Dheeraj Malhotra

Molecular Biology · 2007–2022

A researcher in the Science corpus: 9 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.

Subfields

• Molecular Biology — 130 citations into it

Whom Dheeraj Malhotra trusts overall

Their strongest outbound trust, strongest first, inferred from their citations.

1. M. Lieber

Who trusts Dheeraj Malhotra overall

1. Patrick F. Sullivan

Papers from Dheeraj Malhotra's perspective

Ordered by how strongly the researchers Dheeraj Malhotra trusts endorse each paper. Same corpus, a different order for every researcher.

1. Functional Impact of Global Rare Copy Number Variation in Autism Spectrum Disorder (Nature)
2. Integrated detection and population-genetic analysis of SNPs and copy number variation (Nature Genetics)
3. Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia (Science)
4. Large-Scale Copy Number Polymorphism in the Human Genome (Science)
5. Disruption of two novel genes by a translocation co-segregating with schizophrenia. (Human Molecular Genetics)
6. De Novo Gene Disruptions in Children on the Autistic Spectrum (Neuron)
7. Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets (Nature Genetics)
8. FINEMAP: efficient variable selection using summary data from genome-wide association studies (bioRxiv)
9. Patterns and rates of exonic de novo mutations in autism spectrum disorders
10. Analysis of protein-coding genetic variation in 60,706 humans

Their papers

• muscat detects subpopulation-specific state transitions from multi-sample multi-condition single-cell transcriptomics data (2020) — 376 citations
• Microduplications of 16p11.2 are Associated with Schizophrenia (2009) — 730 citations
• Mapping genomic loci implicates genes and synaptic biology in schizophrenia (2022) — 2,226 citations
• Altered human oligodendrocyte heterogeneity in multiple sclerosis (2019) — 758 citations
• Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects (2016) — 996 citations
• Whole Genome Sequencing in Autism Identifies Hotspots for De Novo Germline Mutation (2012) — 547 citations
• CNVs: Harbinger of a Rare Variant Revolution in Psychiatric Genetics (2012) — 880 citations
• Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia (2008) — 1,770 citations
• Strong Association of De Novo Copy Number Mutations with Autism (2007) — 2,845 citations