Evidence map›Paper›PMID 30567904›Full record

ArticleJournal of medical genetics2019

Comprehensive genomic variation profiling of cervical intraepithelial neoplasia and cervical cancer identifies potential targets for cervical cancer early warning.

Jian Huang, Zhaoyang Qian, Yuhua Gong, Yanzhou Wang, Yanfang Guan, Yingxin Han, Xin Yi, Wanqiu Huang, Liyan Ji, Jiajia Xu and 18 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of medical genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
3.9field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

40 citing papers in PubMed, 61 citations in OpenAlex.

  1. Article
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  7. Advances in cervical cancer: current insights and future directions.Cancer communications (London, England) · 2025
    Review
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  10. Review
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  13. Advances in Mapping Tumor Progression from Precancer Atlases.Cancer prevention research (Philadelphia, Pa.) · 2023
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

28 authors at 7 institutions in 1 country.

Jian Huang *Key Laboratory of Systems Biomedicine (Ministry of Education) and Collaborative Innovation Center of Systems Biomedicine, Shanghai Center for Systems Biomedicine, Shanghai Jiao Tong University, Shanghai, China.ORCID 0000-0002-3153-0296
Zhaoyang Qian *Binhai Genomics Institute, BGI-Tianjin, Tianjin, China.
Yuhua Gong *Geneplus-Beijing, Beijing, China.
Yanzhou Wang *Department of Obstetrics and Gynecology, Southwestern Hospital, Third Military Medical University, Chongqing, China.
Yanfang GuanGeneplus-Beijing, Beijing, China.
Yingxin HanKey Laboratory of Systems Biomedicine (Ministry of Education) and Collaborative Innovation Center of Systems Biomedicine, Shanghai Center for Systems Biomedicine, Shanghai Jiao Tong University, Shanghai, China.
Xin YiGeneplus-Beijing, Beijing, China.
Wanqiu HuangKey Laboratory of Systems Biomedicine (Ministry of Education) and Collaborative Innovation Center of Systems Biomedicine, Shanghai Center for Systems Biomedicine, Shanghai Jiao Tong University, Shanghai, China.
Liyan JiGeneplus-Beijing, Beijing, China.
Jiajia XuBinhai Genomics Institute, BGI-Tianjin, Tianjin, China.
Mengyuan SuBinhai Genomics Institute, BGI-Tianjin, Tianjin, China.
Qing YuanKey Laboratory of Systems Biomedicine (Ministry of Education) and Collaborative Innovation Center of Systems Biomedicine, Shanghai Center for Systems Biomedicine, Shanghai Jiao Tong University, Shanghai, China.
Shujian CuiShanghai-MOST Key Laboratory for Disease and Health Genomics, Chinese National Human Genome at Shanghai, Shanghai, China.
Jinling ZhangShenzhen People's Hospital, Second Clinical Medical College of Jinan University, Shenzhen, China.
Chaohui BaoKey Laboratory of Systems Biomedicine (Ministry of Education) and Collaborative Innovation Center of Systems Biomedicine, Shanghai Center for Systems Biomedicine, Shanghai Jiao Tong University, Shanghai, China.
Weilong LiuShenzhen Key Laboratory of Infection and Immunity, Shenzhen Third People's Hospital, Guangdong Medical University, Shenzhen, Guangdong, China.
Xi ChenBinhai Genomics Institute, BGI-Tianjin, Tianjin, China.
Ming ZhangBinhai Genomics Institute, BGI-Tianjin, Tianjin, China.
Xiaohuan GaoBinhai Genomics Institute, BGI-Tianjin, Tianjin, China.
Renhua WuBinhai Genomics Institute, BGI-Tianjin, Tianjin, China.
Yinxin ZhangKey Laboratory of Systems Biomedicine (Ministry of Education) and Collaborative Innovation Center of Systems Biomedicine, Shanghai Center for Systems Biomedicine, Shanghai Jiao Tong University, Shanghai, China.
Huicheng XuDepartment of Obstetrics and Gynecology, Southwestern Hospital, Third Military Medical University, Chongqing, China.
Shida ZhuBGI-Shenzhen, Shenzhen, Guangdong, China.
Hongmei ZhuBinhai Genomics Institute, BGI-Tianjin, Tianjin, China.
Ling YangGeneplus-Beijing, Beijing, China.
Xun XuBGI-Shenzhen, Shenzhen, Guangdong, China.
Pingyu ZhouSTD Institute, Shanghai Skin Disease Hospital, Tong Ji University, Shanghai, China.
Zhiqing LiangDepartment of Obstetrics and Gynecology, Southwestern Hospital, Third Military Medical University, Chongqing, China.
BGI Group (China) · CNShanghai Jiao Tong University · CNArmy Medical University · CNChinese National Human Genome Center · CNGuangdong Medical College · CNJinan University · CNShanghai Skin Disease Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTo better understand the pathogenesis of cervical cancer (CC), we systematically analysed the genomic variation and human papillomavirus (HPV) integration profiles of cervical intraepithelial neoplasia (CIN) and CC.

methodsWe performed whole-genome sequencing or whole-exome sequencing of 102 tumour-normal pairs and human papillomavirus probe capture sequencing of 45 CCs, 44 CIN samples and 25 normal cervical samples, and constructed strict integrated workflow of genomic analysis.

resultsMutational analysis identified eight significantly mutated genes in CC including four genes (

conclusionOur results lay the foundation for a deep understanding of the molecular mechanisms and finding new diagnostic and therapeutic targets of CC.

Indexed as

Gene Expression ProfilingGenetic VariationBiomarkers, TumorDNA Copy Number VariationsFemaleGenomicsHigh-Throughput Nucleotide SequencingHumansMutationNeoplasm StagingUterine Cervical DysplasiaUterine Cervical NeoplasmsWhole Genome SequencingBiomarkers, Tumorcervical cancergenomic variationhuman papillomavirus integrationpathogenesis

Identifiers

PMID30567904
PMCPMC6581088
OpenAlexW2904296893

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.