Association of the rs3743205 variant of DYX1C1 with dyslexia in Chinese children

Autor: Waye Mary MY, Chou Crystal HN, Ho Connie SH, Lim Cadmon KP

Publikováno v: Behavioral and Brain Functions, Vol 7, Iss 1, p 16 (2011)

Abstract Background Dyslexia is a learning disability that is characterized by difficulties in the acquisition of reading and spelling skills independent of intelligence, motivation or schooling. Studies of western populations have suggested that DYX

Externí odkaz: https://doaj.org/article/d4a7bc639559469686f268beed6ff70f

A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes

Autor: Van Zuydam, Natalie R, Ahlqvist, Emma, Sandholm, Niina, Deshmukh, Harshal, Rayner, N William, Abdalla, Moustafa, Ladenvall, Claes, Ziemek, Daniel, Fauman, Eric, Robertson, Neil R, McKeigue, Paul M, Valo, Erkka, Forsblom, Carol, Harjutsalo, Valma, Finnish Diabetic Nephropathy Study (FinnDiane), Perna, Annalisa, Rurali, Erica, Marcovecchio, M Loredana, Igo, Robert P, Salem, Rany M, Perico, Norberto, Lajer, Maria, Käräjämäki, Annemari, Imamura, Minako, Kubo, Michiaki, Takahashi, Atsushi, Sim, Xueling, Liu, Jianjun, Van Dam, Rob M, Jiang, Guozhi, Tam, Claudia HT, Luk, Andrea OY, Lee, Heung Man, Lim, Cadmon KP, Szeto, Cheuk Chun, So, Wing Yee, Chan, Juliana CN, Group, Hong Kong Diabetes Registry Theme-Based Research Scheme Project, Ang, Su Fen, Dorajoo, Rajkumar, Wang, Ling, Clara, Tan Si Hua, McKnight, Amy-Jayne, Duffy, Seamus, Warren 3 And Genetics Of Kidneys In Diabetes (GoKinD) Study Group, Pezzolesi, Marcus G, GENIE (GEnetics Of Nephropathy An International Effort) Consortium, Marre, Michel, Gyorgy, Beata, Hadjadj, Samy, Hiraki, Linda T, Diabetes Control And Complications Trial (DCCT)/Epidemiology Of Diabetes Interventions And Complications (EDIC) Research Group, Ahluwalia, Tarunveer S, Almgren, Peter, Schulz, Christina-Alexandra, Orho-Melander, Marju, Linneberg, Allan, Christensen, Cramer, Witte, Daniel R, Grarup, Niels, Brandslund, Ivan, Melander, Olle, Paterson, Andrew D, Tregouet, David, Maxwell, Alexander P, Lim, Su Chi, Ma, Ronald CW, Tai, E Shyong, Maeda, Shiro, Lyssenko, Valeriya, Tuomi, Tiinamaija, Krolewski, Andrzej S, Rich, Stephen S, Hirschhorn, Joel N, Florez, Jose C, Dunger, David, Pedersen, Oluf, Hansen, Torben, Rossing, Peter, Remuzzi, Giuseppe, SUrrogate Markers For Micro- And Macrovascular Hard Endpoints For Innovative Diabetes Tools (SUMMIT) Consortium, Brosnan, Mary Julia, Palmer, Colin NA, Groop, Per-Henrik, Colhoun, Helen M, Groop, Leif C, McCarthy, Mark I

Publikováno v: Diabetes, vol 67, iss 7

Identification of sequence variants robustly associated with predisposition to diabetic kidney disease (DKD) has the potential to provide insights into the pathophysiological mechanisms responsible. We conducted a genome-wide association study (GWAS)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1622ca6768b5e956124329f7cbf05537
https://escholarship.org/uc/item/37m0v97n