Xiangqun Zheng-Bradley

Illumina (United Kingdom) — United Kingdom

Biochemistry, Genetics and Molecular Biology · Life Sciences

35h-index168.0kcitations46works18.02yr avg
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Research Topics

Genomics and Phylogenetic Studies(17), Genomics and Rare Diseases(13), Genomic variations and chromosomal abnormalities(10), Genetic Associations and Epidemiology(9), Chromosomal and Genetic Variations(9)

Publications35 total

Transcriptional Analysis of Different Cultivars and Genome-Wide Identification of FAD Gene Family in Tree Peony
Agronomy·2024· 1 citedOpen Access
Genome sequencing as a generic diagnostic strategy for rare disease
Genome Medicine·2024· 35 citedOpen Access
Genome sequencing as a generic diagnostic strategy for rare disease
2023· 3 citedOpen Access
Mucoepidermoid carcinoma of the duodenum: first reported case
Pathology·2023· 1 citedOpen Access
Variant calling on the GRCh38 assembly with the data from phase three of the 1000 Genomes Project
Wellcome Open Research·2019· 118 citedOpen Access
Human-specific tandem repeat expansion and differential gene expression during primate evolution
Proceedings of the National Academy of Sciences·2019· 153 citedOpen Access
Multi-platform discovery of haplotype-resolved structural variation in human genomes
Nature Communications·2019· 983 citedOpen Access
Variant calling on the GRCh38 assembly with the data from phase three of the 1000 Genomes Project
Wellcome Open Research·2019· 7 citedOpen Access
Multi-platform discovery of haplotype-resolved structural variation in human genomes
2017· 157 citedOpen Access
Alignment of 1000 Genomes Project reads to reference assembly GRCh38
GigaScience·2017· 101 citedOpen Access
The international Genome sample resource (IGSR): A worldwide collection of genome variation incorporating the 1000 Genomes Project data
Nucleic Acids Research·2016· 295 citedOpen Access
Applications of the 1000 Genomes Project resources
Briefings in Functional Genomics·2016· 62 citedOpen Access
Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences
Nature Genetics·2016· 347 citedOpen Access
An integrated map of structural variation in 2,504 human genomes_supplement
2016· 1 cited
A global reference for human genetic variation
Civil War Book Review·2015· 612 citedOpen Access
An integrated map of structural variation in 2,504 human genomes
Nature·2015· 2.6k citedOpen Access
A global reference for human genetic variation
Nature·2015· 19.2k citedOpen Access
Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel
Nature Communications·2014· 441 citedOpen Access
The 1000 Genomes Project: data management and community access
Nature Methods·2012· 469 citedOpen Access
Maps for the world of genomic medicine: The 2011 CSHL Personal Genomes meeting
Human Mutation·2012· 1 citedOpen Access
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Frequent Co-authors

Paul Flicek(18), Laura Clarke(15), Andrew G. Clark(8), Evan E. Eichler(8), Charles Lee(8), Gábor Marth(8), Mark D. Adams(8), Goo Jun(7), Susan Fairley(7), Richard A. Gibbs(6), J. Craig Venter(6), Richard Mural(6), Fu Lu(6), Deborah Nusskern(6), Robert E. Handsaker(6), Ankit Malhotra(6), Eliza Cerveira(6), Steven A. McCarroll(6), Ernesto Lowy(6), Adam Auton(5)