D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Genetics D-index 87 Citations 27,227 228 World Ranking 767 National Ranking 114

Research.com Recognitions

Awards & Achievements

2002 - Fellow of the Royal Society, United Kingdom

2001 - Member of Academia Europaea

1993 - Fellow of the Royal Society of Edinburgh

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Genetics
  • DNA

Genetics, Genome-wide association study, Cell biology, Molecular biology and Internal medicine are his primary areas of study. Genetics and Body mass index are frequently intertwined in his study. His study in Genome-wide association study is interdisciplinary in nature, drawing from both Genetic association, Renal function, Kidney disease and Candidate gene.

His Cell biology research includes elements of Embryonic stem cell, Alternative splicing, DNA-binding domain, Regulation of gene expression and Intron. Nicholas D. Hastie has researched Molecular biology in several fields, including ZIC2, DNA binding site, Protein–DNA interaction and Replication protein A. His Internal medicine study incorporates themes from Progenitor cell, Endocrinology and Intermediate mesoderm.

His most cited work include:

  • Modulation of genetic associations with serum urate levels by body-mass-index in humans (1089 citations)
  • Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts (755 citations)
  • New loci associated with kidney function and chronic kidney disease (610 citations)

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

His primary areas of investigation include Genetics, Genome-wide association study, Gene, Cell biology and Molecular biology. Genetics is a component of his Single-nucleotide polymorphism, Genetic association, Locus, Genetic linkage and Alternative splicing studies. His Genome-wide association study research is multidisciplinary, incorporating elements of SNP, Body mass index, Internal medicine and Candidate gene.

Nicholas D. Hastie usually deals with Gene and limits it to topics linked to Wilms' tumor and Cancer research, Carcinogenesis, Tumor suppressor gene, Aniridia and WAGR syndrome. His Cell biology research focuses on Endocrinology and how it relates to Progenitor cell. His work deals with themes such as Regulation of gene expression, Gene expression and Exon, which intersect with Molecular biology.

He most often published in these fields:

  • Genetics (44.64%)
  • Genome-wide association study (21.43%)
  • Gene (18.75%)

What were the highlights of his more recent work (between 2011-2021)?

  • Genome-wide association study (21.43%)
  • Genetics (44.64%)
  • Single-nucleotide polymorphism (11.16%)

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

Nicholas D. Hastie mainly focuses on Genome-wide association study, Genetics, Single-nucleotide polymorphism, Genetic association and Cell biology. His Genome-wide association study study integrates concerns from other disciplines, such as Endocrinology, Internal medicine, Immunology and Locus. His Endocrinology research is multidisciplinary, incorporating perspectives in Progenitor cell and Mesothelium.

His studies deal with areas such as Body mass index and Obesity as well as Genetics. The Single-nucleotide polymorphism study combines topics in areas such as Demography and Allele, Haplotype. His work carried out in the field of Cell biology brings together such families of science as Embryonic stem cell, Zebrafish and Heart morphogenesis.

Between 2011 and 2021, his most popular works were:

  • Modulation of genetic associations with serum urate levels by body-mass-index in humans (1089 citations)
  • GWAS of 126,559 Individuals Identifies Genetic Variants Associated with Educational Attainment (570 citations)
  • Genome-wide association analyses identify 18 new loci associated with serum urate concentrations (488 citations)

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

  • Gene
  • Genetics
  • DNA

His main research concerns Genetics, Genome-wide association study, Single-nucleotide polymorphism, Genetic association and Internal medicine. His Genetics study combines topics from a wide range of disciplines, such as Body mass index, Creatinine and Renal function. His biological study spans a wide range of topics, including Uric acid, Gout, Medical genetics, Genetic variation and Candidate gene.

His work in Single-nucleotide polymorphism addresses issues such as Allele, which are connected to fields such as Blood proteins. He has included themes like SNP genotyping and Tag SNP in his Genetic association study. In his study, which falls under the umbrella issue of Internal medicine, Glycan and Mesothelium is strongly linked to Endocrinology.

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

Modulation of genetic associations with serum urate levels by body-mass-index in humans

Jennifer E. Huffman;Eva Albrecht;Alexander Teumer;Massimo Mangino.
PLOS ONE (2015)

1224 Citations

Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts

Yurii S Aulchenko;Samuli Ripatti;Ida Lindqvist;Dorret Boomsma.
Nature Genetics (2009)

999 Citations

GWAS of 126,559 Individuals Identifies Genetic Variants Associated with Educational Attainment

Cornelius A. Rietveld;Sarah E. Medland;Jaime Lane Derringer;Jian Yang.
Science (2013)

865 Citations

SLC2A9 is a newly identified urate transporter influencing serum urate concentration, urate excretion and gout

Veronique Vitart;Igor Rudan;Igor Rudan;Caroline Hayward;Nicola K Gray;Nicola K Gray.
Nature Genetics (2008)

857 Citations

New loci associated with kidney function and chronic kidney disease

Anna Köttgen;Anna Köttgen;Cristian Pattaro;Carsten A. Böger;Christian Fuchsberger.
Nature Genetics (2010)

810 Citations

Genome-wide association analyses identify 18 new loci associated with serum urate concentrations

Anna Köttgen;Anna Köttgen;Eva Albrecht;Alexander Teumer;Veronique Vitart.
Nature Genetics (2013)

731 Citations

The human PAX6 gene is mutated in two patients with aniridia.

Tim Jordan;Isabel Hanson;Dmitri Zaletayev;Shirley Hodgson.
Nature Genetics (1992)

625 Citations

YAC complementation shows a requirement for Wt1 in the development of epicardium, adrenal gland and throughout nephrogenesis

A W Moore;L McInnes;J Kreidberg;N D Hastie.
Development (1999)

596 Citations

Subnuclear localization of WT1 in splicing or transcription factor domains is regulated by alternative splicing

Stefan H Larsson;Jean-Paul Charlieu;Jean-Paul Charlieu;Kiyoshi Miyagawa;Dieter Engelkamp.
Cell (1995)

575 Citations

Human telomeres contain at least three types of G-rich repeat distributed non-randomly

Robin C Allshire;Maureen Dempster;Nicholas D. Hastie.
Nucleic Acids Research (1989)

516 Citations

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