Publications:

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Comprehensive proteogenomic characterization of early duodenal cancer reveals the carcinogenesis tracks of different subtypes.

Nature Communications

Li, Lingling L; Jiang, Dongxian D; Liu, Hui H; Guo, Chunmei C; Zhao, Rui R; Zhang, Qiao Q; Xu, Chen C; Qin, Zhaoyu Z; Feng, Jinwen J; Liu, Yang Y; Wang, Haixing H; Chen, Weijie W; Zhang, Xue X; Li, Bin B; Bai, Lin L; Tian, Sha S; Tan, Subei S; Yu, Zixiang Z; Chen, Lingli L; Huang, Jie J; Zhao, Jian-Yuan JY; Hou, Yingyong Y; Ding, Chen C

Publication Date: 2023-03-29

Variant appearance in text: rs3765459

PubMed Link: 36991000

Variant Present in the following documents:

• 41467_2023_37221_MOESM5_ESM.xlsx, sheet 3

View BVdb publication page

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Proteogenomic characterization of MiT family translocation renal cell carcinoma.

Nature Communications

Qu, Yuanyuan Y; Wu, Xiaohui X; Anwaier, Aihetaimujiang A; Feng, Jinwen J; Xu, Wenhao W; Pei, Xiaoru X; Zhu, Yu Y; Liu, Yang Y; Bai, Lin L; Yang, Guojian G; Tian, Xi X; Su, Jiaqi J; Shi, Guo-Hai GH; Cao, Da-Long DL; Xu, Fujiang F; Wang, Yue Y; Gan, Hua-Lei HL; Ni, Shujuan S; Sun, Meng-Hong MH; Zhao, Jian-Yuan JY; Zhang, Hailiang H; Ye, Dingwei D; Ding, Chen C

Publication Date: 2022-12-05

Variant appearance in text: rs3765459

PubMed Link: 36470859

Variant Present in the following documents:

• 41467_2022_34460_MOESM5_ESM.xlsx, sheet 2

View BVdb publication page

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Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma.

Scientific Reports

Rauf, Bushra B; Khan, Shahid Y SY; Jiao, Xiaodong X; Irum, Bushra B; Ashfaq, Ramla R; Zehra, Mubashra M; Khan, Asma A AA; Naeem, Muhammad Asif MA; Shahzad, Mohsin M; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA

Publication Date: 2022-10-14

Variant appearance in text: rs3765459

PubMed Link: 36241656

Variant Present in the following documents:

• 41598_2022_20939_MOESM14_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM15_ESM.xlsx, sheet 2

View BVdb publication page

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Distinct non-clock-like signatures of the basal cell carcinomas from three sisters with a lethal Gorlin-Goltz syndrome.

Bmc Medical Genomics

Ye, Lihua L; Wang, Li L; Peng, Kexin K; Fang, Ou O; Tian, Zhen Z; Li, Caihua C; Fu, Xiaopeng X; Chen, Qingdong Q; Chen, Jia J; Luan, Jing J; Zhang, Zhenghua Z; Zhang, Qiaoan Q

Publication Date: 2022-08-05

Variant appearance in text: CD40: 676-114G>A; rs3765459

PubMed Link: 35932013

Variant Present in the following documents:

• 12920_2022_1324_MOESM1_ESM.xlsx, sheet 1

View BVdb publication page

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Genetic overlap between temporomandibular disorders and primary headaches: A systematic review.

The Japanese Dental Science Review

Cruz, Diogo D; Monteiro, Francisca F; Paço, Maria M; Vaz-Silva, Manuel M; Lemos, Carolina C; Alves-Ferreira, Miguel M; Pinho, Teresa T

Publication Date: 2022-11

Variant appearance in text: rs3765459

PubMed Link: 35242249

Variant Present in the following documents:

• main.pdf

View BVdb publication page

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Characterization of Rheumatoid Arthritis Risk-Associated SNPs and Identification of Novel Therapeutic Sites Using an In-Silico Approach.

Biology

Akhtar, Mehran M; Ali, Yasir Y; Islam, Zia-Ul ZU; Arshad, Maria M; Rauf, Mamoona M; Ali, Muhammad M; Maodaa, Saleh N SN; Al-Farraj, Saleh A SA; El-Serehy, Hamed A HA; Jalil, Fazal F

Publication Date: 2021-06-04

Variant appearance in text: rs3765459

PubMed Link: 34199962

Variant Present in the following documents:

• Main text
• biology-10-00501.pdf

View BVdb publication page

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Shared Gene Expression Between Multiple Sclerosis and Ischemic Stroke.

Frontiers In Genetics

Li, He H; Chen, Lin L; Ma, Xiaofeng X; Cui, Pan P; Lang, Wenjing W; Hao, Junwei J

Publication Date: 2018

Variant appearance in text: rs3765459

PubMed Link: 30809253

Variant Present in the following documents:

• Main text
• fgene-09-00598.pdf

View BVdb publication page

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Identification of novel compound heterozygous SPG7 mutations-related hereditary spastic paraplegia in a Chinese family: a case report.

Bmc Neurology

Zhang, Xiaoqian X; Zhang, Lei L; Wu, Yanqing Y; Li, Gang G; Chen, Shengcai S; Xia, Yuanpeng Y; Li, Hongge H

Publication Date: 2018-11-29

Variant appearance in text: rs3765459

PubMed Link: 30497413

Variant Present in the following documents:

• 12883_2018_1199_MOESM5_ESM.xlsx, sheet 1

View BVdb publication page

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Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology

Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P

Publication Date: 2018

Variant appearance in text: CD40: 676-114G>A; rs3765459

PubMed Link: 30319441

Variant Present in the following documents:

• Table_6.xlsx, sheet 1
• Table_5.xlsx, sheet 1

View BVdb publication page

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Population-Specific Associations of Deleterious Rare Variants in Coding Region of P2RY1-P2RY12 Purinergic Receptor Genes in Large-Vessel Ischemic Stroke Patients.

International Journal Of Molecular Sciences

Janicki, Piotr K PK; Eyileten, Ceren C; Ruiz-Velasco, Victor V; Sedeek, Khaled Anwar KA; Pordzik, Justyna J; Czlonkowska, Anna A; Kurkowska-Jastrzebska, Iwona I; Sugino, Shigekazu S; Imamura-Kawasawa, Yuka Y; Mirowska-Guzel, Dagmara D; Postula, Marek M

Publication Date: 2017-12-11

Variant appearance in text: rs3765459

PubMed Link: 29232918

Variant Present in the following documents:

• ijms-18-02678-s001.pdf

View BVdb publication page

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Whole-exome sequencing analysis of Waardenburg syndrome in a Chinese family.

Human Genome Variation

Chen, Dezhong D; Zhao, Na N; Wang, Jing J; Li, Zhuoyu Z; Wu, Changxin C; Fu, Jie J; Xiao, Han H

Publication Date: 2017

Variant appearance in text: rs3765459

PubMed Link: 28690861

Variant Present in the following documents:

• hgv201727-s1.xls, sheet 1

View BVdb publication page

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CD40L and Its Receptors in Atherothrombosis-An Update.

Frontiers In Cardiovascular Medicine

Michel, Nathaly Anto NA; Zirlik, Andreas A; Wolf, Dennis D

Publication Date: 2017

Variant appearance in text: rs3765459

PubMed Link: 28676852

Variant Present in the following documents:

• Main text

View BVdb publication page

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A SNP in 5' untranslated region of CD40 gene is associated with an increased risk of ischemic stroke in a Chinese population: a case-control study.

Genetics And Molecular Biology

Huang, Hua-Tuo HT; Guo, Jing J; Xiang, Yang Y; Chen, Jian-Ming JM; Luo, Hong-Cheng HC; Meng, Lan-Qing LQ; Wei, Ye-Sheng YS

Publication Date: 2017

Variant appearance in text: rs3765459

PubMed Link: 28590502

Variant Present in the following documents:

• Main text
• 1415-4757-gmb-1678-4685-GMB-2016-0212.pdf

View BVdb publication page

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Investigation of DNA repair-related SNPs underlying susceptibility to papillary thyroid carcinoma reveals MGMT as a novel candidate gene in Belarusian children exposed to radiation.

Bmc Cancer

Lonjou, Christine C; Damiola, Francesca F; Moissonnier, Monika M; Durand, Geoffroy G; Malakhova, Irina I; Masyakin, Vladimir V; Le Calvez-Kelm, Florence F; Cardis, Elisabeth E; Byrnes, Graham G; Kesminiene, Ausrele A; Lesueur, Fabienne F

Publication Date: 2017-05-12

Variant appearance in text: rs3765459

PubMed Link: 28499365

Variant Present in the following documents:

• 12885_2017_3314_MOESM1_ESM.xls, sheet 1

View BVdb publication page

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CD40 -1C>T polymorphism and the risk of lung cancer in a Chinese population.

International Journal Of Clinical And Experimental Pathology

Zhou, Gang G; Wang, Ying Y; Fang, Ziyao Z; Liu, Rongrong R; Wang, Anhui A; Zhao, Feng F; Chen, Lihua L

Publication Date: 2015

Variant appearance in text: rs3765459

PubMed Link: 26823861

Variant Present in the following documents:

• Main text

View BVdb publication page

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Generation of a High Number of Healthy Erythroid Cells from Gene-Edited Pyruvate Kinase Deficiency Patient-Specific Induced Pluripotent Stem Cells.

Stem Cell Reports

Garate, Zita Z; Quintana-Bustamante, Oscar O; Crane, Ana M AM; Olivier, Emmanuel E; Poirot, Laurent L; Galetto, Roman R; Kosinski, Penelope P; Hill, Collin C; Kung, Charles C; Agirre, Xabi X; Orman, Israel I; Cerrato, Laura L; Alberquilla, Omaira O; Rodriguez-Fornes, Fatima F; Fusaki, Noemi N; Garcia-Sanchez, Felix F; Maia, Tabita M TM; Ribeiro, Maria L ML; Sevilla, Julian J; Prosper, Felipe F; Jin, Shengfang S; Mountford, Joanne J; Guenechea, Guillermo G; Gouble, Agnes A; Bueren, Juan A JA; Davis, Brian R BR; Segovia, Jose C JC

Publication Date: 2015-12-08

Variant appearance in text: rs3765459

PubMed Link: 26549847

Variant Present in the following documents:

• mmc3.xlsx, sheet 3
• mmc3.xlsx, sheet 2
• mmc3.xlsx, sheet 1

View BVdb publication page

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The SNP rs1883832 in CD40 gene and risk of atherosclerosis in Chinese population: a meta-analysis.

Plos One

Yun, Yan Y; Ma, Chi C; Ma, XiaoChun X

Publication Date: 2014

Variant appearance in text: rs3765459

PubMed Link: 24828072

Variant Present in the following documents:

• Main text
• pone.0097289.pdf

View BVdb publication page

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Apoptosis-Related Single Nucleotide Polymorphisms and the Risk of Non-Small Cell Lung Cancer in Women.

Journal Of Cancer Therapeutics & Research

Pathak, Anand A; Wenzlaff, Angela S AS; Hyland, Paula L PL; Cote, Michele L ML; Keele, Greg R GR; Land, Susan S; Boulton, Matthew L ML; Schwartz, Ann G AG

Publication Date: 2014

Variant appearance in text: rs3765459

PubMed Link: 24790730

Variant Present in the following documents:

• Main text

View BVdb publication page

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Association of CD40 gene polymorphisms with sporadic breast cancer in Chinese Han women of Northeast China.

Plos One

Shuang, Chen C; Dalin, Li L; Weiguang, Yuan Y; Zhenkun, Fu F; Fengyan, Xu X; Da, Pang P; Li, Dianjun D

Publication Date: 2011

Variant appearance in text: rs3765459

PubMed Link: 21912605

Variant Present in the following documents:

• Main text
• pone.0023762.pdf

View BVdb publication page

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The genetics of vascular complications in diabetes mellitus.

Cardiology Clinics

Farbstein, Dan D; Levy, Andrew P AP

Publication Date: 2010-08

Variant appearance in text: rs3765459

PubMed Link: 20621252

Variant Present in the following documents:

• Main text

View BVdb publication page

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STAT2*C related genotypes and allele but not TLR4 and CD40 gene polymorphisms are associated with higher susceptibility for asthma.

International Journal Of Biological Sciences

Hsieh, Yao-Yuan YY; Wan, Lei L; Chang, Chi-Chen CC; Tsai, Chang-Hai CH; Tsai, Fuu-Jen FJ

Publication Date: 2009

Variant appearance in text: rs3765459

PubMed Link: 19159017

Variant Present in the following documents:

• Main text
• ijbsv05p0074.pdf

View BVdb publication page

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