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Author Details

Fuli Yu
East China University of Science and Technology
2002
57
29
PMIDPaper TitleJournal TitlePublished Year
34226836A multi-class COVID-19 segmentation network with pyramid attention and edge loss in CT images.IET Image Process2021
33976457COVID-19 lesion discrimination and localization network based on multi-receptive field attention module on CT images.Optik (Stuttg)2021
32961042REDBot: Natural language process methods for clinical copy number variation reporting in prenatal and products of conception diagnosis.Mol Genet Genomic Med2020
34812359MSD-Net: Multi-Scale Discriminative Network for COVID-19 Lung Infection Segmentation on CT.IEEE Access2020
31673123Mutations in ASH1L confer susceptibility to Tourette syndrome.Mol Psychiatry2020
31023133Prenatal diagnosis and molecular cytogenetic characterisation of hereditary chromosomal deletions with a favourable outcome.J Obstet Gynaecol2019
30828085Clinical utility of noninvasive prenatal screening for expanded chromosome disease syndromes.Genet Med2019
29706352Whole-Exome Sequencing Reveals Uncaptured Variation and Distinct Ancestry in the Southern African Population of Botswana.Am J Hum Genet2018
29997225Rho Guanine Nucleotide Exchange Factor <i>ARHGEF17</i> Is a Risk Gene for Intracranial Aneurysms.Circ Genom Precis Med2018
29852155Prospective chromosome analysis of 3429 amniocentesis samples in China using copy number variation sequencing.Am J Obstet Gynecol2018
30139913Allele-specific epigenome maps reveal sequence-dependent stochastic switching at regulatory loci.Science2018
28532386Extremely low-coverage whole genome sequencing in South Asians captures population genomics information.BMC Genomics2017
28089252Practical Approaches for Whole-Genome Sequence Analysis of Heart- and Blood-Related Traits.Am J Hum Genet2017
28247551Characterization of chromosomal abnormalities in pregnancy losses reveals critical genes and loci for human early development.Hum Mutat2017
27507420Base-Biased Evolution of Disease-Associated Mutations in the Human Genome.Hum Mutat2016
26670213Multiallelic Positions in the Human Genome: Challenges for Genetic Analyses.Hum Mutat2016
27934697The population genomics of rhesus macaques (Macaca mulatta) based on whole-genome sequences.Genome Res2016
27612449A hybrid computational strategy to address WGS variant analysis in &gt;5000 samples.BMC Bioinformatics2016
27584569Association of Single Nucleotide Polymorphisms in the ST3GAL4 Gene with VWF Antigen and Factor VIII Activity.PLoS One2016
25807536Population genomic analysis of 962 whole genome sequences of humans reveals natural selection in non-coding regions.PLoS One2015
26383047Complexity and diversity of F8 genetic variations in the 1000 genomes.J Thromb Haemost2015
26432246An integrated map of structural variation in 2,504 human genomes.Nature2015
25887218PacBio-LITS: a large-insert targeted sequencing method for characterization of human disease-associated chromosomal structural variations.BMC Genomics2015
25765891The distribution and mutagenesis of short coding INDELs from 1,128 whole exomes.BMC Genomics2015
24475911Launching genomics into the cloud: deployment of Mercury, a next generation sequence analysis pipeline.BMC Bioinformatics2014
24465435Possible race and gender divergence in association of genetic variations with plasma von Willebrand factor: a study of ARIC and 1000 genome cohorts.PLoS One2014
23296920An integrative variant analysis pipeline for accurate genotype/haplotype inference in population NGS data.Genome Res2013
29783422The 1000 Genomes Project: paving the way for personalized genomic medicine.Per Med2013
24092746Integrative annotation of variants from 1092 humans: application to cancer genomics.Science2013
23601824Translational signatures and mRNA levels are highly correlated in human stably expressed genes.BMC Genomics2013
23648131Next-generation sequencing study finds an excess of rare, coding single-nucleotide variants of ADAMTS13 in patients with deep vein thrombosis.J Thromb Haemost2013
23770607Whole-genome sequence-based analysis of high-density lipoprotein cholesterol.Nat Genet2013
23743231Whole exome sequencing reveals minimal differences between cell line and whole blood derived DNA.Genomics2013
23216583Characterizing polymorphisms and allelic diversity of von Willebrand factor gene in the 1000 Genomes.J Thromb Haemost2013
22377349Characterizing linkage disequilibrium and evaluating imputation power of human genomic insertion-deletion polymorphisms.Genome Biol2012
23134663Atlas2 Cloud: a framework for personal genome analysis in the cloud.BMC Genomics2012
22219226Influence of single nucleotide polymorphisms in factor VIII and von Willebrand factor genes on plasma factor VIII activity: the ARIC Study.Blood2012
22239737An integrative variant analysis suite for whole exome next-generation sequencing data.BMC Bioinformatics2012
22353194Identification of genetic risk variants for deep vein thrombosis by multiplexed next-generation sequencing of 186 hemostatic/pro-inflammatory genes.BMC Med Genomics2012
21343614Genetic determinants of plasma von Willebrand factor antigen levels: a target gene SNP and haplotype analysis of ARIC cohort.Blood2011
21917140The functional spectrum of low-frequency coding variation.Genome Biol2011
21730125Demographic history and rare allele sharing among human populations.Proc Natl Acad Sci U S A2011
21668978Characterization of single-nucleotide variation in Indian-origin rhesus macaques (Macaca mulatta).BMC Genomics2011
20019143A SNP discovery method to assess variant allele probability from next-generation resequencing data.Genome Res2010
21512588Next-generation sequencing.J Biomed Biotechnol2010
21106085Genetic diversity in India and the inference of Eurasian population expansion.Genome Biol2010
21092284Pash 3.0: A versatile software package for read mapping and integrative analysis of genomic and epigenomic variation using massively parallel DNA sequencing.BMC Bioinformatics2010
20811451Integrating common and rare genetic variation in diverse human populations.Nature2010
19526211Strong association of socioeconomic status with genetic ancestry in Latinos: implications for admixture studies of type 2 diabetes.Diabetologia2009
19783549Detecting natural selection by empirical comparison to random regions of the genome.Hum Mol Genet2009
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Ashok Veeraraghavan
Rice University
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Gil McVean
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Alanna C Morrison
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Changqing Zeng
Institute of Biomedical Sciences, Henan Academy of Sciences
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Charmaine D M Royal
Duke University
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Panos Deloukas
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 3
Li Jin
Fudan University
Co-authored papers 3
Suzanne M Leal
Center for Statistical Genetics, Columbia University Medical Center
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Release 1.2