Human Genome Epidemiology Literature Finder
Records 1 - 20 (of 20 Records) |
Query Trace: SALL1[original query] |
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Common genetic variants associated with open-angle glaucoma. Human molecular genetics 2011 Jun 20 (12): 2464-71. Ramdas Wishal D, van Koolwijk Leonieke M E, Lemij Hans G, Pasutto Francesca, Cree Angela J, Thorleifsson Gudmar, Janssen Sarah F, Jacoline Ten Brink, Amin Najaf, Rivadeneira Fernando, Wolfs Roger C W, Walters G Bragi, Jonasson Fridbert, Weisschuh Nicole, Mardin Christian Y, Gibson Jane, Zegers Richard H C, Hofman Albert, de Jong Paulus T V M, Uitterlinden André G, Oostra Ben A, Thorsteinsdottir Unnur, Gramer Eugen, Welgen-Lüssen Ulrich C, Kirwan James F, Bergen Arthur A B, Reis André, Stefansson Kari, Lotery Andrew J, Vingerling Johannes R, Jansonius Nomdo M, Klaver Caroline C W, van Duijn Cornelia |
Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels.
Circulation 2011 Feb 123 (7): 731-8. Dehghan Abbas, Dupuis Josée, Barbalic Maja, Bis Joshua C, Eiriksdottir Gudny, Lu Chen, Pellikka Niina, Wallaschofski Henri, Kettunen Johannes, Henneman Peter, Baumert Jens, Strachan David P, Fuchsberger Christian, Vitart Veronique, Wilson James F, Paré Guillaume, Naitza Silvia, Rudock Megan E, Surakka Ida, de Geus Eco J C, Alizadeh Behrooz Z, Guralnik Jack, Shuldiner Alan, Tanaka Toshiko, Zee Robert Y L, Schnabel Renate B, Nambi Vijay, Kavousi Maryam, Ripatti Samuli, Nauck Matthias, Smith Nicholas L, Smith Albert V, Sundvall Jouko, Scheet Paul, Liu Yongmei, Ruokonen Aimo, Rose Lynda M, Larson Martin G, Hoogeveen Ron C, Freimer Nelson B, Teumer Alexander, Tracy Russell P, Launer Lenore J, Buring Julie E, Yamamoto Jennifer F, Folsom Aaron R, Sijbrands Eric J G, Pankow James, Elliott Paul, Keaney John F, Sun Wei, Sarin Antti-Pekka, Fontes João D, Badola Sunita, Astor Brad C, Hofman Albert, Pouta Anneli, Werdan Karl, Greiser Karin H, Kuss Oliver, Meyer zu Schwabedissen Henriette E, Thiery Joachim, Jamshidi Yalda, Nolte Ilja M, Soranzo Nicole, Spector Timothy D, Völzke Henry, Parker Alexander N, Aspelund Thor, Bates David, Young Lauren, Tsui Kim, Siscovick David S, Guo Xiuqing, Rotter Jerome I, Uda Manuela, Schlessinger David, Rudan Igor, Hicks Andrew A, Penninx Brenda W, Thorand Barbara, Gieger Christian, Coresh Joe, Willemsen Gonneke, Harris Tamara B, Uitterlinden Andre G, Järvelin Marjo-Riitta, Rice Kenneth, Radke Dörte, Salomaa Veikko, Willems van Dijk Ko, Boerwinkle Eric, Vasan Ramachandran S, Ferrucci Luigi, Gibson Quince D, Bandinelli Stefania, Snieder Harold, Boomsma Dorret I, Xiao Xiangjun, Campbell Harry, Hayward Caroline, Pramstaller Peter P, van Duijn Cornelia M, Peltonen Leena, Psaty Bruce M, Gudnason Vilmundur, Ridker Paul M, Homuth Georg, Koenig Wolfgang, Ballantyne Christie M, Witteman Jacqueline C M, Benjamin Emelia J, Perola Markus, Chasman Daniel |
A genetic epidemiologic study of candidate genes involved in the optic nerve head morphology. Investigative ophthalmology & visual science 2012 Mar 53 (3): 1485-91. Gasten Andrea C, Ramdas Wishal D, Broer Linda, van Koolwijk Leonieke M E, Ikram M Kamran, de Jong Paulus T V M, Aulchenko Yurii S, Wolfs Roger C, Hofman Albert, Rivadeneira Fernando, Uitterlinden Andre G, Oostra Ben A, Lemij Hans G, Klaver Caroline C W, Jansonius Nomdo M, Vingerling Johannes R, van Duijn Cornelia |
Genome-wide association study identifies 8 novel loci associated with blood pressure responses to interventions in Han Chinese.
Circulation. Cardiovascular genetics 2013 Dec 6 (6): 598-607. He Jiang, Kelly Tanika N, Zhao Qi, Li Hongfan, Huang Jianfeng, Wang Laiyuan, Jaquish Cashell E, Sung Yun Ju, Shimmin Lawrence C, Lu Fanghong, Mu Jianjun, Hu Dongsheng, Ji Xu, Shen Chong, Guo Dongshuang, Ma Jixiang, Wang Renping, Shen Jinjin, Li Shengxu, Chen Jing, Mei Hao, Chen Chung-Shiuan, Chen Shufeng, Chen Jichun, Li Jianxin, Cao Jie, Lu Xiangfeng, Wu Xigui, Rice Treva K, Gu C Charles, Schwander Karen, Hamm L Lee, Liu Depei, Rao Dabeeru C, Hixson James E, Gu Dongfe |
Genome-wide association study and mouse expression data identify a highly conserved 32 kb intergenic region between WNT3 and WNT9b as possible susceptibility locus for isolated classic exstrophy of the bladder. Human molecular genetics 2014 Oct 23 (20): 5536-44. Reutter Heiko, Draaken Markus, Pennimpede Tracie, Wittler Lars, Brockschmidt Felix F, Ebert Anne-Karolin, Bartels Enrika, Rösch Wolfgang, Boemers Thomas M, Hirsch Karin, Schmiedeke Eberhard, Meesters Christian, Becker Tim, Stein Raimund, Utsch Boris, Mangold Elisabeth, Nordenskjöld Agneta, Barker Gillian, Kockum Christina Clementsson, Zwink Nadine, Holmdahl Gundula, Läckgren Göran, Jenetzky Ekkehart, Feitz Wouter F J, Marcelis Carlo, Wijers Charlotte H W, Van Rooij Iris A L M, Gearhart John P, Herrmann Bernhard G, Ludwig Michael, Boyadjiev Simeon A, Nöthen Markus M, Mattheisen Manu |
Influence of elevated-CRP level-related polymorphisms in non-rheumatic Caucasians on the risk of subclinical atherosclerosis and cardiovascular disease in rheumatoid arthritis. Scientific reports 2016 6 31979. López-Mejías Raquel, Genre Fernanda, Remuzgo-Martínez Sara, González-Juanatey Carlos, Robustillo-Villarino Montserrat, Llorca Javier, Corrales Alfonso, Vicente Esther, Miranda-Filloy José A, Magro César, Tejera-Segura Beatriz, Ramírez Huaranga Marco A, Pina Trinitario, Blanco Ricardo, Alegre-Sancho Juan J, Raya Enrique, Mijares Verónica, Ubilla Begoña, Mínguez Sánchez María D, Gómez-Vaquero Carmen, Balsa Alejandro, Pascual-Salcedo Dora, López-Longo Francisco J, Carreira Patricia, González-Álvaro Isidoro, Rodríguez-Rodríguez Luis, Fernández-Gutiérrez Benjamín, Ferraz-Amaro Iván, Castañeda Santos, Martín Javier, González-Gay Miguel |
Identification of 8 Novel Mutations in Nephrogenesis-Related Genes in Chinese Han Patients with Unilateral Renal Agenesis. American journal of nephrology 2017 Jun 46 (1): 55-63. Wu Hangdi, Xu Qian, Xie Jingyuan, Ma Jun, Qiao Panpan, Zhang Wen, Yu Haijin, Wang Weiming, Qian Ying, Zhang Qianying, Guo Yiqing, Tang Yonghua, Chen Xiao-Nong, Wang Zhaohui, Chen N |
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 |
Genetic predisposition to uterine leiomyoma is determined by loci for genitourinary development and genome stability. eLife 2018 Sep 7 . Välimäki Niko, Kuisma Heli, Pasanen Annukka, Heikinheimo Oskari, Sjöberg Jari, Bützow Ralf, Sarvilinna Nanna, Heinonen Hanna-Riikka, Tolvanen Jaana, Bramante Simona, Tanskanen Tomas, Auvinen Juha, Uimari Outi, Alkodsi Amjad, Lehtonen Rainer, Kaasinen Eevi, Palin Kimmo, Aaltonen Lauri |
Copy number variants in hypoplastic right heart syndrome. American journal of medical genetics. Part A 2018 10 176 (12): 2760-2767. Giannakou Andreas, Sicko Robert J, Kay Denise M, Zhang Wei, Romitti Paul A, Caggana Michele, Shaw Gary M, Jelliffe-Pawlowski Laura L, Mills James |
miR-181a-2* expression is different amongst carcinomas from the colorectal serrated route. Mutagenesis 2019 12 35 (3): 233-241. Kondelova Alexandra, Alburquerque-González Begoña, Vychytilova-Faltejskova Petra, García-Solano José, Prochazka Vladimir, Kala Zdenek, Pérez Fernando, Slaby Ondrej, Conesa-Zamora Pab |
A Genetics-First Approach Revealed Monogenic Disorders in Patients With ARM and VACTERL Anomalies. Frontiers in pediatrics 2020 7 8 310. van de Putte Romy, Dworschak Gabriel C, Brosens Erwin, Reutter Heiko M, Marcelis Carlo L M, Acuna-Hidalgo Rocio, Kurtas Nehir E, Steehouwer Marloes, Dunwoodie Sally L, Schmiedeke Eberhard, Märzheuser Stefanie, Schwarzer Nicole, Brooks Alice S, de Klein Annelies, Sloots Cornelius E J, Tibboel Dick, Brisighelli Giulia, Morandi Anna, Bedeschi Maria F, Bates Michael D, Levitt Marc A, Peña Alberto, de Blaauw Ivo, Roeleveld Nel, Brunner Han G, van Rooij Iris A L M, Hoischen Alexand |
Next-generation sequencing identifies rare pathogenic and novel candidate variants in a cohort of Chinese patients with syndromic or nonsyndromic hearing loss. Molecular genetics & genomic medicine 2020 Oct e1539. Xiang Yan-Bao, Xu Chen-Yang, Xu Yun-Zhi, Li Huan-Zheng, Zhou Li-Li, Xu Xue-Qin, Chen Zi-Hui, Tang Shao-H |
Inflammatory Pathways Are Impaired in Alzheimer Disease and Differentially Associated With Apolipoprotein E Status. Journal of neuropathology and experimental neurology 2021 9 80 (10): 922-932. Kloske Courtney M, Dugan Adam J, Weekman Erica M, Winder Zachary, Patel Ela, Nelson Peter T, Fardo David W, Wilcock Donna |
GWAS Identifies a Region Containing the SALL1 Gene in Variation of Pigmentation Intensity Within the Chestnut Coat Color of Horses. The Journal of heredity 2021 Aug . Hammons Vada, Ribeiro Leticia, Munyard Kylie, Sadeghi Raheleh, Miller Donald, Antczak Douglas, Brooks Samantha |
Genome-Wide Association Study of Pelvic Organ Prolapse Using the Michigan Genomics Initiative. Female pelvic medicine & reconstructive surgery 2021 May . Cox Caroline K, Pandit Anita, Zawistowski Matthew, Dutta Diptavo, Narla Goutham, Swenson Carolyn |
The Classification of VACTERL Association into 3 Groups According to the Limb Defect. Plastic and reconstructive surgery. Global open 2021 3 9 (2): e3360. Al-Qattan Mohammad |
Pro-inflammatory cytokine polymorphisms and interactions with dietary alcohol and estrogen, risk factors for invasive breast cancer using a post genome-wide analysis for gene-gene and gene-lifestyle interaction. Scientific reports 2021 Jan 11 (1): 1058. Jung Su Yon, Papp Jeanette C, Sobel Eric M, Pellegrini Matteo, Yu Herbert, Zhang Zuo-Fe |
The Enigmatic Etiology of Oculo-Auriculo-Vertebral Spectrum (OAVS): An Exploratory Gene Variant Interaction Approach in Candidate Genes. Life (Basel, Switzerland) 2022 11 12 (11): . Estandia-Ortega Bernardette, Reyna-Fabián Miriam Erandi, Velázquez-Aragón José Antonio, González-Del Angel Ariadna, Fernández-Hernández Liliana, Alcántara-Ortigoza Miguel Ang |
A genotype-first analysis in a cohort of Mullerian anomaly. Journal of human genetics 2022 1 67 (6): 347-352. Tian Weijie, Chen Na, Ye Yang, Ma Congcong, Qin Chenglu, Niu Yuchen, Xiaoxin L, Zhao Lina, Zhao Hengqiang, Liang Ze, Song Shuang, Wang Yuan, Chen Zefu, Lin Jiachen, Yan Zihui, Duan Jiali, Zhao Sen, Zhang Terry Jianguo, Qiu Guixing, Wu Zhihong, Wu Nan, Zhu L |
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