Human Genome Epidemiology Literature Finder
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Query Trace: CPS1[original query] |
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Novel associations of CPS1, MUT, NOX4, and DPEP1 with plasma homocysteine in a healthy population: a genome-wide evaluation of 13 974 participants in the Women's Genome Health Study.
Circulation. Cardiovascular genetics 2009 Apr 2 (2): 142-50. Paré Guillaume, Chasman Daniel I, Parker Alexander N, Zee Robert R Y, Mälarstig Anders, Seedorf Udo, Collins Rory, Watkins Hugh, Hamsten Anders, Miletich Joseph P, Ridker Paul |
The T1405N carbamoyl phosphate synthetase polymorphism does not affect plasma arginine concentrations in preterm infants. PloS one 2010 5 (5): e10792. Moonen Rob M J, Reyes Iballa, Cavallaro Giacomo, González-Luis Gema, Bakker Jaap A, Villamor Eduar |
New loci associated with kidney function and chronic kidney disease.
Nature genetics 2010 May 42 (5): 376-84. Köttgen Anna, Pattaro Cristian, Böger Carsten A, Fuchsberger Christian, Olden Matthias, Glazer Nicole L, Parsa Afshin, Gao Xiaoyi, Yang Qiong, Smith Albert V, O'Connell Jeffrey R, Li Man, Schmidt Helena, Tanaka Toshiko, Isaacs Aaron, Ketkar Shamika, Hwang Shih-Jen, Johnson Andrew D, Dehghan Abbas, Teumer Alexander, Paré Guillaume, Atkinson Elizabeth J, Zeller Tanja, Lohman Kurt, Cornelis Marilyn C, Probst-Hensch Nicole M, Kronenberg Florian, Tönjes Anke, Hayward Caroline, Aspelund Thor, Eiriksdottir Gudny, Launer Lenore J, Harris Tamara B, Rampersaud Evadnie, Mitchell Braxton D, Arking Dan E, Boerwinkle Eric, Struchalin Maksim, Cavalieri Margherita, Singleton Andrew, Giallauria Francesco, Metter Jeffrey, de Boer Ian H, Haritunians Talin, Lumley Thomas, Siscovick David, Psaty Bruce M, Zillikens M Carola, Oostra Ben A, Feitosa Mary, Province Michael, de Andrade Mariza, Turner Stephen T, Schillert Arne, Ziegler Andreas, Wild Philipp S, Schnabel Renate B, Wilde Sandra, Munzel Thomas F, Leak Tennille S, Illig Thomas, Klopp Norman, Meisinger Christa, Wichmann H-Erich, Koenig Wolfgang, Zgaga Lina, Zemunik Tatijana, Kolcic Ivana, Minelli Cosetta, Hu Frank B, Johansson Asa, Igl Wilmar, Zaboli Ghazal, Wild Sarah H, Wright Alan F, Campbell Harry, Ellinghaus David, Schreiber Stefan, Aulchenko Yurii S, Felix Janine F, Rivadeneira Fernando, Uitterlinden Andre G, Hofman Albert, Imboden Medea, Nitsch Dorothea, Brandstätter Anita, Kollerits Barbara, Kedenko Lyudmyla, Mägi Reedik, Stumvoll Michael, Kovacs Peter, Boban Mladen, Campbell Susan, Endlich Karlhans, Völzke Henry, Kroemer Heyo K, Nauck Matthias, Völker Uwe, Polasek Ozren, Vitart Veronique, Badola Sunita, Parker Alexander N, Ridker Paul M, Kardia Sharon L R, Blankenberg Stefan, Liu Yongmei, Curhan Gary C, Franke Andre, Rochat Thierry, Paulweber Bernhard, Prokopenko Inga, Wang Wei, Gudnason Vilmundur, Shuldiner Alan R, Coresh Josef, Schmidt Reinhold, Ferrucci Luigi, Shlipak Michael G, van Duijn Cornelia M, Borecki Ingrid, Krämer Bernhard K, Rudan Igor, Gyllensten Ulf, Wilson James F, Witteman Jacqueline C, Pramstaller Peter P, Rettig Rainer, Hastie Nick, Chasman Daniel I, Kao W H, Heid Iris M, Fox Caroline |
Genome-wide association study of homocysteine levels in Filipinos provides evidence for CPS1 in women and a stronger MTHFR effect in young adults.
Human molecular genetics 2010 May 19 (10): 2050-8. Lange Leslie A, Croteau-Chonka Damien C, Marvelle Amanda F, Qin Li, Gaulton Kyle J, Kuzawa Christopher W, McDade Thomas W, Wang Yunfei, Li Yun, Levy Shawn, Borja Judith B, Lange Ethan M, Adair Linda S, Mohlke Karen |
Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease.
The American journal of clinical nutrition 2013 Sep 98 (3): 668-76. van Meurs Joyce B J, Pare Guillaume, Schwartz Stephen M, Hazra Aditi, Tanaka Toshiko, Vermeulen Sita H, Cotlarciuc Ioana, Yuan Xin, Mälarstig Anders, Bandinelli Stefania, Bis Joshua C, Blom Henk, Brown Morris J, Chen Constance, Chen Yii-Der, Clarke Robert J, Dehghan Abbas, Erdmann Jeanette, Ferrucci Luigi, Hamsten Anders, Hofman Albert, Hunter David J, Goel Anuj, Johnson Andrew D, Kathiresan Sekar, Kampman Ellen, Kiel Douglas P, Kiemeney Lambertus A L M, Chambers John C, Kraft Peter, Lindemans Jan, McKnight Barbara, Nelson Christopher P, O'Donnell Christopher J, Psaty Bruce M, Ridker Paul M, Rivadeneira Fernando, Rose Lynda M, Seedorf Udo, Siscovick David S, Schunkert Heribert, Selhub Jacob, Ueland Per M, Vollenweider Peter, Waeber Gérard, Waterworth Dawn M, Watkins Hugh, Witteman Jacqueline C M, den Heijer Martin, Jacques Paul, Uitterlinden Andre G, Kooner Jaspal S, Rader Dan J, Reilly Muredach P, Mooser Vincent, Chasman Daniel I, Samani Nilesh J, Ahmadi Kourosh |
Genetic variants associated with glycine metabolism and their role in insulin sensitivity and type 2 diabetes.
Diabetes 2013 Feb . Xie W, Wood AR, Lyssenko V, Weedon MN, Knowles JW, Alkayyali S, Assimes TL, Quertermous T, Abbasi F, Paananen J, Häring H, Hansen T, Pedersen O, Smith U, Laakso M, Dekker JM, Nolan JJ, Groop L, Ferrannini E, Adam KP, Gall WE, Frayling TM, Walker M |
4217C>A polymorphism in carbamoyl-phosphate synthase 1 gene may not associate with hyperammonemia development during valproic acid-based therapy. Epilepsy research 2014 Aug 108 (6): 1046-51. Inoue Kazuyuki, Suzuki Eri, Takahashi Toshiki, Yamamoto Yoshiaki, Yazawa Rei, Takahashi Yukitoshi, Imai Katsumi, Miyakawa Kou, Inoue Yushi, Tsuji Daiki, Hayashi Hideki, Itoh Kunihi |
Genome-wide meta-analysis of homocysteine and methionine metabolism identifies five one carbon metabolism loci and a novel association of ALDH1L1 with ischemic stroke.
PLoS genetics 2014 Mar 10 (3): e1004214. Williams Stephen R, Yang Qiong, Chen Fang, Liu Xuan, Keene Keith L, Jacques Paul, Chen Wei-Min, Weinstein Galit, Hsu Fang-Chi, Beiser Alexa, Wang Liewei, Bookman Ebony, Doheny Kimberly F, Wolf Philip A, Zilka Michelle, Selhub Jacob, Nelson Sarah, Gogarten Stephanie M, Worrall Bradford B, Seshadri Sudha, Sale Michèle M, , |
Genetic determinants influencing human serum metabolome among African Americans.
PLoS genetics 2014 Mar 10 (3): e1004212. Yu Bing, Zheng Yan, Alexander Danny, Morrison Alanna C, Coresh Josef, Boerwinkle Er |
Genome-Wide Association Study with Targeted and Non-targeted NMR Metabolomics Identifies 15 Novel Loci of Urinary Human Metabolic Individuality.
PLoS genetics 2015 Sep 11 (9): e1005487. Raffler Johannes, Friedrich Nele, Arnold Matthias, Kacprowski Tim, Rueedi Rico, Altmaier Elisabeth, Bergmann Sven, Budde Kathrin, Gieger Christian, Homuth Georg, Pietzner Maik, Römisch-Margl Werner, Strauch Konstantin, Völzke Henry, Waldenberger Melanie, Wallaschofski Henri, Nauck Matthias, Völker Uwe, Kastenmüller Gabi, Suhre Karst |
Insight in genome-wide association of metabolite quantitative traits by exome sequence analyses.
PLoS genetics 2015 Jan 11 (1): e1004835. Demirkan Ayse, Henneman Peter, Verhoeven Aswin, Dharuri Harish, Amin Najaf, van Klinken Jan Bert, Karssen Lennart C, de Vries Boukje, Meissner Axel, Göraler Sibel, van den Maagdenberg Arn M J M, Deelder André M, C 't Hoen Peter A, van Duijn Cornelia M, van Dijk Ko Wille |
Ayurgenomics for stratified medicine: TRISUTRA consortium initiative across ethnically and geographically diverse Indian populations. Journal of ethnopharmacology 2016 Jul . Prasher Bhavana, Varma Binuja, Kumar Arvind, Khuntia Bharat Krushna, Pandey Rajesh, Narang Ankita, Tiwari Pradeep, Kutum Rintu, Guin Debleena, Kukreti Ritushree, Dash Debasis, , Mukerji Mita |
Cumulative effect of the plasma total homocysteine-related genetic variants on schizophrenia risk. Psychiatry research 2016 Oct . Kinoshita Makoto, Numata Shusuke, Tajima Atsushi, Nishi Akira, Muraki Sho, Tsuchiya Atsushi, Umehara Hidehiro, Watanabe Shin-Ya, Imoto Issei, Ohmori Tetsu |
Association between the p.Thr1406Asn polymorphism of the carbamoyl-phosphate synthetase 1 gene and necrotizing enterocolitis: A prospective multicenter study. Scientific reports 2016 Nov 6 36999. Moonen Rob M, Cavallaro Giacomo, Huizing Maurice J, González-Luis Gema E, Mosca Fabio, Villamor Eduar |
Genome-wide association study and targeted metabolomics identifies sex-specific association of CPS1 with coronary artery disease.
Nature communications 2016 Jan 7 10558. Hartiala Jaana A, Tang W H Wilson, Wang Zeneng, Crow Amanda L, Stewart Alexandre F R, Roberts Robert, McPherson Ruth, Erdmann Jeanette, Willenborg Christina, Hazen Stanley L, Allayee Hoom |
Polymorphisms in urea cycle enzyme genes are associated with persistent pulmonary hypertension of the newborn. Pediatric research 2017 Jun . Kaluarachchi Dinushan C, Smith Caitlin J, Klein Jonathan M, Murray Jeffrey C, Dagle John M, Ryckman Kelli |
Risk Factors for Valproic Acid-induced Hyperammonaemia in Chinese Paediatric Patients with Epilepsy. Basic & clinical pharmacology & toxicology 2018 May . Zhu Xu, Li Xinlin, Zhang Ti, Zhao Lim |
In Silico Preliminary Association of Ammonia Metabolism Genes GLS, CPS1, and GLUL with Risk of Alzheimer's Disease, Major Depressive Disorder, and Type 2 Diabetes. Journal of molecular neuroscience : MN 2018 2 64 (3): 385-396. Griffin Jeddidiah W D, Liu Ying, Bradshaw Patrick C, Wang Keshe |
Genome-wide association study of homocysteine in African Americans from the Jackson Heart Study, the Multi-Ethnic Study of Atherosclerosis, and the Coronary Artery Risk in Young Adults study. Journal of human genetics 2018 Mar 63 (3): 327-337. Raffield Laura M, Ellis Jaclyn, Olson Nels C, Duan Qing, Li Jin, Durda Peter, Pankratz Nathan, Keating Brendan J, Wassel Christina L, Cushman Mary, Wilson James G, Gross Myron D, Tracy Russell P, Rich Stephen S, Reiner Alex P, Li Yun, Willis Monte S, Lange Ethan M, Lange Leslie |
Identification of genetic factors underlying persistent pulmonary hypertension of newborns in a cohort of Chinese neonates. Respiratory research 2019 Aug 20 (1): 174. Liu Xu, Mei Mei, Chen Xiang, Lu Yulan, Dong Xinran, Hu Liyuan, Hu Xiaojing, Cheng Guoqiang, Cao Yun, Yang Lin, Zhou Wenh |
Is there any relationship between mutation in CPS1 Gene and pregnancy loss? International journal of reproductive biomedicine 2019 8 17 (5): 371-4. Talebi Mehrdad, Yahya Vahidi Mehrjardi Mohammad, Kalhor Kambiz, Dehghani Mohammadre |
CPS1 T1405N polymorphism, HDL cholesterol, homocysteine and renal function are risk factors of VPA induced hyperammonemia among epilepsy patients. Epilepsy research 2019 May 154 139-143. Chen Lanlan, Tian Qiuxiang, Zhang Miaoran, Chen Deyu, Gao Xue, Yang Hongqun, Li Haitao, Li Chengnan, Wen Jianping, Li Yulin, Tian Xin, Chen Pe |
Genetic basis for plasma amino acid concentrations based on absolute quantification: a genome-wide association study in the Japanese population.
European journal of human genetics : EJHG 2019 Apr 27 (4): 621-630. Imaizumi Akira, Adachi Yusuke, Kawaguchi Takahisa, Higasa Koichiro, Tabara Yasuharu, Sonomura Kazuhiro, Sato Taka-Aki, Takahashi Meiko, Mizukoshi Toshimi, Yoshida Hiro-O, Kageyama Naoko, Okamoto Chisato, Takasu Mariko, Mori Maiko, Noguchi Yasushi, Shimba Nobuhisa, Miyano Hiroshi, Yamada Ryo, Matsuda Fumihi |
Association of CPS1 rs1047891 SNP and serum lipid levels in two Chinese ethnic groups. International journal of clinical and experimental pathology 2020 1 11 (5): 2887-2900. Yang Shuo, Yin Rui-Xing, Miao Liu, Zhang Qing-Hui, Zhou Yong-Gang, Wu J |
Genetic Predictors for Sinusoidal Obstruction Syndrome-A Systematic Review. Journal of personalized medicine 2021 4 11 (5): . Waespe Nicolas, Strebel Sven, Jurkovic Mlakar Simona, Krajinovic Maja, Kuehni Claudia Elisabeth, Nava Tiago, Ansari Ma |
Possible association between a polymorphism of EPAS1 gene and persistent pulmonary hypertension of the newborn: a case-control study. Jornal de pediatria 2021 Oct . Nakwan Narongsak, Mahasirimongkol Surakameth, Satproedprai Nusara, Chaiyasung Tassamonwan, Kunhapan Punna, Charoenlap Cheep, Singkhamanan Kamonnut, Charalsawadi Chariyaw |
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 |
Liver injury in non-alcoholic fatty liver disease is associated with urea cycle enzyme dysregulation. Scientific reports 2022 3 12 (1): 3418. Gallego-Durán Rocío, Ampuero Javier, Pastor-Ramírez Helena, Álvarez-Amor Leticia, Del Campo Jose Antonio, Maya-Miles Douglas, Montero-Vallejo Rocío, Cárdenas-García Antonio, Pareja Mª Jesús, Gato-Zambrano Sheila, Millán Raquel, Del Carmen Rico María, Luque-Sierra Amparo, Gil-Gómez Antonio, Rojas Ángela, Muñoz-Hernández Rocío, García-Lozano María, Aller Rocío, Andrade Raúl J, García-Monzón Carmelo, Andreola Fausto, Martín Francisco, Jalan Rajiv, Romero-Gómez Manu |
Genetic variants and effect modifiers of QT interval prolongation in patients with sickle cell disease. Gene 2023 9 890 147824. Mengna Zhang, William B Hillegass, Xue Yu, Suvankar Majumdar, J Daryl Pollard, Erin Jackson, Jarrod Knudson, Douglas Wolfe, Gregory J Kato, Joseph F Maher, Hao M |
Underexpression of Carbamoyl Phosphate Synthetase I as Independent Unfavorable Prognostic Factor in Intrahepatic Cholangiocarcinoma: A Potential Theranostic Biomarker. Diagnostics (Basel, Switzerland) 2023 7 13 (13): . Khaa Hoo Ong, Yao-Yu Hsieh, Ding-Ping Sun, Steven Kuan-Hua Huang, Yu-Feng Tian, Chia-Ling Chou, Yow-Ling Shiue, Keva Joseph, I-Wei Cha |
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