Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 43 Records) |
Query Trace: EFEMP1[original query] |
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Mitochondrial DNA variants can mediate methylation status of inflammation, angiogenesis and signaling genes. Human molecular genetics 2015 Aug 24 (16): 4491-503. Atilano Shari R, Malik Deepika, Chwa Marilyn, Cáceres-Del-Carpio Javier, Nesburn Anthony B, Boyer David S, Kuppermann Baruch D, Jazwinski S Michal, Miceli Michael V, Wallace Douglas C, Udar Nitin, Kenney M Cristi |
Association of EFEMP1 gene polymorphisms with the risk of glioma: A hospital-based case-control study in a Chinese Han population. Journal of the neurological sciences 2015 Feb 349 (1-2): 54-9. Zhang Shuo, Ye Zhao, Song Xiao, Chen Gong, Huai Cong, Wang Qihan, Song Jianping, Lu Daru, Zhao Yao, Chen Hongy |
A genome-wide association study identifies four novel susceptibility loci underlying inguinal hernia.
Nature communications 2015 Dec 6 10130. Jorgenson Eric, Makki Nadja, Shen Ling, Chen David C, Tian Chao, Eckalbar Walter L, Hinds David, Ahituv Nadav, Avins Andr |
Polygenic associations of neurodevelopmental genes in suicide attempt. Molecular psychiatry 2015 Dec . Sokolowski M, Wasserman J, Wasserman |
Association between genetic variants of EGF-containing fibulin-like extracellular matrix protein1 gene and sporadic breast cancer in a Chinese Han population. European journal of gynaecological oncology 2016 37 (1): 80-5. Li X, Quan Y, Tang C, Chen |
Whole Exome Sequencing in Patients with the Cuticular Drusen Subtype of Age-Related Macular Degeneration. PloS one 2016 11 (3): e0152047. Duvvari Maheswara R, van de Ven Johannes P H, Geerlings Maartje J, Saksens Nicole T M, Bakker Bjorn, Henkes Arjen, Neveling Kornelia, Rosario Marisol Del, Westra Dineke, van den Heuvel Lambertus P W J, Schick Tina, Fauser Sascha, Boon Camiel J F, Hoyng Carel B, Jong Eiko K de, Hollander Anneke I d |
Assessing the association between EFEMP1 rs3791679 polymorphism and risk of glioma in a Chinese Han population. Genetics and molecular research : GMR 2016 Aug 15 (3): . Jiang N, Peng Y P, Wang X Y, Dou C W, He W |
EFEMP1 rs3791679 polymorphism was associated with susceptibility to glioma. International journal of clinical and experimental pathology 2015 8 (11): 15222-7. Qin Guoqiang, Qi Songtao, Lu Dan, Yu Jiangjun, Huang Weimin, Yu L |
Genome-wide association studies in East Asians identify new loci for waist-hip ratio and waist circumference.
Scientific reports 2016 6 17958. Wen Wanqing, Kato Norihiro, Hwang Joo-Yeon, Guo Xingyi, Tabara Yasuharu, Li Huaixing, Dorajoo Rajkumar, Yang Xiaobo, Tsai Fuu-Jen, Li Shengxu, Wu Ying, Wu Tangchun, Kim Soriul, Guo Xiuqing, Liang Jun, Shungin Dmitry, Adair Linda S, Akiyama Koichi, Allison Matthew, Cai Qiuyin, Chang Li-Ching, Chen Chien-Hsiun, Chen Yuan-Tsong, Cho Yoon Shin, Choi Bo Youl, Gao Yutang, Go Min Jin, Gu Dongfeng, Han Bok-Ghee, He Meian, Hixson James E, Hu Yanling, Huang Tao, Isono Masato, Jung Keum Ji, Kang Daehee, Kim Young Jin, Kita Yoshikuni, Lee Juyoung, Lee Nanette R, Lee Jeannette, Wang Yiqin, Liu Jian-Jun, Long Jirong, Moon Sanghoon, Nakamura Yasuyuki, Nakatochi Masahiro, Ohnaka Keizo, Rao Dabeeru, Shi Jiajun, Sull Jae Woong, Tan Aihua, Ueshima Hirotsugu, Wu Chen, Xiang Yong-Bing, Yamamoto Ken, Yao Jie, Ye Xingwang, Yokota Mitsuhiro, Zhang Xiaomin, Zheng Yan, Qi Lu, Rotter Jerome I, Jee Sun Ha, Lin Dongxin, Mohlke Karen L, He Jiang, Mo Zengnan, Wu Jer-Yuarn, Tai E Shyong, Lin Xu, Miki Tetsuro, Kim Bong-Jo, Takeuchi Fumihiko, Zheng Wei, Shu Xiao- |
Impact of interaction between the G870A and EFEMP1 gene polymorphism on glioma risk in Chinese Han population. Oncotarget 2017 Jun 8 (23): 37561-37567. Yang Libin, Qu Bo, Xia Xun, Kuang Yongqin, Li Jian, Fan Kexia, Guo Heng, Zheng Hui, Ma Yu |
Genome-wide association analysis for chronic venous disease identifies EFEMP1 and KCNH8 as susceptibility loci.
Scientific reports 2017 Apr 7 45652. Ellinghaus Eva, Ellinghaus David, Krusche Petra, Greiner Aljoscha, Schreiber Claudia, Nikolaus Susanna, Gieger Christian, Strauch Konstantin, Lieb Wolfgang, Rosenstiel Philip, Frings Norbert, Fiebig Andreas, Schreiber Stefan, Franke And |
Nine differentially expressed genes from a post mortem study and their association with suicidal status in a sample of suicide completers, attempters and controls. Journal of psychiatric research 2017 Mar 91 98-104. Balestri Martina, Crisafulli Concetta, Donato Luigi, Giegling Ina, Calati Raffaella, Antypa Niki, Schneider Barbara, Marusic Dragan, Tarozzi Maria Eugenia, Marusic Dorjan, Paragi Metka, Hartmann Annette M, Konte Bettina, Marsano Agnese, Serretti Alessandro, Rujescu D |
The associations between common SNPs of EFEMP1 gene and glioma risk in Chinese population. OncoTargets and therapy 2017 10 5297-5302. Hu Jun, Dong Dong, Lu Dand |
A genome-wide association study identifies a susceptibility locus for biliary atresia on 2p16.1 within the gene EFEMP1.
PLoS genetics 2018 08 14 (8): e1007532. Chen Ying, Gilbert Melissa A, Grochowski Christopher M, McEldrew Deborah, Llewellyn Jessica, Waisbourd-Zinman Orith, Hakonarson Hakon, Bailey-Wilson Joan E, Russo Pierre, Wells Rebecca G, Loomes Kathleen M, Spinner Nancy B, Devoto Marcel |
HTRA1, an age-related macular degeneration protease, processes extracellular matrix proteins EFEMP1 and TSP1. Aging cell 2018 5 17 (4): e12710. Lin Michael K, Yang Jin, Hsu Chun Wei, Gore Anuradha, Bassuk Alexander G, Brown Lewis M, Colligan Ryan, Sengillo Jesse D, Mahajan Vinit B, Tsang Stephen |
A genome-wide association analysis identifies 16 novel susceptibility loci for carpal tunnel syndrome.
Nature communications 2019 03 10 (1): 1030. Wiberg Akira, Ng Michael, Schmid Annina B, Smillie Robert W, Baskozos Georgios, Holmes Michael V, Künnapuu K, Mägi R, Bennett David L, Furniss Domin |
Analysis of variants in Chinese individuals with primary open-angle glaucoma using molecular inversion probe (MIP)-based panel sequencing. Molecular vision 2020 26 378-391. Liu Ting, Tang Chao, Shi Xiaolo |
Association of common variation in ADD3 and GPC1 with biliary atresia susceptibility. Aging 2020 4 12 (8): 7163-7182. Bai Mei-Rong, Niu Wei-Bo, Zhou Ying, Gong Yi-Ming, Lu Yan-Jiao, Yu Xian-Xian, Wei Zhi-Liang, Wu Wenjie, Song Huan-Lei, Yu Wen-Wen, Gu Bei-Lin, Cai Wei, Chu X |
Genome-wide association identifies seven loci for pelvic organ prolapse in Iceland and the UK Biobank.
Communications biology 2020 Mar 3 (1): 129. Olafsdottir Thorhildur, Thorleifsson Gudmar, Sulem Patrick, Stefansson Olafur A, Medek Helga, Olafsson Karl, Ingthorsson Orri, Gudmundsson Valur, Jonsdottir Ingileif, Halldorsson Gisli H, Kristjansson Ragnar P, Frigge Michael L, Stefansdottir Lilja, Sigurdsson Jon K, Oddsson Asmundur, Sigurdsson Asgeir, Eggertsson Hannes P, Melsted Pall, Halldorsson Bjarni V, Lund Sigrun H, Styrkarsdottir Unnur, Steinthorsdottir Valgerdur, Gudmundsson Julius, Holm Hilma, Tragante Vinicius, Asselbergs Folkert W, Thorsteinsdottir Unnur, Gudbjartsson Daniel F, Jonsdottir Kristin, Rafnar Thorunn, Stefansson Ka |
Association between Single Nucleotide Polymorphisms and Glioma Risk: A Systematic Literature Review. Cancer investigation 2020 1 38 (3): 169-183. Tavares Cléciton Braga, Gomes-Braga Francisca das Chagas Sheyla Almeida, Sousa Emerson Brandao, Brito José Nazareno Pearce de Oliveira, Melo Mariella de Almeida, Campelo Viriato, Neto Fidelis Manes, de Araújo Ricardo Marques Lopes, Kessler Iruena Moraes, Sousa Júnior Leonardo de Moura, Filho Luís Carlos Carvalho, Aguiar Yousef Qathaf, Lopes Costa Pedro Vitor, da Silva Benedito Borg |
EFEMP1 rare variants cause familial juvenile-onset open-angle glaucoma. Human mutation 2021 12 43 (2): 240-252. Collantes Edward Ryan A, Delfin Manuel S, Fan Baojian, Torregosa Justine May R, Siguan-Bell Christine, Florcruz Nilo Vincent de Guzman, Martinez Jose Maria D, Masna-Hidalgo Barbara Joy, Guzman Vincent Paul T, Anotado-Flores Jewel Faith, Levina Faye D, Hernandez Sophia Raine C, Collantes Anthony A, Sibulo Michael Carreon, Rong Shisong, Wiggs Janey |
A genome-wide association study to investigate genetic loci associated with primary glaucoma in American Cocker Spaniels. American journal of veterinary research 2022 9 83 (11): 1-8. Gomes Filipe Espinheira, Casanova Maria Isabel, Mouttham Lara, Bannasch Danika L, Park Sangwan, Kim Soohyun, Young Laura J, Daley Nicole L, Thomasy Sara M, Castelhano Marta G, Ledbetter Eric C, Holmberg Bradford, Boyd Ryan, Van Der Woerdt Alexandra, McDonald Jessica, Hayward Jessica |
Impact of EFEMP1 on the survival outcome of biliary atresia in Thai infants. Scientific reports 2022 Sep 12 (1): 15603. Laochareonsuk Wison, Kayasut Kanita, Surachat Komwit, Chiengkriwate Piyawan, Sangkhathat Suras |
Your height affects your health: genetic determinants and health-related outcomes in Taiwan.
BMC medicine 2022 07 20 (1): 250. Chiou Jian-Shiun, Cheng Chi-Fung, Liang Wen-Miin, Chou Chen-Hsing, Wang Chung-Hsing, Lin Wei-De, Chiu Mu-Lin, Cheng Wei-Chung, Lin Cheng-Wen, Lin Ting-Hsu, Liao Chiu-Chu, Huang Shao-Mei, Tsai Chang-Hai, Lin Ying-Ju, Tsai Fuu-J |
Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidate. Brain : a journal of neurology 2022 5 145 (6): 1992-2007. Mishra Aniket, Duplaà Cécile, Vojinovic Dina, Suzuki Hideaki, Sargurupremraj Muralidharan, Zilhão Nuno R, Li Shuo, Bartz Traci M, Jian Xueqiu, Zhao Wei, Hofer Edith, Wittfeld Katharina, Harris Sarah E, van der Auwera-Palitschka Sandra, Luciano Michelle, Bis Joshua C, Adams Hieab H H, Satizabal Claudia L, Gottesman Rebecca F, Gampawar Piyush G, Bülow Robin, Weiss Stefan, Yu Miao, Bastin Mark E, Lopez Oscar L, Vernooij Meike W, Beiser Alexa S, Völker Uwe, Kacprowski Tim, Soumare Aicha, Smith Jennifer A, Knopman David S, Morris Zoe, Zhu Yicheng, Rotter Jerome I, Dufouil Carole, Valdés Hernández Maria, Muñoz Maniega Susana, Lathrop Mark, Boerwinkle Erik, Schmidt Reinhold, Ihara Masafumi, Mazoyer Bernard, Yang Qiong, Joutel Anne, Tournier-Lasserve Elizabeth, Launer Lenore J, Deary Ian J, Mosley Thomas H, Amouyel Philippe, DeCarli Charles S, Psaty Bruce M, Tzourio Christophe, Kardia Sharon L R, Grabe Hans J, Teumer Alexander, van Duijn Cornelia M, Schmidt Helena, Wardlaw Joanna M, Ikram M Arfan, Fornage Myriam, Gudnason Vilmundur, Seshadri Sudha, Matthews Paul M, Longstreth William T, Couffinhal Thierry, Debette Stephan |
Shared genetic architecture of hernias: A genome-wide association study with multivariable meta-analysis of multiple hernia phenotypes.
PloS one 2022 12 17 (12): e0272261. Ahmed Waheed Ul-Rahman, Patel Manal I A, Ng Michael, McVeigh James, Zondervan Krina, Wiberg Akira, Furniss Domin |
Ancestry- and sex-specific effects underlying inguinal hernia susceptibility identified in a multiethnic genome-wide association study meta-analysis.
Human molecular genetics 2022 1 31 (13): 2279-2293. Choquet Hélène, Li Weiyu, Yin Jie, Bradley Rachael, Hoffmann Thomas J, Nandakumar Priyanka, , Mostaedi Rouzbeh, Tian Chao, Ahituv Nadav, Jorgenson Er |
Mutations in EFEMP1 in patients with juvenile open-angle glaucoma (JOAG). Ophthalmology. Glaucoma 2023 5 . Aminatta Z Tejan-Kamara, Erin A Boese, Andrew Pouw, Nathan C Sears, Ben R Roos, Edwin M Stone, Todd E Scheetz, John H Finge |
[Expression of CD24 gene in human malignant pleural mesothelioma and its relationship with prognosis]. Zhonghua lao dong wei sheng zhi ye bing za zhi = Zhonghua laodong weisheng zhiyebing zazhi = Chinese journal of industrial hygiene and occupational diseases 2023 4 41 (3): 168-176. Li B, Zhou C X, Pu Y Q, Qiu L, Mei W, Xiong |
Replication study identified EFEMP1 association with varicose vein predisposition among Indians. European journal of medical research 2024 4 29 (1): 232. Rohit Mehra, Vikram Patra, Rishi Dhillan, Anuka Sharma, Sonal Kashyap, Garima Rastogi, Love Gupta, Reena Singh, Chirag Chopra, Varun Shar |
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- Page last updated:Apr 22, 2024
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