Assistant Professor, Medicine-Brigham and Women's Hospital, Harvard Medical School
Internal Medicine
Dr. Soumya Raychaudhuri, MD
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Dr. Soumya Raychaudhuri is an expert in the field of Internal Medicine. He attended Stanford University School of Medicine. Stanford University School of Medicine is one of the top medical schools in the US. Stanford University School of Medicine is ranked 2 in research and 25 in primary care medicine He has 1 awards "Fellow (FACR)". Soumya Raychaudhuri is also published. He has 41 publications published. The lastest publication: "A general framework for meta-analyzing dependent studies with overlapping subjects in association mapping.' He is registered with Medicare.
Publications
- A general framework for meta-analyzing dependent studies with overlapping subjects in association mapping.
- Partitioning heritability by functional annotation using genome-wide association summary statistics.
- Polymorphisms of large effect explain the majority of the host genetic contribution to variation of HIV-1 virus load.
- Functional implications of disease-specific variants in loci jointly associated to coeliac disease and rheumatoid Arthritis.
- Disproportionate Contributions of Select Genomic Compartments and Cell Types to Genetic Risk for Coronary Artery Disease.
- Rare Variants in the Functional Domains of Complement Factor H Are Associated With Age-Related Macular Degeneration.
- Widespread non-additive and interaction effects within HLA loci modulate the risk of autoimmune Diseases.
- Rare Genetic Variants in the CFI Gene are Associated with Advanced Age-Related Macular Degeneration and Commonly Result in Reduced Serum Factor I Levels.
- Risk for ACPA-positive rheumatoid Arthritis is driven by shared HLA amino acid polymorphisms in Asian and European populations.
- HLA-DRB1-Associated Rheumatoid Arthritis Risk at Multiple Levels in African Americans: Hierarchical Classification Systems, Amino Acid Positions, and Residues.
- A role for noncoding variation in schizophrenia.
- A Novel Test for Recessive Contributions to Complex Diseases Implicates Bardet-Biedl Syndrome Gene BBS10 in Idiopathic Type 2 Diabetes and Obesity.
- Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases.
- Genetic variants in the complement system predisposing to age-related macular degeneration: A review.
- Genetic association study of QT interval highlights role for Calcium signaling pathways in myocardial repolarization.
- Regulation of Gene Expression in Autoimmune Disease Loci and the Genetic Basis of Proliferation in CD4+ Effector Memory T Cells.
- Polarization of the effects of autoimmune and neurodegenerative risk alleles in leukocytes.
- Whole-exome sequencing identifies rare, functional CFH variants in families with macular degeneration.
- SNPsea: an algorithm to identify cell types, tissues, and pathways affected by risk loci.
- Fine Mapping Seronegative and Seropositive Rheumatoid Arthritis to Shared and Distinct HLA Alleles by Adjusting for the Effects of Heterogeneity.
- Common genetic variants modulate pathogen-sensing responses in human dendritic cells.
- Quantifying Missing Heritability at Known GWAS Loci.
- Genetics of rheumatoid Arthritis contributes to biology and drug discovery.
- Application of user-guided automated cytometric data analysis to large-scale immunoprofiling of invariant natural killer T cells.
- Using chromatin marks to interpret and localize genetic associations to complex human traits and Diseases.
- Fast Pairwise IBD Association Testing in Genome-wide Association Studies.
- Rare variants in CFI, C3 and C9 are associated with high risk of advanced age-related macular degeneration.
- Granulomatosis with polyangiitis (Wegener's) is associated with HLA-DPB1*04 and SEMA6A gene variants: Evidence from genome-wide analysis.
- Association between low density lipoprotein and rheumatoid Arthritis genetic factors with low density lipoprotein levels in rheumatoid Arthritis and non-rheumatoid art...
- Human Genetics in Rheumatoid Arthritis Guides a High-Throughput Drug Screen of the CD40 Signaling Pathway.
- Common Risk Alleles for Inflammatory Diseases Are Targets of Recent Positive Selection.
- Genome-Wide Association Study and Gene Expression Analysis Identifies CD84 as a Predictor of Response to Etanercept Therapy in Rheumatoid Arthritis.
- Chromatin marks identify critical cell types for fine mapping complex trait variants.
- Rare, low-frequency, and common variants in the protein-coding sequence of biological candidate genes from GWASs contribute to risk of rheumatoid Arthritis.
- Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders.
- Risk for myasthenia gravis maps to a (151) ProâAla change in TNIP1 and to human leukocyte antigen-B*08.
- Heritability and Genome-Wide Association Study to Assess Genetic Differences between Advanced Age-Related Macular Degeneration Subtypes.
- Rheumatoid Arthritis: Evidence for a genetic component to disease severity in RA.
- Bayesian inference analyses of the polygenic architecture of rheumatoid Arthritis.
- Integration of Sequence Data from a Consanguineous Family with Genetic Data from an Outbred Population Identifies PLB1 as a Candidate Rheumatoid Arthritis Risk Gene.
Schools
Stanford Univ Sch Of Med
Brigham and Women39s Hospital
Procedures Preformed
- Joint Drainage
Conditions Treated
- Arthritis
- Calcium Pyrophosphate Dihydrate Deposition Disease (CPPD)
- Low Back Pain
- OsteoArthritis
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Doctors Specialties
- Rheumatology
- Internal Medicine
Accepted Insurances
Awards
- Fellow (FACR)
Education
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Brigham and Women's Hospital -
Stanford University School of Medicine
Hospital
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Brigham and Women's Hospital
Drug Facts
| NPI NUMBER | 1376659144 | |
| NPPES Provider LastName | RAYCHAUDHURI | |
| NPPES Provider FirstName | SOUMYA | |
| NPPES Provider ZIPCode | 02115 | |
| NPPES Provider State | MA | |
| Specialty Description | Rheumatology | |
| Total Claim Count | 69.0 | |
| Distinct Opioid Count | 0.0 | |
| Opioid Claim Count | 0.0 | |
| Percent Opioid Claims | 0.0 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1376659144 |
| Last Name Of The Provider | RAYCHAUDHURI |
| First Name Of The Provider | SOUMYA |
| View All |
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