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.
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.
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.
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.
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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)
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)
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)
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)
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)
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)
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)
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)
Functional significance and clinical phenotype of nontruncating mismatch repair variants of MLH1.
Tiina E. Raevaara;Mari K. Korhonen;Hannes Lohi;Heather Hampel.
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.
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