Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: DAB2[original query] |
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New loci associated with kidney function and chronic kidney disease.
Nature genetics 2010 May 42 (5): 376-84. Köttgen Anna, Pattaro Cristian, Böger Carsten A, Fuchsberger Christian, Olden Matthias, Glazer Nicole L, Parsa Afshin, Gao Xiaoyi, Yang Qiong, Smith Albert V, O'Connell Jeffrey R, Li Man, Schmidt Helena, Tanaka Toshiko, Isaacs Aaron, Ketkar Shamika, Hwang Shih-Jen, Johnson Andrew D, Dehghan Abbas, Teumer Alexander, Paré Guillaume, Atkinson Elizabeth J, Zeller Tanja, Lohman Kurt, Cornelis Marilyn C, Probst-Hensch Nicole M, Kronenberg Florian, Tönjes Anke, Hayward Caroline, Aspelund Thor, Eiriksdottir Gudny, Launer Lenore J, Harris Tamara B, Rampersaud Evadnie, Mitchell Braxton D, Arking Dan E, Boerwinkle Eric, Struchalin Maksim, Cavalieri Margherita, Singleton Andrew, Giallauria Francesco, Metter Jeffrey, de Boer Ian H, Haritunians Talin, Lumley Thomas, Siscovick David, Psaty Bruce M, Zillikens M Carola, Oostra Ben A, Feitosa Mary, Province Michael, de Andrade Mariza, Turner Stephen T, Schillert Arne, Ziegler Andreas, Wild Philipp S, Schnabel Renate B, Wilde Sandra, Munzel Thomas F, Leak Tennille S, Illig Thomas, Klopp Norman, Meisinger Christa, Wichmann H-Erich, Koenig Wolfgang, Zgaga Lina, Zemunik Tatijana, Kolcic Ivana, Minelli Cosetta, Hu Frank B, Johansson Asa, Igl Wilmar, Zaboli Ghazal, Wild Sarah H, Wright Alan F, Campbell Harry, Ellinghaus David, Schreiber Stefan, Aulchenko Yurii S, Felix Janine F, Rivadeneira Fernando, Uitterlinden Andre G, Hofman Albert, Imboden Medea, Nitsch Dorothea, Brandstätter Anita, Kollerits Barbara, Kedenko Lyudmyla, Mägi Reedik, Stumvoll Michael, Kovacs Peter, Boban Mladen, Campbell Susan, Endlich Karlhans, Völzke Henry, Kroemer Heyo K, Nauck Matthias, Völker Uwe, Polasek Ozren, Vitart Veronique, Badola Sunita, Parker Alexander N, Ridker Paul M, Kardia Sharon L R, Blankenberg Stefan, Liu Yongmei, Curhan Gary C, Franke Andre, Rochat Thierry, Paulweber Bernhard, Prokopenko Inga, Wang Wei, Gudnason Vilmundur, Shuldiner Alan R, Coresh Josef, Schmidt Reinhold, Ferrucci Luigi, Shlipak Michael G, van Duijn Cornelia M, Borecki Ingrid, Krämer Bernhard K, Rudan Igor, Gyllensten Ulf, Wilson James F, Witteman Jacqueline C, Pramstaller Peter P, Rettig Rainer, Hastie Nick, Chasman Daniel I, Kao W H, Heid Iris M, Fox Caroline |
Genetic association for renal traits among participants of African ancestry reveals new loci for renal function. PLoS genetics 2011 Sep 7 (9): e1002264. Liu Ching-Ti, Garnaas Maija K, Tin Adrienne, Kottgen Anna, Franceschini Nora, Peralta Carmen A, de Boer Ian H, Lu Xiaoning, Atkinson Elizabeth, Ding Jingzhong, Nalls Michael, Shriner Daniel, Coresh Josef, Kutlar Abdullah, Bibbins-Domingo Kirsten, Siscovick David, Akylbekova Ermeg, Wyatt Sharon, Astor Brad, Mychaleckjy Josef, Li Man, Reilly Muredach P, Townsend Raymond R, Adeyemo Adebowale, Zonderman Alan B, de Andrade Mariza, Turner Stephen T, Mosley Thomas H, Harris Tamara B, , Rotimi Charles N, Liu Yongmei, Kardia Sharon L R, Evans Michele K, Shlipak Michael G, Kramer Holly, Flessner Michael F, Dreisbach Albert W, Goessling Wolfram, Cupples L Adrienne, Kao W Linda, Fox Caroline |
A common genetic variant (97906C>A) of DAB2IP/AIP1 is associated with an increased risk and early onset of lung cancer in Chinese males. PloS one 2011 6 (10): e26944. Yang Lei, Li Yinyan, Ling Xiaoxuan, Liu Lin, Liu Bin, Xu Kevin, Bin Xiaonong, Ji Weidong, Lu Jiach |
Association of eGFR-Related Loci Identified by GWAS with Incident CKD and ESRD. PLoS genetics 2011 Sep 7 (9): e1002292. Böger Carsten A, Gorski Mathias, Li Man, Hoffmann Michael M, Huang Chunmei, Yang Qiong, Teumer Alexander, Krane Vera, O'Seaghdha Conall M, Kutalik Zoltán, Wichmann H-Erich, Haak Thomas, Boes Eva, Coassin Stefan, Coresh Josef, Kollerits Barbara, Haun Margot, Paulweber Bernhard, Köttgen Anna, Li Guo, Shlipak Michael G, Powe Neil, Hwang Shih-Jen, Dehghan Abbas, Rivadeneira Fernando, Uitterlinden André, Hofman Albert, Beckmann Jacques S, Krämer Bernhard K, Witteman Jacqueline, Bochud Murielle, Siscovick David, Rettig Rainer, Kronenberg Florian, Wanner Christoph, Thadhani Ravi I, Heid Iris M, Fox Caroline S, Kao W H, |
Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function. Human molecular genetics 2012 Dec 21 (24): 5329-43. Chasman Daniel I, Fuchsberger Christian, Pattaro Cristian, Teumer Alexander, Böger Carsten A, Endlich Karlhans, Olden Matthias, Chen Ming-Huei, Tin Adrienne, Taliun Daniel, Li Man, Gao Xiaoyi, Gorski Mathias, Yang Qiong, Hundertmark Claudia, Foster Meredith C, O'Seaghdha Conall M, Glazer Nicole, Isaacs Aaron, Liu Ching-Ti, Smith Albert V, O'Connell Jeffrey R, Struchalin Maksim, Tanaka Toshiko, Li Guo, Johnson Andrew D, Gierman Hinco J, Feitosa Mary F, Hwang Shih-Jen, Atkinson Elizabeth J, Lohman Kurt, Cornelis Marilyn C, Johansson Asa, Tönjes Anke, Dehghan Abbas, Lambert Jean-Charles, Holliday Elizabeth G, Sorice Rossella, Kutalik Zoltan, Lehtimäki Terho, Esko Tõnu, Deshmukh Harshal, Ulivi Sheila, Chu Audrey Y, Murgia Federico, Trompet Stella, Imboden Medea, Coassin Stefan, Pistis Giorgio, , , , , Harris Tamara B, Launer Lenore J, Aspelund Thor, Eiriksdottir Gudny, Mitchell Braxton D, Boerwinkle Eric, Schmidt Helena, Cavalieri Margherita, Rao Madhumathi, Hu Frank, Demirkan Ayse, Oostra Ben A, de Andrade Mariza, Turner Stephen T, Ding Jingzhong, Andrews Jeanette S, Freedman Barry I, Giulianini Franco, Koenig Wolfgang, Illig Thomas, Meisinger Christa, Gieger Christian, Zgaga Lina, Zemunik Tatijana, Boban Mladen, Minelli Cosetta, Wheeler Heather E, Igl Wilmar, Zaboli Ghazal, Wild Sarah H, Wright Alan F, Campbell Harry, Ellinghaus David, Nöthlings Ute, Jacobs Gunnar, Biffar Reiner, Ernst Florian, Homuth Georg, Kroemer Heyo K, Nauck Matthias, Stracke Sylvia, Völker Uwe, Völzke Henry, Kovacs Peter, Stumvoll Michael, Mägi Reedik, Hofman Albert, Uitterlinden Andre G, Rivadeneira Fernando, Aulchenko Yurii S, Polasek Ozren, Hastie Nick, Vitart Veronique, Helmer Catherine, Wang Jie Jin, Stengel Bénédicte, Ruggiero Daniela, Bergmann Sven, Kähönen Mika, Viikari Jorma, Nikopensius Tiit, Province Michael, Ketkar Shamika, Colhoun Helen, Doney Alex, Robino Antonietta, Krämer Bernhard K, Portas Laura, Ford Ian, Buckley Brendan M, Adam Martin, Thun Gian-Andri, Paulweber Bernhard, Haun Margot, Sala Cinzia, Mitchell Paul, Ciullo Marina, Kim Stuart K, Vollenweider Peter, Raitakari Olli, Metspalu Andres, Palmer Colin, Gasparini Paolo, Pirastu Mario, Jukema J Wouter, Probst-Hensch Nicole M, Kronenberg Florian, Toniolo Daniela, Gudnason Vilmundur, Shuldiner Alan R, Coresh Josef, Schmidt Reinhold, Ferrucci Luigi, Siscovick David S, van Duijn Cornelia M, Borecki Ingrid B, Kardia Sharon L R, Liu Yongmei, Curhan Gary C, Rudan Igor, Gyllensten Ulf, Wilson James F, Franke Andre, Pramstaller Peter P, Rettig Rainer, Prokopenko Inga, Witteman Jacqueline, Hayward Caroline, Ridker Paul M, Parsa Afshin, Bochud Murielle, Heid Iris M, Kao W H Linda, Fox Caroline S, Köttgen An |
Association of the variant rs2243421 of human DOC-2/DAB2 interactive protein gene (hDAB2IP) with gastric cancer in the Chinese Han population. Gene 2012 Dec . Xu S, Zhou Y, Du WD, Chen G, Zhou FS, Schneider M, Ma XL, Xu HY, Zhang XJ |
Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment.
Genes, brain, and behavior 2014 Apr 13 (4): 418-29. Nudel R, Simpson N H, Baird G, O'Hare A, Conti-Ramsden G, Bolton P F, Hennessy E R, , Ring S M, Davey Smith G, Francks C, Paracchini S, Monaco A P, Fisher S E, Newbury D |
Genetic variations in TP53 binding sites are predictors of clinical outcomes in prostate cancer patients. Archives of toxicology 2014 Apr 88 (4): 901-11. Lin Victor C, Huang Chao-Yuan, Lee Yung-Chin, Yu Chia-Cheng, Chang Ta-Yuan, Lu Te-Ling, Huang Shu-Pin, Bao Bo-Yi |
Importance of prostate androgen-regulated mucin-like protein 1 in development of the bovine blastocyst. BMC developmental biology 2019 7 19 (1): 15. Zolini Adriana M, Negrón-Pérez Verónica M, Hansen Peter |
Exonic variants of genes related to the vitamin D signaling pathway in the families of familial multiple sclerosis using whole-exome next generation sequencing. Brain and behavior 2019 3 9 (4): e01272. Pytel Vanesa, Matías-Guiu Jordi A, Torre-Fuentes Laura, Montero-Escribano Paloma, Maietta Paolo, Botet Javier, Álvarez Sara, Gómez-Pinedo Ulises, Matías-Guiu Jor |
Dab2 gene variant is associated with increased coronary artery disease risk in Chinese Han population. Medicine 2020 Jul 99 (27): e20924. Wang Yinghong, Wang Yongtao, Adi Dilare, He XiaoDong, Liu Fen, Abudesimu Asiya, Fu Zhenyan, Ma Yito |
Genetic polymorphism of the Dab2 gene and its association with Type 2 Diabetes Mellitus in the Chinese Uyghur population. PeerJ 2023 6 11 e15536. Yan-Peng Li, Dilare Adi, Ying-Hong Wang, Yong-Tao Wang, Xiao-Lei Li, Zhen-Yan Fu, Fen Liu, Aibibanmu Aizezi, Jialin Abuzhalihan, Mintao Gai, Xiang Ma, Xiao-Mei Li, Xiang Xie, YiTong |
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