Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 69 Records) |
| Query Trace: Disease and NRG1[original query] |
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| Papillary Thyroid Carcinoma: Association Between Germline DNA Variant Markers and Clinical Parameters. Thyroid : official journal of the American Thyroid Association 2016 09 26 (9): 1276-84. Jendrzejewski Jaroslaw, Liyanarachchi Sandya, Nagy Rebecca, Senter Leigha, Wakely Paul E, Thomas Andrew, Nabhan Fadi, He Huiling, Li Wei, Sworczak Krzysztof, Ringel Matthew D, Kirschner Lawrence S, de la Chapelle Albe |
| Cumulative Risk Impact of RET, SEMA3, and NRG1 Polymorphisms Associated With Hirschsprung Disease in Han Chinese. Journal of pediatric gastroenterology and nutrition 2016 May . Li Qi, Zhang Zhen, Diao Mei, Gan Liang, Cheng Wei, Xiao Ping, Su Lin, Shangguan Shaofang, Jiang Qian, Li Lo |
| Effects of NRG1 genotypes on orbitofrontal sulcogyral patterns in Japanese patients diagnosed with schizophrenia. Psychiatry and clinical neurosciences 2016 Jul 70 (7): 261-8. Yoshimi Asuka, Suda Akira, Hayano Fumi, Nakamura Motoaki, Aoyama-Uehara Kumi, Konishi Jun, Asami Takeshi, Kishida Ikuko, Kawanishi Chiaki, Inoue Tomio, McCarley Robert W, Shenton Martha E, Hirayasu Yosh |
Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease.
Human molecular genetics 2016 Oct . Tang Clara Sze-Man, Gui Hongsheng, Kapoor Ashish, Kim Jeong-Hyun, Luzón-Toro Berta, Pelet Anna, Burzynski Grzegorz, Lantieri Francesca, So Man-Ting, Berrios Courtney, Shin Hyoung Doo, Fernández Raquel M, Le Thuy-Linh, Verheij Joke B G M, Matera Ivana, Cherny Stacey S, Nandakumar Priyanka, Cheong Hyun Sub, Antiñolo Guillermo, Amiel Jeanne, Seo Jeong-Meen, Kim Dae-Yeon, Oh Jung-Tak, Lyonnet Stanislas, Borrego Salud, Ceccherini Isabella, Hofstra Robert M W, Chakravarti Aravinda, Kim Hyun-Young, Sham Pak Chung, Tam Paul K H, Garcia-Barceló Maria-Mer |
| Evaluation of genetic association of neurodevelopment and neuroimmunological genes with antipsychotic treatment response in schizophrenia in Indian populations. Molecular genetics & genomic medicine 2016 Jan 4 (1): 18-27. Jajodia Ajay, Kaur Harpreet, Kumari Kalpana, Kanojia Neha, Gupta Meenal, Baghel Ruchi, Sood Mamta, Jain Sanjeev, Chadda Rakesh K, Kukreti Ritushr |
| Whole-Exome Sequencing Analyses of Inflammatory Bowel Disease-Associated Colorectal Cancers. Gastroenterology 2016 Jan . Robles Ana I, Traverso Giovanni, Zhang Ming, Roberts Nicholas J, Khan Mohammed A, Joseph Christine, Lauwers Gregory Y, Selaru Florin M, Popoli Maria, Pittman Meredith E, Ke Xiquan, Hruban Ralph H, Meltzer Stephen J, Kinzler Kenneth W, Vogelstein Bert, Harris Curtis C, Papadopoulos Nickol |
| Effects of NRG1 Polymorphisms on Hirschsprung's Disease Susceptibility: A Meta-analysis. Scientific reports 2017 Aug 7 (1): 9913. Jiang Meng, Li Changli, Cao Guoqing, Yang Dehua, Zhang Xi, Yang Li, Li Shuai, Tang Shao-T |
| Effects of RET, NRG1 and NRG3 Polymorphisms in a Chinese Population with Hirschsprung Disease. Scientific reports 2017 Mar 7 43222. Yang Dehua, Yang Jun, Li Shuai, Jiang Meng, Cao Guoqing, Yang Li, Zhang Xi, Zhou Ying, Li Kang, Tang Shao-T |
| The association between gene variants and longitudinal structural brain changes in psychosis: a systematic review of longitudinal neuroimaging genetics studies. NPJ schizophrenia 2017 Nov 3 (1): 40. Harari Julia H, Díaz-Caneja Covadonga M, Janssen Joost, Martínez Kenia, Arias Bárbara, Arango Cel |
| Noncoding RET variants explain the strong association with Hirschsprung disease in patients without rare coding sequence variant.
European journal of medical genetics 2018 Jul . Virtanen Valtter B, Salo Perttu P, Cao Jia, Löf-Granström Anna, Milani Lili, Metspalu Andres, Rintala Risto J, Saarenpää-Heikkilä Outi, Paunio Tiina, Wester Tomas, Nordenskjöld Agneta, Perola Markus, Pakarinen Mikko |
| Genome-Wide Association Studies of Autoimmune Thyroid Diseases, Thyroid Function, and Thyroid Cancer. Endocrinology and metabolism (Seoul, Korea) 2018 6 33 (2): 175-184. Hwangbo Yul, Park Young J |
| A Genetic Study of Psychosis in Huntington's Disease: Evidence for the Involvement of Glutamate Signaling Pathways. Journal of Huntington's disease 2018 7 (1): 51-59. Tsuang Debby W, Greenwood Tiffany A, Jayadev Suman, Davis Marie, Shutes-David Andrew, Bird Thomas |
| Combined Genetic Effects of RET and NRG1 Susceptibility Variants on Multifactorial Hirschsprung Disease in Indonesia. The Journal of surgical research 2019 Jan 233 96-99. Gunadi , Iskandar Kristy, Makhmudi Akhmad, Kapoor Ashi |
| Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locus.
European journal of human genetics : EJHG 2018 Jan . Fadista João, Lund Marie, Skotte Line, Geller Frank, Nandakumar Priyanka, Chatterjee Sumantra, Matsson Hans, Granström Anna Löf, Wester Tomas, Salo Perttu, Virtanen Valtter, Carstensen Lisbeth, Bybjerg-Grauholm Jonas, Hougaard David Michael, Pakarinen Mikko, Perola Markus, Nordenskjöld Agneta, Chakravarti Aravinda, Melbye Mads, Feenstra Bjar |
| Association of NRG1 and AUTS2 genetic polymorphisms with Hirschsprung disease in a South Chinese population. Journal of cellular and molecular medicine 2018 Jan . Zhang Yan, Xie Xiaoli, Zeng Jixiao, Wu Qiang, Zhang Ruizhong, Zhu Deli, Xia Huim |
| Distinctive genetic variation of long-segment Hirschsprung's disease in Taiwan. Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society 2019 6 31 (11): e13665. Yang Wendy, Chen Szu-Chieh, Lai Jin-Yao, Ming Yung-Ching, Chen Jeng-Chang, Chen Pei-Lu |
| Association of Neuregulin 1 rs7835688?G?>?C, rs16879552 T?>?C and rs2439302?G?>?C Polymorphisms with Susceptibility to Non-Syndromic Hirschsprung's Disease. Fetal and pediatric pathology 2019 Nov 1-8. Hosseini-Jangjou Seyed Hamed, Dastgheib Seyed Alireza, Aflatoonian Majid, Amooee Abdolhamid, Bahrami Reza, Salehi Elham, Sadeghizadeh-Yazdi Jalal, Neamatzadeh Hosse |
| Genome-Wide Association Analysis of Single-Breath Dl.
American journal of respiratory cell and molecular biology 2019 Jan . Sakornsakolpat Phuwanat, McCormack Meredith, Bakke Per, Gulsvik Amund, Make Barry J, Crapo James D, Cho Michael H, Silverman Edwin |
| Clinical and Clinical-Pharmacogenetic Models for Prediction of the Most Common Psychiatric Complications Due to Dopaminergic Treatment in Parkinson's Disease. The international journal of neuropsychopharmacology 2020 7 23 (8): 496-504. Redenšek Sara, Jenko Bizjan Barbara, Trošt Maja, Dolžan Vi |
| Common variants of NRG1 and ITGB4 confer risk of Hirschsprung disease in Han Chinese population. Journal of pediatric surgery 2020 Apr . Wei Zhiliang, Yu Xianxian, Wu Wenjie, Bai Meirong, Lu Yanjiao, Song Huanlei, Gong Yiming, Gu Beilin, Chu Xun, Cai W |
| Genetic polymorphisms in neuroendocrine disorder-related candidate genes associated with pre-pregnancy obesity in gestational diabetes mellitus patients by using a stratification approach. Annals of translational medicine 2020 11 8 (17): 1060. Lee Kai Wei, Ching Siew Mooi, Devaraj Navin Kumar, Hoo Fan K |
| Early-Onset Schizophrenia: A Special Phenotype of the Disease Characterized by Increased MTHFR Polymorphisms and Aggravating Symptoms. Neuropsychiatric disease and treatment 2021 8 17 2511-2525. Wan Lin, Wei Ji |
| Genetic alteration of Chinese patients with rectal mucosal melanoma. BMC cancer 2021 May 21 (1): 623. Li Huan, Yang Lujing, Lai Yumei, Wang Xintong, Han Xinyin, Liu Siyao, Wang Dongliang, Li Xiaojuan, Hu Nana, Kong Yan, Si Lu, Li Zhong |
| Multiple, independent, common variants at RET, SEMA3 and NRG1 gut enhancers specify Hirschsprung disease risk in European ancestry subjects. Journal of pediatric surgery 2021 Apr . Kapoor Ashish, Nandakumar Priyanka, Auer Dallas R, Sosa Maria X, Ross Holly, Bollinger Juli, Yan Jia, Berrios Courtney, , Chakravarti Aravin |
| Early-Onset Pancreas Cancer: Clinical Descriptors, Genomics, and Outcomes. Journal of the National Cancer Institute 2021 3 113 (9): 1194-1202. Varghese Anna M, Singh Isha, Singh Rituraj, Kunte Siddharth, Chou Joanne F, Capanu Marinela, Wong Winston, Lowery Maeve A, Stadler Zsofia K, Salo-Mullen Erin, Saadat Lily V, Wei Alice C, Reyngold Marsha, Basturk Olca, Benayed Ryma, Mandelker Diana, Iacobuzio-Donahue Christine A, Kelsen David P, Park Wungki, Yu Kenneth H, O'Reilly Eileen |
| Investigating the Association Between rs2439302 Polymorphism and Thyroid Cancer: A Systematic Review and Meta-Analysis. Frontiers in surgery 2022 9 877206. Guo Yawen, Zhang Wanchen, He Ru, Zheng Chuanming, Liu Xuefeng, Ge Minghua, Xu Jiaj |
| Significant Association of rs77493513 Polymorphism in 3'-UTR of the NRG1 Gene with the Risk of Multiple Sclerosis Disease. Metabolic brain disease 2022 Feb . Ghorbani Maedeh, Mohamadynejad Parisa, Moghanibashi Meh |
| Whole genome sequencing reveals epistasis effects within RET for Hirschsprung disease. Scientific reports 2022 11 12 (1): 20423. Wang Yanbing, Mak Timothy Shin Heng, Dattani Saloni, Garcia-Barcelo Maria-Merce, Fu Alexander Xi, Yip Kevin Y, Ngan Elly Sau-Wai, Tam Paul Kwang-Hang, Tang Clara Sze-Man, Sham Pak Chu |
| The interplay of common genetic variants NRG1 rs2439302 and RET rs2435357 increases the risk of developing Hirschsprung's disease. Frontiers in cell and developmental biology 2023 7 11 1184799. Shuiqing Chi, Shuai Li, Guoqing Cao, Jialing Guo, Yunqiao Han, Yun Zhou, Xi Zhang, Yibo Li, Zhibin Luo, Xiangyang Li, Liying Rong, Mengxin Zhang, Linglu Li, Shaotao Ta |
| Neuregulin 1 as a potential biomarker for disease progression in moyamoya disease: A case-control study in Chinese population. Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2024 1 33 (3): 107581. Jie Chen, Hanyue Zheng, Xiaoxin Wu, Xingyang Niu, Yuanyuan Dai, Zhenhua Zhou, Fei |
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