An Association Study of Gamma-Aminobutyric Acid Type A Receptor Variants and Susceptibility to Autism Spectrum Disorders von Adak, Pallabi, Sinha, Swagata, Banerjee, Nilanjana

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Indian ASD probands with 25(OH)D and vitamin D binding protein deficiency exhibited higher severity von Shom, Sayanti, Saha, Sharmistha, Chatterjee, Mahasweta, Sinha, Swagata, Mukhopadhyay, Kanchan

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Metabotropic glutamate receptor genetic variants and peripheral receptor expression affects trait scores of autistic probands von Dutta, Nilanjana, Chatterjee, Mahasweta, Saha, Sharmistha, Sinha, Swagata, Mukhopadhyay, Kanchan

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A pioneering study indicate role of GABRQ rs3810651 in ASD severity of Indo-Caucasoid female probands von Saha, Sharmistha, Chatterjee, Mahasweta, Sinha, Swagata, Mukhopadhyay, Kanchan

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Kainate receptor subunit 1 (GRIK1) risk variants and GRIK1 deficiency were detected in the Indian ADHD probands von Chatterjee, Mahasweta, Saha, Sharmistha, Dutta, Nilanjana, Sinha, Swagata, Mukhopadhyay, Kanchan

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Glutamate receptor genetic variants affected peripheral glutamatergic transmission and treatment induced improvement of Indian ADHD probands von Chatterjee, Mahasweta, Saha, Sharmistha, Shom, Sayanti, Dutta, Nilanjana, Sinha, Swagata, Mukhopadhyay, Kanchan

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Solid lipid nanoparticles for increased oral bioavailability of acalabrutinib in chronic lymphocytic leukaemia von Sinha, Swagata, Ravi, Punna Rao, Somvanshi, Makarand, Rashmi, S. R.

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A three-pronged analysis confirms the association of the serotoninergic system with attention deficit hyperactivity disorder von Chatterjee, Mahasweta, Saha, Sharmistha, Sinha, Swagata, Mukhopadhyay, Kanchan

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Analysis of neurotransmitters validates the importance of the dopaminergic system in autism spectrum disorder von Saha, Sharmistha, Chatterjee, Mahasweta, Dutta, Nilanjana, Sinha, Swagata, Mukhopadhyay, Kanchan

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Functional SLC6A3 polymorphisms differentially affect autism spectrum disorder severity: a study on Indian subjects von Saha, Sharmistha, Chatterjee, Mahasweta, Shom, Sayanti, Sinha, Swagata, Mukhopadhyay, Kanchan

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Analysis of association between components of the folate metabolic pathway and autism spectrum disorder in eastern Indian subjects von Saha, Sharmistha, Saha, Tanusree, Rajamma, Usha, Sinha, Swagata, Mukhopadhyay, Kanchan

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Components of the folate metabolic pathway and ADHD core traits: an exploration in eastern Indian probands von Saha, Tanusree, Chatterjee, Mahasweta, Sinha, Swagata, Rajamma, Usha, Mukhopadhyay, Kanchan

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Cyclin-dependent Kinase 5: Novel role of gene variants identified in ADHD von Maitra, Subhamita, Chatterjee, Mahasweta, Sinha, Swagata, Mukhopadhyay, Kanchan

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Adhesion G protein-coupled receptor L3 gene variants: Statistically significant association observed in the male Indo-caucasoid Attention deficit hyperactivity disorder probands von Chatterjee, Mahasweta, Saha, Sharmistha, Shom, Sayanti, Sinha, Swagata, Mukhopadhyay, Kanchan

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Gender-Specific Effect of 5-HT and 5-HIAA on Threshold Level of Behavioral Symptoms and Sex-Bias in Prevalence of Autism Spectrum Disorder von Chakraborti, Barnali, Verma, Deepak, Guhathakurta, Subhrangshu, Jaiswal, Preeti, Singh, Asem Surindro, Sinha, Swagata, Ghosh, Saurabh, Mukhopadhyay, Kanchan, Mohanakumar, Kochupurackal P, Rajamma, Usha

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A Systematic Review of Interventions Improving University Students’ EFL Writing Competence von Zhang, Dandan, Tan, Joanna Tjin Ai, Sinha Roy, Swagata

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Attention deficit-hyperactivity disorder suffers from mitochondrial dysfunction von Verma, Poonam, Singh, Alpana, Nthenge-Ngumbau, Dominic Ngima, Rajamma, Usha, Sinha, Swagata, Mukhopadhyay, Kanchan, Mohanakumar, Kochupurackal P

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Selective maternal inheritance of risk alleles and genetic interaction between serotonin receptor-1B (5-HTR1B) and serotonin transporter (SLC6A4) in ADHD von Banerjee, Emili, Banerjee, Disha, Chatterjee, Anindita, Sinha, Swagata, Nandagopal, Krishnadas

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Pilot study indicate role of preferentially transmitted monoamine oxidase gene variants in behavioral problems of male ADHD probands von Karmakar, Arijit, Goswami, Rishov, Saha, Tanusree, Maitra, Subhamita, Roychowdhury, Anirban, Panda, Chinmay Kumar, Sinha, Swagata, Ray, Anirban, Mohanakumar, Kochupurackal P, Rajamma, Usha, Mukhopadhyay, Kanchan

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Study on DBH Genetic Polymorphisms and Plasma Activity in Attention Deficit Hyperactivity Disorder Patients from Eastern India von Bhaduri, Nipa, Sarkar, Kanyakumarika, Sinha, Swagata, Chattopadhyay, Anindita, Mukhopadhyay, Kanchan

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