Assistant Professor of Medicine, Brigham and Women's Hospital
Pulmonology
Dr. Benjamin A. Raby, MD
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Benjamin Raby works in the field of Pulmonology. Benjamin Raby is a published doctor as well. He has 83 publications published. The latest was: A Chronic Obstructive Pulmonary Disease Susceptibility Gene, FAM13A, Regulates Protein Stability of β-catenin. Benjamin Raby accepts Medicare payments and is listed with Medicare.gov.
Publications
- Nuclear bioavailability of the glucocorticoid receptor in a pediatric Asthma cohort with variable corticosteroid responsiveness.
- Anticholinergic vs Long-Acting β-Agonist in Combination With Inhaled Corticosteroids in Black Adults With Asthma: The BELT Randomized Clinical Trial.
- Non-invasive Analysis of the Sputum Transcriptome Discriminates Clinical Phenotypes of Asthma.
- A disease module in the interactome explains disease heterogeneity, drug response and captures novel pathways and genes in Asthma.
- Genome-wide association study and admixture mapping reveal new loci associated with total IgE levels in Latinos.
- Glucocorticoid Genes and the Developmental Origins of Asthma Susceptibility and Treatment Response.
- Genome-wide interaction studies reveal sex-specific Asthma risk alleles.
- β-2 Adrenergic receptor gene methylation is associated with decreased Asthma severity in inner-city Schoolchildren: Asthma and Rhinitis.
- Pharmacogenomics: Novel Loci Identification via Integrating Gene Differential Analysis and eQTL Analysis.
- Copy number variation prevalence in known Asthma genes and their impact on Asthma susceptibility.
- A meta-analysis of genome-wide association studies for serum total IgE in diverse study populations.
- Integration of Mouse and Human Genome-Wide Association Data Identifies KCNIP4 as an Asthma Gene.
- Gene expression analysis uncovers novel hedgehog interacting protein (HHIP) effects in human bronchial epithelial cells.
- Different Polymorphisms of the Mineralocorticoid Receptor Gene Are Associated with either Glucocorticoid or Mineralocorticoid Levels in Hypertension.
- Lysine-Specific Demethylase 1: An Epigenetic Regulator of Salt-Sensitive Hypertension.
- Identification of a Chronic obstructive pulmonary disease genetic determinant that regulates HHIP.
- Replication and meta-analysis of the gene-environment interaction between body mass index and the interleukin-6 promoter polymorphism with higher insulin resistance.
- Cystic Fibrosis mutations for p.F508del compound heterozygotes predict sweat chloride levels and pancreatic sufficiency.
- Quantifying differential gene connectivity between Disease states for objective identification of Disease-relevant genes.
- Variants of the Caveolin-1 Gene: A Translational Investigation Linking Insulin Resistance and Hypertension.
- Renin gene polymorphism: its relationship to hypertension, renin levels and vascular responses.
- Association of SERPINE2 with Asthma.
- The impact of self-identified race on epidemiologic studies of gene expression.
- Global analysis of the impact of environmental perturbation on cis-regulation of gene expression.
- Genetic influences on Asthma susceptibility in the developing lung.
- Risk factors and predictive clinical scores for Asthma exacerbations in childhood.
- On the genome-wide analysis of copy number variants in family-based designs: methods for combining family-based and population-based information for testing dichotomou...
- The relationship between peroxisome proliferator-activated receptor-gamma and renin: a human genetics study.
- Pulmonary function and emphysema in Williams-Beuren syndrome.
- A genome-wide association study on African-ancestry populations for Asthma.
- Stronger evidence for replication of NPPA using genome-wide genotyping data.
- Using canonical correlation analysis to discover genetic regulatory variants.
- MMP12, lung function, and COPD in high-risk populations.
- Allele-specific chromatin remodeling in the ZPBP2/GSDMB/ORMDL3 locus associated with the risk of Asthma and autoimmune disease.
- Genome-wide association study implicates chromosome 9q21.31 as a susceptibility locus for Asthma in mexican children.
- Assessing the reproducibility of Asthma candidate gene associations, using genome-wide data.
- Analysis of exonic elastin variants in severe, early-onset Chronic obstructive pulmonary disease.
- Association of VEGF polymorphisms with childhood Asthma, lung function and airway responsiveness.
- Genome-wide association analysis identifies PDE4D as an Asthma-susceptibility gene.
- Variants in TGFB1, dust mite exposure, and disease severity in children with Asthma.
- Genetic association analysis of copy-number variation (CNV) in human Disease pathogenesis.
- High-resolution melting curve analysis of genomic and whole-genome amplified DNA.
- Genomics and genome-wide association studies: an integrative approach to expression QTL mapping.
- Dust mite exposure modifies the effect of functional IL10 polymorphisms on allergy and Asthma exacerbations.
- Sex-stratified linkage analysis identifies a female-specific locus for IgE to cockroach in Costa Ricans.
- On the replication of genetic associations: timing can be everything!
- On the analysis of copy-number variations in genome-wide association studies: a translation of the family-based association test.
- Paternal Asthma, mold exposure, and increased airway responsiveness among children with Asthma in Costa Rica.
- Genes to diseases (G2D) computational method to identify Asthma candidate genes.
- Filaggrin mutations confer susceptibility to atopic dermatitis but not to Asthma.
- Comprehensive testing of positionally cloned Asthma genes in two populations.
- A common mitochondrial haplogroup is associated with elevated total serum IgE levels.
- Polymorphisms in IL13, total IgE, eosinophilia, and Asthma exacerbations in childhood.
- On dichotomizing phenotypes in family-based association tests: quantitative phenotypes are not always the optimal choice.
- The association of a SNP upstream of INSIG2 with body mass index is reproduced in several but not all cohorts.
- Ala92 type 2 deiodinase allele increases risk for the development of hypertension.
- Genetic linkage and association analysis of COPD-related traits on chromosome 8p.
- Beta-2 adrenergic receptor diplotype defines a subset of salt-sensitive hypertension.
- Genetic determinants of functional impairment in Chronic obstructive pulmonary disease.
- Genetic association analysis of functional impairment in Chronic obstructive pulmonary disease.
- Eotaxin polymorphisms and serum total IgE levels in children with Asthma.
- Family-based association test for time-to-onset data with time-dependent differences between the hazard functions.
- T-bet polymorphisms are associated with Asthma and airway hyperresponsiveness.
- A functional mutation in the terminal exon of elastin in severe, early-onset Chronic obstructive pulmonary disease.
- Association of defensin beta-1 gene polymorphisms with Asthma.
- TBX21: a functional variant predicts improvement in Asthma with the use of inhaled corticosteroids.
- Association of vitamin D receptor gene polymorphisms with childhood and adult Asthma.
- TOLL-like receptor 10 genetic variation is associated with Asthma in two independent samples.
- Low-normal gestational age as a predictor of Asthma at 6 years of age.
- Endotoxin exposure and eczema in the first year of life.
- ADAM33: where are we now?
- ADAM33 polymorphisms and phenotype associations in childhood Asthma.
- IL10 gene polymorphisms are associated with Asthma phenotypes in children.
- Transforming growth factor-beta1 promoter polymorphism C-509T is associated with Asthma.
- The molecular basis of glutamate formiminotransferase deficiency.
- Single-nucleotide polymorphisms in the Toll-like receptor 9 gene (TLR9): frequencies, pairwise linkage disequilibrium, and haplotypes in three U.S. ethnic groups and e...
- Polymorphisms in toll-like receptor 4 are not associated with Asthma or atopy-related phenotypes.
- Gene expression profiling in Asthma.
- Circadian rhythm reprogramming during Lung inflammation.
- Metabolomic derangements are associated with mortality in critically ill adult patients.
- Ethnic-specific associations of rare and low-frequency DNA sequence variants with Asthma.
- A Chronic Obstructive Pulmonary Disease Susceptibility Gene, FAM13A, Regulates Protein Stability of β-catenin.
Schools
Harvard Medical School
McGill University Faculty of Medicine
McGill University
Procedures Preformed
- Bronchoscopy
- Ventilation Management
Conditions Treated
- Acidosis
- Asthma
- Atelectasis
- Bronchiectasis
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Doctors Specialties
- Pulmonology
Accepted Insurances
- Aetna HMO
- Choice Plus POS II
- Blue Card PPO
- BlueConnect HMO
- Blue with Managed Care Behavioral Health HMO
- Preferred Blue PPO
- Humana
- Medicare MCR
- MultiPlan PPO
- PHCS Network PPO
- Choice Plus POS
- Navigate HMO
- Navigate POS
- Options PPO
- United Healthcare
Education
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McGill University Faculty of Medicine
Hospital
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Brigham and Women's Hospital
Drug Facts
| NPI NUMBER | 1245299544 | |
| NPPES Provider LastName | RABY | |
| NPPES Provider FirstName | BENJAMIN | |
| NPPES Provider ZIPCode | 021155804 | |
| NPPES Provider State | MA | |
| Specialty Description | Pulmonary Disease | |
| Total Claim Count | 19.0 | |
| Distinct Opioid Count | 0.0 | |
| Opioid Claim Count | 0.0 | |
| Percent Opioid Claims | 0.0 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1245299544 |
| Last Name Of The Provider | RABY |
| First Name Of The Provider | BENJAMIN |
| View All |
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