Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 44 Records) |
Query Trace: TGFB2[original query] |
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Genome-wide association identifies regulatory Loci associated with distinct local histogram emphysema patterns.
American journal of respiratory and critical care medicine 2014 Aug 190 (4): 399-409. Castaldi Peter J, Cho Michael H, San José Estépar Raúl, McDonald Merry-Lynn N, Laird Nan, Beaty Terri H, Washko George, Crapo James D, Silverman Edwin K, |
[Association study between candidate genes on transforming growth factor-ß signaling pathway and the risk of non-syndromic cleft lip with or without cleft palate in Chinese populations]. Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences 2015 Jun 47 (3): 384-9. Wang Zhu-qing, Wang Ping, Wu-Chou Yah-huei, Ye Xiao-qian, Huang Shang-zhi, Shi Bing, Wang Ke, Yuan Yuan, Liu Dong-jing, Wu Tao, Wang Hong, Beaty Terri |
A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry.
BMC genetics 2015 Dec 16 138. Lutz Sharon M, Cho Michael H, Young Kendra, Hersh Craig P, Castaldi Peter J, McDonald Merry-Lynn, Regan Elizabeth, Mattheisen Manuel, DeMeo Dawn L, Parker Margaret, Foreman Marilyn, Make Barry J, Jensen Robert L, Casaburi Richard, Lomas David A, Bhatt Surya P, Bakke Per, Gulsvik Amund, Crapo James D, Beaty Terri H, Laird Nan M, Lange Christoph, Hokanson John E, Silverman Edwin K, , |
Clinically relevant variants identified in thoracic aortic aneurysm patients by research exome sequencing. American journal of medical genetics. Part A 2016 Feb . Schubert Jeffrey A, Landis Benjamin J, Shikany Amy R, Hinton Robert B, Ware Stephanie |
Genetic variants of ADAM17 are implicated in the pathological process of Kawasaki disease and secondary coronary artery lesions via the TGF-ß/SMAD3 signaling pathway. European journal of pediatrics 2016 Feb . Peng Qian, Deng Yan, Yang Xiling, Leng Xiangyou, Yang Yuan, Liu Hanm |
Transforming growth factor-? signaling pathway-associated genes SMAD2 and TGFBR2 are implicated in metabolic syndrome in a Taiwanese population. Scientific reports 2017 Oct 7 (1): 13589. Lin Eugene, Kuo Po-Hsiu, Liu Yu-Li, Yang Albert C, Tsai Shih-J |
Comparison of SNP Genotypes Related to Proliferative Vitreoretinopathy (PVR) across Slovenian and European Subpopulations. Journal of ophthalmology 2018 2018 8761625. Lumi Xhevat, Jelen Mateja M, Jevšinek Skok Daša, Boštjan?i? Emanuela, Ravnik-Glava? Metka, Hawlina Marko, Glava? Damj |
Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases.
Nature communications 2018 May 9 (1): 1864. Iglesias Adriana I, Mishra Aniket, Vitart Veronique, Bykhovskaya Yelena, Höhn René, Springelkamp Henriët, Cuellar-Partida Gabriel, Gharahkhani Puya, Bailey Jessica N Cooke, Willoughby Colin E, Li Xiaohui, Yazar Seyhan, Nag Abhishek, Khawaja Anthony P, Polašek Ozren, Siscovick David, Mitchell Paul, Tham Yih Chung, Haines Jonathan L, Kearns Lisa S, Hayward Caroline, Shi Yuan, van Leeuwen Elisabeth M, Taylor Kent D, , Bonnemaijer Pieter, Rotter Jerome I, Martin Nicholas G, Zeller Tanja, Mills Richard A, Staffieri Sandra E, Jonas Jost B, Schmidtmann Irene, Boutin Thibaud, Kang Jae H, Lucas Sionne E M, Wong Tien Yin, Beutel Manfred E, Wilson James F, , , Uitterlinden André G, Vithana Eranga N, Foster Paul J, Hysi Pirro G, Hewitt Alex W, Khor Chiea Chuen, Pasquale Louis R, Montgomery Grant W, Klaver Caroline C W, Aung Tin, Pfeiffer Norbert, Mackey David A, Hammond Christopher J, Cheng Ching-Yu, Craig Jamie E, Rabinowitz Yaron S, Wiggs Janey L, Burdon Kathryn P, van Duijn Cornelia M, MacGregor Stua |
Genetic basis of hereditary thoracic aortic aneurysms and dissections. Journal of cardiology 2019 4 74 (2): 136-143. Takeda Norifumi, Komuro Iss |
An initial genetic analysis of gemcitabine-induced high-grade neutropenia in pancreatic cancer patients in CALGB 80303 (Alliance).
Pharmacogenetics and genomics 2019 Mar . Innocenti Federico, Jiang Chen, Sibley Alexander B, Denning Stefanie, Etheridge Amy S, Watson Dorothy, Niedzwiecki Donna, Hatch Ace J, Hurwitz Herbert I, Nixon Andrew B, Furukawa Yoichi, Kubo Michiaki, Crona Daniel J, Kindler Hedy L, McLeod Howard L, Ratain Mark J, Owzar Kour |
Significant Association and Increased Risk of Primary Open Angle Glaucoma with TGFB2 Rs991967 Gene Polymorphism in North Eastern Iranian Patients. Reports of biochemistry & molecular biology 2019 Jan 7 (2): 210-216. Derakhshan Akbar, Sadeghi Allah Abadi Javad, Tavakkol-Afshari Jalil, Nikpoor Amin Reza, Daneshvar Ramin, Shokoohi Rad Saeed, Ansari-Astaneh Mohammad-Reza, Ghafarian Sade |
The genetic variants in calcium signaling related genes influence anti-tuberculosis drug induced liver injury: A prospective study. Medicine 2019 Nov 98 (44): e17821. Lyu Mengyuan, Zhou Jian, Chen Hao, Bai Hao, Song Jiajia, Liu Tangyuheng, Cheng Yuhui, Ying Bin |
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 |
Genome-wide association study for circulating fibroblast growth factor 21 and 23.
Scientific reports 2020 Sep 10 (1): 14578. Chuang Gwo-Tsann, Liu Pi-Hua, Chyan Tsui-Wei, Huang Chen-Hao, Huang Yu-Yao, Lin Chia-Hung, Lin Jou-Wei, Hsu Chih-Neng, Tsai Ru-Yi, Hsieh Meng-Lun, Lee Hsiao-Lin, Yang Wei-Shun, Robinson-Cohen Cassianne, Hsiung Chia-Ni, Shen Chen-Yang, Chang Yi-Che |
Variation in genes implicated in B-cell development and antibody production affects susceptibility to pemphigus. Immunology 2020 Sep . Calonga-Solís Verónica, Amorim Leonardo M, Farias Ticiana D J, Petzl-Erler Maria Luiza, Malheiros Danielle, Augusto Danillo |
Corneal thinning and cornea guttata in patients with mutations in TGFB2. Canadian journal of ophthalmology. Journal canadien d'ophtalmologie 2020 4 55 (4): 336-341. Eghrari Allen O, Rasooly Marjohn M, Fliotsos Michael J, Kinard Jessica, Odozor Obinna, Cunningham Denise, Bishop Rachel J, Guerrerio Anthony L, Frischmeyer-Guerrerio Pamela |
Identifying Common Genes Related to Platelet and Immunity for Lung Adenocarcinoma Prognosis Prediction. Frontiers in molecular biosciences 2020 11 7 563142. Zhou Chengmao, Wang Ying, Lei Lei, Ji Mu-Huo, Yang Jian-Jun, Xia Hongpi |
Spontaneous Coronary Artery Dissection: Insights on Rare Genetic Variation From Genome Sequencing. Circulation. Genomic and precision medicine 2020 10 13 (6): e003030. Carss Keren J, Baranowska Anna A, Armisen Javier, Webb Tom R, Hamby Stephen E, Premawardhana Diluka, Al-Hussaini Abtehale, Wood Alice, Wang Quanli, Deevi Sri V V, Vitsios Dimitrios, Lewis Samuel H, Kotecha Deevia, Bouatia-Naji Nabila, Hesselson Stephanie, Iismaa Siiri E, Tarr Ingrid, McGrath-Cadell Lucy, Muller David W, Dunwoodie Sally L, Fatkin Diane, Graham Robert M, Giannoulatou Eleni, Samani Nilesh J, Petrovski Slavé, Haefliger Carolina, Adlam Dav |
Optimising the mutation screening strategy in Marfan syndrome and identifying genotypes with more severe aortic involvement. Orphanet journal of rare diseases 2020 Oct 15 (1): 290. Stengl Roland, Bors András, Ágg Bence, Pólos Miklós, Matyas Gabor, Molnár Mária Judit, Fekete Bálint, Csabán Dóra, Andrikovics Hajnalka, Merkely Béla, Radovits Tamás, Szabolcs Zoltán, Benke Kálm |
Genomic instability-associated lncRNA signature predicts prognosis and distinct immune landscape in gastric cancer. Annals of translational medicine 2021 9 9 (16): 1326. Sun Jie, Jiang Quan, Chen Hao, Zhang Qi, Zhao Junjie, Li Haojie, Wang Xuefei, Fang Yong, Ruan Yuanyuan, Sun Yiho |
Susceptibility loci and polygenic architecture highlight population specific and common genetic features in inguinal hernias: genetics in inguinal hernias. EBioMedicine 2021 8 70 103532. Hikino Keiko, Koido Masaru, Tomizuka Kohei, Liu Xiaoxi, Momozawa Yukihide, Morisaki Takayuki, Murakami Yoshinori, The Biobank Japan Project , Mushiroda Taisei, Terao Chikas |
Association of Myopia and Genetic Variants of TGFB2-AS1 and TGFBR1 in the TGF-? Signaling Pathway: A Longitudinal Study in Chinese School-Aged Children. Frontiers in cell and developmental biology 2021 5 9 628182. Liu Linjie, He Juan, Lu Xiaoyan, Yuan Yimin, Jiang Dandan, Xiao Haishao, Lin Shudan, Xu Liangde, Chen Yany |
A systematic study of mosaicism in heritable thoracic aortic aneurysm and dissection. Genomics 2021 12 114 (1): 196-201. Yang Hang, Zhu Guoyan, Zhou Weizhen, Luo Mingyao, Zhang Yujing, Zhang Yinhui, Shu Chang, Zhou Zh |
Whole Exome Sequencing in Coloboma/Microphthalmia: Identification of Novel and Recurrent Variants in Seven Genes. Genes 2021 1 12 (1): . Haug Patricia, Koller Samuel, Maggi Jordi, Lang Elena, Feil Silke, Wlodarczyk Agnès, Bähr Luzy, Steindl Katharina, Rohrbach Marianne, Gerth-Kahlert Christina, Berger Wolfga |
Comparative Risks of Initial Aortic Events Associated With Genetic Thoracic Aortic Disease. Journal of the American College of Cardiology 2022 Aug 80 (9): 857-869. Regalado Ellen S, Morris Shaine A, Braverman Alan C, Hostetler Ellen M, De Backer Julie, Li Ruosha, Pyeritz Reed E, Yetman Anji T, Cervi Elena, Shalhub Sherene, Jeremy Richmond, LeMaire Scott, Ouzounian Maral, Evangelista Arturo, Boileau Catherine, Jondeau Guillaume, Milewicz Dianna |
Risk prediction of CMV reactivation after allogeneic stem cell transplantation using five non-HLA immunogenetic polymorphisms. Annals of hematology 2022 5 101 (7): 1567-1576. Vallejo Miren, Muñiz Paula, Kwon Mi, Solán Laura, Bailén Rebeca, Carbonell Diego, Chicano María, Suárez-González Julia, Catalán Pilar, Bellón José María, Triviño Juan Carlos, Dorado Nieves, Gallardo David, Díez-Martín José Luis, Ramírez Natalia, Martínez-Laperche Carolina, Buño Isma |
Genome-wide association study reveals novel genetic loci: a new polygenic risk score for mitral valve prolapse.
European heart journal 2022 3 43 (17): 1668-1680. Roselli Carolina, Yu Mengyao, Nauffal Victor, Georges Adrien, Yang Qiong, Love Katie, Weng Lu-Chen, Delling Francesca N, Maurya Svetlana R, Schrölkamp Maren, Tfelt-Hansen Jacob, Hagège Albert, Jeunemaitre Xavier, Debette Stéphanie, Amouyel Philippe, Guan Wyliena, Muehlschlegel Jochen D, Body Simon C, Shah Svati, Samad Zainab, Kyryachenko Sergiy, Haynes Carol, Rienstra Michiel, Le Tourneau Thierry, Probst Vincent, Roussel Ronan, Wijdh-Den Hamer Inez J, Siland Joylene E, Knowlton Kirk U, Jacques Schott Jean, Levine Robert A, Benjamin Emelia J, Vasan Ramachandran S, Horne Benjamin D, Muhlestein Joseph B, Benfari Giovanni, Enriquez-Sarano Maurice, Natale Andrea, Mohanty Sanghamitra, Trivedi Chintan, Shoemaker Moore B, Yoneda Zachary T, Wells Quinn S, Baker Michael T, Farber-Eger Eric, Michelena Hector I, Lundby Alicia, Norris Russell A, Slaugenhaupt Susan A, Dina Christian, Lubitz Steven A, Bouatia-Naji Nabila, Ellinor Patrick T, Milan David |
[Clinical and genetic characteristics of 12 cases of Loeys-Dietz syndrome]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2023 8 40 (9): 1093-1099. Jiaqi Fan, Hairui Sun, Xin Wang, Yuduo Wu, Siyao Zhang, Xiaoyan Hao, Jiancheng Han, Xiaoyan Gu, Ye Zhang, Lin Sun, Yihua |
[Mutational Signatures Analysis of Micropapillary Components and Exploration of ZNF469 Gene in Early-stage Lung Adenocarcinoma with Ground-glass Opacities]. Zhongguo fei ai za zhi = Chinese journal of lung cancer 2023 12 26 (12): 889-900. Youtao Xu, Qinhong Sun, Siwei Wang, Hongyu Zhu, Guozhang Dong, Fanchen Meng, Zhijun Xia, Jing You, Xiangru Kong, Jintao Wu, Peng Chen, Fangwei Yuan, Xinyu Yu, Jinfu Ji, Zhitong Li, Pengcheng Zhu, Yuxiang Sun, Tongyan Liu, Rong Yin, Lin |
Genome-wide association study of varicose veins identifies a protective missense variant in GJD3 enriched in the Finnish population.
Communications biology 2023 1 6 (1): 71. Helkkula Pyry, Hassan Shabbeer, Saarentaus Elmo, Vartiainen Emilia, Ruotsalainen Sanni, Leinonen Jaakko T, , Palotie Aarno, Karjalainen Juha, Kurki Mitja, Ripatti Samuli, Tukiainen Ta |
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