Skip to Main Content

Author Details

Chunlin Xiao
Chongqing Aier Eye Hospital
2000
32
18
PMIDPaper TitleJournal TitlePublished Year
34711123MiRNA-375 inhibits retinoblastoma progression through targeting ERBB2 and inhibiting MAPK1/MAPK3 signalling pathway.Cutan Ocul Toxicol2022
36352452Personalized genome assembly for accurate cancer somatic mutation discovery using tumor-normal paired reference samples.Genome Biol2022
35357935A complete reference genome improves analysis of human genetic variation.Science2022
36380755Towards increased accuracy and reproducibility in SARS-CoV-2 next generation sequence analysis for public health surveillance.bioRxiv2022
36514120Structural variant analysis of a cancer reference cell line sample using multiple sequencing technologies.Genome Biol2022
34980216Assessing reproducibility of inherited variants detected with short-read whole genome sequencing.Genome Biol2022
34711123MiRNA-375 inhibits retinoblastoma progression through targeting ERBB2 and inhibiting MAPK1/MAPK3 signalling pathway.Cutan Ocul Toxicol2022
35132260Curated variation benchmarks for challenging medically relevant autosomal genes.Nat Biotechnol2022
34996510Achieving robust somatic mutation detection with deep learning models derived from reference data sets of a cancer sample.Genome Biol2022
35357935A complete reference genome improves analysis of human genetic variation.Science2022
36514120Structural variant analysis of a cancer reference cell line sample using multiple sequencing technologies.Genome Biol2022
36352452Personalized genome assembly for accurate cancer somatic mutation discovery using tumor-normal paired reference samples.Genome Biol2022
36380755Towards increased accuracy and reproducibility in SARS-CoV-2 next generation sequence analysis for public health surveillance.bioRxiv2022
35132260Curated variation benchmarks for challenging medically relevant autosomal genes.Nat Biotechnol2022
34980216Assessing reproducibility of inherited variants detected with short-read whole genome sequencing.Genome Biol2022
34996510Achieving robust somatic mutation detection with deep learning models derived from reference data sets of a cancer sample.Genome Biol2022
34504346Toward best practice in cancer mutation detection with whole-genome and whole-exome sequencing.Nat Biotechnol2021
33863344Cross-oncopanel study reveals high sensitivity and accuracy with overall analytical performance depending on genomic regions.Genome Biol2021
34504347Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing.Nat Biotechnol2021
34504346Toward best practice in cancer mutation detection with whole-genome and whole-exome sequencing.Nat Biotechnol2021
33863344Cross-oncopanel study reveals high sensitivity and accuracy with overall analytical performance depending on genomic regions.Genome Biol2021
34504347Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing.Nat Biotechnol2021
32559231A crowdsourced set of curated structural variants for the human genome.PLoS Comput Biol2020
32541955A robust benchmark for detection of germline large deletions and insertions.Nat Biotechnol2020
32699374Author Correction: A robust benchmark for detection of germline large deletions and insertions.Nat Biotechnol2020
32559231A crowdsourced set of curated structural variants for the human genome.PLoS Comput Biol2020
32699374Author Correction: A robust benchmark for detection of germline large deletions and insertions.Nat Biotechnol2020
32541955A robust benchmark for detection of germline large deletions and insertions.Nat Biotechnol2020
30936564An open resource for accurately benchmarking small variant and reference calls.Nat Biotechnol2019
31092200Correction to: Similarities and differences between variants called with human reference genome HG19 or HG38.BMC Bioinformatics2019
31201313High-coverage, long-read sequencing of Han Chinese trio reference samples.Sci Data2019
30936564An open resource for accurately benchmarking small variant and reference calls.Nat Biotechnol2019
31201313High-coverage, long-read sequencing of Han Chinese trio reference samples.Sci Data2019
31092200Correction to: Similarities and differences between variants called with human reference genome HG19 or HG38.BMC Bioinformatics2019
29880009Efficacy of acupuncture on pelvic pain in patients with endometriosis: study protocol for a randomized, single-blind, multi-center, placebo-controlled trial.Trials2018
29880009Efficacy of acupuncture on pelvic pain in patients with endometriosis: study protocol for a randomized, single-blind, multi-center, placebo-controlled trial.Trials2018
28302358Elevated ammonium reduces the negative effect of heat stress on the stony coral Pocillopora damicornis.Mar Pollut Bull2017
28302358Elevated ammonium reduces the negative effect of heat stress on the stony coral Pocillopora damicornis.Mar Pollut Bull2017
27271295Extensive sequencing of seven human genomes to characterize benchmark reference materials.Sci Data2016
27271295Extensive sequencing of seven human genomes to characterize benchmark reference materials.Sci Data2016
22543379The 1000 Genomes Project: data management and community access.Nat Methods2012
22543379The 1000 Genomes Project: data management and community access.Nat Methods2012
18278044A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures.Nat Genet2008
18278044A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures.Nat Genet2008
16406193An efficient and high-throughput approach for experimental validation of novel human gene predictions.Genomics2006
16964229The MicroArray Quality Control (MAQC) project shows inter- and intraplatform reproducibility of gene expression measurements.Nat Biotechnol2006
16406193An efficient and high-throughput approach for experimental validation of novel human gene predictions.Genomics2006
16729877Distinct molecular mechanisms underlying clinically relevant subtypes of breast cancer: gene expression analyses across three different platforms.BMC Genomics2006
16729877Distinct molecular mechanisms underlying clinically relevant subtypes of breast cancer: gene expression analyses across three different platforms.BMC Genomics2006
16964229The MicroArray Quality Control (MAQC) project shows inter- and intraplatform reproducibility of gene expression measurements.Nat Biotechnol2006
  • 1 - 50 of 64

Recommended Authors

Broad Institute of MIT and Harvard
Career Start Year 2012
Number of shared co-authors 5
University of Melbourne, The University of Melbourne
Career Start Year 2011
Number of shared co-authors 3
National Center for Tumor Diseases (NCT), German Cancer Research Center (DKFZ)
Career Start Year 2009
Number of shared co-authors 3
Center for Public Health Genomics, University of Virginia
Career Start Year 2008
Number of shared co-authors 11
University of Heidelberg
Career Start Year 2008
Number of shared co-authors 22
Peter MacCallum Cancer Centre
Career Start Year 2007
Number of shared co-authors 2
University of Utah
Career Start Year 2007
Number of shared co-authors 11
Children's Cancer Institute, Lowy Cancer Research Centre
Career Start Year 2006
Number of shared co-authors 1
Ulsan National Institute of Science and Technology (UNIST)
Career Start Year 2005
Number of shared co-authors 3
Baylor College of Medicine
Career Start Year 2004
Number of shared co-authors 27
University of Augsburg
Career Start Year 2004
Number of shared co-authors 4
Uniformed Services University of the Health Sciences
Career Start Year 2004
Number of shared co-authors 2
University of California
Career Start Year 2003
Number of shared co-authors 3
McDonnell Genome Institute, Washington University School of Medicine
Career Start Year 2003
Number of shared co-authors 5
University of British Columbia
Career Start Year 2002
Number of shared co-authors 23
Center for Molecular Medicine, University Medical Center Utrecht
Career Start Year 2001
Number of shared co-authors 6
University of Pennsylvania
Career Start Year 2001
Number of shared co-authors 8
University of Toronto
Career Start Year 2000
Number of shared co-authors 30
Mayo Clinic
Career Start Year 2000
Number of shared co-authors 1
St. Jude Children's Research Hospital
Career Start Year 1999
Number of shared co-authors 4
National Human Genome Research Institute, National Institutes of Health
Career Start Year 1998
Number of shared co-authors 8
QIMR Berghofer Medical Research Institute
Career Start Year 1996
Number of shared co-authors 6
University of British Columbia
Career Start Year 1995
Number of shared co-authors 53
McDonnell Genome Institute, Washington University School of Medicine
Career Start Year 1994
Number of shared co-authors 40
University of British Columbia
Career Start Year 1993
Number of shared co-authors 45
Mayo Clinic
Career Start Year 1991
Number of shared co-authors 0
Baylor College of Medicine
Career Start Year 1991
Number of shared co-authors 30
The Ohio State University
Career Start Year 1988
Number of shared co-authors 28
Baylor College of Medicine
Career Start Year 1984
Number of shared co-authors 42
The Ohio State University
Career Start Year 1983
Number of shared co-authors 41

Collaborators

National Institute of Standards and Technology
Co-authored papers 9
National Center for Biotechnology Information, National Institutes of Health
Co-authored papers 8
Feil Family Brain and Mind Research Institute.
Co-authored papers 8
Co-authored papers 7
Human Phenome Institute and Shanghai Cancer Center, Fudan University
Co-authored papers 7
National Center for Toxicological Research
Co-authored papers 6
Stanford University
Co-authored papers 6
Immuneering Corporation
Co-authored papers 6
Roche Sequencing Solutions Inc.
Co-authored papers 6
National Institute of Standards and Technology
Co-authored papers 6
Georgetown University Medical Center
Co-authored papers 5
Stanford School of Medicine
Co-authored papers 5
Co-authored papers 5
Baylor College of Medicine
Co-authored papers 5
Co-authored papers 5
Co-authored papers 5
National Institute of Standards and Technology
Co-authored papers 4
Co-authored papers 4
David Geffen School of Medicine, university of california los angeles
Co-authored papers 4
Co-authored papers 4
Illumina Inc.
Co-authored papers 4
Google LLC
Co-authored papers 4
Co-authored papers 4
Co-authored papers 4
Institute for Molecular Medicine Finland (FIMM), University of Helsinki
Co-authored papers 4
Stanford University
Co-authored papers 4
Virginia Tech
Co-authored papers 3
Co-authored papers 3
Department of Bioinformatics and Clinical Systems
Co-authored papers 3
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 3