D.R. Rosen - Concepedia

Concepedia

Author

D.R. Rosen

Massachusetts General Hospital

Also Known As

D R Rosen, D Rosen, D. R. Rosen, D. ROSEN, D. Rosen, D.R. Rosen, DANIEL R. ROSEN, DANIEL ROSÉN, Daniel R Rosen, Daniel R. Rosen

54

Publications

8.5K

Citations

17

H-Index

49

Concepts

All Affiliations

Massachusetts General Hospital Howard Hughes Medical Institute Massachusetts Institute of Technology New York State Department of Health Wadsworth Center

DR

About

D.R. Rosen is an author at Massachusetts General Hospital specializing in genetics, medicine, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	7.7K
2	Engineering	1	1	14
3	Health Sciences	1	1	14
4	Social Sciences	1	1	75
5	Biology	1	1	130

D.R. Rosen

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21

Publications

8.5K

Citations

17

H-Index

	Year	Citations
Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis D.R. Rosen, Teepu Siddique, David T. Patterson, Nature Neurodegenerative DiseasesAmyotrophic Lateral SclerosisNeurological DisorderGeneticsMolecular Biology	1993	7K
A Drosophila gene encoding a protein resembling the human beta-amyloid protein precursor. D.R. Rosen, L Martin-Morris, L Q Luo, Proceedings of the National Academy of Sciences Neurodegenerative DiseasesDrosophila Gene CorrespondsDevelopmental BiologyGeneticsGene Structure	1989	212
Rapid Communication: Cu/Zn Superoxide Dismutase Activity in Familial and Sporadic Amyotrophic Lateral Sclerosis Wim Robberecht, Peter C. Sapp, Maria Viaene, Journal of Neurochemistry	1994	163
A frequent ala 4 to val superoxide dismutase-1 mutation is associated with a rapidly progressive familial amyotrophic lateral sclerosis D.R. Rosen, Allen C. Bowling, David Patterson, Human Molecular Genetics	1994	155
A Missense Mutation in the Desmin Rod Domain Is Associated with Autosomal Dominant Distal Myopathy, and Exerts a Dominant Negative Effect on Filament Formation Gunnar Sjöberg, Carlos A. Saavedra‐Matiz, D.R. Rosen, Human Molecular Genetics Filament FormationDevelopmental BiologyMendelian DisorderFirst Point MutationIntermediate Filament Assembly	1999	147
vnd, a gene required for early neurogenesis of Drosophila, encodes a homeodomain protein. F. Jiménez, Linda Martin-Morris, Leonardo Velasco, The EMBO Journal BiologyDevelopmental BiologyDevelopmental GeneticsGeneticsHomeodomain Protein	1995	130
Molecular analysis of the locus elav in Drosophila melanogaster: a gene whose embryonic expression is neural specific. Ana Regina Nascimento Campos, D.R. Rosen, Steven Robinow, The EMBO Journal Drosophila MelanogasterDevelopmental BiologyDevelopmental GeneticsGeneticsMedicine	1987	115
New tumor markers: CA125 and beyond Robert C. Bast, Donna Badgwell, Zhongxin Lu, International Journal of Gynecological Cancer	2005	101
Identification of two novel mutations and a new polymorphism in the gene for Cu/Zn superoxide dismutase in patients with amyotrophic lateral sclerosis Jesús Esteban‐Pérez, D.R. Rosen, Allen C. Bowling, Human Molecular Genetics NeurogenomicsNeurological DisorderGeneticsPathologyGenetic Medicine	1994	75
Genetic linkage analysis of familial amyotrophic lateral sclerosis using human chromosome 21 microsatellite DNA markers D.R. Rosen, Peter C. Sapp, J. O'Regan, American Journal of Medical Genetics	1994	65

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