Publications:

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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: rs4308

PubMed Link: 36443248

Variant Present in the following documents:

• Main text
• JMV-95-0.pdf

View BVdb publication page

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Multi-trait association studies discover pleiotropic loci between Alzheimer's disease and cardiometabolic traits.

Alzheimer'S Research & Therapy

Bone, William P WP; Siewert, Katherine M KM; Jha, Anupama A; Klarin, Derek D; Damrauer, Scott M SM; , ; Chang, Kyong-Mi KM; Tsao, Philip S PS; Assimes, Themistocles L TL; Ritchie, Marylyn D MD; Voight, Benjamin F BF

Publication Date: 2021-02-04

Variant appearance in text: rs4308

PubMed Link: 33541420

Variant Present in the following documents:

• Main text
• 13195_2021_773_MOESM1_ESM.pdf
• 13195_2021_Article_773.pdf

View BVdb publication page

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The Intersection between COVID-19, the Gene Family of ACE2 and Alzheimer's Disease.

Neuroscience Insights

Haghighi, Mahdi Montazer MM; Kakhki, Erfan Ghani EG; Sato, Christine C; Ghani, Mahdi M; Rogaeva, Ekaterina E

Publication Date: 2020

Variant appearance in text: rs4308

PubMed Link: 33283188

Variant Present in the following documents:

• Main text
• 10.1177_2633105520975743.pdf

View BVdb publication page

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Cognitive Decline in Alzheimer's Disease: Limited Clinical Utility for GWAS or Polygenic Risk Scores in a Clinical Trial Setting.

Genes

Euesden, Jack J; Gowrisankar, Sivakumar S; Qu, Angela Xiaoyan AX; Jean, Pamela St PS; Hughes, Arlene R AR; Pulford, David J DJ

Publication Date: 2020-05-02

Variant appearance in text: rs4308

PubMed Link: 32370229

Variant Present in the following documents:

• genes-11-00501-s001.pdf

View BVdb publication page

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Contribution of Four Polymorphisms in Renin-Angiotensin-Aldosterone-Related Genes to Hypertension in a Thai Population.

International Journal Of Hypertension

Charoen, Pimphen P; Eu-Ahsunthornwattana, Jakris J; Thongmung, Nisakron N; Jose, Pedro A PA; Sritara, Piyamitr P; Vathesatogkit, Prin P; Kitiyakara, Chagriya C

Publication Date: 2019

Variant appearance in text: rs4308

PubMed Link: 31511791

Variant Present in the following documents:

• Main text
• IJHY2019-4861081.pdf

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Use of Genetic Variants Related to Antihypertensive Drugs to Inform on Efficacy and Side Effects.

Circulation

Gill, Dipender D; Georgakis, Marios K MK; Koskeridis, Fotios F; Jiang, Lan L; Feng, Qiping Q; Wei, Wei-Qi WQ; Theodoratou, Evropi E; Elliott, Paul P; Denny, Joshua C JC; Malik, Rainer R; Evangelou, Evangelos E; Dehghan, Abbas A; Dichgans, Martin M; Tzoulaki, Ioanna I

Publication Date: 2019-07-23

Variant appearance in text: rs4308

PubMed Link: 31234639

Variant Present in the following documents:

• cir-140-270-s001.pdf

View BVdb publication page

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Genome-Wide Association Studies of Hypertension and Several Other Cardiovascular Diseases.

Pulse (Basel, Switzerland)

Wang, Yan Y; Wang, Ji-Guang JG

Publication Date: 2019-04

Variant appearance in text: rs4308

PubMed Link: 31049317

Variant Present in the following documents:

• Main text

View BVdb publication page

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A multimodal approach to cardiovascular risk stratification in patients with type 2 diabetes incorporating retinal, genomic and clinical features.

Scientific Reports

Fetit, Ahmed E AE; Doney, Alexander S AS; Hogg, Stephen S; Wang, Ruixuan R; MacGillivray, Tom T; Wardlaw, Joanna M JM; Doubal, Fergus N FN; McKay, Gareth J GJ; McKenna, Stephen S; Trucco, Emanuele E

Publication Date: 2019-03-05

Variant appearance in text: rs4308

PubMed Link: 30837638

Variant Present in the following documents:

• Main text
• 41598_2019_Article_40403.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: ACE: 1119-202A>G; rs4308

PubMed Link: 30319441

Variant Present in the following documents:

• Table_5.xlsx, sheet 1

View BVdb publication page

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Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal

Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL

Publication Date: 2019-04

Variant appearance in text: rs4308

PubMed Link: 30214008

Variant Present in the following documents:

• NIHMS1503453-supplement-3.xlsx, sheet 1

View BVdb publication page

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GWAS Reveal Targets in Vessel Wall Pathways to Treat Coronary Artery Disease.

Frontiers In Cardiovascular Medicine

Turner, Adam W AW; Wong, Doris D; Dreisbach, Caitlin N CN; Miller, Clint L CL

Publication Date: 2018

Variant appearance in text: rs4308

PubMed Link: 29988570

Variant Present in the following documents:

• Main text
• fcvm-05-00072.pdf

View BVdb publication page

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Brief Overview of a Decade of Genome-Wide Association Studies on Primary Hypertension.

International Journal Of Endocrinology

Azam, Afifah Binti AB; Azizan, Elena Aisha Binti EAB

Publication Date: 2018

Variant appearance in text: rs4308

PubMed Link: 29666641

Variant Present in the following documents:

• Main text
• IJE2018-7259704.pdf

View BVdb publication page

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Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk.

Nature Genetics

Warren, Helen R HR; Evangelou, Evangelos E; Cabrera, Claudia P CP; Gao, He H; Ren, Meixia M; Mifsud, Borbala B; Ntalla, Ioanna I; Surendran, Praveen P; Liu, Chunyu C; Cook, James P JP; Kraja, Aldi T AT; Drenos, Fotios F; Loh, Marie M; Verweij, Niek N; Marten, Jonathan J; Karaman, Ibrahim I; Lepe, Marcelo P Segura MP; O'Reilly, Paul F PF; Knight, Joanne J; Snieder, Harold H; Kato, Norihiro N; He, Jiang J; Tai, E Shyong ES; Said, M Abdullah MA; Porteous, David D; Alver, Maris M; Poulter, Neil N; Farrall, Martin M; Gansevoort, Ron T RT; Padmanabhan, Sandosh S; Mägi, Reedik R; Stanton, Alice A; Connell, John J; Bakker, Stephan J L SJ; Metspalu, Andres A; Shields, Denis C DC; Thom, Simon S; Brown, Morris M; Sever, Peter P; Esko, Tõnu T; Hayward, Caroline C; van der Harst, Pim P; Saleheen, Danish D; Chowdhury, Rajiv R; Chambers, John C JC; Chasman, Daniel I DI; Chakravarti, Aravinda A; Newton-Cheh, Christopher C; Lindgren, Cecilia M CM; Levy, Daniel D; Kooner, Jaspal S JS; Keavney, Bernard B; Tomaszewski, Maciej M; Samani, Nilesh J NJ; Howson, Joanna M M JM; Tobin, Martin D MD; Munroe, Patricia B PB; Ehret, Georg B GB; Wain, Louise V LV; , ; , ; , ; , ; , ; , ; , ; , ; , ; , ; ,

Publication Date: 2017-03

Variant appearance in text: rs4308

PubMed Link: 28135244

Variant Present in the following documents:

• Main text
• NIHMS70782-supplement-Supplementary_tables.xlsx, sheet 16
• emss-70782.pdf

View BVdb publication page

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