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 44 Citations 28,663 95 World Ranking 4572 National Ranking 2126

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Genetics
  • Mutation

His primary areas of study are Genetics, Genome-wide association study, Disease, Genetic association and Genome. All of his Genetics and Genomics, Candidate gene, Gene and Human genome investigations are sub-components of the entire Genetics study. His study connects Computational biology and Genomics.

His Computational biology study incorporates themes from Exome sequencing, Genetic variation and Human genetic variation. Kasper Lage integrates many fields, such as Genome-wide association study, Allele and Bioinformatics, in his works. His study in Disease is interdisciplinary in nature, drawing from both Phenotype, Proteomics and Gene expression.

His most cited work include:

  • A global reference for human genetic variation. (7825 citations)
  • A global reference for human genetic variation. (7825 citations)
  • A human phenome-interactome network of protein complexes implicated in genetic disorders (812 citations)

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

His primary scientific interests are in Genetics, Gene, Computational biology, Genome-wide association study and Candidate gene. His study in the field of Allele, Exome and Zebrafish also crosses realms of Congenital diaphragmatic hernia. In his research on the topic of Gene, Mutation is strongly related with Cancer.

His Computational biology study integrates concerns from other disciplines, such as Genomics, Disease, Missense mutation and Protein–protein interaction. His Genetic association research extends to Genome-wide association study, which is thematically connected. His Candidate gene study combines topics in areas such as Internal medicine, QRS complex and Gene expression profiling.

He most often published in these fields:

  • Genetics (60.69%)
  • Gene (66.90%)
  • Computational biology (64.14%)

What were the highlights of his more recent work (between 2019-2021)?

  • Gene (66.90%)
  • Computational biology (64.14%)
  • Protein–protein interaction (22.07%)

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

His scientific interests lie mostly in Gene, Computational biology, Protein–protein interaction, Disease and Haploinsufficiency. In his study, Embedding, Identification and Leverage is strongly linked to Cancer, which falls under the umbrella field of Gene. His studies deal with areas such as Missense mutation, CRISPR, Mutagenesis, Interaction network and Protein structure as well as Computational biology.

His studies in Haploinsufficiency integrate themes in fields like Cerebral cortex and Human brain. His Mutation research includes themes of Class, Biological network and Mutation. His Phenotype research is classified as research in Genetics.

Between 2019 and 2021, his most popular works were:

  • BraInMap Elucidates the Macromolecular Connectivity Landscape of Mammalian Brain. (9 citations)
  • BraInMap Elucidates the Macromolecular Connectivity Landscape of Mammalian Brain. (9 citations)
  • Comprehensive characterization of amino acid positions in protein structures reveals molecular effect of missense variants. (3 citations)

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

  • Gene
  • Genetics
  • Mutation

Kasper Lage focuses on Gene, Computational biology, Mutagenesis, Point mutation and Amino acid. His study on Mutation is often connected to Key as part of broader study in Gene. In his papers, Kasper Lage integrates diverse fields, such as Computational biology and Alternative splicing.

His Mutagenesis research incorporates elements of Protein structure and Missense mutation.

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

A global reference for human genetic variation.

Adam Auton;Gonçalo R. Abecasis;David M. Altshuler;Richard M. Durbin.
(2015)

10791 Citations

A global reference for human genetic variation

Adam Auton;Gonçalo R. Abecasis;David M. Altshuler;Richard M. Durbin.
PMC (2015)

1332 Citations

A human phenome-interactome network of protein complexes implicated in genetic disorders

Kasper Lage;E Olof Karlberg;Zenia M Størling;Páll Í Ólason.
Nature Biotechnology (2007)

1023 Citations

Sequencing Chromosomal Abnormalities Reveals Neurodevelopmental Loci that Confer Risk across Diagnostic Boundaries

Michael E. Talkowski;Jill A. Rosenfeld;Ian Blumenthal;Vamsee Pillalamarri.
Cell (2012)

508 Citations

Pervasive sharing of genetic effects in autoimmune disease.

Chris Cotsapas;Benjamin F. Voight;Benjamin F. Voight;Elizabeth Rossin;Kasper Lage;Kasper Lage;Kasper Lage.
PLOS Genetics (2011)

491 Citations

Proteins encoded in genomic regions associated with immune-mediated disease physically interact and suggest underlying biology

Elizabeth J. Rossin;Kasper Lage;Soumya Raychaudhuri;Soumya Raychaudhuri;Soumya Raychaudhuri;Ramnik J. Xavier;Ramnik J. Xavier.
PLOS Genetics (2011)

478 Citations

Proteomic analysis of lysine acetylation sites in rat tissues reveals organ specificity and subcellular patterns

Alicia Lundby;Alicia Lundby;Alicia Lundby;Kasper Lage;Brian T. Weinert;Dorte B. Bekker-Jensen.
Cell Reports (2012)

452 Citations

An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge.

Catherine A. Brownstein;Alan H. Beggs;Nils Homer;Barry Merriman.
(2014)

426 Citations

Integrative Annotation of Variants from 1092 Humans: Application to Cancer Genomics

Ekta Khurana;Yao Fu;Vincenza Colonna;Vincenza Colonna;Xinmeng Jasmine Mu.
Science (2013)

369 Citations

Genome-wide meta-analysis identifies new susceptibility loci for migraine

Verneri Anttila;Bendik S. Winsvold;Bendik S. Winsvold;Padhraig Gormley;Tobias Kurth.
Nature Genetics (2013)

353 Citations

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