Human Genome Epidemiology Literature Finder
Records 1 - 14 (of 14 Records) |
Query Trace: COL13A1[original query] |
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Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.
Gastroenterology 2010 Nov 139 (5): 1567-76, 1576.e1-6. Chalasani Naga, Guo Xiuqing, Loomba Rohit, Goodarzi Mark O, Haritunians Talin, Kwon Soonil, Cui Jinrui, Taylor Kent D, Wilson Laura, Cummings Oscar W, Chen Yii-Der Ida, Rotter Jerome I, |
A genome-wide association study of inflammatory biomarker changes in response to fenofibrate treatment in the Genetics of Lipid Lowering Drug and Diet Network.
Pharmacogenetics and genomics 2012 Mar 22 (3): 191-7. Aslibekyan Stella, Kabagambe Edmond K, Irvin Marguerite R, Straka Robert J, Borecki Ingrid B, Tiwari Hemant K, Tsai Michael Y, Hopkins Paul N, Shen Jian, Lai Chao-Qiang, Ordovas Jose M, Arnett Donna |
Pooled genetic analysis in ultrasound measured non-alcoholic fatty liver disease in Indian subjects: A pilot study. World journal of hepatology 2014 Jun 6 (6): 435-42. Kanth Vishnubhotla Venkata Ravi, Sasikala Mitnala, Rao Padaki Nagaraja, Steffie Avanthi Urmila, Rao Kalashikam Rajender, Nageshwar Reddy Duvvu |
Association of polymorphisms in GCKR and TRIB1 with nonalcoholic fatty liver disease and metabolic syndrome traits. Endocrine journal 2014 61 (7): 683-9. Kitamoto Aya, Kitamoto Takuya, Nakamura Takahiro, Ogawa Yuji, Yoneda Masato, Hyogo Hideyuki, Ochi Hidenori, Mizusawa Seiho, Ueno Takato, Nakao Kazuwa, Sekine Akihiro, Chayama Kazuaki, Nakajima Atsushi, Hotta Kiku |
GWAS-Identified Common Variants With Nonalcoholic Fatty Liver Disease in Chinese Children. Journal of pediatric gastroenterology and nutrition 2015 May 60 (5): 669-74. Shang Xiao-Rui, Song Jie-Yun, Liu Fang-Hong, Ma Jun, Wang Hai-J |
Brief Report: Whole-Exome Sequencing for Identification of Potential Causal Variants for Diffuse Cutaneous Systemic Sclerosis. Arthritis & rheumatology (Hoboken, N.J.) 2016 Apr . Mak Angel Cy, Tang Paul Lf, Cleveland Clare, Smith Melanie H, Connolly M Kari, Katsumoto Tamiko R, Wolters Paul J, Kwok Pui-Yan, Criswell Lindsey |
Monozygotic twins with NASH cirrhosis: cumulative effect of multiple single nucleotide polymorphisms? Annals of hepatology 0 15 (2): 277-82. Grove Jane I, Austin Mark, Tibble Jeremy, Aithal Guruprasad P, Verma Sumi |
Brief Report: Whole-Exome Sequencing to Identify Rare Variants and Gene Networks That Increase Susceptibility to Scleroderma in African Americans. Arthritis & rheumatology (Hoboken, N.J.) 2018 May . Gourh Pravitt, Remmers Elaine F, Boyden Steven E, Alexander Theresa, Morgan Nadia D, Shah Ami A, Mayes Maureen D, Doumatey Ayo, Bentley Amy R, Shriner Daniel, Domsic Robyn T, Medsger Thomas A, Steen Virginia D, Ramos Paula S, Silver Richard M, Korman Benjamin, Varga John, Schiopu Elena, Khanna Dinesh, Hsu Vivien, Gordon Jessica K, Saketkoo Lesley Ann, Gladue Heather, Kron Brynn, Criswell Lindsey A, Derk Chris T, Bridges S Louis, Shanmugam Victoria K, Kolstad Kathleen D, Chung Lorinda, Jan Reem, Bernstein Elana J, Goldberg Avram, Trojanowski Marcin, Kafaja Suzanne, Maksimowicz-McKinnon Kathleen M, Mullikin James C, Adeyemo Adebowale, Rotimi Charles, Boin Francesco, Kastner Daniel L, Wigley Fredrick |
A genome wide association study identifies new genes potentially associated with eyelid sagging.
Experimental dermatology 2018 Apr . Laville Vincent, Le Clerc Sigrid, Ezzedine Khaled, Jdid Randa, Taing Lieng, Labib Toufik, Coulonges Cédric, Ulveling Damien, Galan Pilar, Guinot Christiane, Fezeu Leopold, Morizot Frédérique, Latreille Julie, Malvy Denis, Tschachler Erwin, Zagury Jean-Franço |
Genetic variants in COL13A1, ADIPOQ and SAMM50, in addition to the PNPLA3 gene, confer susceptibility to elevated transaminase levels in an admixed Mexican population. Experimental and molecular pathology 2018 Jan 104 (1): 50-58. Larrieta-Carrasco Elena, Flores Yvonne N, Macías-Kauffer Luis R, Ramírez-Palacios Paula, Quiterio Manuel, Ramírez-Salazar Eric G, León-Mimila Paola, Rivera-Paredez Berenice, Cabrera-Álvarez Guillermo, Canizales-Quinteros Samuel, Zhang Zuo-Feng, López-Pérez Tania V, Salmerón Jorge, Velázquez-Cruz Rafa |
Relationship between N,N-dimethylformamide exposure, PNPLA3, GCKR, COL13A1 and TM6SF2 genes, and liver injury. Ecotoxicology and environmental safety 2019 1 171 347-351. Zhang Xiaoyue, Jiang Haiyue, Shen Jiayang, Zhang Yu, Gu Yiyang, Xiao Jing, Lian Yulo |
Validation of genetic variants associated with metabolic dysfunction-associated fatty liver disease in an ethnic Chinese population. World journal of hepatology 2020 Dec 12 (12): 1228-1238. Lee Guan Huei, Phyo Wah Wah, Loo Wai Mun, Kwok Raymond, Ahmed Taufique, Shabbir Asim, So Jimmy, Koh Calvin Jianyi, Hartono Juanda Leo, Muthiah Mark, Lim Kieron, Tan Poh Seng, Lee Yin Mei, Lim Seng Gee, Dan Yock You |
Alu Deletions in LAMA2 and CDH4 Genes Are Key Components of Polygenic Predictors of Longevity. International journal of molecular sciences 2022 11 23 (21): . Erdman Vera V, Karimov Denis D, Tuktarova Ilsia A, Timasheva Yanina R, Nasibullin Timur R, Korytina Gulnaz |
The clinical and molecular landscape of congenital myasthenic syndromes in Austria: a nationwide study. Journal of neurology 2022 10 270 (2): 909-916. Krenn Martin, Sener Merve, Rath Jakob, Zulehner Gudrun, Keritam Omar, Wagner Matias, Laccone Franco, Iglseder Stephan, Marte Sonja, Baumgartner Manuela, Eisenkölbl Astrid, Liechtenstein Christian, Rudnik Sabine, Quasthoff Stefan, Grinzinger Susanne, Spenger Johannes, Wortmann Saskia B, Löscher Wolfgang N, Zimprich Fritz, Kellersmann Anna, Rappold Mika, Bernert Günther, Freilinger Michael, Cetin Hak |
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- Page last updated:Apr 22, 2024
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