Human Genome Epidemiology Literature Finder
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Records 1 - 9 (of 9 Records) |
| Query Trace: Disease and meta-analysis and ATXN2[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 |
| Identification of novel genetic Loci associated with thyroid peroxidase antibodies and clinical thyroid disease.
PLoS genetics 2014 Feb 10 (2): e1004123. Medici Marco, Porcu Eleonora, Pistis Giorgio, Teumer Alexander, Brown Suzanne J, Jensen Richard A, Rawal Rajesh, Roef Greet L, Plantinga Theo S, Vermeulen Sita H, Lahti Jari, Simmonds Matthew J, Husemoen Lise Lotte N, Freathy Rachel M, Shields Beverley M, Pietzner Diana, Nagy Rebecca, Broer Linda, Chaker Layal, Korevaar Tim I M, Plia Maria Grazia, Sala Cinzia, Völker Uwe, Richards J Brent, Sweep Fred C, Gieger Christian, Corre Tanguy, Kajantie Eero, Thuesen Betina, Taes Youri E, Visser W Edward, Hattersley Andrew T, Kratzsch Jürgen, Hamilton Alexander, Li Wei, Homuth Georg, Lobina Monia, Mariotti Stefano, Soranzo Nicole, Cocca Massimiliano, Nauck Matthias, Spielhagen Christin, Ross Alec, Arnold Alice, van de Bunt Martijn, Liyanarachchi Sandya, Heier Margit, Grabe Hans Jörgen, Masciullo Corrado, Galesloot Tessel E, Lim Ee M, Reischl Eva, Leedman Peter J, Lai Sandra, Delitala Alessandro, Bremner Alexandra P, Philips David I W, Beilby John P, Mulas Antonella, Vocale Matteo, Abecasis Goncalo, Forsen Tom, James Alan, Widen Elisabeth, Hui Jennie, Prokisch Holger, Rietzschel Ernst E, Palotie Aarno, Feddema Peter, Fletcher Stephen J, Schramm Katharina, Rotter Jerome I, Kluttig Alexander, Radke Dörte, Traglia Michela, Surdulescu Gabriela L, He Huiling, Franklyn Jayne A, Tiller Daniel, Vaidya Bijay, de Meyer Tim, Jørgensen Torben, Eriksson Johan G, O'Leary Peter C, Wichmann Eric, Hermus Ad R, Psaty Bruce M, Ittermann Till, Hofman Albert, Bosi Emanuele, Schlessinger David, Wallaschofski Henri, Pirastu Nicola, Aulchenko Yurii S, de la Chapelle Albert, Netea-Maier Romana T, Gough Stephen C L, Meyer Zu Schwabedissen Henriette, Frayling Timothy M, Kaufman Jean-Marc, Linneberg Allan, Räikkönen Katri, Smit Johannes W A, Kiemeney Lambertus A, Rivadeneira Fernando, Uitterlinden André G, Walsh John P, Meisinger Christa, den Heijer Martin, Visser Theo J, Spector Timothy D, Wilson Scott G, Völzke Henry, Cappola Anne, Toniolo Daniela, Sanna Serena, Naitza Silvia, Peeters Robin |
| Genetic variants associated with celiac disease and the risk for coronary artery disease. Molecular genetics and genomics : MGG 2015 Oct 290 (5): 1911-7. Jansen Henning, Willenborg Christina, Schlesinger Sabrina, Ferrario Paola G, König Inke R, Erdmann Jeanette, Samani Nilesh J, Lieb Wolfgang, Schunkert Heribe |
| Genome-wide meta-analysis in alopecia areata resolves HLA associations and reveals two new susceptibility loci.
Nature communications 2015 Jan 6 5966. Betz Regina C, Petukhova Lynn, Ripke Stephan, Huang Hailiang, Menelaou Androniki, Redler Silke, Becker Tim, Heilmann Stefanie, Yamany Tarek, Duvic Madeliene, Hordinsky Maria, Norris David, Price Vera H, Mackay-Wiggan Julian, de Jong Annemieke, DeStefano Gina M, Moebus Susanne, Böhm Markus, Blume-Peytavi Ulrike, Wolff Hans, Lutz Gerhard, Kruse Roland, Bian Li, Amos Christopher I, Lee Annette, Gregersen Peter K, Blaumeiser Bettina, Altshuler David, Clynes Raphael, de Bakker Paul I W, Nöthen Markus M, Daly Mark J, Christiano Angela |
| ATXN2 trinucleotide repeat length correlates with risk of ALS. Neurobiology of aging 2016 12 51 178.e1-178.e9. Sproviero William, Shatunov Aleksey, Stahl Daniel, Shoai Maryam, van Rheenen Wouter, Jones Ashley R, Al-Sarraj Safa, Andersen Peter M, Bonini Nancy M, Conforti Francesca L, Van Damme Philip, Daoud Hussein, Del Mar Amador Maria, Fogh Isabella, Forzan Monica, Gaastra Ben, Gellera Cinzia, Gitler Aaron D, Hardy John, Fratta Pietro, La Bella Vincenzo, Le Ber Isabelle, Van Langenhove Tim, Lattante Serena, Lee Yi-Chung, Malaspina Andrea, Meininger Vincent, Millecamps Stéphanie, Orrell Richard, Rademakers Rosa, Robberecht Wim, Rouleau Guy, Ross Owen A, Salachas Francois, Sidle Katie, Smith Bradley N, Soong Bing-Wen, Sorarù Gianni, Stevanin Giovanni, Kabashi Edor, Troakes Claire, van Broeckhoven Christine, Veldink Jan H, van den Berg Leonard H, Shaw Christopher E, Powell John F, Al-Chalabi Amm |
| Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function.
The Journal of clinical investigation 2017 May 127 (5): 1798-1812. Wild Philipp S, Felix Janine F, Schillert Arne, Teumer Alexander, Chen Ming-Huei, Leening Maarten J G, Völker Uwe, Großmann Vera, Brody Jennifer A, Irvin Marguerite R, Shah Sanjiv J, Pramana Setia, Lieb Wolfgang, Schmidt Reinhold, Stanton Alice V, Malzahn Dörthe, Smith Albert Vernon, Sundström Johan, Minelli Cosetta, Ruggiero Daniela, Lyytikäinen Leo-Pekka, Tiller Daniel, Smith J Gustav, Monnereau Claire, Di Tullio Marco R, Musani Solomon K, Morrison Alanna C, Pers Tune H, Morley Michael, Kleber Marcus E, Aragam Jayashri, Benjamin Emelia J, Bis Joshua C, Bisping Egbert, Broeckel Ulrich, Cheng Susan, Deckers Jaap W, Del Greco M Fabiola, Edelmann Frank, Fornage Myriam, Franke Lude, Friedrich Nele, Harris Tamara B, Hofer Edith, Hofman Albert, Huang Jie, Hughes Alun D, Kähönen Mika, Investigators Knhi, Kruppa Jochen, Lackner Karl J, Lannfelt Lars, Laskowski Rafael, Launer Lenore J, Leosdottir Margrét, Lin Honghuang, Lindgren Cecilia M, Loley Christina, MacRae Calum A, Mascalzoni Deborah, Mayet Jamil, Medenwald Daniel, Morris Andrew P, Müller Christian, Müller-Nurasyid Martina, Nappo Stefania, Nilsson Peter M, Nuding Sebastian, Nutile Teresa, Peters Annette, Pfeufer Arne, Pietzner Diana, Pramstaller Peter P, Raitakari Olli T, Rice Kenneth M, Rivadeneira Fernando, Rotter Jerome I, Ruohonen Saku T, Sacco Ralph L, Samdarshi Tandaw E, Schmidt Helena, Sharp Andrew S P, Shields Denis C, Sorice Rossella, Sotoodehnia Nona, Stricker Bruno H, Surendran Praveen, Thom Simon, Töglhofer Anna M, Uitterlinden André G, Wachter Rolf, Völzke Henry, Ziegler Andreas, Münzel Thomas, März Winfried, Cappola Thomas P, Hirschhorn Joel N, Mitchell Gary F, Smith Nicholas L, Fox Ervin R, Dueker Nicole D, Jaddoe Vincent W V, Melander Olle, Russ Martin, Lehtimäki Terho, Ciullo Marina, Hicks Andrew A, Lind Lars, Gudnason Vilmundur, Pieske Burkert, Barron Anthony J, Zweiker Robert, Schunkert Heribert, Ingelsson Erik, Liu Kiang, Arnett Donna K, Psaty Bruce M, Blankenberg Stefan, Larson Martin G, Felix Stephan B, Franco Oscar H, Zeller Tanja, Vasan Ramachandran S, Dörr Marc |
| Repeat length variations in polyglutamine disease-associated genes affect body mass index. International journal of obesity (2005) 2018 Aug . Gardiner Sarah L, de Mutsert Renée, Trompet Stella, Boogaard Merel W, van Dijk Ko Willems, Jukema P J Wouter, Slagboom P Eline, Roos Raymund A C, Pijl Hanno, Rosendaal Frits R, Aziz N Ahm |
| Genetic risk factors for modulation of age at onset in Machado-Joseph disease/spinocerebellar ataxia type 3: a systematic review and meta-analysis. Journal of neurology, neurosurgery, and psychiatry 2018 10 90 (2): 203-210. de Mattos Eduardo Preusser, Kolbe Musskopf Maiara, Bielefeldt Leotti Vanessa, Saraiva-Pereira Maria Luiza, Jardim Laura Banna |
| Causal Association and Shared Genetics Between Asthma and COVID-19.
Frontiers in immunology 2022 4 13 705379. Baranova Ancha, Cao Hongbao, Chen Jiu, Zhang Fuqu |
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