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List of works by Odity Mukherjee

A Method to Identify and Isolate Pluripotent Human Stem Cells and Mouse Epiblast Stem Cells Using Lipid Body-Associated Retinyl Ester Fluorescence.

scientific article published in August 2016

A method to identify and isolate pluripotent human stem cells and mouse epiblast stem cells using lipid body-associated retinyl ester fluorescence.

scientific article

ApoE4 and late onset depression in Indian population.

scientific article

Apolipoprotein E polymorphism and dementia: a hospital-based study from southern India.

scientific article published in January 2010

Apolipoprotein E4 and brain white matter integrity in Alzheimer's disease: tract-based spatial statistics study under 3-Tesla MRI.

scientific article published on 21 January 2012

Association studies of catechol-O-methyltransferase (COMT) gene with schizophrenia and response to antipsychotic treatment.

scientific article published in March 2009

C9orf72 mutations may be rare in frontotemporal lobar degeneration patients in India.

scientific article published on 14 October 2015

CT60 genotype does not affect CTLA-4 isoform expression despite association to T1D and AITD in northern Sweden

scientific article published on 6 February 2007

Cellular models to study bipolar disorder: A systematic review

scientific article published on 28 May 2015

Common psychiatric diseases and human genetic variation.

scientific article published in January 2002

Detailed Characterization of Human Induced Pluripotent Stem Cells Manufactured for Therapeutic Applications.

scientific article published on 10 June 2016

Effect of CLU and PICALM polymorphisms on AD risk: A study from south India.

scientific article published on 29 December 2016

Evidence of linkage and association on 18p11.2 for psychosis.

scientific article published in December 2006

Genetic polymorphism in the serotonin transporter promoter region and ecological success in macaques.

scientific article published on 22 April 2010

Genotoxic Effects of Culture Media on Human Pluripotent Stem Cells.

scientific article published on 8 February 2017

HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin

scientific article

Haplotype-based association analysis of the MAPT locus in late onset Alzheimer's disease

scientific article published on 31 January 2007

Molecular characterization of novel progranulin (GRN) mutations in frontotemporal dementia

scientific article published on April 2008

Neuropathologic heterogeneity in HDDD1: a familial frontotemporal lobar degeneration with ubiquitin-positive inclusions and progranulin mutation

scientific article published in January 2007

North and South Indian populations share a common ancestral origin of Friedreich's ataxia but vary in age of GAA repeat expansion

scientific article

Phylogenetic analysis and selection pressures of 5-HT receptors in human and non-human primates: receptor of an ancient neurotransmitter.

scientific article

Progranulin mutations and amyotrophic lateral sclerosis or amyotrophic lateral sclerosis-frontotemporal dementia phenotypes

scientific article

Serotonergic candidate genes and puerperal psychosis: an association study.

scientific article published in October 2007

The challenge of detecting epistasis (G x G interactions): Genetic Analysis Workshop 16

scientific article published on January 2009

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