Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: OSR1[original query] |
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The OSR1 rs12329305 polymorphism contributes to the development of congenital malformations in cases of stillborn/neonatal death. Medical science monitor : international medical journal of experimental and clinical research 2014 20 1531-8. Lozi? Bernarda, Krželj Vjekoslav, Kuzmi?-Prusac Ivana, Kuzmani?-Šamija Radenka, ?apkun Vesna, Lasan Ružica, Zemunik Tatija |
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation.
Nature genetics 2015 Sep . Kato Norihiro, Loh Marie, Takeuchi Fumihiko, Verweij Niek, Wang Xu, Zhang Weihua, Kelly Tanika N, Saleheen Danish, Lehne Benjamin, Leach Irene Mateo, Drong Alexander W, Abbott James, Wahl Simone, Tan Sian-Tsung, Scott William R, Campanella Gianluca, Chadeau-Hyam Marc, Afzal Uzma, Ahluwalia Tarunveer S, Bonder Marc Jan, Chen Peng, Dehghan Abbas, Edwards Todd L, Esko Tõnu, Go Min Jin, Harris Sarah E, Hartiala Jaana, Kasela Silva, Kasturiratne Anuradhani, Khor Chiea-Chuen, Kleber Marcus E, Li Huaixing, Yu Mok Zuan, Nakatochi Masahiro, Sapari Nur Sabrina, Saxena Richa, Stewart Alexandre F R, Stolk Lisette, Tabara Yasuharu, Teh Ai Ling, Wu Ying, Wu Jer-Yuarn, Zhang Yi, Aits Imke, Da Silva Couto Alves Alexessander, Das Shikta, Dorajoo Rajkumar, Hopewell Jemma C, Kim Yun Kyoung, Koivula Robert W, Luan Jian'an, Lyytikäinen Leo-Pekka, Nguyen Quang N, Pereira Mark A, Postmus Iris, Raitakari Olli T, Scannell Bryan Molly, Scott Robert A, Sorice Rossella, Tragante Vinicius, Traglia Michela, White Jon, Yamamoto Ken, Zhang Yonghong, Adair Linda S, Ahmed Alauddin, Akiyama Koichi, Asif Rasheed, Aung Tin, Barroso Inês, Bjonnes Andrew, Braun Timothy R, Cai Hui, Chang Li-Ching, Chen Chien-Hsiun, Cheng Ching-Yu, Chong Yap-Seng, Collins Rory, Courtney Regina, Davies Gail, Delgado Graciela, Do Loi D, Doevendans Pieter A, Gansevoort Ron T, Gao Yu-Tang, Grammer Tanja B, Grarup Niels, Grewal Jagvir, Gu Dongfeng, Wander Gurpreet S, Hartikainen Anna-Liisa, Hazen Stanley L, He Jing, Heng Chew-Kiat, Hixson James E, Hofman Albert, Hsu Chris, Huang Wei, Husemoen Lise L N, Hwang Joo-Yeon, Ichihara Sahoko, Igase Michiya, Isono Masato, Justesen Johanne M, Katsuya Tomohiro, Kibriya Muhammad G, Kim Young Jin, Kishimoto Miyako, Koh Woon-Puay, Kohara Katsuhiko, Kumari Meena, Kwek Kenneth, Lee Nanette R, Lee Jeannette, Liao Jiemin, Lieb Wolfgang, Liewald David C M, Matsubara Tatsuaki, Matsushita Yumi, Meitinger Thomas, Mihailov Evelin, Milani Lili, Mills Rebecca, Mononen Nina, Müller-Nurasyid Martina, Nabika Toru, Nakashima Eitaro, Ng Hong Kiat, Nikus Kjell, Nutile Teresa, Ohkubo Takayoshi, Ohnaka Keizo, Parish Sarah, Paternoster Lavinia, Peng Hao, Peters Annette, Pham Son T, Pinidiyapathirage Mohitha J, Rahman Mahfuzar, Rakugi Hiromi, Rolandsson Olov, Ann Rozario Michelle, Ruggiero Daniela, Sala Cinzia F, Sarju Ralhan, Shimokawa Kazuro, Snieder Harold, Sparsø Thomas, Spiering Wilko, Starr John M, Stott David J, Stram Daniel O, Sugiyama Takao, Szymczak Silke, Tang W H Wilson, Tong Lin, Trompet Stella, Turjanmaa Väinö, Ueshima Hirotsugu, Uitterlinden André G, Umemura Satoshi, Vaarasmaki Marja, van Dam Rob M, van Gilst Wiek H, van Veldhuisen Dirk J, Viikari Jorma S, Waldenberger Melanie, Wang Yiqin, Wang Aili, Wilson Rory, Wong Tien-Yin, Xiang Yong-Bing, Yamaguchi Shuhei, Ye Xingwang, Young Robin D, Young Terri L, Yuan Jian-Min, Zhou Xueya, Asselbergs Folkert W, Ciullo Marina, Clarke Robert, Deloukas Panos, Franke Andre, Franks Paul W, Franks Steve, Friedlander Yechiel, Gross Myron D, Guo Zhirong, Hansen Torben, Jarvelin Marjo-Riitta, Jørgensen Torben, Jukema J Wouter, Kähönen Mika, Kajio Hiroshi, Kivimaki Mika, Lee Jong-Young, Lehtimäki Terho, Linneberg Allan, Miki Tetsuro, Pedersen Oluf, Samani Nilesh J, Sørensen Thorkild I A, Takayanagi Ryoichi, Toniolo Daniela, , , , , Ahsan Habibul, Allayee Hooman, Chen Yuan-Tsong, Danesh John, Deary Ian J, Franco Oscar H, Franke Lude, Heijman Bastiaan T, Holbrook Joanna D, Isaacs Aaron, Kim Bong-Jo, Lin Xu, Liu Jianjun, März Winfried, Metspalu Andres, Mohlke Karen L, Sanghera Dharambir K, Shu Xiao-Ou, van Meurs Joyce B J, Vithana Eranga, Wickremasinghe Ananda R, Wijmenga Cisca, Wolffenbuttel Bruce H W, Yokota Mitsuhiro, Zheng Wei, Zhu Dingliang, Vineis Paolo, Kyrtopoulos Soterios A, Kleinjans Jos C S, McCarthy Mark I, Soong Richie, Gieger Christian, Scott James, Teo Yik-Ying, He Jiang, Elliott Paul, Tai E Shyong, van der Harst Pim, Kooner Jaspal S, Chambers John |
Kidney adysplasia and variable hydronephrosis, a new mutation affecting the odd-skipped related 1 gene in the mouse, causes variable defects in kidney development and hydronephrosis. American journal of physiology. Renal physiology 2015 Jun 308 (12): F1335-42. Davisson Muriel T, Cook Susan A, Akeson Ellen C, Liu Don, Heffner Caleb, Gudis Polyxeni, Fairfield Heather, Murray Stephen |
Identification of five novel genetic loci related to facial morphology by genome-wide association studies.
BMC genomics 2018 Jun 19 (1): 481. Cha Seongwon, Lim Ji Eun, Park Ah Yeon, Do Jun-Hyeong, Lee Si Woo, Shin Chol, Cho Nam Han, Kang Ji-One, Nam Jeong Min, Kim Jong-Sik, Woo Kwang-Man, Lee Seung-Hwan, Kim Jong Yeol, Oh Bermse |
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