ArticleNucleic acids research2005
Multiplexed discovery of sequence polymorphisms using base-specific cleavage and MALDI-TOF MS.
Article in Nucleic acids research, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 1 of them a synthesis that pooled it.
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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.
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Who cites it
37 citing papers in PubMed, 1 synthesis or guideline pooled it.
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- Testing candidate genes linked to corolla shape variation of a pollinator shift in Rhytidophyllum (Gesneriaceae).PloS one · 2022Article
- The role of oxytocin signaling in depression and suicidality in returning war veterans.Psychoneuroendocrinology · 2021Article
- Prenatal Maternal Stress From a Natural Disaster and Hippocampal Volumes: Gene-by-Environment Interactions in Young Adolescents From Project Ice Storm.Frontiers in behavioral neuroscience · 2021Article
- Facing the Methodological Challenge in Dissecting the Genetics of ADHD: A Case for Deep Phenotyping and Heterogeneity Reduction.Journal of the Canadian Academy of Child and Adolescent Psychiatry = Journal de l'Academie canadienne de psychiatrie de l'enfant et de l'adolescent · 2020Article
- Analysis of hepatitis B virus-mixed genotype infection by ultra deep pyrosequencing in Sudanese patients, 2015-2016.Infection · 2019Article
- Epigenetically induced ectopic expression of UNCX impairs the proliferation and differentiation of myeloid cells.Haematologica · 2017Article
- Angiogenesis related genes NOS3, CD14, MMP3 and IL4R are associated to VEGF gene expression and circulating levels in healthy adults.BMC medical genetics · 2015Article
- Mendelian randomization supports causality between maternal hyperglycemia and epigenetic regulation of leptin gene in newborns.Epigenetics · 2015Article
- Association of a risk allele of ANK3 with cognitive performance and cortical thickness in patients with first-episode psychosis.Journal of psychiatry & neuroscience : JPN · 2014Article
- Differential methylation relative to breast cancer subtype and matched normal tissue reveals distinct patterns.Breast cancer research and treatment · 2013Article
- Inherited common variants in mitochondrial DNA and invasive serous epithelial ovarian cancer risk.BMC research notes · 2013Article
- Genetic analysis of disheveled 2 and disheveled 3 in human neural tube defects.Journal of molecular neuroscience : MN · 2013Article
- A common variant highly associated with plasma VEGFA levels also contributes to the variation of both LDL-C and HDL-C.Journal of lipid research · 2013Article
- Vimentin DNA methylation predicts survival in breast cancer.Breast cancer research and treatment · 2013Article
- Quantitative DNA methylation analysis of genes coding for kallikrein-related peptidases 6 and 10 as biomarkers for prostate cancer.Epigenetics · 2012Article
- Depression and anxiety symptoms among women who carry the FMR1 premutation: impact of raising a child with fragile X syndrome is moderated by CRHR1 polymorphisms.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2012Article
- Differential association between the norepinephrine transporter gene and ADHD: role of sex and subtype.Journal of psychiatry & neuroscience : JPN · 2012Article
Corrections and comments
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Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The completion of the Human Genome Project provides researchers with a reference sequence that covers about 99% of the gene-containing regions and is more than 99.9% accurate. Sequence drafts and completed sequences for several other species are also available to researchers worldwide. The ongoing effort to provide more and more genomic reference information now enables the detection of deviations from this 'genetic blueprint'. Comparative sequencing projects will play a major role in elucidating the meaning of the genetic code and in establishing a correlation between genotype and phenotype. As part of this effort, a number of projects will focus on distinct functional aspects, like resequencing of exons or HLA determining regions. Typically these target regions are short in length and their analysis does not require long read length. To find an efficient solution for these applications, we developed a novel method that allows simultaneous analysis of multiple independent target regions (Multiplexed Comparative Sequence Analysis) by employing base-specific cleavage biochemistry and MALDI TOF-MS analysis.
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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.