N Narita, H Nishio, Y Kitoh, Y Ishikawa, Y Ishikawa, R Minami, H Nakamura, M Matsuo
Title and authors | Publication | Year |
---|---|---|
Genome-wide analysis of mobile genetic element insertion sites
K Rawal, R Ramaswamy |
Nucleic Acids Research | 2011 |
On the sequence-directed nature of human gene mutation: The role of genomic architecture and the local DNA sequence environment in mediating gene mutations underlying human inherited disease
DN Cooper, A Bacolla, C Férec, KM Vasquez, H Kehrer-Sawatzki, JM Chen |
Human Mutation | 2011 |
L1 Hybridization Enrichment: A Method for Directly Accessing De Novo L1 Insertions in the Human Germline
P Freeman, C Macfarlane, P Collier, AJ Jeffreys, RM Badge |
Human Mutation | 2011 |
Duchenne muscular dystrophy caused by a complex rearrangement between intron 43 of the DMD gene and chromosome 4
B Baskin, WT Gibson, PN Ray |
Neuromuscular Disorders | 2011 |
Pathogenic orphan transduction created by a non-reference LINE-1 retrotransposon
S Solyom, AD Ewing, DC Hancks, Y Takeshima, H Awano, M Matsuo, HH Kazazian |
Human Mutation | 2011 |
LINE-1 elements in structural variation and disease
CR Beck, JL Garcia-Perez, RM Badge, JV Moran |
Annual Review of Genomics and Human Genetics | 2011 |