David S. Rosenblatt - Concepedia

Author

David S. Rosenblatt

Also Known As

Christie Riddell, D Rosenblatt, D S Rosenblatt, D. Rosenblatt, D. S. ROSENBLATT, D. S. Rosenblatt, D.S. ROSENBLATT, D.S. Rosenblatt, DAVID ROSENBLATT, DAVID S. ROSENBLATT

373

Publications

14.6K

Citations

H-Index

182

Concepts

All Affiliations

McGill University McGill University Health Centre Montreal Children's Hospital McGill University and Génome Québec Innovation Centre Royal Victoria Hospital

About

David S. Rosenblatt is an author at McGill University specializing in medicine, genetics, and metabolism.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	42	98	6.2K
2	Natural Sciences	15	15	977
3	Health Sciences	14	17	781
4	Public Health	11	12	682
5	Engineering	2	2	189

David S. Rosenblatt

181

Publications

11.6K

Citations

H-Index

Page 1

	Year	Citations
Cloning and mapping of a cDNA for methionine synthase reductase, a flavoprotein defective in patients with homocystinuria Daniel Leclerc, Aaron Wilson, Renaud Dumas, Proceedings of the National Academy of Sciences	1998	391
Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type Jordan Lerner‐Ellis, Jamie C. Tirone, Peter D. Pawelek, Nature Genetics BiologyCblc TypeMethylmalonic AciduriaGenetic DisorderGenetics	2005	372
Improvement in the Histochemical Localization of Leucine Aminopeptidase with a New Substrate, <i>L</i>-Leucyl-4-Methoxy-2-Naphthylamide Marvin M. Nachlas, Benito Monis, David S. Rosenblatt, The Journal of Cell Biology Bioorganic ChemistrySuperior Enzyme LocalizationBiochemistryCellular EnzymologyHistochemical Localization	1960	318
A Polymorphism (80G->A) in the Reduced Folate Carrier Gene and Its Associations with Folate Status and Homocysteinemia Abalo Chango, Nathalie Emery‐Fillon, G. Potier de Courcy, Molecular Genetics and Metabolism Mendelian DisorderGenetic DisorderGeneticsInherited Metabolic DiseaseGenetic Epidemiology	2000	299
Genetic polymorphisms in methylenetetrahydrofolate reductase and methionine synthase, folate levels in red blood cells, and risk of neural tube defects Benedicte Christensen, Laura Arbour, Pamela V. Tran, American Journal of Medical Genetics Mutant GenotypeGeneticsGenetic EpidemiologyHuman PolymorphismGenetic Medicine	1999	294
Seven novel mutations in the methylenetetrahydrofolate reductase gene and genotype/phenotype correlations in severe methylenetetrahydrofolate reductase deficiency. Philippe Goyette, Phyllis Frosst, David S. Rosenblatt, PubMed	1995	262
Mutations in ABCD4 cause a new inborn error of vitamin B12 metabolism David Coelho, Jaeseung Kim, Isabelle R. Miousse, Nature Genetics Vitamin NutritionGenetic DisorderGeneticsVitamin B12 MetabolismMolecular Biology	2012	233
Correlation of a Common Mutation in the Methylenetetrahydrofolate Reductase Gene With Plasma Homocysteine in Patients With Premature Coronary Artery Disease Benedicte Christensen, Phyllis Frosst, Suzanne Lussier‐Cacan, Arteriosclerosis Thrombosis and Vascular Biology	1997	226
Spectrum of mutations in<i>MMACHC</i>, allelic expression, and evidence for genotypeâphenotype correlations Jordan Lerner‐Ellis, Natascia Anastasio, Junhui Liu, Human Mutation	2009	207
Inborn errors of cobalamin absorption and metabolism David Watkins, David S. Rosenblatt American Journal of Medical Genetics Part C Seminars in Medical Genetics NutritionMetabolic DisorderCbld Variant 1PathologyCbld Variant 2	2011	196

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