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Yuanping Du

The UK10K project identifies rare variants in health and disease
2015 · Writing group, Klaudia Walter, et al. · Nature · 1,039
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Whole-genome sequence variation, population structure and demographic history of the Dutch population
2014 · Laurent C Francioli, Androniki Menelaou, et al. · Nature Genetics · 659
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Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel
2015 · Jie Huang, Bryan Howie, et al. · Nature Communications · 343
The Genome of the Netherlands: design, and project goals
2013 · Dorret I Boomsma, Cisca Wijmenga, et al. · European Journal of Human Genetics · 257
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PrecisionFDA Truth Challenge V2: Calling variants from short and long reads in difficult-to-map regions
2022 · Nathan D. Olson, Justin Wagner, et al. · Cell Genomics · 201
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Whole-Genome Sequencing Uncovers the Genetic Basis of Chronic Mountain Sickness in Andean Highlanders
2013 · Dan Zhou, Nitin Udpa, et al. · The American Journal of Human Genetics · 134
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IMonitor: A Robust Pipeline for TCR and BCR Repertoire Analysis
2015 · Wei Zhang, Yuanping Du, et al. · Genetics · 123
Negative selection in humans and fruit flies involves synergistic epistasis
2017 · Mashaal Sohail, Olga A. Vakhrusheva, et al. · Science · 114
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A high-quality human reference panel reveals the complexity and distribution of genomic structural variants
2016 · Jayne Y. Hehir-Kwa, Tobias Marschall, et al. · Nature Communications · 104
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Whole-genome sequence-based analysis of thyroid function
2015 · Peter N. Taylor, Eleonora Porcu, et al. · Nature Communications · 104
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Whole genome sequencing of Ethiopian highlanders reveals conserved hypoxia tolerance genes
2014 · Nitin Udpa, Roy Ronen, et al. · Genome biology · 92
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Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity
2017 · Audrey E. Hendricks, Elena G. Bochukova, et al. · Scientific Reports · 68
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A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans
2014 · Nicholas J. Timpson, Klaudia Walter, et al. · Nature Communications · 68
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Integrated clinical and omics approach to rare diseases: novel genes and oligogenic inheritance in holoprosencephaly
2018 · Artem Kim, Clara Savary, et al. · Brain · 62
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Systematic Comparative Evaluation of Methods for Investigating the TCRβ Repertoire
2016 · Xiao Liu, Wei Zhang, et al. · PLoS ONE · 62
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Genome of the Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels
2015 · Elisabeth M. van Leeuwen, Lennart C. Karssen, et al. · Nature Communications · 60
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A Cell‐free DNA Barcode‐Enabled Single‐Molecule Test for Noninvasive Prenatal Diagnosis of Monogenic Disorders: Application to β‐Thalassemia
2019 · Xingkun Yang, Qinghua Zhou, et al. · Advanced Science · 47
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Minimal Residual Disease Detection and Evolved IGH Clones Analysis in Acute B Lymphoblastic Leukemia Using IGH Deep Sequencing
2016 · Jinghua Wu, Shan Jia, et al. · Frontiers in Immunology · 46
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Characterization of the B Cell Receptor Repertoire in the Intestinal Mucosa and of Tumor-Infiltrating Lymphocytes in Colorectal Adenoma and Carcinoma
2017 · Wei Zhang, Qiang Feng, et al. · The Journal of Immunology · 39
Low-frequency variation in TP53 has large effects on head circumference and intracranial volume
2019 · Simon Haworth, Chin Yang Shapland, et al. · Nature Communications · 37
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WGS-based telomere length analysis in Dutch family trios implicates stronger maternal inheritance and a role for RRM1 gene
2019 · Lilit Nersisyan, Maria Nikoghosyan, et al. · Scientific Reports · 11
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Low-frequency variation in TP53 has large effects on head circumference and intracranial volume
2019 · Simon Haworth, Chin Yang Shapland, et al. · Newcastle University ePrints (Newcastle Univesity)
Works count: 23
Citation count: 3,670
H-index: 20
I10-index: 21
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