Publications:

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Genetics of type 2 diabetes mellitus in Indian and Global Population: A Review.

The Egyptian Journal Of Medical Human Genetics

Joseph, Anjaly A; Thirupathamma, Maradana M; Mathews, Elezebeth E; Alagu, Manickavelu M

Publication Date: 2022

Variant appearance in text: rs10010131

PubMed Link: 37192883

Variant Present in the following documents:

• Main text
• 43042_2022_Article_346.pdf

View BVdb publication page

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Genetic Variants of HNF4A, WFS1, DUSP9, FTO, and ZFAND6 Genes Are Associated with Prediabetes Susceptibility and Inflammatory Markers in the Saudi Arabian Population.

Genes

Binjawhar, Dalal N DN; Ansari, Mohammed G A MGA; Sabico, Shaun S; Hussain, Syed Danish SD; Alenad, Amal M AM; Alokail, Majed S MS; Al-Masri, Abeer A AA; Al-Daghri, Nasser M NM

Publication Date: 2023-02-21

Variant appearance in text: rs10010131

PubMed Link: 36980809

Variant Present in the following documents:

• Main text
• genes-14-00536.pdf

View BVdb publication page

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Incretin and Pancreatic β-Cell Function in Patients with Type 2 Diabetes.

Endocrinology And Metabolism (Seoul, Korea)

Ahn, Chang Ho CH; Oh, Tae Jung TJ; Min, Se Hee SH; Cho, Young Min YM

Publication Date: 2023-02-13

Variant appearance in text: rs10010131

PubMed Link: 36781163

Variant Present in the following documents:

• Main text
• enm-2023-103.pdf

View BVdb publication page

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Systolic blood pressure as the mediator of the effect of early menarche on the risk of coronary artery disease: A Mendelian randomization study.

Frontiers In Cardiovascular Medicine

Fan, Hsien-Yu HY; Huang, Yen-Tsung YT; Chen, Yun-Yu YY; Hsu, Justin BoKai JB; Li, Hung-Yuan HY; Su, Ta-Chen TC; Lin, Hung-Ju HJ; Chien, Kuo-Liong KL; Chen, Yang-Ching YC

Publication Date: 2022

Variant appearance in text: rs10010131

PubMed Link: 36698922

Variant Present in the following documents:

• Data_Sheet_1.pdf

View BVdb publication page

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The Role of ER Stress in Diabetes: Exploring Pathological Mechanisms Using Wolfram Syndrome.

International Journal Of Molecular Sciences

Morikawa, Shuntaro S; Urano, Fumihiko F

Publication Date: 2022-12-23

Variant appearance in text: rs10010131

PubMed Link: 36613674

Variant Present in the following documents:

• Main text
• ijms-24-00230.pdf

View BVdb publication page

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Mutation analysis of the WFS1 gene in a Chinese family with autosomal-dominant non-syndrome deafness.

Scientific Reports

Zhao, Jing J; Zhang, Siqi S; Jiang, Yuan Y; Liu, Yan Y; Wang, Jiantao J; Zhu, QingWen Q

Publication Date: 2022-12-23

Variant appearance in text: rs10010131

PubMed Link: 36564540

Variant Present in the following documents:

• 41598_2022_26850_MOESM3_ESM.xlsx, sheet 1
• 41598_2022_Article_26850.pdf

View BVdb publication page

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Establishment and characterization of a new mantle cell lymphoma cell line with a NOTCH2 mutation, Arbo.

Ejhaem

Safa, Firas F; Rasmussen, Terri T; Lobelle-Rich, Patricia P; Collier, Stephanie S; Milligan, Nicholas N; Schmeig, John J; Schmid, Janet J; Wiewiorowski, Carol C; Totaro, Denise D; Brown, Theresa C TC; Satyavarapu, Ishwarya I; Badoo, Melody M; Ungerleider, Nathan N; Flemington, Erik K EK; Safah, Hana H; Saba, Nakhle S NS

Publication Date: 2022-11

Variant appearance in text: rs10010131

PubMed Link: 36467812

Variant Present in the following documents:

• JHA2-3-1326-s001.xlsx, sheet 1

View BVdb publication page

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Mutation analysis of the GSDME gene in a Chinese family with non-syndromic hearing loss.

Plos One

Lei, Peiliang P; Zhu, Qingwen Q; Dong, Wenrong W; Zhang, Siqi S; Sun, Yanyan Y; Du, Xitong X; Geng, Meng M; Jiang, Yuan Y

Publication Date: 2022

Variant appearance in text: WFS1: 461-9A>G; rs10010131

PubMed Link: 36350814

Variant Present in the following documents:

• pone.0276233.s004.xlsx, sheet 1

View BVdb publication page

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The PPARGC1A Is the Gene Responsible for Thrifty Metabolism Related Metabolic Diseases: A Scoping Review.

Genes

Aisyah, Riandini R; Sadewa, Ahmad Hamim AH; Patria, Suryono Yudha SY; Wahab, Abdul A

Publication Date: 2022-10-18

Variant appearance in text: rs10010131

PubMed Link: 36292779

Variant Present in the following documents:

• genes-13-01894.pdf

View BVdb publication page

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Genetic Susceptibility to Insulin Resistance and Its Association with Estimated Longevity in the Hungarian General and Roma Populations.

Biomedicines

Piko, Peter P; Werissa, Nardos Abebe NA; Adany, Roza R

Publication Date: 2022-07-14

Variant appearance in text: rs10010131

PubMed Link: 35885008

Variant Present in the following documents:

• biomedicines-10-01703.pdf

View BVdb publication page

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A novel splice site variant c.1183 + 1 G > C in DFNA5 causing autosomal dominant nonsyndromic hearing loss in a Chinese family.

Bmc Medical Genomics

Li, Qiong Q; Wang, Shujuan S; Liang, Pengfei P; Li, Wei W; Wang, Jian J; Fan, Bei B; Yang, Yang Y; An, Xiaogang X; Chen, Jun J; Zha, Dingjun D

Publication Date: 2022-07-21

Variant appearance in text: WFS1: 461-9A>G; rs10010131

PubMed Link: 35864542

Variant Present in the following documents:

• 12920_2022_1315_MOESM2_ESM.xlsx, sheet 3
• 12920_2022_1315_MOESM3_ESM.xlsx, sheet 2
• 12920_2022_1315_MOESM2_ESM.xlsx, sheet 1

View BVdb publication page

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Determinants in Tailoring Antidiabetic Therapies: A Personalized Approach.

Global Medical Genetics

Rizvi, Aliya A AA; Abbas, Mohammad M; Verma, Sushma S; Verma, Shrikant S; Khan, Almas A; Raza, Syed T ST; Mahdi, Farzana F

Publication Date: 2022-06

Variant appearance in text: rs10010131

PubMed Link: 35707783

Variant Present in the following documents:

• Main text

View BVdb publication page

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Type 2 Diabetes-Related Variants Influence the Risk of Developing Prostate Cancer: A Population-Based Case-Control Study and Meta-Analysis.

Cancers

Sánchez-Maldonado, José Manuel JM; Collado, Ricardo R; Cabrera-Serrano, Antonio José AJ; Ter Horst, Rob R; Gálvez-Montosa, Fernando F; Robles-Fernández, Inmaculada I; Arenas-Rodríguez, Verónica V; Cano-Gutiérrez, Blanca B; Bakker, Olivier O; Bravo-Fernández, María Inmaculada MI; García-Verdejo, Francisco José FJ; López, José Antonio López JAL; Olivares-Ruiz, Jesús J; López-Nevot, Miguel Ángel MÁ; Fernández-Puerta, Laura L; Cózar-Olmo, José Manuel JM; Li, Yang Y; Netea, Mihai G MG; Jurado, Manuel M; Lorente, Jose Antonio JA; Sánchez-Rovira, Pedro P; Álvarez-Cubero, María Jesús MJ; Sainz, Juan J

Publication Date: 2022-05-12

Variant appearance in text: rs10010131

PubMed Link: 35625981

Variant Present in the following documents:

• cancers-14-02376.pdf

View BVdb publication page

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The current role of sodium-glucose cotransporter 2 inhibitors in type 2 diabetes mellitus management.

Cardiovascular Diabetology

Xu, Bo B; Li, Shaoqian S; Kang, Bo B; Zhou, Jiecan J

Publication Date: 2022-05-25

Variant appearance in text: rs10010131

PubMed Link: 35614469

Variant Present in the following documents:

• Main text
• 12933_2022_Article_1512.pdf

View BVdb publication page

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A novel missense variant in CEACAM16 gene causes autosomal dominant nonsyndromic hearing loss.

Annals Of Human Genetics

Zhang, Dejun D; Wu, Jie J; Yuan, Yongyi Y; Li, Xiaohong X; Gao, Xue X; Han, Mingyu M; Gao, Song S; Huang, Shasha S; Dai, Pu P

Publication Date: 2022-07

Variant appearance in text: rs10010131

PubMed Link: 35292975

Variant Present in the following documents:

• AHG-86-207-s002.xlsx, sheet 1

View BVdb publication page

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Dapagliflozin plus exenatide on patients with type 2 diabetes awaiting bariatric surgery in the DEXBASU study.

Scientific Reports

López-Cano, Carolina C; Santos, Maria Dolores MD; Sánchez, Enric E; Martí, Raquel R; Bueno, Marta M; Gutiérrez-Carrasquilla, Liliana L; Lecube, Albert A

Publication Date: 2022-02-25

Variant appearance in text: rs10010131

PubMed Link: 35217772

Variant Present in the following documents:

• Main text
• 41598_2022_Article_7250.pdf

View BVdb publication page

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PPARG, TMEM163, UBE2E2, and WFS1 Gene Polymorphisms Are Not Significant Risk Factors for Gestational Diabetes in the Polish Population.

Journal Of Personalized Medicine

Ustianowski, Przemysław P; Malinowski, Damian D; Safranow, Krzysztof K; Dziedziejko, Violetta V; Tarnowski, Maciej M; Pawlik, Andrzej A

Publication Date: 2022-02-08

Variant appearance in text: rs10010131

PubMed Link: 35207731

Variant Present in the following documents:

• jpm-12-00243.pdf

View BVdb publication page

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Circulating Nucleic Acid-Based Biomarkers of Type 2 Diabetes.

International Journal Of Molecular Sciences

Padilla-Martinez, Felipe F; Wojciechowska, Gladys G; Szczerbinski, Lukasz L; Kretowski, Adam A

Publication Date: 2021-12-28

Variant appearance in text: rs10010131

PubMed Link: 35008723

Variant Present in the following documents:

• Main text
• ijms-23-00295.pdf

View BVdb publication page

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Circulating Nucleic Acid-Based Biomarkers of Type 2 Diabetes.

International Journal Of Molecular Sciences

Padilla-Martinez, Felipe F; Wojciechowska, Gladys G; Szczerbinski, Lukasz L; Kretowski, Adam A

Publication Date: 2021-12-28

Variant appearance in text: rs10010131

PubMed Link: 35008723

Variant Present in the following documents:

• Main text
• ijms-23-00295.pdf

View BVdb publication page

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Pharmacogenomics and Personalized Medicine in Type 2 Diabetes Mellitus: Potential Implications for Clinical Practice.

Pharmacogenomics And Personalized Medicine

Venkatachalapathy, Poongothai P; Padhilahouse, Sruthi S; Sellappan, Mohan M; Subramanian, Tharunika T; Kurian, Shilia Jacob SJ; Miraj, Sonal Sekhar SS; Rao, Mahadev M; Raut, Ashwin Ashok AA; Kanwar, Rupinder Kaur RK; Singh, Jitendra J; Khadanga, Sagar S; Mondithoka, Sukumar S; Munisamy, Murali M

Publication Date: 2021

Variant appearance in text: rs10010131

PubMed Link: 34803393

Variant Present in the following documents:

• Main text
• pgpm-14-1441.pdf

View BVdb publication page

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Familial Temperature-Sensitive Auditory Neuropathy: Distinctive Clinical Courses Caused by Variants of the OTOF Gene.

Frontiers In Cell And Developmental Biology

Zhu, Yi-Ming YM; Li, Qi Q; Gao, Xue X; Li, Yan-Fei YF; Liu, You-Li YL; Dai, Pu P; Li, Xiang-Ping XP

Publication Date: 2021

Variant appearance in text: rs10010131

PubMed Link: 34692690

Variant Present in the following documents:

• Table_2.xlsx, sheet 1

View BVdb publication page

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A Clinical-Genetic Score for Predicting Weight Loss after Bariatric Surgery: The OBEGEN Study.

Journal Of Personalized Medicine

Ciudin, Andreea A; Fidilio, Enzamaría E; Gutiérrez-Carrasquilla, Liliana L; Caixàs, Assumpta A; Vilarrasa, Núria N; Pellitero, Silvia S; Simó-Servat, Andreu A; Vilallonga, Ramon R; Ruiz, Amador A; de la Fuente, Maricruz M; Luna, Alexis A; Sánchez, Enric E; Rigla, Mercedes M; Hernández, Cristina C; Salas, Eduardo E; Simó, Rafael R; Lecube, Albert A

Publication Date: 2021-10-17

Variant appearance in text: rs10010131

PubMed Link: 34683180

Variant Present in the following documents:

• Main text
• jpm-11-01040.pdf

View BVdb publication page

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Polygenic risk scores predict diabetes complications and their response to intensive blood pressure and glucose control.

Diabetologia

Tremblay, Johanne J; Haloui, Mounsif M; Attaoua, Redha R; Tahir, Ramzan R; Hishmih, Camil C; Harvey, François F; Marois-Blanchet, François-Christophe FC; Long, Carole C; Simon, Paul P; Santucci, Lara L; Hizel, Candan C; Chalmers, John J; Marre, Michel M; Harrap, Stephen S; Cífková, Renata R; Krajčoviechová, Alena A; Matthews, David R DR; Williams, Bryan B; Poulter, Neil N; Zoungas, Sophia S; Colagiuri, Stephen S; Mancia, Giuseppe G; Grobbee, Diederick E DE; Rodgers, Anthony A; Liu, Liusheng L; Agbessi, Mawussé M; Bruat, Vanessa V; Favé, Marie-Julie MJ; Harwood, Michelle P MP; Awadalla, Philip P; Woodward, Mark M; Hussin, Julie G JG; Hamet, Pavel P

Publication Date: 2021-09

Variant appearance in text: rs10010131

PubMed Link: 34226943

Variant Present in the following documents:

• 125_2021_5491_MOESM1_ESM.pdf

View BVdb publication page

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Associations of TCF7L2 rs11196218 (A/G) and GLP-1R rs761386 (C/T) Gene Polymorphisms with Obesity in Chinese Population.

Diabetes, Metabolic Syndrome And Obesity : Targets And Therapy

Xu, Tiantian T; Liu, Mengmeng M; Liu, Qingjing Q; Wang, Bian B; Wang, Min M; Qu, Minli M; Chen, Xin X; Wu, Jing J

Publication Date: 2021

Variant appearance in text: rs10010131

PubMed Link: 34103955

Variant Present in the following documents:

• Main text
• dmso-14-2465.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: WFS1: 461-9A>G; rs10010131

PubMed Link: 34054912

Variant Present in the following documents:

• Table_2.xlsx, sheet 1

View BVdb publication page

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Pharmacogenetics of new classes of antidiabetic drugs.

Bosnian Journal Of Basic Medical Sciences

Imamovic Kadric, Selma S; Kulo Cesic, Aida A; Dujic, Tanja T

Publication Date: 2021-12-01

Variant appearance in text: rs10010131

PubMed Link: 33974529

Variant Present in the following documents:

• Main text

View BVdb publication page

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Pathological β-Cell Endoplasmic Reticulum Stress in Type 2 Diabetes: Current Evidence.

Frontiers In Endocrinology

Shrestha, Neha N; De Franco, Elisa E; Arvan, Peter P; Cnop, Miriam M

Publication Date: 2021

Variant appearance in text: rs10010131

PubMed Link: 33967960

Variant Present in the following documents:

• Main text

View BVdb publication page

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All thresholds of maternal hyperglycaemia from the WHO 2013 criteria for gestational diabetes identify women with a higher genetic risk for type 2 diabetes.

Wellcome Open Research

Hughes, Alice E AE; Hayes, M Geoffrey MG; Egan, Aoife M AM; Patel, Kashyap A KA; Scholtens, Denise M DM; Lowe, Lynn P LP; Lowe, William L WL; Dunne, Fidelma P FP; Hattersley, Andrew T AT; Freathy, Rachel M RM

Publication Date: 2020

Variant appearance in text: rs10010131

PubMed Link: 33869792

Variant Present in the following documents:

• Main text
• wellcomeopenres-5-18435.pdf

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: rs10010131

PubMed Link: 33791233

Variant Present in the following documents:

• Table_2.xlsx, sheet 1

View BVdb publication page

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Risk assessment of type 2 diabetes in northern China based on the logistic regression model.

Technology And Health Care : Official Journal Of The European Society For Engineering And Medicine

Li, Chunrui C; Liu, Manjiao M; An, Yunhe Y; Tian, Yanjie Y; Guan, Di D; Wu, Huijuan H; Pei, Zhiyong Z

Publication Date: 2021

Variant appearance in text: rs10010131

PubMed Link: 33682772

Variant Present in the following documents:

• Main text
• thc-29-thc218033.pdf

View BVdb publication page

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Methylation status of vault RNA 2-1 promoter is a predictor of glycemic response to glucagon-like peptide-1 analog therapy in type 2 diabetes mellitus.

Bmj Open Diabetes Research & Care

Lin, Chia-Hung CH; Lee, Yun-Shien YS; Huang, Yu-Yao YY; Tsai, Chi-Neu CN

Publication Date: 2021-03

Variant appearance in text: rs10010131

PubMed Link: 33674278

Variant Present in the following documents:

• Main text

View BVdb publication page

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Pharmacogenetics of Type 2 Diabetes-Progress and Prospects.

International Journal Of Molecular Sciences

Nasykhova, Yulia A YA; Tonyan, Ziravard N ZN; Mikhailova, Anastasiia A AA; Danilova, Maria M MM; Glotov, Andrey S AS

Publication Date: 2020-09-18

Variant appearance in text: rs10010131

PubMed Link: 32961860

Variant Present in the following documents:

• Main text
• ijms-21-06842.pdf

View BVdb publication page

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Lack of association between IGF2BP2 rs4402960 polymorphism and gestational diabetes mellitus: a case-control study, meta-analysis and trial sequential analysis.

Bioscience Reports

Liu, Jing J; Song, Guang G; Zhao, Ge G; Meng, Tao T

Publication Date: 2020-07-31

Variant appearance in text: rs10010131

PubMed Link: 32662505

Variant Present in the following documents:

• Main text
• bsr-40-bsr20200990.pdf

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: rs10010131

PubMed Link: 32529721

Variant Present in the following documents:

• JCLA-34-e23418-s003.xls, sheet 1

View BVdb publication page

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Prelingual Sensorineural Hearing Loss Caused by a Novel GJB2 Dominant Mutation in a Chinese Family.

Biomed Research International

Huang, Shasha S; Gao, Xue X; Wang, Yufeng Y; Kang, Dongyang D; Zhang, Xin X; Yang, Suyan S; Dai, Pu P

Publication Date: 2020

Variant appearance in text: rs10010131

PubMed Link: 32090102

Variant Present in the following documents:

• 6370386.f1.xlsx, sheet 2

View BVdb publication page

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Next-generation sequencing identified novel Desmoplakin frame-shift variant in patients with Arrhythmogenic cardiomyopathy.

Bmc Cardiovascular Disorders

Lin, Xiaoping X; Ma, Yuankun Y; Cai, Zhejun Z; Wang, Qiyuan Q; Wang, Lihua L; Huo, Zhaoxia Z; Hu, Dan D; Wang, Jian'an J; Xiang, Meixiang M

Publication Date: 2020-02-11

Variant appearance in text: WFS1: 461-9A>G; rs10010131

PubMed Link: 32046637

Variant Present in the following documents:

• 12872_2020_1369_MOESM1_ESM.xlsx, sheet 1

View BVdb publication page

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Clinical and genetic analysis of two wolfram syndrome families with high occurrence of wolfram syndrome and diabetes type II: a case report.

Bmc Medical Genetics

Sobhani, Maryam M; Tabatabaiefar, Mohammad Amin MA; Ghafouri-Fard, Soudeh S; Rajab, Asadollah A; Hojjat, Asal A; Kajbafzadeh, Abdol-Mohammad AM; Noori-Daloii, Mohammad Reza MR

Publication Date: 2020-01-14

Variant appearance in text: rs10010131

PubMed Link: 31937257

Variant Present in the following documents:

• Main text
• 12881_2020_Article_950.pdf

View BVdb publication page

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Data on a genome-wide association study of type 2 diabetes in a Maya population.

Data In Brief

Totomoch-Serra, Armando A; Domínguez-Cruz, Miriam Givisay MG; Muñoz, María de Lourdes ML; García-Escalante, María Guadalupe MG; Burgueño, Juan J; Díaz-Badillo, Álvaro Á; Valadez-González, Nina N; Escalante, Doris Pinto DP

Publication Date: 2020-02

Variant appearance in text: rs10010131

PubMed Link: 31872004

Variant Present in the following documents:

• Main text

View BVdb publication page

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A diabetes-associated genetic variant is associated with diastolic dysfunction and cardiovascular disease.

Esc Heart Failure

Molvin, John J; Jujic, Amra A; Nilsson, Peter M PM; Leosdottir, Margret M; Lindblad, Ulf U; Daka, Bledar B; Bennet, Louise L; Råstam, Lennart L; Lyssenko, Valeriya V; Magnusson, Martin M

Publication Date: 2020-02

Variant appearance in text: rs10010131

PubMed Link: 31860786

Variant Present in the following documents:

• Main text
• EHF2-7-348.pdf

View BVdb publication page

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Novel mutations identified in Chinese families with autosomal dominant congenital cataracts by targeted next-generation sequencing.

Bmc Medical Genetics

Li, Shan S; Zhang, Jianfei J; Cao, Yixuan Y; You, Yi Y; Zhao, Xiuli X

Publication Date: 2019-12-16

Variant appearance in text: WFS1: 461-9A>G; rs10010131

PubMed Link: 31842807

Variant Present in the following documents:

• 12881_2019_933_MOESM2_ESM.xlsx, sheet 1

View BVdb publication page

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PGG.SNV: understanding the evolutionary and medical implications of human single nucleotide variations in diverse populations.

Genome Biology

Zhang, Chao C; Gao, Yang Y; Ning, Zhilin Z; Lu, Yan Y; Zhang, Xiaoxi X; Liu, Jiaojiao J; Xie, Bo B; Xue, Zhe Z; Wang, Xiaoji X; Yuan, Kai K; Ge, Xueling X; Pan, Yuwen Y; Liu, Chang C; Tian, Lei L; Wang, Yuchen Y; Lu, Dongsheng D; Hoh, Boon-Peng BP; Xu, Shuhua S

Publication Date: 2019-10-22

Variant appearance in text: WFS1: 461-9A>G; rs10010131

PubMed Link: 31640808

Variant Present in the following documents:

• 13059_2019_1838_MOESM3_ESM.xlsx, sheet 1

View BVdb publication page

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Introducing the first whole genomes of nationals from the United Arab Emirates.

Scientific Reports

AlSafar, Habiba S HS; Al-Ali, Mariam M; Elbait, Gihan Daw GD; Al-Maini, Mustafa H MH; Ruta, Dymitr D; Peramo, Braulio B; Henschel, Andreas A; Tay, Guan K GK

Publication Date: 2019-10-11

Variant appearance in text: rs10010131

PubMed Link: 31604968

Variant Present in the following documents:

• Main text
• 41598_2019_50876_MOESM1_ESM.xlsx, sheet 2
• 41598_2019_50876_MOESM1_ESM.xlsx, sheet 1

View BVdb publication page

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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: rs10010131

PubMed Link: 31597922

Variant Present in the following documents:

• 41598_2019_50891_MOESM6_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM9_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM3_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM8_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM7_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM5_ESM.xlsx, sheet 1

View BVdb publication page

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Gene-lifestyle interaction on risk of type 2 diabetes: A systematic review.

Obesity Reviews : An Official Journal Of The International Association For The Study Of Obesity

Dietrich, Stefan S; Jacobs, Simone S; Zheng, Ju-Sheng JS; Meidtner, Karina K; Schwingshackl, Lukas L; Schulze, Matthias B MB

Publication Date: 2019-11

Variant appearance in text: rs10010131

PubMed Link: 31478326

Variant Present in the following documents:

• Main text
• OBR-20-.pdf

View BVdb publication page

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Gene-lifestyle interaction on risk of type 2 diabetes: A systematic review.

Obesity Reviews : An Official Journal Of The International Association For The Study Of Obesity

Dietrich, Stefan S; Jacobs, Simone S; Zheng, Ju-Sheng JS; Meidtner, Karina K; Schwingshackl, Lukas L; Schulze, Matthias B MB

Publication Date: 2019-11

Variant appearance in text: rs10010131

PubMed Link: 31478326

Variant Present in the following documents:

• Main text
• OBR-20-.pdf

View BVdb publication page

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Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls.

Nature

Flannick, Jason J; Mercader, Josep M JM; Fuchsberger, Christian C; Udler, Miriam S MS; Mahajan, Anubha A; Wessel, Jennifer J; Teslovich, Tanya M TM; Caulkins, Lizz L; Koesterer, Ryan R; Barajas-Olmos, Francisco F; Blackwell, Thomas W TW; Boerwinkle, Eric E; Brody, Jennifer A JA; Centeno-Cruz, Federico F; Chen, Ling L; Chen, Siying S; Contreras-Cubas, Cecilia C; Córdova, Emilio E; Correa, Adolfo A; Cortes, Maria M; DeFronzo, Ralph A RA; Dolan, Lawrence L; Drews, Kimberly L KL; Elliott, Amanda A; Floyd, James S JS; Gabriel, Stacey S; Garay-Sevilla, Maria Eugenia ME; García-Ortiz, Humberto H; Gross, Myron M; Han, Sohee S; Heard-Costa, Nancy L NL; Jackson, Anne U AU; Jørgensen, Marit E ME; Kang, Hyun Min HM; Kelsey, Megan M; Kim, Bong-Jo BJ; Koistinen, Heikki A HA; Kuusisto, Johanna J; Leader, Joseph B JB; Linneberg, Allan A; Liu, Ching-Ti CT; Liu, Jianjun J; Lyssenko, Valeriya V; Manning, Alisa K AK; Marcketta, Anthony A; Malacara-Hernandez, Juan Manuel JM; Martínez-Hernández, Angélica A; Matsuo, Karen K; Mayer-Davis, Elizabeth E; Mendoza-Caamal, Elvia E; Mohlke, Karen L KL; Morrison, Alanna C AC; Ndungu, Anne A; Ng, Maggie C Y MCY; O'Dushlaine, Colm C; Payne, Anthony J AJ; Pihoker, Catherine C; , ; Post, Wendy S WS; Preuss, Michael M; Psaty, Bruce M BM; Vasan, Ramachandran S RS; Rayner, N William NW; Reiner, Alexander P AP; Revilla-Monsalve, Cristina C; Robertson, Neil R NR; Santoro, Nicola N; Schurmann, Claudia C; So, Wing Yee WY; Soberón, Xavier X; Stringham, Heather M HM; Strom, Tim M TM; Tam, Claudia H T CHT; Thameem, Farook F; Tomlinson, Brian B; Torres, Jason M JM; Tracy, Russell P RP; van Dam, Rob M RM; Vujkovic, Marijana M; Wang, Shuai S; Welch, Ryan P RP; Witte, Daniel R DR; Wong, Tien-Yin TY; Atzmon, Gil G; Barzilai, Nir N; Blangero, John J; Bonnycastle, Lori L LL; Bowden, Donald W DW; Chambers, John C JC; Chan, Edmund E; Cheng, Ching-Yu CY; Cho, Yoon Shin YS; Collins, Francis S FS; de Vries, Paul S PS; Duggirala, Ravindranath R; Glaser, Benjamin B; Gonzalez, Clicerio C; Gonzalez, Ma Elena ME; Groop, Leif L; Kooner, Jaspal Singh JS; Kwak, Soo Heon SH; Laakso, Markku M; Lehman, Donna M DM; Nilsson, Peter P; Spector, Timothy D TD; Tai, E Shyong ES; Tuomi, Tiinamaija T; Tuomilehto, Jaakko J; Wilson, James G JG; Aguilar-Salinas, Carlos A CA; Bottinger, Erwin E; Burke, Brian B; Carey, David J DJ; Chan, Juliana C N JCN; Dupuis, Josée J; Frossard, Philippe P; Heckbert, Susan R SR; Hwang, Mi Yeong MY; Kim, Young Jin YJ; Kirchner, H Lester HL; Lee, Jong-Young JY; Lee, Juyoung J; Loos, Ruth J F RJF; Ma, Ronald C W RCW; Morris, Andrew D AD; O'Donnell, Christopher J CJ; Palmer, Colin N A CNA; Pankow, James J; Park, Kyong Soo KS; Rasheed, Asif A; Saleheen, Danish D; Sim, Xueling X; Small, Kerrin S KS; Teo, Yik Ying YY; Haiman, Christopher C; Hanis, Craig L CL; Henderson, Brian E BE; Orozco, Lorena L; Tusié-Luna, Teresa T; Dewey, Frederick E FE; Baras, Aris A; Gieger, Christian C; Meitinger, Thomas T; Strauch, Konstantin K; Lange, Leslie L; Grarup, Niels N; Hansen, Torben T; Pedersen, Oluf O; Zeitler, Philip P; Dabelea, Dana D; Abecasis, Goncalo G; Bell, Graeme I GI; Cox, Nancy J NJ; Seielstad, Mark M; Sladek, Rob R; Meigs, James B JB; Rich, Steve S SS; Rotter, Jerome I JI; , ; , ; , ; , ; , ; , ; , ; , ; , ; Altshuler, David D; Burtt, Noël P NP; Scott, Laura J LJ; Morris, Andrew P AP; Florez, Jose C JC; McCarthy, Mark I MI; Boehnke, Michael M

Publication Date: 2019-06

Variant appearance in text: rs10010131

PubMed Link: 31118516

Variant Present in the following documents:

• Main text

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Current Progress in Pharmacogenetics of Second-Line Antidiabetic Medications: Towards Precision Medicine for Type 2 Diabetes.

Journal Of Clinical Medicine

Heo, Chan Uk CU; Choi, Chang-Ik CI

Publication Date: 2019-03-21

Variant appearance in text: rs10010131

PubMed Link: 30901912

Variant Present in the following documents:

• Main text

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Gene x Gene Interactions Highlight the Role of Incretin Resistance for Insulin Secretion.

Frontiers In Endocrinology

Jaghutriz, Benjamin Assad BA; Heni, Martin M; Lutz, Stefan Zoltán SZ; Fritsche, Louise L; Machicao, Fausto F; Staiger, Harald H; Peter, Andreas A; Häring, Hans-Ulrich HU; Fritsche, Andreas A; Wagner, Róbert R

Publication Date: 2019

Variant appearance in text: rs10010131

PubMed Link: 30846969

Variant Present in the following documents:

• Main text
• fendo-10-00072.pdf

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