Human Genome Epidemiology Literature Finder
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Records 1 - 12 (of 12 Records) |
| Query Trace: Disease and SREBF1[original query] |
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| Analysis of lipid pathway genes indicates association of sequence variation near SREBF1/TOM1L2/ATPAF2 with dementia risk. Human molecular genetics 2010 May 19 (10): 2068-78. Reynolds Chandra A, Hong Mun-Gwan, Eriksson Ulrika K, Blennow Kaj, Wiklund Fredrik, Johansson Boo, Malmberg Bo, Berg Stig, Alexeyenko Andrey, Grönberg Henrik, Gatz Margaret, Pedersen Nancy L, Prince Jonathan |
Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease.
PLoS genetics 2011 Jun 7 (6): e1002141. Do Chuong B, Tung Joyce Y, Dorfman Elizabeth, Kiefer Amy K, Drabant Emily M, Francke Uta, Mountain Joanna L, Goldman Samuel M, Tanner Caroline M, Langston J William, Wojcicki Anne, Eriksson Nichol |
| Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence data. Circulation research 2014 Oct 115 (10): 884-96. Glessner Joseph T, Bick Alexander G, Ito Kaoru, Homsy Jason G, Rodriguez-Murillo Laura, Fromer Menachem, Mazaika Erica, Vardarajan Badri, Italia Michael, Leipzig Jeremy, DePalma Steven R, Golhar Ryan, Sanders Stephan J, Yamrom Boris, Ronemus Michael, Iossifov Ivan, Willsey A Jeremy, State Matthew W, Kaltman Jonathan R, White Peter S, Shen Yufeng, Warburton Dorothy, Brueckner Martina, Seidman Christine, Goldmuntz Elizabeth, Gelb Bruce D, Lifton Richard, Seidman Jonathan, Hakonarson Hakon, Chung Wendy |
| [Genetic predisposition to ischemic heart disease in patients with obstructive sleep apnea syndrome (OSAS)]. Polski merkuriusz lekarski : organ Polskiego Towarzystwa Lekarskiego 2014 Apr 36 (214): 229-32. Bielicki Piotr, Brzóska Kamil, P?ywaczewski Robert, Barna? Ma?gorzata, Kumor Marta, Stepkowski Tomasz, Jo?czak Luiza, Chazan Ryszarda, Kruszewski Marcin, Sliwi?ski Paw |
| Association of Parkinson disease risk loci with mild parkinsonian signs in older persons. JAMA neurology 2014 Apr 71 (4): 429-35. Shulman Joshua M, Yu Lei, Buchman Aron S, Evans Denis A, Schneider Julie A, Bennett David A, De Jager Philip |
| Nuclear lamina genetic variants, including a truncated LAP2, in twins and siblings with nonalcoholic fatty liver disease. Hepatology (Baltimore, Md.) 2017 9 67 (5): 1710-1725. Brady Graham F, Kwan Raymond, Ulintz Peter J, Nguyen Phirum, Bassirian Shirin, Basrur Venkatesha, Nesvizhskii Alexey I, Loomba Rohit, Omary M Bis |
| Association analysis of SNP rs11868035 in SREBF1 with sporadic Parkinson's disease, sporadic amyotrophic lateral sclerosis and multiple system atrophy in a Chinese population. Neuroscience letters 2017 Nov . Yuan XiaoQin, Cao Bei, Wu Ying, Chen YongPing, Wei QianQian, Ou RuWei, Yang Jing, Chen XuePing, Zhao Bi, Song Wei, Shang HuiFa |
| Multiethnic Meta-Analysis Identifies RAI1 as a Possible Obstructive Sleep Apnea-related Quantitative Trait Locus in Men.
American journal of respiratory cell and molecular biology 2017 Oct . Chen Han, Cade Brian E, Gleason Kevin J, Bjonnes Andrew C, Stilp Adrienne M, Sofer Tamar, Conomos Matthew P, Ancoli-Israel Sonia, Arens Raanan, Azarbarzin Ali, Bell Graeme I, Below Jennifer E, Chun Sung, Evans Daniel S, Ewert Ralf, Frazier-Wood Alexis C, Gharib Sina A, Haba-Rubio José, Hagen Erika W, Heinzer Raphael, Hillman David R, Johnson W Craig, Kutalik Zoltan, Lane Jacqueline M, Larkin Emma K, Lee Seung Ku, Liang Jingjing, Loredo Jose S, Mukherjee Sutapa, Palmer Lyle J, Papanicolaou George J, Penzel Thomas, Peppard Paul E, Post Wendy S, Ramos Alberto R, Rice Ken, Rotter Jerome I, Sands Scott A, Shah Neomi A, Shin Chol, Stone Katie L, Stubbe Beate, Sul Jae Hoon, Tafti Mehdi, Taylor Kent D, Teumer Alexander, Thornton Timothy A, Tranah Gregory J, Wang Chaolong, Wang Heming, Warby Simon C, Wellman D Andrew, Zee Phyllis C, Hanis Craig L, Laurie Cathy C, Gottlieb Daniel J, Patel Sanjay R, Zhu Xiaofeng, Sunyaev Shamil R, Saxena Richa, Lin Xihong, Redline Sus |
| The polymorphism of SREBF1 gene rs11868035?G/A is associated with susceptibility to Parkinson's disease in a Chinese population. The International journal of neuroscience 2018 Sep 1-18. Lou Fan, Li Ming, Liu Na, Li Xiaohong, Ren Yan, Luo Xiaogua |
| Genetic variation in 117 myelination-related genes in schizophrenia: Replication of association to lipid biosynthesis genes. Scientific reports 2018 May 8 (1): 6915. Stokowy Tomasz, Polushina Tatiana, Sønderby Ida E, Karlsson Robert, Giddaluru Sudheer, Le Hellard Stephanie, Bergen Sarah E, Sullivan Patrick F, Andreassen Ole A, Djurovic Srdjan, Hultman Christina M, Steen Vidar |
| A replication study of GWAS-genetic risk variants associated with Parkinson's disease in a Spanish population. Neuroscience letters 2019 Aug 134425. Tejera-Parrado Cristina, Jesús Silvia, Periñán María Teresa, Buiza-Rueda Dolores, Oliva-Ariza Guillermo, Adarmes-Gómez Astrid D, Macías-García Daniel, Gómez-Garre Pilar, Mir Pab |
| Genome-wide association meta-analysis identifies 17 loci associated with nonalcoholic fatty liver disease. Nature genetics 2023 9 . Yanhua Chen, Xiaomeng Du, Annapurna Kuppa, Mary F Feitosa, Lawrence F Bielak, Jeffrey R O'Connell, Solomon K Musani, Xiuqing Guo, Bratati Kahali, Vincent L Chen, Albert V Smith, Kathleen A Ryan, Gudny Eirksdottir, Matthew A Allison, Donald W Bowden, Matthew J Budoff, John Jeffrey Carr, Yii-Der I Chen, Kent D Taylor, Antonino Oliveri, Adolfo Correa, Breland F Crudup, Sharon L R Kardia, Thomas H Mosley, Jill M Norris, James G Terry, Jerome I Rotter, Lynne E Wagenknecht, Brian D Halligan, Kendra A Young, John E Hokanson, George R Washko, Vilmundur Gudnason, Michael A Province, Patricia A Peyser, Nicholette D Palmer, Elizabeth K Speliot |
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