Anuranjan Anand

Bengaluru, KA, India

Last Updated: 09/26/2026

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Found 13 publications

Clinico-genetic Analysis of Adenosine Signaling Pathway in Drug-Resistant Epilepsy.

Clinico-genetic Analysis of Adenosine Signaling Pathway in Drug-Resistant Epilepsy.

Journal: Annals of Indian Academy of Neurology
Published: May 04, 2024

Exome sequencing and functional analyses revealed CETN1 variants leads to impaired cell division and male fertility.

Exome sequencing and functional analyses revealed CETN1 variants leads to impaired cell division and male fertility.

Journal: Human molecular genetics
Published: June 06, 2022

Novel NR5A1 Pathogenic Variants Cause Phenotypic Heterogeneity in 46,XY Disorders of Sex Development.

Novel NR5A1 Pathogenic Variants Cause Phenotypic Heterogeneity in 46,XY Disorders of Sex Development.

Journal: Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation
Published: December 09, 2019

A linkage and exome study implicates rare variants of KANK4 and CAP2 in bipolar disorder in a multiplex family.

A linkage and exome study implicates rare variants of KANK4 and CAP2 in bipolar disorder in a multiplex family.

Journal: Bipolar disorders
Published: August 11, 2019

A genetic locus for sensory epilepsy precipitated by contact with hot water maps to chromosome 9p24.3-p23.

A genetic locus for sensory epilepsy precipitated by contact with hot water maps to chromosome 9p24.3-p23.

Journal: Journal of genetics
Published: June 23, 2018

Mutations in OTOF, CLDN14 & SLC26A4 genes as major causes of hearing impairment in Dhadkai village, Jammu & Kashmir, India.

Mutations in OTOF, CLDN14 & SLC26A4 genes as major causes of hearing impairment in Dhadkai village, Jammu & Kashmir, India.

Journal: The Indian journal of medical research
Published: February 13, 2018

Identification of a novel homozygous mutation in transmembrane channel like 1 (TMC1) gene, one of the second-tier hearing loss genes after GJB2 in India.

Identification of a novel homozygous mutation in transmembrane channel like 1 (TMC1) gene, one of the second-tier hearing loss genes after GJB2 in India.

Journal: The Indian journal of medical research
Published: September 02, 2017

Rare SLC1A1 variants in hot water epilepsy.

Rare SLC1A1 variants in hot water epilepsy.

Journal: Human genetics
Published: December 28, 2016

Microtubule-associated defects caused by EFHC1 mutations in juvenile myoclonic epilepsy.

Microtubule-associated defects caused by EFHC1 mutations in juvenile myoclonic epilepsy.

Journal: Human mutation
Published: November 22, 2016

Functional Analysis of a Novel Connexin30 Mutation in a Large Family with Hearing Loss, Pesplanus, Ichthyosis, Cutaneous Nodules, and Keratoderma.

Functional Analysis of a Novel Connexin30 Mutation in a Large Family with Hearing Loss, Pesplanus, Ichthyosis, Cutaneous Nodules, and Keratoderma.

Journal: Annals of human genetics
Published: December 24, 2014

Non-syndromic hearing impairment in India: high allelic heterogeneity among mutations in TMPRSS3, TMC1, USHIC, CDH23 and TMIE.

Non-syndromic hearing impairment in India: high allelic heterogeneity among mutations in TMPRSS3, TMC1, USHIC, CDH23 and TMIE.

Journal: PloS one
Published: June 22, 2013

Sex determining signal in Drosophila melanogaster.

Sex determining signal in Drosophila melanogaster.

Journal: Journal of genetics
Published: November 13, 2004
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Last Updated: 09/26/2026