| scholarly article | Q13442814 |
| P50 | author | Peter Aplan | Q89272233 |
| P2093 | author name string | Masahiro Onozawa | |
| Liat Goldberg | |||
| P2860 | cites work | Initial sequencing and analysis of the human genome | Q21045365 |
| Retrotransposition of gene transcripts leads to structural variation in mammalian genomes | Q21183991 | ||
| An integrated map of genetic variation from 1,092 human genomes | Q22122153 | ||
| Mitochondrial DNA and human evolution | Q22122407 | ||
| The human genome browser at UCSC | Q24672361 | ||
| Y chromosome sequence variation and the history of human populations | Q28142979 | ||
| Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays | Q28263829 | ||
| LINE-1 retrotransposition activity in human genomes | Q28743798 | ||
| Pattern of organization of human mitochondrial pseudogenes in the nuclear genome | Q28768380 | ||
| Millions of years of evolution preserved: a comprehensive catalog of the processed pseudogenes in the human genome | Q28775887 | ||
| The origin and evolution of mutations in acute myeloid leukemia | Q29614630 | ||
| Natural mutagenesis of human genomes by endogenous retrotransposons | Q29619443 | ||
| Nuclear pseudogenes of mitochondrial DNA as a variable part of the human genome | Q30831922 | ||
| Efficient repair of DNA double-strand breaks in malignant cells with structural instability | Q33554472 | ||
| Repair of DNA double-strand breaks by templated nucleotide sequence insertions derived from distant regions of the genome | Q33694621 | ||
| Ubiquitinated sperm mitochondria, selective proteolysis, and the regulation of mitochondrial inheritance in mammalian embryos. | Q33910756 | ||
| Structure and chromosomal distribution of human mitochondrial pseudogenes | Q33959798 | ||
| Chromosomal aberrations induced by double strand DNA breaks | Q34049453 | ||
| A recent common ancestry for human Y chromosomes | Q34288673 | ||
| Comprehensive genomic analysis of rhabdomyosarcoma reveals a landscape of alterations affecting a common genetic axis in fusion-positive and fusion-negative tumors | Q35711420 | ||
| The origin, evolution, and functional impact of short insertion-deletion variants identified in 179 human genomes | Q36800421 | ||
| Mobile interspersed repeats are major structural variants in the human genome | Q42423737 | ||
| Molecular evolution and tempo of amplification of human LINE-1 retrotransposons since the origin of primates. | Q43192302 | ||
| Novel mitochondrial DNA insertion polymorphism and its usefulness for human population studies. | Q47814777 | ||
| Human genetic disease caused by de novo mitochondrial-nuclear DNA transfer. | Q54793719 | ||
| Germ line insertion of mtDNA at the breakpoint junction of a reciprocal constitutional translocation | Q64388078 | ||
| P433 | issue | 4 | |
| P304 | page(s) | 960-968 | |
| P577 | publication date | 2015-03-04 | |
| P1433 | published in | Genome Biology and Evolution | Q15817736 |
| P1476 | title | Landscape of insertion polymorphisms in the human genome | |
| P478 | volume | 7 |
| Q98466776 | Current Understanding of the Genetics of Intervertebral Disc Degeneration |
| Q44807078 | FGF4 retrogene on CFA12 is responsible for chondrodystrophy and intervertebral disc disease in dogs |
| Q37471101 | Nuclear Noncoding RNAs and Genome Stability. |
| Q39355640 | Public antibodies to malaria antigens generated by two LAIR1 insertion modalities |
| Q28078682 | Templated Sequence Insertion Polymorphisms in the Human Genome |
| Q47830580 | Widening the spectrum of deletions and molecular mechanisms underlying alpha-thalassemia. |
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