-Stylianos E Antonarakis Researcher Activity Profile

Research Author Detailed Information 

Stylianos E Antonarakis Publication Rate By Year

Stylianos E Antonarakis has published 1 paper(s) in 2005, 1 paper(s) in 2006, 16 paper(s) in 2007, 2 paper(s) in 2008, for a total of 20 research publications in total.

Stylianos E Se Antonarakis Author Information

LAST NAME: antonarakis

FIRST NAME: Stylianos E

INITIALS: se

AFFILIATION:

Papers

Stylianos E Antonarakis's Publication Record

1. Different mechanisms preclude mutant CLDN14 proteins from forming tight junctions in vitro. Year Published: 2005
Department of Genetic Medicine and Development, University of Geneva Medical School and Geneva University Hospitals, Geneva, Switzerland.
2. The challenge of Down syndrome. Year Published: 2006
Department of Genetic Medicine and Development, University of Geneva Medical School, University Hospitals of Geneva, 1 rue Michel-Servet, 1211 Geneva, Switzerland.
3. Abnormal cortical activation during response inhibition in 22q11.2 deletion syndrome. Year Published: 2007
The Behavioral Neurogenetics Center, Child Psychiatry Department, Schneider Children's Medical Center of Israel, Petah Tiqwa, Israel. gothelf@post.tau.ac.il
4. Prominent use of distal 5' transcription start sites and discovery of a large number of additional exons in ENCODE regions. Year Published: 2007
5. Pseudogenes in the ENCODE regions: consensus annotation, analysis of transcription, and evolution. Year Published: 2007
Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, Connecticut 06520, USA. deyou.zheng@yale.edu
6. Structured RNAs in the ENCODE selected regions of the human genome. Year Published: 2007
Institute for Theoretical Chemistry, University of Vienna, A-1090 Wien, Austria. wash@tbi.univie.ac.at
7. Natural gene-expression variation in Down syndrome modulates the outcome of gene-dosage imbalance. Year Published: 2007
Department of Genetic Medicine and Development, University of Geneva Medical School and University Hospitals of Geneva, Geneva, Switzerland.
8. Gene duplication: a drive for phenotypic diversity and cause of human disease. Year Published: 2007
Department of Genetic Medicine & Development, University of Geneva Medical School and Geneva University Hospitals, CH-1211 Geneva 4, Switzerland. bernard.conrad@insel.ch
9. Islands of euchromatin-like sequence and expressed polymorphic sequences within the short arm of human chromosome 21. Year Published: 2007
Department of Genetic Medicine and Development, University of Geneva Medical School, and University Hospitals, 1211 Geneva, Switzerland. Robert.Lyle@medisin.uio.no
10. TMPRSS3, a type II transmembrane serine protease mutated in non-syndromic autosomal recessive deafness. Year Published: 2007
Division of Medical Genetics, University Hospital of Geneva, Geneva, Switzerland. Michel.Guipponi@hcuge.ch
11. TMPRSS3, a type II transmembrane serine protease mutated in non-syndromic autosomal recessive deafness. Year Published: 2007
Division of Medical Genetics, University Hospital of Geneva, Geneva, Switzerland. Michel.Guipponi@hcuge.ch
12. Promoter polymorphisms and allelic imbalance in ABCB1 expression. Year Published: 2007
Institute of Microbiology, University Hospital, Lausanne, Switzerland.
13. Gene duplication: a drive for phenotypic diversity and cause of human disease. Year Published: 2007
Department of Genetic Medicine & Development, University of Geneva Medical School and Geneva University Hospitals, CH-1211 Geneva 4, Switzerland. bernard.conrad@insel.ch
14. Life-history traits drive the evolutionary rates of mammalian coding and noncoding genomic elements. Year Published: 2007
Department of Genetic Medicine and Development, University of Geneva Medical School, 1 Rue Michel-Servet, 1211 Geneva, Switzerland. sergey.nikolaev@medecine.unige.ch
15. Islands of euchromatin-like sequence and expressed polymorphic sequences within the short arm of human chromosome 21. Year Published: 2007
Department of Genetic Medicine and Development, University of Geneva Medical School, and University Hospitals, 1211 Geneva, Switzerland. Robert.Lyle@medisin.uio.no
16. Promoter polymorphisms and allelic imbalance in ABCB1 expression. Year Published: 2007
Institute of Microbiology, University Hospital, Lausanne, Switzerland.
17. Primary ciliary dyskinesia associated with normal axoneme ultrastructure is caused by DNAH11 mutations. Year Published: 2008
18. Life-history traits drive the evolutionary rates of mammalian coding and noncoding genomic elements. Year Published: 2007
Department of Genetic Medicine and Development, University of Geneva Medical School, 1 Rue Michel-Servet, 1211 Geneva, Switzerland. sergey.nikolaev@medecine.unige.ch
19. Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project. Year Published: 2007
20. Primary ciliary dyskinesia associated with normal axoneme ultrastructure is caused by DNAH11 mutations. Year Published: 2008
Department for General Pediatrics, Charité University Hospital, Campus Virchow, Berlin, Germany. georg.schwabe@charite.de