-David N Cooper Researcher Activity Profile

Research Author Detailed Information 

David N Cooper Publication Rate By Year

David N Cooper has published 1 paper(s) in 2006, 8 paper(s) in 2007, 5 paper(s) in 2008, for a total of 14 research publications in total.

David N Dn Cooper Author Information

LAST NAME: cooper

FIRST NAME: David N

INITIALS: dn

AFFILIATION:

Papers

David N Cooper's Publication Record

1. Evolutionary and biomedical insights from the rhesus macaque genome. Year Published: 2007
Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX 77030, USA. agibbs@bcm.edu
2. LINE-1 Endonuclease-Dependent Retrotranspositional Events Causing Human Genetic Disease: Mutation Detection Bias and Multiple Mechanisms of Target Gene Disruption. Year Published: 2006
3. Diversity of cystathionine beta-synthase haplotypes bearing the most common homocystinuria mutation c.833T>C: a possible role for gene conversion. Year Published: 2007
Center for Applied Genomics, Institute of Inherited Metabolic Disorders, Charles University 1st Faculty of Medicine, Prague, Czech Republic.
4. Co-inheritance of a novel deletion of the entire SPINK1 gene with a CFTR missense mutation (L997F) in a family with chronic pancreatitis. Year Published: 2007
INSERM, U613, 29220 Brest, France.
5. Compound heterozygosity for two novel mutations (1203insG/Y1456X) in the von Willebrand factor gene causing type 3 von Willebrand disease. Year Published: 2007
Shanghai Institute of Hematology, Ruijin Hospital, Shanghai Jiaotong University, Shanghai, China. topxiefei@126.com
6. Editorial. Year Published: 2007
Institute of Medical Genetics, Cardiff University, Heath Park, Cardiff, CF14 4XN, UK, humangenetics@oicr.on.ca.
7. Type 2 NF1 deletions are highly unusual by virtue of the absence of nonallelic homologous recombination hotspots and an apparent preference for female mitotic recombination. Year Published: 2007
Institute of Human Genetics, University of Ulm, Ulm, Germany.
8. Compound heterozygosity for two novel mutations (1203insG/Y1456X) in the von Willebrand factor gene causing type 3 von Willebrand disease. Year Published: 2007
Shanghai Institute of Hematology, Ruijin Hospital, Shanghai Jiaotong University, Shanghai, China. topxiefei@126.com
9. Type 2 NF1 deletions are highly unusual by virtue of the absence of nonallelic homologous recombination hotspots and an apparent preference for female mitotic recombination. Year Published: 2007
Institute of Human Genetics, University of Ulm, Ulm, Germany.
10. Detection of two Alu insertions in the CFTR gene. Year Published: 2008
11. Human Gene Mutation Database: towards a comprehensive central mutation database. Year Published: 2008
P Stenson, Institute of Medical Genetics, Cardiff University, Heath Park, Cardiff CF15 8DW, UK; StensonPD@cardiff.ac.uk.
12. Human Gene Mutation Database: towards a comprehensive central mutation database. Year Published: 2008
13. Molecular mechanisms of chromosomal rearrangement during primate evolution. Year Published: 2008
Institute of Human Genetics, University of Ulm, Ulm, Germany, hildegard.kehrer-sawatzki@uni-ulm.de.
14. Molecular mechanisms of chromosomal rearrangement during primate evolution. Year Published: 2008
Institute of Human Genetics, University of Ulm, Ulm, Germany. hildegard.kehrer-sawatzki@uni-ulm.de