Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: HS6ST1[original query] |
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Genome-wide Association Studies Identify Genetic Loci Associated With Albuminuria in Diabetes.
Diabetes 2015 Dec . Teumer Alexander, Tin Adrienne, Sorice Rossella, Gorski Mathias, Yeo Nan Cher, Chu Audrey Y, Li Man, Li Yong, Mijatovic Vladan, Ko Yi-An, Taliun Daniel, Luciani Alessandro, Chen Ming-Huei, Yang Qiong, Foster Meredith C, Olden Matthias, Hiraki Linda T, Tayo Bamidele O, Fuchsberger Christian, Dieffenbach Aida Karina, Shuldiner Alan R, Smith Albert V, Zappa Allison M, Lupo Antonio, Kollerits Barbara, Ponte Belen, Stengel Bénédicte, Krämer Bernhard K, Paulweber Bernhard, Mitchell Braxton D, Hayward Caroline, Helmer Catherine, Meisinger Christa, Gieger Christian, Shaffer Christian M, Müller Christian, Langenberg Claudia, Ackermann Daniel, Siscovick David, , Boerwinkle Eric, Kronenberg Florian, Ehret Georg B, Homuth Georg, Waeber Gerard, Navis Gerjan, Gambaro Giovanni, Malerba Giovanni, Eiriksdottir Gudny, Li Guo, Wichmann H Erich, Grallert Harald, Wallaschofski Henri, Völzke Henry, Brenner Herrmann, Kramer Holly, Leach I Mateo, Rudan Igor, Hillege J L, Beckmann Jacques S, Lambert Jean Charles, Luan Jian'an, Zhao Jing Hua, Chalmers John, Coresh Josef, Denny Joshua C, Butterbach Katja, Launer Lenore J, Ferrucci Luigi, Kedenko Lyudmyla, Haun Margot, Metzger Marie, Woodward Mark, Hoffman Matthew J, Nauck Matthias, Waldenberger Melanie, Pruijm Menno, Bochud Murielle, Rheinberger Myriam, Verweij N, Wareham Nicholas J, Endlich Nicole, Soranzo Nicole, Polasek Ozren, van der Harst P, Pramstaller Peter Paul, Vollenweider Peter, Wild Philipp S, Gansevoort R T, Rettig Rainer, Biffar Reiner, Carroll Robert J, Katz Ronit, Loos Ruth J F, Hwang Shih-Jen, Coassin Stefan, Bergmann Sven, Rosas Sylvia E, Stracke Sylvia, Harris Tamara B, Corre Tanguy, Zeller Tanja, Illig Thomas, Aspelund Thor, Tanaka Toshiko, Lendeckel Uwe, Völker Uwe, Gudnason Vilmundur, Chouraki Vincent, Koenig Wolfgang, Kutalik Zoltan, O'Connell Jeffrey R, Parsa Afshin, Heid Iris M, Paterson Andrew D, de Boer Ian H, Devuyst Olivier, Lazar Jozef, Endlich Karlhans, Susztak Katalin, Tremblay Johanne, Hamet Pavel, Jacob Howard J, Böger Carsten A, Fox Caroline S, Pattaro Cristian, Köttgen An |
Prevalence and associated phenotypes of PLXNA1 variants in normosmic and anosmic idiopathic hypogonadotropic hypogonadism. Clinical genetics 2019 Feb 95 (2): 320-324. Kotan Leman D, Isik Emregul, Turan Ihsan, Mengen Eda, Akkus Gamze, Tastan Mehmet, Gurbuz Fatih, Yuksel Bilgin, Topaloglu A Kem |
Clinical characteristics and molecular genetic analysis of a cohort with idiopathic congenital hypogonadism. Journal of pediatric endocrinology & metabolism : JPEM 2021 4 34 (6): 771-780. Turkyilmaz Ayberk, Cayir Atilla, Yarali Oguzhan, Kurnaz Erdal, Kartal Baykan Emine, Arslan Ates Esra, Demirbilek Husey |
Exploring the Genetic Diversity of Isolated Hypogonadotropic Hypogonadism and Its Phenotypic Spectrum: A Case Series. Journal of reproduction & infertility 2021 3 22 (1): 38-46. Danda Vijay Sheker Reddy, Paidipelly Srinivas Rao, Verepula Madhavi, Lodha Piyush, Thaduri Krishna Reddy, Konda Chaitanya, Ruhi Aps |
Correlation Analysis of Genotypes and Phenotypes in Chinese Male Pediatric Patients With Congenital Hypogonadotropic Hypogonadism. Frontiers in endocrinology 2022 13 846801. Wang Yi, Qin Miao, Fan Lijun, Gong Chunx |
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- Page last updated:Apr 16, 2024
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