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Author Details
Full Name
Samuela Pollack
Affiliation
Harvard T.H. Chan School of Public Health
ORCID
Career Start Year
2010
Papers
18
H Index
12
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
34166655
Gene Set Enrichment Analsyes Identify Pathways Involved in Genetic Risk for Diabetic Retinopathy.
Am J Ophthalmol
2022
35659450
Erratum to Gene Set Enrichment Analyses Identify Pathways Involved in Genetic Risk for Diabetic Retinopathy. Am J Ophthalmol 2022;233:111-123.
Am J Ophthalmol
2022
34166655
Gene Set Enrichment Analsyes Identify Pathways Involved in Genetic Risk for Diabetic Retinopathy.
Am J Ophthalmol
2022
35659450
Erratum to Gene Set Enrichment Analyses Identify Pathways Involved in Genetic Risk for Diabetic Retinopathy. Am J Ophthalmol 2022;233:111-123.
Am J Ophthalmol
2022
30487263
Multiethnic Genome-Wide Association Study of Diabetic Retinopathy Using Liability Threshold Modeling of Duration of Diabetes and Glycemic Control.
Diabetes
2019
30487263
Multiethnic Genome-Wide Association Study of Diabetic Retinopathy Using Liability Threshold Modeling of Duration of Diabetes and Glycemic Control.
Diabetes
2019
30828438
restfulSE: A semantically rich interface for cloud-scale genomics with Bioconductor.
F1000Res
2019
30828438
restfulSE: A semantically rich interface for cloud-scale genomics with Bioconductor.
F1000Res
2019
29632380
Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types.
Nat Genet
2018
30178632
A genome-wide association study suggests new evidence for an association of the NADPH Oxidase 4 (NOX4) gene with severe diabetic retinopathy in type 2 diabetes.
Acta Ophthalmol
2018
29632380
Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types.
Nat Genet
2018
30178632
A genome-wide association study suggests new evidence for an association of the NADPH Oxidase 4 (NOX4) gene with severe diabetic retinopathy in type 2 diabetes.
Acta Ophthalmol
2018
28017371
Mixed Model Association with Family-Biased Case-Control Ascertainment.
Am J Hum Genet
2017
28951389
Genetically Determined Plasma Lipid Levels and Risk of Diabetic Retinopathy: A Mendelian Randomization Study.
Diabetes
2017
28017371
Mixed Model Association with Family-Biased Case-Control Ascertainment.
Am J Hum Genet
2017
28951389
Genetically Determined Plasma Lipid Levels and Risk of Diabetic Retinopathy: A Mendelian Randomization Study.
Diabetes
2017
25892111
Mixed model with correction for case-control ascertainment increases association power.
Am J Hum Genet
2015
25892111
Mixed model with correction for case-control ascertainment increases association power.
Am J Hum Genet
2015
26523775
Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis.
Nat Genet
2015
26523775
Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis.
Nat Genet
2015
25383972
Leveraging population admixture to characterize the heritability of complex traits.
Nat Genet
2014
25383972
Leveraging population admixture to characterize the heritability of complex traits.
Nat Genet
2014
23539302
Improved ancestry inference using weights from external reference panels.
Bioinformatics
2013
23666277
Replication and fine mapping of asthma-associated loci in individuals of African ancestry.
Hum Genet
2013
23539302
Improved ancestry inference using weights from external reference panels.
Bioinformatics
2013
23737753
Using extended genealogy to estimate components of heritability for 23 quantitative and dichotomous traits.
PLoS Genet
2013
23666277
Replication and fine mapping of asthma-associated loci in individuals of African ancestry.
Hum Genet
2013
23737753
Using extended genealogy to estimate components of heritability for 23 quantitative and dichotomous traits.
PLoS Genet
2013
22556366
Analysis of case-control association studies with known risk variants.
Bioinformatics
2012
22556366
Analysis of case-control association studies with known risk variants.
Bioinformatics
2012
23144628
Informed conditioning on clinical covariates increases power in case-control association studies.
PLoS Genet
2012
23144628
Informed conditioning on clinical covariates increases power in case-control association studies.
PLoS Genet
2012
21907010
Genome-wide comparison of African-ancestry populations from CARe and other cohorts reveals signals of natural selection.
Am J Hum Genet
2011
21907010
Genome-wide comparison of African-ancestry populations from CARe and other cohorts reveals signals of natural selection.
Am J Hum Genet
2011
20811451
Integrating common and rare genetic variation in diverse human populations.
Nature
2010
20811451
Integrating common and rare genetic variation in diverse human populations.
Nature
2010
1 - 36 of 36
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