SERPINE1 c.*722T>G

Variant ID: 7-100781445-T-G

NM_000602.4(SERPINE1):c.*722T>G

This variant was identified in 42 publications

View GRCh38 version.




Publications:


Association between PAI-1 Polymorphisms and Ischemic Stroke in a South Korean Case-Control Cohort.

International Journal Of Molecular Sciences
Choi, Gun Ho GH; Cho, Sung Hwan SH; An, Hui Jeong HJ; Park, Han Sung HS; Lee, Jeong Yong JY; Ko, Eun Ju EJ; Oh, Seung Hun SH; Kim, Ok Joon OJ; Kim, Nam Keun NK
Publication Date: 2023-04-28

Variant appearance in text: rs7242
PubMed Link: 37175749
Variant Present in the following documents:
  • Main text
  • ijms-24-08041.pdf
View BVdb publication page



Laboratory biomarkers of delayed cerebral ischemia following subarachnoid hemorrhage: A systematic review.

Journal Of Circulating Biomarkers
Tjerkstra, Maud A MA; Labib, Homeyra H; Coert, Bert A BA; Spijker, René R; Coutinho, Jonathan M JM; Vandertop, W Peter WP; Verbaan, Dagmar D
Publication Date: 2023

Variant appearance in text: rs7242
PubMed Link: 37056917
Variant Present in the following documents:
  • Main text
  • jcb-12-17.pdf
View BVdb publication page



Association of SNPs in the PAI1 Gene with Disease Recurrence and Clinical Outcome in Bladder Cancer.

International Journal Of Molecular Sciences
Murakami, Kaoru K; Furuya, Hideki H; Hokutan, Kanani K; Goodison, Steve S; Pagano, Ian I; Chen, Runpu R; Shen, Cheng-Huang CH; Chan, Michael W Y MWY; Ng, Chi Fai CF; Kobayashi, Takashi T; Ogawa, Osamu O; Miyake, Makito M; Thornquist, Mark M; Shimizu, Yoshiko Y; Hayashi, Kazukuni K; Wang, Zhangwei Z; Yu, Herbert H; Rosser, Charles J CJ
Publication Date: 2023-03-03

Variant appearance in text: rs7242
PubMed Link: 36902377
Variant Present in the following documents:
  • Main text
  • ijms-24-04943.pdf
View BVdb publication page



A Review of Genetic Polymorphisms and Susceptibilities to Complications after Aneurysmal Subarachnoid Hemorrhage.

International Journal Of Molecular Sciences
Medina-Suárez, Jose J; Rodríguez-Esparragón, Francisco F; Sosa-Pérez, Coralia C; Cazorla-Rivero, Sara S; Torres-Mata, Laura B LB; Jiménez-O'Shanahan, Aruma A; Clavo, Bernardino B; Morera-Molina, Jesús J
Publication Date: 2022-12-06

Variant appearance in text: rs7242
PubMed Link: 36499752
Variant Present in the following documents:
  • Main text
  • ijms-23-15427.pdf
View BVdb publication page



JAK-STAT signaling in inflammatory breast cancer enables chemotherapy-resistant cell states.

Cancer Research
Stevens, Laura E LE; Peluffo, Guillermo G; Qiu, Xintao X; Temko, Daniel D; Fassl, Anne A; Li, Zheqi Z; Trinh, Anne A; Seehawer, Marco M; Jovanovic, Bojana B; Aleckovic, Masa M; Wilde, Callahan M CM; Geck, Renee C RC; Shu, Shaokun S; Kingston, Natalie L NL; Harper, Nicholas W NW; Almendro, Vanessa V; Pyke, Alanna L AL; Egri, Shawn B SB; Papanastasiou, Malvina M; Clement, Kendell K; Zhou, Ningxuan N; Walker, Sarah S; Salas, Jacqueline J; Park, So Yeon SY; Frank, David A DA; Meissner, Alexander A; Jaffe, Jacob D JD; Sicinski, Piotr P; Toker, Alex A; Michor, Franziska F; Long, Henry W HW; Overmoyer, Beth A BA; Polyak, Kornelia K
Publication Date: 2022-11-21

Variant appearance in text: rs7242
PubMed Link: 36409824
Variant Present in the following documents:
  • can-22-0423_supplementary_table_s3_suppst3.xlsx, sheet 1
View BVdb publication page



Promising Biomarkers of Radiation-Induced Lung Injury: A Review.

Biomedicines
Liu, Xinglong X; Shao, Chunlin C; Fu, Jiamei J
Publication Date: 2021-09-08

Variant appearance in text: rs7242
PubMed Link: 34572367
Variant Present in the following documents:
  • Main text
  • biomedicines-09-01181.pdf
View BVdb publication page



Severity of radiation pneumonitis, from clinical, dosimetric and biological features: a pilot study.

Radiation Oncology (London, England)
Aso, Samantha S; Navarro-Martin, Arturo A; Castillo, Richard R; Padrones, Susana S; Castillo, Edward E; Montes, Ana A; Martínez, José Ignacio JI; Cubero, Noelia N; López, Rosa R; Rodríguez, Laura L; Palmero, Ramon R; Manresa, Federico F; Guerrero, Thomas T; Molina, María M
Publication Date: 2020-10-27

Variant appearance in text: rs7242
PubMed Link: 33109238
Variant Present in the following documents:
  • Main text
  • 13014_2020_Article_1694.pdf
View BVdb publication page



Association between Five Common Plasminogen Activator Inhibitor-1 (PAI-1) Gene Polymorphisms and Colorectal Cancer Susceptibility.

International Journal Of Molecular Sciences
Oh, Jisu J; An, Hui Jeong HJ; Kim, Jung Oh JO; Jun, Hak Hoon HH; Kim, Woo Ram WR; Kim, Eo Jin EJ; Oh, Doyeun D; Kim, Jong Woo JW; Kim, Nam Keun NK
Publication Date: 2020-06-18

Variant appearance in text: rs7242
PubMed Link: 32570732
Variant Present in the following documents:
  • Main text
  • ijms-21-04334.pdf
View BVdb publication page



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: rs7242
PubMed Link: 32529721
Variant Present in the following documents:
  • JCLA-34-e23418-s003.xls, sheet 1
View BVdb publication page



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: rs7242
PubMed Link: 32046637
Variant Present in the following documents:
  • 12872_2020_1369_MOESM1_ESM.xlsx, sheet 1
View BVdb publication page



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: rs7242
PubMed Link: 31640808
Variant Present in the following documents:
  • 13059_2019_1838_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page



Haplotype analysis of SERPINE1 gene: Risk for aneurysmal subarachnoid hemorrhage and clinical outcomes.

Molecular Genetics & Genomic Medicine
Lin, Mingkuan M; Griessenauer, Christoph J CJ; Starke, Robert M RM; Tubbs, R Shane RS; Shoja, Mohammadali M MM; Foreman, Paul M PM; Vyas, Nilesh A NA; Walters, Beverly C BC; Harrigan, Mark R MR; Hendrix, Philipp P; Fisher, Winfield S WS; Pittet, Jean-Francois JF; Mathru, Mali M; Lipsky, Robert H RH
Publication Date: 2019-08

Variant appearance in text: rs7242
PubMed Link: 31268630
Variant Present in the following documents:
  • Main text
View BVdb publication page



Sex-Specific Genetic Susceptibility to Adverse Neurodevelopmental Outcome in Offspring of Pregnancies at Risk of Early Preterm Delivery.

American Journal Of Perinatology
Varner, Michael W MW; Costantine, Maged M MM; Jablonski, Kathleen A KA; Rouse, Dwight J DJ; Mercer, Brian M BM; Leveno, Kenneth J KJ; Reddy, Uma M UM; Buhimschi, Catalin C; Wapner, Ronald J RJ; Sorokin, Yoram Y; Thorp, John M JM; Ramin, Susan M SM; Malone, Fergal D FD; Carpenter, Marshall M; O'sullivan, Mary J MJ; Peaceman, Alan M AM; Dudley, Donald J DJ; Caritis, Steve N SN; ,
Publication Date: 2020-02

Variant appearance in text: rs7242
PubMed Link: 30731481
Variant Present in the following documents:
  • Main text
View BVdb publication page



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: rs7242
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_7.xlsx, sheet 1
  • Table_5.xlsx, sheet 1
  • Table_6.xlsx, sheet 1
View BVdb publication page



Genetic Variation, Magnesium Sulfate Exposure, and Adverse Neurodevelopmental Outcomes Following Preterm Birth.

American Journal Of Perinatology
Clark, Erin A S EAS; Weiner, Steven J SJ; Rouse, Dwight J DJ; Mercer, Brian M BM; Reddy, Uma M UM; Iams, Jay D JD; Wapner, Ronald J RJ; Sorokin, Yoram Y; Malone, Fergal D FD; O'Sullivan, Mary J MJ; Peaceman, Alan M AM; Hankins, Gary D V GDV; Dudley, Donald J DJ; Caritis, Steve N SN; ,
Publication Date: 2018-08

Variant appearance in text: rs7242
PubMed Link: 29510423
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic and epigenetic variations associated with idiopathic recurrent pregnancy loss.

Journal Of Assisted Reproduction And Genetics
Arias-Sosa, Luis Alejandro LA; Acosta, Iván Darío ID; Lucena-Quevedo, Elkin E; Moreno-Ortiz, Harold H; Esteban-Pérez, Clara C; Forero-Castro, Maribel M
Publication Date: 2018-03

Variant appearance in text: rs7242
PubMed Link: 29313278
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association between plasminogen activator inhibitor gene polymorphisms and osteonecrosis of the femoral head susceptibility: A case-control study.

Medicine
Li, Yi Y; Liu, Feng-Xia FX; Yuan, Chao C; Meng, Lingguo L
Publication Date: 2017-10

Variant appearance in text: rs7242
PubMed Link: 29049169
Variant Present in the following documents:
  • Main text
View BVdb publication page



Biological networks in Parkinson's disease: an insight into the epigenetic mechanisms associated with this disease.

Bmc Genomics
Chatterjee, Paulami P; Roy, Debjani D; Bhattacharyya, Malay M; Bandyopadhyay, Sanghamitra S
Publication Date: 2017-09-12

Variant appearance in text: rs7242
PubMed Link: 28899360
Variant Present in the following documents:
  • Main text
  • 12864_2017_Article_4098.pdf
View BVdb publication page



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: rs7242
PubMed Link: 28690861
Variant Present in the following documents:
  • hgv201727-s1.xls, sheet 1
View BVdb publication page



Genetic variants in the plasminogen activator inhibitor-1 gene are associated with an increased risk of radiation pneumonitis in lung cancer patients.

Cancer Medicine
Liu, Bo B; Tang, Yang Y; Yi, Minxiao M; Liu, Qingxu Q; Xiong, Huihua H; Hu, Guangyuan G; Yuan, Xianglin X
Publication Date: 2017-03

Variant appearance in text: rs7242
PubMed Link: 28211612
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association of Plasminogen Activator Inhibitor-1 (PAI-1) Gene Polymorphisms with Osteoporotic Vertebral Compression Fractures (OVCFs) in Postmenopausal Women.

International Journal Of Molecular Sciences
Kim, Jung Oh JO; Han, Soo Hong SH; Lee, Yeon Ho YH; Ahn, Tae Keun TK; Lim, Jae Joon JJ; Chung, Young Sun YS; Shin, Dong Eun DE; Lee, Woo Sik WS; Han, In Bo IB; Kim, Nam Keun NK
Publication Date: 2016-12-09

Variant appearance in text: rs7242
PubMed Link: 27941685
Variant Present in the following documents:
  • Main text
  • ijms-17-02062.pdf
View BVdb publication page



Plasminogen Activator Inhibitor-1 in depression: Results from Animal and Clinical Studies.

Scientific Reports
Jiang, Haitang H; Li, Xiaoli X; Chen, Suzhen S; Lu, Na N; Yue, Yingying Y; Liang, Jinfeng J; Zhang, Zhijun Z; Yuan, Yonggui Y
Publication Date: 2016-07-26

Variant appearance in text: rs7242
PubMed Link: 27456456
Variant Present in the following documents:
  • Main text
  • srep30464.pdf
View BVdb publication page



Genetic polymorphisms and the development of invasive bacterial infections in children.

International Journal Of Immunopathology And Pharmacology
Esposito, Susanna S; Bosis, Samantha S; Orenti, Annalisa A; Spena, Silvia S; Montinaro, Valentina V; Bianchini, Sonia S; Zampiero, Alberto A; Principi, Nicola N
Publication Date: 2016-03

Variant appearance in text: rs7242
PubMed Link: 26684632
Variant Present in the following documents:
  • Main text
View BVdb publication page



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: rs7242
PubMed Link: 26549847
Variant Present in the following documents:
  • mmc3.xlsx, sheet 3
  • mmc3.xlsx, sheet 1
  • mmc3.xlsx, sheet 2
View BVdb publication page



Principles Governing A-to-I RNA Editing in the Breast Cancer Transcriptome.

Cell Reports
Fumagalli, Debora D; Gacquer, David D; Rothé, Françoise F; Lefort, Anne A; Libert, Frederick F; Brown, David D; Kheddoumi, Naima N; Shlien, Adam A; Konopka, Tomasz T; Salgado, Roberto R; Larsimont, Denis D; Polyak, Kornelia K; Willard-Gallo, Karen K; Desmedt, Christine C; Piccart, Martine M; Abramowicz, Marc M; Campbell, Peter J PJ; Sotiriou, Christos C; Detours, Vincent V
Publication Date: 2015-10-13

Variant appearance in text: rs7242
PubMed Link: 26440892
Variant Present in the following documents:
  • mmc3.xlsx, sheet 1
View BVdb publication page



Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair.

Nature Genetics
Day, Felix R FR; Ruth, Katherine S KS; Thompson, Deborah J DJ; Lunetta, Kathryn L KL; Pervjakova, Natalia N; Chasman, Daniel I DI; Stolk, Lisette L; Finucane, Hilary K HK; Sulem, Patrick P; Bulik-Sullivan, Brendan B; Esko, Tõnu T; Johnson, Andrew D AD; Elks, Cathy E CE; Franceschini, Nora N; He, Chunyan C; Altmaier, Elisabeth E; Brody, Jennifer A JA; Franke, Lude L LL; Huffman, Jennifer E JE; Keller, Margaux F MF; McArdle, Patrick F PF; Nutile, Teresa T; Porcu, Eleonora E; Robino, Antonietta A; Rose, Lynda M LM; Schick, Ursula M UM; Smith, Jennifer A JA; Teumer, Alexander A; Traglia, Michela M; Vuckovic, Dragana D; Yao, Jie J; Zhao, Wei W; Albrecht, Eva E; Amin, Najaf N; Corre, Tanguy T; Hottenga, Jouke-Jan JJ; Mangino, Massimo M; Smith, Albert V AV; Tanaka, Toshiko T; Abecasis, Goncalo G; Andrulis, Irene L IL; Anton-Culver, Hoda H; Antoniou, Antonis C AC; Arndt, Volker V; Arnold, Alice M AM; Barbieri, Caterina C; Beckmann, Matthias W MW; Beeghly-Fadiel, Alicia A; Benitez, Javier J; Bernstein, Leslie L; Bielinski, Suzette J SJ; Blomqvist, Carl C; Boerwinkle, Eric E; Bogdanova, Natalia V NV; Bojesen, Stig E SE; Bolla, Manjeet K MK; Borresen-Dale, Anne-Lise AL; Boutin, Thibaud S TS; Brauch, Hiltrud H; Brenner, Hermann H; Brüning, Thomas T; Burwinkel, Barbara B; Campbell, Archie A; Campbell, Harry H; Chanock, Stephen J SJ; Chapman, J Ross JR; Chen, Yii-Der Ida YI; Chenevix-Trench, Georgia G; Couch, Fergus J FJ; Coviello, Andrea D AD; Cox, Angela A; Czene, Kamila K; Darabi, Hatef H; De Vivo, Immaculata I; Demerath, Ellen W EW; Dennis, Joe J; Devilee, Peter P; Dörk, Thilo T; Dos-Santos-Silva, Isabel I; Dunning, Alison M AM; Eicher, John D JD; Fasching, Peter A PA; Faul, Jessica D JD; Figueroa, Jonine J; Flesch-Janys, Dieter D; Gandin, Ilaria I; Garcia, Melissa E ME; García-Closas, Montserrat M; Giles, Graham G GG; Girotto, Giorgia G GG; Goldberg, Mark S MS; González-Neira, Anna A; Goodarzi, Mark O MO; Grove, Megan L ML; Gudbjartsson, Daniel F DF; Guénel, Pascal P; Guo, Xiuqing X; Haiman, Christopher A CA; Hall, Per P; Hamann, Ute U; Henderson, Brian E BE; Hocking, Lynne J LJ; Hofman, Albert A; Homuth, Georg G; Hooning, Maartje J MJ; Hopper, John L JL; Hu, Frank B FB; Huang, Jinyan J; Humphreys, Keith K; Hunter, David J DJ; Jakubowska, Anna A; Jones, Samuel E SE; Kabisch, Maria M; Karasik, David D; Knight, Julia A JA; Kolcic, Ivana I; Kooperberg, Charles C; Kosma, Veli-Matti VM; Kriebel, Jennifer J; Kristensen, Vessela V; Lambrechts, Diether D; Langenberg, Claudia C; Li, Jingmei J; Li, Xin X; Lindström, Sara S; Liu, Yongmei Y; Luan, Jian'an J; Lubinski, Jan J; Mägi, Reedik R; Mannermaa, Arto A; Manz, Judith J; Margolin, Sara S; Marten, Jonathan J; Martin, Nicholas G NG; Masciullo, Corrado C; Meindl, Alfons A; Michailidou, Kyriaki K; Mihailov, Evelin E; Milani, Lili L; Milne, Roger L RL; Müller-Nurasyid, Martina M; Nalls, Michael M; Neale, Ben M BM; Nevanlinna, Heli H; Neven, Patrick P; Newman, Anne B AB; Nordestgaard, Børge G BG; Olson, Janet E JE; Padmanabhan, Sandosh S; Peterlongo, Paolo P; Peters, Ulrike U; Petersmann, Astrid A; Peto, Julian J; Pharoah, Paul D P PDP; Pirastu, Nicola N NN; Pirie, Ailith A; Pistis, Giorgio G; Polasek, Ozren O; Porteous, David D; Psaty, Bruce M BM; Pylkäs, Katri K; Radice, Paolo P; Raffel, Leslie J LJ; Rivadeneira, Fernando F; Rudan, Igor I; Rudolph, Anja A; Ruggiero, Daniela D; Sala, Cinzia F CF; Sanna, Serena S; Sawyer, Elinor J EJ; Schlessinger, David D; Schmidt, Marjanka K MK; Schmidt, Frank F; Schmutzler, Rita K RK; Schoemaker, Minouk J MJ; Scott, Robert A RA; Seynaeve, Caroline M CM; Simard, Jacques J; Sorice, Rossella R; Southey, Melissa C MC; Stöckl, Doris D; Strauch, Konstantin K; Swerdlow, Anthony A; Taylor, Kent D KD; Thorsteinsdottir, Unnur U; Toland, Amanda E AE; Tomlinson, Ian I; Truong, Thérèse T; Tryggvadottir, Laufey L; Turner, Stephen T ST; Vozzi, Diego D; Wang, Qin Q; Wellons, Melissa M; Willemsen, Gonneke G; Wilson, James F JF; Winqvist, Robert R; Wolffenbuttel, Bruce B H R BBHR; Wright, Alan F AF; Yannoukakos, Drakoulis D; Zemunik, Tatijana T; Zheng, Wei W; Zygmunt, Marek M; Bergmann, Sven S; Boomsma, Dorret I DI; Buring, Julie E JE; Ferrucci, Luigi L; Montgomery, Grant W GW; Gudnason, Vilmundur V; Spector, Tim D TD; van Duijn, Cornelia M CM; Alizadeh, Behrooz Z BZ; Ciullo, Marina M; Crisponi, Laura L; Easton, Douglas F DF; Gasparini, Paolo P PP; Gieger, Christian C; Harris, Tamara B TB; Hayward, Caroline C; Kardia, Sharon L R SLR; Kraft, Peter P; McKnight, Barbara B; Metspalu, Andres A; Morrison, Alanna C AC; Reiner, Alex P AP; Ridker, Paul M PM; Rotter, Jerome I JI; Toniolo, Daniela D; Uitterlinden, André G AG; Ulivi, Sheila S; Völzke, Henry H; Wareham, Nicholas J NJ; Weir, David R DR; Yerges-Armstrong, Laura M LM; , ; , ; , ; , ; , ; , ; Price, Alkes L AL; Stefansson, Kari K; Visser, Jenny A JA; Ong, Ken K KK; Chang-Claude, Jenny J; Murabito, Joanne M JM; Perry, John R B JRB; Murray, Anna A
Publication Date: 2015-11

Variant appearance in text: rs7242
PubMed Link: 26414677
Variant Present in the following documents:
  • NIHMS64932-supplement-Supplementary_Tables.xlsx, sheet 15
  • NIHMS64932-supplement-Supplementary_Tables.xlsx, sheet 16
View BVdb publication page



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: rs7242
PubMed Link: 25944692
Variant Present in the following documents:
  • oncotarget-06-15375-s005.xlsx, sheet 2
View BVdb publication page



Association of CVD candidate gene polymorphisms with ischemic stroke and cerebral hemorrhage in Chinese individuals.

Plos One
Ou, Wenjing W; Liu, Xin X; Shen, Yue Y; Li, Jiana J; He, Lingbin L; Yuan, Yuan Y; Tan, Xuerui X; Liu, Lisheng L; Zhao, Jingbo J; Wang, Xingyu X
Publication Date: 2014

Variant appearance in text: rs7242
PubMed Link: 25144711
Variant Present in the following documents:
  • Main text
  • pone.0105516.pdf
View BVdb publication page



Integrated mRNA and microRNA transcriptome sequencing characterizes sequence variants and mRNA-microRNA regulatory network in nasopharyngeal carcinoma model systems.

Febs Open Bio
Szeto, Carol Ying-Ying CY; Lin, Chi Ho CH; Choi, Siu Chung SC; Yip, Timothy T C TT; Ngan, Roger Kai-Cheong RK; Tsao, George Sai-Wah GS; Li Lung, Maria M
Publication Date: 2014

Variant appearance in text: rs7242
PubMed Link: 24490137
Variant Present in the following documents:
  • mmc5.xlsx, sheet 2
View BVdb publication page



Using a multi-staged strategy based on machine learning and mathematical modeling to predict genotype-phenotype risk patterns in diabetic kidney disease: a prospective case-control cohort analysis.

Bmc Nephrology
Leung, Ross K K RK; Wang, Ying Y; Ma, Ronald C W RC; Luk, Andrea O Y AO; Lam, Vincent V; Ng, Maggie M; So, Wing Yee WY; Tsui, Stephen K W SK; Chan, Juliana C N JC
Publication Date: 2013-07-23

Variant appearance in text: rs7242
PubMed Link: 23879411
Variant Present in the following documents:
View BVdb publication page



Single nucleotide polymorphisms of metabolic syndrome-related genes in primary open angle glaucoma.

International Journal Of Ophthalmology
Zhou, Gang G; Liu, Bin B
Publication Date: 2010

Variant appearance in text: rs7242
PubMed Link: 22553514
Variant Present in the following documents:
  • Main text
View BVdb publication page



Candidate genes and risk for CP: a population-based study.

Pediatric Research
Wu, Yvonne W YW; Croen, Lisa A LA; Vanderwerf, Andrew A; Gelfand, Amy A AA; Torres, Anthony R AR
Publication Date: 2011-12

Variant appearance in text: rs7242
PubMed Link: 21857382
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association of fetal inflammation and coagulation pathway gene polymorphisms with neurodevelopmental delay at age 2 years.

American Journal Of Obstetrics And Gynecology
Clark, Erin A S EA; Mele, Lisa L; Wapner, Ronald J RJ; Spong, Catherine Y CY; Sorokin, Yoram Y; Peaceman, Alan A; Iams, Jay D JD; Leveno, Kenneth J KJ; Harper, Margaret M; Caritis, Steve N SN; Miodovnik, Menachem M; Mercer, Brian M BM; Thorp, John M JM; Ramin, Susan M SM; Carpenter, Marshall M; Rouse, Dwight J DJ; ,
Publication Date: 2010-07

Variant appearance in text: rs7242
PubMed Link: 20417488
Variant Present in the following documents:
  • Main text
View BVdb publication page



High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta.

Bmc Genetics
Daelemans, Caroline C; Ritchie, Matthew E ME; Smits, Guillaume G; Abu-Amero, Sayeda S; Sudbery, Ian M IM; Forrest, Matthew S MS; Campino, Susana S; Clark, Taane G TG; Stanier, Philip P; Kwiatkowski, Dominic D; Deloukas, Panos P; Dermitzakis, Emmanouil T ET; Tavaré, Simon S; Moore, Gudrun E GE; Dunham, Ian I
Publication Date: 2010-04-19

Variant appearance in text: rs7242
PubMed Link: 20403199
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association of congenital cardiovascular malformations with 33 single nucleotide polymorphisms of selected cardiovascular disease-related genes.

Birth Defects Research. Part A, Clinical And Molecular Teratology
Kuehl, Karen K; Loffredo, Christopher C; Lammer, Edward J EJ; Iovannisci, David M DM; Shaw, Gary M GM
Publication Date: 2010-02

Variant appearance in text: rs7242
PubMed Link: 19764075
Variant Present in the following documents:
  • Main text
View BVdb publication page



A candidate gene association study of 77 polymorphisms in migraine.

The Journal Of Pain
Schürks, Markus M; Kurth, Tobias T; Buring, Julie E JE; Zee, Robert Y L RY
Publication Date: 2009-07

Variant appearance in text: rs7242
PubMed Link: 19559392
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Genetic evidence implicating multiple genes in the MET receptor tyrosine kinase pathway in autism spectrum disorder.

Autism Research : Official Journal Of The International Society For Autism Research
Campbell, Daniel B DB; Li, Chun C; Sutcliffe, James S JS; Persico, Antonio M AM; Levitt, Pat P
Publication Date: 2008-06

Variant appearance in text: rs7242
PubMed Link: 19360663
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Association of 77 polymorphisms in 52 candidate genes with blood pressure progression and incident hypertension: the Women's Genome Health Study.

Journal Of Hypertension
Conen, David D; Cheng, Suzanne S; Steiner, Lori L LL; Buring, Julie E JE; Ridker, Paul M PM; Zee, Robert Y L RY
Publication Date: 2009-03

Variant appearance in text: rs7242
PubMed Link: 19330901
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Genetic risk factors in recurrent venous thromboembolism: A multilocus, population-based, prospective approach.

Clinica Chimica Acta; International Journal Of Clinical Chemistry
Zee, Robert Y L RY; Bubes, Vadim V; Shrivastava, Sanjay S; Ridker, Paul M PM; Glynn, Robert J RJ
Publication Date: 2009-04

Variant appearance in text: rs7242
PubMed Link: 19263529
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A meta-analysis of candidate gene polymorphisms and ischemic stroke in 6 study populations: association of lymphotoxin-alpha in nonhypertensive patients.

Stroke
Wang, Xingyu X; Cheng, Suzanne S; Brophy, Victoria H VH; Erlich, Henry A HA; Mannhalter, Christine C; Berger, Klaus K; Lalouschek, Wolfgang W; Browner, Warren S WS; Shi, Yu Y; Ringelstein, E Bernd EB; Kessler, Christof C; Luedemann, Jan J; Lindpaintner, Klaus K; Liu, Lisheng L; Ridker, Paul M PM; Zee, Robert Y L RY; Cook, Nancy R NR; ,
Publication Date: 2009-03

Variant appearance in text: rs7242
PubMed Link: 19131662
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New application of intelligent agents in sporadic amyotrophic lateral sclerosis identifies unexpected specific genetic background.

Bmc Bioinformatics
Penco, Silvana S; Buscema, Massimo M; Patrosso, Maria Cristina MC; Marocchi, Alessandro A; Grossi, Enzo E
Publication Date: 2008-05-30

Variant appearance in text: rs7242
PubMed Link: 18513389
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  • 1471-2105-9-254.pdf
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Association of polymorphisms in platelet and hemostasis system genes with acute myocardial infarction.

American Heart Journal
Knowles, Joshua W JW; Wang, Huijan H; Itakura, Haruka H; Southwick, Audrey A; Myers, Richard M RM; Iribarren, Carlos C; Fortmann, Stephen P SP; Go, Alan S AS; Quertermous, Thomas T; Hlatky, Mark A MA
Publication Date: 2007-12

Variant appearance in text: rs7242
PubMed Link: 18035074
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