| Issue Date | Title | Author(s) |
| 2014 | Connecting the paralogs: contribution of EFHC1 and EFHC2 in juvenile myoclonic epilepsy | Anand, Anuranjan; Pedabaliyarasimhuni, P K Raju |
| 2021 | Dissecting the molecular genetic basis of juvenile myoclonic epilepsy | Anand, Anuranjan; Barak, Pooja |
| 2016 | Functional Analysis of a Novel Connexin30 Mutation in a Large Family with Hearing Loss, Pesplanus, Ichthyosis, Cutaneous Nodules, and Keratoderma | Pandey, Nishtha; Xavier, Dennis F.; Chatterjee, Arunima; Mani, Ram-Shankar; Hiremagalore, Ravi; Tharakan, Ajith; Rajashekhar, B.; Anand, Anuranjan |
| 2013-12-02 | Genetic analysis of the 5q34 locus for juvenile myoclonic epilepsy | Anand, Anuranjan; Jaishankar, Shveta |
| 2022-02 | Genetic and cellular analysis of genes and variants for juvenile myoclonic epilepsy | Anand, Anuranjan; Joshi, Shrilaxmi V. |
| 2015 | Identification of genetic loci and mutations in SLC1A1 for a sensory epilepsy triggered by touch and temperature stimuli | Anand, Anuranjan; Karan, Kalpita Rashmi |
| 2009 | Identification of genetic loci for human epilepsies | Anand, Anuranjan; Ratnapriya, R. |
| 2006 | Molecular genetic aspects of non-syndromic hearing loss in India | Anand, Anuranjan; Ram Shankar, M. |
| 2014 | Non-Syndromic Hearing Impairment in India: High Allelic Heterogeneity among Mutations in TMPRSS3, TMC1, USHIC, CDH23 and TMIE | Ganapathy, Aparna; Pandey, Nishtha; Srisailapathy, C. R. Srikumari; Jalvi, Rajeev; Malhotra, Vikas; Venkatappa, Mohan; Chatterjee, Arunima; Sharma, Meenakshi; Santhanam, Rekha; Chadha, Shelly; Ramesh, Arabandi; Agarwal, Arun K.; Rangasayee, Raghunath R.; Anand, Anuranjan |
| 2018 | On genetic aspects of hot water epilepsy, a sensory epilepsy triggered by touch and temperature stimuli | Anand, Anuranjan; Choudhury, Shalini Roy |
| 2014-12-02; 2012 | On genetic aspects of non-syndromic hearing loss | Anand, Anuranjan; Pandey, Nishtha |
| 2021 | On molecular genetic analysis of juvenile myoclonic epilepsy | Anand, Anuranjan; Jaishankar, Shveta |
| 2014 | Prospective causal genes for genetic generalized epilepsy | Anand, Anuranjan; Kaur, Manpreet |
| 2014 | A search for novel genes for juvenile myoclonic epilepsy | Anand, Anuranjan; Barak, Pooja |
| 2006 | Studies on molecular genetic aspects of idiopathic generalized epilepsies | Anand, Anuranjan; Kapoor, Ashish |
| 2009 | Studies on molecular genetic aspects of nonsyndromic hereditary hearing loss | Anand, Anuranjan; G., Aparna |
| 2014 | Towards identifying a potentially causal gene for hot water epilepsy | Anand, Anuranjan; Abdullah, Mariyam |
| 2021 | Towards understanding molecular and cellular attributes of potential genes for hot water epilepsy | Anand, Anuranjan; Puri, Sambhavi |
