Publications:

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Single-nucleotide polymorphisms of matrix metalloproteinase genes are associated with graft fibrosis after kidney transplantation.

Translational Andrology And Urology

Zhang, Hengcheng H; Gao, Xiang X; Gui, Zeping Z; Suo, Chuanjian C; Tao, Jun J; Han, Zhijian Z; Ju, Xiaobin X; Tan, Ruoyun R; Gu, Min M; Wang, Zijie Z

Publication Date: 2023-03-31

Variant appearance in text: rs2236416

PubMed Link: 37032759

Variant Present in the following documents:

• tau-12-03-375.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: rs2236416

PubMed Link: 36991000

Variant Present in the following documents:

• 41467_2023_37221_MOESM5_ESM.xlsx, sheet 3

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: rs2236416

PubMed Link: 36467812

Variant Present in the following documents:

• JHA2-3-1326-s001.xlsx, sheet 1

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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: rs2236416

PubMed Link: 36241656

Variant Present in the following documents:

• 41598_2022_20939_MOESM14_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM15_ESM.xlsx, sheet 2

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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

View BVdb publication page

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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: 2022-02

Variant appearance in text: rs2236416

PubMed Link: 34973089

Variant Present in the following documents:

• Main text
• 192_2021_Article_4917.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: MMP9: 997+189A>G; rs2236416

PubMed Link: 34054912

Variant Present in the following documents:

• Table_2.xlsx, sheet 1

View BVdb publication page

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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

View BVdb publication page

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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
• jpm-10-00044.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: MMP9: 997+189A>G; rs2236416

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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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
• fmed-04-00186.pdf

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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
• pone.0168550.pdf

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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
• MI2015-569714.pdf

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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

View BVdb publication page

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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

View BVdb publication page

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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

View BVdb publication page

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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

View BVdb publication page

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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
• 1471-2350-11-7.pdf

View BVdb publication page

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