-Steven A Fisher Researcher Activity Profile

Research Author Detailed Information 

Steven A Fisher Publication Rate By Year

Steven A Fisher has published 3 paper(s) in 2006, 16 paper(s) in 2007, 3 paper(s) in 2008, for a total of 22 research publications in total.

Steven A Sa Fisher Author Information

LAST NAME: fisher

FIRST NAME: Steven A

INITIALS: sa

AFFILIATION:

Papers

Steven A Fisher's Publication Record

1. Myosin phosphatase isoform switching in vascular smooth muscle development. Year Published: 2006
Department of Medicine, 422 BRB, 2109 Adelbert Road, Case Western Reserve School of Medicine, Cleveland, OH 44106-4958, USA.
2. Meta-analysis of genome-wide linkage studies of systemic lupus erythematosus. Year Published: 2006
Department of Medical and Molecular Genetics, King's College London School of Medicine at Guy's, King's College and St Thomas' Hospitals, London, UK.
3. Investigation of association of the DLG5 gene with phenotypes of inflammatory bowel disease in the British population. Year Published: 2007
Department of Medical & Molecular Genetics, King's College London School of Medicine, 8th Floor Guy's Tower, Guy's Hospital, London SE1 9RT, UK.
4. Role of hypoxia in the evolution and development of the cardiovascular system. Year Published: 2007
Case Western Reserve School of Medicine, Cleveland, Ohio 44106-7290, USA. Steven.Fisher@Case.Edu
5. Workshop report on the extraction of foetal DNA from maternal plasma. Year Published: 2007
6. Identification, evolution, and association study of a novel promoter and first exon of the human NOD2 (CARD15) gene. Year Published: 2007
Department of Medical and Molecular Genetics, King's College London School of Medicine, Guy's Hospital, London, UK.
7. Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants. Year Published: 2007
Genetic Epidemiology Group, Department of Health Sciences, University of Leicester, Adrian Building, University Road, Leicester LE1 7RH, UK.
8. The developing embryonic cardiac outflow tract is highly sensitive to oxidant stress. Year Published: 2007
Department of Medicine (Cardiology) and Physiology and Biophysics, Case Western Reserve University, Cleveland, Ohio.
9. Identification, evolution, and association study of a novel promoter and first exon of the human NOD2 (CARD15) gene. Year Published: 2007
Department of Medical and Molecular Genetics, King's College London School of Medicine, Guy's Hospital, London, UK.
10. Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A. Year Published: 2007
Juvenile Diabetes Research Foundation/Wellcome Trust Diabetes and Inflammation Laboratory, Department of Medical Genetics, Cambridge Institute of Medical Research, University of Cambridge, CB2 0XY, UK.
11. Investigation of association of the DLG5 gene with phenotypes of inflammatory bowel disease in the British population. Year Published: 2007
Department of Medical & Molecular Genetics, King's College London School of Medicine, 8th Floor Guy's Tower, Guy's Hospital, London SE1 9RT, UK.
12. Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants. Year Published: 2007
Genetic Epidemiology Group, Department of Health Sciences, University of Leicester, Adrian Building, University Road, Leicester LE1 7RH, UK.
13. Gender-stratified analysis of DLG5 R30Q in 4707 patients with Crohn disease and 4973 controls from 12 Caucasian cohorts. Year Published: 2008
14. Workshop report on the extraction of foetal DNA from maternal plasma. Year Published: 2007
15. Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants. Year Published: 2007
Genetic Epidemiology Group, Department of Health Sciences, University of Leicester, Adrian Building, University Road, Leicester LE1 7RH, UK.
16. The developing embryonic cardiac outflow tract is highly sensitive to oxidant stress. Year Published: 2007
Department of Medicine (Cardiology) and Physiology and Biophysics, Case Western Reserve University, Cleveland, Ohio 44106-7290, USA. steven.fisher@case.edu
17. Diverse effects of the CARD15 and IBD5 loci on clinical phenotype in 630 patients with Crohn's disease. Year Published: 2007
Division of Genetics and Molecular Medicine, King's College London School of Medicine, Guy's Hospital, London, UK.
18. Gender-stratified analysis of DLG5 R30Q in 4707 patients with Crohn disease and 4973 controls from 12 Caucasian cohorts. Year Published: 2008
19. Myosin phosphatase isoform switching in vascular smooth muscle development. Year Published: 2006
Department of Medicine, 422 BRB, 2109 Adelbert Road, Case Western Reserve School of Medicine, Cleveland, OH 44106-4958, USA.
20. A nonsynonymous SNP in ATG16L1 predisposes to ileal Crohn's disease and is independent of CARD15 and IBD5. Year Published: 2007
Department of Medical and Molecular Genetics, King's College London School of Medicine, Guy's Hospital, London, UK.
21. Uterine artery myosin phosphatase isoform switching and increased sensitivity to SNP in a rat L-NAME model of hypertension of pregnancy. Year Published: 2008
Dept. of Medicine (Cardiology 4-533 Wolstein Research Bldg., 2103 Cornell Rd., Case Western Reserve School of Medicine, Cleveland, OH 44106-7290. saf9@po.cwru.edu).
22. Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility. Year Published: 2007
Inflammatory Bowel Disease Research Group, Addenbrooke's Hospital, University of Cambridge, Cambridge CB2 2QQ, UK. miles.parkes@addenbrookes.nhs.uk