H-Index & Metrics Best Publications

H-Index & Metrics

Discipline name H-index Citations Publications World Ranking National Ranking
Genetics and Molecular Biology D-index 107 Citations 44,386 533 World Ranking 335 National Ranking 5
Medicine D-index 91 Citations 31,255 450 World Ranking 5537 National Ranking 63

Research.com Recognitions

Awards & Achievements

Member of the European Molecular Biology Organization (EMBO)

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Mutation
  • Genetics

Genetics, Haplotype, Gene, Immunology and Locus are his primary areas of study. In his articles, Juha Kere combines various disciplines, including Genetics and Dyslexia. His Haplotype research integrates issues from Genetic marker, Neuropeptide S receptor and Gene mapping.

His work is dedicated to discovering how Gene, Molecular biology are connected with Alternative splicing, Ectodysplasin A receptor, Ectodysplasin A, Ectodysplasins and Gene expression profiling and other disciplines. His studies deal with areas such as Genetic determinism and Genetic linkage as well as Locus. His research in Asthma intersects with topics in Methylation, Epigenetics and DNA methylation, CpG site.

His most cited work include:

  • A promoter-level mammalian expression atlas (1307 citations)
  • A promoter-level mammalian expression atlas (1307 citations)
  • A Genome-Wide Association Study Identifies New Psoriasis Susceptibility Loci and an Interaction Between HLA-C and ERAP1 (768 citations)

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

His primary areas of investigation include Genetics, Immunology, Gene, Candidate gene and Haplotype. His work is connected to Locus, Single-nucleotide polymorphism, Genetic association, Genetic linkage and Allele, as a part of Genetics. His Single-nucleotide polymorphism research includes themes of Internal medicine and Genetic variation.

His studies in Gene integrate themes in fields like Molecular biology and Cell biology. He undertakes multidisciplinary studies into Candidate gene and Dyslexia in his work. Juha Kere studies Haplotype, namely Linkage disequilibrium.

He most often published in these fields:

  • Genetics (76.69%)
  • Immunology (34.03%)
  • Gene (31.15%)

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

  • Genetics (76.69%)
  • Immunology (34.03%)
  • Gene (31.15%)

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

Juha Kere spends much of his time researching Genetics, Immunology, Gene, Cell biology and Genome-wide association study. His studies in Candidate gene, Medical genetics, Single-nucleotide polymorphism, Genetic linkage and Genome are all subfields of Genetics research. His Immunology research is multidisciplinary, incorporating elements of Phenotype and Genetic predisposition.

As part of the same scientific family, Juha Kere usually focuses on Gene, concentrating on Computational biology and intersecting with Cap analysis gene expression. His research integrates issues of Meta-analysis, Genetic association, Locus, Molecular genetics and Haplotype in his study of Genome-wide association study. His Asthma research is multidisciplinary, relying on both Methylation, Epigenetics and DNA methylation.

Between 2016 and 2021, his most popular works were:

  • DNA methylation in childhood asthma: an epigenome-wide meta-analysis (93 citations)
  • DNA methylation in childhood asthma: an epigenome-wide meta-analysis (93 citations)
  • FANTOM5 CAGE profiles of human and mouse samples (82 citations)

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

  • Gene
  • Mutation
  • Internal medicine

His scientific interests lie mostly in Genetics, DNA methylation, Immunology, Epigenetics and Genome-wide association study. His research in Candidate gene and Genetic linkage are components of Genetics. He works mostly in the field of DNA methylation, limiting it down to topics relating to Pregnancy and, in certain cases, Physiology, Cord blood, dNaM and Gene expression, as a part of the same area of interest.

The Immunology study combines topics in areas such as Phenotype, Single-nucleotide polymorphism, Disease and Allele. His study explores the link between Epigenetics and topics such as Methylation that cross with problems in CpG site. His Genome-wide association study research includes elements of Meta-analysis and SNP.

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 promoter-level mammalian expression atlas

Alistair R.R. Forrest;Hideya Kawaji;Michael Rehli;J. Kenneth Baillie.
Nature (2014)

1134 Citations

X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein.

Juha Kere;Anand K. Srivastava;Outi Montonen;Jonathan Zonana.
Nature Genetics (1996)

951 Citations

A Genome-Wide Association Study Identifies New Psoriasis Susceptibility Loci and an Interaction Between HLA-C and ERAP1

Amy Strange;Francesca Capon;Chris C A Spencer.
Nature Genetics (2010)

841 Citations

Differential DNA Methylation in Purified Human Blood Cells: Implications for Cell Lineage and Studies on Disease Susceptibility

Lovisa E. Reinius;Nathalie Acevedo;Maaike Joerink;Göran Pershagen.
PLOS ONE (2012)

823 Citations

Epigenome-wide association data implicate DNA methylation as an intermediary of genetic risk in rheumatoid arthritis

Yun Liu;Martin J Aryee;Leonid Padyukov;M Daniele Fallin;M Daniele Fallin.
Nature Biotechnology (2013)

812 Citations

Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity

Lam C. Tsoi;Sarah L. Spain;Sarah L. Spain;Jo Knight;Eva Ellinghaus;Eva Ellinghaus.
Nature Genetics (2012)

749 Citations

Polymorphisms in the Tyrosine Kinase 2 and Interferon Regulatory Factor 5 Genes Are Associated with Systemic Lupus Erythematosus

Snaevar Sigurdsson;Gunnel Nordmark;Harald H.H. Göring;Katarina Lindroos.
American Journal of Human Genetics (2005)

656 Citations

Mutations in the gene encoding the 3'-5' DNA exonuclease TREX1 are associated with systemic lupus erythematosus.

Min Ae Lee-Kirsch;Maolian Gong;Dipanjan Chowdhury;Lydia Senenko.
Nature Genetics (2007)

621 Citations

Characterization of a Common Susceptibility Locus for Asthma-Related Traits

Tarja Laitinen;Anne Polvi;Pia Rydman;Johanna Vendelin.
Science (2004)

558 Citations

Mutations of the Down–regulated in adenoma ( DRA ) gene cause congenital chloride diarrhoea

Höglund P;Haila S;Socha J;Tomaszewski L.
Nature Genetics (1996)

532 Citations

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