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Author Details
Full Name
Sameer Chavan
Affiliation
University of Colorado
ORCID
Career Start Year
2014
Papers
17
H Index
10
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37683082
Thyroid Cancer Polygenic Risk Score Improves Classification of Thyroid Nodules as Benign or Malignant.
J Clin Endocrinol Metab
2024
37683082
Thyroid Cancer Polygenic Risk Score Improves Classification of Thyroid Nodules as Benign or Malignant.
J Clin Endocrinol Metab
2024
36702996
Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing.
Nat Genet
2023
37662265
WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE.
medRxiv
2023
36702996
Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing.
Nat Genet
2023
37662265
WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE.
medRxiv
2023
34111454
Polygenic prediction of atopic dermatitis improves with atopic training and filaggrin factors.
J Allergy Clin Immunol
2022
35927319
Rare genetic variants explain missing heritability in smoking.
Nat Hum Behav
2022
35385311
Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential.
Sci Adv
2022
36477530
Genetic diversity fuels gene discovery for tobacco and alcohol use.
Nature
2022
34111454
Polygenic prediction of atopic dermatitis improves with atopic training and filaggrin factors.
J Allergy Clin Immunol
2022
35385311
Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential.
Sci Adv
2022
36477530
Genetic diversity fuels gene discovery for tobacco and alcohol use.
Nature
2022
35927319
Rare genetic variants explain missing heritability in smoking.
Nat Hum Behav
2022
34536413
Multiethnic genome-wide and HLA association study of total serum IgE level.
J Allergy Clin Immunol
2021
33713768
Genome-wide association study of asthma, total IgE, and lung function in a cohort of Peruvian children.
J Allergy Clin Immunol
2021
33548076
Whole genome sequencing identifies novel genetic mutations in patients with eczema herpeticum.
Allergy
2021
34582791
Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program.
Am J Hum Genet
2021
34536413
Multiethnic genome-wide and HLA association study of total serum IgE level.
J Allergy Clin Immunol
2021
33548076
Whole genome sequencing identifies novel genetic mutations in patients with eczema herpeticum.
Allergy
2021
33713768
Genome-wide association study of asthma, total IgE, and lung function in a cohort of Peruvian children.
J Allergy Clin Immunol
2021
34582791
Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program.
Am J Hum Genet
2021
31981624
Association of HLA-DRB1â¿¿09:01 with tIgE levels among African-ancestry individuals with asthma.
J Allergy Clin Immunol
2020
31981624
Association of HLA-DRB1â¿¿09:01 with tIgE levels among African-ancestry individuals with asthma.
J Allergy Clin Immunol
2020
30455414
Assembly of a pan-genome from deep sequencing of 910 humans of African descent.
Nat Genet
2019
30825465
The MALT1 locus and peanut avoidance in the risk for peanut allergy.
J Allergy Clin Immunol
2019
30455414
Assembly of a pan-genome from deep sequencing of 910 humans of African descent.
Nat Genet
2019
31443688
Replicated methylation changes associated with eczema herpeticum and allergic response.
Clin Epigenetics
2019
31443688
Replicated methylation changes associated with eczema herpeticum and allergic response.
Clin Epigenetics
2019
30825465
The MALT1 locus and peanut avoidance in the risk for peanut allergy.
J Allergy Clin Immunol
2019
28437440
Synthesizer: Expediting synthesis studies from context-free data with information retrieval techniques.
PLoS One
2017
28437440
Synthesizer: Expediting synthesis studies from context-free data with information retrieval techniques.
PLoS One
2017
24907368
Preserving biological heterogeneity with a permuted surrogate variable analysis for genomics batch correction.
Bioinformatics
2014
24907368
Preserving biological heterogeneity with a permuted surrogate variable analysis for genomics batch correction.
Bioinformatics
2014
1 - 34 of 34
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