Publications:

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Matrix metalloproteinases in coronary artery disease and myocardial infarction.

Basic Research In Cardiology

Bräuninger, Hanna H; Krüger, Saskia S; Bacmeister, Lucas L; Nyström, Alexander A; Eyerich, Kilian K; Westermann, Dirk D; Lindner, Diana D

Publication Date: 2023-05-09

Variant appearance in text: rs17576

PubMed Link: 37160529

Variant Present in the following documents:

• Main text
• 395_2023_Article_987.pdf

View BVdb publication page

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Methodological quality assessment of genetic studies on brain arteriovenous malformation related hemorrhage: A cross-sectional study.

Frontiers In Genetics

Jiang, Junhao J; Qin, Zhuo Z; Yan, Junxia J; Liu, Junyu J

Publication Date: 2023

Variant appearance in text: MMP9: Q279R; rs17576

PubMed Link: 37065486

Variant Present in the following documents:

• Main text
• fgene-14-1123898.pdf

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Increased levels of a subset of angiogenesis-related plasma proteins in essential thrombocythemia.

Upsala Journal Of Medical Sciences

Vikman, Sofia S; Larsson, Anders A; Thulin, Måns M; Karlsson, Torbjörn T

Publication Date: 2023

Variant appearance in text: MMP9: Gln279Arg

PubMed Link: 37051288

Variant Present in the following documents:

• Main text
• UJMS-128-9194.pdf

View BVdb publication page

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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: rs17576

PubMed Link: 37032759

Variant Present in the following documents:

• tau-12-03-375.pdf

View BVdb publication page

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Workflow enabling deepscale immunopeptidome, proteome, ubiquitylome, phosphoproteome, and acetylome analyses of sample-limited tissues.

Nature Communications

Abelin, Jennifer G JG; Bergstrom, Erik J EJ; Rivera, Keith D KD; Taylor, Hannah B HB; Klaeger, Susan S; Xu, Charles C; Verzani, Eva K EK; Jackson White, C C; Woldemichael, Hilina B HB; Virshup, Maya M; Olive, Meagan E ME; Maynard, Myranda M; Vartany, Stephanie A SA; Allen, Joseph D JD; Phulphagar, Kshiti K; Harry Kane, M M; Rachimi, Suzanna S; Mani, D R DR; Gillette, Michael A MA; Satpathy, Shankha S; Clauser, Karl R KR; Udeshi, Namrata D ND; Carr, Steven A SA

Publication Date: 2023-04-03

Variant appearance in text: MMP9: Q279R

PubMed Link: 37012232

Variant Present in the following documents:

• 41467_2023_37547_MOESM12_ESM.xlsx, sheet 3
• 41467_2023_37547_MOESM12_ESM.xlsx, sheet 2

View BVdb publication page

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New Genetically Determined Markers of the Functional State of the Cardiovascular System.

Genes

Kondakova, Elena V EV; Ilina, Valeria M VM; Ermakova, Lyubov M LM; Krivonosov, Mikhail I MI; Kuchin, Kirill V KV; Vedunova, Maria V MV

Publication Date: 2023-01-10

Variant appearance in text: MMP9: Gln279Arg; rs17576

PubMed Link: 36672926

Variant Present in the following documents:

• Main text
• genes-14-00185.pdf

View BVdb publication page

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Molecular Genetics of Thrombotic Myeloproliferative Neoplasms: Implications in Precision Oncology.

Diagnostics (Basel, Switzerland)

Chia, Yuh Cai YC; Siti Asmaa, Mat Jusoh MJ; Ramli, Marini M; Woon, Peng Yeong PY; Johan, Muhammad Farid MF; Hassan, Rosline R; Islam, Md Asiful MA

Publication Date: 2023-01-03

Variant appearance in text: MMP9: Gln279Arg

PubMed Link: 36611455

Variant Present in the following documents:

• Main text
• diagnostics-13-00163.pdf

View BVdb publication page

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Zinc in Prostate Health and Disease: A Mini Review.

Biomedicines

Karunasinghe, Nishi N

Publication Date: 2022-12-10

Variant appearance in text: rs17576

PubMed Link: 36551962

Variant Present in the following documents:

• Main text
• biomedicines-10-03206.pdf

View BVdb publication page

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Serum matrix metalloproteinase-9 (MMP-9) as a biomarker in paediatric and adult tick-borne encephalitis patients.

Virus Research

Fortova, Andrea A; Hönig, Vaclav V; Salat, Jiri J; Palus, Martin M; Pychova, Martina M; Krbkova, Lenka L; Barkhash, Andrey V AV; Kriha, Michal F MF; Chrdle, Ales A; Lipoldova, Marie M; Ruzek, Daniel D

Publication Date: 2022-12-14

Variant appearance in text: MMP9: Gln279Arg; rs17576

PubMed Link: 36528170

Variant Present in the following documents:

• Main text
• main.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: MMP9: Q279R; rs17576

PubMed Link: 36467812

Variant Present in the following documents:

• JHA2-3-1326-s001.xlsx, sheet 1

View BVdb publication page

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Chronic Cadmium Exposure and Genetic Polymorphisms of MMP-2 and MMP-9 in a Population Exposed to Steel Slag in the State of Rio de Janeiro, Brazil: A Cross-Sectional Study.

International Journal Of Environmental Research And Public Health

Perini, Jamila A JA; Silva, Mayara C da MCD; Correa, Lorena V LV; Silva, Yasmin M YM; Borges, Renato M RM; Moreira, Maria de Fátima R MFR

Publication Date: 2022-11-19

Variant appearance in text: rs17576

PubMed Link: 36430020

Variant Present in the following documents:

• Main text
• ijerph-19-15304.pdf

View BVdb publication page

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Single Nucleotide Polymorphisms and Dental Fluorosis: A Systematic Review.

Dentistry Journal

González-Casamada, Carlos C; Nevarez-Rascón, Martina M; Nevarez-Rascón, Alfredo A; González-Galván, María M; Isiordia-Espinoza, Mario Alberto MA; Bologna-Molina, Ronell R; Sánchez-Pérez, Leonor L; Molina-Frechero, Nelly N

Publication Date: 2022-11-06

Variant appearance in text: rs17576

PubMed Link: 36354656

Variant Present in the following documents:

• dentistry-10-00211.pdf

View BVdb publication page

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The Modifying Effect of Obesity on the Association of Matrix Metalloproteinase Gene Polymorphisms with Breast Cancer Risk.

Biomedicines

Pavlova, Nadezhda N; Demin, Sergey S; Churnosov, Mikhail M; Reshetnikov, Evgeny E; Aristova, Inna I; Churnosova, Maria M; Ponomarenko, Irina I

Publication Date: 2022-10-18

Variant appearance in text: MMP9: 836A>G; Q279R; rs17576

PubMed Link: 36289879

Variant Present in the following documents:

• Main text
• biomedicines-10-02617.pdf

View BVdb publication page

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Gene polymorphisms of cyclin-dependent kinase inhibitor and matrix metalloproteinase-9 in Sudanese patients with esophageal squamous cell carcinoma.

Molecular Genetics & Genomic Medicine

Eltayeb, Majdolin Mohammed MM; Ali, Mohamed M MM; Omar, Saeed M SM; Mohamed, Nouh Saad NS; Adam, Ishag I; Hamdan, Hamdan Z HZ

Publication Date: 2022-10-19

Variant appearance in text: MMP9: 836A>G; Gln279Arg; rs17576

PubMed Link: 36259348

Variant Present in the following documents:

• Main text
• MGG3-10-e2074.pdf

View BVdb publication page

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Genetic susceptibility of bladder cancer in the Lebanese population.

Bmc Medical Genomics

Kourie, Hampig Raphael HR; Succar, Bahaa B; Chouery, Eliane E; Mehawej, Cybel C; Ahmadieh, Nizar N; Zouein, Joseph J; Mardirossian, Avedis A; Jalkh, Nadine N; Sleilaty, Ghassan G; Kattan, Joseph J; Nemr, Elie E

Publication Date: 2022-10-17

Variant appearance in text: MMP9: 836A>G; Q279R; rs17576

PubMed Link: 36253817

Variant Present in the following documents:

• 12920_2022_1372_MOESM1_ESM.xlsx, sheet 1

View BVdb publication page

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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: MMP9: Q279R

PubMed Link: 36241656

Variant Present in the following documents:

• 41598_2022_20939_MOESM10_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM11_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM2_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM9_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM8_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM7_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM6_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM3_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM14_ESM.xlsx, sheet 2

View BVdb publication page

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A genomic deletion encompassing CRYBB2-CRYBB2P1 is responsible for autosomal recessive congenital cataracts.

Human Genome Variation

Irum, Bushra B; Kabir, Firoz F; Shoshany, Nadav N; Khan, Shahid Y SY; Rauf, Bushra B; Naeem, Muhammad Asif MA; Qaiser, Tanveer A TA; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA

Publication Date: 2022-09-08

Variant appearance in text: MMP9: Q279R; rs17576

PubMed Link: 36075891

Variant Present in the following documents:

• 41439_2022_208_MOESM4_ESM.xlsx, sheet 2
• 41439_2022_208_MOESM5_ESM.xlsx, sheet 2

View BVdb publication page

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Molecular Genetic Mechanisms in Age-Related Macular Degeneration.

Genes

Shughoury, Aumer A; Sevgi, Duriye Damla DD; Ciulla, Thomas A TA

Publication Date: 2022-07-12

Variant appearance in text: rs17576

PubMed Link: 35886016

Variant Present in the following documents:

• Main text
• genes-13-01233.pdf

View BVdb publication page

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Effects of TIMP1 rs4898 Gene Polymorphism on Early-Onset Preeclampsia Development and Placenta Weight.

Diagnostics (Basel, Switzerland)

Mrozikiewicz, Aleksandra E AE; Kurzawińska, Grażyna G; Goździewicz-Szpera, Agata A; Potograbski, Michał M; Ożarowski, Marcin M; Karpiński, Tomasz M TM; Barlik, Magdalena M; Jędrzejczak, Piotr P; Drews, Krzysztof K

Publication Date: 2022-07-05

Variant appearance in text: MMP9: Q279R; rs17576

PubMed Link: 35885543

Variant Present in the following documents:

• Main text
• diagnostics-12-01637.pdf

View BVdb publication page

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Genomic, transcriptomic, and metabolomic profiles of hiPSC-derived dopamine neurons from clinically discordant brothers with identical PRKN deletions.

Npj Parkinson'S Disease

Cukier, Holly N HN; Kim, Hyunjin H; Griswold, Anthony J AJ; Codreanu, Simona G SG; Prince, Lisa M LM; Sherrod, Stacy D SD; McLean, John A JA; Dykxhoorn, Derek M DM; Ess, Kevin C KC; Hedera, Peter P; Bowman, Aaron B AB; Neely, M Diana MD

Publication Date: 2022-06-29

Variant appearance in text: MMP9: Q279R; rs17576

PubMed Link: 35768426

Variant Present in the following documents:

• 41531_2022_346_MOESM2_ESM.xlsx, sheet 1

View BVdb publication page

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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: rs17576

PubMed Link: 35647299

Variant Present in the following documents:

• Main text
• biol-2022-0055.pdf

View BVdb publication page

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Asian Race and Primary Open-Angle Glaucoma: Where Do We Stand?

Journal Of Clinical Medicine

Belamkar, Aditya A; Harris, Alon A; Oddone, Francesco F; Verticchio Vercellin, Alice A; Fabczak-Kubicka, Anna A; Siesky, Brent B

Publication Date: 2022-04-28

Variant appearance in text: rs17576

PubMed Link: 35566612

Variant Present in the following documents:

• jcm-11-02486.pdf

View BVdb publication page

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Germline Variants in Angiogenesis-Related Genes Contribute to Clinical Outcome in Head and Neck Squamous Cell Carcinoma.

Cancers

Butkiewicz, Dorota D; Gdowicz-Kłosok, Agnieszka A; Krześniak, Małgorzata M; Rutkowski, Tomasz T; Łasut-Szyszka, Barbara B; Składowski, Krzysztof K

Publication Date: 2022-04-06

Variant appearance in text: rs17576

PubMed Link: 35406617

Variant Present in the following documents:

• Main text
• cancers-14-01844.pdf

View BVdb publication page

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Single-nucleotide polymorphisms as important risk factors of diabetes among Middle East population.

Human Genomics

Akhlaghipour, Iman I; Bina, Amir Reza AR; Mogharrabi, Mohammad Reza MR; Fanoodi, Ali A; Ebrahimian, Amir Reza AR; Khojasteh Kaffash, Soroush S; Babazadeh Baghan, Atefeh A; Khorashadizadeh, Mohammad Erfan ME; Taghehchian, Negin N; Moghbeli, Meysam M

Publication Date: 2022-04-02

Variant appearance in text: rs17576

PubMed Link: 35366956

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genetic markers for non-syndromic orofacial clefts in populations of European ancestry: a meta-analysis.

Scientific Reports

Slavec, Lara L; Karas Kuželički, Nataša N; Locatelli, Igor I; Geršak, Ksenija K

Publication Date: 2022-01-24

Variant appearance in text: rs17576

PubMed Link: 35075162

Variant Present in the following documents:

• Main text
• 41598_2021_Article_2159.pdf

View BVdb publication page

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Genetic markers for non-syndromic orofacial clefts in populations of European ancestry: a meta-analysis.

Scientific Reports

Slavec, Lara L; Karas Kuželički, Nataša N; Locatelli, Igor I; Geršak, Ksenija K

Publication Date: 2022-01-24

Variant appearance in text: rs17576

PubMed Link: 35075162

Variant Present in the following documents:

• Main text
• 41598_2021_Article_2159.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: 2022-01-01

Variant appearance in text: MMP9: Q279R; rs17576

PubMed Link: 34973089

Variant Present in the following documents:

• Main text
• 192_2021_Article_4917.pdf
• 192_2021_4917_MOESM1_ESM.xls, sheet 1

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: MMP9: Q279R; rs17576

PubMed Link: 34973089

Variant Present in the following documents:

• Main text
• 192_2021_Article_4917.pdf
• 192_2021_4917_MOESM1_ESM.xls, sheet 1

View BVdb publication page

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Association of Matrix Metalloproteinase (MMP) Gene Polymorphisms With Knee Osteoarthritis: A Review of the Literature.

Cureus

Milaras, Christos C; Lepetsos, Panagiotis P; Dafou, Dimitra D; Potoupnis, Michael M; Tsiridis, Eleftherios E

Publication Date: 2021-10

Variant appearance in text: rs17576

PubMed Link: 34765365

Variant Present in the following documents:

• Main text

View BVdb publication page

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Potential underlying genetic associations between keratoconus and diabetes mellitus.

Advances In Ophthalmology Practice And Research

Ates, Kristin M KM; Estes, Amy J AJ; Liu, Yutao Y

Publication Date: 2021-11

Variant appearance in text: rs17576

PubMed Link: 34746916

Variant Present in the following documents:

• Main text
• nihms-1746551.pdf

View BVdb publication page

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Selected Biomarkers of Tick-Borne Encephalitis: A Review.

International Journal Of Molecular Sciences

Gudowska-Sawczuk, Monika M; Mroczko, Barbara B

Publication Date: 2021-09-30

Variant appearance in text: rs17576

PubMed Link: 34638953

Variant Present in the following documents:

• Main text

View BVdb publication page

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Matrix Metalloproteinases as Biomarkers and Treatment Targets in Mesothelioma: A Systematic Review.

Biomolecules

Štrbac, Danijela D; Dolžan, Vita V

Publication Date: 2021-08-25

Variant appearance in text: rs17576

PubMed Link: 34572485

Variant Present in the following documents:

• Main text
• biomolecules-11-01272.pdf

View BVdb publication page

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The Genetic Basis of Moyamoya Disease.

Translational Stroke Research

Mertens, R R; Graupera, M M; Gerhardt, H H; Bersano, A A; Tournier-Lasserve, E E; Mensah, M A MA; Mundlos, S S; Vajkoczy, P P

Publication Date: 2021-09-16

Variant appearance in text: rs17576

PubMed Link: 34529262

Variant Present in the following documents:

• Main text
• 12975_2021_Article_940.pdf

View BVdb publication page

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The Genetic Basis of Moyamoya Disease.

Translational Stroke Research

Mertens, R R; Graupera, M M; Gerhardt, H H; Bersano, A A; Tournier-Lasserve, E E; Mensah, M A MA; Mundlos, S S; Vajkoczy, P P

Publication Date: 2022-02

Variant appearance in text: rs17576

PubMed Link: 34529262

Variant Present in the following documents:

• Main text
• 12975_2021_Article_940.pdf

View BVdb publication page

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Association of the functionally significant polymorphisms of the MMP9 gene with H. pylori-positive gastric ulcer in the Caucasian population of Central Russia.

Plos One

Dvornyk, Volodymyr V; Ponomarenko, Irina I; Minyaylo, Oksana O; Reshetnikov, Evgeny E; Churnosov, Mikhail M

Publication Date: 2021

Variant appearance in text: MMP9: Gln279Arg; rs17576

PubMed Link: 34492072

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genetic Variation of Inflammatory Genes to Ischemic Stroke Risk in a Chinese Han Population.

Pharmacogenomics And Personalized Medicine

Zhang, Zhongqiu Z; Mei, Yanping Y; Xiong, Mengqiu M; Lu, Fang F; Zhao, Xianghong X; Zhu, Junrong J; He, Bangshun B

Publication Date: 2021

Variant appearance in text: rs17576

PubMed Link: 34413669

Variant Present in the following documents:

• Main text
• pgpm-14-977.pdf

View BVdb publication page

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Treatment outcome clustering patterns correspond to discrete asthma phenotypes in children.

Asthma Research And Practice

Banić, Ivana I; Lovrić, Mario M; Cuder, Gerald G; Kern, Roman R; Rijavec, Matija M; Korošec, Peter P; Turkalj, Mirjana M

Publication Date: 2021-08-03

Variant appearance in text: rs17576

PubMed Link: 34344475

Variant Present in the following documents:

• Main text
• 40733_2021_Article_77.pdf

View BVdb publication page

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Functionally significant polymorphisms of the MMP-9 gene are associated with peptic ulcer disease in the Caucasian population of Central Russia.

Scientific Reports

Minyaylo, Oksana O; Ponomarenko, Irina I; Reshetnikov, Evgeny E; Dvornyk, Volodymyr V; Churnosov, Mikhail M

Publication Date: 2021-06-29

Variant appearance in text: rs17576

PubMed Link: 34188075

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genetic Predictors of Early-Onset Spinal Intervertebral Disc Degeneration: Part Two of Two.

Cureus

Fiani, Brian B; Covarrubias, Claudia C; Jarrah, Ryan R

Publication Date: 2021-05-22

Variant appearance in text: rs17576

PubMed Link: 34178504

Variant Present in the following documents:

• Main text
• cureus-0013-00000015183.pdf

View BVdb publication page

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Predicting Treatment Outcomes Using Explainable Machine Learning in Children with Asthma.

Children (Basel, Switzerland)

Lovrić, Mario M; Banić, Ivana I; Lacić, Emanuel E; Pavlović, Kristina K; Kern, Roman R; Turkalj, Mirjana M

Publication Date: 2021-05-10

Variant appearance in text: rs17576

PubMed Link: 34068718

Variant Present in the following documents:

• Main text

View BVdb publication page

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