Human Genome Epidemiology Literature Finder
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Records 1 - 15 (of 15 Records) |
| Query Trace: Disease and MADD[original query] |
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Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.
Nature genetics 2009 Jan 41 (1): 47-55. Aulchenko Yurii S, Ripatti Samuli, Lindqvist Ida, Boomsma Dorret, Heid Iris M, Pramstaller Peter P, Penninx Brenda W J H, Janssens A Cecile J W, Wilson James F, Spector Tim, Martin Nicholas G, Pedersen Nancy L, Kyvik Kirsten Ohm, Kaprio Jaakko, Hofman Albert, Freimer Nelson B, Jarvelin Marjo-Riitta, Gyllensten Ulf, Campbell Harry, Rudan Igor, Johansson Asa, Marroni Fabio, Hayward Caroline, Vitart Veronique, Jonasson Inger, Pattaro Cristian, Wright Alan, Hastie Nick, Pichler Irene, Hicks Andrew A, Falchi Mario, Willemsen Gonneke, Hottenga Jouke-Jan, de Geus Eco J C, Montgomery Grant W, Whitfield John, Magnusson Patrik, Saharinen Juha, Perola Markus, Silander Kaisa, Isaacs Aaron, Sijbrands Eric J G, Uitterlinden Andre G, Witteman Jacqueline C M, Oostra Ben A, Elliott Paul, Ruokonen Aimo, Sabatti Chiara, Gieger Christian, Meitinger Thomas, Kronenberg Florian, Döring Angela, Wichmann H-Erich, Smit Johannes H, McCarthy Mark I, van Duijn Cornelia M, Peltonen Leena, |
| Clinical and genetic analysis of lipid storage myopathies. Muscle & nerve 2009 Mar 39 (3): 333-42. Ohkuma Aya, Noguchi Satoru, Sugie Hideo, Malicdan May Christine V, Fukuda Tokiko, Shimazu Kunio, López Luis Carlos, Hirano Michio, Hayashi Yukiko K, Nonaka Ikuya, Nishino Ichi |
| High frequency of ETFDH c.250G>A mutation in Taiwanese patients with late-onset lipid storage myopathy. Clinical genetics 2010 Dec 78 (6): 565-9. Lan M-Y, Fu M-H, Liu Y-F, Huang C-C, Chang Y-Y, Liu J-S, Peng C-H, Chen S |
| Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes.
Diabetes 2011 Oct 60 (10): 2624-34. Strawbridge Rona J, Dupuis Josée, Prokopenko Inga, Barker Adam, Ahlqvist Emma, Rybin Denis, Petrie John R, Travers Mary E, Bouatia-Naji Nabila, Dimas Antigone S, Nica Alexandra, Wheeler Eleanor, Chen Han, Voight Benjamin F, Taneera Jalal, Kanoni Stavroula, Peden John F, Turrini Fabiola, Gustafsson Stefan, Zabena Carina, Almgren Peter, Barker David J P, Barnes Daniel, Dennison Elaine M, Eriksson Johan G, Eriksson Per, Eury Elodie, Folkersen Lasse, Fox Caroline S, Frayling Timothy M, Goel Anuj, Gu Harvest F, Horikoshi Momoko, Isomaa Bo, Jackson Anne U, Jameson Karen A, Kajantie Eero, Kerr-Conte Julie, Kuulasmaa Teemu, Kuusisto Johanna, Loos Ruth J F, Luan Jian'an, Makrilakis Konstantinos, Manning Alisa K, Martínez-Larrad María Teresa, Narisu Narisu, Nastase Mannila Maria, Ohrvik John, Osmond Clive, Pascoe Laura, Payne Felicity, Sayer Avan A, Sennblad Bengt, Silveira Angela, Stancáková Alena, Stirrups Kathy, Swift Amy J, Syvänen Ann-Christine, Tuomi Tiinamaija, van 't Hooft Ferdinand M, Walker Mark, Weedon Michael N, Xie Weijia, Zethelius Björn, , , , , , Ongen Halit, Mälarstig Anders, Hopewell Jemma C, Saleheen Danish, Chambers John, Parish Sarah, Danesh John, Kooner Jaspal, Ostenson Claes-Göran, Lind Lars, Cooper Cyrus C, Serrano-Ríos Manuel, Ferrannini Ele, Forsen Tom J, Clarke Robert, Franzosi Maria Grazia, Seedorf Udo, Watkins Hugh, Froguel Philippe, Johnson Paul, Deloukas Panos, Collins Francis S, Laakso Markku, Dermitzakis Emmanouil T, Boehnke Michael, McCarthy Mark I, Wareham Nicholas J, Groop Leif, Pattou François, Gloyn Anna L, Dedoussis George V, Lyssenko Valeriya, Meigs James B, Barroso Inês, Watanabe Richard M, Ingelsson Erik, Langenberg Claudia, Hamsten Anders, Florez Jose |
| Family-based genome scan for age at onset of late-onset Alzheimer's disease in whole exome sequencing data. Genes, brain, and behavior 2015 Sep . Saad M, Brkanac Z, Wijsman E |
| Associations of lipid levels susceptibility loci with coronary artery disease in Chinese population. Lipids in health and disease 2015 14 (1): 80. Wang Xue-Bin, Han Ya-di, Cui Ning-Hua, Gao Jia-Jia, Yang Jie, Huang Zhu-Liang, Zhu Qiang, Zheng Fa |
| MADD-FOLH1 Polymorphisms and Their Haplotypes with Serum Lipid Levels and the Risk of Coronary Heart Disease and Ischemic Stroke in a Chinese Han Population. Nutrients 2016 8 (4): . Wu Dong-Feng, Yin Rui-Xing, Cao Xiao-Li, Huang Feng, Wu Jin-Zhen, Chen Wu-Xi |
| A novel mutation in ETFDH manifesting as severe neonatal-onset multiple acyl-CoA dehydrogenase deficiency. Journal of the neurological sciences 2017 12 384 121-125. van der Westhuizen Francois H, Smuts Izelle, Honey Engela, Louw Roan, Schoonen Maryke, Jonck Lindi-Maryn, Dercksen Mar |
| Association between genetic loci linked to HDL-C levels and Indian patients with CAD: a pilot study. Heart Asia 2017 9 (1): 9-13. Stanley Ashley, Ponde C K, Rajani R M, Ashavaid T |
| GWAS-Top Polymorphisms Associated With Late-Onset Alzheimer Disease in Brazil: Pointing Out Possible New Culprits Among Non-Coding RNAs. Frontiers in molecular biosciences 2021 8 632314. Kretzschmar Gabriela Canalli, Alencar Nina Moura, da Silva Saritha Suellen Lopes, Sulzbach Carla Daniela, Meissner Caroline Grisbach, Petzl-Erler Maria Luiza, Souza Ricardo Lehtonen R, Boldt Angelica Beate Wint |
| Phenotype and genotype spectrum of variants in guanine nucleotide exchange factor genes in a broad cohort of Iranian patients. Molecular genetics & genomic medicine 2022 2 10 (4): e1894. Mosallaei Meysam, Ehtesham Naeim, Beheshtian Maryam, Khoshbakht Shahrouz, Davarnia Behzad, Kahrizi Kimia, Najmabadi Hosse |
| Large-scale exome sequence analysis identifies sex- and age-specific determinants of obesity. Cell genomics 2023 8 3 (8): 100362. Lena R Kaisinger, Katherine A Kentistou, Stasa Stankovic, Eugene J Gardner, Felix R Day, Yajie Zhao, Alexander Mörseburg, Christopher J Carnie, Guido Zagnoli-Vieira, Fabio Puddu, Stephen P Jackson, Stephen O'Rahilly, I Sadaf Farooqi, Laura Dearden, Lucas C Pantaleão, Susan E Ozanne, Ken K Ong, John R B Per |
| Co-existence of multiple functional variants and genes underlie genetic risk locus 11p11.2 of Alzheimer's disease. Biological psychiatry 2023 6 . Min Xu, Qianjin Liu, Rui Bi, Yu Li, Hongli Li, Wei-Bo Kang, Zhongjiang Yan, Quanzhen Zheng, Chunli Sun, Maosen Ye, Bo-Lin Xiang, Xiong-Jian Luo, Ming Li, Deng-Feng Zhang, Yong-Gang Y |
| Newborn screening for fatty acid oxidation disorders in a southern Chinese population. Heliyon 2024 1 10 (1): e23671. Yiming Lin, Chunmei Lin, Bangbang Lin, Zhenzhu Zheng, Weihua Lin, Yanru Chen, Dongmei Chen, Weilin Pe |
| Clinical, biochemical, and genetic spectrum of MADD in a South African cohort: an ICGNMD study. Orphanet journal of rare diseases 2024 1 19 (1): 15. Michelle Bisschoff, Izelle Smuts, Marli Dercksen, Maryke Schoonen, Barend C Vorster, George van der Watt, Careni Spencer, Kireshnee Naidu, Franclo Henning, Surita Meldau, Robert McFarland, Robert W Taylor, Krutik Patel, Mahmoud R Fassad, Jana Vandrovcova, , Ronald J A Wanders, Francois H van der Westhuiz |
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