Search Results - "MALHOTRA, Dheeraj"
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CNVs: Harbingers of a Rare Variant Revolution in Psychiatric Genetics
Published in Cell (16-03-2012)“…The genetic bases of neuropsychiatric disorders are beginning to yield to scientific inquiry. Genome-wide studies of copy number variation (CNV) have given…”
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muscat detects subpopulation-specific state transitions from multi-sample multi-condition single-cell transcriptomics data
Published in Nature communications (30-11-2020)“…Single-cell RNA sequencing (scRNA-seq) has become an empowering technology to profile the transcriptomes of individual cells on a large scale. Early analyses…”
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An intelligent approach to design of E-Commerce metasearch and ranking system using next-generation big data analytics
Published in Journal of King Saud University. Computer and information sciences (01-02-2021)“…The purpose of this research work is to explore various limitations of conventional search and page ranking systems in an E-Commerce environment. The key…”
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Whole-Genome Sequencing in Autism Identifies Hot Spots for De Novo Germline Mutation
Published in Cell (21-12-2012)“…De novo mutation plays an important role in autism spectrum disorders (ASDs). Notably, pathogenic copy number variants (CNVs) are characterized by high…”
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Tau Pathology Drives Dementia Risk-Associated Gene Networks toward Chronic Inflammatory States and Immunosuppression
Published in Cell reports (Cambridge) (17-11-2020)“…To understand how neural-immune-associated genes and pathways contribute to neurodegenerative disease pathophysiology, we performed a systematic functional…”
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Machine Learning and Artificial Intelligence in the Food Industry: A Sustainable Approach
Published in Journal of food quality (12-05-2022)“…The goal of this research was to look into how artificial intelligence (AI) and machine learning (ML) techniques are being used in food industry and to come up…”
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High Frequencies of De Novo CNVs in Bipolar Disorder and Schizophrenia
Published in Neuron (Cambridge, Mass.) (22-12-2011)“…While it is known that rare copy-number variants (CNVs) contribute to risk for some neuropsychiatric disorders, the role of CNVs in bipolar disorder is…”
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Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia
Published in Science (American Association for the Advancement of Science) (25-04-2008)“…Schizophrenia is a devastating neurodevelopmental disorder whose genetic influences remain elusive. We hypothesize that individually rare structural variants…”
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Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia
Published in Nature (London) (24-03-2011)“…Rare copy number variants (CNVs) have a prominent role in the aetiology of schizophrenia and other neuropsychiatric disorders. Substantial risk for…”
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Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism
Published in Nature communications (11-04-2014)“…Increased risk for autism spectrum disorders (ASD) is attributed to hundreds of genetic loci . The convergence of ASD variants have been investigated using…”
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IMSS-P: An intelligent approach to design & development of personalized meta search & page ranking system
Published in Journal of King Saud University. Computer and information sciences (01-02-2022)“…The proposed research work aims to discuss and explore various constraints of traditional web page search and ranking systems primarily in the present…”
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Machine Learning Integrated Multivariate Water Quality Control Framework for Prawn Harvesting from Fresh Water Ponds
Published in Journal of food quality (23-01-2023)“…Water contamination, temperature imbalance, feed, space, and cost are key issues that traditional fish farming encounters. The aquaculture business still…”
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Author Correction: Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism
Published in Nature communications (02-02-2023)Get full text
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Reduced transcript expression of genes affected by inherited and de novo CNVs in autism
Published in European journal of human genetics : EJHG (01-06-2011)“…Individuals with autism are more likely to carry rare inherited and de novo copy number variants (CNVs). However, further research is needed to establish which…”
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Data structures and program design using C: a self-teaching introduction / Dheeraj Malhotra, Neha Malhotra
Published 2019“…"Data structures provide a means to manage large amounts of information such as large databases, using SEO, and creating Internet/Web indexing services. The…”
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The Influence of Microdeletions and Microduplications of 16p11.2 on Global Transcription Profiles
Published in Journal of child neurology (01-12-2015)“…Copy number variants (CNVs) of a 600 kb region on 16p11.2 are associated with neurodevelopmental disorders and changes in brain volume. The authors hypothesize…”
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Divergent Levels of Marker Chromosomes in an hiPSC-Based Model of Psychosis
Published in Stem cell reports (14-03-2017)“…In the process of generating presumably clonal human induced pluripotent stem cells (hiPSCs) from two carriers of a complex structural rearrangement, each…”
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Big data analytics for retail industry using MapReduce-Apriori framework
Published in Journal of management analytics (02-07-2020)“…Presently, retailing has changed its face from unordered stacked traditional stores to beautifully decorated and appropriately managed merchandise stores or…”
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Altered human oligodendrocyte heterogeneity in multiple sclerosis
Published in Nature (London) (01-02-2019)“…Oligodendrocyte pathology is increasingly implicated in neurodegenerative diseases as oligodendrocytes both myelinate and provide metabolic support to axons…”
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Cell-type-specific cis-eQTLs in eight human brain cell types identify novel risk genes for psychiatric and neurological disorders
Published in Nature neuroscience (01-08-2022)“…To date, most expression quantitative trait loci (eQTL) studies, which investigate how genetic variants contribute to gene expression, have been performed in…”
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