Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 40 Records) |
Query Trace: TNXB[original query] |
---|
A Genome-Wide Association Study Identified Novel Genetic Susceptibility Loci for Oral Cancer in Taiwan.
International journal of molecular sciences 2023 2 24 (3): . Bau Da-Tian, Liu Ting-Yuan, Tsai Chia-Wen, Chang Wen-Shin, Gu Jian, Yang Jai-Sing, Shih Liang-Chun, Tsai Fuu-J |
Associations of 6p21.3 Region with Age-related Macular Degeneration and Polypoidal Choroidal Vasculopathy. Scientific reports 2016 6 20914. Ye Zimeng, Shuai Ping, Zhai Yaru, Li Fang, Jiang Lingxi, Lu Fang, Wen Feng, Huang Lulin, Zhang Dingding, Liu Xiaoqi, Lin Ying, Luo Huaichao, Zhang Houbin, Zhu Xianjun, Wu Zhengzheng, Yang Zhenglin, Gong Bo, Shi |
Genetic similarities and differences between discoid and systemic lupus erythematosus patients within the Polish population. Postepy dermatologii i alergologii 2017 Jun 34 (3): 228-232. Skonieczna Katarzyna, Czajkowski Rafa?, Kaszewski Sebastian, Gawrych Mariusz, Jakubowska Aneta, Grzybowski Toma |
Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney.
Hypertension (Dallas, Tex. : 1979) 2017 Jul . Wain Louise V, Vaez Ahmad, Jansen Rick, Joehanes Roby, van der Most Peter J, Erzurumluoglu A Mesut, O'Reilly Paul F, Cabrera Claudia P, Warren Helen R, Rose Lynda M, Verwoert Germaine C, Hottenga Jouke-Jan, Strawbridge Rona J, Esko Tonu, Arking Dan E, Hwang Shih-Jen, Guo Xiuqing, Kutalik Zoltan, Trompet Stella, Shrine Nick, Teumer Alexander, Ried Janina S, Bis Joshua C, Smith Albert V, Amin Najaf, Nolte Ilja M, Lyytikäinen Leo-Pekka, Mahajan Anubha, Wareham Nicholas J, Hofer Edith, Joshi Peter K, Kristiansson Kati, Traglia Michela, Havulinna Aki S, Goel Anuj, Nalls Mike A, Sõber Siim, Vuckovic Dragana, Luan Jian'an, Del Greco M Fabiola, Ayers Kristin L, Marrugat Jaume, Ruggiero Daniela, Lopez Lorna M, Niiranen Teemu, Enroth Stefan, Jackson Anne U, Nelson Christopher P, Huffman Jennifer E, Zhang Weihua, Marten Jonathan, Gandin Ilaria, Harris Sarah E, Zemunik Tatijana, Lu Yingchang, Evangelou Evangelos, Shah Nabi, de Borst Martin H, Mangino Massimo, Prins Bram P, Campbell Archie, Li-Gao Ruifang, Chauhan Ganesh, Oldmeadow Christopher, Abecasis Gonçalo, Abedi Maryam, Barbieri Caterina M, Barnes Michael R, Batini Chiara, Beilby John, Blake Tineka, Boehnke Michael, Bottinger Erwin P, Braund Peter S, Brown Morris, Brumat Marco, Campbell Harry, Chambers John C, Cocca Massimiliano, Collins Francis, Connell John, Cordell Heather J, Damman Jeffrey J, Davies Gail, de Geus Eco J, de Mutsert Renée, Deelen Joris, Demirkale Yusuf, Doney Alex S F, Dörr Marcus, Farrall Martin, Ferreira Teresa, Frånberg Mattias, Gao He, Giedraitis Vilmantas, Gieger Christian, Giulianini Franco, Gow Alan J, Hamsten Anders, Harris Tamara B, Hofman Albert, Holliday Elizabeth G, Hui Jennie, Jarvelin Marjo-Riitta, Johansson Åsa, Johnson Andrew D, Jousilahti Pekka, Jula Antti, Kähönen Mika, Kathiresan Sekar, Khaw Kay-Tee, Kolcic Ivana, Koskinen Seppo, Langenberg Claudia, Larson Marty, Launer Lenore J, Lehne Benjamin, Liewald David C M, Lin Li, Lind Lars, Mach François, Mamasoula Chrysovalanto, Menni Cristina, Mifsud Borbala, Milaneschi Yuri, Morgan Anna, Morris Andrew D, Morrison Alanna C, Munson Peter J, Nandakumar Priyanka, Nguyen Quang Tri, Nutile Teresa, Oldehinkel Albertine J, Oostra Ben A, Org Elin, Padmanabhan Sandosh, Palotie Aarno, Paré Guillaume, Pattie Alison, Penninx Brenda W J H, Poulter Neil, Pramstaller Peter P, Raitakari Olli T, Ren Meixia, Rice Kenneth, Ridker Paul M, Riese Harriëtte, Ripatti Samuli, Robino Antonietta, Rotter Jerome I, Rudan Igor, Saba Yasaman, Saint Pierre Aude, Sala Cinzia F, Sarin Antti-Pekka, Schmidt Reinhold, Scott Rodney, Seelen Marc A, Shields Denis C, Siscovick David, Sorice Rossella, Stanton Alice, Stott David J, Sundström Johan, Swertz Morris, Taylor Kent D, Thom Simon, Tzoulaki Ioanna, Tzourio Christophe, Uitterlinden André G, Völker Uwe, Vollenweider Peter, Wild Sarah, Willemsen Gonneke, Wright Alan F, Yao Jie, Thériault Sébastien, Conen David, Attia John, Sever Peter, Debette Stéphanie, Mook-Kanamori Dennis O, Zeggini Eleftheria, Spector Tim D, van der Harst Pim, Palmer Colin N A, Vergnaud Anne-Claire, Loos Ruth J F, Polasek Ozren, Starr John M, Girotto Giorgia, Hayward Caroline, Kooner Jaspal S, Lindgren Cecila M, Vitart Veronique, Samani Nilesh J, Tuomilehto Jaakko, Gyllensten Ulf, Knekt Paul, Deary Ian J, Ciullo Marina, Elosua Roberto, Keavney Bernard D, Hicks Andrew A, Scott Robert A, Gasparini Paolo, Laan Maris, Liu YongMei, Watkins Hugh, Hartman Catharina A, Salomaa Veikko, Toniolo Daniela, Perola Markus, Wilson James F, Schmidt Helena, Zhao Jing Hua, Lehtimäki Terho, van Duijn Cornelia M, Gudnason Vilmundur, Psaty Bruce M, Peters Annette, Rettig Rainer, James Alan, Jukema J Wouter, Strachan David P, Palmas Walter, Metspalu Andres, Ingelsson Erik, Boomsma Dorret I, Franco Oscar H, Bochud Murielle, Newton-Cheh Christopher, Munroe Patricia B, Elliott Paul, Chasman Daniel I, Chakravarti Aravinda, Knight Joanne, Morris Andrew P, Levy Daniel, Tobin Martin D, Snieder Harold, Caulfield Mark J, Ehret Georg |
Generating testable hypotheses for schizophrenia and rheumatoid arthritis pathogenesis by integrating epidemiological, genomic, and protein interaction data. NPJ schizophrenia 2017 3 11. Malavia Tulsi A, Chaparala Srilakshmi, Wood Joel, Chowdari Kodavali, Prasad Konasale M, McClain Lora, Jegga Anil G, Ganapathiraju Madhavi K, Nimgaonkar Vishwajit |
Involvement of the bone morphogenic protein/SMAD signaling pathway in the etiology of congenital anomalies of the kidney and urinary tract accompanied by cryptorchidism. BMC urology 2017 12 17 (1): 112. Mizuno Kentaro, Nakane Akihiro, Nishio Hidenori, Moritoki Yoshinobu, Kamisawa Hideyuki, Kurokawa Satoshi, Kato Taiki, Ando Ryosuke, Maruyama Tetsuji, Yasui Takahiro, Hayashi Yuta |
Targeted Sequencing of Lung Function Loci in Chronic Obstructive Pulmonary Disease Cases and Controls. PloS one 2017 1 12 (1): e0170222. Artigas María Soler, Wain Louise V, Shrine Nick, McKeever Tricia M, , Sayers Ian, Hall Ian P, Tobin Martin |
Whole-exome sequencing reveals known and novel variants in a cohort of intracranial vertebral-basilar artery dissection (IVAD). Journal of human genetics 2018 Aug . Wang Kun, Zhao Sen, Zhang Qianqian, Yuan Jian, Liu Jiaqi, Ding Xinghuan, Song Xiaofei, Lin Jiachen, Du Renqian, Zhou Yangzhong, Sugimoto Michihiko, Chen Weisheng, Yuan Bo, Liu Jian, Yan Zihui, Liu Bowen, Zhang Yisen, Li Xiaoxin, Niu Yuchen, Long Bo, Shen Yiping, Zhang Shuyang, Abe Kuniya, Su Jianzhong, Wu Zhihong, Wu Nan, Liu Pengfei, Yang Xinjian, |
Revisiting the association of HLA alleles and haplotypes with CYP21A2 mutations in a large cohort of patients with congenital adrenal hyperplasia. Gene 2018 11 687 30-34. Jayakrishnan Rahul, Lao Qizong, Adams Sharon D, Ward William W, Merke Deborah |
Exome-wide analyses identify low-frequency variant in CYP26B1 and additional coding variants associated with esophageal squamous cell carcinoma. Nature genetics 2018 Jan . Chang Jiang, Zhong Rong, Tian Jianbo, Li Jiaoyuan, Zhai Kan, Ke Juntao, Lou Jiao, Chen Wei, Zhu Beibei, Shen Na, Zhang Yi, Zhu Ying, Gong Yajie, Yang Yang, Zou Danyi, Peng Xiating, Zhang Zhi, Zhang Xuemei, Huang Kun, Wu Tangchun, Wu Chen, Miao Xiaoping, Lin Dongx |
Measurement of Serum Tenascin-X in Joint Hypermobility Syndrome Patients. Biological & pharmaceutical bulletin 2019 42 (9): 1596-1599. Yamada Kazuo, Watanabe Atsushi, Takeshita Haruo, Fujita Atsushi, Miyake Noriko, Matsumoto Naomichi, Matsumoto Ken-Ic |
Genetic Alleles Associated with SLE Susceptibility and Clinical Manifestations in Hispanic Patients from the Dominican Republic. Current molecular medicine 2019 Apr . Liu Zheng, Yu Yangsheng, Yue Yinshi, Hearth-Holmes Michelene, Lopez Persio David, Tineo Carmen, Paulino Glenny, Fu Wei-Neng, Loyo Esthela, Su Kaiho |
Identification of Rare Copy Number Variants Associated With Pulmonary Atresia With Ventricular Septal Defect. Frontiers in genetics 2019 10 15. Xie Huilin, Hong Nanchao, Zhang Erge, Li Fen, Sun Kun, Yu |
Children with vesicoureteric reflux have joint hypermobility and occasional tenascin XB sequence variants. Canadian Urological Association journal = Journal de l'Association des urologues du Canada 2019 Nov . Tokhmafshan Fatima, El Andalousi Jasmine, Murugapoopathy Vasikar, Fillion Marie-Lyne, Campillo Sarah, Capolicchio John-Paul, Jednak Roman, El Sherbiny Mohamed, Turpin Sophie, Schalkwijk Joost, Matsumoto Ken-Ichi, Brophy Patrick D, Gbadegesin Rasheed A, Gupta Indra |
Measurement of serum tenascin-X in patients with congenital adrenal hyperplasia at risk for Ehlers-Danlos contiguous gene deletion syndrome CAH-X. BMC research notes 2019 Oct 12 (1): 711. Kolli Vipula, Kim Hannah, Rao Hamsini, Lao Qizong, Gaynor Alison, Milner Joshua D, Merke Deborah |
A genome wide association study for lung function in the Korean population using an exome array. The Korean journal of internal medicine 2020 Apr . Lee Kyu-Sun, Kim Kun Hee, Oh Yeon-Mok, Han Buhm, Kim Woo J |
The Prevalence of the Chimeric TNXA/TNXB Gene and Clinical Symptoms of Ehlers-Danlos Syndrome with 21-Hydroxylase Deficiency. The Journal of clinical endocrinology and metabolism 2020 Apr . Gao Yinjie, Lu Lin, Yu Bingqing, Mao Jiangfeng, Wang Xi, Nie Min, Wu Xuey |
A rare CYP21A2 haplotype clarifies the phenotype-genotype discrepancy in an Italian patient with Non Classical Congenital Adrenal Hyperplasia (NC-CAH). Molecular biology reports 2020 3 47 (4): 3049-3052. Concolino Pao |
A functional variant in TNXB promoter associates with the risk of esophageal squamous-cell carcinoma. Molecular carcinogenesis 2020 Feb . Yang Nan, Tian Jianbo, Wang Xiaoyang, Mei Shufang, Zou Danyi, Peng Xiating, Zhu Ying, Yang Yang, Gong Yajie, Ke Juntao, Zhong Rong, Chang Jiang, Miao Xiaopi |
Familial genetic and environmental risk profile and high blood pressure event: a prospective cohort of cardio-metabolic and genetic study. Blood pressure 2021 Apr 1-9. Kolifarhood Goodarz, Daneshpour Maryam S, Zahedi Asiyeh Sadat, Khosravi Nasim, Sedaghati-Khayat Bahareh, Guity Kamran, Rasekhi Dehkordi Saeid, Amiri Roudbar Mahmoud, Ghanbari Forough, Hadaegh Farzad, Azizi Fereidoun, Akbarzadeh Mahdi, Sabour Siam |
[Clinical Characteristics and Genetic Analysis of Klippel-Feil Syndrome]. Zhongguo yi xue ke xue yuan xue bao. Acta Academiae Medicinae Sinicae 2021 3 43 (1): 25-31. Li Zi Quan, Geng Mo Zhao, Zhao Sen, Wu Zhi Hong, Zhang Jian Guo, Wu Nan, Wang Yi Pe |
Resequencing of candidate genes for Keratoconus reveals a role for Ehlers-Danlos Syndrome genes. European journal of human genetics : EJHG 2021 3 29 (12): 1745-1755. Fransen Erik, Valgaeren Hanne, Janssens Katleen, Sommen Manou, De Ridder Raphael, Vandeweyer Geert, Bisceglia Luigi, Soler Vincent, Hoischen Alexander, Mortier Geert, Malecaze François, Koppen Carina, Van Camp G |
Ehlers-Danlos Syndrome: Molecular and Clinical Characterization of TNXA/TNXB Chimeras in Congenital Adrenal Hyperplasia. The Journal of clinical endocrinology and metabolism 2021 1 106 (7): e2789-e2802. Marino Roxana, Garrido Natalia Perez, Ramirez Pablo, Notaristéfano Guillermo, Moresco Angélica, Touzon Maria Sol, Vaiani Elisa, Finkielstain Gabriela, Obregón María Gabriela, Balbi Viviana, Soria Ianina, Belgorosky Alic |
Prevalence of CAH-X Syndrome in Italian Patients with Congenital Adrenal Hyperplasia (CAH) Due to 21-Hydroxylase Deficiency. Journal of clinical medicine 2022 7 11 (13): . Paragliola Rosa Maria, Perrucci Alessia, Foca Laura, Urbani Andrea, Concolino Pao |
The AGT epistasis pattern proposed a novel role for ZBED9 in regulating blood pressure: Tehran Cardiometabolic genetic study (TCGS). Gene 2022 Jul 831 146560. Akbarzadeh Mahdi, Riahi Parisa, Kolifarhood Goodarz, Lanjanian Hossein, Alipour Nadia, Najd Hassan Bonab Leila, Reza Moghadas Mohammad, Sabour Siamak, Azizi Fereidoun, Daneshpour Maryam |
Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic Diagnosis. Journal of the American Society of Nephrology : JASN 2023 3 . Ahram Dina F, Lim Tze Y, Ke Juntao, Jin Gina, Verbitsky Miguel, Bodria Monica, Kil Byum Hee, Chatterjee Debanjana, Piva Stacy E, Marasa Maddalena, Zhang Jun Y, Cocchi Enrico, Caridi Gianluca, Gucev Zoran, Lozanovski Vladimir J, Pisani Isabella, Izzi Claudia, Savoldi Gianfranco, Gnutti Barbara, Capone Valentina P, Morello William, Guarino Stefano, Esposito Pasquale, Lambert Sarah, Radhakrishnan Jai, Appel Gerald B, Uy Natalie S, Rao Maya K, Canetta Pietro A, Bomback Andrew S, Nestor Jordan G, Hays Thomas, Cohen David J, Finale Na Carolina, van Wijk Joanna A E, La Scola Claudio, Baraldi Olga, Tondolo Francesco, Di Renzo Dacia, Jamry-Dziurla Anna, Pezzutto Alessandro, Manca Valeria, Mitrotti Adele, Santoro Domenico, Conti Giovanni, Martino Marida, Giordano Mario, Gesualdo Loreto, Zibar Lada, Masnata Giuseppe, Bonomini Mario, Alberti Daniele, La Manna Gaetano, Caliskan Yasar, Ranghino Andrea, Marzuillo Pierluigi, Kiryluk Krzysztof, Krzemie? Gra?yna, Miklaszewska Monika, Lin Fangming, Montini Giovanni, Scolari Francesco, Fiaccadori Enrico, Arapovi? Adela, Saraga Marijan, McKiernan James, Alam Shumyle, Zaniew Marcin, Szczepa?ska Maria, Szmigielska Agnieszka, Sikora Przemys?aw, Dro?d? Dorota, Mizerska-Wasiak Malgorzata, Mane Shrikant, Lifton Richard P, Tasic Velibor, Latos-Bielenska Anna, Gharavi Ali G, Ghiggeri Gian Marco, Materna-Kiryluk Anna, Westland Rik, Sanna-Cherchi Simo |
Pseudogene TNXA Variants May Interfere with the Genetic Testing of CAH-X. Genes 2023 2 14 (2): . Lao Qizong, Zhou Kiet, Parker Megan, Faucz Fabio R, Merke Deborah |
Genetic determinants of complement activation in the general population. Cell reports 2023 12 43 (1): 113611. Damia Noce, Luisa Foco, Dorothea Orth-Höller, Eva König, Giulia Barbieri, Maik Pietzner, Dariush Ghasemi-Semeskandeh, Stefan Coassin, Christian Fuchsberger, Martin Gögele, Fabiola Del Greco M, Alessandro De Grandi, Monika Summerer, Eleanor Wheeler, Claudia Langenberg, Cornelia Lass-Flörl, Peter Paul Pramstaller, Florian Kronenberg, Reinhard Würzner, Cristian Patta |
A cross-trait study of lung cancer and its related respiratory diseases based on large-scale exome sequencing population. Translational lung cancer research 2024 4 13 (3): 512-525. Yunke Jiang, Hongru Li, Zaiming Li, Sha Du, Ruyang Zhang, Yang Zhao, David C Christiani, Sipeng Shen, Feng Ch |
Whole-Genome Sequencing Analysis Reveals New Susceptibility Loci and Structural Variants Associated with Progressive Supranuclear Palsy. medRxiv : the preprint server for health sciences 2024 1 . Hui Wang, Timothy S Chang, Beth A Dombroski, Po-Liang Cheng, Vishakha Patil, Leopoldo Valiente-Banuet, Kurt Farrell, Catriona Mclean, Laura Molina-Porcel, Alex Rajput, Peter Paul De Deyn, Nathalie Le Bastard, Marla Gearing, Laura Donker Kaat, John C Van Swieten, Elise Dopper, Bernardino F Ghetti, Kathy L Newell, Claire Troakes, Justo G de Yébenes, Alberto Rábano-Gutierrez, Tina Meller, Wolfgang H Oertel, Gesine Respondek, Thomas Arzberger, Sigrun Roeber, Pau Pastor, Alexis Brice, Alexandra Durr, Isabelle Le Ber, Thomas G Beach, Geidy E Serrano, Lili-Naz Hazrati, Irene Litvan, Rosa Rademakers, Owen A Ross, Douglas Galasko, Adam L Boxer, Bruce L Miller, Willian W Seeley, Vivanna M Van Deerlin, Charles L White, Huw Morris, Rohan de Silva, John F Crary, Alison M Goate, Jeffrey S Friedman, Yuk Yee Leung, Giovanni Coppola, Adam C Naj, Li-San Wang, Dennis W Dickson, Günter U Höglinger, Gerard D Schellenberg, Daniel H Geschwind, Wan-Ping L |
- Page last reviewed:Feb 1, 2024
- Page last updated:May 06, 2024
- Content source: