GWAS identifies population-specific new regulatory variants in FUT6 associated with plasma B12 concentrations in Indians

Hum Mol Genet. 2017 Jul 1;26(13):2589. doi: 10.1093/hmg/ddx156.

2017

A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk

Diabetes. 2017 Jul;66(7):2019-2032. doi: 10.2337/db16-1329. Epub 2017 Mar 24.

2017

GWAS identifies population-specific new regulatory variants in FUT6 associated with plasma B12 concentrations in Indians

Hum Mol Genet. 2017 Jul 1;26(13):2551-2564. doi: 10.1093/hmg/ddx071.

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

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

&sdquo;Like sugar in milk&sdquo: reconstructing the genetic history of the Parsi population.

Genome Biol. 18:110.

2017

Geographical distribution of complement receptor type 1 variants and their associated disease risk.

PLoS One. 2017 12(5):e0175973.

2017

Clinicopathologic and molecular spectrum of RNASEH1-related mitochondrial disease.

Neurol Genet. 2017 3(3):e149.

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

Origin and spread of human mitochondrial DNA haplogroup U7.

Sci Rep; 7:46044.

2017

Ancient DNA Reveals Late Pleistocene Existence of Ostriches in Indian Sub-Continent.

PLoS One. 12:e0164823.

2017

Reconstructing the population history of the largest tribe of India: the Dravidian speaking Gond.

Eur J Hum Genet. 25:493-498.

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

Mitochondrial oxidative phosphorylation disorders in children: Phenotypic, genotypic and biochemical correlations in 85 patients from South India.

Mitochondrion 32:42-49.

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