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
Biology and Biochemistry D-index 53 Citations 9,011 259 World Ranking 11639 National Ranking 83

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Mutation
  • Internal medicine

Hannes Lohi mostly deals with Genetics, Biochemistry, Genome-wide association study, Gene and SLC26A3. His Genetics study is mostly concerned with Single-nucleotide polymorphism, Locus, Haplotype, MLH1 and DNA mismatch repair. In Locus, Hannes Lohi works on issues like Candidate gene, which are connected to SNP genotyping and Bioinformatics.

His Genome-wide association study research includes themes of Kufs disease, Cerebellar ataxia and Parkinsonism, Kufor Rakeb syndrome. His study in the fields of Structural variation, Copy-number variation and Comparative genomic hybridization under the domain of Gene overlaps with other disciplines such as PRDM9 and Genome instability. His SLC26A3 research integrates issues from Congenital chloride diarrhea, Inflammation and Inflammatory bowel disease.

His most cited work include:

  • A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome. (276 citations)
  • Identification of Genomic Regions Associated with Phenotypic Variation between Dog Breeds using Selection Mapping (259 citations)
  • Mapping of five new putative anion transporter genes in human and characterization of SLC26A6, a candidate gene for pancreatic anion exchanger. (179 citations)

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

Hannes Lohi mainly investigates Genetics, Genome-wide association study, Gene, Breed and Locus. His studies in Candidate gene, Haplotype, Single-nucleotide polymorphism, Allele and Genotype are all subfields of Genetics research. His Haplotype study frequently draws connections between adjacent fields such as Genetic association.

His Genome-wide association study research incorporates elements of SNP and Progressive retinal atrophy, Retinitis pigmentosa. His study in Frameshift mutation, Exon, Phenotype, Mutation and Missense mutation is carried out as part of his studies in Gene. His Breed research includes elements of Internal medicine and Physiology.

He most often published in these fields:

  • Genetics (41.76%)
  • Genome-wide association study (14.56%)
  • Gene (13.79%)

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

  • Genetics (41.76%)
  • Gene (13.79%)
  • Genome-wide association study (14.56%)

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

His primary areas of investigation include Genetics, Gene, Genome-wide association study, Locus and Internal medicine. Retinitis pigmentosa, Phenotype, Missense mutation, Whole genome sequencing and Exome sequencing are the primary areas of interest in his Genetics study. The various areas that Hannes Lohi examines in his Genome-wide association study study include Lupus erythematosus, Autoimmunity and Autosomal recessive trait.

The Locus study combines topics in areas such as Chromosome 13, Physical exam, Fructosamine, Cohort and Candidate gene. The Candidate gene study which covers Breed that intersects with Clinical psychology. In his research on the topic of Internal medicine, Valine is strongly related with Endocrinology.

Between 2019 and 2021, his most popular works were:

  • Prevalence, comorbidity, and breed differences in canine anxiety in 13,700 Finnish pet dogs. (15 citations)
  • Inadequate socialisation, inactivity, and urban living environment are associated with social fearfulness in pet dogs (15 citations)
  • Mutations in the Kinesin-2 Motor KIF3B Cause an Autosomal-Dominant Ciliopathy. (9 citations)

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

  • Gene
  • Mutation
  • Internal medicine

His main research concerns Genetics, Genome-wide association study, Gene, Distress and Socialization. His research on Genetics often connects related topics like Cerebellum. His research in Genome-wide association study intersects with topics in Genetic testing, Haplotype, Progressive retinal atrophy and Locus.

His work deals with themes such as Lupus erythematosus, Autoimmunity, Autosomal recessive trait and Immunology, which intersect with Locus. His Gene research is multidisciplinary, incorporating perspectives in Ataxia and Cerebellar ataxia. His studies deal with areas such as Neutering, Logistic regression and Female sex as well as Socialization.

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 previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome.

Gevork N Mnatzakanian;Hannes Lohi;Iulia Munteanu;Simon E Alfred.
Nature Genetics (2004)

392 Citations

Identification of Genomic Regions Associated with Phenotypic Variation between Dog Breeds using Selection Mapping

Amaury Vaysse;Abhirami Ratnakumar;Thomas Derrien;Erik Axelsson.
PLOS Genetics (2011)

372 Citations

Out of southern East Asia: the natural history of domestic dogs across the world.

Guo-Dong Wang;Weiwei Zhai;He-Chuan Yang;He-Chuan Yang;He-Chuan Yang;Lu Wang.
Cell Research (2016)

284 Citations

Genome-Wide Analysis Reveals Selection for Important Traits in Domestic Horse Breeds

Jessica L. Petersen;James R. Mickelson;Aaron K. Rendahl;Stephanie J. Valberg.
PLOS Genetics (2013)

237 Citations

FEELnc: a tool for long non-coding RNA annotation and its application to the dog transcriptome.

Valentin Wucher;Fabrice Legeai;Benoît Hédan;Guillaume Rizk.
Nucleic Acids Research (2017)

234 Citations

Functional Characterization of Three Novel Tissue-specific Anion Exchangers SLC26A7, -A8, and -A9

Hannes Lohi;Minna Kujala;Siru Mäkelä;Eero Lehtonen.
Journal of Biological Chemistry (2002)

226 Citations

Genetic diversity in the modern horse illustrated from genome-wide SNP data

Jessica L. Petersen;James R. Mickelson;E. Gus Cothran;Lisa S. Andersson.
PLOS ONE (2013)

224 Citations

The Novel Neuronal Ceroid Lipofuscinosis Gene MFSD8 Encodes a Putative Lysosomal Transporter

Eija Siintola;Meral Topcu;Nina Aula;Hannes Lohi.
American Journal of Human Genetics (2007)

219 Citations

Functional significance and clinical phenotype of nontruncating mismatch repair variants of MLH1.

Tiina E. Raevaara;Mari K. Korhonen;Hannes Lohi;Heather Hampel.
Gastroenterology (2005)

215 Citations

Mapping of five new putative anion transporter genes in human and characterization of SLC26A6, a candidate gene for pancreatic anion exchanger.

Hannes Lohi;Minna Kujala;Erja Kerkelä;Ulpu Saarialho-Kere.
Genomics (2000)

215 Citations

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