Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 204 Records) |
| Query Trace: Disease and ABCA1[original query] |
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| Exome Sequencing of 5 Families with Severe Early-Onset Periodontitis. Journal of dental research 2021 9 101 (2): 151-157. Richter G M, Wagner G, Reichenmiller K, Staufenbiel I, Martins O, Löscher B S, Holtgrewe M, Jepsen S, Dommisch H, Schaefer A |
| Coronary Artery Disease: Association Study of 5 Loci with Angiographic Indices of Disease Severity. Disease markers 2021 2021 5522539. Bogari Neda M, Allam Reem M, Bouazzaoui Abdellatif, Elkhateeb Osama, Porqueddu Massimo, Colombo Gualtiero |
| A comprehensive analysis of copy number variation in a Turkish dementia cohort. Human genomics 2021 Jul 15 (1): 48. Dehghani Nadia, Guven Gamze, Kun-Rodrigues Celia, Gouveia Catarina, Foster Kalina, Hanagasi Hasmet, Lohmann Ebba, Samanci Bedia, Gurvit Hakan, Bilgic Basar, Bras Jose, Guerreiro Ri |
| Epigenomic Profiles of African-American Transthyretin Val122Ile Carriers Reveals Putatively Dysregulated Amyloid Mechanisms. Circulation. Genomic and precision medicine 2021 1 14 (1): e003011. Pathak Gita A, Wendt Frank R, De Lillo Antonella, Nunez Yaira Z, Goswami Aranyak, De Angelis Flavio, Fuciarelli Maria, Kranzler Henry R, Gelernter Joel, Polimanti Rena |
| Association between LXR-? and ABCA1 Gene Polymorphisms and the Risk of Diabetic Kidney Disease in Patients with Type 2 Diabetes Mellitus in a Chinese Han Population. Journal of diabetes research 2021 1 2020 8721536. Liu Peng, Ma Liang, Zhao Hailing, Shen Zhengri, Zhou Xuefeng, Yan Meihua, Zhao Tingting, Zhang Haojun, Qiu Xinping, Li Pi |
| Association of novel MUC16, MAP3K15 and ABCA1 mutation with giant congenital melanocytic nevus. Hereditas 2022 9 159 (1): 33. Zhou Renpeng, Wang Qirui, Hou Jialin, Wang Danru, Liang Yim |
| Association Between ABCA1 Gene Polymorphisms and the Risk of Hypertension in the Chinese Han Population. Frontiers in public health 2022 10 878610. Ren Yanli, Tong Enyu, Di Chunhong, Zhang Yunheng, Xu Liangwen, Tan Xiaohua, Yang L |
| Bioinformatic Prioritization and Functional Annotation of GWAS-Based Candidate Genes for Primary Open-Angle Glaucoma. Genes 2022 Jun 13 (6): . Asefa Nigus G, Kamali Zoha, Pereira Satyajit, Vaez Ahmad, Jansonius Nomdo, Bergen Arthur A, Snieder Haro |
| Evaluation of ABCA1 and FNDC3B Gene Polymorphisms Associated With Pseudoexfoliation Glaucoma and Primary Angle-Closure Glaucoma in a Saudi Cohort. Frontiers in genetics 2022 13 877174. Kondkar Altaf A, Sultan Tahira, Azad Taif A, Osman Essam A, Almobarak Faisal A, Lobo Glenn P, Al-Obeidan Saleh |
| Whole-exome sequencing reveals damaging gene variants associated with hypoalphalipoproteinemia. Journal of lipid research 2022 4 63 (6): 100209. Dong Weilai, Wong Karen H Y, Liu Youbin, Levy-Sakin Michal, Hung Wei-Chien, Li Mo, Li Boyang, Jin Sheng Chih, Choi Jungmin, Lopez-Giraldez Francesc, Vaka Dedeepya, Poon Annie, Chu Catherine, Lao Richard, Balamir Melek, Movsesyan Irina, Malloy Mary J, Zhao Hongyu, Kwok Pui-Yan, Kane John P, Lifton Richard P, Pullinger Clive |
| Rare missense mutations in ABCA7 might increase Alzheimer's disease risk by plasma membrane exclusion. Acta neuropathologica communications 2022 4 10 (1): 43. Bossaerts Liene, Hendrickx Van de Craen Elisabeth, Cacace Rita, Asselbergh Bob, Van Broeckhoven Christi |
| Regulation of ABCA1 by AMD-Associated Genetic Variants and Hypoxia in iPSC-RPE. International journal of molecular sciences 2022 3 23 (6): . Peters Florian, Ebner Lynn J A, Atac David, Maggi Jordi, Berger Wolfgang, den Hollander Anneke I, Grimm Christi |
| Polymorphic Variants of AGT, ABCA1, and CYBA Genes Influence the Survival of Patients with Coronary Artery Disease: A Prospective Cohort Study. Genes 2022 11 13 (11): . Balcerzyk-Mati? Anna, Nowak Tomasz, Mizia-Stec Katarzyna, Iwanicka Joanna, Iwanicki Tomasz, Ba?ka Pawe?, Jarosz Alicja, Filipecki Artur, ?ak Iwona, Krauze Jolanta, Niemiec Paw |
| ABCA1 Polymorphism R1587K in Chronic Hepatitis C Is Gender-Specific and Modulates Liver Disease Severity through Its Influence on Cholesterol Metabolism and Liver Function: A Preliminary Study. Genes 2022 11 13 (11): . Ferreira Joana, Bicho Manuel, Serejo Fáti |
| Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's disease. Nature genetics 2022 11 54 (12): 1786-1794. Holstege Henne, Hulsman Marc, Charbonnier Camille, Grenier-Boley Benjamin, Quenez Olivier, Grozeva Detelina, van Rooij Jeroen G J, Sims Rebecca, Ahmad Shahzad, Amin Najaf, Norsworthy Penny J, Dols-Icardo Oriol, Hummerich Holger, Kawalia Amit, Amouyel Philippe, Beecham Gary W, Berr Claudine, Bis Joshua C, Boland Anne, Bossù Paola, Bouwman Femke, Bras Jose, Campion Dominique, Cochran J Nicholas, Daniele Antonio, Dartigues Jean-François, Debette Stéphanie, Deleuze Jean-François, Denning Nicola, DeStefano Anita L, Farrer Lindsay A, Fernández Maria Victoria, Fox Nick C, Galimberti Daniela, Genin Emmanuelle, Gille Johan J P, Le Guen Yann, Guerreiro Rita, Haines Jonathan L, Holmes Clive, Ikram M Arfan, Ikram M Kamran, Jansen Iris E, Kraaij Robert, Lathrop Marc, Lemstra Afina W, Lleó Alberto, Luckcuck Lauren, Mannens Marcel M A M, Marshall Rachel, Martin Eden R, Masullo Carlo, Mayeux Richard, Mecocci Patrizia, Meggy Alun, Mol Merel O, Morgan Kevin, Myers Richard M, Nacmias Benedetta, Naj Adam C, Napolioni Valerio, Pasquier Florence, Pastor Pau, Pericak-Vance Margaret A, Raybould Rachel, Redon Richard, Reinders Marcel J T, Richard Anne-Claire, Riedel-Heller Steffi G, Rivadeneira Fernando, Rousseau Stéphane, Ryan Natalie S, Saad Salha, Sanchez-Juan Pascual, Schellenberg Gerard D, Scheltens Philip, Schott Jonathan M, Seripa Davide, Seshadri Sudha, Sie Daoud, Sistermans Erik A, Sorbi Sandro, van Spaendonk Resie, Spalletta Gianfranco, Tesi Niccolo', Tijms Betty, Uitterlinden André G, van der Lee Sven J, Visser Pieter Jelle, Wagner Michael, Wallon David, Wang Li-San, Zarea Aline, Clarimon Jordi, van Swieten John C, Greicius Michael D, Yokoyama Jennifer S, Cruchaga Carlos, Hardy John, Ramirez Alfredo, Mead Simon, van der Flier Wiesje M, van Duijn Cornelia M, Williams Julie, Nicolas Gaël, Bellenguez Céline, Lambert Jean-Charl |
| Association Between ABCA1 R219K Variant and Alzheimer's Disease: An Updated Meta-Analysis and Systematic Review. Current Alzheimer research 2022 11 19 (10): 734-741. Zhao Jinrong, Wang Jinpei, Zhao Dong, Wang Lin, Luo Xia |
| Assessment of genetic polymorphism associated with ATP-binding cassette transporter A1 (ABCA1) gene and fluctuations in serum lipid profile levels in patients with coronary artery disease. Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society 2022 1 29 (12): 1458-1465. Bogari Neda M, Babalghith Ahmad O, Bouazzaoui Abdellatif, Aljohani Ashwag, Dannoun Anas, Elkhateeb Osama, Amin Amr A, Bogari Mazin K, Mazhar Abdulbari A, Porqueddu Massimo, Khan Imran A |
| Coronary artery disease, its associations with ocular, genetic and blood lipid parameters. Eye (London, England) 2023 8 . Indr? Matulevi?i?t?, Vacis Tatar?nas, Vilius Skipskis, Ieva ?iapien?, Audron? Veikutien?, Vaiva Lesauskait?, Olivija Dobilien?, Dalia Žali?nie |
| Association of ABCA1 R219K polymorphism and telomere length in a Chinese rural population: possible linking to systemic inflammation. Journal of genetics 2023 5 102 . Shutan Liao, Qing Zhou, Yang Zha |
| Lipoprotein lipids and apolipoproteins in primary immune thrombocytopenia: Results from a clinical characteristics and causal relationship verification, potential drug target identification by Mendelian randomization analyses. British journal of haematology 2023 11 . Yang Ou, Yanxia Zhan, Xia Shao, Pengcheng Xu, Lili Ji, Xibing Zhuang, Hao Chen, Yunfeng Che |
| Evaluation of the participation of ABCA1 transporter in epicardial and mediastinal adipose tissue from patients with coronary artery disease. Archives of endocrinology and metabolism 2023 11 68 e230188. Giovanny Fuentevilla-Álvarez, Claudia Huesca-Gómez, Yazmín Estela Paz-Torres, Nadia González-Moyotl, María Elena Soto, José Antonio García-Valdivia, Reyna Sámano, Martín Martínez-Rosas, Sergio Enrique Meza-Toledo, Ricardo Gamb |
| Deletion of miR-33, a regulator of the ABCA1-APOE pathway, ameliorates neuropathological phenotypes in APP/PS1 mice. Alzheimer's & dementia : the journal of the Alzheimer's Association 2024 9 . Mason Tate, H R Sagara Wijeratne, Byungwook Kim, Stéphanie Philtjens, Yanwen You, Do-Hun Lee, Daniela A Gutierrez, Daniel Sharify, Megan Wells, Magdalena Perez-Cardelo, Emma H Doud, Carlos Fernandez-Hernando, Cristian Lasagna-Reeves, Amber L Mosley, Jungsu K |
| Association between high-density lipoprotein and functional outcome of ischemic stroke patients in a Taiwanese population. Lipids in health and disease 2024 8 23 (1): 275. Ting-Chun Lin, Chun-Yao Huang, Yu-Ling Li, Hung-Yi Chiou, Chaur-Jong Hu, Jiann-Shing Jeng, Sung-Chun Tang, Lung Chan, Li-Ming Lien, Huey-Juan Lin, Chu-Chien Lin, Yi-Chen Hsi |
| High-Density Lipoprotein Particle Concentration and Size Predict Incident Coronary Artery Disease Events in a Cohort With Type 1 Diabetes. Journal of the American Heart Association 2024 7 e034763. Tina Costacou, Tomas Vaisar, Rachel G Miller, W Sean Davidson, Jay W Heinecke, Trevor J Orchard, Karin E Bornfel |
| The Expression of Genes Related to Reverse Cholesterol Transport and Leptin Receptor Pathways in Peripheral Blood Mononuclear Cells Are Decreased in Morbid Obesity and Related to Liver Function. International journal of molecular sciences 2024 7 25 (14): . Carlos Jiménez-Cortegana, Soledad López-Enríquez, Gonzalo Alba, Consuelo Santa-María, Gracia M Martín-Núñez, Francisco J Moreno-Ruiz, Sergio Valdés, Sara García-Serrano, Cristina Rodríguez-Díaz, Ailec Ho-Plágaro, María I Fontalba-Romero, Eduardo García-Fuentes, Lourdes Garrido-Sánchez, Víctor Sánchez-Margal |
| Identification and Molecular Simulation of Genetic Variants in ABCA1 Gene Associated with Susceptibility to Dyslipidemia in Type 2 Diabetes. International journal of molecular sciences 2024 6 25 (12): . Asifa Majeed, Zunaira Ali Baig, Amir Rash |
| Targeted next-generation sequencing panel to investigate antiplatelet adverse reactions in acute coronary syndrome patients undergoing percutaneous coronary intervention with stenting. Thrombosis research 2024 6 240 109060. Alba Antúnez-Rodríguez, Sonia García-Rodríguez, Ana Pozo-Agundo, Jesús Gabriel Sánchez-Ramos, Eduardo Moreno-Escobar, José Matías Triviño-Juárez, Luis Javier Martínez-González, Cristina Lucía Dávila-Fajar |
| Input of exome sequencing in early-onset cerebral amyloid angiopathy. Alzheimer's & dementia (Amsterdam, Netherlands) 2024 11 16 (4): e70027. Lou Grangeon, Camille Charbonnier, Stéphane Rousseau, Anne Claire Richard, Olivier Quenez, Aline Zarea, Anne Boland, Robert Olaso, Jean-François Deleuze, , Elisabeth Tournier-Lasserve, Gael Nicolas, David Wall |
| Genetic and Anthropometric Interplay: How Waist-to-Hip Ratio Modulates LDL-c Levels in Mexican Population. Nutrients 2024 10 16 (19): . César Hernández-Guerrero, Erika Arenas, Jaime García-Mena, Edgar J Mendivil, Omar Ramos-Lopez, Graciela Teru |
| ABCA1 variant rs9282541 is associated with metabolic syndrome in Maya children. Annals of human genetics 2024 1 . Barbara I Peña-Espinoza, Emmanuel Torre-Horta, María G Ortiz-López, Marta Menjiv |
- Page last reviewed:Feb 1, 2024
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