Publications:

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SNPs in 3'UTR miRNA Target Sequences Associated with Individual Drug Susceptibility.

International Journal Of Molecular Sciences

Rykova, Elena E; Ershov, Nikita N; Damarov, Igor I; Merkulova, Tatiana T

Publication Date: 2022-11-08

Variant appearance in text: rs10211

PubMed Link: 36430200

Variant Present in the following documents:

• Main text
• ijms-23-13725.pdf

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Caffeine Therapy for Apnea of Prematurity: Role of the Circadian CLOCK Gene Polymorphism.

Frontiers In Pharmacology

Guo, Hong-Li HL; Long, Jia-Yi JY; Hu, Ya-Hui YH; Liu, Yun Y; He, Xin X; Li, Ling L; Xia, Ying Y; Ding, Xuan-Sheng XS; Chen, Feng F; Xu, Jing J; Cheng, Rui R

Publication Date: 2021

Variant appearance in text: rs10211

PubMed Link: 35145399

Variant Present in the following documents:

• Main text
• fphar-12-724145.pdf

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An accessible insight into genetic findings for transplantation recipients with suspected genetic kidney disease.

Npj Genomic Medicine

Wang, Zhigang Z; Xu, Hongen H; Xiang, Tianchao T; Liu, Danhua D; Xu, Fei F; Zhao, Lixiang L; Feng, Yonghua Y; Xu, Linan L; Liu, Jialu J; Fang, Ye Y; Liu, Huanfei H; Li, Ruijun R; Hu, Xinxin X; Guan, Jingyuan J; Liu, Longshan L; Feng, Guiwen G; Shen, Qian Q; Xu, Hong H; Frishman, Dmitrij D; Tang, Wenxue W; Guo, Jiancheng J; Rao, Jia J; Shang, Wenjun W

Publication Date: 2021-07-02

Variant appearance in text: rs10211

PubMed Link: 34215756

Variant Present in the following documents:

• 41525_2021_219_MOESM1_ESM.pdf

View BVdb publication page

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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: rs10211

PubMed Link: 34054912

Variant Present in the following documents:

• Table_2.xlsx, sheet 1

View BVdb publication page

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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: rs10211

PubMed Link: 33791233

Variant Present in the following documents:

• Table_2.xlsx, sheet 1

View BVdb publication page

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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: rs10211

PubMed Link: 32529721

Variant Present in the following documents:

• JCLA-34-e23418-s003.xls, sheet 1

View BVdb publication page

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Influence of Genetic Variants on Steady-State Etonogestrel Concentrations Among Contraceptive Implant Users.

Obstetrics And Gynecology

Lazorwitz, Aaron A; Aquilante, Christina L CL; Oreschak, Kris K; Sheeder, Jeanelle J; Guiahi, Maryam M; Teal, Stephanie S

Publication Date: 2019-04

Variant appearance in text: rs10211

PubMed Link: 30870275

Variant Present in the following documents:

• Main text

View BVdb publication page

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Whole exome sequencing for the identification of CYP3A7 variants associated with tacrolimus concentrations in kidney transplant patients.

Scientific Reports

Sohn, Minji M; Kim, Myeong Gyu MG; Han, Nayoung N; Kim, In-Wha IW; Gim, Jungsoo J; Min, Sang-Il SI; Song, Eun Young EY; Kim, Yon Su YS; Jung, Hun Soon HS; Shin, Young Kee YK; Ha, Jongwon J; Oh, Jung Mi JM

Publication Date: 2018-12-24

Variant appearance in text: rs10211

PubMed Link: 30584253

Variant Present in the following documents:

• Main text
• 41598_2018_Article_36085.pdf

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: rs10211

PubMed Link: 30319441

Variant Present in the following documents:

• Table_6.xlsx, sheet 1
• Table_5.xlsx, sheet 1
• Table_7.xlsx, sheet 1

View BVdb publication page

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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: rs10211

PubMed Link: 29221171

Variant Present in the following documents:

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

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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: rs10211

PubMed Link: 28690861

Variant Present in the following documents:

• hgv201727-s1.xls, sheet 1

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: rs10211

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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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: rs10211

PubMed Link: 25944692

Variant Present in the following documents:

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

View BVdb publication page

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Genotype and age at Parkinson disease diagnosis.

International Journal Of Molecular Epidemiology And Genetics

Searles Nielsen, Susan S; Bammler, Theo K TK; Gallagher, Lisa G LG; Farin, Federico M FM; Longstreth, Wt W; Franklin, Gary M GM; Swanson, Phillip D PD; Checkoway, Harvey H

Publication Date: 2013

Variant appearance in text: rs10211

PubMed Link: 23565323

Variant Present in the following documents:

• Main text

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Impact of the Interaction between 3'-UTR SNPs and microRNA on the Expression of Human Xenobiotic Metabolism Enzyme and Transporter Genes.

Frontiers In Genetics

Wei, Rongrong R; Yang, Fan F; Urban, Thomas J TJ; Li, Lang L; Chalasani, Naga N; Flockhart, David A DA; Liu, Wanqing W

Publication Date: 2012

Variant appearance in text: rs10211

PubMed Link: 23181071

Variant Present in the following documents:

• Main text

View BVdb publication page

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Shared ancestral susceptibility to colorectal cancer and other nutrition related diseases.

Bmc Medical Genetics

Huhn, Stefanie S; Bevier, Melanie M; Rudolph, Anja A; Pardini, Barbara B; Naccarati, Alessio A; Hein, Rebecca R; Hoffmeister, Michael M; Vodickova, Ludmila L; Novotny, Jan J; Brenner, Hermann H; Chang-Claude, Jenny J; Hemminki, Kari K; Vodicka, Pavel P; Försti, Asta A

Publication Date: 2012-10-05

Variant appearance in text: rs10211

PubMed Link: 23036011

Variant Present in the following documents:

• Main text

View BVdb publication page

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Analysis of pharmacogenetic traits in two distinct South African populations.

Human Genomics

Ikediobi, Ogechi O; Aouizerat, Bradley B; Xiao, Yuanyuan Y; Gandhi, Monica M; Gebhardt, Stefan S; Warnich, Louise L

Publication Date: 2011-05

Variant appearance in text: rs10211

PubMed Link: 21712189

Variant Present in the following documents:

• Main text
• 1479-7364-5-4-265.pdf

View BVdb publication page

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Survey of allelic expression using EST mining.

Genome Research

Ge, Bing B; Gurd, Scott S; Gaudin, Tiffany T; Dore, Carole C; Lepage, Pierre P; Harmsen, Eef E; Hudson, Thomas J TJ; Pastinen, Tomi T

Publication Date: 2005-11

Variant appearance in text: rs10211

PubMed Link: 16251468

Variant Present in the following documents:

• Main text

View BVdb publication page

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