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Possible role of rare variants in Trace amine associated receptor 1 in schizophrenia

Schizophrenia research, 2017-11, Vol.189, p.190-195

2017

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447. Large-Scale Mendelian Randomization Study Reveals Circulating Blood-Based Proteomic Biomarkers for Psychopathology and Cognitive Task Performance

Biological psychiatry (1969), 2024-05, Vol.95 (10), p.S282-S283

2024

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402. Using Cognitive Phenotypes to Parse Biological Pathways in Schizophrenia

Biological psychiatry (1969), 2024-05, Vol.95 (10), p.S264-S264

2024

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425. Integrative Analysis of Neuroimaging Phenotypes and Genetic Associations in the UK Biobank

Biological psychiatry (1969), 2024-05, Vol.95 (10), p.S274-S274

2024

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Association of common and rare genetic variants with cognition in schizophrenia

Canadian Journal of Biotechnology, 2017-10, Vol.1 (Special Issue), p.89-89

2017

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89. PLEIOTROPIC META-ANALYSIS WITH COGNITIVE ENDOPHENOTYPES DIFFERENTIATES NEURODEVELOPMENTAL, SYNAPTIC, AND APOPTOTIC PATHWAYS IN SCHIZOPHRENIA

European neuropsychopharmacology, 2023-10, Vol.75, p.S103-S104

2023

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F85. PROTEOMIC MENDELIAN RANDOMIZATION REVEALS NOVEL MOLECULAR PATHWAYS IN SCHIZOPHRENIA

European neuropsychopharmacology, 2023-10, Vol.75, p.S265-S266

2023

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Illumination Compensated images for surface roughness evaluation using machine vision in grinding process

Procedia manufacturing, 2019, Vol.34, p.969-977

2019

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Whole exome sequencing in familial primary comitant exotropia

Journal of AAPOS, 2018-08, Vol.22 (4), p.e68-e68

2018

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Rare Variants in Tissue Inhibitor of Metalloproteinase 2 as a Risk Factor for Schizophrenia: Evidence From Familial and Cohort Analysis

Schizophrenia bulletin, 2019-01, Vol.45 (1), p.256-263

2019

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Multiple rare inherited variants in a four generation schizophrenia family offer leads for complex mode of disease inheritance

Schizophrenia research, 2020-02, Vol.216, p.288-294

2020

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Rare And Ultra-Rare Variants In Familial Schizophrenia - An Update From India

European neuropsychopharmacology, 2019, Vol.29, p.S744-S745

2019

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SA120FAMILY BASED RARE VARIANT STUDY SUPPORTS THE CUMULATIVE CONTRIBUTION OF NEURODEVELOPMENTAL PATHWAY GENES IN SCHIZOPHRENIA ETIOLOGY

European neuropsychopharmacology, 2019, Vol.29, p.S1254-S1255

2019

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Rare variant based evidence for oligogenic contribution of neurodevelopmental pathway genes to schizophrenia

Schizophrenia research, 2019-08, Vol.210, p.296-298

2019

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Rare variants in Protein tyrosine phosphatase, receptor type A (PTPRA) in schizophrenia: Evidence from a family based study

Schizophrenia research, 2019-04, Vol.206, p.75-81

2019

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Smart Resource Planning for Live Migration in Edge Computing for Industrial Scenario

2019 7th IEEE International Conference on Mobile Cloud Computing, Services, and Engineering (MobileCloud), 2019, p.30-37

2019

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Findings From Continuing Gene Hunt In Families With Schizophrenia

European neuropsychopharmacology, 2017, Vol.27, p.S490-S490

2017

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Association study of MiRSNPs with schizophrenia, tardive dyskinesia and cognition

Schizophrenia research, 2016-07, Vol.174 (1-3), p.29-34

2016

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A Prospective Study Of Prescription Pattern and Assessing the Psychiatric Co-Morbidities In Dementia Patients In A Tertiary Care Hospital In South Kerala

American journal of pharmacy and health research, 2020-09, Vol.8 (9), p.1-17

2020

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Pedigree Analysis of Familial Primary Concomitant Horizontal Strabismus in Northern India

Strabismus, 2017-10, Vol.25 (4), p.200-213

2017

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Role of miRNA binding site SNPs in candidate genes in a North Indian schizophrenia cohort

Molecular cytogenetics, 2014-01, Vol.7 (Suppl 1), p.P91-P91

2014

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Awareness of treatment options for dengue fever among the patients and their relatives attending a tertiary care hospital in central Kerala

Journal of current research in scientific medicine, 2018, Vol.4 (1), p.30-36

2018

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Hardware Implementation of Machine Vision System for Component Detection

Emerging Research in Computing, Information, Communication and Applications, 2022, Vol.928, p.519-535

2022

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Variations in management of A3 and A4 cervical spine fractures as designated by the AO Spine Subaxial Injury Classification System

Journal of neurosurgery. Spine, 2022-01, Vol.36 (1), p.99

2022

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A new (q, S) policy to manage inventory for low shelf life products facing deterioration in quality and age differentiated requirements

Computers & industrial engineering, 2022-11, Vol.173, p.108706, Article 108706

2022

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Possible role of rare variants in Trace amine associated receptor 1 in schizophrenia

447. Large-Scale Mendelian Randomization Study Reveals Circulating Blood-Based Proteomic Biomarkers for Psychopathology and Cognitive Task Performance

402. Using Cognitive Phenotypes to Parse Biological Pathways in Schizophrenia

425. Integrative Analysis of Neuroimaging Phenotypes and Genetic Associations in the UK Biobank

Association of common and rare genetic variants with cognition in schizophrenia

89. PLEIOTROPIC META-ANALYSIS WITH COGNITIVE ENDOPHENOTYPES DIFFERENTIATES NEURODEVELOPMENTAL, SYNAPTIC, AND APOPTOTIC PATHWAYS IN SCHIZOPHRENIA

F85. PROTEOMIC MENDELIAN RANDOMIZATION REVEALS NOVEL MOLECULAR PATHWAYS IN SCHIZOPHRENIA

Illumination Compensated images for surface roughness evaluation using machine vision in grinding process

Whole exome sequencing in familial primary comitant exotropia

Rare Variants in Tissue Inhibitor of Metalloproteinase 2 as a Risk Factor for Schizophrenia: Evidence From Familial and Cohort Analysis

Multiple rare inherited variants in a four generation schizophrenia family offer leads for complex mode of disease inheritance

Rare And Ultra-Rare Variants In Familial Schizophrenia - An Update From India

SA120FAMILY BASED RARE VARIANT STUDY SUPPORTS THE CUMULATIVE CONTRIBUTION OF NEURODEVELOPMENTAL PATHWAY GENES IN SCHIZOPHRENIA ETIOLOGY

Rare variant based evidence for oligogenic contribution of neurodevelopmental pathway genes to schizophrenia

Rare variants in Protein tyrosine phosphatase, receptor type A (PTPRA) in schizophrenia: Evidence from a family based study

Smart Resource Planning for Live Migration in Edge Computing for Industrial Scenario

Findings From Continuing Gene Hunt In Families With Schizophrenia

Association study of MiRSNPs with schizophrenia, tardive dyskinesia and cognition

A Prospective Study Of Prescription Pattern and Assessing the Psychiatric Co-Morbidities In Dementia Patients In A Tertiary Care Hospital In South Kerala

Pedigree Analysis of Familial Primary Concomitant Horizontal Strabismus in Northern India

Role of miRNA binding site SNPs in candidate genes in a North Indian schizophrenia cohort

Awareness of treatment options for dengue fever among the patients and their relatives attending a tertiary care hospital in central Kerala

Hardware Implementation of Machine Vision System for Component Detection

Variations in management of A3 and A4 cervical spine fractures as designated by the AO Spine Subaxial Injury Classification System

A new (q, S) policy to manage inventory for low shelf life products facing deterioration in quality and age differentiated requirements

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