James Scott
#160,503
Most Influential Person Now
Professor of Cardiovascular Medicine
James Scott 's AcademicInfluence.com Rankings
James Scott philosophy Degrees
Philosophy
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#18117
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Logic
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World Rank
#12725
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Philosophy
James Scott 's Degrees
- Doctorate Medicine Harvard University
- PhD Cardiovascular Medicine Stanford University
Why Is James Scott Influential?
(Suggest an Edit or Addition)According to Wikipedia, James Scott FRCP, FIBiol, FMedSci, FRS is a British cardiologist. Scott undertook training at the London Hospital and in Birmingham, then in 1975 took up a position the Academic Department of Medicine at the Royal Free Hospital.
James Scott '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
- Biological, Clinical, and Population Relevance of 95 Loci for Blood Lipids (2010) (3485)
- Genetic Variants in Novel Pathways Influence Blood Pressure and Cardiovascular Disease Risk (2011) (1928)
- Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility (2014) (933)
- The genetic architecture of type 2 diabetes (2016) (927)
- Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries (2018) (735)
- A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease (2011) (638)
- Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity (2016) (634)
- Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease. (2009) (614)
- Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma (2011) (526)
- Common genetic variation near MC4R is associated with waist circumference and insulin resistance (2008) (523)
- Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci (2011) (518)
- Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure (2011) (424)
- Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. (2008) (424)
- New gene functions in megakaryopoiesis and platelet formation (2011) (423)
- Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function (2016) (388)
- Seventy-five genetic loci influencing the human red blood cell (2012) (357)
- Epigenome-wide association of DNA methylation markers in peripheral blood from Indian Asians and Europeans with incident type 2 diabetes: a nested case-control study. (2015) (347)
- Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides (2008) (334)
- Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation (2015) (285)
- Genetic variation in SCN10A influences cardiac conduction (2010) (285)
- Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption (2011) (270)
- Genetic loci influencing kidney function and chronic kidney disease (2010) (266)
- A coherent approach for analysis of the Illumina HumanMethylation450 BeadChip improves data quality and performance in epigenome-wide association studies (2015) (264)
- Genome-wide association study identifies variants in TMPRSS6 associated with hemoglobin levels (2009) (240)
- Large-Scale Gene-Centric Analysis Identifies Novel Variants for Coronary Artery Disease (2011) (228)
- Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study (2011) (185)
- The South Asian Genome (2014) (131)
- Genome-Wide Meta-Analysis for Serum Calcium Identifies Significantly Associated SNPs near the Calcium-Sensing Receptor (CASR) Gene (2010) (110)
- Common Genetic Variation Near Melatonin Receptor MTNR1B Contributes to Raised Plasma Glucose and Increased Risk of Type 2 Diabetes Among Indian Asians and European Caucasians (2009) (103)
- A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure. (2018) (100)
- Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids (2019) (93)
- Causal Effect of Plasminogen Activator Inhibitor Type 1 on Coronary Heart Disease (2017) (78)
- Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. (2019) (77)
- A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk (2017) (43)
- A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure. (2019) (28)
- Sequence data and association statistics from 12,940 type 2 diabetes cases and controls (2017) (25)
- Coronary heart disease in Indian Asians (2014) (16)
- Investigation of Genetic Variation Underlying Central Obesity amongst South Asians (2016) (15)
- Genetic association study of childhood aggression across raters, instruments, and age (2021) (12)
- Genome-wide association reveals that common genetic variation in the kallikrein-kinin system is associated with serum L-arginine levels (2016) (8)
- Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption (Proceedings of the National Academy Sciences of the United States of America (2011) 108, 17, (7119-7124)) (2011) (6)
- Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls (2018) (4)
- Correction for Schumann et al., Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption (2011) (3)
- Erratum to: A coherent approach for analysis of the Illumina HumanMethylation450 BeadChip improves data quality and performance in epigenome-wide association studies (2016) (3)
- Abstract 3970: Obesity and risk of Type 2 Diabetes in UK Indian Asians and Northern Europeans in the London Life Sciences Population (LOLIPOP) study (2006) (3)
- 114 Whole genome sequencing to identify genetic variants underlying cardiovascular disease among Indian Asians (2012) (3)
- Abstract 4144: Physical Activity and Risk of Type 2 Diabetes in UK Indian Asian and Northern European Subjects in the London Life Sciences Population (LOLIPOP) Study (2006) (2)
- Multi-ancestry genome-wide gene–smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids (2019) (2)
- Genetic loci influencing C-reactive protein levels and coronary heart disease risk: results of genetic association and Mendelian randomisation study with meta-analysis in 80 614 people (2009) (2)
- Interethnic analyses of blood pressure loci in populations of East Asian and European descent (2018) (2)
- Abstract 1969: Genetic Variation in SCN10a is Associated With Cardiac Conduction, Heart Block and Risk of Ventricular Fibrillation (2009) (1)
- Multi-ancestry genome-wide smoking interaction study of 387,272 individuals identifies novel lipid loci. (2019) (1)
- Abstract 2320: A Genome-wide Scan Identifies Novel And Known DNA Variants Associated With Component Phenotypes Of Metabolic Syndrome (2007) (0)
- Epigenome-wide association reveals extensive perturbations in DNA methylation associated with adiposity and its adverse metabolic consequences. Authors (2015) (0)
- Abstract P224: Whole Genome Sequencing of 8 Indian Asians (2012) (0)
- Nature Genetics | Article (2015) (0)
- Erratum: A coherent approach for analysis of the Illumina HumanMethylation450 BeadChip improves data quality and performance in epigenome-wide association studies (vol 16, 37, 2015) (2016) (0)
- Genetic association study of childhood aggression across raters, instruments, and age. (2021) (0)
- A coherent approach for analysis of the Illumina HumanMethylation450 BeadChip improves data quality and performance in epigenome-wide association studies (2015) (0)
- Abstract 4115: Transcription factor 7-like-2 polymorphisms and risk of Type 2 Diabetes in Indian Asians and Northern Europeans (2006) (0)
- Periodontitis, Atherosclerotic Cardiovascular Disease and Vitamin D (2009) (0)
- Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity Authors (2016) (0)
- Abstract 19090: Assessing the Contribution of Dietary Factors to the Increased Prevalence of Insulin Resistance Amongst Uk Indian Asians Compared to Europeans (2013) (0)
- Abstract 4181: The Age and Gender Related Patterns of Insulin Resistance in UK Indian Asians and Northern Europeans: the London Life Sciences Population (LOLIPOP) Study (2006) (0)
- Estimating heritabilities and genetic correlations of insulin resistance and related metabolic traits in Indian families using a multivariate maximum likelihood approach (2007) (0)
- Are Indian Asians genetically homogeneous? Implications for genetic association studies (2008) (0)
- Common genetic variation near MTNR1B contributes to raised plasma glucose and increased risk of type-2 diabetes among Indian Asians (2009) (0)
- Does genetic variation in FTO account for the increased risk of obesity and type 2 diabetes in UK Indian Asians (2008) (0)
- Erratum to: A coherent approach for analysis of the Illumina HumanMethylation450 BeadChip improves data quality and performance in epigenome-wide association studies (2016) (0)
- Supplementary Material (nature09270-s1) (2012) (0)
- Explorer The South Asian Genome (2017) (0)
- 111 Investigation of the Validity of Cardiovascular Death Certification Amongst Uk Indian Asians and Europeans (2014) (0)
- Does CRP Play a Causal Role in the Development of Coronary Heart Disease: Results of a Mendelian Randomisation Experiment Involving 128,935 People (2009) (0)
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