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HG 007022

Funded outputs count: 30
Funder award ID: HG 007022
OpenAlex ID: G1050708039
Robust, flexible, and scalable tests for Hardy–Weinberg equilibrium across diverse ancestries
2021 · Alan M Kwong, Thomas W Blackwell, et al. · Genetics · 26
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Ancestry-agnostic estimation of DNA sample contamination from sequence reads
2020 · Fan Zhang, Matthew Flickinger, et al. · Genome Research · 89
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Estimation of DNA contamination and its sources in genotyped samples
2019 · Gregory J. M. Zajac, Lars G. Fritsche, et al. · Genetic Epidemiology · 14
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Overexpression of the Cytokine BAFF and Autoimmunity Risk
2017 · Maristella Steri, Valeria Orrù, et al. · New England Journal of Medicine · 383
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Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair
2015 · Felix R Day, kConFab Investigators, et al. · Nature Genetics · 413
Genome-wide association analyses based on whole-genome sequencing in Sardinia provide insights into regulation of hemoglobin levels
2015 · Fabrice Danjou, Magdalena Zoledziewska, et al. · Nature Genetics · 73
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Height-reducing variants and selection for short stature in Sardinia
2015 · Magdalena Zoledziewska, The Understanding Society Scientific Group, et al. · Nature Genetics · 103
Genome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markers
2015 · Carlo Sidore, Fabio Busonero, et al. · Nature Genetics · 377
Correcting for Sample Contamination in Genotype Calling of DNA Sequence Data
2015 · Matthew Flickinger, Goo Jun, et al. · The American Journal of Human Genetics · 42
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Assessing Mitochondrial DNA Variation and Copy Number in Lymphocytes of ~2,000 Sardinians Using Tailored Sequencing Analysis Tools
2015 · Jun Ding, Carlo Sidore, et al. · PLoS Genetics · 163
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Whole-genome sequencing of uropathogenic Escherichia coli reveals long evolutionary history of diversity and virulence
2015 · Yancy Lo, Lixin Zhang, et al. · Infection Genetics and Evolution · 20
Cross-Population Joint Analysis of eQTLs: Fine Mapping and Functional Annotation
2015 · Xiaoquan Wen, Francesca Luca, et al. · PLoS Genetics · 87
Comparing variant calling algorithms for target-exon sequencing in a large sample
2015 · Yancy Lo, Hyun M Kang, et al. · BMC Bioinformatics · 5
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Unified representation of genetic variants
2015 · Adrian Tan, Gonçalo R. Abecasis, et al. · Bioinformatics · 403
Genetic associations of nonsynonymous exonic variants with psychophysiological endophenotypes
2014 · Scott I. Vrieze, Stephen M. Malone, et al. · Psychophysiology · 21
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Genome‐wide scans of genetic variants for psychophysiological endophenotypes: A methodological overview
2014 · William. G. Iacono, Stephen. M. Malone, et al. · Psychophysiology · 24
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In search of rare variants: Preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes
2014 · Scott I. Vrieze, Stephen M. Malone, et al. · Psychophysiology · 28
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Knowns and unknowns for psychophysiological endophenotypes: Integration and response to commentaries
2014 · William G. Iacono, Uma Vaidyanathan, et al. · Psychophysiology · 57
Rare variant genotype imputation with thousands of study-specific whole-genome sequences: implications for cost-effective study designs
2014 · Giorgio Pistis, Eleonora Porcu, et al. · European Journal of Human Genetics · 99
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Rare-Variant Association Analysis: Study Designs and Statistical Tests
2014 · Seunggeun Lee, Gonçalo R. Abecasis, et al. · The American Journal of Human Genetics · 1,042
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RAREMETAL: fast and powerful meta-analysis for rare variants
2014 · Shuang Feng, Dajiang Liu, et al. · Bioinformatics · 108
Ancestry estimation and control of population stratification for sequence-based association studies
2014 · The FUSION Study, Chaolong Wang, et al. · Nature Genetics · 139
Bayesian model selection in complex linear systems, as illustrated in genetic association studies
2013 · Xiaoquan Wen · Biometrics · 29
Accurate Local-Ancestry Inference in Exome-Sequenced Admixed Individuals via Off-Target Sequence Reads
2013 · Youna Hu, Cristen Willer, et al. · The American Journal of Human Genetics · 34
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Identification of a rare coding variant in complement 3 associated with age-related macular degeneration
2013 · Xiaowei Zhan, David E Larson, et al. · Nature Genetics · 179
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