Publications:

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COVID-19: Focusing on the Link between Inflammation, Vitamin D, MAPK Pathway and Oxidative Stress Genetics.

Antioxidants (Basel, Switzerland)

Cusato, Jessica J; Manca, Alessandra A; Palermiti, Alice A; Mula, Jacopo J; Costanzo, Martina M; Antonucci, Miriam M; Chiara, Francesco F; De Vivo, Elisa Delia ED; Maiese, Domenico D; Ferrara, Micol M; Bonora, Stefano S; Di Perri, Giovanni G; D'Avolio, Antonio A; Calcagno, Andrea A

Publication Date: 2023-05-20

Variant appearance in text: rs4343

PubMed Link: 37237997

Variant Present in the following documents:

• Main text
• antioxidants-12-01133.pdf

View BVdb publication page

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Association between Interactions among ACE Gene Polymorphisms and Essential Hypertension in Patients in the Hefei Region, Anhui, China.

Journal Of The Renin-Angiotensin-Aldosterone System : Jraas

Wang, Li L; Song, Ting-Ting TT; Dong, Chang-Wu CW

Publication Date: 2023

Variant appearance in text: rs4343

PubMed Link: 37091860

Variant Present in the following documents:

• JRAAS2023-1159973.pdf

View BVdb publication page

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Genetic polymorphisms of ACE1, ACE2, IFTM3, TMPRSS2 and TNFα genes associated with susceptibility and severity of SARS-CoV-2 infection: a systematic review and meta-analysis.

Clinical And Experimental Medicine

Pecoraro, Valentina V; Cuccorese, Michela M; Trenti, Tommaso T

Publication Date: 2023-04-13

Variant appearance in text: rs4343

PubMed Link: 37055652

Variant Present in the following documents:

• Main text
• 10238_2023_Article_1038.pdf

View BVdb publication page

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Single Nucleotide Variants (SNVs) of Angiotensin-Converting Enzymes (ACE1 and ACE2): A Plausible Explanation for the Global Variation in COVID-19 Prevalence.

Journal Of The Renin-Angiotensin-Aldosterone System : Jraas

Atiku, Saad Mahjub SM; Kasozi, Dennis D; Campbell, Katrina K

Publication Date: 2023

Variant appearance in text: rs4343

PubMed Link: 37051471

Variant Present in the following documents:

• JRAAS2023-9668008.pdf

View BVdb publication page

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Relevance of TMPRSS2, CD163/CD206, and CD33 in clinical severity stratification of COVID-19.

Frontiers In Immunology

Martínez-Diz, Silvia S; Marín-Benesiu, Fernando F; López-Torres, Ginesa G; Santiago, Olivia O; Díaz-Cuéllar, José F JF; Martín-Esteban, Sara S; Cortés-Valverde, Ana I AI; Arenas-Rodríguez, Verónica V; Cuenca-López, Sergio S; Porras-Quesada, Patricia P; Ruiz-Ruiz, Carmen C; Abadía-Molina, Ana C AC; Entrala-Bernal, Carmen C; Martínez-González, Luis J LJ; Álvarez-Cubero, Maria Jesus MJ

Publication Date: 2022

Variant appearance in text: rs4343

PubMed Link: 36969980

Variant Present in the following documents:

• fimmu-13-1094644.pdf

View BVdb publication page

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The effect of ACE2 receptor, IFN-γ, and TNF-α polymorphisms on the severity and prognosis of the disease in SARS-CoV-2 infection.

Journal Of Investigative Medicine : The Official Publication Of The American Federation For Clinical Research

Esen, Sayın Gülensoy SG; Basak, Celtikci C; Leyla, Özer Ö; Aslıhan, Alhan A; Evrim Eylem, Akpınar A

Publication Date: 2023-03-06

Variant appearance in text: rs4343

PubMed Link: 36876951

Variant Present in the following documents:

• Main text
• 10.1177_10815589231158379.pdf

View BVdb publication page

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Polymorphisms in ACE1, TMPRSS2, IFIH1, IFNAR2, and TYK2 Genes Are Associated with Worse Clinical Outcomes in COVID-19.

Genes

Dieter, Cristine C; de Almeida Brondani, Leticia L; Lemos, Natália Emerim NE; Schaeffer, Ariell Freires AF; Zanotto, Caroline C; Ramos, Denise Taurino DT; Girardi, Eliandra E; Pellenz, Felipe Mateus FM; Camargo, Joiza Lins JL; Moresco, Karla Suzana KS; da Silva, Lucas Lima LL; Aubin, Mariana Rauback MR; de Oliveira, Mayara Souza MS; Rech, Tatiana Helena TH; Canani, Luís Henrique LH; Gerchman, Fernando F; Leitão, Cristiane Bauermann CB; Crispim, Daisy D

Publication Date: 2022-12-22

Variant appearance in text: rs4343

PubMed Link: 36672770

Variant Present in the following documents:

• genes-14-00029.pdf

View BVdb publication page

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Genetic studies of plasma analytes identify novel potential biomarkers for several complex traits.

Scientific Reports

Deming, Yuetiva Y; Xia, Jian J; Cai, Yefei Y; Lord, Jenny J; Del-Aguila, Jorge L JL; Fernandez, Maria Victoria MV; Carrell, David D; Black, Kathleen K; Budde, John J; Ma, ShengMei S; Saef, Benjamin B; Howells, Bill B; Bertelsen, Sarah S; Bailey, Matthew M; Ridge, Perry G PG; , ; Holtzman, David D; Morris, John C JC; Bales, Kelly K; Pickering, Eve H EH; Lee, Jin-Moo JM; Heitsch, Laura L; Kauwe, John J; Goate, Alison A; Piccio, Laura L; Cruchaga, Carlos C

Publication Date: 2016-01-04

Variant appearance in text: rs4343

PubMed Link: 36647296

Variant Present in the following documents:

• srep18092-s1.pdf
• srep18092.pdf

View BVdb publication page

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Pre-Existing Diabetes Mellitus, Hypertension and KidneyDisease as Risk Factors of Pre-Eclampsia: A Disease of Theories and Its Association with Genetic Polymorphism.

International Journal Of Environmental Research And Public Health

Alanazi, Abdullah Salah AS; Victor, Francis F; Rehman, Kanwal K; Khan, Yusra Habib YH; Yunusa, Ismaeel I; Alzarea, Abdulaziz Ibrahim AI; Akash, Muhammad Sajid Hamid MSH; Mallhi, Tauqeer Hussain TH

Publication Date: 2022-12-12

Variant appearance in text: rs4343

PubMed Link: 36554576

Variant Present in the following documents:

• Main text
• ijerph-19-16690.pdf

View BVdb publication page

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ACE2 polymorphisms impact COVID-19 severity in obese patients.

Scientific Reports

Jalaleddine, Nour N; Bouzid, Amal A; Hachim, Mahmood M; Sharif-Askari, Narjes Saheb NS; Mahboub, Bassam B; Senok, Abiola A; Halwani, Rabih R; Hamoudi, Rifat A RA; Al Heialy, Saba S

Publication Date: 2022-12-13

Variant appearance in text: rs4343

PubMed Link: 36513710

Variant Present in the following documents:

• 41598_2022_Article_26072.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: ACE: T776T; rs4343

PubMed Link: 36467812

Variant Present in the following documents:

• JHA2-3-1326-s001.xlsx, sheet 1

View BVdb publication page

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Haplotypic variants of COVID-19 related genes are associated with blood pressure and metabolites levels.

Journal Of Medical Virology

Gholami, Morteza M; Zoughi, Marziyeh M; Hasanzad, Mandana M; Larijani, Bagher B; Amoli, Mahsa M MM

Publication Date: 2022-11-28

Variant appearance in text: rs4343

PubMed Link: 36443248

Variant Present in the following documents:

• Main text
• JMV-95-0.pdf

View BVdb publication page

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Analysis of Gene Single Nucleotide Polymorphisms in COVID-19 Disease Highlighting the Susceptibility and the Severity towards the Infection.

Diagnostics (Basel, Switzerland)

Balzanelli, Mario Giosuè MG; Distratis, Pietro P; Lazzaro, Rita R; Pham, Van Hung VH; Tran, Toai Cong TC; Dipalma, Gianna G; Bianco, Angelica A; Serlenga, Emilio Maria EM; Aityan, Sergey Khachatur SK; Pierangeli, Valentina V; Nguyen, Kieu Cao Diem KCD; Inchingolo, Francesco F; Tomassone, Diego D; Isacco, Ciro Gargiulo CG

Publication Date: 2022-11-16

Variant appearance in text: rs4343

PubMed Link: 36428884

Variant Present in the following documents:

• Main text
• diagnostics-12-02824.pdf

View BVdb publication page

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A protective erythropoietin evolutionary landscape, NLRP3 inflammasome regulation, and multisystem inflammatory syndrome in children.

Human Cell

Papadopoulos, Konstantinos I KI; Papadopoulou, Alexandra A; Aw, Tar-Choon TC

Publication Date: 2022-10-31

Variant appearance in text: rs4343

PubMed Link: 36310304

Variant Present in the following documents:

• Main text
• 13577_2022_Article_819.pdf

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: ACE: T776T; rs4343

PubMed Link: 36241656

Variant Present in the following documents:

• 41598_2022_20939_MOESM6_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM15_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM3_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM13_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM5_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM2_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM14_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM7_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM12_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM11_ESM.xlsx, sheet 2

View BVdb publication page

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Inflammasome Genetic Variants Are Associated with Protection to Clinical Severity of COVID-19 among Patients from Rio de Janeiro, Brazil.

Biomed Research International

de Sá, Nathalia Beatriz Ramos NBR; Neira-Goulart, Milena M; Ribeiro-Alves, Marcelo M; Perazzo, Hugo H; Geraldo, Kim Mattos KM; Ribeiro, Maria Pia Diniz MPD; Cardoso, Sandra Wagner SW; Grinsztejn, Beatriz B; Veloso, Valdiléa G VG; Capão, Artur A; Siqueira, Marilda Mendonça MM; de Lima Bezerra, Ohanna Cavalcanti OC; Garcia, Cristiana Couto CC; Gomes, Larissa Rodrigues LR; da Silva Cazote, Andressa A; de Almeida, Dalziza Victalina DV; Giacoia-Gripp, Carmem Beatriz Wagner CBW; Côrtes, Fernanda Heloise FH; Morgado, Mariza Gonçalves MG

Publication Date: 2022

Variant appearance in text: rs4343

PubMed Link: 36105941

Variant Present in the following documents:

• BMRI2022-9082455.pdf

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: ACE: T776T; rs4343

PubMed Link: 36075891

Variant Present in the following documents:

• 41439_2022_208_MOESM5_ESM.xlsx, sheet 2

View BVdb publication page

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Systematic review and meta-analysis of human genetic variants contributing to COVID-19 susceptibility and severity.

Gene

Gupta, Kajal K; Kaur, Gaganpreet G; Pathak, Tejal T; Banerjee, Indranil I

Publication Date: 2022-11-30

Variant appearance in text: rs4343

PubMed Link: 35987511

Variant Present in the following documents:

• Main text
• main.pdf

View BVdb publication page

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Association of AGTR1 gene methylation and its genetic variant in Chinese farmer with hypertension: A case-control study.

Medicine

Li, Zhi-Yuan ZY; Ma, Qiang Q; Li, Xing X; Yu, Shui-Yuan SY; Zuo, Juan J; Wang, Chong-Jian CJ; Li, Wen-Jie WJ; Ba, Yue Y; Yu, Fang-Fang FF

Publication Date: 2022-07-22

Variant appearance in text: rs4343

PubMed Link: 35866766

Variant Present in the following documents:

• Main text
• medi-101-e29712.pdf

View BVdb publication page

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Clinical Utility of Amplification Refractory Mutation System-Based PCR and Mutation-Specific PCR for Precise and Rapid Genotyping of Angiotensin-Converting Enzyme 1 (ACE1-rs4646996 D>I) and Angiotensin-Converting Enzyme 2 (ACE2-rs4240157T>C) Gene Variations in Coronary Artery Disease and Their Strong Association with Its Disease Susceptibility and Progression.

Diagnostics (Basel, Switzerland)

Yousif, Aadil A; Mir, Rashid R; Javid, Jamsheed J; Barnawi, Jameel J; Jalal, Mohammed M MM; Altayar, Malik A MA; Albalawi, Salem Owaid SO; Abuduhier, Faisel M FM

Publication Date: 2022-05-26

Variant appearance in text: rs4343

PubMed Link: 35741131

Variant Present in the following documents:

• Main text
• diagnostics-12-01321.pdf

View BVdb publication page

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Transmembrane protease serine 2 (TMPRSS2) rs75603675, comorbidity, and sex are the primary predictors of COVID-19 severity.

Life Science Alliance

Villapalos-García, Gonzalo G; Zubiaur, Pablo P; Rivas-Durán, Rebeca R; Campos-Norte, Pilar P; Arévalo-Román, Cristina C; Fernández-Rico, Marta M; García-Fraile Fraile, Lucio L; Fernández-Campos, Paula P; Soria-Chacartegui, Paula P; Fernández de Córdoba-Oñate, Sara S; Delgado-Wicke, Pablo P; Fernández-Ruiz, Elena E; González-Álvaro, Isidoro I; Sanz, Jesús J; Abad-Santos, Francisco F; de Los Santos, Ignacio I

Publication Date: 2022-10

Variant appearance in text: rs4343

PubMed Link: 35636966

Variant Present in the following documents:

• Main text
• LSA-2022-01396.pdf

View BVdb publication page

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SNPs of ACE1 (rs4343) and ACE2 (rs2285666) genes are linked to SARS-CoV-2 infection but not with the severity of disease.

Virology Journal

Alimoradi, Nahid N; Sharqi, Moein M; Firouzabadi, Dena D; Sadeghi, Mohammad Moein MM; Moezzi, Mohammad Iman MI; Firouzabadi, Negar N

Publication Date: 2022-03-19

Variant appearance in text: rs4343

PubMed Link: 35305693

Variant Present in the following documents:

• Main text
• 12985_2022_Article_1782.pdf

View BVdb publication page

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Genetically proxied therapeutic inhibition of antihypertensive drug targets and risk of common cancers: A mendelian randomization analysis.

Plos Medicine

Yarmolinsky, James J; Díez-Obrero, Virginia V; Richardson, Tom G TG; Pigeyre, Marie M; Sjaarda, Jennifer J; Paré, Guillaume G; Walker, Venexia M VM; Vincent, Emma E EE; Tan, Vanessa Y VY; Obón-Santacana, Mireia M; Albanes, Demetrius D; Hampe, Jochen J; Gsur, Andrea A; Hampel, Heather H; Pai, Rish K RK; Jenkins, Mark M; Gallinger, Steven S; Casey, Graham G; Zheng, Wei W; Amos, Christopher I CI; , ; , ; , ; Smith, George Davey GD; Martin, Richard M RM; Moreno, Victor V

Publication Date: 2022-02

Variant appearance in text: rs4343

PubMed Link: 35113855

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genetically proxied therapeutic inhibition of antihypertensive drug targets and risk of common cancers: A mendelian randomization analysis.

Plos Medicine

Yarmolinsky, James J; Díez-Obrero, Virginia V; Richardson, Tom G TG; Pigeyre, Marie M; Sjaarda, Jennifer J; Paré, Guillaume G; Walker, Venexia M VM; Vincent, Emma E EE; Tan, Vanessa Y VY; Obón-Santacana, Mireia M; Albanes, Demetrius D; Hampe, Jochen J; Gsur, Andrea A; Hampel, Heather H; Pai, Rish K RK; Jenkins, Mark M; Gallinger, Steven S; Casey, Graham G; Zheng, Wei W; Amos, Christopher I CI; , ; , ; , ; Smith, George Davey GD; Martin, Richard M RM; Moreno, Victor V

Publication Date: 2022-02

Variant appearance in text: rs4343

PubMed Link: 35113855

Variant Present in the following documents:

• Main text

View BVdb publication page

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Association of MTHFD1 gene polymorphisms and maternal smoking with risk of congenital heart disease: a hospital-based case-control study.

Bmc Pregnancy And Childbirth

Song, Xinli X; Li, Qiongxuan Q; Diao, Jingyi J; Li, Jinqi J; Li, Yihuan Y; Zhang, Senmao S; Zhao, Lijuan L; Chen, Letao L; Wei, Jianhui J; Shu, Jing J; Liu, Yiping Y; Sun, Mengting M; Huang, Peng P; Wang, Tingting T; Qin, Jiabi J

Publication Date: 2022-01-31

Variant appearance in text: rs4343

PubMed Link: 35100977

Variant Present in the following documents:

• 12884_2022_Article_4419.pdf

View BVdb publication page

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Association of MTHFD1 gene polymorphisms and maternal smoking with risk of congenital heart disease: a hospital-based case-control study.

Bmc Pregnancy And Childbirth

Song, Xinli X; Li, Qiongxuan Q; Diao, Jingyi J; Li, Jinqi J; Li, Yihuan Y; Zhang, Senmao S; Zhao, Lijuan L; Chen, Letao L; Wei, Jianhui J; Shu, Jing J; Liu, Yiping Y; Sun, Mengting M; Huang, Peng P; Wang, Tingting T; Qin, Jiabi J

Publication Date: 2022-01-31

Variant appearance in text: rs4343

PubMed Link: 35100977

Variant Present in the following documents:

• 12884_2022_Article_4419.pdf

View BVdb publication page

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Two Opposing Functions of Angiotensin-Converting Enzyme (ACE) That Links Hypertension, Dementia, and Aging.

International Journal Of Molecular Sciences

Le, Duc D; Brown, Lindsay L; Malik, Kundan K; Murakami, Shin S

Publication Date: 2021-12-07

Variant appearance in text: rs4343

PubMed Link: 34947975

Variant Present in the following documents:

• Main text
• ijms-22-13178.pdf

View BVdb publication page

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Two Opposing Functions of Angiotensin-Converting Enzyme (ACE) That Links Hypertension, Dementia, and Aging.

International Journal Of Molecular Sciences

Le, Duc D; Brown, Lindsay L; Malik, Kundan K; Murakami, Shin S

Publication Date: 2021-12-07

Variant appearance in text: rs4343

PubMed Link: 34947975

Variant Present in the following documents:

• Main text
• ijms-22-13178.pdf

View BVdb publication page

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Strong Association of Angiotensin Converting Enzyme-2 Gene Insertion/Deletion Polymorphism with Susceptibility to SARS-CoV-2, Hypertension, Coronary Artery Disease and COVID-19 Disease Mortality.

Journal Of Personalized Medicine

Mir, Mohammad Muzaffar MM; Mir, Rashid R; Alghamdi, Mushabab Ayed Abdullah MAA; Alsayed, Badr Abdulmohsin BA; Wani, Javed Iqbal JI; Alharthi, Muffarah Hamid MH; Al-Shahrani, Abdullah M AM

Publication Date: 2021-10-27

Variant appearance in text: rs4343

PubMed Link: 34834450

Variant Present in the following documents:

• Main text

View BVdb publication page

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The Renin-Angiotensin System: A Key Role in SARS-CoV-2-Induced COVID-19.

Molecules (Basel, Switzerland)

El-Arif, George G; Farhat, Antonella A; Khazaal, Shaymaa S; Annweiler, Cédric C; Kovacic, Hervé H; Wu, Yingliang Y; Cao, Zhijian Z; Fajloun, Ziad Z; Khattar, Ziad Abi ZA; Sabatier, Jean Marc JM

Publication Date: 2021-11-17

Variant appearance in text: rs4343

PubMed Link: 34834033

Variant Present in the following documents:

• Main text

View BVdb publication page

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Angiotensin-converting enzyme polymorphisms AND Alzheimer's disease susceptibility: An updated meta-analysis.

Plos One

Xin, Xiao-Yu XY; Lai, Ze-Hua ZH; Ding, Kai-Qi KQ; Zeng, Li-Li LL; Ma, Jian-Fang JF

Publication Date: 2021

Variant appearance in text: rs4343

PubMed Link: 34818351

Variant Present in the following documents:

• Main text

View BVdb publication page

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Angiotensin-converting enzyme polymorphisms AND Alzheimer's disease susceptibility: An updated meta-analysis.

Plos One

Xin, Xiao-Yu XY; Lai, Ze-Hua ZH; Ding, Kai-Qi KQ; Zeng, Li-Li LL; Ma, Jian-Fang JF

Publication Date: 2021

Variant appearance in text: rs4343

PubMed Link: 34818351

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genetic analysis of pharmacogenomic VIP variants in the Wa population from Yunnan Province of China.

Bmc Genomic Data

Li, Dandan D; Peng, Linna L; Xing, Shishi S; He, Chunjuan C; Jin, Tianbo T

Publication Date: 2021-11-19

Variant appearance in text: rs4343

PubMed Link: 34798807

Variant Present in the following documents:

• Main text
• 12863_2021_Article_999.pdf

View BVdb publication page

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Population Genetic Polymorphism of Skeletal Muscle Strength Related Genes in Five Ethnic Minorities in North China.

Frontiers In Genetics

Dong, Bonan B; Li, Qiuyan Q; Zhang, Tingting T; Liang, Xiao X; Jia, Mansha M; Fu, Yansong Y; Bai, Jing J; Fu, Songbin S

Publication Date: 2021

Variant appearance in text: rs4343

PubMed Link: 34745225

Variant Present in the following documents:

• Main text
• fgene-12-756802.pdf

View BVdb publication page

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Systematic Review and Bioinformatic Analysis of microRNA Expression in Autism Spectrum Disorder Identifies Pathways Associated With Cancer, Metabolism, Cell Signaling, and Cell Adhesion.

Frontiers In Psychiatry

Huang, Zhi-Xiong ZX; Chen, Yanhui Y; Guo, Hong-Ru HR; Chen, Guo-Feng GF

Publication Date: 2021

Variant appearance in text: rs4343

PubMed Link: 34744804

Variant Present in the following documents:

• Table_4.xlsx, sheet 2

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: rs4343

PubMed Link: 34683180

Variant Present in the following documents:

• Main text
• jpm-11-01040.pdf

View BVdb publication page

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A systematic review of common genetic variation and biological pathways in autism spectrum disorder.

Bmc Neuroscience

Rodriguez-Gomez, Diego Alejandro DA; Garcia-Guaqueta, Danna Paola DP; Charry-Sánchez, Jesús David JD; Sarquis-Buitrago, Elias E; Blanco, Mariana M; Velez-van-Meerbeke, Alberto A; Talero-Gutiérrez, Claudia C

Publication Date: 2021-10-09

Variant appearance in text: rs4343

PubMed Link: 34627165

Variant Present in the following documents:

• 12868_2021_662_MOESM1_ESM.xlsx, sheet 1

View BVdb publication page

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ACE Gene Variants Rise the Risk of Severe COVID-19 in Patients With Hypertension, Dyslipidemia or Diabetes: A Spanish Pilot Study.

Frontiers In Endocrinology

Íñiguez, María M; Pérez-Matute, Patricia P; Villoslada-Blanco, Pablo P; Recio-Fernandez, Emma E; Ezquerro-Pérez, Diana D; Alba, Jorge J; Ferreira-Laso, M Lourdes ML; Oteo, José A JA

Publication Date: 2021

Variant appearance in text: rs4343

PubMed Link: 34489863

Variant Present in the following documents:

• Main text

View BVdb publication page

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Haematological Indicators of Response to Erythropoietin Therapy in Chronic Renal Failure Patients on Haemodialysis: Impact of Angiotensin-Converting Enzyme rs4343 Gene Polymorphism.

Pharmacogenomics And Personalized Medicine

Hamdan Almaeen, Abdulrahman A; Mostafa-Hedeab, Gomaa G

Publication Date: 2021

Variant appearance in text: rs4343

PubMed Link: 34483678

Variant Present in the following documents:

• Main text

View BVdb publication page

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COVID-19 in pregnancy: What we know from the first year of the pandemic.

Biochimica Et Biophysica Acta. Molecular Basis Of Disease

Arthurs, Anya Lara AL; Jankovic-Karasoulos, Tanja T; Roberts, Claire Trelford CT

Publication Date: 2021-12-01

Variant appearance in text: rs4343

PubMed Link: 34461257

Variant Present in the following documents:

• Main text
• main.pdf

View BVdb publication page

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Genetics of Diabetic Retinopathy, a Leading Cause of Irreversible Blindness in the Industrialized World.

Genes

Bhatwadekar, Ashay D AD; Shughoury, Aumer A; Belamkar, Ameya A; Ciulla, Thomas A TA

Publication Date: 2021-07-31

Variant appearance in text: rs4343

PubMed Link: 34440374

Variant Present in the following documents:

• Main text
• genes-12-01200.pdf

View BVdb publication page

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The Genetic Contribution to Drug Response in Spondyloarthritis: A Systematic Literature Review.

Frontiers In Genetics

Ortolan, Augusta A; Cozzi, Giacomo G; Lorenzin, Mariagrazia M; Galozzi, Paola P; Doria, Andrea A; Ramonda, Roberta R

Publication Date: 2021

Variant appearance in text: rs4343

PubMed Link: 34354741

Variant Present in the following documents:

• Main text
• fgene-12-703911.pdf

View BVdb publication page

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Genetic polymorphisms associated with obesity in the Arab world: a systematic review.

International Journal Of Obesity (2005)

Younes, Salma S; Ibrahim, Amal A; Al-Jurf, Rana R; Zayed, Hatem H

Publication Date: 2021-09

Variant appearance in text: rs4343

PubMed Link: 34131278

Variant Present in the following documents:

• 41366_2021_Article_867.pdf

View BVdb publication page

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A systematic review of nonsynonymous single nucleotide polymorphisms in the renin-angiotensin-aldosterone system.

Cardiology Journal

Rechciński, Tomasz T; Kasprzak, Jarosław D JD

Publication Date: 2021-06-01

Variant appearance in text: rs4343

PubMed Link: 34060646

Variant Present in the following documents:

• Main text
• cardj-29-6-1020.pdf

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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: ACE: 2328G>A; T776T; rs4343

PubMed Link: 34054912

Variant Present in the following documents:

• Table_2.xlsx, sheet 1

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An intron variant of the GLI family zinc finger 3 (GLI3) gene differentiates resistance training-induced muscle fiber hypertrophy in younger men.

Faseb Journal : Official Publication Of The Federation Of American Societies For Experimental Biology

Vann, Christopher G CG; Morton, Robert W RW; Mobley, Christopher B CB; Vechetti, Ivan J IJ; Ferguson, Brian K BK; Haun, Cody T CT; Osburn, Shelby C SC; Sexton, Casey L CL; Fox, Carlton D CD; Romero, Matthew A MA; Roberson, Paul A PA; Oikawa, Sara Y SY; McGlory, Chris C; Young, Kaelin C KC; McCarthy, John J JJ; Phillips, Stuart M SM; Roberts, Michael D MD

Publication Date: 2021-05

Variant appearance in text: rs4343

PubMed Link: 33891350

Variant Present in the following documents:

• Main text

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