Browse by Fellow

Anjanappa, Ram M. ; Nayak, Sourav ; Moily, Nagaraj S. ; Manduva, Vallikiran ; Nadella, Ravi K. ; Viswanath, Biju ; Reddy, Yemmiganur C. J. ; Jain, Sanjeev ; Anand, Anuranjan (2020) A linkage and exome study implicates rare variants of KANK4 and CAP2 in bipolar disorder in a multiplex family Bipolar Disorders, 22 (1). pp. 70-78. ISSN 1398-5647

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 (2019) Novel NR5A1 Pathogenic Variants Cause Phenotypic Heterogeneity in 46,XY Disorders of Sex Development Sexual Development, 13 (4). pp. 178-186. ISSN 1661-5425

Karan, Kalpita R. ; Satishchandra, Parthasarthy ; Sinha, Sanjib ; Anand, Anuranjan (2018) A genetic locus for sensory epilepsy precipitated by contact with hot water maps to chromosome 9p24.3-p23 Journal of Genetics, 97 (2). pp. 391-398. ISSN 0022-1333

Raju, Praveen K ; Satishchandra, Parthasarathy ; Nayak, Sourav ; Iyer, Vishwanathan ; Sinha, Sanjib ; Anand, Anuranjan (2017) Microtubule-associated defects caused by EFHC1 mutations in juvenile myoclonic epilepsy Human Mutation, 38 (7). pp. 816-826. ISSN 10597794

Karan, Kalpita Rashimi ; Satishchandra, P. ; Sinha, Sanjib ; Anand, Anuranjan (2017) Rare SLC1A1 variants in hot water epilepsy Human Genetics, 136 (6). pp. 693-703. ISSN 0340-6717

Pandey, Nishtha ; Xavier, Dennis F. ; Chatterjee, Arunima ; Mani, Ram-Shankar ; Hiremagalore, Ravi ; Tharakan, Ajith ; Rajashekhar, B. ; Anand, Anuranjan (2015) Functional Analysis of a Novel Connexin30 Mutation in a Large Family with Hearing Loss, Pesplanus, Ichthyosis, Cutaneous Nodules, and Keratoderma Annals of Human Genetics, 80 (1). pp. 11-19. ISSN 00034800

Hoheisel, Jörg D. ; 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 (2014) Non-Syndromic Hearing Impairment in India: High Allelic Heterogeneity among Mutations in TMPRSS3, TMC1, USHIC, CDH23 and TMIE PLoS ONE, 9 (1). e84773. ISSN 1932-6203

Ratnapriya, Rinki ; Vijai, Joseph ; Kadandale, Jayaram S. ; Iyer, Rajesh S. ; Radhakrishnan, Kurupath ; Anand, Anuranjan (2010) A locus for juvenile myoclonic epilepsy maps to 2q33–q36 Human Genetics, 128 (2). pp. 123-130. ISSN 0340-6717

Ratnapriya, Rinki ; Satishchandra, Parthasarthy ; Dilip, S. ; Gadre, Girish ; Anand, Anuranjan (2009) Familial autosomal dominant reflex epilepsy triggered by hot water maps to 4q24-q28 Human Genetics, 126 (5). pp. 677-683. ISSN 0340-6717

Mani, Ram Shankar ; Ganapathy, Aparna ; Jalvi, Rajeev ; Srikumari Srisailapathy, C. R. ; Malhotra, Vikas ; Chadha, Shelly ; Agarwal, Arun ; Ramesh, Arabandi ; Rangasayee, Raghunath Rao ; Anand, Anuranjan (2009) Functional consequences of novel connexin 26 mutations associated with hereditary hearing loss European Journal of Human Genetics, 17 (4). pp. 502-509. ISSN 1018-4813

Ratnapriya, Rinki ; Satishchandra, Parthasarthy ; Dilip Kumar, S. ; Gadre, Girish ; Reddy, Ramesh ; Anand, Anuranjan (2009) A locus for autosomal dominant reflex epilepsy precipitated by hot water maps at chromosome 10q21.3-q22.3 Human Genetics, 125 (5-6). pp. 541-549. ISSN 0340-6717

Chatterjee, Arunima ; Jalvi, Rajeev ; Pandey, Nishtha ; Rangasayee, R. ; Anand, Anuranjan (2009) A novel locus DFNA59 for autosomal dominant nonsyndromic hearing loss maps at chromosome 11p14.2-q12.3 Human Genetics, 124 (6). pp. 669-675. ISSN 0340-6717

Kapoor, Ashish ; Satishchandra, Parthasarathy ; Ratnapriya, Rinki ; Reddy, Ramesh ; Kadandale, Jayaram ; Shankar, Susarla K. ; Anand, Anuranjan (2008) An idiopathic epilepsy syndrome linked to 3q13.3-q21 and missense mutations in the extracellular calcium sensing receptor gene Annals of Neurology, 64 (2). 158–167. ISSN 0364-5134

Shekhawat, Giriraj Singh ; Ramshankar, M. ; Jalvi, Rajeev R. ; Rangasayee, R. ; Anand, Anuranjan (2007) Implications in disclosing auditory genetic mutation to a family: a case study International Journal of Audiology, 46 (7). pp. 384-387. ISSN 1499-2027

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. (2007) A multicenter study of BRD2 as a risk factor for juvenile myoclonic epilepsy Epilepsia, 48 (4). pp. 706-712. ISSN 0013-9580

Kapoor, Ashish ; Ratnapriya, R. ; Kuruttukulam, Gigy ; Anand, Anuranjan (2007) A novel genetic locus for juvenile myoclonic epilepsy at chromosome 5q12-q14 Human Genetics, 121 (6). pp. 655-662. ISSN 0340-6717

Madegowda, R. H. ; Kishore, A. ; Anand, A. (2005) Mutational screening of the Parkin gene among South Indians with early onset Parkinson's disease Journal of Neurology, Neurosurgery & Psychiatry, 76 (11). pp. 1588-1590. ISSN 0022-3050

Vijai, J. ; Cherian, P. J. ; Sylaja, P. N. ; Anand, A. ; Radhakrishnan, K. (2003) Clinical characteristics of a South Indian cohort of juvenile myoclonic epilepsy probands Seizure, 12 (7). pp. 490-496. ISSN 1059-1311

RamShankar, M. ; Girirajan, S. ; Dagan, O. ; Ravi Shankar, H. M. ; Jalvi, R. ; Rangasayee, R. ; Avraham, K. B. ; Anand, A. (2003) Contribution of connexin26 (GJB2) mutations and founder effect to non-syndromic hearing loss in India Journal of Medical Genetics, 40 (5). e68_1-e68_6. ISSN 0022-2593

Vijai, J. ; Kapoor, A. ; Ravishankar, H. M. ; Cherian, P. J. ; Girija, A. S. ; Rajendran, B. ; Rangan, G. ; Jayalakshmi, S. ; Mohandas, S. ; Radhakrishnan, K. (2003) Genetic association analysis of KCNQ3 and juvenile myoclonic epilepsy in a South Indian population Human Genetics, 113 (5). pp. 461-463. ISSN 0340-6717

Mukherjee, O. ; Saleem, Q. ; Purushottam, M. ; Anand, A. ; Brahmachari, S. K. ; Jain, S. (2002) Common psychiatric diseases and human genetic variation Community Genetics, 5 (3). pp. 171-177. ISSN 1422-2795

Murgod, Uday A. ; Saleem, Quasar ; Anand, A. ; Brahmachari, S. K. ; Jain, Sanjeev ; Muthane, Uday B. (2001) A clinical study of patients with genetically confirmed Huntington's disease from India Journal of the Neurological Sciences, 190 (1-2). pp. 73-78. ISSN 0022-510X

Shaikh, Kauser J. ; Naveen, Daniel ; Sherrin, Tessi ; Murthy, Ashlesh ; Thennarasu, K. ; Anand, Anuranjan ; Benegal, Vivek ; Jain, Sanjeev (2001) Polymorphisms at the DRD2 locus in early-onset alcohol dependence in the Indian population Addiction Biology, 6 (4). 331–335. ISSN 1355-6215

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. (2001) Molecular genetic dissection of the sex-specific and vital functions of the Drosophila melanogaster sex determination gene fruitless Genetics, 158 (4). pp. 1569-1595. ISSN 0016-6731

Saleem, Quasar ; Anand, Anuranjan ; Jain, Sanjeev ; Brahmachari, Samir K. (2001) The polyglutamine motif is highly conserved at the Clock locus in various organisms and is not polymorphic in humans Human Genetics, 109 (2). pp. 136-142. ISSN 0340-6717

Saleem, Quasar ; Sreevidya, V. S. ; Sudhir, J. ; Vijaya Savithri, J. ; Gowda, Y. ; Rao, Chandrika B. ; Benegal, V. ; Majumder, Partha P. ; Anand, Anuranjan ; Brahmachari, Samir K. ; Jain, Sanjeev (2000) Association analysis of CAG repeats at the KCNN3 locus in Indian patients with bipolar disorder and schizophrenia American Journal of Medical Genetics, 96 (6). pp. 744-748. ISSN 0148-7299

Anand, Anuranjan ; Dasgupta, Aindrilla ; Sudha, S. ; Raghavan, S. ; Sharat Chandra, H. (1998) A search for additional X-linked genes affecting sex determination in Drosophila melanogaster Journal of Genetics, 77 (1). pp. 27-36. ISSN 0022-1333

Anand, Anuranjan ; Sharat Chandra, H. (1994) Synergistic interaction between particular X-chromosome deletions and Sex-lethal causes female lethality in Drosophila melanogaster Journal of Genetics, 73 (2-3). pp. 81-90. ISSN 0022-1333