Soumya Raychaudhuri

Statistics and Probability · 2009–2021

A researcher in the Science corpus: 28 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.

Subfields

Statistics and Probability — 9 citations into it

Whom Soumya Raychaudhuri trusts overall

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

Who trusts Soumya Raychaudhuri overall

Papers from Soumya Raychaudhuri's perspective

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

Association between microdeletion and microduplication at 16p11.2 and autism. (New England Journal of Medicine)
Principal components analysis corrects for stratification in genome-wide association studies
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease (Nature Genetics)
The human genome browser at UCSC.
The PANTHER database of protein families, subfamilies, functions and pathways (Nucleic Acids Res.)
Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia (Science)
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes (Nature Genetics)
Gradient-based learning applied to document recognition
Deep Residual Learning for Image Recognition (Computer Vision and Pattern Recognition)
A linear complexity phasing method for thousands of genomes (Nature Methods)

Their papers

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes (2012) — 1,982 citations
Fast, sensitive, and accurate integration of single cell data with Harmony (2019) — 8,178 citations
Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease (2012) — 4,566 citations
Partitioning heritability by functional annotation using genome-wide association summary statistics (2015) — 2,445 citations
Biological interpretation of genome-wide association studies using predicted gene functions (2015) — 821 citations
Chromatin marks identify critical cell types for fine mapping complex trait variants (2012) — 604 citations
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis (2010) — 1,860 citations
Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci (2009) — 835 citations
Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types (2017) — 984 citations
Mapping the human genetic architecture of COVID-19 (2021) — 807 citations
The immune cell landscape in kidneys of patients with lupus nephritis (2019) — 693 citations
Distinct fibroblast subsets drive inflammation and damage in arthritis (2019) — 808 citations
Defining inflammatory cell states in rheumatoid arthritis joint synovial tissues by integrating single-cell transcriptomics and mass cytometry (2019) — 1,117 citations
Pathologically expanded peripheral T helper cell subset drives B cells in rheumatoid arthritis (2017) — 995 citations
Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci (2016) — 719 citations
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways (2015) — 750 citations
Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases. (2014) — 595 citations
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility (2014) — 1,017 citations
Imputing Amino Acid Polymorphisms in Human Leukocyte Antigens (2013) — 651 citations
Genetics of rheumatoid arthritis contributes to biology and drug discovery (2013) — 742 citations