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B. Strober · SciRah

Researcher profile · Semantic Scholar

B. Strober

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B. Strober — researcher profile on SciRah

h-index: 15
Works: 44
Citations: 8,789

Most-cited papers

The GTEx Consortium atlas of genetic regulatory effects across human tissues
F. Aguet, A. Barbeira, Rodrigo Bonazzola, A. Brown +48 more
2019Science5,221 citations Open access
Semantic Scholar
Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics
A. Barbeira, Scott P. Dickinson, Rodrigo Bonazzola, Jiamao Zheng +241 more
2016Nature Communications1,077 citations Open access
Semantic Scholar
A method to predict the impact of regulatory variants from DNA sequence
Dongwon Lee, David U. Gorkin, Maggie Baker, B. Strober +3 more
2015Nature Genetics459 citations Open access
Semantic Scholar
A Quantitative Proteome Map of the Human Body
Lihua Jiang, Meng Wang, Shin Lin, Rui-Qi Jian +170 more
2020Cell407 citations Open access
Semantic Scholar
Identification of rare-disease genes using blood transcriptome sequencing and large control cohorts
L. Frésard, Craig Smail, N. Ferraro, Nicole A. Teran +30 more
2019Nature Medicine298 citations Open access
Semantic Scholar
The impact of rare variation on gene expression across tissues
Xin Li, Yungil Kim, Emily K. Tsang, Joe R. Davis +71 more
2016Nature253 citations Open access
Semantic Scholar
Dynamic genetic regulation of gene expression during cellular differentiation
B. Strober, Reem Elorbany, Katherine L. Rhodes, N. Krishnan +3 more
2019Science205 citations Open access
Semantic Scholar
Genetic effects on gene expression across human tissues
A. Brown, S. Castel, Joe R. Davis, Brian Jo +89 more
2018200 citations
Semantic Scholar
Population-scale tissue transcriptomics maps long non-coding RNAs to complex disease
Olivia M. de Goede, D. Nachun, N. Ferraro, M. Gloudemans +23 more
2021Cell160 citations Open access
Semantic Scholar
Transcriptomic signatures across human tissues identify functional rare genetic variation
N. Ferraro, B. Strober, Jonah Einson, Nathan S. Abell +33 more
2020Science152 citations Open access
Semantic Scholar
Redefining tissue specificity of genetic regulation of gene expression in the presence of allelic heterogeneity
Marios Arvanitis, Karl Tayeb, B. Strober, A. Battle
2021medRxiv76 citations Open access
Semantic Scholar
Local genetic effects on gene expression across 44 human tissues
F. Aguet, A. Brown, S. Castel, Joe R. Davis +46 more
2016bioRxiv74 citations Open access
Semantic Scholar
Single-cell sequencing reveals lineage-specific dynamic genetic regulation of gene expression during human cardiomyocyte differentiation
Reem Elorbany, Joshua M. Popp, Katherine L. Rhodes, B. Strober +4 more
2021bioRxiv65 citations Open access
Semantic Scholar
Human embryoid bodies as a novel system for genomic studies of functionally diverse cell types
Katherine L. Rhodes, Kenneth A. Barr, Joshua M. Popp, B. Strober +2 more
2021bioRxiv31 citations Open access
Semantic Scholar
Single-cell allele-specific expression analysis reveals dynamic and cell-type-specific regulatory effects
Guang-Hao Qi, B. Strober, Joshua M. Popp, Rebecca Keener +2 more
2022bioRxiv29 citations Open access
Semantic Scholar
MultiSuSiE improves multi-ancestry fine-mapping in All of Us whole-genome sequencing data
J. Rossen, Huwenbo Shi, B. Strober, M. Zhang +5 more
2024medRxiv14 citations Open access
Semantic Scholar
SURGE: uncovering context-specific genetic-regulation of gene expression from single-cell RNA sequencing using latent-factor models
B. Strober, Karl Tayeb, Joshua M. Popp, Guang-Hao Qi +4 more
2022bioRxiv14 citations Open access
Semantic Scholar
The functional impact of rare variation across the regulatory cascade
Tai-Bo Li, N. Ferraro, B. Strober, F. Aguet +34 more
2022bioRxiv13 citations Open access
Semantic Scholar
Fine-mapping causal tissues and genes at disease-associated loci
B. Strober, M. Zhang, T. Amariuta, J. Rossen +1 more
2025Nature Genetics11 citations Open access
Semantic Scholar
Fine-mapping causal tissues and genes at disease-associated loci
B. Strober, M. Zhang, T. Amariuta, J. Rossen +1 more
2023medRxiv11 citations Open access
Semantic Scholar
Identification of rare-disease genes in diverse undiagnosed cases using whole blood transcriptome sequencing and large control cohorts
L. Frésard, Craig Smail, Kevin S. Smith, N. Ferraro +29 more
2018bioRxiv11 citations Open access
Semantic Scholar
Long non-coding RNA gene regulation and trait associations across human tissues
O. M. de Goede, N. Ferraro, D. Nachun, Abhiram S. Rao +17 more
2019bioRxiv9 citations Open access
Semantic Scholar
Trans-eQTLs reveal the architecture of human gene regulatory networks
C.A. Robert Warmerdam, H. Westra, A. van der Graaf, M. Bonder +127 more
2026medRxiv8 citations Open access
Semantic Scholar
Distant regulatory effects of genetic variation in multiple human tissues 1
Brian Jo, Yuan He, B. Strober, P. Parsana +32 more
20168 citations
Semantic Scholar
Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genes
Rebecca Keener, Surya B. Chhetri, C. Connelly, M. Taub +94 more
2024Nature Communications7 citations Open access
Semantic Scholar
Pervasive correlations between causal disease effects of proximal SNPs vary with functional annotations and implicate stabilizing selection
M. Zhang, Arun Durvasula, Colby Chiang, E. Koch +9 more
2023medRxiv7 citations Open access
Semantic Scholar
MultiSuSiE improves multi-ancestry fine-mapping in All of Us whole-genome sequencing data
J. Rossen, Huwenbo Shi, B. Strober, M. Zhang +5 more
2026Nature Genetics5 citations
Semantic Scholar
Mapping disease loci to biological processes via joint pleiotropic and epigenomic partitioning
Gaspard Kerner, Nolan Kamitaki, B. Strober, Alkes L. Price
2025medRxiv4 citations Open access
Semantic Scholar
Distant regulatory effects of genetic variation in multiple human tissues
Brian Jo, Yuan He, B. Strober, P. Parsana +29 more
2016bioRxiv3 citations Open access
Semantic Scholar
Per-allele disease and complex trait effect sizes are predominantly African MAF-dependent in European populations
J. Rossen, B. Strober, Kang-Cheng Hou, Gaspard Kerner +1 more
2026medRxiv2 citations
Semantic Scholar
Abstract 11946: Prioritization of Multiomic Rare Variants (RVs) Underlying Electrocardiogram (EKG) Traits Using Bayesian Hierarchical Modeling (“Watershed”)
Tai-Bo Li, Nicole Ersaro, B. Strober, Marios Arvanitis +10 more
2022Circulation2 citations
Semantic Scholar
Validation of human telomere length trans-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as novel human telomere length regulation genes
Rebecca Keener, Surya B. Chhetri, C. Connelly, M. Taub +92 more
2023bioRxiv1 citations Open access
Semantic Scholar
Exploring the Phenotypic Consequences of Tissue Specific Gene Exploring the Phenotypic Consequences of Tissue Specific Gene Expression Variation Inferred from GWAS Summary Statistics Expression Variation Inferred from GWAS Summary Statistics
F. Aguet, K. Ardlie, B. Cummings, E. Gelfand +92 more
20211 citations
Semantic Scholar
Sharing Aggregated Patient Counts in Place of Line-Level EHR Data: Analytic Fidelity and the Limits of Count Suppression for Privacy
Y. Chen, A. Mcmurry, D. Gottlieb, J. Jones +2 more
2026medRxiv0 citations Open access
Semantic Scholar
Pleiotropic shared heritability quantifies the shared genetic variance of common diseases
Yu-Jie Zhao, B. Strober, Kang-Cheng Hou, Gaspard Kerner +6 more
2026Nature Genetics0 citations Open access
Semantic Scholar
Functionally informed cis and trans proteome-wide association studies prioritize disease-critical genes
Kang-Cheng Hou, Ali Pazokitoroudi, B. Strober, Xi-Lin Jiang +1 more
2026medRxiv0 citations Open access
Semantic Scholar
Mapping disease loci to biological processes via joint pleiotropic and epigenomic partitioning
Gaspard Kerner, Nolan Kamitaki, B. Strober, Alkes L. Price
2026Cell Genomics0 citations Open access
Semantic Scholar
Correlations between causal effect sizes of proximal SNPs vary with functional annotations and implicate stabilizing selection
M. Zhang, Arun Durvasula, C. Chiang, E. Koch +9 more
2026Nature Genetics0 citations Open access
Semantic Scholar
Functionally informed cis and trans proteome-wide association studies prioritize disease-critical genes
Kangcheng Hou, Ali Pazokitoroudi, B. Strober, Xi-Lin Jiang +1 more
2026Research Square0 citations Open access
Semantic Scholar
Pleiotropic heritability quantifies the shared genetic variance of common diseases
Yu-Jie Zhao, B. Strober, Kang-Cheng Hou, Gaspard Kerner +6 more
2025medRxiv0 citations Open access
Semantic Scholar
Pervasive correlations between causal disease effects of proximal SNPs vary with functional annotations and implicate stabilizing selection
M. Zhang, Arun Durvasula, Colby Chiang, E. Koch +9 more
2023Research Square0 citations Open access
Semantic Scholar
Author response: Human embryoid bodies as a novel system for genomic studies of functionally diverse cell types
Katherine L. Rhodes, Kenneth A. Barr, Joshua M. Popp, B. Strober +2 more
20210 citations Open access
Semantic Scholar
A framework for predicting tissue-specific 1 effects of rare genetic variants 2
Farhan N. Damani, Yungil Kim, Xin Li, Emily K. Tsang +10 more
20170 citations
Semantic Scholar
The impact of rare variation on gene expression across tissues 1
Xin Li, Yungil Kim, Emily K. Tsang, Joe R. Davis +10 more
20160 citations
Semantic Scholar

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