Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 91 Records) |
Query Trace: ABCG5[original query] |
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Heterozygous ABCG5 Gene Deficiency and Risk of Coronary Artery Disease. Circulation. Genomic and precision medicine 2020 9 13 (5): 417-423. Nomura Akihiro, Emdin Connor A, Won Hong Hee, Peloso Gina M, Natarajan Pradeep, Ardissino Diego, Danesh John, Schunkert Heribert, Correa Adolfo, Bown Matthew J, Samani Nilesh J, Erdmann Jeanette, McPherson Ruth, Watkins Hugh, Saleheen Danish, Elosua Roberto, Kawashiri Masa-Aki, Tada Hayato, Gupta Namrata, Shah Svati H, Rader Daniel J, Gabriel Stacey, Khera Amit V, Kathiresan Sek |
Targeted Genetic Analysis in a Chinese Cohort of 208 Patients Related to Familial Hypercholesterolemia. Journal of atherosclerosis and thrombosis 2020 Aug . Wang Hao, Yang Hang, Liu Zhaohui, Cui Kai, Zhang Yinhui, Zhang Yujing, Zhao Kun, Yin Kunlun, Li Wenke, Zhou Zh |
Next-generation sequencing to confirm clinical familial hypercholesterolemia. European journal of preventive cardiology 2020 Jul 2047487320942996. Reeskamp Laurens F, Tromp Tycho R, Defesche Joep C, Grefhorst Aldo, Stroes Erik Sg, Hovingh G Kees, Zuurbier Lin |
Recent Advances in the Critical Role of the Sterol Efflux Transporters ABCG5/G8 in Health and Disease. Advances in experimental medicine and biology 2020 7 1276 105-136. Wang Helen H, Liu Min, Portincasa Piero, Wang David Q |
Genetic variability in the absorption of dietary sterols affects the risk of coronary artery disease. European heart journal 2020 Jul 41 (28): 2618-2628. Helgadottir Anna, Thorleifsson Gudmar, Alexandersson Kristjan F, Tragante Vinicius, Thorsteinsdottir Margret, Eiriksson Finnur F, Gretarsdottir Solveig, Björnsson Eythór, Magnusson Olafur, Sveinbjornsson Gardar, Jonsdottir Ingileif, Steinthorsdottir Valgerdur, Ferkingstad Egil, Jensson Brynjar Ö, Stefansson Hreinn, Olafsson Isleifur, Christensen Alex H, Torp-Pedersen Christian, Køber Lars, Pedersen Ole B, Erikstrup Christian, Sørensen Erik, Brunak Søren, Banasik Karina, Hansen Thomas F, Nyegaard Mette, Eyjolfssson Gudmundur I, Sigurdardottir Olof, Thorarinsson Bjorn L, Matthiasson Stefan E, Steingrimsdottir Thora, Bjornsson Einar S, Danielsen Ragnar, Asselbergs Folkert W, Arnar David O, Ullum Henrik, Bundgaard Henning, Sulem Patrick, Thorsteinsdottir Unnur, Thorgeirsson Gudmundur, Holm Hilma, Gudbjartsson Daniel F, Stefansson Ka |
Evaluation of ABC gene polymorphisms on the pharmacokinetics and pharmacodynamics of capecitabine in colorectal patients: Implications for dosing recommendations. British journal of clinical pharmacology 2020 6 87 (3): 905-915. Sáez-Belló Marina, Mangas-Sanjuán Víctor, Martínez-Gómez Mª Amparo, López-Montenegro Soria Mª Ángeles, Climente-Martí Mónica, Merino-Sanjuán Matil |
Serum sitosterol level predicting ABCG5 or ABCG8 genetic mutations. Clinica chimica acta; international journal of clinical chemistry 2020 4 507 11-16. Kojima Nobuko, Tada Hayato, Usui Soichiro, Sakata Kenji, Hayashi Kenshi, Nohara Atsushi, Inazu Akihiro, Takamura Masayuki, Kawashiri Masa-A |
Features of Sitosterolemia in Children. The American journal of cardiology 2020 3 125 (9): 1312-1316. Xu Liyuan, Wen Wenhui, Yang Ya, Xie Jinjie, Li Rongjuan, Wu Yue, Hu Yifei, Wang Luya, Chong M |
ABCG5 and ABCG8 genetic variants in familial hypercholesterolemia. Journal of clinical lipidology 2020 Jan . Reeskamp Laurens F, Volta Andrea, Zuurbier Linda, Defesche Joep C, Hovingh G Kees, Grefhorst Al |
Cascade screening and genetic diagnosis of familial hypercholesterolemia in clusters of the Southeastern region from Brazil. Molecular biology reports 2020 11 47 (12): 9279-9288. de Paiva Silvino Júnea Paolucci, Jannes Cinthia Elim, Tada Mauricio Teruo, Lima Isabella Ramos, Silva Iêda de Fátima Oliveira, Pereira Alexandre Costa, Gomes Karina Bra |
Effects of SNVs in ABCA1, ABCG1, ABCG5, ABCG8, and SCARB1 Genes on Plasma Lipids, Lipoproteins, and Adiposity Markers in a Brazilian Population. Biochemical genetics 2021 Sep . Zago Vanessa Helena Souza, Scherrer Daniel Zanetti, Parra Eliane Soler, Vieira Isabela Calanca, Marson Fernando Augusto Lima, de Faria Eliana Cot |
Genetic basis and hematologic manifestations of sitosterolemia in a group of Turkish patients. Journal of clinical lipidology 2021 Jul . Kaya Zühre, Sal Ertan, Yorulmaz Asl?, Hsieh Yu-Ping, Gülen Hüseyin, Y?ld?r?m Ay?en Türedi, Niu Dau-Ming, Tekin Az |
Next-generation sequencing to confirm clinical familial hypercholesterolemia. European journal of preventive cardiology 2021 7 28 (8): 875-883. Reeskamp Laurens F, Tromp Tycho R, Defesche Joep C, Grefhorst Aldo, Stroes Erik S G, Hovingh G Kees, Zuurbier Lin |
An association of ABCG8: rs11887534 polymorphism and HDL-cholesterol response to statin treatment in the Polish population. Pharmacological reports : PR 2021 Jun . Sa?acka A, Boro? A, Gor?cy I, Hornowska I, Safranow K, Ciechanowicz |
Genetic Analysis of Japanese Children Clinically Diagnosed with Familial Hypercholesterolemia. Journal of atherosclerosis and thrombosis 2021 5 29 (5): 667-677. Nagahara Keiko, Nishibukuro Tsuyoshi, Ogiwara Yasuko, Ikegawa Kento, Tada Hayato, Yamagishi Masakazu, Kawashiri Masa-Aki, Ochi Ayako, Toyoda Junya, Nakano Yuya, Adachi Masanori, Mizuno Katsumi, Hasegawa Yukihiro, Dobashi Kazushi |
Analysis of Rare Variants in Genes Related to Lipid Metabolism in Patients with Familial Hypercholesterolemia in Western Siberia (Russia). Journal of personalized medicine 2021 11 11 (11): . Shakhtshneider Elena, Ivanoshchuk Dinara, Timoshchenko Olga, Orlov Pavel, Semaev Sergey, Valeev Emil, Goonko Andrew, Ladygina Nataliya, Voevoda Mikha |
Associations between SNPs in Intestinal Cholesterol Absorption and Endogenous Cholesterol Synthesis Genes with Cholesterol Metabolism. Biomedicines 2021 Oct 9 (10): . Schroor Maite M, Mokhtar Fatma B A, Plat Jogchum, Mensink Ronald |
Population-based meta-analysis and gene-set enrichment identifies FXR/RXR pathway as common to fatty liver disease and serum lipids. Hepatology communications 2022 Sep . Handelman Samuel K, Puentes Yindra M, Kuppa Annapurna, Chen Yanhua, Du Xiaomeng, Feitosa Mary F, Palmer Nicholette D, Speliotes Elizabeth |
Identification of genetic variants related to metabolic syndrome by next-generation sequencing. Diabetology & metabolic syndrome 2022 Aug 14 (1): 119. Lee Sanghoo, Kim Seol-A, Hong Jeonghoon, Kim Yejin, Hong Gayeon, Baik SaeYun, Choi Kyeonghwan, Lee Mi-Kyeong, Lee Kyoung-Ry |
[Identification of genetic variants associated with familial hypercholesterolemia in Chilean children and adolescents]. Revista medica de Chile 2022 3 149 (9): 1267-1274. Sánchez Andrea, Bustos Paulina, Honorato Paula, Sáez Katia, Elim-Jannes Cinthia, Barriga Natalia, Ibieta Guillermo, Pérez Luis, Alonso Rodrigo, Radojkovic Claudia, Asenjo Sylv |
Improvement of Definite Diagnosis of Familial Hypercholesterolemia Using an Expanding Genetic Analysis. JACC. Asia 2022 11 1 (1): 82-89. Cao Ye-Xuan, Sun Di, Liu Hui-Hui, Jin Jing-Lu, Li Sha, Guo Yuan-Lin, Wu Na-Qiong, Zhu Cheng-Gang, Liu Geng, Dong Qian, Sun Jing, Chen Xie-Hui, Li Jian-J |
Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis.
Nature communications 2022 1 13 (1): 143. Scholz Markus, Horn Katrin, Pott Janne, Gross Arnd, Kleber Marcus E, Delgado Graciela E, Mishra Pashupati Prasad, Kirsten Holger, Gieger Christian, Müller-Nurasyid Martina, Tönjes Anke, Kovacs Peter, Lehtimäki Terho, Raitakari Olli, Kähönen Mika, Gylling Helena, Baber Ronny, Isermann Berend, Stumvoll Michael, Loeffler Markus, März Winfried, Meitinger Thomas, Peters Annette, Thiery Joachim, Teupser Daniel, Ceglarek U |
A polymorphism in ABCA2 is associated with neutropenia induced by capecitabine in Japanese patients with colorectal cancer. Cancer chemotherapy and pharmacology 2023 8 . Yukitaka Shibata, Natsumi Matsumoto, Remi Murase, Yutaro Kubota, Hiroo Ishida, Ken Shimada, Ken-Ichi Fuji |
Genetic Characteristics of Latvian Patients with Familial Hypercholesterolemia: The First Analysis from Genome-Wide Sequencing. Journal of clinical medicine 2023 8 12 (15): . Gustavs Latkovskis, Raimonds Rescenko-Krums, Georgijs Nesterovics, Monta Briviba, Vita Saripo, Dainus Gilis, Elizabete Terauda, Ruta Meiere, Gunda Skudrina, Andrejs Erglis, Joana Rita Chora, Mafalda Bourbon, Janis Klovi |
Unravelling the genetic background of individuals with a clinical Familial Hypercholesterolemia phenotype. Journal of lipid research 2023 12 100490. Ana Margarida Medeiros, Ana Catarina Alves, Beatriz Miranda, Joana Rita Chora, Mafalda Bourbon, |
Causal effect of gallstone disease on the risk of coronary heart disease or acute myocardial infarction: a Mendelian randomization study. Scientific reports 2023 11 13 (1): 18807. Qingan Fu, Tianzhou Shen, Qingyun Yu, Long Jiang, Renqiang Ya |
Searching for new genes associated with the familial hypercholesterolemia phenotype using whole-genome sequencing and machine learning. Vavilovskii zhurnal genetiki i selektsii 2023 10 27 (5): 522-529. D E Ivanoshchuk, A B Kolker, O V Timoshchenko, S E Semaev, E V Shakhtshneid |
Association of CELSR2, APOB100, ABCG5/8, LDLR, and APOE polymorphisms and their genetic risks with lipids among the Thai subjects. Saudi journal of biological sciences 2023 1 30 (2): 103554. Nuinoon Manit, Saiphak Wutthichai, Nawaka Nantiya, Rattanawan Chutima, Pussadhamma Burabha, Jeenduang Nutjar |
Targeted sequencing of a gene panel in patients with Familial Hypercholesterolemia from Southern Poland. Polish archives of internal medicine 2023 1 . Toto?-?ura?ska Justyna, Wo?kow Pawe?, Kapusta Maria, Wójcik Ma?gorzata, Starzyk Jerzy, Kawalec Ewa, Idzior-Walu? Barbara, Walu?-Miarka Ma?gorza |
Proteome-Wide Mendelian Randomization Identifies Causal Links Between Blood Proteins and Acute Pancreatitis.
Gastroenterology 2023 2 . Bourgault Jérôme, Abner Erik, Manikpurage Hasanga D, Pujol-Gualdo Natàlia, Laisk Triin, , Gobeil Émilie, Gagnon Eloi, Girard Arnaud, Mitchell Patricia L, Thériault Sébastien, Esko Tõnu, Mathieu Patrick, Arsenault Benoit |
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