H-Index & Metrics Best Publications

H-Index & Metrics

Discipline name H-index Citations Publications World Ranking National Ranking
Genetics and Molecular Biology D-index 76 Citations 19,547 219 World Ranking 1141 National Ranking 618
Medicine D-index 77 Citations 26,495 291 World Ranking 10845 National Ranking 5793

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Internal medicine
  • Genetics

Alexander P. Reiner spends much of his time researching Genetics, Genome-wide association study, Genetic association, Internal medicine and Single-nucleotide polymorphism. Genotype, Gene, Exome, Allele and Allele frequency are the subjects of his Genetics studies. The Genome-wide association study study combines topics in areas such as SNP, Bioinformatics, Medical genetics, Meta-analysis and Locus.

His research in Genetic association intersects with topics in Phenome, Genomics, Pacific islanders and Genetic variation. His study in Internal medicine is interdisciplinary in nature, drawing from both Gastroenterology, Endocrinology and Type 2 diabetes. His studies deal with areas such as Polymorphism and Gene mapping as well as Single-nucleotide polymorphism.

His most cited work include:

  • Effect of VKORC1 haplotypes on transcriptional regulation and warfarin dose. (1222 citations)
  • Loss-of-function mutations in APOC3, triglycerides, and coronary disease (660 citations)
  • Loss-of-function mutations in APOC3, triglycerides, and coronary disease (660 citations)

What are the main themes of his work throughout his whole career to date?

Alexander P. Reiner mostly deals with Genetics, Genome-wide association study, Internal medicine, Genetic association and Single-nucleotide polymorphism. His study in Genetics focuses on Gene, Allele, Locus, Exome and Minor allele frequency. His research in Genome-wide association study focuses on subjects like Bioinformatics, which are connected to Disease.

He has included themes like Endocrinology and Cardiology in his Internal medicine study. His biological study spans a wide range of topics, including Evolutionary biology, Genetic variation, Linkage disequilibrium, Meta-analysis and Computational biology. The concepts of his Single-nucleotide polymorphism study are interwoven with issues in Polymorphism, Immunology, Heritability, Haplotype and Candidate gene.

He most often published in these fields:

  • Genetics (55.66%)
  • Genome-wide association study (55.85%)
  • Internal medicine (39.73%)

What were the highlights of his more recent work (between 2018-2021)?

  • Genome-wide association study (55.85%)
  • Genetics (55.66%)
  • Internal medicine (39.73%)

In recent papers he was focusing on the following fields of study:

Alexander P. Reiner mainly investigates Genome-wide association study, Genetics, Internal medicine, Genetic association and Disease. His Genome-wide association study study improves the overall literature in Single-nucleotide polymorphism. Alexander P. Reiner interconnects Endocrinology and Cardiology in the investigation of issues within Internal medicine.

His Genetic association study incorporates themes from Mendelian randomization, Genome, Meta-analysis, ABO blood group system and Computational biology. His Disease study integrates concerns from other disciplines, such as Telomere, Precision medicine, Cholesterol and Bioinformatics. Within one scientific family, he focuses on topics pertaining to Minor allele frequency under Whole genome sequencing, and may sometimes address concerns connected to Exome.

Between 2018 and 2021, his most popular works were:

  • Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use (385 citations)
  • Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use (385 citations)
  • DNA methylation GrimAge strongly predicts lifespan and healthspan (231 citations)

In his most recent research, the most cited papers focused on:

  • Gene
  • Internal medicine
  • Genetics

His primary areas of study are Genome-wide association study, Genetics, Genetic association, Genetic architecture and Disease. Alexander P. Reiner has researched Genome-wide association study in several fields, including Evolutionary biology, Heritability, Mendelian randomization, Cardiology and Human genetics. Genetics is closely attributed to Lipid profile in his work.

His Genetic association research includes themes of SNP and Genomics. His Genetic architecture study combines topics in areas such as Precision medicine, Genome, Reference genome, Blood cell and Computational biology. Internal medicine covers Alexander P. Reiner research in Disease.

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.

Best Publications

Effect of VKORC1 haplotypes on transcriptional regulation and warfarin dose.

Mark J. Rieder;Alexander P. Reiner;Brian F. Gage;Deborah A. Nickerson.
The New England Journal of Medicine (2005)

1713 Citations

The interleukin-6 receptor as a target for prevention of coronary heart disease: a mendelian randomisation analysis.

D I Swerdlow;M V Holmes;K B Kuchenbaecker.
The Lancet (2012)

686 Citations

Loss-of-function mutations in APOC3, triglycerides, and coronary disease

Jacy Crosby;Gina M. Peloso;Gina M. Peloso;Paul L. Auer;David R. Crosslin.
The New England Journal of Medicine (2014)

660 Citations

Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction

Ron Do;Ron Do;Nathan O. Stitziel;Hong Hee Won;Hong Hee Won;Anders Berg Jørgensen.
Nature (2015)

574 Citations

Association between C reactive protein and coronary heart disease: mendelian randomisation analysis based on individual participant data

G. Eiriksdottir;T. B. Harris;L. J. Launer;V. Gudnason.
web science (2011)

563 Citations

HMG-coenzyme A reductase inhibition, type 2 diabetes, and bodyweight: evidence from genetic analysis and randomised trials.

Daniel I Swerdlow;David Preiss;Karoline B Kuchenbaecker;Michael Holmes.
The Lancet (2015)

547 Citations

DNA methylation-based measures of biological age: meta-analysis predicting time to death

Brian H. Chen;Riccardo E. Marioni;Riccardo E. Marioni;Elena Colicino;Marjolein J. Peters.
Aging (Albany NY) , 8 (9) pp. 1844-1865. (2016) (2016)

522 Citations

Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use

Mengzhen Liu;Yu Jiang;Robbee Wedow;Yue Li;Yue Li.
Nature Genetics (2019)

514 Citations

Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies.

Matthew Traylor;Martin Farrall;Elizabeth G Holliday;Cathie Sudlow.
Lancet Neurology (2012)

504 Citations

Inactivating mutations in NPC1L1 and protection from coronary heart disease

Nathan O. Stitziel;Hong Hee Won;Alanna C. Morrison;Gina M. Peloso.
The New England Journal of Medicine (2014)

465 Citations

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