Michael Olivier
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Michael Olivierbiology Degrees
Biology
#12316
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#15785
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Bioinformatics
#151
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#153
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Computational Biology
#270
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#271
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Genetics
#1353
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#1455
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Biology
Michael Olivier's Degrees
- PhD Genetics Stanford University
Why Is Michael Olivier Influential?
(Suggest an Edit or Addition)Michael Olivier's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- A haplotype map of the human genome (2003) (4991)
- A haplotype map of the human genome. (2003) (4032)
- An Apolipoprotein Influencing Triglycerides in Humans and Mice Revealed by Comparative Sequencing (2001) (923)
- Two independent apolipoprotein A5 haplotypes influence human plasma triglyceride levels. (2002) (415)
- Relative contribution of variation within the APOC3/A4/A5 gene cluster in determining plasma triglycerides. (2002) (399)
- High-throughput genotyping with single nucleotide polymorphisms. (2001) (365)
- Integration of cytogenetic landmarks into the draft sequence of the human genome (2001) (316)
- Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations (2015) (286)
- Integrated Omics: Tools, Advances, and Future Approaches. (2019) (227)
- The Need for Multi-Omics Biomarker Signatures in Precision Medicine (2019) (200)
- A High-Resolution Radiation Hybrid Map of the Human Genome Draft Sequence (2001) (149)
- Genetic linkage and association of the growth hormone secretagogue receptor (ghrelin receptor) gene in human obesity. (2005) (106)
- Haplotype analysis of the apolipoprotein gene cluster on human chromosome 11. (2004) (105)
- Linkage and Association Between Distinct Variants of the APOA1/C3/A4/A5 Gene Cluster and Familial Combined Hyperlipidemia (2004) (105)
- The Invader assay for SNP genotyping. (2005) (97)
- Y chromosome haplotyping in Scandinavian wolves (Canis lupus) based on microsatellite markers (2001) (97)
- High-throughput genotyping of single nucleotide polymorphisms using new biplex invader technology. (2002) (88)
- Current analysis platforms and methods for detecting copy number variation. (2013) (85)
- Improved method for the analysis of membrane proteins by mass spectrometry. (2007) (74)
- ZoomQuant: An application for the quantitation of stable isotope labeled peptides (2005) (74)
- Insights into Dahl salt-sensitive hypertension revealed by temporal patterns of renal medullary gene expression. (2003) (73)
- Genetic variation in aldosterone synthase predicts plasma glucose levels (2001) (57)
- Tree-structured supervised learning and the genetics of hypertension. (2004) (55)
- Methods and approaches for the comprehensive characterization and quantification of cellular proteomes using mass spectrometry. (2008) (54)
- Fatty acid binding protein 3 (fabp3) is associated with insulin, lipids and cardiovascular phenotypes of the metabolic syndrome through epigenetic modifications in a northern european family population (2013) (52)
- The glycine allele of a glycine/arginine polymorphism in the beta2-adrenergic receptor gene is associated with essential hypertension in a population of Chinese origin. (2001) (52)
- Genetic variation in cannabinoid receptor 1 (CNR1) is associated with derangements in lipid homeostasis, independent of body mass index. (2008) (51)
- Single nucleotide polymorphisms in protein tyrosine phosphatase 1β (PTPN1) are associated with essential hypertension and obesity (2004) (50)
- Genetic Variation in the Peroxisome Proliferator Activated Receptor-Gamma Gene Is Associated with Histologically Advanced NAFLD (2012) (47)
- Nonhuman Primates and Translational Research-Cardiovascular Disease. (2017) (43)
- Hepatic Gene Networks in Morbidly Obese Patients With Nonalcoholic Fatty Liver Disease (2010) (38)
- 18O labeling over a coffee break: a rapid strategy for quantitative proteomics. (2008) (37)
- INSIG1 influences obesity-related hypertriglyceridemia in humans (2010) (36)
- Genetic determinants of obesity-related lipid traits Published, JLR Papers in Press, February 1, 2004. DOI 10.1194/jlr.M300474-JLR200 (2004) (35)
- Sequence-Specific Capture of Protein-DNA Complexes for Mass Spectrometric Protein Identification (2011) (34)
- Comparison of linkage disequilibrium patterns between the HapMap CEPH samples and a family-based cohort of Northern European descent. (2006) (29)
- Obesity-related dyslipidemia associated with FAAH, independent of insulin response, in multigenerational families of Northern European descent. (2009) (28)
- Integrated approach for the comprehensive characterization of lipoproteins from human plasma using FPLC and nano-HPLC-tandem mass spectrometry. (2010) (27)
- Gene expression reveals vulnerability to oxidative stress and interstitial fibrosis of renal outer medulla to nonhypertensive elevations of ANG II. (2003) (27)
- Genomic and geographic distribution of private SNPs and pathways in human populations. (2009) (27)
- Simultaneous quantification and identification using 18O labeling with an ion trap mass spectrometer and the analysis software application “ZoomQuant” (2005) (27)
- Parallel single nucleotide polymorphism genotyping by surface invasive cleavage with universal detection. (2005) (27)
- A comprehensive analysis of adiponectin QTLs using SNP association, SNP cis-effects on peripheral blood gene expression and gene expression correlation identified novel metabolic syndrome (MetS) genes with potential role in carcinogenesis and systemic inflammation (2013) (25)
- Proteomic characterization of high-density lipoprotein particles in patients with non-alcoholic fatty liver disease (2018) (24)
- Complex high-resolution linkage disequilibrium and haplotype patterns of single-nucleotide polymorphisms in 2.5 Mb of sequence on human chromosome 21. (2001) (23)
- Serotonin (5-HT) receptor 5A sequence variants affect human plasma triglyceride levels. (2010) (23)
- From SNPs to function: the effect of sequence variation on gene expression. Focus on "a survey of genetic and epigenetic variation affecting human gene expression". (2004) (22)
- Relative quantification of peptide phosphorylation in a complex mixture using 18O labeling. (2007) (21)
- Obesity and its therapy: from genes to community action. (2006) (21)
- Analysis of concordance of different haplotype block partitioning algorithms (2005) (20)
- Heritability of the Severity of the Metabolic Syndrome in Whites and Blacks in 3 Large Cohorts (2017) (19)
- Discovery of Chromatin-Associated Proteins via Sequence-Specific Capture and Mass Spectrometric Protein Identification in Saccharomyces cerevisiae (2014) (19)
- Single nucleotide polymorphisms in protein tyrosine phosphatase 1beta (PTPN1) are associated with essential hypertension and obesity. (2004) (18)
- High Resolution GC-Orbitrap-MS Metabolomics using both Electron Ionization (EI) and Chemical Ionization (CI) for Analysis of Human Plasma. (2020) (18)
- High-resolution gas chromatography/mass spectrometry metabolomics of non-human primate serum (2018) (17)
- Quantitative comparison of lipoprotein fractions derived from human plasma and serum by liquid chromatography-tandem mass spectrometry (2010) (17)
- Proteomics in non-human primates: utilizing RNA-Seq data to improve protein identification by mass spectrometry in vervet monkeys (2017) (17)
- Analysis of serum changes in response to a high fat high cholesterol diet challenge reveals metabolic biomarkers of atherosclerosis (2019) (17)
- Optimized GC–MS metabolomics for the analysis of kidney tissue metabolites (2018) (14)
- Association of TMTC2 With Human Nonsyndromic Sensorineural Hearing Loss. (2016) (14)
- A novel procedure for genotyping of single nucleotide polymorphisms in trisomy with genomic DNA and the invader assay (2008) (12)
- QTL-based association analyses reveal novel genes influencing pleiotropy of Metabolic Syndrome (MetS) (2013) (12)
- HyCCAPP as a tool to characterize promoter DNA-protein interactions in Saccharomyces cerevisiae. (2016) (11)
- Elucidating Protein-DNA Interactions in Human Alphoid Chromatin via Hybridization Capture and Mass Spectrometry. (2017) (11)
- Identification of cell surface markers to differentiate rat endothelial and fibroblast cells using lectin arrays and LC-ESI-MS/MS. (2008) (11)
- Nonhuman primate breath volatile organic compounds associate with developmental programming and cardio-metabolic status (2018) (10)
- Quantitative characterization of changes in the cardiac mitochondrial proteome during anesthetic preconditioning and ischemia. (2013) (10)
- Characterization of vascular endothelial growth factor receptors on the endothelial cell surface during hypoxia using whole cell binding arrays. (2007) (10)
- Variant discovery in targeted resequencing using whole genome amplified DNA (2013) (9)
- Corrigendum: Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations (2016) (8)
- High Resolution GC/MS Metabolomics of Non-Human Primate Serum. (2018) (8)
- TMTC2 variant associated with sensorineural hearing loss and auditory neuropathy spectrum disorder in a family dyad (2018) (7)
- To understand the whole, you must know the parts: unraveling the roles of protein-DNA interactions in genome regulation. (2011) (7)
- Visualizing Quantitative Proteomics Datasets using Treemaps (2007) (7)
- Advanced methods for the analysis of chromatin-associated proteins. (2014) (5)
- Automated SNP Genotype Clustering Algorithm to Improve Data Completeness in High-Throughput SNP Genotyping Datasets from Custom Arrays (2008) (5)
- Comparison of a GC-Orbitrap-MS with Parallel GC-FID Capabilities for Metabolomics of Human Serum (2019) (4)
- Optimization of Imputation Strategies for High-Resolution Gas Chromatography–Mass Spectrometry (HR GC–MS) Metabolomics Data (2022) (4)
- Sequential abundant ion fragmentation analysis (SAIFA): an alternative approach for phosphopeptide identification using an ion trap mass spectrometer. (2011) (3)
- Body fat distribution, lipoprotein metabolism, and insulin resistance: a lifetime of research on the pathophysiology of the human metabolic syndrome. (2012) (3)
- Accounting for a Quantitative Trait Locus for Plasma Triglyceride Levels: Utilization of Variants in Multiple Genes (2012) (3)
- A novel method, the Variant Impact On Linkage Effect Test (VIOLET), leads to improved identification of causal variants in linkage regions (2013) (3)
- The rocky road toward clinical genetic testing: insights into the physio-genetic basis of hearing loss. (2009) (3)
- Integrated omics analysis reveals sirtuin signaling is central to hepatic response to a high fructose diet (2021) (2)
- Assessment of label-free quantification and missing value imputation for proteomics in non-human primates (2021) (2)
- Using SNPs to unravel the genetic basis of obesity (2006) (1)
- Putting the Invader assay to work: laboratory application and data management. (2009) (1)
- Publisher Correction: Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations (2020) (1)
- Metabolite Extraction and Derivatization of Plasma/ Serum Samples for High Resolution GC-MS- based Metabolomics v1 (2019) (1)
- Genetic Markers and Genotyping Analyses for Genetic Disease Studies (2010) (1)
- Efficiency of whole‐exome sequencing in old world and new world primates using human capture reagents (2021) (1)
- Metabolic Reprogramming: Short-term Western Diet Exposure Induces Sustained Changes in Plasma Metabolites (2019) (1)
- A comprehensive analysis of adiponectin QTLs using SNP association, SNP cis-effects on peripheral blood gene expression and gene expression correlation identified novel metabolic syndrome (MetS) genes with potential role in carcinogenesis and systemic inflammation (2013) (1)
- Abstract 504: Association of Exercise-Induced Changes in Cholesterol Efflux Capacity with Changes in the HDL Proteome (2019) (0)
- Human Genome Draft Sequence A High-Resolution Radiation Hybrid Map of the (2010) (0)
- 2392: Detecting cardiometabolic disease through breath analysis: A metabolomic approach (2017) (0)
- expressionpatterns of renal medullary gene Insights into Dahl salt-sensitive hypertension revealed (2015) (0)
- Proteomics in non-human primates: utilizing RNA-Seq data to improve protein identification by mass spectrometry in vervet monkeys (2017) (0)
- Linkage and association of haplotypes at the APOA1/C3/A4/A5 gene cluster to familial combined hyperlipidemia (2002) (0)
- Genetic Variation in the Peroxisome Proliferator Activated Receptor-gamma Gene Is Associated with NAFLD and Its Histological Phenotypes: 358 (2007) (0)
- Adaptation of Hybridization Capture of Chromatin-associated Proteins for Proteomics to Mammalian Cells. (2018) (0)
- Fatty acid binding protein 3 (fabp3) is associated with insulin, lipids and cardiovascular phenotypes of the metabolic syndrome through epigenetic modifications in a northern european family population (2013) (0)
- Linkage and Association of Haplotypes at the APOA 1 / C 3 / A 4 / A 5 Gene Cluster to Familial Combined Hyperlipidemia (2002) (0)
- Linkage and association of haplotypes at the APOA1/C3/A4/A5 gene cluster to familial combined hyperlipidemia - eScholarship (2002) (0)
- Polymorphisms High-Throughput Genotyping with Single Nucleotide Material (2001) (0)
- Linkage and association of haplotypes at the APOA1/C3/A4/A5 genecluster to familial combined hyperlipidemia (2002) (0)
- Abstract 1456: Proteomic Analysis Of Proteins Bound By D-4F In Plasma From C57bl/6 And ApoA-I KO Mice (2007) (0)
- Abstract 16370: Hexokinase-Induced Residue Specific Phosphorylation of Cardiac Mitochondrial Voltage-Dependent Anion Channel (2011) (0)
- 2392 (2017) (0)
- epigenetic variation affecting human gene expression'' . Focus on ''A survey of genetic and on gene expression From SNPs to function: the effect of sequence variation (2015) (0)
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What Schools Are Affiliated With Michael Olivier?
Michael Olivier is affiliated with the following schools:
