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Adduri, R.S.R. and George, S.A. and Padmavathi, K. and Bashyam, M.D. (2020) SMARCD1 is a transcriptional target of specific non‐hotspot mutant p53 forms. Journal of Cellular Physiology, 235 (5). pp. 4559-4570. ISSN 0021-9541

Adduri, R.S.R. and Katamoni, R. and Pandilla, R. and Madana, S.N. and Paripati, A.K. and Kotapalli, V. and Bashyam, M.D. (2014) TP53 Pro72 allele is enriched in oral tongue cancer and frequently mutated in esophageal cancer in India. PloS one, 9 (12). e114002. ISSN 1932-6203

Aggarwal, Shagun and Coutinho, M.F. and Dalal, Ashwin and Jain, S.J.M.N. and Prata, M.J. and Alves, S. (2014) Prenatal skeletal dysplasia phenotype in severe MLII alpha/beta with novel GNPTAB mutation. Gene, 542 (2). pp. 266-268. ISSN 1879-0038

Aggarwal, Shagun and Kar, A. and Bland, P. and Kelsell, D. and Dalal, Ashwin (2015) Novel ABCA12 mutations in harlequin ichthyosis: a journey from photo diagnosis to prenatal diagnosis. Gene, 556 (2). pp. 254-256. ISSN 1879-0038

Aggarwal, Shagun and Vineeth, V.S. and Das Bhowmik, A. and Tandon, A. and Kulkarni, A. and Dhanya Lakshmi, N. and Bhattacherjee, Amrita and Dalal, Ashwin (2020) Exome sequencing for perinatal phenotypes: the significance of deep phenotyping. Prenatal Diagnosis, 40 (2). pp. 260-273. ISSN 0197-3851

Ali, Nida and Gowrishankar, J. (2020) Cross-subunit catalysis and a new phenomenon of recessive resurrection in Escherichia coli RNase E. Nucleic Acids Research, 48 (2). pp. 847-861. ISSN 0305-1048

Arora, Veronica and Setia, Nitika and Dalal, Ashwin and Vanaja, M.C. and Gupta, Deepti and Razdan, Tinku and Phadke, S.R. and Saxena, Renu and Rohtagi, Anshu and Verma, I.C. and Puri, R.D. (2020) Sialidosis type II: Expansion of phenotypic spectrum and identification of a common mutation in seven patients. Molecular Genetics and Metabolism Reports, 22. p. 100561. ISSN 2214-4269

B

Bashyam, M.D. (2002) Understanding cancer metastasis. Cancer, 94 (6). pp. 1821-1829. ISSN 0008-543X

Bashyam, M.D. and Chaudhary, A.K. and Kiran, M. and Nagarajaram, H.A. and Radha Rama Devi, A. and Ranganath, P. and Dalal, Ashwin and Bashyam, L. and Gupta, N. and Kabra, M. and Muranjan, M. and Puri, R.D. and Verma, I.C. and Nampoothiri, S. and Kadandale, J.S. (2014) Splice, insertion-deletion and nonsense mutations that perturb the phenylalanine hydroxylase transcript cause phenylketonuria in India. Journal of Cellular Biochemistry, 115 (3). pp. 566-74. ISSN 1097-4644

Bashyam, M.D. and Kotapalli, V. and Raman, R. and Chaudhary, A.K. and Yadav, B.K. and Gowrishankar, S. and Uppin, S.G. and Kongara, R. and Sastry, R.A. and Mohana Vamsy, C. and Patnaik, S. and Rao, S. and Dsouza, S. and Desai, D.C. and Tester, A. (2015) Evidence for presence of mismatch repair gene expression positive Lynch syndrome cases in India. Molecular Carcinogenesis, 54 (12). pp. 1807-1814. ISSN 0899-1987

Bashyam, M.D. and Srinivas, A. and Pratyusha, B. and Ashmala, N. and Sara , A.G. (2019) The Yin and Yang of cancer genes. Gene, 704. pp. 121-133. ISSN 0378-1119

Bashyam, M.D. and Chaudhary, A.K. and Kiran, M. and Reddy, V. and Nagarajaram, H.A. and Dalal, Ashwin and Bashyam, L. and Sun, D. and Gupta, A. and Gupta, N. and Kabra, M. and Puri, R.D. and Radha Rama Devi, A. and Kapoor, S. and Danda, S. (2014) Molecular analyses of novel ASAH1 mutations causing Farber lipogranulomatosis: analyses of exonic splicing enhancer inactivating mutation. Clinical Genetics, 86 (6). pp. 530-538. ISSN 1399-0004

Basu, A. and Dasari, V. and Mishra, R.K. and Khosla, Sanjeev (2014) The CpG island encompassing the promoter and first exon of human DNMT3L gene is a PcG/TrX response element (PRE). PloS one, 9. e93561. ISSN 1932-6203

Bhattacherjee, Amrita and Ranganath, P. and Divya, Pasumarthi and Dalal, Ashwin (2019) Identification and in-silico analysis of a novel disease-causing variant in the GUSB gene for Mucopolysaccharidosis VII presenting as non-immune fetal hydrops. Gene Reports, 16. p. 100437. ISSN 2452-0144

Bidchol, A.M. and Dalal, Ashwin and Shah, H. and Suryanarayana, S. and Nampoothiri, S. and Kabra, M. and Gupta, N. and Danda, S. and Gowrishankar, K. and Phadke, S.R. and Kapoor, S. and Kamate, M. and Verma, I.C. and Puri, R.D. and Sankar, V.H. and Radha Rama Devi, A. and Patil, S.J. and Ranganath, P. and Jain, S.J.M.N. and Agarwal, Meenal and Singh, Ankur and Mishra, P. and Tamhankar, P.M. and Gopinath, P.M. and Nagarajaram, H.A. and Satyamoorthy, K. and Girisha, K.M. (2014) GALNS Mutations in Indian Patients With Mucopolysaccharidosis IVA. American Journal of Medical Genetics Part A, 164A (11). pp. 2793-2801. ISSN 1552-4833

Borah, S. and Shivarathri, R. and Srivastava, V.K. and Ferrari, S. and Sanglard, D. and Kaur, Rupinder (2014) Pivotal Role for a Tail Subunit of the RNA Polymerase II Mediator Complex CgMed2 in Azole Tolerance and Adherence in Candida glabrata. Antimicrobial Agents and Chemotherapy, 58 (10). pp. 5976-5986. ISSN 0066-4804

C

Chaudhary, Neelam and Subba Reddy, Maddika (2014) WWP2-WWP1 Ubiquitin Ligase Complex Coordinated by PPM1G Maintains the Balance between Cellular p73 and Delta Np73 Levels. Molecular and Cellular Biology, 34 (19). pp. 3754-3764. ISSN 0270-7306

Chauhan, R. and Mande, S.C. (2002) Site-directed mutagenesis reveals a novel catalytic mechanism of Mycobacterium tuberculosis alkylhydroperoxidase C. Biochemical Journal, 367 (Pt 1). pp. 255-61. ISSN 0264-6021

D

Dalal, Ashwin (2014) Molecular cytogenetic characterization of chromosomal rearrangements - utility in genetic counseling and research. Molecular Cytogenetics, 7 (Suppl ). I12. ISSN 1755-8166

Das Bhowmik, A. and Rangaswamaiah, S. and Srinivas, G. and Dalal, Ashwin (2015) Molecular genetic analysis of trinucleotide repeat disorders (TRDs) in Indian population and application of repeat primed PCR. European journal of Medical Genetics, 58 (3). pp. 160-167. ISSN 1878-0849

Dhanya Lakshmi, N. and Ranganath, P. and Aggarwal , Shagun and Dalal, Ashwin and Phadke, S.R. and Mandal, K. (2019) Computer-aided Facial Analysis in Diagnosing Dysmorphic Syndromes in Indian Children. Indian Pediatrics, 56 (12). pp. 1017-1019. ISSN 0019-6061

Dhanya Lakshmi, N. and Ranganath, P. and Balakrishnan, S. and Dalal, Ashwin (2019) Mosaic paternal uniparental isodisomy of 15q11-q13 region causing Angelman phenotype. Clinical Dysmorphology, 28 (4). pp. 202-204. ISSN 0962-8827

Divya, Pasumarthi and Gupta, N. and Sheth, J. and Jain, J.M.N. and Rungsung, I. and Kabra, M. and Ranganath, Prajnya and Aggarwal, Shagun and Phadke, S.R. and Girisha, K.M. and Shukla, A. and Datar, C. and Verma, I.C. and Puri, R.D. and Bhavsar, R. and Mistry, M. and Sankar, V.H. and Gowrishankar, K. and Agrawal, Divya and Nair, M. and Danda, S. and Soni, J.P. and Dalal, Ashwin (2020) Identification and characterization of 30 novel pathogenic variations in 69 unrelated Indian patients with Mucolipidosis Type II and Type III. Journal of Human Genetics, 65 (11). pp. 971-984. ISSN 1434-5161

Dutta, Usha and Hansmann, I. and Schlote, D. (2015) Molecular cytogenetic characterization of a familial pericentric inversion 3 associated with short stature. European Journal of Medical Genetics, 58 (3). pp. 154-159. ISSN 1878-0849

Dutta, Usha and Rao, S.N. and Vijaya Kumar, P. and Vineeth, V.S. and Bhattacherjee, Amrita and Das Bhowmik, A. and Ramaswamy, S.K. and Singh, K.G. and Dalal, Ashwin (2019) Breakpoint mapping of a novel de novo translocation t(X;20)(q11.1;p13) by positional cloning and long read sequencing. Genomics, 111 (5). pp. 1108-1114. ISSN 0888-7543

Dutta, Usha and Suttur, M.S. and Vineeth, V.S. and Laxmi Priyanka, P. and Sravani, G. and Talwar, S. and Suhana, A. and Sushmita, B. and Rachel, J.A. and Dalal, Ashwin (2020) Cytogenetic and molecular study of 370 infertile men in South India highlighting the importance of copy number variations by multiplex ligation‐dependent probe amplification. Andrologia. ISSN 0303-4569 (In Press)

Dutta, Usha and Swamy, Venugopala and Rajitha, Ponnala and Aggarwal, Shagun and Dalal, Ashwin (2019) Determining the Cause of Recurrent Miscarriages in a Couple: Importance of NOR in the Era of NGS. Journal of Reproduction and Infertility, 20 (2). pp. 109-114. ISSN 2228-5482

Dutta, Usha and Vempally, S. and Ranganath, P. and Dalal, Ashwin (2014) A novel combined 15q11.2 duplication and a bisatellited supernumerary marker derived from chromosome 22: molecular characterization of the marker. Gene, 539 (1). pp. 162-7. ISSN 1879-0038

Dutta, Usha and Rajitha, Ponnala and Dalal, Ashwin (2014) A Novel de novo Balanced Reciprocal Translocation t(18;22) Associated with Recurrent Miscarriages: A Case Report. Journal of Reproduction and Infertility, 15 (2). pp. 113-116. ISSN 2251-676X

G

Giri, D.A. and Pankajam, A.V. and Nishant, K.T. and Kasbekar, D.P. (2019) The Neurospora crassa Standard Oak Ridge Background Exhibits Atypically Efficient Meiotic Silencing by Unpaired DNA. G3 Genes Genomes Genetics, 9 (5). pp. 1487-1496. ISSN 2160-1836

Girisha, K.M. and Pande, Shruti and Dalal, Ashwin and Phadke, S.R. (2020) Untapped opportunities for rare disease gene discovery in India. American Journal of Medical Genetics Part A. ISSN 1552-4825 (In Press)

Gowrishankar, J. (2015) End of the Beginning: Elongation and Termination Features of Alternative Modes of Chromosomal Replication Initiation in Bacteria. PLOS Genetics, 11 (1). e1004909. ISSN 1553-7390

Gupta, A. and Uttarilli, Anusha and Dalal, Ashwin and Girisha, K.M. (2015) Hunter syndrome with late age of presentation: clinical description of a case and review of the literature. BMJ Case Reports, 2015. ISSN 1757-790X

H

Hegde, S.R. and Pal, K. and Mande, S.C. (2014) Differential enrichment of regulatory motifs in the composite network of protein-protein and gene regulatory interactions. BMC Systems Biology, 8. p. 26. ISSN 1752-0509

K

Kalyani, B.S. and Kunamneni, R. and Wal, Megha and Ranjan, Amitabh and Sen, Ranjan (2015) A NusG paralogue from Mycobacterium tuberculosis, Rv0639, has evolved to interact with ribosomal protein S10 (Rv0700) but not to function as a transcription elongation-termination factor. Microbiology (Reading, England), 161 (Pt 1). pp. 67-83. ISSN 1465-2080

Kantaputra, P.N. and Kayserili, H. and Guven, Y. and Kantaputra, W. and Balci, M.C. and Tanpaiboon, P. and Tananuvat, N. and Uttarilli, Anusha and Dalal, Ashwin (2014) Clinical manifestations of 17 patients affected with mucopolysaccharidosis type VI and eight novelARSBmutations. American Journal of Medical Genetics Part A, 164 (6). pp. 1443-1453. ISSN 1552-4825

Kantaputra, P.N. and Kayserili, H. and Guven, Y. and Kantaputra, W. and Balci, M.C. and Tanpaiboon, P. and Uttarilli, Anusha and Dalal, Ashwin (2014) Oral manifestations of 17 patients affected with mucopolysaccharidosis type VI. Journal of Inherited Metabolic Disease, 37 (2). pp. 263-8. ISSN 1573-2665

Karthik, T. and Ranganath, P. and Ramachandran, A. and Uppin, M.S. and Sreeja, P. and Aggarwal, Shagun and Lakshmi, D. and Meena, A.K. and Dalal, Ashwin (2019) Molecular and Histopathological Characterization of Patients Presenting with the Duchenne Muscular Dystrophy Phenotype in a Tertiary Care Center in Southern India. Indian Pediatrics, 56 (7). pp. 556-559. ISSN 0019-6061

Kasbekar, D.P. (2020) Fungal senescence induced by the Neurospora sen mutation and mitochondrial plasmids - the contributions of Ramesh Maheshwari. International Journal of Developmental Biology, 64 (1-3). pp. 29-34. ISSN 0214-6282

Kasbekar, D.P. (2020) Neurospora exhibits the highest known non-viral mutation rate. Current Science, 119 (5). p. 737. ISSN 0011-3891

Kasbekar, D.P. (2019) A cross-eyed geneticist’s view III. Mouse chromosomes take a drive. Journal of Biosciences, 44 (2). p. 51. ISSN 0250-5991

Kasbekar, D.P. (2019) A cross-eyed geneticist’s view IV. Neurospora genes and inversions collude to cheat Mendel. Journal of Biosciences, 44 (4). p. 83. ISSN 0250-5991

Kasbekar, D.P. (2019) A cross-eyed geneticist’s view V. How Sydney Brenner, Leslie Barnett, Eugene Katz, and Francis Crick inferred that UGA is a nonsense codon. Journal of Biosciences, 44 (6). pp. 134-135. ISSN 0250-5991

Kasbekar, D.P. (2020) A cross-eyed geneticist’s view VI. Segregation distortion in Drosophila melanogaster: Recent progress in solving ‘an esoteric puzzle’. Journal of Biosciences, 45. e0139. ISSN 0250-5991

Komaravalli, Prasanna Latha and Vasantha Rani, S. and Dalal, Ashwin and Jahan, Parveen (2020) Association analysis of FMR1 genetic variants and Primary Ovarian Insufficiency in South Indian women with a novel approach of CGG repeats classification. European Journal of Medical Genetics, 63 (12). p. 104081. ISSN 1769-7212

Kumari, Sonam and Kumar, Mohit and Khandelwal, N.K. and Pandey, A.K. and Bhakt, Priyanka and Kaur, Rupinder and Prasad, Rajendra and Gaur, N.A. (2020) A homologous overexpression system to study roles of drug transporters in Candida glabrata. FEMS Yeast Research, 20 (4). foaa032. ISSN 1567-1356

L

Love, J.M. and Prosser, D. and Love, D.R. and Krishnaprasad, C. and Dalal, Ashwin and Aggarwal, Shagun (2014) A novel glycine decarboxylase gene mutation in an Indian family with nonketotic hyperglycinemia. Journal of Child Neurology, 29 (1). pp. 122-7. ISSN 1708-8283

M

Meccariello, A. and Salvemini, M. and Primo, P. and Hall, B. and Koskinioti, P. and Dalíková, M. and Gravina, A. and Gucciardino, M.A. and Forlenza, F. and Gregoriou, M.-E. and Ippolito, D. and Monti, S.M. and Petrella, V. and Perrotta, M.M. and Schmeing, S. and Ruggiero, A. and Scolari, F. and Giordano, E. and Tsoumani, K.T. and Marec, F. and Windbichler, N. and Arunkumar, K.P. and Bourtzis, K. and Mathiopoulos, K.D. and Ragoussis, J. and Vitagliano, L. and Tu, Z. and Papathanos, P.A. and Robinson, M.D. and Saccone, G. (2019) Maleness-on-the-Y (MoY) orchestrates male sex determination in major agricultural fruit fly pests. Science, 365 (6460). pp. 1457-1460. ISSN 0036-8075

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Nagaraju, J. (2002) Application of genetic principles for improving silk production. Current Science, 83 (4). pp. 409-414. ISSN 0011-3891

Nagaraju, J. (2000) Recent advances in the silkworm, Bombyx mori. Current Science , 78 (2). pp. 151-161. ISSN 0011-3891

Nagaraju, J. and Goldsmith, M.R. (2002) Silkworm genomics - progress and prospects. Current Science, 83 (4). pp. 415-425. ISSN 0011-3891

Nagaraju, J. and Gopinath, G. and Sharma, V. and Shukla, J.N. (2014) Lepidopteran sex determination: a cascade of surprises. Sexual Development, 8 (1-3). pp. 104-12. ISSN 1661-5433

Nagaraju, J. and Kathirvel, M. and Kumar, R.R. and Siddiq, E.A. and Hasnain, S.E. (2002) Genetic analysis of traditional and evolved Basmati and non-Basmati rice varieties by using fluorescence-based ISSR-PCR and SSR markers. Proceedings of the National Academy of Sciences, 99 (9). pp. 5836-5841. ISSN 0027-8424

Nagaraju, J. and Singh, Lalji (1997) Assessment of genetic diversity by DNA profiling and its significance in silkworm,Bombyx mori. Electrophoresis, 18 (9). pp. 1676-1681. ISSN 0173-0835

Nampoothiri, S. and Yesodharan, D. and Bhattacherjee, Amrita and Ahamed, H. and Puri, R.D. and Gupta, N. and Kabra, M. and Ranganath, Prajnya and Bhat, M. and Phadke, S.R. and Radha Rama Devi, A. and Jagadeesh, S. and Danda, S. and Sylaja, P.N. and Mandal, K. and Bijarnia‐Mahay, S. and Makkar, R. and Verma, I.C. and Dalal, Ashwin and Ramaswami, U. (2020) Fabry disease in India: A multicenter study of the clinical and mutation spectrum in 54 patients. JIMD Reports, 56 (1). pp. 82-94. ISSN 2192-8312

Naushad, S.M. and Krishnaprasad, C. and Radha Rama Devi, A. (2014) Adaptive developmental plasticity in methylene tetrahydrofolate reductase (MTHFR) C677T polymorphism limits its frequency in South Indians. Molecular Biology Reports, 41 (5). pp. 3045-50. ISSN 1573-4978

Nerakh, Gayatri and Tandon, A. and Dalal, Ashwin and Aggarwal, Shagun (2019) Exome Sequencing Identifies RET Associated Hirschsprung Disease in a Fetus with Echogenic Bowel. Journal of Fetal Medicine, 6 (3). pp. 151-154. ISSN 2348-1153

P

Pan, Y.E. and Tibbe, D. and Harms, F.L. and Reißner, C. and Becker, K. and Dingmann, B. and Mirzaa, G. and Kattentidt‐Mouravieva, A.A. and Shoukier, M. and Aggarwal, Shagun and Missler, M. and Kutsche, K. and Kreienkamp, H.J. (2020) Missense mutations in CASK, coding for the calcium‐/calmodulin‐dependent serine protein kinase, interfere with neurexin binding and neurexin‐induced oligomerization. Journal of Neurochemistry. ISSN 0022-3042 (In Press)

Pandey, S.D. and Choudhury, Mitali and Yousuf, S. and Wheeler, P.R. and Gordon, S.V. and Ranjan, Akash and Sritharan, Manjula (2014) Iron-Regulated Protein HupB of Mycobacterium tuberculosis Positively Regulates Siderophore Biosynthesis and Is Essential for Growth in Macrophages. Journal of Bacteriology, 196 (10). pp. 1853-1865. ISSN 0021-9193

Panicker, S.G. and Reddy, A.B.M. and Mandal, A.K. and Ahmed, N. and Nagarajaram, H.A. and Hasnain, S.E. and Balasubramanian, D. (2002) Identification of novel mutations causing familial primary congenital glaucoma in Indian pedigrees. Investigative Ophthalmology & Visual Science, 43 (5). pp. 1358-66. ISSN 0146-0404

Panicker, S.G. and Sampath, S. and Mandal, A.K. and Reddy, A.B.M. and Ahmed, N. and Hasnain, S.E. (2002) Novel mutation in FOXC1 wing region causing Axenfeld-Rieger anomaly. Investigative Ophthalmology & Visual Science, 43 (12). pp. 3613-3616. ISSN 0146-0404

Patil, S.J. and Rai, G.K. and Bhat, V. and Ramesh, V.A. and Nagarajaram, H.A. and Matalia, J. and Phadke, S.R. (2014) Distal Arthrogryposis Type 5D With a Novel ECEL1 Gene Mutation. American Journal of Medical Genetics Part A, 164A (11). pp. 2857-2862. ISSN 1552-4833

Prabhakara, K. and Dutta, Usha and Radha Rama Devi, A. (2002) A partial 15q22 trisomy arising due to segregation of maternal 10;15 reciprocal translocation. Indian Pediatrics, 39 (11). pp. 1050-1054. ISSN 0019-6061

Pradhan, B.B. and Chatterjee, Subhadeep (2014) Reversible non-genetic phenotypic heterogeneity in bacterial quorum sensing. Molecular Microbiology, 92 (3). pp. 557-69. ISSN 1365-2958

Prasad, M.D. and Nurminsky, D.L. and Nagaraju, J. (2002) Characterization and molecular phylogenetic analysis of mariner elements from wild and domesticated species of silkmoths. Molecular Phylogenetics and Evolution, 25 (1). pp. 210-17. ISSN 1055-7903

R

Radha Rama Devi, A. and Prabhakara, K. and Dutta, Usha (2002) Familial (11;21)(p13;q22)pat balanced reciprocal translocation in a female child with regression of milestones. Annales de Génétique, 45 (1). pp. 13-5. ISSN 0003-3995

Raghavendra, V. and Chatterjee, Nirupama and Haldar, Devyani (2020) Cellular environment controls the dynamics of histone H3 lysine 56 acetylation in response to DNA damage in mammalian cells. Journal of Biosciences, 45 (1). p. 19. ISSN 0250-5991

Ram, B.M. and Ramakrishna, Gayatri (2014) Endoplasmic reticulum vacuolation and unfolded protein response leading to paraptosis like cell death in cyclosporine A treated cancer cervix cells is mediated by cyclophilin B inhibition. Biochimica et Biophysica Acta - Molecular Cell Research , 1843 (11). pp. 2497-2512. ISSN 0167-4889

Raman, R. and Kotapalli, V. and Adduri, R.S.R. and Gowrishankar, S. and Bashyam, L. and Chaudhary, A. and Mohana Vamsy, C. and Patnaik, S. and Srinivasulu, M. and Sastry, R.A. and Rao, S. and Vasala, A. and Kalidindi, N.R. and Pollack, J.R. and Murthy, S. and Bashyam, M.D. (2014) Evidence for possible non-canonical pathway(s) driven early-onset colorectal cancer in India. Molecular Carcinogenesis, 53 (S1). E181-E186. ISSN 1098-2744

Ranganath, Prajnya and Sreeja, P. and Nair, Lekshmi and Pramod Kumar, P. and Aparna , Shankar and Sakthivel, M. and Dalal, Ashwin (2020) A newly recognized multiple malformation syndrome with caudal regression associated with a biallelic c.402G>A variant in TBX4. European Journal of Human Genetics, 28 (5). pp. 669-673. ISSN 1018-4813

Reddy, A.B.M. and Panicker, S.G. and Mandal, A.K. and Hasnain, S.E. and Balasubramanian, D. (2003) Identification of R368H as a PredominantCYP1B1Allele Causing Primary Congenital Glaucoma in Indian Patients. Investigative Opthalmology & Visual Science, 44 (10). p. 4200. ISSN 1552-5783

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Rekha, Selvam and Kasbekar, D.P. (2020) A transmission ratio distortion and the ‘max-4’ ascus phenotype: Do both reflect the same Bateson-Dobzhansky-Muller Incompatibility emerging during trans-species introgression of translocations in Neurospora? Journal of Biosciences, 45 (1). p. 24. ISSN 0250-5991

Rungsung, I. and Sahay, M. and Dalal, Ashwin (2020) Digenic variations of human COL4A3 and COL4A4 genes result in early onset renal failure. Gene Reports, 19. p. 100602. ISSN 2452-0144

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Sackton, T.B. and Corbett-Detig, R.B. and Nagaraju, J. and Vaishna, L. and Arunkumar, K.P. and Hartl, D.L.. (2014) Positive selection drives faster-Z evolution in silkmoths. Evolution, 68 (8). pp. 2331-2342. ISSN 0014-3820

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Samaranayake, N. and Dissanayaka, P. and Gunarathna, I. and Gonawala, L. and Wijekoon, N. and Rathnayake, P. and Sirisena, D. and Gunasekara, H. and Dissanayake, A. and Senanayake, S. and Anand, Akshay and Satyamoorthy, K. and Dalal, Ashwin and de Silva, K.R.D. (2020) What We Fail to See in Neuro-Genetic Diseases: A Bird’s Eye View from the Developing World. Annals of Neurosciences. 097275312095006. ISSN 0972-7531 (In Press)

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Sanyal, Rajeshree and Singh, Vani and Harinarayanan, R. (2019) A novel gene contributing to the initiation of fatty acid biosynthesis in Escherichia coli. Journal of Bacteriology, 201 (19). e00354-19. ISSN 0021-9193

Sanyal, Rajeshree and Vimala, A. and Harinarayanan, R. (2020) Studies on the Regulation of (p)ppGpp Metabolism and Its Perturbation Through the Over-Expression of Nudix Hydrolases in Escherichia coli. Frontiers in Microbiology, 11. e562804. ISSN 1664-302X

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Sharma, G. and Upadhyay, S. and Srilalitha, M. and Nandicoori, V.K. and Khosla, Sanjeev (2015) The interaction of mycobacterial protein Rv2966c with host chromatin is mediated through non-CpG methylation and histone H3/H4 binding. Nucleic Acids Research, 43 (8). pp. 3922-37. ISSN 1362-4962

Sharma, V. and Nandineni, M.R. (2014) Assessment of genetic diversity among Indian potato (Solanum tuberosum L.) collection using microsatellite and retrotransposon based marker systems. Molecular Phylogenetics and Evolution, 73. pp. 10-7. ISSN 1095-9513

Shetty, K. and Sarma, A.S. and Devan, Meera and Dalal, Ashwin and Dash, G.K. and Jannabhatla, A. and Patil, S.J. (2020) Recurrent <i>ADCY5</i> Mutation in Mosaic Form with Nocturnal Paroxysmal Dyskinesias and Video Electroencephalography Documentation of Dramatic Response to Caffeine Treatment. Journal of Movement Disorders, 13 (3). pp. 238-240. ISSN 2005-940X

Siddiqi, N. and Shamim, M. and Amin, A. and Chauhan, D.S. and Das, R. and Srivastava, K. and Singh, D. and Sharma, V.D. and Katoch, V.M. and Sharma, S.K. and Hanief, M. and Hasnain, S.E. (2001) Typing of drug resistant isolates of Mycobacterium tuberculosis from India using the IS6110 element reveals substantive polymorphism. Infection, Genetics and Evolution, 1 (2). pp. 109-116. ISSN 1567-1348

Singh, C.P. and Singh, J. and Nagaraju, J. (2014) bmnpv-miR-3 facilitates BmNPV infection by modulating the expression of viral P6.9 and other late genes in Bombyx mori. Insect Biochemistry and Molecular Biology, 49. pp. 59-69. ISSN 1879-0240

Singh, C.P. and Vaishna, L. and Kakkar, Akanksha and Arunkumar, K.P. and Nagaraju, J. (2014) Characterization of antiviral and antibacterial activity of Bombyx mori seroin proteins. Cellular Microbiology, 16 (9). pp. 1354-1365. ISSN 1462-5822

Singh, Mugdha and Sarkar, A. and Kumar, Devinder and Nandineni, M.R. (2020) The genetic affinities of Gujjar and Ladakhi populations of India. Scientific Reports, 10 (1). p. 2055. ISSN 2045-2322

Singh, S. and Kumar, P.U. and Thakur, S. and Shashi Kiran, and Sen, B. and Sharma, S. and Rao, V.V. and Poongothai , A.R. and Ramakrishna, Gayatri (2015) Expression/localization patterns of sirtuins (SIRT1, SIRT2, and SIRT7) during progression of cervical cancer and effects of sirtuin inhibitors on growth of cervical cancer cells. Tumor Biology, 36 (8). pp. 6159-6171. ISSN 1010-4283

Srivastava, Varsha and Prabhakar Rao, K. and Surekha Rani, H. and Kumawat, R.K. and Mishra, Aditi and Shrivastava, Pankaj (2020) Genomic diversity in the Goud population of Telangana, India inferred using twenty three autosomal marker PowerPlex® Fusion 6C System. Meta Gene, 25. p. 100718. ISSN 2214-5400

Srivastava, Varsha and Surekha Rani, H. and Kumawat, R.K. and Chaubey, Gyaneshwer and Shrivastava, Pankaj (2020) Genomic diversity of the Muslim population from Telangana (India) inferred from 23 autosomal STRs. Annals of Human Biology. ISSN 0301-4460 (In Press)

Stephen, J. and Girisha, K.M. and Dalal, Ashwin and Shukla, A. and Shah, H. and Srivastava, P. and Kornak, U. and Phadke, S.R. (2015) Mutations in patients with osteogenesis imperfecta from consanguineous Indian families. European Journal of Medical Genetics, 58 (1). pp. 21-27. ISSN 1878-0849

Stephen, J. and Shukla, A. and Dalal, Ashwin and Girisha, K.M. and Shah, H. and Gupta, N. and Kabra, M. and Dabadghao, P. and Phadke, S.R. (2014) Mutation spectrum of COL1A1 and COL1A2 genes in Indian patients with osteogenesis imperfecta. American Journal of Medical Genetics. Part A, 164A (6). pp. 1482-1489. ISSN 1552-4833

T

Thamban, Thushara and Agarwaal, Viplove and Khosla, Sanjeev (2020) Role of genomic imprinting in mammalian development. Journal of Biosciences, 45 (1). p. 20. ISSN 0250-5991

Tsurusaki, Y. and Okamoto, N. and Ohashi, H. and Mizuno, S. and Matsumoto, N. and Makita, Y. and Fukuda, M. and Isidor, B. and Perrier, J. and Aggarwal, Shagun and Dalal, Ashwin and Al-Kindy, A. and Liebelt, J. and Mowat, D. and Nakashima, M. and Saitsu, H. and Miyake, N. and Matsumoto, N. (2014) Coffin-Siris syndrome is a SWI/SNF complex disorder. Clinical Genetics, 85 (6). pp. 548-554. ISSN 1399-0004

Tyagi, Rahul and Kumar, Sumit and Dalal, Ashwin and Mohammed, Faruq and Mohanty, Manju and Kaur, Paramvir and Anand , Akshay (2019) Repurposing Pathogenic Variants of DMD Gene and its Isoforms for DMD Exon Skipping Intervention. Current Genomics, 20 (7). pp. 519-530. ISSN 1389-2029

V

Vignesh, Pandiarajan and Sharma, Madhubala and Pilania, R.K. and Shandilya, J.K. and Kaur, Anit and Goel, Shubham and Kaur, Anupriya and Suri, Deepti and Rawat, Amit and Dalal, Ashwin and Sarma, A.S. and Singh, Surjit (2019) Myriad Faces of Chronic Granulomatous Disease: All in an Indian Family with Novel CYBB Defect. Journal of Clinical Immunology, 39 (6). pp. 611-615. ISSN 0271-9142