| Year |
Citation |
Score |
| 2014 |
Metsu S, Rainger JK, Debacker K, Bernhard B, Rooms L, Grafodatskaya D, Weksberg R, Fombonne E, Taylor MS, Scherer SW, Kooy RF, FitzPatrick DR. A CGG-repeat expansion mutation in ZNF713 causes FRA7A: association with autistic spectrum disorder in two families. Human Mutation. 35: 1295-300. PMID 25196122 DOI: 10.1002/Humu.22683 |
0.455 |
|
| 2007 |
Debacker K, Winnepenninckx B, Longman C, Colgan J, Tolmie J, Murray R, van Luijk R, Scheers S, Fitzpatrick D, Kooy F. The molecular basis of the folate-sensitive fragile site FRA11A at 11q13. Cytogenetic and Genome Research. 119: 9-14. PMID 18160775 DOI: 10.1159/000109612 |
0.481 |
|
| 2007 |
Debacker K, Kooy RF. Fragile sites and human disease. Human Molecular Genetics. 16: R150-8. PMID 17567780 DOI: 10.1093/Hmg/Ddm136 |
0.49 |
|
| 2007 |
Debacker K, Winnepenninckx B, Ben-Porat N, FitzPatrick D, Van Luijk R, Scheers S, Kerem B, Frank Kooy R. FRA18C: a new aphidicolin-inducible fragile site on chromosome 18q22, possibly associated with in vivo chromosome breakage. Journal of Medical Genetics. 44: 347-52. PMID 17475918 DOI: 10.1136/Jmg.2006.044628 |
0.464 |
|
| 2007 |
Winnepenninckx B, Debacker K, Ramsay J, Smeets D, Smits A, FitzPatrick DR, Kooy RF. CGG-repeat expansion in the DIP2B gene is associated with the fragile site FRA12A on chromosome 12q13.1. American Journal of Human Genetics. 80: 221-31. PMID 17236128 DOI: 10.1086/510800 |
0.506 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2012 |
Debacker K, Frizzell A, Gleeson O, Kirkham-McCarthy L, Mertz T, Lahue RS. Histone deacetylase complexes promote trinucleotide repeat expansions. Plos Biology. 10: e1001257. PMID 22363205 DOI: 10.1371/Journal.Pbio.1001257 |
0.285 |
|
| Hide low-probability matches. |