Human Genome Epidemiology Literature Finder
Records 1 - 17 (of 17 Records) |
Query Trace: WDR72[original query] |
---|
A genome-wide association study identifies a novel major locus for glycemic control in type 1 diabetes, as measured by both A1C and glucose. Diabetes 2010 Feb 59 (2): 539-49. Paterson Andrew D, Waggott Daryl, Boright Andrew P, Hosseini S Mohsen, Shen Enqing, Sylvestre Marie-Pierre, Wong Isidro, Bharaj Bhupinder, Cleary Patricia A, Lachin John M, , Below Jennifer E, Nicolae Dan, Cox Nancy J, Canty Angelo J, Sun Lei, Bull Shelley B, |
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 |
Evaluation of four novel genetic variants affecting hemoglobin A1c levels in a population-based type 2 diabetes cohort (the HUNT2 study). BMC medical genetics 2011 12 (1): 20. Hertel Jens K, Johansson Stefan, Ræder Helge, Platou Carl G P, Midthjell Kristian, Hveem Kristian, Molven Anders, Njølstad Pål |
Genome-wide study identifies PTPRO and WDR72 and FOXQ1-SUMO1P1 interaction associated with neurocognitive function.
Journal of psychiatric research 2012 Feb 46 (2): 271-8. LeBlanc Marissa, Kulle Bettina, Sundet Kjetil, Agartz Ingrid, Melle Ingrid, Djurovic Srdjan, Frigessi Arnoldo, Andreassen Ole |
Generalization of associations of kidney-related genetic loci to American Indians. Clinical journal of the American Society of Nephrology : CJASN 2013 Dec . Franceschini N, Haack K, Almasy L, Laston S, Lee ET, Best LG, Fabsitz RR, Maccluer JW, Howard BV, Umans JG, Cole SA |
Analysis of Polymorphisms in Genes Differentially Expressed in the Enamel of Mice with Different Genetic Susceptibilities to Dental Fluorosis. Caries research 2018 8 53 (2): 228-233. Charone Senda, Küchler Erika Calvano, Leite Aline de Lima, Silva Fernandes Mileni, Taioqui Pelá Vinicius, Martini Tatiana, Brondino Bárbara Margarido, Magalhães Ana Carolina, Dionisio Thiago J, F Santos Carlos, Buzalaf Marília Afonso Rabe |
Clinical and genetic associations of renal function and diabetic kidney disease in the United Arab Emirates: a cross-sectional study. BMJ open 2018 12 8 (12): e020759. Osman Wael M, Jelinek Herbert F, Tay Guan K, Khandoker Ahsan H, Khalaf Kinda, Almahmeed Wael, Hassan Mohamed H, Alsafar Habiba |
Sequence variants associating with urinary biomarkers.
Human molecular genetics 2019 04 28 (7): 1199-1211. Benonisdottir Stefania, Kristjansson Ragnar P, Oddsson Asmundur, Steinthorsdottir Valgerdur, Mikaelsdottir Evgenia, Kehr Birte, Jensson Brynjar O, Arnadottir Gudny A, Sulem Gerald, Sveinbjornsson Gardar, Kristmundsdottir Snaedis, Ivarsdottir Erna V, Tragante Vinicius, Gunnarsson Bjarni, Runolfsdottir Hrafnhildur Linnet, Arthur Joseph G, Deaton Aimee M, Eyjolfsson Gudmundur I, Davidsson Olafur B, Asselbergs Folkert W, Hreidarsson Astradur B, Rafnar Thorunn, Thorleifsson Gudmar, Edvardsson Vidar, Sigurdsson Gunnar, Helgadottir Anna, Halldorsson Bjarni V, Masson Gisli, Holm Hilma, Onundarson Pall T, Indridason Olafur S, Benediktsson Rafn, Palsson Runolfur, Gudbjartsson Daniel F, Olafsson Isleifur, Thorsteinsdottir Unnur, Sulem Patrick, Stefansson Ka |
Genome-wide association study for proliferative diabetic retinopathy in Africans.
NPJ genomic medicine 2019 4 20. Liu Chang, Chen Guanjie, Bentley Amy R, Doumatey Ayo, Zhou Jie, Adeyemo Adebowale, Yang Jinkui, Rotimi Charl |
Genetic variants of calcium and vitamin D metabolism in kidney stone disease.
Nature communications 2019 Nov 10 (1): 5175. Howles Sarah A, Wiberg Akira, Goldsworthy Michelle, Bayliss Asha L, Gluck Anna K, Ng Michael, Grout Emily, Tanikawa Chizu, Kamatani Yoichiro, Terao Chikashi, Takahashi Atsushi, Kubo Michiaki, Matsuda Koichi, Thakker Rajesh V, Turney Benjamin W, Furniss Domin |
Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline.
Kidney international 2020 11 99 (4): 926-939. Gorski Mathias, Jung Bettina, Li Yong, Matias-Garcia Pamela R, Wuttke Matthias, Coassin Stefan, Thio Chris H L, Kleber Marcus E, Winkler Thomas W, Wanner Veronika, Chai Jin-Fang, Chu Audrey Y, Cocca Massimiliano, Feitosa Mary F, Ghasemi Sahar, Hoppmann Anselm, Horn Katrin, Li Man, Nutile Teresa, Scholz Markus, Sieber Karsten B, Teumer Alexander, Tin Adrienne, Wang Judy, Tayo Bamidele O, Ahluwalia Tarunveer S, Almgren Peter, Bakker Stephan J L, Banas Bernhard, Bansal Nisha, Biggs Mary L, Boerwinkle Eric, Bottinger Erwin P, Brenner Hermann, Carroll Robert J, Chalmers John, Chee Miao-Li, Chee Miao-Ling, Cheng Ching-Yu, Coresh Josef, de Borst Martin H, Degenhardt Frauke, Eckardt Kai-Uwe, Endlich Karlhans, Franke Andre, Freitag-Wolf Sandra, Gampawar Piyush, Gansevoort Ron T, Ghanbari Mohsen, Gieger Christian, Hamet Pavel, Ho Kevin, Hofer Edith, Holleczek Bernd, Xian Foo Valencia Hui, Hutri-Kähönen Nina, Hwang Shih-Jen, Ikram M Arfan, Josyula Navya Shilpa, Kähönen Mika, Khor Chiea-Chuen, Koenig Wolfgang, Kramer Holly, Krämer Bernhard K, Kühnel Brigitte, Lange Leslie A, Lehtimäki Terho, Lieb Wolfgang, , , Loos Ruth J F, Lukas Mary Ann, Lyytikäinen Leo-Pekka, Meisinger Christa, Meitinger Thomas, Melander Olle, Milaneschi Yuri, Mishra Pashupati P, Mononen Nina, Mychaleckyj Josyf C, Nadkarni Girish N, Nauck Matthias, Nikus Kjell, Ning Boting, Nolte Ilja M, O'Donoghue Michelle L, Orho-Melander Marju, Pendergrass Sarah A, Penninx Brenda W J H, Preuss Michael H, Psaty Bruce M, Raffield Laura M, Raitakari Olli T, Rettig Rainer, Rheinberger Myriam, Rice Kenneth M, Rosenkranz Alexander R, Rossing Peter, Rotter Jerome I, Sabanayagam Charumathi, Schmidt Helena, Schmidt Reinhold, Schöttker Ben, Schulz Christina-Alexandra, Sedaghat Sanaz, Shaffer Christian M, Strauch Konstantin, Szymczak Silke, Taylor Kent D, Tremblay Johanne, Chaker Layal, van der Harst Pim, van der Most Peter J, Verweij Niek, Völker Uwe, Waldenberger Melanie, Wallentin Lars, Waterworth Dawn M, White Harvey D, Wilson James G, Wong Tien-Yin, Woodward Mark, Yang Qiong, Yasuda Masayuki, Yerges-Armstrong Laura M, Zhang Yan, Snieder Harold, Wanner Christoph, Böger Carsten A, Köttgen Anna, Kronenberg Florian, Pattaro Cristian, Heid Iris |
Genome-Wide Association Study Identifies Eight Novel Loci for Susceptibility of Scrub Typhus and Highlights Immune-Related Signaling Pathways in Its Pathogenesis. Cells 2021 Mar 10 (3): . Kim Yong-Chan, Kim Soriul, Kim Hee-Kwon, Lee Yi, Shin Chol, Lee Chang-Seop, Jeong Byung-Ho |
Multivariate GWAS of Structural Dental Anomalies and Dental Caries in a Multi-Ethnic Cohort.
Frontiers in dental medicine 2021 1 2 . Alotaibi Rasha N, Howe Brian J, Moreno Uribe Lina M, Ramirez Consuelo Valencia, Restrepo Claudia, Deleyiannis Frederic W B, Padilla Carmencita, Orioli Ieda M, Buxó Carmen J, Hecht Jacqueline T, Wehby George L, Neiswanger Katherine, Murray Jeffery C, Shaffer John R, Weinberg Seth M, Marazita Mary |
A Genetic Polymorphism in the WDR72 Gene is Associated With Calcium Nephrolithiasis in the Chinese Han Population. Frontiers in genetics 2022 13 897051. Wang Lujia, Zhou Zijian, Yang Yuanyuan, Gao Peng, Lin Xiaoling, Wu Zho |
Meta-GWAS Reveals Novel Genetic Variants Associated with Urinary Excretion of Uromodulin.
Journal of the American Society of Nephrology : JASN 2022 3 33 (3): 511-529. Joseph Christina B, Mariniello Marta, Yoshifuji Ayumi, Schiano Guglielmo, Lake Jennifer, Marten Jonathan, Richmond Anne, Huffman Jennifer E, Campbell Archie, Harris Sarah E, Troyanov Stephan, Cocca Massimiliano, Robino Antonietta, Thériault Sébastien, Eckardt Kai-Uwe, Wuttke Matthias, Cheng Yurong, Corre Tanguy, Kolcic Ivana, Black Corrinda, Bruat Vanessa, Concas Maria Pina, Sala Cinzia, Aeschbacher Stefanie, Schaefer Franz, Bergmann Sven, Campbell Harry, Olden Matthias, Polasek Ozren, Porteous David J, Deary Ian J, Madore Francois, Awadalla Philip, Girotto Giorgia, Ulivi Sheila, Conen David, Wuehl Elke, Olinger Eric, Wilson James F, Bochud Murielle, Köttgen Anna, Hayward Caroline, Devuyst Olivi |
Association between malocclusions and amelogenesis imperfecta genotype and phenotype: A systematic review. International orthodontics 2023 7 21 (4): 100789. Alice Broutin, Angélique K Bidi-Lebihan, Thibault Canceill, Frédéric Vaysse, Agnès Bloch-Zupan, Isabelle Bailleul-Forestier, Emmanuelle Noirrit-Esclass |
Hearing Loss Related to Gene Mutations in Distal Renal Tubular Acidosis. Audiology & neuro-otology 2023 4 1-10. Ezgi Ay, Emre Gurses, Filiz Aslan, Bora Gulhan, Asuman Alniacik, Ali Duzova, Munir Demir Bajin, Levent Sennaroglu, Gulsum Aydan Genc, Fatih Ozaltin, Rezan Topalog |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 16, 2024
- Content source: