Lack of replication of association of THSD7A with obesity

Int J Obes (Lond). 2016 Apr;40(4):725-6. doi: 10.1038/ijo.2016.15. Epub 2016 Feb 23.

2016

Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

Nat Commun. 2016 Jan 21;7:10023. doi: 10.1038/ncomms10023.

2016

Association Analysis of PRSS1-PRSS2 and CLDN2-MORC4 Variants in Nonalcoholic Chronic Pancreatitis Using Tropical Calcific Pancreatitis as Model

Pancreas. 2016 Sep;45(8):1153-7. doi: 10.1097/MPA.0000000000000608.

2016

c.*84G>A Mutation in CETP Is Associated with Coronary Artery Disease in South Indians.

PLoS One. 11:e0164151.

2016

The Simons Genome Diversity Project: 300 genomes from 142 diverse populations.

Nature. 538: 201-206

2016

Cryptic Eimeria genotypes are common across the southern but not northern hemisphere.

Int J Parasitol. Jun 28

2016

Audiological manifestations in mitochondrial encephalomyopathy lactic acidosis and stroke like episodes (MELAS) syndrome.

Clin Neurol Neurosurg. 148: 17-21

2016

Whole Exome Screening Identifies Novel and Recurrent WISP3 Mutations Causing Progressive Pseudorheumatoid Dysplasia in Jammu and Kashmir-India.

Sci Rep. 6: 27684.

2016

Optimization of purification method and characterization of recombinant human Centrin-1.

Protein Expr. Purif. 124: 48-54.

2016

Reply to `Lack of replication of association of THSD7A with obesity`

Int J Obes (Lond). Feb 2. doi: 10.1038

2016

Is MTHFR 677 C>T Polymorphism Clinically Important in Polycystic Ovarian Syndrome (PCOS)? A Case-Control Study, Meta-Analysis and Trial Sequential Analysis.

PLoS One. 11(3):e0151510.

2016

Peripheral neuropathy in genetically characterized patients with mitochondrial disorders: A study from south India.

Mitochondrion. 27:1-5

2016

Genetic affinities of the Jewish populations of India.

Sci Rep. 6:19166

2016

Dissecting the influence of Neolithic demic diffusion on Indian Y-chromosome pool through J2-M172 haplogroup.

Sci Rep. 6:19157

2016

Novel mutation in C10orf2 associated with multiple mtDNA deletions, chronic progressive external ophthalmoplegia and premature aging.

Mitochondrion. 26:81-85.

2016