Delusions, Hallucinations, and Cognitive Decline in Middle Age: A Case of Dementia, GIGYF2 Gene Mutation, and 22q11 Duplication
Nadella, Ravi Kumar, Pulaparambil, Vani, Vemula, Alekhya, Swathi Lakshmi P., Saini, Jitender, Nagaraj, Chandana, Purushottam, Meera, Viswanath, Biju, Sullivan, Patrick F., Jain, Sanjeev
Published in Indian journal of psychological medicine (01.05.2023)
Published in Indian journal of psychological medicine (01.05.2023)
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Journal Article
Whole exome sequencing in dense families suggests genetic pleiotropy amongst Mendelian and complex neuropsychiatric syndromes
Ganesh, Suhas, Vemula, Alekhya, Bhattacharjee, Samsiddhi, Mathew, Kezia, Ithal, Dhruva, Navin, Karthick, Nadella, Ravi Kumar, Viswanath, Biju, Sullivan, Patrick F, Jain, Sanjeev, Purushottam, Meera
Published in Scientific reports (07.12.2022)
Published in Scientific reports (07.12.2022)
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Journal Article
Analysis of whole exome sequencing in severe mental illness hints at selection of brain development and immune related genes
Mahadevan, Jayant, Pathak, Ajai Kumar, Vemula, Alekhya, Nadella, Ravi Kumar, Viswanath, Biju, Jain, Sanjeev, Purushottam, Meera, Mondal, Mayukh
Published in Scientific reports (26.10.2021)
Published in Scientific reports (26.10.2021)
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Journal Article
Abnormalities in the migration of neural precursor cells in familial bipolar disorder
Sukumaran, Salil K, Paul, Pradip, Guttal, Vishwesha, Holla, Bharath, Vemula, Alekhya, Bhatt, Harsimar, Bisht, Piyush, Mathew, Kezia, Nadella, Ravi K, Varghese, Anu Mary, Kalyan, Vijayalakshmi, Purushottam, Meera, Jain, Sanjeev, Consortium, Adbs, Sud, Reeteka, Viswanath, Biju
Published in Disease models & mechanisms (01.10.2022)
Published in Disease models & mechanisms (01.10.2022)
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W60. ANALYSIS OF WHOLE EXOME SEQUENCING IN SEVERE MENTAL ILLNESS HINTS AT SELECTION OF BRAIN DEVELOPMENT AND IMMUNE RELATED GENES
Mahadevan, Jayant, Pathak, Ajai Kumar, Vemula, Alekhya, Nadella, Ravikumar, Viswanath, Biju, Purushottam, Meera, Jain, Sanjeev, Mondal, Mayukh
Published in European neuropsychopharmacology (01.10.2021)
Published in European neuropsychopharmacology (01.10.2021)
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Exome hits demystified: The next frontier
Ithal, Dhruva, Sukumaran, Salil K., Bhattacharjee, Debanjan, Vemula, Alekhya, Nadella, Ravi, Mahadevan, Jayant, Sud, Reeteka, Viswanath, Biju, Purushottam, Meera, Jain, Sanjeev
Published in Asian journal of psychiatry (01.05.2021)
Published in Asian journal of psychiatry (01.05.2021)
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TU82. WHOLE EXOME SEQUENCING IN FAMILIES WITH SERIOUS MENTAL ILLNESSES IDENTIFIES POTENTIALLY DELETERIOUS RARE VARIANTS IN GENES IMPLICATED IN NEURODEVELOPMENT
Jain, Sanjeev, Ganesh, Suhas, Bhattacharjee, Samsiddhi, Vemula, Alekhya, Nadella, Ravikumar, Ithal, Dhruva, Mathew, Kezia, Viswanath, Biju, Purushottam, Meera
Published in European neuropsychopharmacology (01.10.2021)
Published in European neuropsychopharmacology (01.10.2021)
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