Department of Biotechnology
inStem (Institute for Stem Cell Science and Regenerative Medicine)

Exome sequencing in families with severe mental illness identifies novel and rare variants in genes implicated in Mendelian neuropsychiatric syndromes.

Publication Type

Journal Article

Date of Publication

January 1, 2019

Journal

Psychiatry and clinical neurosciences

Volume/Issue

73/1

ISSN

1440-1819

Severe mental illnesses (SMI), such as bipolar disorder and schizophrenia, are highly heritable, and have a complex pattern of inheritance. Genome-wide association studies detect a part of the heritability, which can be attributed to common genetic variation. Examination of rare variants with next-generation sequencing may add to the understanding of the genetic architecture of SMI.

Alternate Journal

Psychiatry Clin Neurosci

PubMed ID

30367527

PubMed Central ID

PMC7380025

Authors

Suhas Ganesh
Husayn Ahmed P
Ravi K Nadella
Ravi P More
Manasa Seshadri
Biju Viswanath
Mahendra Rao
Sanjeev Jain
Odity Mukherjee

Keywords

Humans
Exome
Bipolar Disorder
Schizophrenia
Genetic Predisposition to Disease
Phenotype
Genetic Variation
Genome-Wide Association Study
Pedigree
Female
Male