Personal information

Emails & domains

Verified email addresses

Keywords

RNA-Seq, Population genetics, Genomic medicine, Bioinformatics, WGS, Medical genetics, WES, Genetic counseling, Bioinformatics, Herb

Countries

China

Activities

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Employment (7)

Westlake University: Hangzhou, Zhejiang, CN

2022-03-02 to present | Assistant Researcher
Employment
Source: Self-asserted source
Peikuan Cong

Westlake Institute for Advanced Study: Hangzhou, Zhejiang, CN

2020-01-06 to 2022-03-01 | Postdoc
Employment
Source: Self-asserted source
Peikuan Cong

Westlake University: Hangzhou, Zhejiang, CN

2017-09-01 to 2020-01-05 | Assistant Researcher
Employment
Source: Self-asserted source
Peikuan Cong

Hangzhou Beingen Biotechnoloy Co.,Ltd: Hangzhou, Zhejiang, CN

2015-05-02 to 2017-08-01 | Technical Director
Employment
Source: Self-asserted source
Peikuan Cong

Novogene Bioinformatics Institute: Beijing, CN

2014-07-01 to 2015-04-30 | Bioinformatics Engineer
Employment
Source: Self-asserted source
Peikuan Cong

Leiden University Medical Center: Leiden, NL

2013-01-01 to 2013-05-31 | exchange PhD student
Employment
Source: Self-asserted source
Peikuan Cong

BGI Tech Solutions Co Ltd: Shenzhen, Guangdong, CN

2011-03-01 to 2012-01-31 | Intern
Employment
Source: Self-asserted source
Peikuan Cong

Education and qualifications (3)

Zhejiang University: Hangzhou, Zhejiang, CN

2010-09-01 to 2014-06-30 | Phd
Education
Source: Self-asserted source
Peikuan Cong

Zhejiang University: Hangzhou, Zhejiang, CN

2006-09-01 to 2008-06-30 | Master
Education
Source: Self-asserted source
Peikuan Cong

Shandong Agricultural University: Taian, Shandong, CN

2002-09-01 to 2006-06-30 | Bachelor
Education
Source: Self-asserted source
Peikuan Cong

Works (20)

SEAD reference panel with 22,134 haplotypes boosts rare variant imputation and genome-wide association analysis in Asian populations

Nature Communications
2024-12-30 | Journal article | Author
DOI: 10.1038/s41467-024-55147-4
Part of ISSN: 2041-1723
Contributors: Meng-Yuan Yang; Jia-Dong Zhong; Xin Li; Geng Tian; Wei-Yang Bai; Yi-Hu Fang; Mo-Chang Qiu; Cheng-Da Yuan; Chun-Fu Yu; Nan Li et al.
Source: Self-asserted source
Peikuan Cong

A novel pathogenic splicing mutation of RPGR in a Chinese family with X-linked retinitis pigmentosa verified by minigene splicing assay

International journal of ophthalmology
2023-10-18 | Journal article
DOI: 10.18240/ijo.2023.10.06
PMID: 37854381
PMC: PMC10559041
Contributors: Wang HQ; Cong PK; He T; Yu XF; Huo YN
Source: Self-asserted source
Peikuan Cong

The causal mutation in ARR3 gene for high myopia and progressive color vision defect

Scientific Reports
2023-06-02 | Journal article
DOI: 10.1038/s41598-023-36141-0
Part of ISSN: 2045-2322
Contributors: Lei Gu; Peikuan Cong; Qingyao Ning; Bo Jiang; Jianyong Wang; Hongguang Cui
Source: Self-asserted source
Peikuan Cong via Crossref Metadata Search

Identification of clinically actionable secondary genetic variants from whole‐genome sequencing in a large‐scale Chinese population

Clinical and Translational Medicine
2022-05 | Journal article
DOI: 10.1002/ctm2.866
Contributors: Pei‐Kuan Cong; Saber Khederzadeh; Cheng‐Da Yuan; Rui‐Jie Ma; Yi‐Yao Zhang; Jun‐Quan Liu; Shi‐Hui Yu; Lin Xu; Jian‐Hua Gao; Hong‐Xu Pan et al.
Source: check_circle
Crossref

Genomic analyses of 10,376 individuals in the Westlake BioBank for Chinese (WBBC) pilot project

Nature Communications
2022-05-26 | Journal article
DOI: 10.1038/s41467-022-30526-x
Contributors: Pei-Kuan Cong; Wei-Yang Bai; Jin-Chen Li; Meng-Yuan Yang; Saber Khederzadeh; Si-Rui Gai; Nan Li; Yu-Heng Liu; Shi-Hui Yu; Wei-Wei Zhao et al.
Source: check_circle
Crossref

Integrative analysis of genomic and epigenomic data reveal underlying superenhancer-mediated microRNA regulatory network for human bone mineral density.

Human molecular genetics
2021-11 | Journal article
DOI: 10.1093/hmg/ddab181
PMID: 34230965
PMC: PMC8561425
Contributors: Bai WY; Xia JW; Rong XL; Cong PK; Khederzadeh S; Zheng HF
Source: Self-asserted source
Peikuan Cong via Europe PubMed Central

Observational and genetic evidence highlight the association of human sleep behaviors with the incidence of fracture

Communications Biology
2021-11-26 | Journal article
DOI: 10.1038/s42003-021-02861-0
Contributors: Yu Qian; Jiangwei Xia; Ke-Qi Liu; Lin Xu; Shu-Yang Xie; Guo-Bo Chen; Pei-Kuan Cong; Saber Khederzadeh; Hou-Feng Zheng
Source: check_circle
Crossref

Cohort profile: the Westlake BioBank for Chinese (WBBC) pilot project.

BMJ open
2021-06 | Journal article
DOI: 10.1136/bmjopen-2020-045564
PMID: 34183340
PMC: PMC8240579
Contributors: Zhu XW; Liu KQ; Wang PY; Liu JQ; Chen JY; Xu XJ; Xu JJ; Qiu MC; Sun Y; Liu C et al.
Source: Self-asserted source
Peikuan Cong via Europe PubMed Central

Systemic evaluation of the relationship between psoriasis, psoriatic arthritis and osteoporosis: observational and Mendelian randomisation study.

Annals of the rheumatic diseases
2020-07 | Journal article
DOI: 10.1136/annrheumdis-2020-217892
PMID: 32737104
PMC: PMC7970448
Contributors: Xia J; Xie SY; Liu KQ; Xu L; Zhao PP; Gai SR; Guan PL; Zhao JQ; Zhu YP; Tsoi LC et al.
Source: Self-asserted source
Peikuan Cong via Europe PubMed Central

Identification of PIEZO1 polymorphisms for human bone mineral density.

Bone
2020-01 | Journal article
DOI: 10.1016/j.bone.2020.115247
PMID: 31968281
Contributors: Bai WY; Wang L; Ying ZM; Hu B; Xu L; Zhang GQ; Cong PK; Zhu X; Zou W; Zheng HF
Source: Self-asserted source
Peikuan Cong via Europe PubMed Central

Genotype imputation and reference panel: a systematic evaluation on haplotype size and diversity.

Briefings in bioinformatics
2019-11 | Journal article
DOI: 10.1093/bib/bbz108
PMID: 32002535
Contributors: Bai WY; Zhu XW; Cong PK; Zhang XJ; Richards JB; Zheng HF
Source: Self-asserted source
Peikuan Cong via Europe PubMed Central

LOVD-DASH: A comprehensive LOVD database coupled with diagnosis and an at-risk assessment system for hemoglobinopathies.

Human mutation
2019-09 | Journal article
DOI: 10.1002/humu.23863
PMID: 31286593
PMC: PMC6899610
Contributors: Zhang L; Zhang Q; Tang Y; Cong P; Ye Y; Chen S; Zhang X; Chen Y; Zhu B; Cai W et al.
Source: Self-asserted source
Peikuan Cong via Europe PubMed Central

A Chinese patient with KBG syndrome and a 9q31.2-33.1 microdeletion.

European journal of medical genetics
2013-01 | Journal article
DOI: 10.1016/j.ejmg.2013.01.007
PMID: 23369839
Contributors: Xu M; Zhou H; Yong J; Cong P; Li C; Yu Y; Qi M
Source: Self-asserted source
Peikuan Cong via Europe PubMed Central

Exome sequencing identifies NMNAT1 mutations as a cause of Leber congenital amaurosis.

Nature genetics
2012-07 | Journal article
DOI: 10.1038/ng.2370
PMID: 22842231
Contributors: Chiang PW; Wang J; Chen Y; Fu Q; Zhong J; Chen Y; Yi X; Wu R; Gan H; Shi Y et al.
Source: Self-asserted source
Peikuan Cong via Europe PubMed Central

A large deletion/insertion-induced frameshift mutation of the androgen receptor gene in a family with a familial complete androgen insensitivity syndrome.

Gene
2012-03 | Journal article
DOI: 10.1016/j.gene.2012.02.028
PMID: 22487869
Contributors: Cong P; Ye Y; Wang Y; Lu L; Yong J; Yu P; Joseph KK; Jin F; Qi M
Source: Self-asserted source
Peikuan Cong via Europe PubMed Central

Preimplantation and prenatal genetic diagnosis for androgen insensitivity syndrome resulting from a novel deletion/insertion mutation.

Clinical genetics
2012-02 | Journal article
DOI: 10.1111/j.1399-0004.2012.01847.x
PMID: 22332610
Contributors: Ye Y; Cong P; Yu P; Qi M; Jin F
Source: Self-asserted source
Peikuan Cong via Europe PubMed Central

Novel LOVD databases for hereditary breast cancer and colorectal cancer genes in the Chinese population.

Human mutation
2011-10 | Journal article
DOI: 10.1002/humu.21588
PMID: 21901790
Contributors: Pan M; Cong P; Wang Y; Lin C; Yuan Y; Dong J; Banerjee S; Zhang T; Chen Y; Zhang T et al.
Source: Self-asserted source
Peikuan Cong via Europe PubMed Central

LQTS gene LOVD database.

Human mutation
2010-11 | Journal article
DOI: 10.1002/humu.21341
PMID: 20809527
PMC: PMC3037562
Contributors: Zhang T; Moss A; Cong P; Pan M; Chang B; Zheng L; Fang Q; Zareba W; Robinson J; Lin C et al.
Source: Self-asserted source
Peikuan Cong via Europe PubMed Central

Familial syndrome resembling Aarskog syndrome.

American journal of medical genetics. Part A
2010-08 | Journal article
DOI: 10.1002/ajmg.a.33487
PMID: 20607856
Contributors: Xu M; Qi M; Zhou H; Yong J; Qiu H; Cong P; Hong X; Li C; Jiang Y; Chen X et al.
Source: Self-asserted source
Peikuan Cong via Europe PubMed Central

Genomic organization and promoter analysis of the Trichomonas vaginalis core histone gene families.

Parasitology international
2009-09 | Journal article
DOI: 10.1016/j.parint.2009.08.010
PMID: 19744576
Contributors: Cong P; Luo Y; Bao W; Hu S
Source: Self-asserted source
Peikuan Cong via Europe PubMed Central
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