Skip to Main Content

Author Details

Xiaoming Liu
College of Electronic Science and Engineering, Jilin University
1997
73
30
PMIDPaper TitleJournal TitlePublished Year
33418499Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium.EBioMedicine2021
34336661Advanced Deep Learning Approach to Automatically Segment Malignant Tumors and Ablation Zone in the Liver With Contrast-Enhanced CT.Front Oncol2021
32190566Development and assessment of an individualized nomogram to predict colorectal cancer liver metastases.Quant Imaging Med Surg2020
32728489Analysis of conserved miRNAs in cynomolgus macaque genome using small RNA sequencing and homology searching.PeerJ2020
32487083Noninvasive KRAS mutation estimation in colorectal cancer using a deep learning method based on CT imaging.BMC Med Imaging2020
30972448Genome-wide analysis of differentially expressed lncRNA in sporadic parathyroid tumors.Osteoporos Int2019
31242253Pharmacogenomics of statin-related myopathy: Meta-analysis of rare variants from whole-exome sequencing.PLoS One2019
30712509Investigation of multi-trait associations using pathway-based analysis of GWAS summary statistics.BMC Genomics2019
30704510The International Conference on Intelligent Biology and Medicine (ICIBM) 2018: genomics meets medicine.BMC Med Genomics2019
31004712Automated and accurate quantification of subcutaneous and visceral adipose tissue from magnetic resonance imaging based on machine learning.Magn Reson Imaging2019
31087327Accurate colorectal tumor segmentation for CT scans based on the label assignment generative adversarial network.Med Phys2019
29264654Genetic variants in microRNA genes and targets associated with cardiovascular disease risk factors in the African-American population.Hum Genet2018
30577731The International Conference on Intelligent Biology and Medicine (ICIBM) 2018: systems biology on diverse data types.BMC Syst Biol2018
29445242Colorectal Cancer-Associated Genes Are Associated with Tooth Agenesis and May Have a Role in Tooth Development.Sci Rep2018
29610217Sequence-Based Analysis of Lipid-Related Metabolites in a Multiethnic Study.Genetics2018
29679242Automatic Organ Segmentation for CT Scans Based on Super-Pixel and Convolutional Neural Networks.J Digit Imaging2018
29193502FOXP3 mutations causing early-onset insulin-requiring diabetes but without other features of immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome.Pediatr Diabetes2018
27709577In Silico Prediction of Deleteriousness for Nonsynonymous and Splice-Altering Single Nucleotide Variants in the Human Genome.Methods Mol Biol2017
28089252Practical Approaches for Whole-Genome Sequence Analysis of Heart- and Blood-Related Traits.Am J Hum Genet2017
28125085The next generation of population-based spinal muscular atrophy carrier screening: comprehensive pan-ethnic SMN1 copy-number and sequence variant analysis by massively parallel sequencing.Genet Med2017
28347562Automatic segmentation of liver tumors from multiphase contrast-enhanced CT images based on FCNs.Artif Intell Med2017
29178643Role of WNT10A in failure of tooth development in humans and zebrafish.Mol Genet Genomic Med2017
29074945Analysis commons, a team approach to discovery in a big-data environment for genetic epidemiology.Nat Genet2017
28813562Polygenic Scores for Major Depressive Disorder and Risk of Alcohol Dependence.JAMA Psychiatry2017
28854705Whole-genome sequencing study of serum peptide levels: the Atherosclerosis Risk in Communities study.Hum Mol Genet2017
28903421Development and validation of a preoperative prediction model for colorectal cancer T-staging based on MDCT images and clinical information.Oncotarget2017
27999115The performance of deleteriousness prediction scores for rare non-protein-changing single nucleotide variants in human genes.J Med Genet2017
26773050FLAGS: A Flexible and Adaptive Association Test for Gene Sets Using Summary Statistics.Genetics2016
26555599dbNSFP v3.0: A One-Stop Database of Functional Predictions and Annotations for Human Nonsynonymous and Splice-Site SNVs.Hum Mutat2016
26395054WGSA: an annotation pipeline for human genome sequencing studies.J Med Genet2016
27934697The population genomics of rhesus macaques (Macaca mulatta) based on whole-genome sequences.Genome Res2016
28007024iCAGES: integrated CAncer GEnome Score for comprehensively prioritizing driver genes in personal cancer genomes.Genome Med2016
27884205Whole genome sequence analysis of serum amino acid levels.Genome Biol2016
27256581Identification of Rare Variants in Metabolites of the Carnitine Pathway by Whole Genome Sequencing Analysis.Genet Epidemiol2016
27284292GS/DBM/PLA porous composite biomaterial for the treatment of infective femoral condyle defect in rats.Exp Ther Med2016
25552646Comparison and integration of deleteriousness prediction methods for nonsynonymous SNVs in whole exome sequencing studies.Hum Mol Genet2015
25915599Analysis of loss-of-function variants and 20 risk factor phenotypes in 8,554 individuals identifies loci influencing chronic disease.Nat Genet2015
25848749Exploring population size changes using SNP frequency spectra.Nat Genet2015
25807536Population genomic analysis of 962 whole genome sequences of humans reveals natural selection in non-coding regions.PLoS One2015
23914949Neonatal diabetes, gallbladder agenesis, duodenal atresia, and intestinal malrotation caused by a novel homozygous mutation in RFX6.Pediatr Diabetes2014
25416802In silico prediction of splice-altering single nucleotide variants in the human genome.Nucleic Acids Res2014
25136813Gene-specific function prediction for non-synonymous mutations in monogenic diabetes genes.PLoS One2014
24733182Tendon allograft sterilized by peracetic acid/ethanol combined with gamma irradiation.J Orthop Sci2014
24951662Sequencing of 2 subclinical atherosclerosis candidate regions in 3669 individuals: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study.Circ Cardiovasc Genet2014
24951659Strategies to design and analyze targeted sequencing data: cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study.Circ Cardiovasc Genet2014
24959832Associations of NINJ2 sequence variants with incident ischemic stroke in the Cohorts for Heart and Aging in Genomic Epidemiology (CHARGE) consortium.PLoS One2014
24442821The effects of different crossing-linking conditions of genipin on type I collagen scaffolds: an in vitro evaluation.Cell Tissue Bank2014
24263461In silico tools for splicing defect prediction: a survey from the viewpoint of end users.Genet Med2014
23514131Significantly fewer protein functional changing variants for lipid metabolism in Africans than in Europeans.J Transl Med2013
24268660Integrating GWASs and human protein interaction networks identifies a gene subnetwork underlying alcohol dependence.Am J Hum Genet2013
  • 1 - 50 of 73

Recommended Authors

Xiaowei Zhan
Southwestern Medical Center, University of Texas
Career Start Year 2012
Number of shared co-authors 15
Jiayin Wang
Xi'an Jiaotong University
Career Start Year 2012
Number of shared co-authors 5
Hao Hu
Aerospace Center Hospital
Career Start Year 2011
Number of shared co-authors 10
Monnat Pongpanich
Chulalongkorn University
Career Start Year 2010
Number of shared co-authors 2
Aakrosh Ratan
Center for Public Health Genomics, University of Virginia
Career Start Year 2008
Number of shared co-authors 19
Martin Kircher
Berlin Institute of Health (BIH) at Charite-Universitatsmedizin Berlin
Career Start Year 2008
Number of shared co-authors 6
Chad D Huff
University of Texas M.D. Anderson Cancer Center
Career Start Year 2007
Number of shared co-authors 22
Akihiro Fujimoto
Graduate School of Medicine, The University of Tokyo
Career Start Year 2007
Number of shared co-authors 2
Ali Torkamani
Scripps Science Institute
Career Start Year 2005
Number of shared co-authors 8
Vikas Bansal
University of California San Diego
Career Start Year 2004
Number of shared co-authors 8
Qingrun Zhang
University of Calgary
Career Start Year 2003
Number of shared co-authors 17
Lachlan J M Coin
The Peter Doherty Institute for Infection and Immunity, The University of Melbourne
Career Start Year 2003
Number of shared co-authors 24
Daniel G MacArthur
Broad Institute of MIT and Harvard
Career Start Year 2003
Number of shared co-authors 34
Yufeng Shen
Columbia University
Career Start Year 2002
Number of shared co-authors 40
Yungang He
Shanghai Fifth People's Hospital, Institutes of Biomedical Sciences, Fudan University
Career Start Year 2002
Number of shared co-authors 13
Sean D Mooney
University of Washington
Career Start Year 2001
Number of shared co-authors 10
Yosuke Kawai
Research Institute, National Center for Global Health and Medicine
Career Start Year 2001
Number of shared co-authors 4
Nancy F Hansen
National Human Genome Research Institute, National Institutes of Health
Career Start Year 2000
Number of shared co-authors 20
Chao Xing
University of Texas Southwestern Medical Center
Career Start Year 1999
Number of shared co-authors 5
Vineet Bafna
University of California San Diego
Career Start Year 1998
Number of shared co-authors 101
Yan Cui
University of Tennessee Health Science Center
Career Start Year 1998
Number of shared co-authors 0
Jared C Roach
Institute for Systems Biology
Career Start Year 1995
Number of shared co-authors 14
Jean-Pierre A Kocher
Mayo Clinic
Career Start Year 1991
Number of shared co-authors 2
Gustavo Glusman
Institute for Systems Biology
Career Start Year 1988
Number of shared co-authors 21
Li Jin
Fudan University
Career Start Year 1988
Number of shared co-authors 22
Pui-Yan Kwok
Cardiovascular Research Institute, University of California San Francisco
Career Start Year 1987
Number of shared co-authors 31
David Haussler
Genomics Institute, University of California Santa Cruz
Career Start Year 1986
Number of shared co-authors 67
James C Mullikin
National Human Genome Research Institute, National Institutes of Health
Career Start Year 1985
Number of shared co-authors 54
Tatsuhiko Tsunoda
The University of Tokyo
Career Start Year 1984
Number of shared co-authors 29
Kelly A Frazer
University of California, USA Institute for Genomic Medicine
Career Start Year 1967
Number of shared co-authors 22

Collaborators

Eric Boerwinkle
Baylor College of Medicine
Co-authored papers 31
Richard A Gibbs
Baylor College of Medicine
Co-authored papers 16
Donna M Muzny
Baylor College of Medicine
Co-authored papers 14
Alanna C Morrison
Co-authored papers 11
Bruce M Psaty
Co-authored papers 8
Jennifer A Brody
Co-authored papers 8
Joshua C Bis
Co-authored papers 7
Laura Adrienne Cupples
Co-authored papers 7
Ginger A Metcalf
Co-authored papers 5
Andrew D Johnson
and Blood Institute
Co-authored papers 5
Kenneth Rice
Co-authored papers 4
Scott M Lippman
Moores Cancer Center, university of california san diego
Co-authored papers 4
Fuli Yu
East China University of Science and Technology
Co-authored papers 4
Thomas Lumley
Co-authored papers 3
Zhongming Zhao
Center for Precision Health, The University of Texas Health Science Center at Houston
Co-authored papers 3
James B Potash
University Hospital Frankfurt
Co-authored papers 3
Susan R Heckbert
Co-authored papers 3
Christie L Kovar
Baylor College of Medicine
Co-authored papers 3
Taylor J Maxwell
Computational Biology Institute, The George Washington University
Co-authored papers 3
Christopher J O'Donnell
Brigham and Women's Hospital, Harvard Medical School
Co-authored papers 3
Paul S de Vries
Co-authored papers 2
Stacey Gabriel
Broad Institute of MIT and Harvard
Co-authored papers 2
Stephen S Rich
Co-authored papers 2
Jennifer E Below
Vanderbilt Genetics Institute, Vanderbilt University Medical Center
Co-authored papers 2
Nora Franceschini
University of North Carolina
Co-authored papers 2
Braxton D Mitchell
Co-authored papers 2
Craig L Hanis
Co-authored papers 2
Charles C White
University of Tennessee College of Medicine Chattanooga
Co-authored papers 2
Thomas H Mosley
Co-authored papers 2
Irene F Newsham
MD Anderson Cancer Center
Co-authored papers 2
Release 1.2