Publications:

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S100 proteins in cardiovascular diseases.

Molecular Medicine (Cambridge, Mass.)

Zhou, Yue Y; Zha, Yiwen Y; Yang, Yongqi Y; Ma, Tan T; Li, Hongliang H; Liang, Jingyan J

Publication Date: 2023-05-22

Variant appearance in text: rs9722

PubMed Link: 37217870

Variant Present in the following documents:

• Main text
• 10020_2023_Article_662.pdf

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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: rs9722

PubMed Link: 36991000

Variant Present in the following documents:

• 41467_2023_37221_MOESM5_ESM.xlsx, sheet 3

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Overlap between genetic variants associated with schizophrenia spectrum disorders and intelligence quotient: a systematic review.

Journal Of Psychiatry & Neuroscience : Jpn

Murillo-García, Nancy N; Barrio-Martínez, Sara S; Setién-Suero, Esther E; Soler, Jordi J; Papiol, Sergi S; Fatjó-Vilas, Mar M; Ayesa-Arriola, Rosa R

Publication Date: 2022

Variant appearance in text: rs9722

PubMed Link: 36414327

Variant Present in the following documents:

• 47-6-E393.pdf

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Impact of cognition-related single nucleotide polymorphisms on brain imaging phenotype in Parkinson's disease.

Neural Regeneration Research

Shen, Ting T; Pu, Jia-Li JL; Jiang, Ya-Si YS; Yue, Yu-Mei YM; He, Ting-Ting TT; Qu, Bo-Yi BY; Zhao, Shuai S; Yan, Ya-Ping YP; Lai, Hsin-Yi HY; Zhang, Bao-Rong BR

Publication Date: 2023-05

Variant appearance in text: rs9722

PubMed Link: 36255006

Variant Present in the following documents:

• Main text

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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: rs9722

PubMed Link: 36241656

Variant Present in the following documents:

• 41598_2022_20939_MOESM14_ESM.xlsx, sheet 2

View BVdb publication page

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Editorial: Relationship Between Cardiovascular Disease and Other Chronic Conditions.

Frontiers In Cardiovascular Medicine

Vassalle, Cristina C; Xiao, Junjie J; Sabatino, Laura L

Publication Date: 2022

Variant appearance in text: rs9722

PubMed Link: 35548438

Variant Present in the following documents:

• Main text
• fcvm-09-875551.pdf

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Contributions of common genetic variants to specific languages and to when a language is learned.

Scientific Reports

Wong, Patrick C M PCM; Kang, Xin X; So, Hon-Cheong HC; Choy, Kwong Wai KW

Publication Date: 2022-01-12

Variant appearance in text: rs9722

PubMed Link: 35022429

Variant Present in the following documents:

• Main text
• 41598_2021_Article_4163.pdf

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Contributions of common genetic variants to specific languages and to when a language is learned.

Scientific Reports

Wong, Patrick C M PCM; Kang, Xin X; So, Hon-Cheong HC; Choy, Kwong Wai KW

Publication Date: 2022-01-12

Variant appearance in text: rs9722

PubMed Link: 35022429

Variant Present in the following documents:

• Main text
• 41598_2021_Article_4163.pdf

View BVdb publication page

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Longitudinal assessment of S100B serum levels and clinical factors in youth patients with mood disorders.

Scientific Reports

Rajewska-Rager, Aleksandra A; Dmitrzak-Weglarz, Monika M; Kapelski, Pawel P; Lepczynska, Natalia N; Pawlak, Joanna J; Twarowska-Hauser, Joanna J; Skibinska, Maria M

Publication Date: 2021-06-07

Variant appearance in text: rs9722

PubMed Link: 34099858

Variant Present in the following documents:

• Main text
• 41598_2021_Article_91577.pdf

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The Polygenic Nature and Complex Genetic Architecture of Specific Learning Disorder.

Brain Sciences

Georgitsi, Marianthi M; Dermitzakis, Iasonas I; Soumelidou, Evgenia E; Bonti, Eleni E

Publication Date: 2021-05-14

Variant appearance in text: rs9722

PubMed Link: 34068951

Variant Present in the following documents:

• Main text
• brainsci-11-00631.pdf

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Case Report: A Variant Non-ketotic Hyperglycinemia With GLRX5 Mutations: Manifestation of Deficiency of Activities of the Respiratory Chain Enzymes.

Frontiers In Genetics

Feng, Wei-Xing WX; Zhuo, Xiu-Wei XW; Liu, Zhi-Mei ZM; Li, Jiu-Wei JW; Zhang, Wei-Hua WH; Wu, Yun Y; Han, Tong-Li TL; Fang, Fang F

Publication Date: 2021

Variant appearance in text: rs9722

PubMed Link: 34054912

Variant Present in the following documents:

• Table_2.xlsx, sheet 1

View BVdb publication page

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S100B gene polymorphisms are associated with the S100B level and Alzheimer's disease risk by altering the miRNA binding capacity.

Aging

Wang, Jiafeng J; Zhou, Yulan Y; Yang, Yixia Y; Gao, Xiang X; Liu, Zhibin Z; Hong, Guanhao G; Yao, Lifen L; Yin, Jingwen J; Gu, Xuefeng X; Li, Keshen K

Publication Date: 2021-05-12

Variant appearance in text: rs9722

PubMed Link: 33982673

Variant Present in the following documents:

• Main text

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Role of Neutrophil-Derived S100B in Acute Myocardial Infarction Patients From the Han Chinese Population.

Frontiers In Cardiovascular Medicine

Cheng, Minghui M; Su, Xu X; Liu, Dan D; Tian, Xiaoxiang X; Yan, Chenghui C; Zhang, Xiaolin X; Han, Yaling Y

Publication Date: 2020

Variant appearance in text: rs9722

PubMed Link: 33796567

Variant Present in the following documents:

• Main text
• fcvm-07-595446.pdf

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Disseminated Talaromyces marneffei Infection in a Non-HIV Infant With a Homozygous Private Variant of RELB.

Frontiers In Cellular And Infection Microbiology

Ding, Xiaofang X; Huang, Han H; Zhong, Lili L; Chen, Min M; Peng, Fang F; Zhang, Bing B; Cui, Xinyu X; Yang, Xiu-An XA

Publication Date: 2021

Variant appearance in text: rs9722

PubMed Link: 33791233

Variant Present in the following documents:

• Table_2.xlsx, sheet 1

View BVdb publication page

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Association of S100B 3'UTR polymorphism with risk of chronic heart failure in a Chinese Han population.

Medicine

Chen, Yuewu Y; Chen, Xianghong X; Yao, Maozhong M; Chen, Lei L; Chen, Weiwei W; Liu, Xianxia X

Publication Date: 2020-06-26

Variant appearance in text: rs9722

PubMed Link: 32590820

Variant Present in the following documents:

• Main text
• medi-99-e21018.pdf

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Identification of a nonsense mutation in TNNI3K associated with cardiac conduction disease.

Journal Of Clinical Laboratory Analysis

Liu, Jiang J; Liu, Da D; Li, Muzheng M; Wu, Keke K; Liu, Na N; Zhao, Chenyu C; Shi, Xiaoliu X; Liu, Qiming Q

Publication Date: 2020-09

Variant appearance in text: rs9722

PubMed Link: 32529721

Variant Present in the following documents:

• JCLA-34-e23418-s003.xls, sheet 1

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S100B single nucleotide polymorphisms exhibit sex-specific associations with chronic pain in sickle cell disease in a largely African-American cohort.

Plos One

Jhun, Ellie H EH; Sadhu, Nilanjana N; He, Ying Y; Yao, Yingwei Y; Wilkie, Diana J DJ; Molokie, Robert E RE; Wang, Zaijie Jim ZJ

Publication Date: 2020

Variant appearance in text: rs9722

PubMed Link: 32379790

Variant Present in the following documents:

• Main text
• pone.0232721.pdf

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Distinctive mutational spectrum and karyotype disruption in long-term cisplatin-treated urothelial carcinoma cell lines.

Scientific Reports

Skowron, Margaretha A MA; Petzsch, Patrick P; Hardt, Karin K; Wagner, Nicholas N; Beier, Manfred M; Stepanow, Stefanie S; Drechsler, Matthias M; Rieder, Harald H; Köhrer, Karl K; Niegisch, Günter G; Hoffmann, Michèle J MJ; Schulz, Wolfgang A WA

Publication Date: 2019-10-09

Variant appearance in text: rs9722

PubMed Link: 31597922

Variant Present in the following documents:

• 41598_2019_50891_MOESM6_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM7_ESM.xlsx, sheet 1

View BVdb publication page

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Association of S100B polymorphisms and serum S100B with risk of systemic lupus erythematous in a Chinese population.

Genetics And Molecular Biology

Lu, Yulan Y; Huang, Huatuo H; Liu, Chunhong C; Zeng, Yonglong Y; Wang, Rong R; Wang, Chunfang C; Wei, Yesheng Y; Lan, Yan Y

Publication Date: 2019

Variant appearance in text: rs9722

PubMed Link: 31271591

Variant Present in the following documents:

• Main text

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A functional polymorphism in the promoter of TUG1 is associated with an increased risk of ischaemic stroke.

Journal Of Cellular And Molecular Medicine

Wei, Ye-Sheng YS; Yang, Jun J; He, Yong-Ling YL; Shi, Xiang X; Zeng, Zhi-Neng ZN

Publication Date: 2019-09

Variant appearance in text: rs9722

PubMed Link: 31264779

Variant Present in the following documents:

• Main text

View BVdb publication page

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A functional variant rs12904 in the miR-200c binding site was associated with a decreased risk of ischemic stroke.

Lipids In Health And Disease

Zeng, Zhi-Neng ZN; Liu, Ling-Ling LL; He, Yong-Ling YL; Shi, Xiang X; Wei, Ye-Sheng YS

Publication Date: 2019-05-10

Variant appearance in text: rs9722

PubMed Link: 31077198

Variant Present in the following documents:

• Main text
• 12944_2019_Article_1060.pdf

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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: rs9722

PubMed Link: 30319441

Variant Present in the following documents:

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

View BVdb publication page

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Neuroplasticity, Neurotransmission and Brain-Related Genes in Major Depression and Bipolar Disorder: Focus on Treatment Outcomes in an Asiatic Sample.

Advances In Therapy

Calabrò, Marco M; Mandelli, Laura L; Crisafulli, Concetta C; Lee, Soo-Jung SJ; Jun, Tae-Youn TY; Wang, Sheng-Min SM; Patkar, Ashwin A AA; Masand, Prakash S PS; Benedetti, Francesco F; Han, Changsu C; Pae, Chi-Un CU; Serretti, Alessandro A

Publication Date: 2018-10

Variant appearance in text: rs9722

PubMed Link: 30178121

Variant Present in the following documents:

• Main text
• 12325_2018_Article_781.pdf

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S100B polymorphisms are associated with age of onset of Parkinson's disease.

Bmc Medical Genetics

Fardell, Camilla C; Zettergren, Anna A; Ran, Caroline C; Carmine Belin, Andrea A; Ekman, Agneta A; Sydow, Olof O; Bäckman, Lars L; Holmberg, Björn B; Dizdar, Nil N; Söderkvist, Peter P; Nissbrandt, Hans H

Publication Date: 2018-03-12

Variant appearance in text: rs9722

PubMed Link: 29529989

Variant Present in the following documents:

• Main text

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Association of S100B polymorphisms and serum S100B with risk of ischemic stroke in a Chinese population.

Scientific Reports

Lu, Yu-Lan YL; Wang, Rong R; Huang, Hua-Tuo HT; Qin, Hai-Mei HM; Liu, Chun-Hong CH; Xiang, Yang Y; Wang, Chun-Fang CF; Luo, Hong-Cheng HC; Wang, Jun-Li JL; Lan, Yan Y; Wei, Ye-Sheng YS

Publication Date: 2018-01-17

Variant appearance in text: rs9722

PubMed Link: 29343763

Variant Present in the following documents:

• Main text
• 41598_2018_Article_19156.pdf

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Proteogenomic analysis prioritises functional single nucleotide variants in cancer samples.

Oncotarget

Ma, Shiyong S; Menon, Ranjeeta R; Poulos, Rebecca C RC; Wong, Jason W H JWH

Publication Date: 2017-11-10

Variant appearance in text: rs9722

PubMed Link: 29221171

Variant Present in the following documents:

• oncotarget-08-95841-s002.xlsx, sheet 4

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[Association between S100B gene polymorphisms and hand, foot and mouth disease caused by enterovirus 71 infection].

Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal Of Contemporary Pediatrics

Li, Jing J; Shan, Ruo-Bing RB; Liu, Rui-Hai RH; Xu, Ying-Jun YJ; Qu, Ni-Yan NY; Pan, Gui-Mei GM; Zhang, Na N; Yang, Na N; Chen, Zhen-Zhen ZZ; Zhang, Wen-Xiang WX; Li, Zi-Pu ZP

Publication Date: 2017-08

Variant appearance in text: rs9722

PubMed Link: 28774366

Variant Present in the following documents:

• Main text

View BVdb publication page

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Validation of single nucleotide polymorphisms in invasive aspergillosis following hematopoietic cell transplantation.

Blood

Fisher, Cynthia E CE; Hohl, Tobias M TM; Fan, Wenhong W; Storer, Barry E BE; Levine, David M DM; Zhao, Lu Ping LP; Martin, Paul J PJ; Warren, Edus H EH; Boeckh, Michael M; Hansen, John A JA

Publication Date: 2017-05-11

Variant appearance in text: rs9722

PubMed Link: 28270451

Variant Present in the following documents:

• Main text

View BVdb publication page

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[Research advances in susceptible genes for developmental dyslexia in children].

Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal Of Contemporary Pediatrics

Kong, Rui R; Song, Ran-Ran RR

Publication Date: 2016-12

Variant appearance in text: rs9722

PubMed Link: 27974128

Variant Present in the following documents:

• Main text

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Genome-Wide Expression Profiling Reveals S100B as Biomarker for Invasive Aspergillosis.

Frontiers In Microbiology

Dix, Andreas A; Czakai, Kristin K; Springer, Jan J; Fliesser, Mirjam M; Bonin, Michael M; Guthke, Reinhard R; Schmitt, Anna L AL; Einsele, Hermann H; Linde, Jörg J; Löffler, Jürgen J

Publication Date: 2016

Variant appearance in text: rs9722

PubMed Link: 27047454

Variant Present in the following documents:

• Main text
• fmicb-07-00320.pdf

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Proteogenomic analysis reveals exosomes are more oncogenic than ectosomes.

Oncotarget

Keerthikumar, Shivakumar S; Gangoda, Lahiru L; Liem, Michael M; Fonseka, Pamali P; Atukorala, Ishara I; Ozcitti, Cemil C; Mechler, Adam A; Adda, Christopher G CG; Ang, Ching-Seng CS; Mathivanan, Suresh S

Publication Date: 2015-06-20

Variant appearance in text: rs9722

PubMed Link: 25944692

Variant Present in the following documents:

• oncotarget-06-15375-s005.xlsx, sheet 2

View BVdb publication page

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Polymorphisms in DCDC2 and S100B associate with developmental dyslexia.

Journal Of Human Genetics

Matsson, Hans H; Huss, Mikael M; Persson, Helena H; Einarsdottir, Elisabet E; Tiraboschi, Ettore E; Nopola-Hemmi, Jaana J; Schumacher, Johannes J; Neuhoff, Nina N; Warnke, Andreas A; Lyytinen, Heikki H; Schulte-Körne, Gert G; Nöthen, Markus M MM; Leppänen, Paavo H T PH; Peyrard-Janvid, Myriam M; Kere, Juha J

Publication Date: 2015-07

Variant appearance in text: rs9722

PubMed Link: 25877001

Variant Present in the following documents:

• Main text

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RACK1 is a candidate gene associated with the prognosis of patients with early stage non-small cell lung cancer.

Oncotarget

Choi, Yi-Young YY; Lee, Shin Yup SY; Lee, Won Kee WK; Jeon, Hyo-Sung HS; Lee, Eung Bae EB; Lee, Hyun Cheol HC; Choi, Jin Eun JE; Kang, Hyo-Gyoung HG; Lee, Eun Jin EJ; Bae, Eun Young EY; Yoo, Seung Soo SS; Lee, Jaehee J; Cha, Seung Ick SI; Kim, Chang Ho CH; Kim, In-San IS; Lee, Myung Hoon MH; Kim, Young Tae YT; Jheon, Sanghoon S; Park, Jae Yong JY

Publication Date: 2015-02-28

Variant appearance in text: rs9722

PubMed Link: 25686824

Variant Present in the following documents:

• Main text
• oncotarget-06-4451.pdf

View BVdb publication page

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Human genetic susceptibility to invasive aspergillosis.

Plos Pathogens

Cunha, Cristina C; Aversa, Franco F; Romani, Luigina L; Carvalho, Agostinho A

Publication Date: 2013

Variant appearance in text: rs9722

PubMed Link: 23950708

Variant Present in the following documents:

• Main text

View BVdb publication page

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Serum S100B represents a new biomarker for mood disorders.

Current Drug Targets

Schroeter, Matthias L ML; Sacher, Julia J; Steiner, Johann J; Schoenknecht, Peter P; Mueller, Karsten K

Publication Date: 2013-10

Variant appearance in text: rs9722

PubMed Link: 23701298

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genetically-determined hyperfunction of the S100B/RAGE axis is a risk factor for aspergillosis in stem cell transplant recipients.

Plos One

Cunha, Cristina C; Giovannini, Gloria G; Pierini, Antonio A; Bell, Alain S AS; Sorci, Guglielmo G; Riuzzi, Francesca F; Donato, Rosario R; Rodrigues, Fernando F; Velardi, Andrea A; Aversa, Franco F; Romani, Luigina L; Carvalho, Agostinho A

Publication Date: 2011

Variant appearance in text: rs9722

PubMed Link: 22114731

Variant Present in the following documents:

• Main text
• pone.0027962.pdf

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Serum S100B: a potential biomarker for suicidality in adolescents?

Plos One

Falcone, Tatiana T; Fazio, Vincent V; Lee, Catherine C; Simon, Barry B; Franco, Kathleen K; Marchi, Nicola N; Janigro, Damir D

Publication Date: 2010-06-14

Variant appearance in text: rs9722

PubMed Link: 20559426

Variant Present in the following documents:

• Main text
• pone.0011089.pdf

View BVdb publication page

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