Publications by Centre's Scientists

1.Perumal G, Kulshrestha PS, Prabu P, Tarigopula A, Kadandale JS, Samuel CR;Analysis of complex chromosomal abnormalities in a case of multiple myeloma using spectral karyotyping.Asian J Pharm Clin Res (AJPCR). 2018; 11(9):9-11
2.Zahavi A, Harris KD and Nanjundiah V.An individuallevel selection model for the apparent altruism exhibited by cellular slime moulds.J Biosci. 2018; 43(1): 49-58.
3.Linda B, Sumathy A, Indumathi M, Shetty S, Kandandale J, Kar B;Localization of the SRY gene on chromosome 3 in a patient with azoospermia having a complex karyotype 45,X/46,X,i(Y)(q10)/46,XX/ 47,XX,i(Y)(q10).Cytogenet Genome Res. 2018;156(3):134-139. doi: 10.1159/000494464
4.Sathe V and Nanjundiah V;Complex interactions underpin social behaviour in Dictyostelium giganteum.Behavioral Ecology and Sociobiology. 2018; 72(10):167.doi: 10.1007/s00265-018-2572-9
5.Rao V and Nanjundiah V;Haldane's view of natural selection.J Genet. 2017; 96(5): 965-972.
6.Nakatsuka N, Moorjani P, Rai N, Sarkar B, Tandon A, Patterson N, Bhavani GS, Girisha KM, Mustak MS, Srinivasan S et al;The promise of discovering population-specific disease-associated genes in South Asia.Nat Genet. 49(9):1403-1407, 2017 [IF: 27.95]
7.Han X, Ranganathan P, Tzimas C, Weaver KL, Jin K, Astudillo L, Zhou W, Zhu X, Li B, Robbins DJ et al;Notch represses transcription by PRC2 recruitment to the ternary complex.Mol Cancer Res. 15 (9), 1173-1183, 2017. [IF:4.51]
8.Muthusamy B, Selvan LDN, Nguyen TT, Manoj J, Stawiski EW, Jaiswal BS, Wang W, Raja R, Ramprasad VL, Gupta R, Murugan S, Kadandale JS et al;Next-generation sequencing reveals novel mutations in Xlinked intellectual disability.OMICS. 21(5):295-303,2017 [IF:2.273]
9.Kantheti P, Kubba A, Prabhu A, Batrani M, Hiremagalore R;Two novel mutations in KIND1 in Indian patients with Kindler syndrome.Clin Exp Dermatol. 42(1):95-97, 2017 [IF:1.315]
10.Sanjeeva GN, Maganthi M, Kodishala H, Marol RKR, Kulshreshtha PS, Lorenzetto E, Kadandale JS, Hladnik U, Raghupathy P, Bhat M;Clinical and molecular characterization of Prader-Willi syndrome.Indian J Pediatr 2017. [IF:0.808]
11.Pandey N, Xavier DF, Chatterjee A, Mani RS, Hiremagalore R, Tharakan A, Rajashekhar B, Anand A;Functional analysis of a novel Connexin30 mutation in a large family with hearing loss, pesplanus, ichthyosis, cutaneous nodules, and keratoderma.Ann Hum Genet. 80(1):11-19,2016 [IF:1.889]
12.Ranganath P, Matta D, Bhavani GS, Wangnekar S, Jain JM, Verma IC, Kabra M, Puri RD, Danda S, Gupta N , Girisha KM, Sankar VH, Patil SJ, Ramadevi AR, Bhat M et al;Spectrum of SMPD1 mutations in Asian- Indian patients with acid sphingomyelinase (ASM)-deficient Niemann-Pick disease.Am J Med Genet A. 170(10):2719-2730, 2016 [IF:1.163]
13.Rao V, Nanjundiah V;Ernst Mayr's interactions with JBS Haldane.Hist Philos Life Sci. 38(1):138-150, 2016 [IF:0.349]
14.Shetty M, Kadandale J, Hegde S;Pre- and postnatal analysis of chromosome 15q26.1 and 8p23.1 deletions in congenital diaphragmatic hernia.Mol Syndromol. 6(5):248-253, 2016[IF: 2.03]
15.Shetty M, Srikanth A, Kadandale J, Hegde S;Pre- and postnatal diagnosis of 10p14 deletion and 22q11.2 deletion syndrome and significance of non-cardiac markers.Cytogenet Genome Res. 148(4):249-255, 2016[IF:1.354]
16.Shetty M, Srikanth A, Kulshreshtha P, Kadandale J, Hegde S;Pre- and postnatal diagnosis of 5q35.1 and 8p23.1 deletion in congenital heart disease.Indian J Pediatr. 83(12-13):1484-1485,2016[IF:0.945]
17.Sivasankaran A, Srikanth A, Kulshreshtha PS, Anuradha D, Kadandale JS, Samuel CR;Split hand/foot malformation associated with 7q21.3 microdeletion:A case report.Mol Syndromol.6(6):287-296,2016[IF: 2.03]
18.Uttarilli A, Ranganath P, Matta D, Md Nurul Jain J, Prasad K, Babu AS, Girisha KM, Verma IC, Phadke SR, Mandal, Puri RD, Aggarwal S, Danda S, Sankar VH, Kapoor S, Bhat M K et al;Identification and characterization of 20 novel pathogenic variants in 60 unrelated Indian patients with mucopolysaccharidoses type I and type II.Clin Genet.90(6):496-508, 2016 [IF:3.892]
19.Sanyal D, Bhairi V, Kadandale JS;Practice of consanguinity and unusual cases of inherited familial chromosome abnormalities.Int J Mol Cell Med. 5(1): 57-63, 2016[IF: 2.77]
20.Nanjundiah V and Morange M;Aging, sex ratio, and genomic imprinting: functional and evolutionary explanations in biology.Biol. Theory. 10, 125-133, 2015[IF:1.02]
21.Ragunatha S, Ramesh M, Anupama P, Kapoor M, Bhat M;Papillon-Lefvre syndrome with homozygous nonsense mutation of cathepsin C gene presenting with late-onset periodontitis.Pediatr Dermatol. 32(2):292-4, 2015 [IF:1.163]
22.Sanyal Debarshi and Kadandale JS;Clinical and haematological evidence of a rare case of polycythemia vera by conventional cytogenetics.Journal of Rare Disorders. 38-41, 3(2), 2015[IF: 3.507]
23.Vogel D, Nicolis SC, Perez-Escudero A, Nanjundiah V, Sumpter DJ, Dussutour A;Phenotypic variability in unicellular organisms: from calcium signalling to social behaviour.Proc Biol Sci . 282(1819), 2015 [IF:4.823]
24.Shetty M, Srikanth A, Kadandale J, Hegde S;Pre- and postnatal analysis of chromosome 1q44 deletion in agenesis of corpus callosum.Mol Syndromol. 6(4):187-192, 2015[IF: 2.03]
25.Mathew J, Jagadeesh SM, Bhat M, Udhaya Kumar S, Thiyagarajan S, Srinivasan S;Mutations in ARSB in MPS VI patients in India.Mol Genet Metab Rep. 4:53-61,2015[IF: 3.769]
26.Hiremagalore R, Kubba A, Bansel S, Jerajani H;Immunofluorescence mapping in inherited epidermolysis bullosa: a study of 86 cases from India.Br J Dermatol. 172(2):384-391, 2015 [IF:4.317]
27.Dwarakanathan A, Bhat M, Gn S, Shetty S;Missense and deletion mutations in GJA1 causing oculodentodigital dysplasia in two Indian families.Clin Dysmorphol.24(4):159- 162, 2015 [IF:0.518]
28.Bhavani GS, Shah H, Dalal AB, Shukla A, Danda S, Aggarwal S, Phadke SR, Gupta N, Kabra M, Gowrishankar K et al;Novel and recurrent mutations in WISP3 and an atypical phenotype.Am J Med Genet A. 167A(10):2481-2484, 2015 [IF:2.082]
29.Bhat, M;Social and cultural issues in genetic counselling.J Biosci. 40(2):217-220, 2015 [IF:1.419]
30.Bashyam MD, Chaudhary AK, Kiran M, Nagarajaram HA, Devi RR, Ranganath P, Dalal A, Bashyam L, Gupta N, Kabra M et al;Splice, insertion-deletion and nonsense mutations that perturb the phenylalanine hydroxylase transcript cause phenylketonuria in India.J Cell Biochem. 115(3):566-574, 2014 [IF:3.446]
31.Rajasimha HK, Shirol PB, Ramamoorthy P, Hegde M, Barde S, Chandru V, Ravinandan ME, Ramchandran R, Haldar K, Lin JC et al;Organization for rare diseases India (ORDI) - addressing the challenges and opportunities for the Indian rare diseases' community.Genet Res (Camb).96:e009,2014 [IF:0.743]
32.Bhat, M;Anomalies of Nipple.Perinatology. 15 (1), 2014
33.Nanjundiah V, Newman SA;Introducton: e pluribus unum.J Biosci. 39(2): 171-176, 2014 [IF:1.419]
34.Dimopoulou A, Fischer B, Gardeitchik T, Schroter P, Kayserili H, Schlack C, Li Y, Brum JM, Barisic I, Castori M et al;Genotypephenotype spectrum of PYCR1-related autosomal recessive cutis laxa.Mol Genet Metab.110(3):352-361, 2013 [IF:3.093]
35.Makrythanasis P, van Bon BW, Steehouwer M, Rodriguez-Santiago B, Simpson M, Dias P, Anderlid BM, Arts P, Bhat M, Augello B et al;MLL2 mutation detection in 86 patients with Kabuki syndrome: a genotype-phenotype study.Clin Genet. 84(6):539-545,2013 [IF:3.892]
36.Raj SM, Halebeedu P, Kadandale JS, Mirazon Lahr M, Gallego Romero I, Yadhav JR, Iliescu M, Rai N, Crivellaro F, Chaubey G et al;Variation at diabetes- and obesity-associated loci may mirror neutral patterns of human population diversity and diabetes prevalence in India.Ann Hum Genet. 77(5):392-408, 2013 [IF:1.889]
37.Bhat M;Ear anomalies in dysmorphic syndromes.Perinatology. 13(4): 149-152, 2013
38.Pandey N, Sharma M, Rashid T, Jalvi R, Andrabi R, Rangasayee R, Anand A;Mutations in OTOF, CLDN14 and SLC26A4 are a major cause of hearing impairment in Dhadhaki village, Jammu and Kashmir, India.Indian Journal of Medical Research. 146(4): 489-497, [IF: 1.446] (2017)
39.Nanjundiah V;Introduction to Obaid Siddiqi Memoirs.Indian National Science Academy, New Delhi (2016)
40.Chandra HS;The Principle of Respect for Human Vulnerability and Personal Integrity.Report of the International Bioethics Committee, UNESCO (2013)
41.Chandra HS;On Social Responsibility and Health.Report of the International Bioethics Committee, UNESCO (2013)
42.Human Diversity and Ancestry in India.Eds. Majumder PP and Nanjundiah V, Special Issue, Journal of Biosciences, Vol. 44, July 2019
43.Nanjundiah V;The Origin of Species after 150 years - One Hundred and Fifty years Without Darwin Are Enough.Page 15-33. From so simple a beginning.. The Expansion of Evolutionary Thought, Indian Academy of Sciences, 2019; Ed. TNC Vidya

BOOKS, CHAPTERS, MONOGRAPHS

1.Nanjundiah V, Ruiz-Trillo I and Kirk D; (2017).Protists and multiple routes to the evolution of multicellularity.History of Evolutionary Cell Biology, Eds: B Hall and S Moody, CRC Press.
2.Bhat M; (2017)Genetic counseling after diagnosis of fetal congenital heart disease.Fetal Echocardiography, pp.181-189. Eds: Sejal Shah, Sunita Maheshwari, PV Suresh, Jaypee Brothers Medical Publishers (P) Ltd.
3.Srinivasan S, Berg JN, Marchuk DA; (2016)ENG, ACVRL1, SMAD4 and hereditary haemorrhagic telangiectasia (Osler-Weber- Rendu syndrome).Epstein's Inborn Errors of Development: the Molecular Basis of Clinical Disorders of Morphogenesis; Erickson RP and Wynshaw-Boris A, Eds. 3rd edition, pp: 393- 400, Oxford University Press. 4.Nanjundiah V;Foreword,Biochemical Evolution: The pursuit of Perfection' by A. Cornish Bowden. 2nd Edition, Garland Science. 2016. 5.Nanjundiah V;Cellular slime mold development as a paradigm for the transition from unicellular to multicellular life.Multicellularity: Origins and Evolution. 2016: 105-128. 6.Hiremagalore R;Epidermolysis Bullosa.IADVL Textbook of Dermatology, Chapter 26, 2015 7.Hiremagalore R, Lokre S, Bishnoi P;Papulosquamous disorders in children.Textbook of Pediatrics for Postgraduates, Section 48, chapter 48.14, 2015 8.Bhat M;An approach to the diagnosis of skeletal dysplasia.Genetics in Clinical Practice: symptoms, diagnosis & therapy. pp.25- 36. Ed: Jayesh and Freny Sheth, Jaypee Brothers Medical Publishers (P) Ltd, (2014) 9.Kadandale J, Shetty S and Pooja K;Cytogenetics and Molecular Genetics of male infertility.Text book of Infertility. Jaypee Brothers Medical Publishers, India (2013) 10.Bhat M;The practice of genetic counseling in India.Genomics and Health in the Developing World, Ed. Dhavendra Kumar, Cardiff University School of Medicine, UK, Oxford Monographs in Medical Genetics, Oxford University Press, New York (2012)