Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 75 Records) |
Query Trace: Coronary artery disease and LDLR[original query] |
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Impact of LDLR and PCSK9 pathogenic variants in Japanese heterozygous familial hypercholesterolemia patients. Atherosclerosis 2019 Aug 289 101-108. Hori Mika, Ohta Naotaka, Takahashi Atsushi, Masuda Hiroaki, Isoda Rieko, Yamamoto Suguru, Son Cheol, Ogura Masatsune, Hosoda Kiminori, Miyamoto Yoshihiro, Harada-Shiba Mari |
Polymorphisms in PCSK9, LDLR, BCMO1, SLC12A3, and KCNJ1 are Associated with Serum Lipid Profile in Chinese Han Population. International journal of environmental research and public health 2019 Sep 16 (17): . Li Zheng, Zhao Tianyu, Tan Xiaohua, Lei Song, Huang Liu, Yang L |
Low-density lipoprotein receptor gene mutation at Exon 2 and 4 in premature coronary artery disease in our population. Pakistan journal of medical sciences 2019 8 35 (4): 1143-1148. Rehman Saqibah, Ahmad Tariq Mahmood, Hayat Asma, Tahir Sufy |
LDLR Gene Polymorphisms (rs5925 and rs1529729) Are Associated with Susceptibility to Coronary Artery Disease in a South Indian Population. Medical sciences (Basel, Switzerland) 2019 Jul 7 (7): . K Jha Chandan, Mir Rashid, Elfaki Imadeldin, Banu Shaheena, Chahal S M |
A cross-national investigation of cardiovascular survival in homozygous familial hypercholesterolemia: The Sino-Roman Study. Journal of clinical lipidology 2019 7 13 (4): 608-617. Stefanutti Claudia, Pang Jing, Di Giacomo Serafina, Wu Xue, Wang Xumin, Morozzi Claudia, Watts Gerald F, Lin J |
Genetic Testing and Risk Scores: Impact on Familial Hypercholesterolemia. Frontiers in cardiovascular medicine 2019 6 5. Sarraju Ashish, Knowles Joshua |
Heterozygosity in LDLR rs2228671 and rs72658855 Gene is Associated with Increased Risk of Developing Coronary Artery Disease in India -A Case-Control Study. Endocrine, metabolic & immune disorders drug targets 2019 Oct . Jha Chandan K, Mir Rashid, Banu Shaheena, Elfaki Imadeldin, Chahal Sukh M |
Dab2 gene variant is associated with increased coronary artery disease risk in Chinese Han population. Medicine 2020 Jul 99 (27): e20924. Wang Yinghong, Wang Yongtao, Adi Dilare, He XiaoDong, Liu Fen, Abudesimu Asiya, Fu Zhenyan, Ma Yito |
Common gene variants in ASGR1 gene locus associate with reduced cardiovascular risk in absence of pleiotropic effects. Atherosclerosis 2020 Jul 306 15-21. Ali Lubna, Cupido Arjen J, Rijkers Maaike, Hovingh G Kees, Holleboom Adriaan G, Dallinga-Thie Geesje M, Stroes Erik S G, van den Boogert Marjolein A |
NBEAL1 controls SREBP2 processing and cholesterol metabolism and is a susceptibility locus for coronary artery disease. Scientific reports 2020 3 10 (1): 4528. Bindesbøll Christian, Aas Aleksander, Ogmundsdottir Margret Helga, Pankiv Serhiy, Reine Trine, Zoncu Roberto, Simonsen An |
Genetic analysis of familial hypercholesterolemia in Asian Indians: A single-center study. Journal of clinical lipidology 2020 2 14 (1): 35-45. Setia Nitika, Movva Sireesha, Balakrishnan Prahlad, Biji Ishpreet K, Sawhney Jitendra Pal Singh, Puri Raman, Arora Anjali, Puri Ratna D, Saxena Renu, Mishra Sanghamitra, Apte Sanika, Kulshrestha Samarth, Ramprasad Vedam Lakshmi, Verma Ishwar |
Phenotypic and Genetic Analyses of Korean Patients with Familial Hypercholesterolemia: Results from the KFH Registry 2020. Journal of atherosclerosis and thrombosis 2021 8 29 (8): 1176-1187. Kim Hyoeun, Lee Chan Joo, Kim Sang-Hyun, Kim Jang Young, Choi Sung Hee, Kang Hyun-Jae, Park Kyong Soo, Cho Byung Ryul, Kim Byung Jin, Sung Ki Chul, Jeong In-Kyung, Jeong Jin-Ok, Bae Jang-Whan, Park Jung Mi, Lee Yunbeom, Jeong Ilecheon, Han Hyojun, Lee Ji Hyun, Lee Sang-H |
Cholesterol-related gene variants are associated with diabetes in coronary artery disease patients. Molecular biology reports 2021 May . Ozuynuk Aybike Sena, Erkan Aycan Fahri, Ekici Berkay, Erginel-Unaltuna Nihan, Coban Neslih |
Screening of PCSK9 and LDLR genetic variants in Familial Hypercholesterolemia (FH) patients in India. Journal of human genetics 2021 Apr . Reddy Lakshmi Lavanya, Shah Swarup A V, Ponde Chandrashekhar K, Dalal Jamshed J, Jatale Raj G, Dalal Reeta J, Rajani Rajesh M, Pillai Sudhir K, Vanjani Chander V, Ashavaid Tester |
Mutational Spectrum of LDLR and PCSK9 Genes Identified in Iranian Patients With Premature Coronary Artery Disease and Familial Hypercholesterolemia. Frontiers in genetics 2021 3 12 625959. Moradi Arman, Maleki Majid, Ghaemmaghami Zahra, Khajali Zahra, Noohi Feridoun, Moghadam Maryam Hosseini, Kalyinia Samira, Mowla Seyed Javad, Seidah Nabil G, Malakootian Mahsh |
Relations of physical signs to genotype, lipid and inflammatory markers, coronary stenosis or calcification, and outcomes in patients with heterozygous familial hypercholesterolemia. Journal of translational medicine 2021 12 19 (1): 498. Liu Ming-Ming, Peng Jia, Guo Yuan-Lin, Zhu Cheng-Gang, Wu Na-Qiong, Xu Rui-Xia, Dong Qian, Li Jian-J |
Pharmacogenetic loci for rosuvastatin are associated with intima-media thickness change and coronary artery disease risk. Pharmacogenomics 2021 12 23 (1): 15-34. Kononov Stanislav, Mal Galina, Azarova Iuliia, Klyosova Elena, Bykanova Marina, Churnosov Mikhail, Polonikov Alex |
Exome sequencing identifies rare mutations of LDLR and QTRT1 conferring risk for early-onset coronary artery disease in Chinese. National science review 2022 9 9 (8): nwac102. Yao Kang, Dai Yuxiang, Shen Juan, Wang Yi, Yang Huanjie, Wu Runda, Liao Qijun, Wu Hongyi, Fang Xiaodong, Shali Shalaimaiti, Xu Lili, Hao Meng, Lin Chenhao, Sun Zhonghan, Liu Yilian, Li Mengxin, Wang Zhen, Gao Qiang, Zhang Shuning, Li Chenguang, Gao Wei, Ge Lei, Zou Yunzeng, Sun Aijun, Qian Juying, Jin Li, Hong Shangyu, Zheng Yan, Ge Jun |
The impact of gene variants on the thickness and softness of the Achilles tendon in familial hypercholesterolemia. Atherosclerosis 2022 Oct 358 41-46. Michikura Masahito, Hori Mika, Ogura Masatsune, Hosoda Kiminori, Harada-Shiba Mari |
Coronary Artery Disease Risk of Familial Hypercholesterolemia Genetic Variants Independent of Clinically Observed Longitudinal Cholesterol Exposure. Circulation. Genomic and precision medicine 2022 Feb CIRCGEN121003501. Clarke Shoa L, Tcheandjieu Catherine, Hilliard Austin T, Lee Kyung Min, Lynch Julie, Chang Kyong-Mi, Miller Donald, Knowles Joshua W, O'Donnell Christopher, Tsao Philip S, Rader Daniel J, Wilson Peter W, Sun Yan V, Gaziano J Michael, Assimes Themistocles L, |
Whole genome sequence analysis of blood lipid levels in >66,000 individuals.
![]() Nature communications 2022 10 13 (1): 5995. Selvaraj Margaret Sunitha, Li Xihao, Li Zilin, Pampana Akhil, Zhang David Y, Park Joseph, Aslibekyan Stella, Bis Joshua C, Brody Jennifer A, Cade Brian E, Chuang Lee-Ming, Chung Ren-Hua, Curran Joanne E, de Las Fuentes Lisa, de Vries Paul S, Duggirala Ravindranath, Freedman Barry I, Graff Mariaelisa, Guo Xiuqing, Heard-Costa Nancy, Hidalgo Bertha, Hwu Chii-Min, Irvin Marguerite R, Kelly Tanika N, Kral Brian G, Lange Leslie, Li Xiaohui, Lisa Martin, Lubitz Steven A, Manichaikul Ani W, Michael Preuss, Montasser May E, Morrison Alanna C, Naseri Take, O'Connell Jeffrey R, Palmer Nicholette D, Peyser Patricia A, Reupena Muagututia S, Smith Jennifer A, Sun Xiao, Taylor Kent D, Tracy Russell P, Tsai Michael Y, Wang Zhe, Wang Yuxuan, Bao Wei, Wilkins John T, Yanek Lisa R, Zhao Wei, Arnett Donna K, Blangero John, Boerwinkle Eric, Bowden Donald W, Chen Yii-Der Ida, Correa Adolfo, Cupples L Adrienne, Dutcher Susan K, Ellinor Patrick T, Fornage Myriam, Gabriel Stacey, Germer Soren, Gibbs Richard, He Jiang, Kaplan Robert C, Kardia Sharon L R, Kim Ryan, Kooperberg Charles, Loos Ruth J F, Viaud-Martinez Karine A, Mathias Rasika A, McGarvey Stephen T, Mitchell Braxton D, Nickerson Deborah, North Kari E, Psaty Bruce M, Redline Susan, Reiner Alexander P, Vasan Ramachandran S, Rich Stephen S, Willer Cristen, Rotter Jerome I, Rader Daniel J, Lin Xihong, , Peloso Gina M, Natarajan Prade |
Gene Sequencing Identifies Perturbation in Nitric Oxide Signaling as a Nonlipid Molecular Subtype of Coronary Artery Disease. Circulation. Genomic and precision medicine 2022 Oct 101161CIRCGEN121003598. Khera Amit V, Wang Minxian, Chaffin Mark, Emdin Connor A, Samani Nilesh J, Schunkert Heribert, Watkins Hugh, McPherson Ruth, Erdmann Jeanette, Elosua Roberto, Boerwinkle Eric, Ardissino Diego, Butterworth Adam S, Di Angelantonio Emanuele, Naheed Aliya, Danesh John, Chowdhury Rajiv, Krumholz Harlan M, Sheu Wayne H-H, Rich Stephen S, Rotter Jerome I, Chen Yii-der Ida, Gabriel Stacey, Lander Eric S, Saleheen Danish, Kathiresan Sek |
Genetic Testing Enables the Diagnosis of Familial Hypercholesterolemia Underdiagnosed by Clinical Criteria: Analysis of Japanese Early-Onset Coronary Artery Disease Patients. Cardiology research and practice 2023 5 2023 2236422. Hiroshi Miyama, Yoshinori Katsumata, Mizuki Momoi, Genki Ichihara, Taishi Fujisawa, Jin Endo, Takashi Kawakami, Masaharu Kataoka, Shinsuke Yuasa, Motoaki Sano, Kazuki Sato, Keiichi Fuku |
Dynamics of the personalities of PCSK9 on missense variants (rs505151 and rs562556) from elderly cohort studies in Brazil. Journal of biomolecular structure & dynamics 2023 4 1-9. Galvão Lopes Vitor, Fernandes de Oliveira Victor, Mendonça Munhoz Dati Livia, Naslavsky Michel Satya, Ferreira Glaucio Monteiro, Hirata Mario Hiroyu |
Calling and Phasing of Single-Nucleotide and Structural Variants of the LDLR Gene Using Oxford Nanopore MinION. International journal of molecular sciences 2023 3 24 (5): . Nazarenko Maria S, Sleptcov Aleksei A, Zarubin Aleksei A, Salakhov Ramil R, Shevchenko Alexander I, Tmoyan Narek A, Elisaphenko Eugeny A, Zubkova Ekaterina S, Zheltysheva Nina V, Ezhov Marat V, Kukharchuk Valery V, Parfyonova Yelena V, Zakian Suren M, Zakharova Irina |
Novel Finnish-enriched variants causing severe hypercholesterolemia and their clinical impact on coronary artery disease. Atherosclerosis 2023 10 117327. Nella Junna, Sanni Ruotsalainen, Pietari Ripatti, FinnGen, Samuli Ripatti, Elisabeth Wid |
Polygenic risk of high LDL cholesterol and ischemic heart disease in the general population. Atherosclerosis 2024 9 397 118574. Tim Møller Eyrich, Nawar Dalila, Mette Christoffersen, Anne Tybjærg-Hansen, Stefan Stend |
Prevalence of genetically diagnosed familial hypercholesterolemia in Vietnamese patients with premature acute myocardial infarction. Medicine 2024 9 103 (39): e39939. Kha Minh Nguyen, Sy Van Hoa |
Genetic testing for familial hypercholesterolemia in a Finnish cohort of patients with premature coronary artery disease and elevated LDL-C levels. Frontiers in cardiovascular medicine 2024 8 11 1433042. Antti Jokiniitty, Markku Eskola, Saara Metso, Martin Bogsrud, Heini Huhtala, Tanja Saare |
Identifying genetic susceptibility loci associated with human coronary artery disease. PloS one 2025 1 20 (1): e0315460. Aqsa Zahid, Andleeb Batool, Abdul Wajid, Yurong Wu, Chun Liang, Muhammad Ajmal Khan, Amin Ullah, Kashif Iqbal Sahibzada, Hong X |
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