Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 36 Records) |
Query Trace: SREBF1[original query] |
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Genetic variation in genes of the fatty acid synthesis pathway and breast cancer risk. Breast cancer research and treatment 2009 Dec 118 (3): 565-74. Campa Daniele, McKay James, Sinilnikova Olga, Hüsing Anika, Vogel Ulla, Hansen Rikke Dalgaard, Overvad Kim, Witt Petra Mariann, Clavel-Chapelon Françoise, Boutron-Ruault Marie-Christine, Chajes Veronique, Rohrmann Sabine, Chang-Claude Jenny, Boeing Heiner, Fisher Eva, Trichopoulou Antonia, Trichopoulos Dimitrios, Palli Domenico, Villarini Anna, Sacerdote Carlotta, Mattiello Amalia, Tumino Rosario, Peeters Petra H M, van Gils Carla H, Bas Bueno-de-Mesquita H, Lund Eiliv, Chirlaque María Dolores, Sala Núria, Suarez Laudina Rodriguez, Barricarte Aurelio, Dorronsoro Miren, Sánchez Maria-José, Lenner Per, Hallmans Göran, Tsilidis Kostas, Bingham Sheila, Khaw Kay-Tee, Gallo Valentina, Norat Teresa, Riboli Elio, Rinaldi Sabina, Lenoir Gilbert, Tavtigian Sean V, Canzian Federico, Kaaks Rudo |
Obesity-related polymorphisms and their associations with the ability to regulate fat oxidation in obese Europeans: the NUGENOB study. Obesity (Silver Spring, Md.) 2010 Jul 18 (7): 1369-77. Corpeleijn Eva, Petersen Liselotte, Holst Claus, Saris Wim H, Astrup Arne, Langin Dominique, MacDonald Ian, Martinez J Alfredo, Oppert Jean-Michel, Polak Jan, Pedersen Oluf, Froguel Philippe, Arner Peter, Sørensen Thorkild I A, Blaak Ellen |
Common sequence variants in pharmacodynamic and pharmacokinetic pathway-related genes conferring LDL cholesterol response to statins. Pharmacogenomics 2010 Mar 11 (3): 309-17. Chien Kuo-Liong, Wang Kuei-Chen, Chen Yen-Ching, Chao Chia-Lung, Hsu Hsiu-Ching, Chen Ming-Fong, Chen Wei |
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 |
Associations between polymorphisms in genes involved in fatty acid metabolism and dietary fat intakes. Journal of nutrigenetics and nutrigenomics 2012 5 (1): 1-12. Bouchard-Mercier Annie, Paradis Ann-Marie, Pérusse Louis, Vohl Marie-Clau |
Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci. American journal of human genetics 2012 Feb . Saxena R, Elbers CC, Guo Y, Peter I, Gaunt TR, Mega JL, Lanktree MB, Tare A, Castillo BA, Li YR, Johnson T, Bruinenberg M, Gilbert-Diamond D, Rajagopalan R, Voight BF, Balasubramanyam A, Barnard J, Bauer F, Baumert J, Bhangale T, Böhm BO, Braund PS, Burton PR, Chandrupatla HR, Clarke R, Cooper-Dehoff RM, Crook ED, Davey-Smith G, Day IN, de Boer A, de Groot MC, Drenos F, Ferguson J, Fox CS, Furlong CE, Gibson Q, Gieger C, Gilhuijs-Pederson LA, Glessner JT, Goel A, Gong Y, Grant SF, Grobbee DE, Hastie C, Humphries SE, Kim CE, Kivimaki M, Kleber M, Meisinger C, Kumari M, Langaee TY, Lawlor DA, Li M, Lobmeyer MT, Maitland-van der Zee AH, Meijs MF, Molony CM, Morrow DA, Murugesan G, Musani SK, Nelson CP, Newhouse SJ, O'Connell JR, Padmanabhan S, Palmen J, Patel SR, Pepine CJ, Pettinger M, Price TS, Rafelt S, Ranchalis J, Rasheed A, Rosenthal E, Ruczinski I, Shah S, Shen H, Silbernagel G, Smith EN, Spijkerman AW, Stanton A, Steffes MW, Thorand B, Trip M, van der Harst P, van der A DL, van Iperen EP, van Setten J, van Vliet-Ostaptchouk JV, Verweij N, Wolffenbuttel BH, Young T, Zafarmand MH, Zmuda JM, Boehnke M, Altshuler D, McCarthy M, Kao WH, Pankow JS, Cappola TP, Caulfield M, Dominiczak A, Shields DC, Bhatt D, Zhang L, Curtis SP, Danesh J, Casas JP, van der Schouw YT, Onland-Moret NC, Doevendans PA, Dorn GW, Farrall M, Fitzgerald GA, Hamsten A, Hegele R, Hingorani AD, Hofker MH, Huggins GS, Illig T, Jarvik GP, Johnson JA, Klungel OH, Knowler WC, Koenig W, März W, Meigs JB, Melander O, Munroe PB, Mitchell BD, Bielinski SJ, Rader DJ, Reilly MP, Rich SS, Rotter JI, Saleheen D, Samani NJ, Schadt EE, Shuldiner AR, Silverstein R, Kottke-Marchant K, Talmud PJ, Watkins H, Asselbergs F, de Bakker PI, McCaffery J, Wijmenga C, Sabatine MS, Wilson JG, Reiner A, Bowden DW, Hakonarson H, Siscovick DS, Keating BJ |
Polymorphisms, de novo lipogenesis, and plasma triglyceride response following fish oil supplementation. Journal of lipid research 2013 Oct 54 (10): 2866-73. Bouchard-Mercier Annie, Rudkowska Iwona, Lemieux Simone, Couture Patrick, Vohl Marie-Clau |
The Association Study between Twenty One Polymorphisms in Seven Candidate Genes and Coronary Heart Diseases in Chinese Han Population. PloS one 2013 8 (6): e66976. Alobeidy Barrak F, Li Cong, Alzobair Alya A, Liu Tao, Zhao Junzhang, Fang Yuan, Zheng Fa |
Pharmacogenomics of sterol synthesis and statin use in schizophrenia subjects treated with antipsychotics. Pharmacogenomics 2014 Jan 15 (1): 61-7. Vassas Thomas J, Burghardt Kyle J, Ellingrod Vicki |
Genetic polymorphisms of the main transcription factors for adiponectin gene promoter in regulation of adiponectin levels: association analysis in three European cohorts. PloS one 2012 7 (12): 12. Kedenko L, Lamina C, Kiesslich T, Kapur K, Bergmann S, Waterworth D, Heid IM, Wichmann HE, Kedenko I, Kronenberg F, Paulweber B |
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 |
A gene variant in the transcription factor 7-like 2 (TCF7L2) is associated with an increased risk of gestational diabetes mellitus. European journal of obstetrics, gynecology, and reproductive biology 2014 Sep 180 77-82. Pagán Ana, Sabater-Molina María, Olza Josune, Prieto-Sánchez María T, Blanco-Carnero Jose E, Parrilla Juan J, Gil Ángel, Larqué Elvi |
[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 |
SREBF1 gene variations modulate insulin sensitivity in response to a fish oil supplementation. Lipids in health and disease 2014 13 152. Bouchard-Mercier Annie, Rudkowska Iwona, Lemieux Simone, Couture Patrick, Pérusse Louis, Vohl Marie-Clau |
Association between SCAP and SREBF1 gene polymorphisms and metabolic syndrome in schizophrenia patients treated with atypical antipsychotics. The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry 2016 Mar 1-26. Yang Lin, Chen Jianhua, Li Yan, Wang Yan, Liang Shiqiao, Shi Yongyong, Shi Shenxun, Xu Yife |
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 |
Bivariate genome-wide association meta-analysis of pediatric musculoskeletal traits reveals pleiotropic effects at the SREBF1/TOM1L2 locus.
Nature communications 2017 Jul 8 (1): 121. Medina-Gomez Carolina, Kemp John P, Dimou Niki L, Kreiner Eskil, Chesi Alessandra, Zemel Babette S, Bønnelykke Klaus, Boer Cindy G, Ahluwalia Tarunveer S, Bisgaard Hans, Evangelou Evangelos, Heppe Denise H M, Bonewald Lynda F, Gorski Jeffrey P, Ghanbari Mohsen, Demissie Serkalem, Duque Gustavo, Maurano Matthew T, Kiel Douglas P, Hsu Yi-Hsiang, C J van der Eerden Bram, Ackert-Bicknell Cheryl, Reppe Sjur, Gautvik Kaare M, Raastad Truls, Karasik David, van de Peppel Jeroen, Jaddoe Vincent W V, Uitterlinden André G, Tobias Jonathan H, Grant Struan F A, Bagos Pantelis G, Evans David M, Rivadeneira Fernan |
Dietary cholesterol interacts with SREBF1 to modulate obesity in Chinese children. Molecular nutrition & food research 2017 09 61 (9): . Zhang Shixiu, Lin Xinying, Lynn Henry, Xu Guifa, Li Jun, Zhao Changfeng, Li Mingm |
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 |
Impact of polymorphism of selected genes on the diagnosis of type 2 diabetes in patients with obstructive sleep apnea. Polish archives of internal medicine 2019 1 129 (1): 6-11. Bielicki Piotr, P?ywaczewski Robert, Brzóska Kamil, Kumor Marta, Barna? Ma?gorzata, Jonczak Luiza, St?pkowski Tomasz M, Piechuta Aleksandra, Chazan Ryszarda, ?liwi?ski Pawe?, Kruszewski Marc |
Genetic variants associated with expression of TCF19 contribute to the risk of head and neck cancer in Chinese population. Journal of medical genetics 2021 Mar . Ji Pei, Chang Jiang, Wei Xiaoyu, Song Xueyao, Yuan Hua, Gong Linnan, Li Yuancheng, Ding Dongsheng, Zhang Erbao, Yan Caiwang, Zhu Meng, Miao Xiaoping, Wu Chen, Jin Guangfu, Hu Zhibin, Shen Hongbing, Ma Hongx |
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 |
By characterizing metabolic and immune microenvironment reveal potential prognostic markers in the development of colorectal cancer. Frontiers in bioengineering and biotechnology 2022 8 10 822835. Liao Liangliang, Gao Yongjian, Su Jie, Feng |
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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