Professor, Medicine, UCLA School of Medicine
Medical Genetics
Dr. Jerome I. Rotter, MD
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Jerome Rotter works in the field of Medical Genetics. He went to David Geffen School of Medicine at UCLA. David Geffen School of Medicine at UCLA is a top medical university. David Geffen School of Medicine at UCLA has a rank of 13 in research and a 7 in primary care He received 1 awards: "Elected Member". Doctor Jerome I. Rotter, MD is also a published physician. He has 88 publication published. The most recent publication is: Detailed analysis of association between common single nucleotide polymorphisms and subclinical atherosclerosis: The Multi-ethnic Study of Atherosclerosis.
Publications
- GWAS for executive function and processing speed suggests involvement of the CADM2 gene.
- Common genetic variants and subclinical atherosclerosis: The Multi-Ethnic Study of Atherosclerosis (MESA).
- Genome-wide Association Study of Platelet Count Identifies Ancestry-Specific Loci in Hispanic/Latino Americans.
- Incidence of Age-Related Macular Degeneration in a Multi-Ethnic United States Population: The Multi-Ethnic Study of Atherosclerosis.
- Characterization of Genetic Loci That Affect Susceptibility to Inflammatory Bowel Diseases in African Americans.
- Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair.
- A genome-wide association study of chronic obstructive pulmonary disease in hispanics.
- Actionable exomic incidental findings in 6503 participants: challenges of variant classification.
- A novel Alzheimer disease locus located near the gene encoding tau protein.
- Association of a 62 Variant Type 2 Diabetes Genetic Risk Score with Markers of Subclinical Atherosclerosis: A Transethnic, Multicenter Study.
- Multi-Ethnic Genome-Wide Association Study of Cerebral White Matter Hyperintensities on MRI.
- Dietary fatty acids modulate associations between genetic variants and circulating fatty acids in plasma and erythrocyte membranes: Meta-analysis of nine studies in th...
- Empirical characteristics of family-based linkage to a complex trait: the ADIPOQ region and adiponectin levels.
- Erratum to: Empirical characteristics of family-based linkage to a complex trait: the ADIPOQ region and adiponectin levels.
- Genetic Variants Associated with Quantitative Glucose Homeostasis Traits Translate to Type 2 Diabetes in Mexican Americans: The GUARDIAN (Genetics Underlying Diabetes ...
- Genome-wide Studies of Verbal Declarative Memory in Nondemented Older People: The Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium.
- Ancestry and other genetic associations with plasma PCSK9 response to simvastatin.
- Air Pollution and Percent Emphysema Identified by Computed Tomography in the Multi-Ethnic Study of Atherosclerosis.
- Further Investigation in Europeans of Susceptibility Variants for Polycystic Ovary Syndrome Discovered in Genome-wide Association Studies of Chinese Individuals.
- GWAS of Longevity in CHARGE Consortium Confirms APOE and FOXO3 Candidacy.
- Effects of long-term averaging of quantitative blood pressure traits on the detection of genetic associations.
- Whole-exome imputation of sequence variants identified two novel alleles associated with adult body height in African Americans.
- Genome-wide association analysis identifies six new loci associated with forced vital capacity.
- Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.
- Gene-Age Interactions in Blood Pressure Regulation: A Large-Scale Investigation with the CHARGE, Global BPgen, and ICBP Consortia.
- Pleiotropic genes for metabolic syndrome and inflammation.
- Leptin-Mediated Increases in Catecholamine Signaling Reduce Adipose Tissue Inflammation via Activation of Macrophage HDAC4.
- Genome-Wide Family-Based Linkage Analysis of Exome Chip Variants and Cardiometabolic Risk.
- Associations of Pentraxin 3 with Cardiovascular Disease: The Multi-Ethnic Study of Atherosclerosis.
- Large multiethnic Candidate Gene Study for C-reactive protein levels: identification of a novel association at CD36 in African Americans.
- Common variation in fatty acid metabolic genes and risk of incident sudden cardiac arrest.
- Clinical, serologic, and genetic factors associated with pyoderma gangrenosum and erythema nodosum in inflammatory bowel disease patients.
- Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval.
- Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks.
- Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol.
- Linkage Analysis of High-density SNPs Confirms Keratoconus Locus at 5q Chromosomal Region.
- Elevated plasma free fatty acids are associated with sudden death: A prospective community-based evaluation at the time of cardiac arrest.
- Novel Genetic Markers Associate with Atrial Fibrillation Risk in Europeans and Japanese.
- Genetic analysis of adiponectin variation and its association with type 2 diabetes in African Americans.
- Discovery and refinement of loci associated with lipid levels.
- Common variants associated with plasma triglycerides and risk for coronary artery disease.
- Statin-induced changes in gene expression in EBV-transformed and native B-cells.
- Targeted sequencing in candidate genes for atrial fibrillation: the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Targeted Sequencing Study.
- Challenges in Elucidating the Genetics of Diabetic Retinopathy.
- Insulin Sensitivity and Insulin Clearance are Heritable and Have Strong Genetic Correlation in Mexican Americans.
- Pooled analysis of iron-related genes in Parkinson's disease: Association with transferrin.
- Characterization of Statin Dose Response in Electronic Medical Records.
- Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease.
- No association of 9p21 with arterial elasticity and retinal microvascular findings.
- Genome-wide Association Analysis of Blood-Pressure Traits in African-Ancestry Individuals Reveals Common Associated Genes in African and Non-African Populations.
- Lipoprotein receptor-related protein 1 variants and dietary fatty acids: meta-analysis of European origin and African American studies.
- Trans-ethnic fine mapping identifies a novel independent locus at the 3' end of CDKAL1 and novel variants of several susceptibility loci for type 2 diabetes in a Han C...
- A statin-dependent QTL for GATM expression is associated with statin-induced myopathy.
- Association of heat shock proteins with all-cause mortality.
- Genome-wide association study in a Chinese population with diabetic retinopathy.
- Associations of Candidate Genes to Age-Related Macular Degeneration Among Racial/Ethnic Groups in the Multi-Ethnic Study of Atherosclerosis.
- Genome-wide association of body fat distribution in african ancestry populations suggests new Loci.
- The M694V mutation in Armenian-Americans: a 10-year retrospective study of MEFV mutation testing for familial Mediterranean fever at UCLA.
- Meta-Analysis of Genome-wide Association Studies in 5 cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive er...
- APOM and high-density lipoprotein are associated with lung function and percent emphysema.
- Genome-wide meta-analysis of observational studies shows common genetic variants associated with macronutrient intake.
- Multidimensional Prognostic Risk Assessment Identifies Association Between IL12B Variation and Surgery in Crohn's Disease.
- Genetic ancestry and the relationship of cigarette smoking to lung function and per cent emphysema in four race/ethnic groups: a cross-sectional study.
- Genetic variants associated with VLDL, LDL and HDL particle size differ with race/ethnicity.
- Transferability and fine mapping of type 2 diabetes loci in African Americans: the Candidate Gene Association Resource Plus Study.
- Trans-ethnic fine-mapping of lipid Loci identifies population-specific signals and allelic heterogeneity that increases the trait variance explained.
- Genetic association of COL5A1 variants in keratoconus patients suggests a complex connection between corneal thinning and keratoconus.
- Systematic evaluation of validated type 2 diabetes and glycaemic trait loci for association with insulin clearance.
- An Association Between the Calpastatin (CAST) Gene and Keratoconus.
- Linkage of Crohn's disease-related serological phenotypes: NFKB1 haplotypes are associated with anti-CBir1 and ASCA, and show reduced NF-kappaB activation.
- Association of the Kir6.2 E23K variant with reduced acute insulin response in African-Americans.
- The transcriptional landscape of age in human peripheral blood.
- Drug-Gene Interactions of Antihypertensive Medications and Risk of Incident Cardiovascular Disease: A Pharmacogenomics Study from the CHARGE Consortium.
- Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility.
- Genome of the Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels.
- Association of fasting insulin and C peptide with diabetic retinopathy in Latinos with type 2 diabetes.
- A generalized least-squares framework for rare-variant analysis in family data.
- Association of NOD2 and IL23R with Inflammatory Bowel Disease in Puerto Rico.
- Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 Loci.
- Large-scale genome-wide association studies and meta-analyses of longitudinal change in adult lung function.
- Gene expression in thiazide diuretic or statin users in relation to incident type 2 diabetes.
- Genetics of coronary artery calcification among African Americans, a meta-analysis.
- Best Practices and Joint Calling of the HumanExome BeadChip: The CHARGE Consortium.
- Novel Loci associated with increased risk of sudden cardiac death in the context of coronary artery disease.
- A genome-wide association study of central corneal thickness in Latinos.
- Detailed analysis of association between common single nucleotide polymorphisms and subclinical atherosclerosis: The Multi-ethnic Study of Atherosclerosis.
- CELF4 Variant and Anthracycline-Related Cardiomyopathy: A Children's Oncology Group Genome-Wide Association Study.
Schools
D Geffen Sch Of MedUcla
La Co Harbor UCLA Med Center
Wadsworth Va Hospital
Doctors Specialties
- Clinical Genetics
- Internal Medicine
- Medical Genetics
Accepted Insurances
Awards
- Elected Member
Education
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VA Greater Los Angeles Healthcare System -
Harbor - UCLA Medical Center -
David Geffen School of Medicine at UCLA
Hospital
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Ronald Reagan UCLA Medical Center -
Cedars-Sinai Medical Center
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