Mutations in OTOF, CLDN14 & SLC26A4 genes as major causes of hearing impairment in Dhadkai village, Jammu & Kashmir, India von Pandey, Nishtha, Rashid, Tabassum, Jalvi, Rajeev, Sharma, Meenakshi, Rangasayee, Raghunath, Andrabi, Khurshid, Anand, Anuranjan

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A linkage and exome study implicates rare variants of KANK4 and CAP2 in bipolar disorder in a multiplex family von Anjanappa, Ram M., Nayak, Sourav, Moily, Nagaraj S., Manduva, Vallikiran, Nadella, Ravi K., Viswanath, Biju, Reddy, Yemmiganur C. J., Jain, Sanjeev, Anand, Anuranjan

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A genetic locus for sensory epilepsy precipitated by contact with hot water maps to chromosome 9p24.3-p23 von Karan, Kalpita R., Satishchandra, Parthasarthy, Sinha, Sanjib, Anand, Anuranjan

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

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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 von Singh, Pawan Kumar, Ghosh, Manju, Sharma, Shipra, Shastri, Shivaram, Gupta, Neerja, Chowdhury, Madhumita Roy, Anand, Anuranjan, Kabra, Madhulika

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An idiopathic epilepsy syndrome linked to 3q13.3-q21 and missense mutations in the extracellular calcium sensing receptor gene von Kapoor, Ashish, Satishchandra, Parthasarathy, Ratnapriya, Rinki, Reddy, Ramesh, Kadandale, Jayaram, Shankar, Susarla K., Anand, Anuranjan

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A Multicenter Study of BRD2 as a Risk Factor for Juvenile Myoclonic Epilepsy von Cavalleri, Gianpiero L., Walley, Nicole M., Soranzo, Nicole, Mulley, John, Doherty, Colin P., Kapoor, Ashish, Depondt, Chantal, Lynch, John M., Scheffer, Ingrid E., Heils, Armin, Gehrmann, Anne, Kinirons, Peter, Gandhi, Sonia, Satishchandra, Parthasarathy, Wood, Nicholas W., Anand, Anuranjan, Sander, Thomas, Berkovic, Samuel F., Delanty, Norman, Goldstein, David B., Sisodiya, Sanjay M.

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Control of Male Sexual Behavior and Sexual Orientation in Drosophila by the fruitless Gene von Ryner, Lisa C, Goodwin, Stephen F, Castrillon, Diego H, Anand, Anuranjan, Villella, Adriana, Baker, Bruce S, Hall, Jeffrey C, Taylor, Barbara J, Wasserman, Steven A

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A novel genetic locus for juvenile myoclonic epilepsy at chromosome 5q12-q14 von KAPOOR, Ashish, RATNAPRIYA, R, KURUTTUKULAM, Gigy, ANAND, Anuranjan

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Molecular Genetic Dissection of the Sex-Specific and Vital Functions of the Drosophila melanogaster Sex Determination Gene fruitless von Anand, Anuranjan, Villella, Adriana, Ryner, Lisa C, Carlo, Troy, Goodwin, Stephen F, Song, Ho-Juhn, Gailey, Donald A, Morales, Ana, Hall, Jeffrey C, Baker, Bruce S, Taylor, Barbara J

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Sex determining signal inDrosophila melanogaster von Anand, Anuranjan

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Exome sequencing and functional analyses revealed CETN1 variants leads to impaired cell division and male fertility von Sudhakar, Digumarthi V S, Phanindranath, Regur, Jaishankar, Shveta, Ramani, Anand, Kalamkar, Kaustubh P, Kumar, Umesh, Pawar, Asmita D, Dada, Rima, Singh, Rajender, Gupta, Nalini J, Deenadayal, Mamata, Tolani, Aarti Deenadayal, Sharma, Yogendra, Anand, Anuranjan, Gopalakrishnan, Jay, Thangaraj, Kumarasamy

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Rare SLC1A1 variants in hot water epilepsy von Karan, Kalpita Rashimi, Satishchandra, P., Sinha, Sanjib, Anand, Anuranjan

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Microtubule‐associated defects caused by EFHC1 mutations in juvenile myoclonic epilepsy von Raju, Praveen K, Satishchandra, Parthasarathy, Nayak, Sourav, Iyer, Vishwanathan, Sinha, Sanjib, Anand, Anuranjan

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Microtubule-associated defects caused by EFHC1 mutations in juvenile myoclonic epilepsy: RAJU et al von Raju, Praveen K, Satishchandra, Parthasarathy, Nayak, Sourav, Iyer, Vishwanathan, Sinha, Sanjib, Anand, Anuranjan

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Familial autosomal dominant reflex epilepsy triggered by hot water maps to 4q24-q28 von Ratnapriya, Rinki, Satishchandra, Parthasarthy, Dilip, S, Gadre, Girish, Anand, Anuranjan

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Novel NR5A1 Pathogenic Variants Cause Phenotypic Heterogeneity in 46,XY Disorders of Sex Development von Sudhakar, Digumarthi V.S., Jaishankar, Shveta, Regur, Phanindranath, Kumar, Umesh, Singh, Raghvendra, Kabilan, Usha, Namduri, Sree, Dhyani, Jaishree, Gupta, Nalini J., Chakravarthy, Baidyanath, Vaman, Khadilkar, Shabir, Iram, Khadgawat, Rajesh, Deenadayal, Mamata, Chaitanya A, Datar, Dada, Rima, Sharma, Yogendra, Anand, Anuranjan, Thangaraj, Kumarasamy

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Functional Analysis of a Novel Connexin30 Mutation in a Large Family with Hearing Loss, Pesplanus, Ichthyosis, Cutaneous Nodules, and Keratoderma: Cx30 Mutation for Syndromic Heari... von Pandey, Nishtha, Xavier, Dennis F., Chatterjee, Arunima, Mani, Ram-Shankar, Hiremagalore, Ravi, Tharakan, Ajith, Rajashekhar, B., Anand, Anuranjan

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Functional consequences of novel connexin 26 mutations associated with hereditary hearing loss von RAM SHANKAR MANI, GANAPATHY, Aparna, JALVI, Rajeev, SRIKUMARI SRISAILAPATHY, C. R, MALHOTRA, Vikas, CHADHA, Shelly, AGARWAL, Arun, RAMESH, Arabandi, RAGHUNATH RAO RANGASAYEE, ANAND, Anuranjan

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locus for autosomal dominant reflex epilepsy precipitated by hot water maps at chromosome 10q21.3-q22.3 von Ratnapriya, Rinki, Satishchandra, Parthasarthy, Kumar, S. Dilip, Gadre, Girish, Reddy, Ramesh, Anand, Anuranjan

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