2010Article
- Homozygosity mapping reveals mutations of GRXCR1 as a cause of autosomal-recessive nonsyndromic hearing impairment.American journal of human genetics · 2010Article
- Ectodermal dysplasia-cutaneous syndactyly syndrome maps to chromosome 7p21.1-p14.3.Human genetics · 2009Article
- Most parsimonious haplotype allele sharing determination.BMC bioinformatics · 2009Article
- Localization of a gene for keratoconus to a 5.6-Mb interval on 13q32.Investigative ophthalmology & visual science · 2009Article
18 more citing papers are in PubMed but not listed here.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
Abstract
PubMed holds no abstract for this paper.
Indexed as
Identifiers
7762577PMC1801078What 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.