Physician
Medical Genetics
Dr. Arno G. Motulsky, MD
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Arno G. Motulsky, MD is an expert in the field of Medical Genetics. He has 1 awards "Elected Member". Arno G. Motulsky, MD is also a published doctor. He has 99 paper published. The most recent paper is: Preventing coronary heart disease: B vitamins and homocysteine.
Publications
- Actionable exomic incidental findings in 6503 participants: challenges of variant classification.
- Joint Linkage and Association Analysis with Exome Sequence Data Implicates SLC25A40 in Hypertriglyceridemia.
- Actionable, Pathogenic Incidental Findings in 1,000 Participants' Exomes.
- Response of serum and red blood cell folate concentrations to folic acid supplementation depends on methylenetetrahydrofolate reductase C677T genotype: Results from a ...
- Garrod's fourth inborn error of metabolism solved by the identification of mutations causing pentosuria.
- Linkage and association of phospholipid transfer protein activity to LASS4.
- Genetic and nongenetic sources of variation in phospholipid transfer protein activity.
- Genome-environment interactions and prospective technology assessment: evolution from pharmacogenomics to nutrigenomics and ecogenomics.
- Frequent detection of familial hypercholesterolemia mutations in familial combined hyperlipidemia.
- Enhancing recruitment of healthy African American volunteers in a city with a small African American community: results from a dietary supplement crossover trial.
- Priorities and standards in pharmacogenetic research.
- Equal proportion of adult male and female homozygous for the 677C --> T mutation in the methylenetetrahydrofolate reductase polymorphism.
- Low-density lipoprotein particle size loci in familial combined hyperlipidemia: evidence for multiple loci from a genome scan.
- X-linked high myopia associated with cone dysfunction.
- Genome-wide scan for quantitative trait loci influencing LDL size and plasma triglyceride in familial hypertriglyceridemia.
- Small, dense LDL and elevated apolipoprotein B are the common characteristics for the three major lipid phenotypes of familial combined hyperlipidemia.
- Human genetics. Mapping human history.
- 2001 William Allan Award Address. Introductory speech for Charles J. Epstein.
- The beta-delta thalassemias.
- General remarks on genetic factors in anesthesia.
- New clinical implications of molecular genetics.
- Special award lecture: biochemical genetics and psychiatry.
- Hyperlipidemia in coronary heart disease. I. Lipid levels in 500 survivors of myocardial infarction.
- Impact of genetic manipulation on society and medicine.
- Effect of chronologic age on induction of cystathionine synthase, uroporphyrinogen I synthase, and glucose-6-phosphate dehydrogenase activities in lymphocytes.
- Nonrandom patterns of codon usage and of nucleotide substitutions in human alpha- and beta-globin genes: an evolutionary strategy reducing the rate of mutations with d...
- Negro variant of glucose-6-phosphate dehydrogenase deficiency (A-) in man.
- Predominance of hemoglobin Gower 1 in early human embryonic development.
- Autosomal phosphogluconic dehydrogenase polymorphism in the cat (Felis catus L.).
- Genetics by nation.
- Historical genetics.
- Brain, genetics, and behavior.
- DEVELOPMENTAL HEMOGLOBIN ANOMALIES IN A CHROMOSOMAL TRIPLICATION: D1 TRISOMY SYNDROME.
- Developmental variation in the isoenzymes of human liver and gastric alchhol dehydrogenase.
- Screening for sickle cell hemoglobinopathy and thalassemia.
- Phylogenetic relationships of human populations in sub-Saharan Africa.
- Risk counselling in autosomal dominant disorders with undetermined penetrance.
- Hemoglobin tacoma--a beta-chain variant associated with increased hb A2.
- The HLA complex and disease: some interpretations and new data in cardiomyopathy.
- Human genetic variation and nutrition.
- Medical genetics and adoption.
- Human genetics, society, ad medicine.
- Variants of glucose-6-phosphate dehydrogenase.
- Drugs and genes.
- Serum paraoxonase and its influence on paraoxon and chlorpyrifos-oxon toxicity in rats.
- Glutathione S-transferase and epoxide hydrolase activity in human leukocytes in relation to risk of lung cancer and other smoking-related cancers.
- Current concepts in genetics. The genetic hyperlipidemias.
- Public health and long-term genetic implications of intrauterine diagnosis and selective abortion.
- Genetics of hyperlipidemia in coronary heart disease.
- Multifactorial inheritance and heritability in pharmacogenetics.
- Medical genetics.
- Significance of genetic diseases for population studies.
- The distribution of glucose-6-phosphate dehydrogenase deficiency in Greece.
- Methemoglobin reduction and the inactive X hypothesis.
- Jewish diseases and origins.
- Paraoxon hydrolysis in human serum mediated by a genetically variable arylesterase and albumin.
- Vernon M.
- A pseudocholinesterase variant (E Cynthiana) associated with elevated plasma enzyme activity.
- Gene frequencies at loci determining blood-group and serum-protein polymorphisms in two villages of northwestern Greece.
- Population genetic studies in the Congo. 3. Blood groups (ABO, MNSs, Rh, Jsa).
- Spectrophotometric assays for the enzymatic hydrolysis of the active metabolites of chlorpyrifos and parathion by plasma paraoxonase/arylesterase.
- Analbuminemia in an American Indian girl.
- Genetic research in coronary heart disease.
- Preventing coronary heart disease: B vitamins and homocysteine.
- Werner''s syndrome; caricature of aging. A genetic model for the study of degenerative diseases.
- Evolutionary origins of human proteins.
- Hereditary dysplasia of bone with kyphoscoliosis, contractures, and abnormally shaped ears.
- Hypertension: some unanswered questions.
- Molecular genetics of apolipoproteins and coronary heart disease.
- Linkage disequilibrium and evolutionary relationships of DNA variants (restriction enzyme fragment length polymorphisms) at the serum albumin locus.
- Genetic control mechanisms in man and other mammals.
- Atypical cholinesterase gene E1a: rarity in Negroes and most Orientals.
- Brave new world?
- The 1985 Nobel Prize in physiology or medicine.
- Genetics of hemochromatosis.
- Molecular genetics of human serum albumin: restriction enzyme fragment length polymorphisms and analbuminemia.
- Linkage disequilibrium of plasminogen polymorphisms and assignment of the gene to human chromosome 6q26-6q27.
- Societal problems in human and medical genetics.
- Genetics of protan and deutan color-vision anomalies: an instructive family.
- Human genetic individuality and risk assessment.
- The glutathione S-transferase mu polymorphism as a marker for susceptibility to lung carcinoma.
- Population genetic studies in the Congo. I. Glucose-6-phosphate dehydrogenase deficiency, hemoglobin S, and malaria.
- Predictive genetic diagnosis.
- Plasma paraoxonase polymorphism: a new enzyme assay, population, family, biochemical, and linkage studies.
- Medical and human genetics 1977: trends and directions.
- Hyperlipidemia in coronary heart disease. 3. Evaluation of lipoprotein phenotypes of 156 genetically defined survivors of myocardial infarction.
- Drug reactions enzymes, and biochemical genetics.
- Pharmacogenetics and ecogenetics in 1991.
- Familial hypercholesterolemia in a large indred. Evidence for a monogenic mechanism.
- Bioethical problems in pharmacogenetics and ecogenetics.
- Werner''s syndrome a review of its symptomatology, natural history, pathologic features, genetics and relationship to the natural aging process.
- Hyperlipidemia in coronary heart disease. II. Genetic analysis of lipid levels in 176 families and delineation of a new inherited disorder, combined hyperlipidemia.
- Nutritional ecogenetics: homocysteine-related arteriosclerotic vascular disease, neural tube defects, and folic acid.
- Pharmacogenetics and ecogenetics: the problem and its scope.
- Measurable linkage between ocular albinism and Xg.
- Role of genetic polymorphism of human plasma paraoxonase/arylesterase in hydrolysis of the insecticide metabolites chlorpyrifos oxon and paraoxon.
- Nutrition and genetic susceptibility to common diseases.
- Different patterns of X inactivation in MZ twins discordant for red-green color-vision deficiency.
Schools
University of Illinois At Chicago College of Medicine
Doctors Specialties
- Clinical Genetics
- Internal Medicine
- Medical Genetics
Accepted Insurances
Awards
- Elected Member
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