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Author

Tanja Smith

Observed name: Josh Smith
ORCID: 0000-0001-6111-6312
Observed ORCID: 0000-0001-6111-6312
OpenAlex ID: A5036837505
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
2021 · Daniel Taliun, Daniel N. Harris, et al. · Nature · 2,198
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Inherited causes of clonal haematopoiesis in 97,691 whole genomes
2020 · Alexander G. Bick, Joshua S. Weinstock, et al. · Nature · 730
Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data
2022 · Pierrick Wainschtein, Deepti Jain, et al. · Nature Genetics · 514
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Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale
2020 · Xihao Li, Zilin Li, et al. · Nature Genetics · 263
Clonal haematopoiesis and risk of chronic liver disease
2023 · Waihay J. Wong, Connor Emdin, et al. · Nature · 212
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A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response
2021 · Yang Luo, Masahiro Kanai, et al. · Nature Genetics · 187
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Deep-coverage whole genome sequences and blood lipids among 16,324 individuals
2018 · Pradeep Natarajan, Gina M. Peloso, et al. · Nature Communications · 183
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Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis
2023 · Joshua S. Weinstock, Jayakrishnan Gopakumar, et al. · Nature · 114
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A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies
2022 · Zilin Li, Xihao Li, et al. · Nature Methods · 105
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Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries
2018 · Seyedeh M. Zekavat, Sanni Ruotsalainen, et al. · Nature Communications · 105
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Whole genome sequence analysis of blood lipid levels in >66,000 individuals
2022 · Margaret Sunitha Selvaraj, Xihao Li, et al. · Nature Communications · 69
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Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies
2022 · Xihao Li, Corbin Quick, et al. · Nature Genetics · 59
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Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals
2022 · Usman A. Tahir, Daniel H. Katz, et al. · Nature Communications · 53
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Genome sequencing unveils a regulatory landscape of platelet reactivity
2021 · Ali R. Keramati, Ming-Huei Chen, et al. · Nature Communications · 50
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Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices
2021 · Pradeep Natarajan, Akhil Pampana, et al. · Nature Communications · 38
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Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program
2021 · Brian E. Cade, Jiwon Lee, et al. · Genome Medicine · 33
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Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk
2025 · Seung Hoan Choi, Sean J. Jurgens, et al. · Nature Genetics · 31
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Epigenome-wide DNA methylation association study of circulating IgE levels identifies novel targets for asthma
2023 · Kathryn Recto, Priyadarshini Kachroo, et al. · EBioMedicine · 20
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Variant-specific inflation factors for assessing population stratification at the phenotypic variance level
2021 · Tamar Sofer, Xiuwen Zheng, et al. · Nature Communications · 20
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A statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studies
2025 · Xihao Li, Han Chen, et al. · Nature Computational Science · 15
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Whole Genome Sequencing Identifies CRISPLD2 as a Lung Function Gene in Children With Asthma
2019 · Priyadarshini Kachroo, Julian Hecker, et al. · CHEST Journal · 10
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cellSTAAR: incorporating single-cell-sequencing-based functional data to boost power in rare variant association testing of noncoding regions
2025 · Eric Van Buren, Yi Zhang, et al. · Nature Methods · 4
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Author Correction: A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response
2021 · Yang Luo, Masahiro Kanai, et al. · Nature Genetics · 4
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Author Correction: Clonal haematopoiesis and risk of chronic liver disease
2023 · Waihay J. Wong, Connor Emdin, et al. · Nature · 2
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Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries
2020 · Seyedeh M. Zekavat, Sanni Ruotsalainen, et al. · Nature Communications · 2
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Works count: 27
Citation count: 7,219
H-index: 20
I10-index: 22
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