1966 - Fellow of the American Statistical Association (ASA)
His main research concerns Genetics, Internal medicine, Endocrinology, Methionine synthase and Homocystinuria. Genetics is closely attributed to Molecular biology in his research. David S. Rosenblatt interconnects Teratology and Gestation in the investigation of issues within Internal medicine.
The study incorporates disciplines such as Pregnancy and Cobalamin metabolism in addition to Endocrinology. His Methionine synthase study is focused on Methionine and Biochemistry. The Methionine study combines topics in areas such as Cobalamin and Homocysteine.
David S. Rosenblatt focuses on Internal medicine, Genetics, Endocrinology, Biochemistry and Cobalamin. Internal medicine is closely attributed to Gastroenterology in his work. His work deals with themes such as Molecular biology and Methylmalonic aciduria, which intersect with Genetics.
His Molecular biology research focuses on subjects like Complementation, which are linked to Methylmalonyl-CoA mutase. His research integrates issues of Homocystinuria, Prenatal diagnosis and Methylenetetrahydrofolate reductase in his study of Endocrinology. His studies deal with areas such as Genetic heterogeneity and Severe combined immunodeficiency as well as Cobalamin.
David S. Rosenblatt mainly investigates Genetics, Cobalamin, Gene, Methylmalonic aciduria and Internal medicine. His work on DNA sequencing, Mutation, Missense mutation and Zebrafish as part of general Genetics research is frequently linked to Identification, bridging the gap between disciplines. The study incorporates disciplines such as Sanger sequencing, Methionine synthase and Severe combined immunodeficiency in addition to Cobalamin.
His Gene research includes themes of Genetic testing and Bioinformatics. He combines subjects such as GTPase, Genome, Chaperone, Mutase and G protein with his study of Methylmalonic aciduria. David S. Rosenblatt focuses mostly in the field of Internal medicine, narrowing it down to matters related to Endocrinology and, in some cases, Transient receptor potential channel.
David S. Rosenblatt mostly deals with Gene, Genetics, Mutation, Cobalamin and Biochemistry. The concepts of his Genetics study are interwoven with issues in Vitamin B12, Methylmalonic acid and Medical diagnosis. His Mutation research incorporates elements of Internal medicine, Genetic testing, Endocrinology and DNA sequencing.
His work in the fields of Procollagen peptidase overlaps with other areas such as SEC23A. His Cobalamin study frequently involves adjacent topics like Methionine synthase. Much of his study explores Biochemistry relationship to Molecular biology.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Human methionine synthase: cDNA cloning and identification of mutations in patients of the cblG complementation group of folate/cobalamin disorders.
D. Leclerc;E. Campeau;P. Goyette;C. E. Adjalla.
Human Molecular Genetics (1996)
Cloning and mapping of a cDNA for methionine synthase reductase, a flavoprotein defective in patients with homocystinuria
D. Leclerc;A. Wilson;R. Dumas;C. Gafuik.
Proceedings of the National Academy of Sciences of the United States of America (1998)
Seven novel mutations in the methylenetetrahydrofolate reductase gene and genotype/phenotype correlations in severe methylenetetrahydrofolate reductase deficiency.
P Goyette;P Frosst;D S Rosenblatt;R Rozen.
American Journal of Human Genetics (1995)
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 Tran;Daniel Leclerc.
American Journal of Medical Genetics (1999)
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;Jacob Selhub.
Arteriosclerosis, Thrombosis, and Vascular Biology (1997)
Novel Reductant for Determination of Total Plasma Homocysteine
Brian M. Gilfix;David W. Blank;David S. Rosenblatt.
Clinical Chemistry (1997)
Adverse Effect of Nitrous Oxide in a Child with 5,10-Methylenetetrahydrofolate Reductase Deficiency
Rebecca R Selzer;David S Rosenblatt;Renata Laxova;Kirk Hogan.
The New England Journal of Medicine (2003)
The effect of 677C-->T and 1298A-->C mutations on plasma homocysteine and 5,10-methylenetetrahydrofolate reductase activity in healthy subjects.
A. Chango;F. Boisson;F. Barbé;D. Quilliot.
British Journal of Nutrition (2000)
Functional methionine synthase deficiency (cblE and cblG): clinical and biochemical heterogeneity.
D Watkins;D S Rosenblatt.
American Journal of Medical Genetics (1989)
Severe and mild mutations in cis for the methylenetetrahydrofolate reductase (MTHFR) gene, and description of five novel mutations in MTHFR.
Goyette P;Christensen B;Rosenblatt Ds;Rozen R.
American Journal of Human Genetics (1996)
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