_{THE NALLUR B. RAMACHANDRA LABORATORY
Genetics and Genomics Lab- University of Mysore}

09

1. Publications in peer-reviewed journals ……………………..141
2. Publications in conference proceedings ……………………09
3. Gene / DNA sequences in NCBI, USA……………………...63
4. Research notes in Drosophila Information Service, USA…14
5. Protocols / Methods developed………………………………05
6. Books / Documentation……………………………………….14

246

Presentation in Seminars and Conferences…………………...…..

h-index :

 i10-index:

Total citations:

249

24

60

2000+

Details of publications

Koushik Ponnanna, Stafny DSouza and Ramachandra Nallur

De novo assembly,annotation and gene expression profiles of gonods of Cytoraces3, a hybrid lineage of Drosophila nasuta nasuta and D.n. albomicans,Genomics and Informatics ( in Press).

StafnyDSouza, Koushik Ponnanna, Amruthavalli Chokkanna, Ramachandra Nallur

Illumina short-read sequencing data, de novo assembly and annotations of the Drosophila nasuta nasuta genome, Data in Brief, https://doi.org/10.1016/j/dib/2020.106674

DSouza, S., Ponnanna, K., Chokkanna, A., Ramachandra, N

Drosophila nasuta nasuta whole genome: Illumina sequencing & data analysis, Mendeley Data, V2, [dataset] ,http://dx.doi.org/10.17632/3s7tft6vgb.2

TejaswiniPrakash , and Nallur B. Ramachandra

Integrated Network and Gene Ontology Analysis Identifies Key Genes and Pathways for Coronary Artery Diseases, Avicenna Journal of Medical Biotechnology (In Press).(IF: 1.690)

Swati Agrawala, Avinash M Veerappa and Nallur B. Ramachandra

Identification of primary Copy Number Variations reveals enrichment of Calcium, and MAPK pathways sensitizing secondary sites for autism, Egyptian Journal Medical Human Genetics(In Press). (IF:0.77)

Ashitha SNM, Raviraj VS and Nallur B. Ramachandra

Comprehensive in silico mutational-sensitivity analysis of PTEN establishes signature regions implicated in pathogenesis of Autism Spectrum Disorders, Genomics, doi.org/10.1016/j.ygeno.2020.10.035,(IF: 6.2)

Koushik Ponnanna, StafnyM.D.Souza, C.Amruthavalli and Nallur B. Ramachandra

Allopatric sibling species pair Drosophila nasuta nasuta and Drosophila nasuta albomicans exhibit expression divergence in ovarian transcriptomes, Gene,doi.org/10.1016/j.gene.2020.145189. (IF: 2.984)

Rahim Gholipoorfeshkecheh, Swati Agarwala, Kavya G, Santhosh Krishnappa, Mysore R. Savitha and Nallur B. Ramachandra

Whole exome sequencing and homozygosity mapping identify variants in NCOR1 and MAP2K3 associated with non- syndromic Congenital Heart Defects,Egyptian Journal of Medical Human Genetics,doi: 10.1186/s43042-020-00101-4. (IF:0.77)

Malek Abbaspourkharyeki, Naveen J Anvekar and Nallur B. Ramachandra

The possible role of point mutations and activation of the CDC27 gene in progression of Multiple Myeloma Meta Gene,https://doi.org/10.1016/j.mgene.2020.100761

Ashitha SNM and Nallur B. Ramachandra

Integrated Functional Analysis implicates Syndromic and Rare Copy Number Variation genes as prominent molecular players in pathogenesis of Autism Spectrum Disorders, Neuroscience 438:25-40 (IF: 3.244)

Malek Abbaspourkharyeki, Naveen Jayaram Anvekar and Nallur B. Ramachandra

Genomic Landscape of a Case of Multiple Myeloma by Whole Exome Sequencing, Bio-Science Research Bulletin (Microbiology & Bio-technology), 36 (1): 1-8.

Tejaswini Prakash, MS. Basavaraj and Nallur B. Ramachandra

Evaluation of Nonsynonymous Single Nucleotide Variations in NOS2 Gene Identified Through Whole Exome Sequencing: A Bioinformatics Approach Bulletin of Pure and Applied Sciences(Zoology),39A(1): 1-17

Rahim G, Swati A,Santhosh K, M.R.Savitha,D. Narayanappa and NB Ramachandra

Nuclear Co-repressor 1, a Potential Candidate Gene in the Manifestation of Congenital Heart Diseases, Int J Hum Genet, 20(2): 55-65 (IF: 0.265)

S Nachappa, S Neelambike, A Sarikhani, and N Ramachandra

Simultaneous detection of drug-resistant mutations in Mycobacterium tuberculosis and determining their role through in silico docking. Infectious disorders drug targets, 18 Mar 2020, DOI: 10.2174/1871526520666200318111140

Rahim G, Swati A,Santhosh K, M.R.Savitha,D. Narayanappa and NB Ramachandra

Variants in HEY genes manifest in Ventricular Septal Defects of Congenital Heart Disease, Gene Reports,1-6, doi.org/10.1016/j.genrep.2020.100613 (IF: 0.610)

Sangeetha V, Avinash MV, Mahesh PA, Jayaraj  BS, Chaya SK,  and NB Ramachandra

Haplotype analysis of ADAM33 polymorphisms in Asthma: A pilot study from South Indian population. Indian J Med Res, Accepted

Megha N Murthy and NB Ramachandra

Prioritization of differentially expressed genes in Substantia nigra transcriptomes of Parkinsons's disease reveals key protein interactions and pathways, Meta Gene, 14:12-18 (IF:1.27)

Ashitha SNM, Avinash M Veerappa and  NB Ramachandra

Whole exome sequencing of discordant diseases in monozygotic twins with Down syndrome reveals mutations for Congenital Heart Defect and Epileptic seizures, Meta Gene, 12: 134-137 (IF:1.27)

Tejaswini Prakash, Avinash M Veerappa and  NB Ramachandra

Complex interaction between HNRNPD mutations and risk polymorphisms is associated with discordant Crohn’s disease in monozygotic twins, Autoimmunity (IAUT) DOI: 10.1080/08916934.2017.1300883 (IF:2.9).

Raviraj V Suresh, Narayanappa D , Savitha R. M., Ambika S. Udupa, Kusuma Lingaiah, Sunil Kumar Polapalli and  NB Ramachandra

Association of RFC1 A80G gene polymorphism with advanced maternal age in risk of Down syndrome,  Current Medicine Research and Practice, 7:6-10

Raviraj V Suresh, Kusuma Lingaiah , Avinash M Veerappa and

NB Ramachandra

Identifying the risk of producing aneuploids using meiotic recombination genes as biomarkers: A Copy Number Variation approach. Indian J Med Res , 145: 39-50 (IF:2.061).

Avinash M. Veerappa, Prakash Padakannaya,and NB Ramachandra

Copy Number Variation of UGT 2B Genes in Indian Families Using Whole Genome Scans. Journal of Nucleic Acids, ID 1648527, 7 pages, On line: http://dx.doi.org/10.1155/2016/1648527. (IF: 2.0) Citation:01

Sinam YM, Chatterjee A, Ranjini MS, Poojari A, Nagarajan A, Ramachandra NB and U. Nongthomba

A newly evolved Drosophila Cytorace-9 shows trade-off between longevity and immune response. Infection, Genetics and Evolution 44 :1–7. (IF: 2.5) Citation:01

Megha N Murthy , Avinash M Veerappa and NB Ramachandra

High-resolution arrays reveal burden of Copy Number Variations on Parkinson Disease genes associated with increased disease risk in random cohorts. Neurological Research , 38 (9), 775-785 (IF: 1.439)

Manasa Prabhanjan, Raviraj V. Suresh  Megha N. Murthy, NB Ramachandra 

Type 2 diabetes mellitus disease risk genes identified by genome wide copy number variation scan in normal populations.  Diabetes Res Clin Pract, http://dx.doi.org/10.1016/j.diabres.2015.12.01 (IF:3.045).

Manjegowda,  D. S., P. Karunakar and  NB Ramachandra

 Effect of Structural Changes in Proteins Derived from GATA4 Nonsynonymous Single Nucleotide Polymorphisms in Congenital Heart Disease. Indian J Pharm Sci 2015;77(6):735-741.

Parisa Davoodi, Mahesh P, Amrutha D Holla and NB Ramachandra

A preliminary study of the association of single nucleotide polymorphisms of IL4, IL13, IL4R and TLR4 with asthma in Indian adults. Indian J Med  Res. 142: 675-680, DOI:10.4103/0971-5916.174551 (IF: 2.061).

Veerappa AM, Raviraj VS, Sangeetha V, Kusuma L, Megha Murthy, Dinesh SM,Prakash P and  NB Ramachandra

Global patterns of large copy number variations in the human genome reveal complexity in chromosome organization.  Genet. Res., Camb. vol. 97, e18. doi:10.1017/S0016672315000191. (IF=2.2)

IL-10 and IL-17F Promoter Single Nucleotide Polymorphism and Asthma: A Case-Control Study in South India, Lung,193:739-747  (IF:2.271).

Parisa Davoodi, Mahesh P, Amrutha D Holla and NB Ramachandra

Family history and the risk for adult onset asthma. Indian J Med  Res.  141:361-363 (IF: 2.061).

Ramachandra NB and Kusuma L  

An understanding of spinocerebellar ataxia. Indian J. of Med Res. 141:10-12 (Commentary) (IF: 2.061).

Avinash M V, Sangeetha V, Kusuma L, Megha M,  Raviraj V S, , Dinesh S M, and NB Ramachandra

Global spectrum of Copy Number Variations reveals genome organizational plasticity and proposes new migration routes. PLoS ONE 10(4): e0121846. doi:10.1371/journal.pone.0121846 (IF: 4.09).

Kusuma L and  NB Ramachandra

An insight into the understanding of 5-HTR2A variants leading to schizophrenia. Indian J. of Med Res. 140: 713-715 (Commentary) (IF: 2.061)

Avinash M Veerappa, Kusuma Lingaiah, SangeethaVishweswaraiah, Megha N Murthy, Raviraj V Suresh, Dinesh S Manjegowda, and NB Ramachandra

Impact of Copy Number Variations Burden on Coding Genome in Humans Using Integrated High Resolution Arrays. Genet. Res., Camb. 96, e17. doi:10.1017/S0016672314000202  (IF=2.2)

Dinesh S Manjegowda, Manu Prasad, Avinash M Veerappa, and NB Ramachandra

Genome-wide Copy Number Scan Identifies IRF6 Involvement in Van der Woude Syndrome in an Indian Family. Genet. Res., Camb. 96, e12  doi.org/10.1017/S0016672314000159 (IF=2.2)

Sangeetha Vishweswaraiah, Avinash M Veerappa, Padukudru A Mahesh, Sareh R Jahromi and NB Ramachandra

Copy Number Variation burden on Asthma sub-genome in normal cohorts identifies susceptibility markers. Allergy, Asthma & Immunology Research, Dec;7:e2. :1-15 (IF= 3.084)

Anand Siddaiah · Marita Saldanha · Shyamala K. Venkatesh, Ramachandra NB and Prakash Padakannaya

Development of Rapid Automatized Naming (RAN) in Simultaneous Kannada-English Biliterate Children, J Psycholinguist Res DOI 10.1007/s10936-014-9338-y (IF=0.653)

Sangeetha V, Avinash MV, Mahesh PA, Jayaraj  BS, Chaya SK,  and NB Ramachandra

Molecular interaction network and pathway studies of ADAM33 potentially relevant to asthma, Annals of Allergy, Asthma & Immunology  (113 (4):418–424.e1. (IF: 3.1).

Avinash MV, Marieta S, Prakash P and NB Ramachandra

Family based genome-wide copy number scan identifies complex rearrangements at 17q21.31 in dyslexics, American Journal of Medical Genetics. Part B: Psychiatry Genetics, 165(7): 572-580 (IF: 3.270)

Jahromi SR, Mahesh PA, Jayaraj  BS, Subbarao MV, Holla AD,  Sangeetha V,  and NB Ramachandra

Serum Levels of IL-10, IL-17F and IL-33 in Patients with Asthma: A Case-Control Study, Journal of Asthma,  51(10): 1004-1013. (IF:1.848)

Salam Herojeet Singh, Prabodh Kumar, NB Ramachandra, Upendra Nongthomba.

Roles of the Troponin isoforms during indirect flight muscle development in Drosophila, J Genet.,93(2):379-88 (IF: 0.876).

Salam Herojeet Singh, NB Ramachandra, Upendra Nongthomba. 

Egg-derived tyrosine phosphatase as a potential biomarker for muscle ageing and degeneration in Drosophila melanogaster , J. Genet Genomics  41:221-224 (IF:1.883)

Radhika P and NB Ramachandra,

Divergence of the gene aly in experimentally evolved Cytoraces, the members of nasuta-albomicans complex of Drosophila, Insect Molecular Biology, 23(4):435-443, DOI: 10.1111/imb.12091 (IF:3.044).

Avinash M V, Megha M, Sangeetha V, Kusuma L, Raviraj V S, Somanna A N, Nelchi P, Sangeetha N U, Manjula A S, Dinesh S M, B S Keshava and NB Ramachandra

Copy Number Variations burden on miRNA genes reveals layers of complexities involved in the regulation of pathways and phenotypic expression. PLoS ONE9 (2): e90391 (IF:4.09).

Venkatesh, S K., Siddaiah, A., Padakannaya, P. and NB Ramachandra

Association of SNPs of DYX1C1 with Developmental Dyslexia in Indian population. Psychiatric Genetics, 24:10-20 (IF: 2.581).

Avinash MV, Sangeetha V, Kusuma L, Megha M, Raviraj VS, Tejaswini, Niveditha P, Supriya GPK, Keshava B S, and NB Ramachandra 

Insertion-Deletions burden in Copy Number Polymorphisms of the Tibetan Population, Indian journal of Human Genet  20:166-174

Marita Saldanha, Anand Siddaiah, Avinash M. Veerappa, Ramachandra NB ,and Prakash Padakannaya

Catch Them Before They Fall : A Simple Test of Sight-Word and Pseudo-Word Reading in Kannada for a Quick and Early Assessment. Sage Open  DOI: 10.1177/2158244014560524Published 21 December 2014

Jahromi SR, Mahesh PA, Jayaraj  BS, Subbarao MV, Holla AD,  Sangeetha V, and  NB Ramachandra

Single Nucleotide Polymorphism and Asthma: From Conformational Variations to Structural Alternations. Molecular and Biochemical Diagnosis (Journal) 1(2) : 63-75.

Avinash MV, Marieta S, Prakash P and NB Ramachandra

Genome-wide copy number scan identifies disruption of PCDH11X in developmental dyslexia.  American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 9999:1–9. (IF: 3.270)  DOI 10.1002/ajmg.b.32199.

Venkatesh, S K., Siddaiah, A., Padakannaya, P. and NB Ramachandra

Lack of association between genetic polymorphisms in ROBO1, MRPL19/C2ORF3 and THEM2 with Developmental Dyslexia.  Gene, 529: 215–219 (IF: 2.196)

Parisa Davoodi, P A Mahesh, Amrutha D Holla and NB Ramachandra

 Association of socio-economic status with family history in adult patients with Asthma. Indian J Med  Res, 138: 497-503 (IF:2.061)

Avinash M V, Sangeetha V, Kusuma L, Megha Murthy, Dinesh S M, Radhika Nayaka, and NB Ramachandra

Unraveling the complexity of Human Olfactory Receptor repertoire by Copy Number analysis across population using high resolution arrays
PLOS ONE 8(7): e66843. doi:10.1371/journal.pone.0066843 (IF: 4.09)

Avinash MV, Marieta S, Prakash P and NB Ramachandra

Family based genome-wide copy number scan identifies five new genes of dyslexia involved in dendritic spinal plasticity. Journal of Human Genetics, 1434-5161/13 (IF: 2.570)

Venkatesh, S. K., Siddaiah, A., Padakannaya, P.and NB Ramachandra

Analysis of genetic variants of Dyslexia candidate genes KIAA0319 and DCDC2 in Indian population. Journal of Human Genetics , 1434-5161/13  (IF: 2.570)

Avinash M Veerappa, Marita Saldanha, Prakash Padakannaya and NB Ramachandra

Copy Number Variation analysis in humans reveal previously identified X chromosome Transposed Region (XTR) in Y-chromosome to be a pseudoautosomal region 3 (PAR3). Functional & Integrative Genomics  (DOI: 10.1007/s10142-013-0323-6)   (IF:3.3).

Mysore S. Ranjini and NB Ramachandra    

Rapid evolution of a few members of nasuta-albomicans complex of Drosophila: Study on two candidate genes, Sod1 and Rpd3. Journal of Molecular Evolution ,  J. Mol. Evol. 76(5): 311—323, DOI 10.1007 /s00239-013-9560-5 (IF:2.274).

Parisa Davoodi, P A Mahesh, Amrutha D Holla,  G S Vijayakumar,  B S Jayaraj,  Chandrashekar S, and NB Ramachandra

Serum levels of Interleukin-13 and Interferon-gamma from adult patients with asthma in Mysore. Cytokine, 431–437Doi.org/10.1016/j.cyto.2012.05.012   (IF: 3.53)

Bijaya T. and NB Ramachandra

Genomic Introgression in Laboratory Evolved Hybrid Races, Cytorace 1 and  Fissioncytorace-1 of Nasuta-Albomicans Complex (NAC) of Drosophila as  Revealed by RAPD and ISSR Markers.  Italian Journal of Zoology, 2012,  iFirst, 1–10  (IF=0.939).

Salvi SS, Kumar RP, Ramachandra NB, Sparrow JC,  Nongthomba U.

Mutations in Drosophila myosin rod cause defects in myofibril assembly. J Mol. Bio.   419(1-2):22-40. (IF: 4.008)

Santhosh Kumar K, Kusuma L, Ramachandra NB and Nair Vijay Mala

Genetic variations among ecologically diverse species of Anurans at the level of Genus based on ISSR Marker. I. Res. J. Biological Sci. 1(7): 11-19 

Suttur S Malini, Mysore R Savitha, and NB Ramachandra

Maternal grandmothers with advanced age reproduction are more likely to have Down syndrome grandchildren. J. Paramedical Sciences (JPS), 2 (3):8-15  

Bijanzadeh Mahdi , Mahesh  PA, and NB Ramachandra

An understanding of the genetic basis of Asthma. Review- Indian J. Med Res.   134:149-161  (IF: 2.031)

Kusuma L, Dinesh S. M., Savitha M.R, Krishnamurthy B., Narayanappa D.   and NB Ramachandra

 Mutations of TFAP2B in congenital heart disease patients of Mysore, South  India, Indian Journal of Medical Research, 134: 621-626 (IF:2.031).

Ranjini MS, Ravikumar H, Muralidhara and NB Ramachandra

Differential susceptibility of a few members of nasuta-albomicans complex of Drosophila to paraquat induced lethality and oxidative stress. Genome,  54(10): 829-835, 10.1139/g11-049  (IF: 1.971).

Sosalagere M. Dinesh, Kusuma Lingaiah, Mysore R. Savitha, B Krishnamurthy, D Narayanappa and NB Ramachandra

GATA4  Specific Nonsynonymous Single Nucleotide Polymorphisms in Congenital Heart Disease Patients of Mysore, India, Genetic Testing and Molecular Biomarkers , 15(10): 715-720. (IF= 1.617)

Kusuma L, Dinesh S. M., Savitha M.R, Krishnamurthy B., Narayanappa D. and  NB Ramachandra

A maiden report on CRELD1 Single Nucleotide Polymorphism association in congenital heart disease patients of Mysore, South India.  Genetic Testing and Molecular Biomarkers, doi:10.1089/gtmb.2010.0246. (IF= 1.617)

Shyamala K. Venkatesh, Anand Siddaiah, Prakash Padakannaya and NB  Ramachandra

An examination of candidate gene SNPs for Dyslexia in an Indian  sample, Behavior genetics,  2011;41(1):105-109. (IF=3.1)

Dinesh S.M., Kusuma L., Smitha R., Savitha M.R., Krishnamurthy B., Narayanappa D.,  and NB Ramachnadra  

Single Nucleotide Polymorphisms of NKX2.5 found in Congenital Heart Disease patients of Mysore, South India. Genetic Testing and Molecular Biomarkers 14 (6):1-7. (IF= 1.617)

Ranjini,M.S  and NB Ramachandra

Differential response to hormosis by laboratory evolved short-lived and long-lived cytoraces of nasuta-albomicans complex of Drosophila, Italian J. Zoology iFirst, 1-12. (IF=0.939)

Bijanzadeh Mahdi , Mahesh  PA, Savitha Mysore R.,  Pradeep Kumar,  Jayaraj  B S,  and NB Ramachandra

Inheritance patterns, Consanguinity and Risk for Asthma, Indian J. Med Res  132:48-55. (IF =2.031)

Mahdi Bijanzadeh, NB. Ramachandra, P. A. Mahesh,  M R. Savitha, B. S. Manjunath and B. S. Jayaraj

Association of IL-4 and ADAM33 gene polymorphisms with asthma in an Indian population, Lung 188:415-422 (IF=1.899)

Smitha Rame Gowda, Harshavardhan M. Gawde, Abbas Hyderi, Mysore R.Savitha, Balasundaram Krishnamurthy, Sameul C. Karat, Narayanappa, Doddaiah, Zareen M. Patel and NB Ramachandra

Chromosomal Anomalies and Congenital Heart Disease in Mysore, South India. Int. J. Hum. Genet. 10(1-3):131-139. (IF:0.183)

Suttur S. Malini   and NB Ramachandra

Young Mothers Produce More Chromosomal Syndrome Babies in Mysore, South India. Int. J. Hum. Genet. 10(1-3):105-112. (IF:0.183)

Bijaya T. and NB Ramachandra

Racial divergence of a rare laboratory evolved centromeric fission Cytorace of nasuta-albomicans complex of Drosophila. Indian J. Exp. Biol. 48:511-517.(IF 1.295)

Dinesh S M,  Kusuma L, and NB Ramachandra

 The most frequent 239 A>G SNP of NKX2.5 is not involved in Congenital Heart Disease. New York Science Journal, 3(8): 43-47.

Dinesh S. M, Prashantha Karunakar, C. Amruthavalli and NB Ramachandra

 Analysis and homology modeling of proteins derived from NKX2.5 non-synonymous single nucleotide polymorphisms involved in congenital heart disease, Nature and Science, 8(9); 27-38

Bijaya T. and NB Ramachandra

Genetic Variability Assessed by Competitive Ability and ISSR Markers in the Members of the nasuta-albomicans Complex of Drosophila. Nature and Science, 8(12); 29-42.

Kusuma L, Bharath A. P., Savitha R. M., Krishnamurthy B. and  NB Ramachandra

A rare case of congenital heart disease with ambiguous genitalia. Indian J. Hum Genet. 53: 100-102.

Mahdi Bijanzadeh, Ramachandra,NB, P. A. Mahesh, Mysore R. Savitha,  B. S. Manjunath and B. S. Jayaraj

 Lack of Association Between Asthma and ABO Blood Group. Lung, 187(6):389-392. (IF=1.899) 

Mahdi Bijanzadeh, Ramachandra,NB, P. A. Mahesh, Mysore R. Savitha,  G. S. Vijayakumar, Pradeep Kumar, B. S. Manjunath and  B. S. Jayaraj

Soluble Intercellular Adhesion Molecule-1 and E-selectin in Patients with  

 Asthma Exacerbation. Lung, 187(5):315-320. (IF=1.899) 

Pushpa Saviour, Prakash Padakannaya, Surendranath Nishanimutt and NB Ramachandra

Familial Patterns and Biological Markers of Dyslexia. . Int. J. Hum. Genet.  9(1):21-29. (IF:0.183)  

Malini S. Suttur, Savitha R. Mysore, Balasundaram Krishnamurthy,   NB Ramachandra.

 Rare association of Turner syndrome with neurofibromatosis type 1 and tuberous sclerosis complex. Indian J. Hum. Genet 15(2): 75-77. (IF=0.469)

Ranjini,M.S  and NB Ramachandra

Evolution of short-lived and long-lived races of Drosophila in the environs of laboratory. Indian J. of Gerontology, 23(4):381-298.

Ramachandra NB and Ranjini M.S 

Experiments to Demonstrate Change in Allelic Frequency by Genetic Drift.

Resonance, 14 (11): 1110-1118.

Prakash Padakannaya, Ramachandra NB and Nandini C. Singh

  Dyslexia, orthography and brain. Curr. Sci., 95(10):1381(IF= 0.935)

Ponnappa K.C., Pushpa Saviour, Ramachandra, NB. Manjunatha Kini, R and T. Veerabasappa Gowda

INN-toxin, a highly lethal peptide from the venom of Indian cobra (Naja naja) venom—Isolation, characterization and pharmacological actions. Peptides,   29(11):1893-1900. (IF=2.654)

Sajesh Babu and NB Ramachandra

Recombination mapping of mutations involved in the development of indirect flight muscles in Drosophila melanogaster. J. Cytol. and Genet. 9(NS):7-11.

Pushpa Saviour, Satish Kumar, U Kiran, Rajasekhara Reddy Ravuri, VR Rao,  NB Ramachandra

 Allelic variants of DYX1C1 are not associated with dyslexia in India. Indian J.  Hum. Genet 14(3):99-102. (IF=0.469)

Suttur S Malini, Mysore R. Savitha, Balasundaram Krishnamurthy and NB Ramachandra

 Advanced maternal grandmother age is a risk factor in causing sex

 chromosomal aneupolidy. Int. J. Hum. Genet. 7(4): 289-296. (IF:0.183)

Smitha R, Savitha MR, Krishnamurthy B, Doddaiah N, Prasanth SN and

NB Ramachandra

Association between pericentric inversion in chromosome 9 and congenital heart defects.  Int. J. Hum. Genet. 7(3): 241-248.  (IF:0.183)

Harini B.P. and NB Ramachandra

Newly evolved races live better: a study of life – history traits in the four members of nasuta – albomicans complex of Drosophila at different temperatures. Curr. Sci.  93: 348-356. (IF=0.897)

Sajesh Babu and NB Ramachandra

Screen for new Mutations on the 2^nd Chromosome Involved in Indirect Flight Muscle Development in Drosophila melanogaster.  Genome, 50(4): 343–350. (IF= 1.971) 

Smitha R, Arun K, Savitha MR, Krishnamurthy B, Narayanappa D and Ramachandra NB.

Missense mutation G296S in GATA4 is not responsible for cardiac septal defects. Indian J. Hum. Genet. 13(1):30-32.

Suttur. S. Malini, Smitha Ramegowda and NB Ramachandra

Evolution of Phenylthiocarbamide taster trait in Mysore. South India, Indian J. hum. Genet.13 (1): 16-20.

Pushpa Saviour, Smitha Ramegowda and NB Ramachandra

 Satellite associations in human acrocentric chromosomes: An insight into the evolution of biarmed chromosomes. J. Cytol. and Genet. 8:47-55.

Suttur S Malini and NB Ramachandra

 Possible risk factors for Down syndrome and sex chromosomal aneuploidy in Mysore, South India. Indian J. Hum. Genet. 13(3):102-108.

Savitha MR, Krishnamurthy B, Ashok DA and NB Ramachandra

Self-abortion of attacks in patients with Hot water epilepsy. Indian Pediatrics, 44:295-298. (IF=0.956) 

Saviour P and NB Ramachandra

 Biological basis of dyslexia: A maturing perspective. Curr. Sci. 90(2):168-175.   Review article.  (IF= 0.935) 

Smitha R, Gawde HM, Hyderi A, Savitha MR, Patel ZM, Krishnamurthy B and NB Ramachandra

De novo isochromosome 18p in a female dysmorphic child. J. Appl. Genet. 47(4):397-401.  (IF= 1.482)

Smitha R and NB Ramachandra

Parental consanguinity increases Congenital Heart Diseases in South India. Annals of Hum. Biol. 33(5/6):519-928.   (IF=1.713) 

Savitha MR, Krishnamurthy B, Hyderi A, Farhan-Ul-Haque and NB Ramachandra

Myotonia congenital- a successful response to carbamazepine. Ind. J. Pediatrics,73:431-433. (IF= 0.52) 

Smitha R, Karat SC, Narayanappa D, Krishnamurthy B, Prasanth SN and  NB Ramachandra

Prevalence of Congenital Heart Diseases in Mysore. Indian  J. Hum. Genet. 12(1):12-17.

Malini S S and NB Ramachandra

Influence of advanced age of maternal grandmothers on Down syndrome. BMC Medical genetics. 7: 4 ( 8 pages) Feb. 14^th (IF=2.84)

Saviour P and NB Ramachandra

Modes of genetic transmission of dyslexia in south Indian families. Indian  J. Human Genetics . 11(3):135-140.

Smitha R and NB Ramachandra

An understanding the basis of congenital heart disease. Ind. J. Human Genetics 11: 14-23. Review article (IF=0.469)

Morros J, Ramachandra NB, Ladurner P., Egger B, Rieger R and V.                     Hartenstein

The embryonic development of flatworm Macrostomum sp.  Dev. Genes Evol. 214:220-239    (IF=2.146)

Harini BP and NB Ramachandra

Racial divergence in the foreleg bristles of four members of the nasuta-                albomicans complex of Drosophila, Curr. Sci. 85(10) : 1444-1450. (IF= 0.935)

Harini BP and NB Ramachandra

Evolutionary experimentation through hybridization under laboratory condition in Drosophila: Evidence for Recombinational Speciation. BMC

Evolutionary Biology, 3,20 (1-19)  (IF= 3.52. )

Tanuja MT., Ramachandra  NB and  HA Ranganath

Hybridization and introgression of the genomes of Drosophila nasuta and Drosophila albomicans: Evolution of new karyotypes.  Genome 46:605-611.  (IF= 1.971) 

Ramachandra NB., Gates RD.,  Ladurner P.,  Jacobs JK  and  Hartenstein V.

Embryonic development in the primitive bilaterian Neochildia fusca: normal morphogenesis and isolation of POU genes Brn-1 and Brn-2. Dev.genes Evol.  212: 55-69.  (IF=2.146)

Tanuja MT., Ramachandra  NB and  HA Ranganath

Incipient sexual isolation in the nasuta-albomicans complex of Drosophila: Mating preference in male-, female- and multiple-choice mating experiments J. Biosci., 26:365-371 (IF=1.888)

Tanuja MT., Ramachandra  NB and  HA Ranganath

Incipient sexual isolation in the nasuta-albomicans complex of Drosophila: No- Choice experiments,  J. Biosci., 26:71-76. (IF=1.888)

Mahesh G., Ramachandra NB and H. A. Ranganath

Autoradiographic study of transcription and dosage compensation in the sex and neo- sex chromosome of D. n. nasuta and D. n. albomicans. Genome. 44:71-78. (IF= 1.971)

Harini BP and NB Ramachandra

Racial divergence in abdominal bristles among parental races and newly  

Evolved Cytoraces of nasuta-albomicans complex of Drosophila, Indian.J. Exp.Biol., 38:1263-1266. (IF=1.295)

Mahesh G., Ramachandra NB and H. A. Ranganath

Patterns of replication in the neo-sex chromosomes of Drosophila nasuta  

albomicans. J. Biosci. 25 (3): 229-234. (IF=1.888) 

Harini BP and NB Ramachandra.

Racial divergence in body weight: A study in the four members of the newly evolved  nasuta-albomicans complex of Drosophila, Curr. Sci. 78 (3): 342-344.  (IF= 0.935)

Tanuja M. T., Ramachandra NB and H. A. Ranganath.

Evolution of a new chromosomal lineage in a laboratory population of Drosophila through centric fission. J. Biosci. 24(4):421-426. (IF= 1.888)

1999

Tanuja MT., Ramachandra NB and HA Ranganath.

Evolution of a recent neo-Y sex chromosome in a laboratory population of Drosophila. J. Genet. 78:81-85. (IF=1.338) 

Upendra Nongthomba and NB Ramachandra.

A direct screen identifies new flight muscle mutants on the Drosophila second chromosome. Genetics, USA, 71-83. (IF= 4.836)

Harini BP and  NB Ramachandra

Does evolution reduce the body size?: A study in four members of nasuta- albomicans complex of Drosophila. Genetica, 105: 1-6. (IF=2.358)

Harini BP and  NB Ramachandra.

Racial divergence in sternopleural bristles among the parental races and the newly evolved Cytorace 1 and 2 of the nasuta-albomicans complex of Drosophila. Curr. Sci. 76(7):1017-1019. (IF= 0.935)

Tanuja MT., NB Ramachandra and  HA Ranganath

Creation of a hybrid zone in Drosophila with allo-sympatric races. Curr. Sci., 75(11): 1116-1117. (IF= 0.935)

Ramachandra NB

A simple and rapid method for isolation of cellular DNA. Resonance - J.

Science Education 3(7): 71-73.

Ramachandra, NB and HA Ranganath.

Evolution of the Nasuta - Albomicans complex of Drosophila. Curr. Sci.,

 71(7): 515-517.  (IF= 0.935)

Ramachandra NB and Ranganath HA

Population differentiation: A study with two strains of Drosophila albomicans. J. Mysore University, Sec. B, 34:12-27.

Ranganath HA and Ramachandra NB

Drosophila albomicans – a unique karyotype. Nucleus, Calcutta, International Journal of Cytology 37(3): 105-112. Citation – 05

Ramachandra, NB and HA Ranganath

 Estimation of inter-genotypic competitive ability of the parental races 

 (Drosophila nasuta nasuta and D. n.  albomicana) and   of the newly evolved  Cytoraces (I and II).  Journal of Zoological Systematics and Evolutionary  Research (Germany), 32: 73-78.  (IF= 2.740)

Ramachandra, NB and HA Ranganath.

Pattern of sexual isolation between parental races (Drosophila nasuta nasuta and D. n. albomicans) and the newly evolved races (Cytoraces I & II). Indian J. Exp. Biol. 32:98-102. (IF 1.295) 

Ramachandra, NB and HA Ranganath.

Analysis of intergenotypic resource utilization divergence in the parental races (D. n. nasuta and D.n.albomicana) and of the newly evolved Cytoraces (I and II). J. Mysore University, sec,B, Platinum Jubilee Special Issue, 32: 308-315.

Ramachandra, NB and HA Ranganath.

The chromosomes of two Drosophila races: D. nasuta nasuta and D. nasuta albomicana: V.  Introgression and the evolution of new karyotypes. Journal of Zoological Systematics and Evolutionary Research (Germany), 28 (1): 62-68.  (IF= 2.740)

Ramachandra, NB and HA Ranganath.

Estimation of population fitness of the parental races (D. n.nasuta and D. n.albomicana) and of the newly evolved Cytoraces (I and II) - the products of parental interracial hybridization. Genome, 30(1): 58-62.

(IF= 1.971)

Ramachandra, NB and HA Ranganath.

 A comparative study on the microchromosomes of six Drosophila members.The Nucleus, Calcutta, International Journal of Cytology, 31(3):102-106.

Ranganath,HA and NB Ramachandra.

Chromosomal basis of raciation in Drosophila : A study with Drosophila  nasuta and D. albomicans, Proc. Indian Acad. Sci. ( Anim. Sci.) 96(5): 451-  459 (Review). (IF=1.703)

Ramachandra, NB and HA Ranganath.

Accumulation of B-chromosomes in Drosophila nasuta albomicana. Curr.Sci. 56(16): 850-852. (IF= 0.935) 

Ramachandra, NB and HA Ranganath.

Mating preference between Drosophila nasuta nasuta and D.n. albomicana. Indian J. Exp. Biol. 25:55-57. (IF= 1.295) 

Ramachandra, NB and HA Ranganath.

Characterization of heterochromatin in the B-chromosomes of Drosophila  nasuta albomicana. Chromosoma, 95:223-226. (IF=4.979)

Ramachandra, NB and HA Ranganath.

Population fitness of Drosophila nasuta albomicana with and without B-Chromosomes at three different temperatures. Indian J. Exp. Biol. 24: 779- 782. (IF= 1.295) 

Ramachandra, NB and HA Ranganath.

Analysis of resource utilization divergence in two strains of Drosophila  nasuta albomicana with and without B-chromosomes. Indian J. Exp. Biol. 24: 404- 407. (IF= 1.295)

Ramachandra NB and HA Ranganath

Estimation of population fitness in two strains of D. nasuta albomicana and without B-chromosomes. Indian J. Exp.

Biol. 24: 137-141. (IF =1.295)

Ramachandra, NB and HA Ranganath.

The Chromosomes of two Drosophila races: D. nasuta nasuta and D. nasuta albomicana.  IV. Hybridization and karyotype repatterning. Chromosoma, 93: 243-248. (IF= 4.979)

Ramachandra, NB and HA Ranganath.

 Ecogenetics of Drosophila_- Exploitation of media with different sugars by two cosmopolitan and sympatric species of Drosophila. J. Mysore University, sec. B, 31:108-116.

Ramachandra, NB and HA Ranganath.

Supernumerary chromosomes in Drosophila nasuta albomicana.  

(Experientia) Cellular and molecular Life Sciences, 1: 680-681.

 (IF = 7.047)

Dinesh SM,  Amruthhavalli C, Kusuma L and NB Ramachandra

Genotype-Phenotype analysis of NKX 2.5. single nucleotide polymorphisms involved in the Congenital Heart Disease patients of Mysore, India.  Proc. Of National Conference on Information Technology and its applications held on 21-22 Nov.2009, Eds. C Basavaraju,CN Ravikumar and C Amruthavall ,Centre for Information Science and technology & DOS in Computer Science,  University of Mysore, Mysore. pp: 148-152.

Avinash MV, Bhanu priya R  and NB Ramachandra

Designing  a Biosoftware: Human phenopaedia and Genome sequence analyzer. Proc. of National Conference on Information Technology and its applications  held on 21-22 Nov. 2009, Eds. C Basavaraju,CN Ravikumar and C  Amruthavalli ,Centre for Information Science and technology & DOS in Computer Science,  University of Mysore, Mysore. pp: 153-157.

Ranjini MS, Amruthhavalli C and NB Ramachandra

Molecular perspective of Sod 1 in Drosophila nasuta nasuta. Proc. Of National Conference on Information Technology and its applications held on 21-22 Nov. 2009, Eds. C Basavaraju,CN Ravikumar and C Amruthavalli, Centre for Information Science and technology & DOS in Computer Science, University of Mysore, Mysore. pp: 97-105.

Radhey S. Gupta, Ramachandra NB, Timothy Bowes and Bhag Singh

Unusual cellular disposition of the mitochondrial molecular chaperones Hsp60, Hsp70 and Hsp10. The Biology of extracellular molecular chaperones, Wiley, Chichester (Novartis Foundation Symposium 291) p59-73. Citation – 36

Ranjini, MS  and NB Ramachandra

Recombination influences longevity in karyotypically similar hybrid races of nasuta-albomicans complex of Drosophila. Proc. Nat. Symp. RTIBS, 90-96.

Kusuma Lingaiah  and NB Ramachandra

Genes Involved in Congenital Heart Diseases: A Review Proc. Nat. Symp. RTIBS, 22-28.

Mahdi Bijanzadeh, NB Ramachandra

Possible causes of Asthma in Mysore, South India. Proc. Nat. Symp. RTIBS, 74-77.

Tanuja MT., Ramachandra NB and HA Ranganath.

Hybridization and Raciation in Drosophila. DST SERC Research highlights:17-21.

Ramachandra, NB and HA Ranganath.

 Population cytogenetics of supernumerary chromosomes in Drosophila nasuta albomicana. In commemorative volume of advances in Cytology and Genetics. edited by VS Bhatnagar: 115-121.