Variant ID: 20-44640575-A-G

NM_004994.2(MMP9):c.997+189A>G

This variant was identified in 19 publications

View GRCh38 version.




Publications:


Genetic susceptibility to high myopia in Han Chinese population.

Open Life Sciences
Li, Yufei Y; Zhang, Yong Y; Zhang, Ping P; Gao, Lei L; Ma, Qingyue Q; Li, Jin J; Wang, Shengxia S; Liu, Bing B; Wang, Xinye X; Meng, Chao C
Publication Date: 2022

Variant appearance in text: rs2236416
PubMed Link: 35647299
Variant Present in the following documents:
  • Main text
  • biol-2022-0055.pdf
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The polymorphisms of extracellular matrix-remodeling genes are associated with pelvic organ prolapse.

International Urogynecology Journal
Li, Lei L; Ma, Yidi Y; Yang, Hua H; Sun, Zhijing Z; Chen, Juan J; Zhu, Lan L
Publication Date: 2022-01-01

Variant appearance in text: rs2236416
PubMed Link: 34973089
Variant Present in the following documents:
  • Main text
  • 192_2021_Article_4917.pdf
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Systematic review and meta-analysis of genetic association studies of pelvic organ prolapse.

International Urogynecology Journal
Allen-Brady, Kristina K; Chua, John W F JWF; Cuffolo, Romana R; Koch, Marianne M; Sorrentino, Felice F; Cartwright, Rufus R
Publication Date: 2021-04-24

Variant appearance in text: rs2236416
PubMed Link: 33893823
Variant Present in the following documents:
  • Main text
  • 192_2021_Article_4782.pdf
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Genetic Variants of ANGPT1, CD39, FGF2 and MMP9 Linked to Clinical Outcome of Bevacizumab Plus Chemotherapy for Metastatic Colorectal Cancer.

International Journal Of Molecular Sciences
Gaibar, María M; Galán, Miguel M; Romero-Lorca, Alicia A; Antón, Beatriz B; Malón, Diego D; Moreno, Amalia A; Fernández-Santander, Ana A; Novillo, Apolonia A
Publication Date: 2021-01-30

Variant appearance in text: rs2236416
PubMed Link: 33573134
Variant Present in the following documents:
  • Main text
  • ijms-22-01381.pdf
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Bruxism Throughout the Lifespan and Variants in MMP2, MMP9 and COMT.

Journal Of Personalized Medicine
Vieira, Alexandre R AR; Scariot, Rafaela R; Gerber, Jennifer T JT; Arid, Juliana J; Küchler, Erika C EC; Sebastiani, Aline M AM; Palinkas, Marcelo M; Díaz-Serrano, Kranya V KV; Torres, Carolina P CP; Regalo, Simone C H SCH; Nelson-Filho, Paulo P; Bussaneli, Diego G DG; Deeley, Kathleen K; Modesto, Adriana A
Publication Date: 2020-05-27

Variant appearance in text: rs2236416
PubMed Link: 32471213
Variant Present in the following documents:
  • Main text
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A Pragmatic Study Shows Failure of Dental Composite Fillings Is Genetically Determined: A Contribution to the Discussion on Dental Amalgams.

Frontiers In Medicine
Vieira, Alexandre R AR; Silva, Marília B MB; Souza, Kesia K A KKA; Filho, Arnôldo V A AVA; Rosenblatt, Aronita A; Modesto, Adriana A
Publication Date: 2017

Variant appearance in text: rs2236416
PubMed Link: 29164121
Variant Present in the following documents:
  • Main text
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[Research advances in immunological pathogenesis of immunoglobulin A vasculitis].

Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal Of Contemporary Pediatrics
Liu, Ya-Ting YT; Lu, Si-Guang SG
Publication Date: 2017-07

Variant appearance in text: rs2236416
PubMed Link: 28697842
Variant Present in the following documents:
  • Main text
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Germline Genetic Variants in TEK, ANGPT1, ANGPT2, MMP9, FGF2 and VEGFA Are Associated with Pathologic Complete Response to Bevacizumab in Breast Cancer Patients.

Plos One
Makhoul, Issam I; Todorova, Valentina K VK; Siegel, Eric R ER; Erickson, Stephen W SW; Dhakal, Ishwori I; Raj, Vinay R VR; Lee, Jeannette Y JY; Orloff, Mohammed S MS; Griffin, Robert J RJ; Henry-Tillman, Ronda S RS; Klimberg, Suzanne S; Hutchins, Laura F LF; Kadlubar, Susan A SA
Publication Date: 2017

Variant appearance in text: rs2236416
PubMed Link: 28045923
Variant Present in the following documents:
  • Main text
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An Inflammatory Polymorphisms Risk Scoring System for the Differentiation of Ischemic Stroke Subtypes.

Mediators Of Inflammation
Muiño, Elena E; Krupinski, Jurek J; Carrera, Caty C; Gallego-Fabrega, Cristina C; Montaner, Joan J; Fernández-Cadenas, Israel I
Publication Date: 2015

Variant appearance in text: rs2236416
PubMed Link: 26355258
Variant Present in the following documents:
  • Main text
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Systematic review and metaanalysis of genetic association studies of urinary symptoms and prolapse in women.

American Journal Of Obstetrics And Gynecology
Cartwright, Rufus R; Kirby, Anna C AC; Tikkinen, Kari A O KA; Mangera, Altaf A; Thiagamoorthy, Gans G; Rajan, Prabhakar P; Pesonen, Jori J; Ambrose, Chris C; Gonzalez-Maffe, Juan J; Bennett, Phillip P; Palmer, Tom T; Walley, Andrew A; Järvelin, Marjo-Riitta MR; Chapple, Chris C; Khullar, Vik V
Publication Date: 2015-02

Variant appearance in text: rs2236416
PubMed Link: 25111588
Variant Present in the following documents:
  • Main text
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Genetic epidemiology of pelvic organ prolapse: a systematic review.

American Journal Of Obstetrics And Gynecology
Ward, Renée M RM; Velez Edwards, Digna R DR; Edwards, Todd T; Giri, Ayush A; Jerome, Rebecca N RN; Wu, Jennifer M JM
Publication Date: 2014-10

Variant appearance in text: rs2236416
PubMed Link: 24721264
Variant Present in the following documents:
  • Main text
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Single nucleotide polymorphisms and risk of recurrence of renal-cell carcinoma: a cohort study.

The Lancet. Oncology
Schutz, Fabio A B FA; Pomerantz, Mark M MM; Gray, Kathryn P KP; Atkins, Michael B MB; Rosenberg, Jonathan E JE; Hirsch, Michelle S MS; McDermott, David F DF; Lampron, Megan E ME; Lee, Gwo-Shu Mary GS; Signoretti, Sabina S; Kantoff, Philip W PW; Freedman, Matthew L ML; Choueiri, Toni K TK
Publication Date: 2013-01

Variant appearance in text: rs2236416
PubMed Link: 23219378
Variant Present in the following documents:
  • Main text
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A genome-wide association study of variations in maternal cardiometabolic genes and risk of placental abruption.

International Journal Of Molecular Epidemiology And Genetics
Moore, Amy A; Enquobahrie, Daniel A DA; Sanchez, Sixto E SE; Ananth, Cande V CV; Pacora, Percy N PN; Williams, Michelle A MA
Publication Date: 2012

Variant appearance in text: rs2236416
PubMed Link: 23205182
Variant Present in the following documents:
  • Main text
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Matrix metalloproteinase-9 genetic polymorphisms and the risk for advanced pelvic organ prolapse.

Obstetrics And Gynecology
Wu, Jennifer M JM; Visco, Anthony G AG; Grass, Elizabeth A EA; Craig, Damian M DM; Fulton, Rebekah G RG; Haynes, Carol C; Weidner, Alison C AC; Shah, Svati H SH
Publication Date: 2012-09

Variant appearance in text: rs2236416
PubMed Link: 22914468
Variant Present in the following documents:
  • Main text
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MMP9 polymorphisms and breast cancer risk: a report from the Shanghai Breast Cancer Genetics Study.

Breast Cancer Research And Treatment
Beeghly-Fadiel, Alicia A; Lu, Wei W; Shu, Xiao-Ou XO; Long, Jirong J; Cai, Qiuyin Q; Xiang, Yongbin Y; Gao, Yu-Tang YT; Zheng, Wei W
Publication Date: 2011-04

Variant appearance in text: rs2236416
PubMed Link: 20725776
Variant Present in the following documents:
  • Main text
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Association of matrix metalloproteinase gene polymorphisms with refractive error in Amish and Ashkenazi families.

Investigative Ophthalmology & Visual Science
Wojciechowski, Robert R; Bailey-Wilson, Joan E JE; Stambolian, Dwight D
Publication Date: 2010-10

Variant appearance in text: rs2236416
PubMed Link: 20484597
Variant Present in the following documents:
  • Main text
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Variants of the Matrix Metalloproteinase-2 but not the Matrix Metalloproteinase-9 genes significantly influence functional outcome after stroke.

Bmc Medical Genetics
Manso, Helena H; Krug, Tiago T; Sobral, João J; Albergaria, Isabel I; Gaspar, Gisela G; Ferro, José M JM; Oliveira, Sofia A SA; Vicente, Astrid M AM
Publication Date: 2010-03-11

Variant appearance in text: rs2236416
PubMed Link: 20222942
Variant Present in the following documents:
  • Main text
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MMP-9 gene variants increase the risk for non-atopic asthma in children.

Respiratory Research
Pinto, Leonardo A LA; Depner, Martin M; Klopp, Norman N; Illig, Thomas T; Vogelberg, Christian C; von Mutius, Erika E; Kabesch, Michael M
Publication Date: 2010-02-24

Variant appearance in text: rs2236416
PubMed Link: 20181264
Variant Present in the following documents:
  • Main text
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Association of MMP-2 polymorphisms with severe and very severe COPD: a case control study of MMPs-1, 9 and 12 in a European population.

Bmc Medical Genetics
Haq, Imran I; Chappell, Sally S; Johnson, Simon R SR; Lotya, Juzer J; Daly, Leslie L; Morgan, Kevin K; Guetta-Baranes, Tamar T; Roca, Josep J; Rabinovich, Roberto R; Millar, Ann B AB; Donnelly, Seamas C SC; Keatings, Vera V; MacNee, William W; Stolk, Jan J; Hiemstra, Pieter S PS; Miniati, Massimo M; Monti, Simonetta S; O'Connor, Clare M CM; Kalsheker, Noor N
Publication Date: 2010-01-15

Variant appearance in text: rs2236416
PubMed Link: 20078883
Variant Present in the following documents:
  • Main text
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