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 and Molecular Biology D-index 40 Citations 42,866 52 World Ranking 5123 National Ranking 534

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Genetics
  • Internal medicine

His primary scientific interests are in Genetics, Genome-wide association study, Genetic association, Linkage disequilibrium and Single-nucleotide polymorphism. In general Genetics study, his work on Haplotype and International HapMap Project often relates to the realm of Bipolar disorder and Psychosis, thereby connecting several areas of interest. While the research belongs to areas of Haplotype, he spends his time largely on the problem of Human genome, intersecting his research to questions surrounding Selection and Natural selection.

The concepts of his Genome-wide association study study are interwoven with issues in Allele, Allele frequency, Genotyping, Disease and ANK3. His Genetic association research incorporates elements of Genetic architecture, Psoriasis, Immunology and Genetic predisposition. His research in Linkage disequilibrium intersects with topics in Sample size determination, Bioinformatics and Pruning.

His most cited work include:

  • Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls (7922 citations)
  • A haplotype map of the human genome (5144 citations)
  • Biological insights from 108 schizophrenia-associated genetic loci (4834 citations)

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

His scientific interests lie mostly in Genetics, Genome-wide association study, Genetic association, Linkage disequilibrium and Single-nucleotide polymorphism. His studies in Haplotype, Allele, Copy-number variation, Gene and Genome are all subfields of Genetics research. In his study, Mutation is strongly linked to Natural selection, which falls under the umbrella field of Haplotype.

His Genome-wide association study study incorporates themes from Case-control study, Immunology, Disease, Genetic architecture and Candidate gene. His Genetic association research is multidisciplinary, incorporating elements of Psoriasis, Genetic predisposition, Bioinformatics, Genetic heterogeneity and Genetic variation. His Linkage disequilibrium study also includes

  • International HapMap Project which connect with Haplotype estimation,
  • Imputation that connect with fields like Data mining.

He most often published in these fields:

  • Genetics (59.05%)
  • Genome-wide association study (53.33%)
  • Genetic association (33.33%)

What were the highlights of his more recent work (between 2016-2021)?

  • Genetics (59.05%)
  • Genome-wide association study (53.33%)
  • Genetic association (33.33%)

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

His main research concerns Genetics, Genome-wide association study, Genetic association, Copy-number variation and Disease. Chris C. A. Spencer conducted interdisciplinary study in his works that combined Genetics and Bipolar disorder. His research in Genome-wide association study intersects with topics in Odds ratio, Biobank, Computational biology and Case-control study.

His Biobank research integrates issues from Phenome and Single-nucleotide polymorphism. His Genetic association research is multidisciplinary, relying on both Meta-analysis, Bayesian probability and Frequentist inference. Chris C. A. Spencer focuses mostly in the field of Copy-number variation, narrowing it down to topics relating to Structural variation and, in certain cases, Locus, 1000 Genomes Project, Haplotype and Red blood cell.

Between 2016 and 2021, his most popular works were:

  • Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects (475 citations)
  • Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes (328 citations)
  • Excessive burden of lysosomal storage disorder gene variants in Parkinson's disease (163 citations)

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

  • Gene
  • Genetics
  • Internal medicine

Chris C. A. Spencer spends much of his time researching Genome-wide association study, Genetics, Copy-number variation, Virology and Hepatitis C virus. His study in Genome-wide association study is interdisciplinary in nature, drawing from both Odds ratio, Phenotype and Case-control study. Chris C. A. Spencer combines topics linked to Disease with his work on Genetics.

His studies in Copy-number variation integrate themes in fields like Structural variation, GYPA, 1000 Genomes Project, Haplotype and GYPB. His research integrates issues of Acquired immune system, Genetic variability and Innate immune system in his study of Virology. His Hepatitis C virus study integrates concerns from other disciplines, such as Genome and Immune system.

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

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

Paul R. Burton;David G. Clayton;Lon R. Cardon;Nick Craddock.
Nature (2007)

7828 Citations

A haplotype map of the human genome

John W. Belmont;Andrew Boudreau;Suzanne M. Leal;Paul Hardenbol.
Nature (2003)

5062 Citations

A second generation human haplotype map of over 3.1 million SNPs

Kelly A. Frazer;Dennis G. Ballinger;David R. Cox;David A. Hinds.
Nature (2007)

4739 Citations

Biological insights from 108 schizophrenia-associated genetic loci

Stephan Ripke;Stephan Ripke;Benjamin M. Neale;Benjamin M. Neale;Aiden Corvin;James T. R. Walters.
Nature (2014)

4139 Citations

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

Stephen Sawcer;Garrett Hellenthal;Matti Pirinen;Chris C. A. Spencer.
Nature (2011)

2262 Citations

Genome-wide detection and characterization of positive selection in human populations

Pardis C. Sabeti;Pardis C. Sabeti;Patrick Varilly;Patrick Varilly;Ben Fry;Jason Lohmueller.
(2007)

1972 Citations

Genome-wide association study identifies five new schizophrenia loci

Stephan Ripke;Alan R. Sanders;Kenneth S. Kendler;Douglas F. Levinson.
Nature Genetics (2011)

1603 Citations

Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

Paul R Burton;David G Clayton;Lon R Cardon;Nick Craddock.
Nature Genetics (2007)

1230 Citations

Identification of loci associated with schizophrenia by genome-wide association and follow-up

Michael C. O'Donovan;Nicholas Craddock;Nadine Norton;Hywel Williams.
Nature Genetics (2008)

1180 Citations

Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores

Bjarni J. Vilhjálmsson;Jian Yang;Hilary K. Finucane;Alexander Gusev.
American Journal of Human Genetics (2015)

960 Citations

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