Simple Sequence repeats showing \\\"length preference have regulatory functions in humans.\\\"
Gene
2017
MSDB:A Comperhensive Database of Simple Sequence Repeats
Genome Biol Evol
2017
Mutations in the prostate specific antigen (PSA/KLK3) correlate with male infertility
Sci. Rep. 7:11225
2017
Leber\\\'s Hereditary Optic Neuropathy-Specific Mutation m.11778G>A Exists on Diverse Mitochondrial Haplogroups in India
Invest. Ophthalmol. Vis. Sci. 58: 3923-3930
2017
Mitochondrial oxidative phosphorylation disorders in children: Phenotypic, genotypic and biochemical correlations in 85 patients from South India.
Mitochondrion 32:42-49.
2017
Genotype-Phenotype Study of the Middle Gangetic Plain in India Shows Association of rs2470102 with Skin Pigmentation.
J Invest Dermatol. 137:670-677.
2017
Reconstructing the population history of the largest tribe of India: the Dravidian speaking Gond.
Eur J Hum Genet. 25:493-498.
2017
Ancient DNA Reveals Late Pleistocene Existence of Ostriches in Indian Sub-Continent.
PLoS One. 12:e0164823.
2017
Origin and spread of human mitochondrial DNA haplogroup U7.
Sci Rep; 7:46044.
2017
3`-UTR SNP rs2229611 in G6PC1 affects mRNA stability, expression and Glycogen Storage Disease type-Ia risk.
Clin Chim Acta. 471:46-54.
2017
Clinicopathologic and molecular spectrum of RNASEH1-related mitochondrial disease.
Neurol Genet. 2017 3(3):e149.
2017
Geographical distribution of complement receptor type 1 variants and their associated disease risk.
PLoS One. 2017 12(5):e0175973.
2017
&sdquo;Like sugar in milk&sdquo: reconstructing the genetic history of the Parsi population.
Genome Biol. 18:110.
2017
MPV17 hepatocerebral mitochondrial DNA depletion syndrome presenting as acute flaccid paralysis - A case report. Mitochondrion.
Jun 30. doi: 10.1016/j.mito.2017.06.006. [Epub ahead of print].
2017
The promise of discovering population-specific disease-associated genes in South Asia.
Nat Genet. Jul 17. doi: 10.1038/ng.3917. [Epub ahead of print].
2017
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