194 related articles for article (PubMed ID: 25886137)
1. Detecting non-allelic homologous recombination from high-throughput sequencing data.
Parks MM; Lawrence CE; Raphael BJ
Genome Biol; 2015 Apr; 16(1):72. PubMed ID: 25886137
[TBL] [Abstract][Full Text] [Related]
2. Correlation between frequency of non-allelic homologous recombination and homology properties: evidence from homology-mediated CNV mutations in the human genome.
Peng Z; Zhou W; Fu W; Du R; Jin L; Zhang F
Hum Mol Genet; 2015 Mar; 24(5):1225-33. PubMed ID: 25324539
[TBL] [Abstract][Full Text] [Related]
3. Optical mapping of the 22q11.2DS region reveals complex repeat structures and preferred locations for non-allelic homologous recombination (NAHR).
Pastor S; Tran O; Jin A; Carrado D; Silva BA; Uppuluri L; Abid HZ; Young E; Crowley TB; Bailey AG; McGinn DE; McDonald-McGinn DM; Zackai EH; Xie M; Taylor D; Morrow BE; Xiao M; Emanuel BS
Sci Rep; 2020 Jul; 10(1):12235. PubMed ID: 32699385
[TBL] [Abstract][Full Text] [Related]
4. Alu-mediated diverse and complex pathogenic copy-number variants within human chromosome 17 at p13.3.
Gu S; Yuan B; Campbell IM; Beck CR; Carvalho CM; Nagamani SC; Erez A; Patel A; Bacino CA; Shaw CA; Stankiewicz P; Cheung SW; Bi W; Lupski JR
Hum Mol Genet; 2015 Jul; 24(14):4061-77. PubMed ID: 25908615
[TBL] [Abstract][Full Text] [Related]
5. Human endogenous retroviral elements promote genome instability via non-allelic homologous recombination.
Campbell IM; Gambin T; Dittwald P; Beck CR; Shuvarikov A; Hixson P; Patel A; Gambin A; Shaw CA; Rosenfeld JA; Stankiewicz P
BMC Biol; 2014 Sep; 12():74. PubMed ID: 25246103
[TBL] [Abstract][Full Text] [Related]
6. Frequency of nonallelic homologous recombination is correlated with length of homology: evidence that ectopic synapsis precedes ectopic crossing-over.
Liu P; Lacaria M; Zhang F; Withers M; Hastings PJ; Lupski JR
Am J Hum Genet; 2011 Oct; 89(4):580-8. PubMed ID: 21981782
[TBL] [Abstract][Full Text] [Related]
7. The role of gene conversion in preserving rearrangement hotspots in the human genome.
Fawcett JA; Innan H
Trends Genet; 2013 Oct; 29(10):561-8. PubMed ID: 23953668
[TBL] [Abstract][Full Text] [Related]
8. NAHR-mediated copy-number variants in a clinical population: mechanistic insights into both genomic disorders and Mendelizing traits.
Dittwald P; Gambin T; Szafranski P; Li J; Amato S; Divon MY; Rodríguez Rojas LX; Elton LE; Scott DA; Schaaf CP; Torres-Martinez W; Stevens AK; Rosenfeld JA; Agadi S; Francis D; Kang SH; Breman A; Lalani SR; Bacino CA; Bi W; Milosavljevic A; Beaudet AL; Patel A; Shaw CA; Lupski JR; Gambin A; Cheung SW; Stankiewicz P
Genome Res; 2013 Sep; 23(9):1395-409. PubMed ID: 23657883
[TBL] [Abstract][Full Text] [Related]
9. A chromosomal rearrangement hotspot can be identified from population genetic variation and is coincident with a hotspot for allelic recombination.
Lindsay SJ; Khajavi M; Lupski JR; Hurles ME
Am J Hum Genet; 2006 Nov; 79(5):890-902. PubMed ID: 17033965
[TBL] [Abstract][Full Text] [Related]
10. Identification of recurrent type-2 NF1 microdeletions reveals a mitotic nonallelic homologous recombination hotspot underlying a human genomic disorder.
Vogt J; Mussotter T; Bengesser K; Claes K; Högel J; Chuzhanova N; Fu C; van den Ende J; Mautner VF; Cooper DN; Messiaen L; Kehrer-Sawatzki H
Hum Mutat; 2012 Nov; 33(11):1599-609. PubMed ID: 22837079
[TBL] [Abstract][Full Text] [Related]
11. Human Structural Variation: Mechanisms of Chromosome Rearrangements.
Weckselblatt B; Rudd MK
Trends Genet; 2015 Oct; 31(10):587-599. PubMed ID: 26209074
[TBL] [Abstract][Full Text] [Related]
12. Fine characterisation of a recombination hotspot at the DPY19L2 locus and resolution of the paradoxical excess of duplications over deletions in the general population.
Coutton C; Abada F; Karaouzene T; Sanlaville D; Satre V; Lunardi J; Jouk PS; Arnoult C; Thierry-Mieg N; Ray PF
PLoS Genet; 2013 Mar; 9(3):e1003363. PubMed ID: 23555282
[TBL] [Abstract][Full Text] [Related]
13. Genome-wide signatures of 'rearrangement hotspots' within segmental duplications in humans.
Uddin M; Sturge M; Peddle L; O'Rielly DD; Rahman P
PLoS One; 2011; 6(12):e28853. PubMed ID: 22194928
[TBL] [Abstract][Full Text] [Related]
14. The rate of nonallelic homologous recombination in males is highly variable, correlated between monozygotic twins and independent of age.
MacArthur JA; Spector TD; Lindsay SJ; Mangino M; Gill R; Small KS; Hurles ME
PLoS Genet; 2014 Mar; 10(3):e1004195. PubMed ID: 24603440
[TBL] [Abstract][Full Text] [Related]
15. Analysis of meiotic recombination in 22q11.2, a region that frequently undergoes deletions and duplications.
Torres-Juan L; Rosell J; Sánchez-de-la-Torre M; Fibla J; Heine-Suñer D
BMC Med Genet; 2007 Apr; 8():14. PubMed ID: 17397557
[TBL] [Abstract][Full Text] [Related]
16. Fine mapping of meiotic NAHR-associated crossovers causing large NF1 deletions.
Hillmer M; Wagner D; Summerer A; Daiber M; Mautner VF; Messiaen L; Cooper DN; Kehrer-Sawatzki H
Hum Mol Genet; 2016 Feb; 25(3):484-96. PubMed ID: 26614388
[TBL] [Abstract][Full Text] [Related]
17. Annotation of pseudogenic gene segments by massively parallel sequencing of rearranged lymphocyte receptor loci.
Dean J; Emerson RO; Vignali M; Sherwood AM; Rieder MJ; Carlson CS; Robins HS
Genome Med; 2015 Nov; 7():123. PubMed ID: 26596423
[TBL] [Abstract][Full Text] [Related]
18. Ionizing radiation and genetic risks XIV. Potential research directions in the post-genome era based on knowledge of repair of radiation-induced DNA double-strand breaks in mammalian somatic cells and the origin of deletions associated with human genomic disorders.
Sankaranarayanan K; Wassom JS
Mutat Res; 2005 Oct; 578(1-2):333-70. PubMed ID: 16084534
[TBL] [Abstract][Full Text] [Related]
19. Sequencing individual genomes with recurrent genomic disorder deletions: an approach to characterize genes for autosomal recessive rare disease traits.
Yuan B; Schulze KV; Assia Batzir N; Sinson J; Dai H; Zhu W; Bocanegra F; Fong CT; Holder J; Nguyen J; Schaaf CP; Yang Y; Bi W; Eng C; Shaw C; Lupski JR; Liu P
Genome Med; 2022 Sep; 14(1):113. PubMed ID: 36180924
[TBL] [Abstract][Full Text] [Related]
20. Characterization of the nonallelic homologous recombination hotspot PRS3 associated with type-3 NF1 deletions.
Zickler AM; Hampp S; Messiaen L; Bengesser K; Mussotter T; Roehl AC; Wimmer K; Mautner VF; Kluwe L; Upadhyaya M; Pasmant E; Chuzhanova N; Kestler HA; Högel J; Legius E; Claes K; Cooper DN; Kehrer-Sawatzki H
Hum Mutat; 2012 Feb; 33(2):372-83. PubMed ID: 22045503
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
