Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 53 Records) |
Query Trace: RP1[original query] |
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Possible association of IL-4 VNTR polymorphism with susceptibility to preeclampsia. BioMed research international 2014 2014 497031. Salimi Saeedeh, Mohammadoo-Khorasani Milad, Yaghmaei Minoo, Mokhtari Mojgan, Moossavi Mary |
High risk association of IL-4 VNTR polymorphism with asthma in a North Indian population. Cytokine 2014 Mar 66 (1): 87-94. Birbian Niti, Singh Jagtar, Jindal Surinder Kumar, Sobti Ranbir Chand |
Association between interleukin-4 gene intron 3 VNTR polymorphism and cancer risk. Cancer cell international 2014 14 (1): 131. Duan Yin, Pan Chi, Shi Jinan, Chen Hailong, Zhang Suzh |
A genome-wide association study for diabetic retinopathy in a Japanese population: potential association with a long intergenic non-coding RNA.
PloS one 2014 9 (11): e111715. Awata Takuya, Yamashita Hisakuni, Kurihara Susumu, Morita-Ohkubo Tomoko, Miyashita Yumi, Katayama Shigehiro, Mori Keisuke, Yoneya Shin, Kohda Masakazu, Okazaki Yasushi, Maruyama Taro, Shimada Akira, Yasuda Kazuki, Nishida Nao, Tokunaga Katsushi, Koike Asa |
Interleukin-1ß (IL-1ß) & IL-4 gene polymorphisms in patients with systemic lupus erythematosus (SLE) & their association with susceptibility to SLE. The Indian journal of medical research 2016 May 143 (5): 591-6. Mohammadoo-Khorasani Milad, Salimi Saeedeh, Tabatabai Ehsan, Sandoughi Mahnaz, Zakeri Zahra, Farajian-Mashhadi Farzan |
Genome-wide time-to-event analysis on smoking progression stages in a family-based study. Brain and behavior 2016 Apr e00462. He Liang, Pitkäniemi Janne, Heikkilä Kauko, Chou Yi-Ling, Madden Pamela A F, Korhonen Tellervo, Sarin Antti-Pekka, Ripatti Samuli, Kaprio Jaakko, Loukola A |
RP1-13D10.2 Is a Novel Modulator of Statin-Induced Changes in Cholesterol. Circulation. Cardiovascular genetics 2016 Apr . Mitchel Katrina, Theusch Elizabeth, Cubitt Celia, Dosé Andréa C, Stevens Kristen, Naidoo Devesh, Medina Marisa |
Genome-wide Regional Heritability Mapping Identifies a Locus Within the TOX2 Gene Associated With Major Depressive Disorder. Biological psychiatry 2016 Dec . Zeng Yanni, Navarro Pau, Shirali Masoud, Howard David M, Adams Mark J, Hall Lynsey S, Clarke Toni-Kim, Thomson Pippa A, Smith Blair H, Murray Alison, Padmanabhan Sandosh, Hayward Caroline, Boutin Thibaud, MacIntyre Donald J, Lewis Cathryn M, Wray Naomi R, Mehta Divya, Penninx Brenda W J H, Milaneschi Yuri, Baune Bernhard T, Air Tracy, Hottenga Jouke-Jan, Mbarek Hamdi, Castelao Enrique, Pistis Giorgio, Schulze Thomas G, Streit Fabian, Forstner Andreas J, Byrne Enda M, Martin Nicholas G, Breen Gerome, Müller-Myhsok Bertram, Lucae Susanne, Kloiber Stefan, Domenici Enrico, , Deary Ian J, Porteous David J, Haley Chris S, McIntosh Andrew |
A founder mutation in CERKL is a major cause of retinal dystrophy in Finland. Acta ophthalmologica 2017 10 96 (2): 183-191. Avela Kristiina, Sankila Eeva-Marja, Seitsonen Sanna, Kuuluvainen Liina, Barton Stephanie, Gillies Stuart, Aittomäki Kristii |
Mutations in Splicing Factor Genes Are a Major Cause of Autosomal Dominant Retinitis Pigmentosa in Belgian Families. PloS one 2017 1 12 (1): e0170038. Van Cauwenbergh Caroline, Coppieters Frauke, Roels Dimitri, De Jaegere Sarah, Flipts Helena, De Zaeytijd Julie, Walraedt Sophie, Claes Charlotte, Fransen Erik, Van Camp Guy, Depasse Fanny, Casteels Ingele, de Ravel Thomy, Leroy Bart P, De Baere Elfri |
Toward the Mutational Landscape of Autosomal Dominant Retinitis Pigmentosa: A Comprehensive Analysis of 258 Spanish Families. Investigative ophthalmology & visual science 2018 5 59 (6): 2345-2354. Martin-Merida Inmaculada, Aguilera-Garcia Domingo, Fernandez-San Jose P, Blanco-Kelly Fiona, Zurita Olga, Almoguera Berta, Garcia-Sandoval Blanca, Avila-Fernandez Almudena, Arteche Ana, Minguez Pablo, Carballo Miguel, Corton Marta, Ayuso Carm |
Targeted Next-Generation Sequencing Reveals Novel RP1 Mutations in Autosomal Recessive Retinitis Pigmentosa. Genetic testing and molecular biomarkers 2018 2 22 (2): 109-114. Li Shujin, Yang Mu, Liu Wenjing, Liu Yuqing, Zhang Lin, Yang Yeming, Sundaresan Periasamy, Yang Zhenglin, Zhu Xianj |
Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels.
Circulation 2019 Jan 139 (5): 620-635. Sabater-Lleal Maria, Huffman Jennifer E, de Vries Paul S, Marten Jonathan, Mastrangelo Michael A, Song Ci, Pankratz Nathan, Ward-Caviness Cavin K, Yanek Lisa R, Trompet Stella, Delgado Graciela E, Guo Xiuqing, Bartz Traci M, Martinez-Perez Angel, Germain Marine, de Haan Hugoline G, Ozel Ayse B, Polasek Ozren, Smith Albert V, Eicher John D, Reiner Alex P, Tang Weihong, Davies Neil M, Stott David J, Rotter Jerome I, Tofler Geoffrey H, Boerwinkle Eric, de Maat Moniek P M, Kleber Marcus E, Welsh Paul, Brody Jennifer A, Chen Ming-Huei, Vaidya Dhananjay, Soria José Manuel, Suchon Pierre, van Hylckama Vlieg Astrid, Desch Karl C, Kolcic Ivana, Joshi Peter K, Launer Lenore J, Harris Tamara B, Campbell Harry, Rudan Igor, Becker Diane M, Li Jun Z, Rivadeneira Fernando, Uitterlinden André G, Hofman Albert, Franco Oscar H, Cushman Mary, Psaty Bruce M, Morange Pierre-Emmanuel, McKnight Barbara, Chong Michael R, Fernandez-Cadenas Israel, Rosand Jonathan, Lindgren Arne, , Gudnason Vilmundur, Wilson James F, Hayward Caroline, Ginsburg David, Fornage Myriam, Rosendaal Frits R, Souto Juan Carlos, Becker Lewis C, Jenny Nancy S, März Winfried, Jukema J Wouter, Dehghan Abbas, Trégouët David-Alexandre, Morrison Alanna C, Johnson Andrew D, O'Donnell Christopher J, Strachan David P, Lowenstein Charles J, Smith Nicholas |
Analysis of 12 variants in the development of gastric and colorectal cancers. World journal of gastroenterology 2017 Dec 23 (48): 8533-8543. Cavalcante Giovanna C, Amador Marcos At, Ribeiro Dos Santos André M, Carvalho Darlen C, Andrade Roberta B, Pereira Esdras Eb, Fernandes Marianne R, Costa Danielle F, Santos Ney Pc, Assumpção Paulo P, Ribeiro Dos Santos Ândrea, Santos Sidn |
A frequent variant in the Japanese population determines quasi-Mendelian inheritance of rare retinal ciliopathy. Nature communications 2019 6 10 (1): 2884. Nikopoulos Konstantinos, Cisarova Katarina, Quinodoz Mathieu, Koskiniemi-Kuendig Hanna, Miyake Noriko, Farinelli Pietro, Rehman Atta Ur, Khan Muhammad Imran, Prunotto Andrea, Akiyama Masato, Kamatani Yoichiro, Terao Chikashi, Miya Fuyuki, Ikeda Yasuhiro, Ueno Shinji, Fuse Nobuo, Murakami Akira, Wada Yuko, Terasaki Hiroko, Sonoda Koh-Hei, Ishibashi Tatsuro, Kubo Michiaki, Cremers Frans P M, Kutalik Zoltán, Matsumoto Naomichi, Nishiguchi Koji M, Nakazawa Toru, Rivolta Car |
Associations among Genetic Variants and Intracranial Aneurysm in a Chinese Population. Yonsei medical journal 2019 Jul 60 (7): 651-658. Li Bingyang, Hu Chongyu, Liu Junyu, Liao Xin, Xun Jiayu, Xiao Manqian, Yan Junx |
Genetic characteristics of retinitis pigmentosa in 1204 Japanese patients. Journal of medical genetics 2019 Jun . Koyanagi Yoshito, Akiyama Masato, Nishiguchi Koji M, Momozawa Yukihide, Kamatani Yoichiro, Takata Sadaaki, Inai Chihiro, Iwasaki Yusuke, Kumano Mikako, Murakami Yusuke, Omodaka Kazuko, Abe Toshiaki, Komori Shiori, Gao Dan, Hirakata Toshiaki, Kurata Kentaro, Hosono Katsuhiro, Ueno Shinji, Hotta Yoshihiro, Murakami Akira, Terasaki Hiroko, Wada Yuko, Nakazawa Toru, Ishibashi Tatsuro, Ikeda Yasuhiro, Kubo Michiaki, Sonoda Koh-H |
Genomewide association study of C-peptide surfaces key regulatory genes in Indians.
Journal of genetics 2019 Mar 98 (1): . Bandesh Khushdeep, Prasad Gauri, Giri Anil Kumar, Saroja Voruganti V, Butte Nancy F, Cole Shelley A, Comuzzie Anthony G, , Tandon Nikhil, Bharadwaj Dwaipay |
IL-1RN VNTR, IL-2(-330), and IL-4 VNTR gene polymorphisms in patients with chronic rhinosinusitis with sinonasal polyposis. Turkish journal of medical sciences 2019 Oct 49 (5): 1411-1417. Kuran Gökhan, Aslan Hüseyin, Hayto?lu Süheyl, Özalp Yüre?ir Özge, Tu? Bozdo?an Sevc |
Complement C4 Gene Copy Number Variation Genotyping by High Resolution Melting PCR. International journal of molecular sciences 2020 Aug 21 (17): . Jaimes-Bernal Claudia P, Trujillo Monte, Márquez Francisco José, Caruz Anton |
A founder Alu insertion in RP1 gene in Japanese patients with retinitis pigmentosa. Japanese journal of ophthalmology 2020 3 64 (4): 346-350. Nishiguchi Koji Miura, Fujita Kosuke, Ikeda Yasuhiro, Kunikata Hiroshi, Koyanagi Yoshito, Akiyama Masato, Abe Toshiaki, Wada Yuko, Sonoda Koh-Hei, Nakazawa To |
Genetic and clinical findings of panel-based targeted exome sequencing in a northeast Chinese cohort with retinitis pigmentosa. Molecular genetics & genomic medicine 2020 2 8 (4): e1184. Sun Yan, Li Wei, Li Jian-Kang, Wang Zhuo-Shi, Bai Jin-Yue, Xu Ling, Xing Bo, Yang Wen, Wang Zi-Wei, Wang Lu-Sheng, He Wei, Chen Fa |
EYS is a major gene involved in retinitis pigmentosa in Japan: genetic landscapes revealed by stepwise genetic screening. Scientific reports 2020 11 10 (1): 20770. Numa Shogo, Oishi Akio, Higasa Koichiro, Oishi Maho, Miyata Manabu, Hasegawa Tomoko, Ikeda Hanako Ohashi, Otsuka Yuki, Matsuda Fumihiko, Tsujikawa Akita |
In Silico identification of a common mobile element insertion in exon 4 of RP1. Scientific reports 2021 6 11 (1): 13381. Won Dongju, Hwang Joo-Yeon, Shim Yeeun, Byeon Suk Ho, Lee Junwon, Lee Christopher Seungkyu, Kim Min, Lim Hyun Taek, Choi Jong Rak, Lee Seung-Tae, Han Ji |
Genotype-Phenotype Correlations in RP1-Associated Retinal Dystrophies: A Multi-Center Cohort Study in JAPAN. Journal of clinical medicine 2021 6 10 (11): . Mizobuchi Kei, Hayashi Takaaki, Oishi Noriko, Kubota Daiki, Kameya Shuhei, Higasa Koichiro, Futami Takuma, Kondo Hiroyuki, Hosono Katsuhiro, Kurata Kentaro, Hotta Yoshihiro, Yoshitake Kazutoshi, Iwata Takeshi, Matsuura Tomokazu, Nakano Tadas |
Epidermal Growth Factor Receptor Mutation Mechanisms in Nonsmall Cell Lung Cancer by Transcriptome Sequencing. Cancer biotherapy & radiopharmaceuticals 2021 5 37 (7): 560-568. Yu Min, Huo Shufen, Sun Li, Gao Jinglong, Liu Yi, Yu Jiao, Liu Fuqiang, Sheng Sen, Nie Xinyu, Nan Qiaofeng, Tian Yingxu |
Regional differences in genes and variants causing retinitis pigmentosa in Japan. Japanese journal of ophthalmology 2021 2 65 (3): 338-343. Koyanagi Yoshito, Akiyama Masato, Nishiguchi Koji M, Momozawa Yukihide, Kamatani Yoichiro, Takata Sadaaki, Inai Chihiro, Iwasaki Yusuke, Kumano Mikako, Murakami Yusuke, Komori Shiori, Gao Dan, Kurata Kentaro, Hosono Katsuhiro, Ueno Shinji, Hotta Yoshihiro, Murakami Akira, Terasaki Hiroko, Wada Yuko, Nakazawa Toru, Ishibashi Tatsuro, Ikeda Yasuhiro, Kubo Michiaki, Sonoda Koh-H |
Variant Profiling of a Large Cohort of 138 Chinese Families With Autosomal Dominant Retinitis Pigmentosa. Frontiers in cell and developmental biology 2021 2 8 629994. Xiao Ting, Xie Yue, Zhang Xin, Xu Ke, Zhang Xiaohui, Jin Zi-Bing, Li Ya |
Genetic epidemiology of inherited retinal diseases in a large patient cohort followed at a single center in Italy. Scientific reports 2022 12 12 (1): 20815. Karali Marianthi, Testa Francesco, Di Iorio Valentina, Torella Annalaura, Zeuli Roberta, Scarpato Margherita, Romano Francesca, Onore Maria Elena, Pizzo Mariateresa, Melillo Paolo, Brunetti-Pierri Raffaella, Passerini Ilaria, Pelo Elisabetta, Cremers Frans P M, Esposito Gabriella, Nigro Vincenzo, Simonelli Francesca, Banfi Sand |
LncRNA RP1-276N6.2 Expression and RP1-276N6.2 Gene Polymorphisms Contribute to the Risk of Coronary Artery Disease in Chinese Han Population. DNA and cell biology 2023 10 . Lijuan Chen, Mingming Zhao, Mingsha Zhou, Jia Luo, Shan Li, Xing Liu, Zheng Cheng, Yang Zhuo, Weiqi Zeng, Zhiyu Zhang, Li Zh |
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- Page last updated:Apr 22, 2024
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