Human Genome Epidemiology Literature Finder
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Records 1 - 18 (of 18 Records) |
| Query Trace: Disease and TGFB2[original query] |
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| Investigation of TGFB2 as a candidate gene in multiple sclerosis and Parkinson's disease. Journal of neurology 2007 Jul 254 (7): 846-8. Goris A, Williams-Gray C H, Foltynie T, Brown J, Maranian M, Walton A, Compston D A S, Barker R A, Sawcer S |
| Association of TGFBR2 polymorphism with risk of sudden cardiac arrest in patients with coronary artery disease. Heart rhythm : the official journal of the Heart Rhythm Society 2009 Dec 6 (12): 1745-50. Tseng Zian H, Vittinghoff Eric, Musone Stacy L, Lin Feng, Whiteman Dean, Pawlikowska Ludmila, Kwok Pui-Yan, Olgin Jeffrey E, Aouizerat Bradley |
| Transforming growth factor-beta signaling pathway in patients with Kawasaki disease. Circulation. Cardiovascular genetics 2011 Feb 4 (1): 16-25. Shimizu Chisato, Jain Sonia, Davila Sonia, Hibberd Martin L, Lin Kevin O, Molkara Delaram, Frazer Jeffrey R, Sun Shelly, Baker Annette L, Newburger Jane W, Rowley Anne H, Shulman Stanford T, Davila Sonia, Burgner David, Breunis Willemijn B, Kuijpers Taco W, Wright Victoria J, Levin Michael, Eleftherohorinou Hariklia, Coin Lachlan, Popper Stephen J, Relman David A, Fury Wen, Lin Calvin, Mellis Scott, Tremoulet Adriana H, Burns Jane |
Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.
Nature genetics 2011 Sep 43 (11): 1082-90. Soler Artigas María, Loth Daan W, Wain Louise V, Gharib Sina A, Obeidat Ma'en, Tang Wenbo, Zhai Guangju, Zhao Jing Hua, Smith Albert Vernon, Huffman Jennifer E, Albrecht Eva, Jackson Catherine M, Evans David M, Cadby Gemma, Fornage Myriam, Manichaikul Ani, Lopez Lorna M, Johnson Toby, Aldrich Melinda C, Aspelund Thor, Barroso Inês, Campbell Harry, Cassano Patricia A, Couper David J, Eiriksdottir Gudny, Franceschini Nora, Garcia Melissa, Gieger Christian, Gislason Gauti Kjartan, Grkovic Ivica, Hammond Christopher J, Hancock Dana B, Harris Tamara B, Ramasamy Adaikalavan, Heckbert Susan R, Heliövaara Markku, Homuth Georg, Hysi Pirro G, James Alan L, Jankovic Stipan, Joubert Bonnie R, Karrasch Stefan, Klopp Norman, Koch Beate, Kritchevsky Stephen B, Launer Lenore J, Liu Yongmei, Loehr Laura R, Lohman Kurt, Loos Ruth J F, Lumley Thomas, Al Balushi Khalid A, Ang Wei Q, Barr R Graham, Beilby John, Blakey John D, Boban Mladen, Boraska Vesna, Brisman Jonas, Britton John R, Brusselle Guy G, Cooper Cyrus, Curjuric Ivan, Dahgam Santosh, Deary Ian J, Ebrahim Shah, Eijgelsheim Mark, Francks Clyde, Gaysina Darya, Granell Raquel, Gu Xiangjun, Hankinson John L, Hardy Rebecca, Harris Sarah E, Henderson John, Henry Amanda, Hingorani Aroon D, Hofman Albert, Holt Patrick G, Hui Jennie, Hunter Michael L, Imboden Medea, Jameson Karen A, Kerr Shona M, Kolcic Ivana, Kronenberg Florian, Liu Jason Z, Marchini Jonathan, McKeever Tricia, Morris Andrew D, Olin Anna-Carin, Porteous David J, Postma Dirkje S, Rich Stephen S, Ring Susan M, Rivadeneira Fernando, Rochat Thierry, Sayer Avan Aihie, Sayers Ian, Sly Peter D, Smith George Davey, Sood Akshay, Starr John M, Uitterlinden André G, Vonk Judith M, Wannamethee S Goya, Whincup Peter H, Wijmenga Cisca, Williams O Dale, Wong Andrew, Mangino Massimo, Marciante Kristin D, McArdle Wendy L, Meibohm Bernd, Morrison Alanna C, North Kari E, Omenaas Ernst, Palmer Lyle J, Pietiläinen Kirsi H, Pin Isabelle, Pola Sbreve Ek Ozren, Pouta Anneli, Psaty Bruce M, Hartikainen Anna-Liisa, Rantanen Taina, Ripatti Samuli, Rotter Jerome I, Rudan Igor, Rudnicka Alicja R, Schulz Holger, Shin So-Youn, Spector Tim D, Surakka Ida, Vitart Veronique, Völzke Henry, Wareham Nicholas J, Warrington Nicole M, Wichmann H-Erich, Wild Sarah H, Wilk Jemma B, Wjst Matthias, Wright Alan F, Zgaga Lina, Zemunik Tatijana, Pennell Craig E, Nyberg Fredrik, Kuh Diana, Holloway John W, Boezen H Marike, Lawlor Debbie A, Morris Richard W, Probst-Hensch Nicole, , , Kaprio Jaakko, Wilson James F, Hayward Caroline, Kähönen Mika, Heinrich Joachim, Musk Arthur W, Jarvis Deborah L, Gläser Sven, Järvelin Marjo-Riitta, Ch Stricker Bruno H, Elliott Paul, O'Connor George T, Strachan David P, London Stephanie J, Hall Ian P, Gudnason Vilmundur, Tobin Martin |
| Multiple single-nucleotide polymorphism-based risk model for clinical outcomes after allogeneic stem-cell transplantation, especially for acute graft-versus-host disease. Transplantation 2012 Nov . Kim DD, Yun J, Won HH, Cheng L, Su J, Xu W, Uhm J, Gupta V, Kuruvilla J, Messner HA, Lipton JH |
| 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, |
| Risk loci for chronic obstructive pulmonary disease: a genome-wide association study and meta-analysis.
The Lancet. Respiratory medicine 2014 Mar 2 (3): 214-25. Cho Michael H, McDonald Merry-Lynn N, Zhou Xiaobo, Mattheisen Manuel, Castaldi Peter J, Hersh Craig P, Demeo Dawn L, Sylvia Jody S, Ziniti John, Laird Nan M, Lange Christoph, Litonjua Augusto A, Sparrow David, Casaburi Richard, Barr R Graham, Regan Elizabeth A, Make Barry J, Hokanson John E, Lutz Sharon, Dudenkov Tanda Murray, Farzadegan Homayoon, Hetmanski Jacqueline B, Tal-Singer Ruth, Lomas David A, Bakke Per, Gulsvik Amund, Crapo James D, Silverman Edwin K, Beaty Terri H, |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| Identification of differentially expressed genes to predict the risk of heart failure in older patients with hypertrophic cardiomyopathy. Aging 2024 7 16 . Hao Dong, Chufan Yin, Dongping Xiao, Yong Ta |
- Page last reviewed:Feb 1, 2024
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