ACE c.1488-58T>C

Variant ID: 17-61560763-T-C

NM_000789.3(ACE):c.1488-58T>C

This variant was identified in 45 publications

View GRCh38 version.




Publications:


Association of candidate genetic variants and circulating levels of ApoE/ApoJ with common neuroimaging features of cerebral amyloid angiopathy.

Frontiers In Aging Neuroscience
Bonaterra-Pastra, Anna A; Benítez, Sònia S; Pancorbo, Olalla O; Rodríguez-Luna, David D; Vert, Carla C; Rovira, Alex A; Freijo, M Mar MM; Tur, Silvia S; Martínez-Zabaleta, Maite M; Cardona Portela, Pere P; Vera, Rocío R; Lebrato-Hernández, Lucia L; Arenillas, Juan F JF; Pérez-Sánchez, Soledad S; Domínguez-Mayoral, Ana A; Fàbregas, Joan Martí JM; Mauri, Gerard G; Montaner, Joan J; Sánchez-Quesada, Jose Luis JL; Hernández-Guillamon, Mar M
Publication Date: 2023

Variant appearance in text: rs4311
PubMed Link: 37113571
Variant Present in the following documents:
  • Main text
  • fnagi-15-1134399.pdf
View BVdb publication page



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: rs4311
PubMed Link: 36876951
Variant Present in the following documents:
  • Main text
  • 10.1177_10815589231158379.pdf
View BVdb publication page



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: rs4311
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



Deep learning approaches for noncoding variant prioritization in neurodegenerative diseases.

Frontiers In Aging Neuroscience
Lan, Alexander Y AY; Corces, M Ryan MR
Publication Date: 2022

Variant appearance in text: rs4311
PubMed Link: 36466610
Variant Present in the following documents:
  • Main text
  • fnagi-14-1027224.pdf
View BVdb publication page



JAK-STAT signaling in inflammatory breast cancer enables chemotherapy-resistant cell states.

Cancer Research
Stevens, Laura E LE; Peluffo, Guillermo G; Qiu, Xintao X; Temko, Daniel D; Fassl, Anne A; Li, Zheqi Z; Trinh, Anne A; Seehawer, Marco M; Jovanovic, Bojana B; Aleckovic, Masa M; Wilde, Callahan M CM; Geck, Renee C RC; Shu, Shaokun S; Kingston, Natalie L NL; Harper, Nicholas W NW; Almendro, Vanessa V; Pyke, Alanna L AL; Egri, Shawn B SB; Papanastasiou, Malvina M; Clement, Kendell K; Zhou, Ningxuan N; Walker, Sarah S; Salas, Jacqueline J; Park, So Yeon SY; Frank, David A DA; Meissner, Alexander A; Jaffe, Jacob D JD; Sicinski, Piotr P; Toker, Alex A; Michor, Franziska F; Long, Henry W HW; Overmoyer, Beth A BA; Polyak, Kornelia K
Publication Date: 2022-11-21

Variant appearance in text: ACE: 1488-58T>C; rs4311
PubMed Link: 36409824
Variant Present in the following documents:
  • can-22-0423_supplementary_table_s3_suppst3.xlsx, sheet 1
View BVdb publication page



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: rs4311
PubMed Link: 36241656
Variant Present in the following documents:
  • 41598_2022_20939_MOESM15_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM14_ESM.xlsx, sheet 2
View BVdb publication page



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: rs4311
PubMed Link: 36075891
Variant Present in the following documents:
  • 41439_2022_208_MOESM5_ESM.xlsx, sheet 2
View BVdb publication page



Outcomes of Genetic Testing-Based Cardiac Rehabilitation Program in Patients with Acute Myocardial Infarction after Percutaneous Coronary Intervention.

Cardiology Research And Practice
Yu, Xing X; Fan, Yuxuan Y; Sun, Xiaopeng X; Wang, Xiaojing X; Guo, Qi Q; Fan, Zhiqing Z
Publication Date: 2022

Variant appearance in text: rs4311
PubMed Link: 36032316
Variant Present in the following documents:
  • 9742071.f1.xlsx, sheet 1
  • CRP2022-9742071.pdf
View BVdb publication page



Antihypertensive drugs and brain function: mechanisms underlying therapeutically beneficial and harmful neuropsychiatric effects.

Cardiovascular Research
Carnovale, Carla C; Perrotta, Cristiana C; Baldelli, Sara S; Cattaneo, Dario D; Montrasio, Cristina C; Barbieri, Silvia S SS; Pompilio, Giulio G; Vantaggiato, Chiara C; Clementi, Emilio E; Pozzi, Marco M
Publication Date: 2022-07-27

Variant appearance in text: rs4311
PubMed Link: 35895876
Variant Present in the following documents:
  • Main text
  • cvac110.pdf
View BVdb publication page



Association of the angiotensin I converting enzyme (ACE) gene polymorphisms with recurrent aphthous stomatitis in the Czech population: case-control study.

Bmc Oral Health
Bartakova, Julie J; Deissova, Tereza T; Slezakova, Simona S; Bartova, Jirina J; Petanova, Jitka J; Kuklinek, Pavel P; Fassmann, Antonin A; Borilova Linhartova, Petra P; Dušek, Ladislav L; Izakovicova Holla, Lydie L
Publication Date: 2022-03-19

Variant appearance in text: rs4311
PubMed Link: 35305614
Variant Present in the following documents:
  • Main text
  • 12903_2022_Article_2115.pdf
View BVdb publication page



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: 1488-58T>C; rs4311
PubMed Link: 34054912
Variant Present in the following documents:
  • Table_2.xlsx, sheet 1
View BVdb publication page



Using Mendelian randomization study to assess the renal effects of antihypertensive drugs.

Bmc Medicine
Zhao, Jie V JV; Schooling, C Mary CM
Publication Date: 2021-03-26

Variant appearance in text: rs4311
PubMed Link: 33766008
Variant Present in the following documents:
  • Main text
  • 12916_2021_Article_1951.pdf
View BVdb publication page



Genome-wide meta-analysis, fine-mapping and integrative prioritization implicate new Alzheimer's disease risk genes.

Nature Genetics
Schwartzentruber, Jeremy J; Cooper, Sarah S; Liu, Jimmy Z JZ; Barrio-Hernandez, Inigo I; Bello, Erica E; Kumasaka, Natsuhiko N; Young, Adam M H AMH; Franklin, Robin J M RJM; Johnson, Toby T; Estrada, Karol K; Gaffney, Daniel J DJ; Beltrao, Pedro P; Bassett, Andrew A
Publication Date: 2021-03

Variant appearance in text: rs4311
PubMed Link: 33589840
Variant Present in the following documents:
  • Main text
  • EMS118040-supplement-Supplementary_Tables_1_14.xlsx, sheet 2
View BVdb publication page



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: rs4311
PubMed Link: 33541420
Variant Present in the following documents:
  • 13195_2021_773_MOESM1_ESM.pdf
View BVdb publication page



A Non-APOE Polygenic Risk Score for Alzheimer's Disease Is Associated With Cerebrospinal Fluid Neurofilament Light in a Representative Sample of Cognitively Unimpaired 70-Year Olds.

The Journals Of Gerontology. Series A, Biological Sciences And Medical Sciences
Skoog, Ingmar I; Kern, Silke S; Najar, Jenna J; Guerreiro, Rita R; Bras, Jose J; Waern, Margda M; Zetterberg, Henrik H; Blennow, Kaj K; Zettergren, Anna A
Publication Date: 2021-05-22

Variant appearance in text: rs4311
PubMed Link: 33512503
Variant Present in the following documents:
  • glab030_suppl_supplementary_table_1.pdf
View BVdb publication page



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: rs4311
PubMed Link: 33283188
Variant Present in the following documents:
  • Main text
  • 10.1177_2633105520975743.pdf
View BVdb publication page



The genetic map of diabetic nephropathy: evidence from a systematic review and meta-analysis of genetic association studies.

Clinical Kidney Journal
Tziastoudi, Maria M; Stefanidis, Ioannis I; Zintzaras, Elias E
Publication Date: 2020-10

Variant appearance in text: rs4311
PubMed Link: 33123356
Variant Present in the following documents:
  • Main text
  • sfaa077.pdf
View BVdb publication page



A Generic Sure Independence Screening Procedure.

Journal Of The American Statistical Association
Pan, Wenliang W; Wang, Xueqin X; Xiao, Weinan W; Zhu, Hongtu H
Publication Date: 2019

Variant appearance in text: rs4311
PubMed Link: 31692981
Variant Present in the following documents:
  • Main text
View BVdb publication page



Common pathways and communication between the brain and heart: connecting post-traumatic stress disorder and heart failure.

Stress (Amsterdam, Netherlands)
Wilson, Marlene A MA; Liberzon, Israel I; Lindsey, Merry L ML; Lokshina, Yana Y; Risbrough, Victoria B VB; Sah, Renu R; Wood, Susan K SK; Williamson, John B JB; Spinale, Francis G FG
Publication Date: 2019-09

Variant appearance in text: rs4311
PubMed Link: 31161843
Variant Present in the following documents:
  • Main text
View BVdb publication page



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: 1488-58T>C; rs4311
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_7.xlsx, sheet 1
  • Table_6.xlsx, sheet 1
  • Table_5.xlsx, sheet 1
View BVdb publication page



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: rs4311
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Mendelian randomization: a novel approach for the prediction of adverse drug events and drug repurposing opportunities.

International Journal Of Epidemiology
Walker, Venexia M VM; Davey Smith, George G; Davies, Neil M NM; Martin, Richard M RM
Publication Date: 2017-12-01

Variant appearance in text: rs4311
PubMed Link: 29040597
Variant Present in the following documents:
  • Main text
  • dyx207.pdf
View BVdb publication page



Whole-exome sequencing analysis of Waardenburg syndrome in a Chinese family.

Human Genome Variation
Chen, Dezhong D; Zhao, Na N; Wang, Jing J; Li, Zhuoyu Z; Wu, Changxin C; Fu, Jie J; Xiao, Han H
Publication Date: 2017

Variant appearance in text: rs4311
PubMed Link: 28690861
Variant Present in the following documents:
  • hgv201727-s1.xls, sheet 1
View BVdb publication page



A Bayesian group sparse multi-task regression model for imaging genetics.

Bioinformatics (Oxford, England)
Greenlaw, Keelin K; Szefer, Elena E; Graham, Jinko J; Lesperance, Mary M; Nathoo, Farouk S FS; ,
Publication Date: 2017-08-15

Variant appearance in text: rs4311
PubMed Link: 28419235
Variant Present in the following documents:
  • Main text
View BVdb publication page



Influence of angiotensin converting enzyme (ACE) gene rs4362 polymorphism on the progression of kidney failure in patients with autosomal dominant polycystic kidney disease (ADPKD).

The Indian Journal Of Medical Research
Ramanathan, Gnanasambandan G; Ghosh, Santu S; Elumalai, Ramprasad R; Periyasamy, Soundararajan S; Lakkakula, Bhaskar V K S BV
Publication Date: 2016-06

Variant appearance in text: rs4311
PubMed Link: 27748299
Variant Present in the following documents:
  • Main text
  • IJMR-143-748.pdf
View BVdb publication page



EDN1 Gene Variant is Associated with Neonatal Persistent Pulmonary Hypertension.

Scientific Reports
Mei, Mei M; Cheng, Guoqiang G; Sun, Bijun B; Yang, Lin L; Wang, Huijun H; Sun, Jinqiao J; Zhou, Wenhao W
Publication Date: 2016-07-18

Variant appearance in text: rs4311
PubMed Link: 27425626
Variant Present in the following documents:
  • Main text
View BVdb publication page



Shared genetic variants between serum levels of high-density lipoprotein cholesterol and wheezing in a cohort of children from Cyprus.

Italian Journal Of Pediatrics
Yiallouros, Panayiotis K PK; Kouis, Panayiotis P; Kolokotroni, Ourania O; Youhanna, Sonia S; Savva, Savvas C SC; Dima, Kleanthi K; Zerva, Aikaterini A; Platt, Danielle D; Middleton, Nicos N; Zalloua, Pierre P
Publication Date: 2016-07-13

Variant appearance in text: rs4311
PubMed Link: 27411394
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association of Genetic Polymorphisms of Renin-Angiotensin-Aldosterone System-Related Genes with Arterio-Venous Fistula Malfunction in Hemodialysis Patients.

International Journal Of Molecular Sciences
Chen, Yu-Wei YW; Wu, Yu-Te YT; Lin, Jhin-Shyaun JS; Yang, Wu-Chang WC; Hsu, Yung-Ho YH; Lee, Kuo-Hua KH; Ou, Shou-Ming SM; Chen, Yung-Tai YT; Shih, Chia-Jen CJ; Lee, Pui-Ching PC; Chan, Chia-Hao CH; Chung, Ming-Yi MY; Lin, Chih-Ching CC
Publication Date: 2016-05-27

Variant appearance in text: rs4311
PubMed Link: 27240348
Variant Present in the following documents:
  • Main text
  • ijms-17-00833.pdf
View BVdb publication page



Generation of a High Number of Healthy Erythroid Cells from Gene-Edited Pyruvate Kinase Deficiency Patient-Specific Induced Pluripotent Stem Cells.

Stem Cell Reports
Garate, Zita Z; Quintana-Bustamante, Oscar O; Crane, Ana M AM; Olivier, Emmanuel E; Poirot, Laurent L; Galetto, Roman R; Kosinski, Penelope P; Hill, Collin C; Kung, Charles C; Agirre, Xabi X; Orman, Israel I; Cerrato, Laura L; Alberquilla, Omaira O; Rodriguez-Fornes, Fatima F; Fusaki, Noemi N; Garcia-Sanchez, Felix F; Maia, Tabita M TM; Ribeiro, Maria L ML; Sevilla, Julian J; Prosper, Felipe F; Jin, Shengfang S; Mountford, Joanne J; Guenechea, Guillermo G; Gouble, Agnes A; Bueren, Juan A JA; Davis, Brian R BR; Segovia, Jose C JC
Publication Date: 2015-12-08

Variant appearance in text: rs4311
PubMed Link: 26549847
Variant Present in the following documents:
  • mmc3.xlsx, sheet 3
  • mmc3.xlsx, sheet 1
  • mmc3.xlsx, sheet 2
View BVdb publication page



Autonomic and inflammatory consequences of posttraumatic stress disorder and the link to cardiovascular disease.

American Journal Of Physiology. Regulatory, Integrative And Comparative Physiology
Brudey, Chevelle C; Park, Jeanie J; Wiaderkiewicz, Jan J; Kobayashi, Ihori I; Mellman, Thomas A TA; Marvar, Paul J PJ
Publication Date: 2015-08-15

Variant appearance in text: rs4311
PubMed Link: 26062635
Variant Present in the following documents:
  • Main text
View BVdb publication page



Pleiotropic effect of common variants at ABO Glycosyltranferase locus in 9q32 on plasma levels of pancreatic lipase and angiotensin converting enzyme.

Plos One
,
Publication Date: 2014

Variant appearance in text: rs4311
PubMed Link: 24586218
Variant Present in the following documents:
  • Main text
View BVdb publication page



Angiotensin-converting enzyme gene variants are associated with both cortisol secretion and late-life depression.

Translational Psychiatry
Ancelin, M L ML; Carrière, I I; Scali, J J; Ritchie, K K; Chaudieu, I I; Ryan, J J
Publication Date: 2013-11-05

Variant appearance in text: rs4311
PubMed Link: 24193727
Variant Present in the following documents:
  • Main text
  • tp201395a.pdf
View BVdb publication page



Influence of genetic variation on plasma protein levels in older adults using a multi-analyte panel.

Plos One
Kim, Sungeun S; Swaminathan, Shanker S; Inlow, Mark M; Risacher, Shannon L SL; Nho, Kwangsik K; Shen, Li L; Foroud, Tatiana M TM; Petersen, Ronald C RC; Aisen, Paul S PS; Soares, Holly H; Toledo, Jon B JB; Shaw, Leslie M LM; Trojanowski, John Q JQ; Weiner, Michael W MW; McDonald, Brenna C BC; Farlow, Martin R MR; Ghetti, Bernardino B; Saykin, Andrew J AJ; ,
Publication Date: 2013

Variant appearance in text: rs4311
PubMed Link: 23894628
Variant Present in the following documents:
  • Main text
View BVdb publication page



Fine-mapping angiotensin-converting enzyme gene: separate QTLs identified for hypertension and for ACE activity.

Plos One
Chung, Chia-Min CM; Wang, Ruey-Yun RY; Fann, Cathy S J CS; Chen, Jaw-Wen JW; Jong, Yuh-Shiun YS; Jou, Yuh-Shan YS; Yang, Hsin-Chou HC; Kang, Chih-Sen CS; Chen, Chien-Chung CC; Chang, Huan-Cheng HC; Pan, Wen-Harn WH
Publication Date: 2013

Variant appearance in text: rs4311
PubMed Link: 23469169
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic predictors of response to serotonergic and noradrenergic antidepressants in major depressive disorder: a genome-wide analysis of individual-level data and a meta-analysis.

Plos Medicine
Tansey, Katherine E KE; Guipponi, Michel M; Perroud, Nader N; Bondolfi, Guido G; Domenici, Enrico E; Evans, David D; Hall, Stephanie K SK; Hauser, Joanna J; Henigsberg, Neven N; Hu, Xiaolan X; Jerman, Borut B; Maier, Wolfgang W; Mors, Ole O; O'Donovan, Michael M; Peters, Tim J TJ; Placentino, Anna A; Rietschel, Marcella M; Souery, Daniel D; Aitchison, Katherine J KJ; Craig, Ian I; Farmer, Anne A; Wendland, Jens R JR; Malafosse, Alain A; Holmans, Peter P; Lewis, Glyn G; Lewis, Cathryn M CM; Stensbøl, Tine Bryan TB; Kapur, Shitij S; McGuffin, Peter P; Uher, Rudolf R
Publication Date: 2012

Variant appearance in text: rs4311
PubMed Link: 23091423
Variant Present in the following documents:
  • pmed.1001326.s001.pdf
View BVdb publication page



Genetic polymorphisms located in genes related to immune and inflammatory processes are associated with end-stage renal disease: a preliminary study.

Bmc Medical Genetics
Jimenez-Sousa, Ma Angeles MA; López, Elisabeth E; Fernandez-Rodríguez, Amanda A; Tamayo, Eduardo E; Fernández-Navarro, Pablo P; Segura-Roda, Laura L; Heredia, María M; Gómez-Herreras, José I JI; Bustamante, Jesús J; García-Gómez, Juan Miguel JM; Bermejo-Martin, Jesús F JF; Resino, Salvador S
Publication Date: 2012-07-20

Variant appearance in text: rs4311
PubMed Link: 22817530
Variant Present in the following documents:
  • Main text
  • 1471-2350-13-58.pdf
View BVdb publication page



The link between angiotensin II-mediated anxiety and mood disorders with NADPH oxidase-induced oxidative stress.

International Journal Of Physiology, Pathophysiology And Pharmacology
Liu, Feng F; Havens, Jennifer J; Yu, Qi Q; Wang, Gang G; Davisson, Robin L RL; Pickel, Virginia M VM; Iadecola, Costantino C
Publication Date: 2012

Variant appearance in text: rs4311
PubMed Link: 22461954
Variant Present in the following documents:
  • Main text
View BVdb publication page



ACE variants and association with brain Aβ levels in Alzheimer's disease.

American Journal Of Translational Research
Miners, J Scott JS; van Helmond, Zoë Z; Raiker, Merryn M; Love, Seth S; Kehoe, Patrick G PG
Publication Date: 2010-10-15

Variant appearance in text: rs4311
PubMed Link: 21139807
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic risk factors for hepatopulmonary syndrome in patients with advanced liver disease.

Gastroenterology
Roberts, Kari E KE; Kawut, Steven M SM; Krowka, Michael J MJ; Brown, Robert S RS; Trotter, James F JF; Shah, Vijay V; Peter, Inga I; Tighiouart, Hocine H; Mitra, Nandita N; Handorf, Elizabeth E; Knowles, James A JA; Zacks, Steven S; Fallon, Michael B MB; ,
Publication Date: 2010-07

Variant appearance in text: rs4311
PubMed Link: 20346360
Variant Present in the following documents:
  • Main text
View BVdb publication page



Polymorphisms in the ACE and ADRB2 genes and risks of aging-associated phenotypes: the case of myocardial infarction.

Rejuvenation Research
Kulminski, Alexander M AM; Culminskaya, Irina V IV; Ukraintseva, Svetlana V SV; Arbeev, Konstantin G KG; Akushevich, Igor I; Land, Kenneth C KC; Yashin, Anatoli I AI
Publication Date: 2010-02

Variant appearance in text: rs4311
PubMed Link: 20230274
Variant Present in the following documents:
  • Main text
View BVdb publication page



Renin angiotensin system gene polymorphisms and cerebral blood flow regulation: the MOBILIZE Boston study.

Stroke
Hajjar, Ihab I; Sorond, Farzaneh F; Hsu, Yi-Hsiang YH; Galica, Andrew A; Cupples, L Adrienne LA; Lipsitz, Lewis A LA
Publication Date: 2010-04

Variant appearance in text: rs4311
PubMed Link: 20185782
Variant Present in the following documents:
  • Main text
View BVdb publication page



Visual exploration of genetic association with voxel-based imaging phenotypes in an MCI/AD study.

Annual International Conference Of The Ieee Engineering In Medicine And Biology Society. Ieee Engineering In Medicine And Biology Society. Annual International Conference
Kim, Sungeun S; Shen, Li L; Saykin, Andrew J AJ; West, John D JD
Publication Date: 2009

Variant appearance in text: rs4311
PubMed Link: 19963597
Variant Present in the following documents:
  • Main text
View BVdb publication page



An association analysis of Alzheimer disease candidate genes detects an ancestral risk haplotype clade in ACE and putative multilocus association between ACE, A2M, and LRRTM3.

American Journal Of Medical Genetics. Part B, Neuropsychiatric Genetics : The Official Publication Of The International Society Of Psychiatric Genetics
Edwards, Todd L TL; Pericak-Vance, Margaret M; Gilbert, Johnny R JR; Haines, Jonathan L JL; Martin, Eden R ER; Ritchie, Marylyn D MD
Publication Date: 2009-07-05

Variant appearance in text: rs4311
PubMed Link: 19105203
Variant Present in the following documents:
  • Main text
View BVdb publication page



Confronting complexity in late-onset Alzheimer disease: application of two-stage analysis approach addressing heterogeneity and epistasis.

Genetic Epidemiology
Thornton-Wells, Tricia A TA; Moore, Jason H JH; Martin, Eden R ER; Pericak-Vance, Margaret A MA; Haines, Jonathan L JL
Publication Date: 2008-04

Variant appearance in text: rs4311
PubMed Link: 18076107
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association of polymorphisms in the Angiotensin-converting enzyme gene with Alzheimer disease in an Israeli Arab community.

American Journal Of Human Genetics
Meng, Yan Y; Baldwin, Clinton T CT; Bowirrat, Abdalla A; Waraska, Kristin K; Inzelberg, Rivka R; Friedland, Robert P RP; Farrer, Lindsay A LA
Publication Date: 2006-05

Variant appearance in text: rs4311
PubMed Link: 16642441
Variant Present in the following documents:
  • Main text
View BVdb publication page