| 1. |
The Missing Heritability Puzzle of Schizophrenia: Hypothesis and Plausible Sources. Kiran Kumar HalagurBhogegowda, Rama Thyloor,MukundaSuryanarayana, SajeedaNiketh.Indian Journal of Genetics and Molecular Research.Volume 13. Number 1, January - June 2024. |
2024 |
| 2. |
Bioinformatics analysis of 5HT2C gene Cys23ser polymorphism and Epigenetics insights into the HTR2C receptor gene regulation: implications for physiological roles in brain.Kiran Kumar HalagurBhogegowda,Sajeedaniketh, Sowmyashreebs.(Journal of Advances in Biology & BiotechnologyVolume 27, Issue 8, Page 185-210, 2024) |
2024 |
| 3. |
Mating receptivity peptides in Helicoverpaarmigera: Molecular and evolutionary perspectives.RamaThyloor , Kiran Kumar HalagurBhogegowda,SaraswathiSaraswathi, DoddamaneManjulakumari. (Journal of Advances in Biology & Biotechnology Volume 27, Issue 8, Page 185-210, 2024) |
2024 |
| 4. |
Characterization of seminal fluid peptides of male Helicoverpaarmigeraand their plausiblerole in post-copulatory modulation of female reproductive behavoiur Rama Thyloor, Kiran Kumar HalagurBhogegowda, DoddamaneManjulakumari. (Under review Indian journal of entomology ) |
2024 |
| 5. |
Insights into the role of cis-regulatory elements of 5-HT2A gene in gene expression and regulation: an in silico approach. Kiran Kumar HalagurBhogegowda,SajeedaNiketh, Rama Thyloor,Rajeev R Kolgi(Journal of Biotechnology 2024, 15: 1-14). |
2024 |
| 6. |
A plausible role of 5HT2A gene SNPs on chromatin and 5’UTR related genomic architecture: insights from Bioinformatics methods.Sajeedaniketh,Kiran Kumar HalagurBhogegowda,,Sowmyashreebs. Rajeev kolgi.(Accepted for publication Bioscene September 2024). |
2024 |
| 7. |
Possible role of T102C polymorphism in RNA folding during transcription of 5HT2A gene. Kiran Kumar HB.IJMRI, 2016;Vol.2(3): 305-307. |
2016 |
| 8. |
In silico analysis of Dysbindin (DTNBP1) invariants and their plausible role in splicing. Kiran Kumar HB. Intl. jnrl rec. Biotech 2015 :1(2). |
2015 |
| 9. |
Search for missing schizophrenia genes will require a new developmental neurogenomic perspective. Kiran Kumar HB, Christina Castellani, SujitMaiti, Richard O'Reilly and Shiva M. Singh.Journal of Genetics.( PMID-23970094 ) |
2014 |
| 10. |
Gene-hormone interactions: Biological and genetic implications in mood disorders. Kiran Kumar HB. Intl. jnrl rec. Biotech 2014 :2(1) 24-32 |
2014 |
| 11. |
In silico analysis of SERTpromoter (5HTTLPR) and intronic(5HTTVNTR) and their putative role in gene regulation.Kiran Kumar HB. Intl. jnrl rec. Biotech 2014 :2(2) 51-66. |
2014 |
| 12. |
Novel deletion at 13q:clinical and molecular findings. Kiran Kumar HB, SujitMaiti, Christina Castellani, Richard O'Reilly and Shiva M. Singh. Indian Journal of Human Genetics.Jan-March 2013 volume 19 issue 1.( PMID-23901202 ) |
2013 |
| 13. |
Association study of tsnax/disc1 locus for Schizophrenia and Bipolar affective disorder in south Indian population. Ram Murthy Anjanappa, MeeraPurushottam, Kiran KumarHB. et al., J Hum Genet. 2012 Jun 7. (PMID:22673686). |
2012 |
| 14. |
Molecular analysis of Candidate genes at the 22q region in Schizophrenia subjects. Kiran KumarHalagurBhoge Gowda, Jay Rao,Richard O'Reillyand Shiva M. Singh.Research inbiotechnology3(6): 24-32, 2012. |
2012 |
| 15. |
Ontogenetic de novo Copy Number Variations (CNVs) as a Source of Genetic Individuality: Studies on Two Families with MZD Twins for Schizophrenia SujitMaiti, Kiran KH, Christina Castelani, Richard O'Reilly, and Shiva Singh.PLoS One. 2011 Mar 2;6(3):e17125.(PMID:21399695).Highlighted Article.Faculty of 1000 Biology and Science Daily. |
2011 |
| 16. |
Duchenne Muscular Dystrophy: A clinical, histopathological and genetic study at a Neurology tertiary care centre in Southern India.BhairaviSwaminathan, Shubha GN, Shubha D, Kiran Kumar HB, Rammurthy,et al., Neurology India (PMID: 20139501). |
2010 |
| 17. |
Phylogenetic and selection pressure analysis of 5-HT receptors in human and non-human primates. PadmanabhanAnbazhagan,MeeraPurushottam,H. B. Kiran Kumar,Odity Mukherjee et al., Journal of Biomolecular Dynamics and Structure(PMID: 20085376). |
2010 |
| 18. |
Association of serotonin transporter gene polymorphisms with obsessive–compulsive disorder (OCD) in a southern Indian population.Prashant Tibrewal, Kiran Kumar H B, Shubha G N, Subhashree D, MeeraPurushottam et al., Indian Journal Of Medical Research(PMID:21245616). |
2010 |
| 19. |
Identification of interaction between serotonin transporter and glycogen synthase kinase-3β gene polymorphisms: role in susceptibility to bipolar disorder D Subhashree, HB Kiran Kumar,MeeraPurushottam, GN Shubha, M Vallikiran, et al., Future Neurology, May 2009, Vol. 4, No. 3, Pages 363-370 |
2009 |
| 20. |
Evolutionary analysis of PHLPP1 gene in humans and non-human primates. PadmanabhanAnbazghan,Meera P, HB Kiran Kumar, Odity Mukherjee, Shobanakubendran, et al., Bioinformation (Volume 2, Issue 10 (2008).(PMID-18841245). |
2008 |
| 21. |
Serotonergic candidate genes and postpartum psychosis : an association study. H.B. Kiran Kumar,Meera P, Shobanakubendran, Praveenagayathri, VivekBenegal, et al., Psychiatric Genetics . 2007 Oct;17(5):253-260. (PMID-17728663). |
2007 |
| 22. |
SCA 1, SCA 2 & SCA3 / MJD mutations in ataxia syndromes in Southern India. Nithin Krishna, Surendra Mohan, BS Yashavantha, A Rammurthy, HB Kiran Kumar, et al., (Indian J Med Res 2007;November(126), pp 465- 70). (PMID -18160752). |
2007 |
| 23. |
Evidence of linkage and association on 18p11.2 for psychoses. Mukherjee O, Meera P, Ghosh S, Kubendran S, Kiran Kumar HB, et al., Am J Med Genet B Neuropsychiatr Genet. 2006 Dec 5;141(8):868-73.(PMID-16941653). |
2006 |