Novel Glioblastoma Markers with Diagnostic and Prognostic Value Identified through Transcriptome Analysis von Reddy, Sreekanth P, Britto, Ramona, Vinnakota, Katyayni, Aparna, Hebbar, Sreepathi, Hari Kishore, Thota, Balaram, Kumari, Arpana, Shilpa, B M, Vrinda, M, Umesh, Srikantha, Samuel, Cini, Shetty, Mitesh, Tandon, Ashwani, Pandey, Paritosh, Hegde, Sridevi, Hegde, A S, Balasubramaniam, Anandh, Chandramouli, B A, Santosh, Vani, Kondaiah, Paturu, Somasundaram, Kumaravel, Rao, M R Satyanarayana

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Inadequate Pre-conception Counseling is a Major Challenge for Antenatal Management of β-Thalassemia: Experience from a Referral Centre in India von Shetty, Mitesh, Balakrishna, Sharath, Hegde, Sridevi

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Upregulation of ASCL1 and inhibition of Notch signaling pathway characterize progressive astrocytoma von SOMASUNDARAM, Kumaravel, REDDY, Sreekanth P, SANTOSH, Vani, ALANGAR SATHYARANJANDAS HEGDE, HEGDE, Sridevi, KONDAIAH, Paturu, RAO, M. R. S, VINNAKOTA, Katyayni, BRITTO, Ramona, SUBBARAYAN, Madhavan, NAMBIAR, Sandeep, HEBBAR, Aparna, SAMUEL, Cini, SHETTY, Mitesh, HARI KISHORE SREEPATHI

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Pre- and Postnatal Analysis of Chromosome 1q44 Deletion in Agenesis of Corpus Callosum von Shetty, Mitesh, Srikanth, Ambika, Kadandale, Jayarama, Hegde, Sridevi

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Generation of Induced Pluripotent Stem Cells from Turner Syndrome (45XO) Fetal Cells for Downstream Modelling of Neurological Deficits Associated with the Syndrome von Veerasubramanian, Nivedha, Karthikeyan, Vaishnavi, Hegde, Sridevi, Dhanushkodi, Anandh, Parveen, Shagufta

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Generation of Induced Pluripotent Stem Cells from Turner Syndrome (45XO) Fetal Cells for Downstream Modelling of Neurological Deficits Associated with the Syndrome von Veerasubramanian, Nivedha, Karthikeyan, Vaishnavi, Hegde, Sridevi, Dhanushkodi, Anandh, Parveen, Shagufta

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Shift in AP-2α localization characterizes astrocytoma progression von Britto, Ramona, Umesh, S., Hegde, A., Hegde, Sridevi, Santosh, Vani, Chandramouli, B., Somasundaram, Kumaravel

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Freeman-Sheldon syndrome-prenatal and postnatal diagnosis von Hegde, Sridevi S., Shetty, Mitesh S., Rama Murthy, B. S.

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Culturing Human Tumor Cells: One Source for All von Hegde, Sridevi, Somasundaram, Kumaravel

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Exonic microdeletions in the X-linked PQBP1 gene in mentally retarded patients : a pathogenic mutation and in-frame deletions of uncertain effect von COSSE, Mireille, DEMEER, Bénédicte, HEGDE, Sridevi, SPRINGELL, Kelly, THELMA, B. K, WOODS, Geoffrey, KALSCHEUER, Vera, MANDEL, Jean-Louis, BLANCHET, Patricia, ECHENNE, Bernard, SINGH, Deepika, HAGENS, Olivier, ANTIN, Manuela, FINCK, Sonja, VALLEE, Louis, DOLLFUS, Hélène

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Pre- and Postnatal Diagnosis of 10p14 Deletion and 22q11.2 Deletion Syndrome and Significance of Non-Cardiac Markers von Shetty, Mitesh, Srikanth, Ambika, Kadandale, Jayarama, Hegde, Sridevi

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A Homozygous Missense Variant in INPP5E Associated with Joubert Syndrome and Related Disorders von Shetty, Mitesh, Ramdas, Nimmy, Sahni, Shubhi, Mullapudi, Nandita, Hegde, Sridevi

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Pre- and Postnatal Analysis of Chromosome 15q26.1 and 8p23.1 Deletions in Congenital Diaphragmatic Hernia von Shetty, Mitesh, Kadandale, Jayarama, Hegde, Sridevi

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Pre- and Postnatal Diagnosis of 5q35.1 and 8p23.1 Deletion in Congenital Heart Disease von Shetty, Mitesh, Srikanth, Ambika, Kulshreshtha, Pooja, Kadandale, Jayarama, Hegde, Sridevi

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The A1298C Methylenetetrahydrofolate Reductase Gene Variant as a Susceptibility Gene for Non-Syndromic Conotruncal Heart Defects in an Indian Population von Koshy, Teena, Venkatesan, Vettriselvi, Perumal, Venkatachalam, Hegde, Sridevi, Paul, Solomon Franklin Durairaj

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Effects of an Integrated Yoga Program in Modulating Psychological Stress and Radiation-Induced Genotoxic Stress in Breast Cancer Patients Undergoing Radiotherapy von Banerjee, Birendranath, Vadiraj, H.S., Ram, Amritanshu, Rao, Raghavendra, Jayapal, Manikandan, Gopinath, Kodaganur S., Ramesh, B.S., Rao, Nalini, Kumar, Ajay, Raghuram, Nagarathna, Hegde, Sridevi, Nagendra, H.R., Prakash Hande, M.

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A novel de novo heterozygous deletion at 13q14.2-q21.1 in two siblings with mild intellectual disability von Mittal, Kirti, Kirola, Laxmi, Hegde, Sridevi, Shetty, Mitesh, Kabra, Madhulika, Thelma, B.K.

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Sporadic spinocerebellar ataxia, type 5: First report from India von Mahale, Rohan, Mehta, Anish, Hegde, Sridevi, Buddaraju, Kiran, Javali, Mahendra, Acharya, Purushottam, Srinivasa, Rangasetty

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Differential protein expression in human gliomas and molecular insights von Chumbalkar, Vaibhav C., Subhashini, Chanumolu, Dhople, Vishnu M., Sundaram, Curam S., Jagannadham, Medicharla V., Kumar, Kafnam N., Srinivas, Pasumarti N. B. S., Mythili, Ravinutala, Rao, Mulla K., Kulkarni, Mahesh J., Hegde, Sridevi, Hegde, Alangar S., Samual, Cini, Santosh, Vani, Singh, Lalji, Sirdeshmukh, Ravi

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Single Nucleotide Polymorphism-Based Noninvasive Prenatal Testing: Experience in India von Verma, Ishwar Chander, Puri, Ratna, Venkataswamy, Eswarachary, Tayal, Tulika, Nampoorthiri, Sheela, Andrew, Chitra, Kabra, Madhulika, Bagga, Rashmi, Gowda, Mamatha, Batra, Meenu, Hegde, Sridevi, Kaul, Anita, Gupta, Neerja, Mishra, Pallavi, Subramanian, Jayshree Ganapathi, Lingaiah, Shruti, Akhtar, Riyaz, Kidangan, Francis, Chandran, R., Kiran, C., Ravi Kumar, G. R., Ramprasad, V. L., Kadam, Priya

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