Meharji Arumilli
Helsinki, 02900, Finland
Last Updated: 09/26/2026
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Found 31 publications
Author Correction: Genome sequencing of 2000 canids by the Dog10K consortium advances the understanding of demography, genome function and architecture.
Journal: Genome biology
Published: November 08, 2023
The DoGA consortium expression atlas of promoters and genes in 100 canine tissues.
Journal: Nature communications
Published: March 14, 2023
Genome sequencing of 2000 canids by the Dog10K consortium advances the understanding of demography, genome function and architecture.
Journal: Genome biology
Published: November 23, 2022
Dominant Distal Myopathy 3 (MPD3) Caused by a Deletion in the HNRNPA1 Gene.
Journal: Neurology. Genetics
Published: July 21, 2021
Missense variant in LOXHD1 is associated with canine nonsyndromic hearing loss.
Journal: Human genetics
Published: March 03, 2021
Dog colour patterns explained by modular promoters of ancient canid origin.
Journal: Nature ecology & evolution
Published: February 04, 2021
Intronic variant in POU1F1 associated with canine pituitary dwarfism.
Journal: Human genetics
Published: December 21, 2020
In-frame deletion in canine PITRM1 is associated with a severe early-onset epilepsy, mitochondrial dysfunction and neurodegeneration.
Journal: Human genetics
Published: December 21, 2020
A missense variant in IFT122 associated with a canine model of retinitis pigmentosa.
Journal: Human genetics
Published: December 16, 2020
Improved Criteria for the Classification of Titin Variants in Inherited Skeletal Myopathies.
Journal: Journal of neuromuscular diseases
Published: February 11, 2020
webGQT: A Shiny Server for Genotype Query Tools for Model-Based Variant Filtering.
Journal: Frontiers in genetics
Published: September 06, 2019
A putative silencer variant in a spontaneous canine model of retinitis pigmentosa.
Journal: PLoS genetics
Published: June 11, 2019
Last Updated: 09/26/2026