Human Genome Epidemiology Literature Finder
Heart, Lung, Blood and Sleep Disorders
Records 1 - 11 (of 11 Records) |
Query Trace: Restless Legs Syndrome[original query] |
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A genetic risk factor for periodic limb movements in sleep.
The New England journal of medicine 2007 Aug 357 (7): 639-47. Stefansson Hreinn, Rye David B, Hicks Andrew, Petursson Hjorvar, Ingason Andres, Thorgeirsson Thorgeir E, Palsson Stefan, Sigmundsson Thordur, Sigurdsson Albert P, Eiriksdottir Ingibjorg, Soebech Emilia, Bliwise Donald, Beck Joseph M, Rosen Ami, Waddy Salina, Trotti Lynn M, Iranzo Alex, Thambisetty Madhav, Hardarson Gudmundur A, Kristjansson Kristleifur, Gudmundsson Larus J, Thorsteinsdottir Unnur, Kong Augustine, Gulcher Jeffrey R, Gudbjartsson Daniel, Stefansson Ka |
Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions.
Nature genetics 2007 Aug 39 (8): 1000-6. Winkelmann Juliane, Schormair Barbara, Lichtner Peter, Ripke Stephan, Xiong Lan, Jalilzadeh Shapour, Fulda Stephany, Pütz Benno, Eckstein Gertrud, Hauk Stephanie, Trenkwalder Claudia, Zimprich Alexander, Stiasny-Kolster Karin, Oertel Wolfgang, Bachmann Cornelius G, Paulus Walter, Peglau Ines, Eisensehr Ilonka, Montplaisir Jacques, Turecki Gustavo, Rouleau Guy, Gieger Christian, Illig Thomas, Wichmann H-Erich, Holsboer Florian, Müller-Myhsok Bertram, Meitinger Thom |
PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome.
Nature genetics 2008 Aug 40 (8): 946-8. Schormair Barbara, Kemlink David, Roeske Darina, Eckstein Gertrud, Xiong Lan, Lichtner Peter, Ripke Stephan, Trenkwalder Claudia, Zimprich Alexander, Stiasny-Kolster Karin, Oertel Wolfgang, Bachmann Cornelius G, Paulus Walter, Högl Birgit, Frauscher Birgit, Gschliesser Viola, Poewe Werner, Peglau Ines, Vodicka Pavel, Vávrová Jana, Sonka Karel, Nevsimalova Sona, Montplaisir Jacques, Turecki Gustavo, Rouleau Guy, Gieger Christian, Illig Thomas, Wichmann H-Erich, Holsboer Florian, Müller-Myhsok Bertram, Meitinger Thomas, Winkelmann Julia |
Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1.
PLoS genetics 2011 Jul 7 (7): e1002171. Winkelmann Juliane, Czamara Darina, Schormair Barbara, Knauf Franziska, Schulte Eva C, Trenkwalder Claudia, Dauvilliers Yves, Polo Olli, Högl Birgit, Berger Klaus, Fuhs Andrea, Gross Nadine, Stiasny-Kolster Karin, Oertel Wolfgang, Bachmann Cornelius G, Paulus Walter, Xiong Lan, Montplaisir Jacques, Rouleau Guy A, Fietze Ingo, Vávrová Jana, Kemlink David, Sonka Karel, Nevsimalova Sona, Lin Siong-Chi, Wszolek Zbigniew, Vilariño-Güell Carles, Farrer Matthew J, Gschliesser Viola, Frauscher Birgit, Falkenstetter Tina, Poewe Werner, Allen Richard P, Earley Christopher J, Ondo William G, Le Wei-Dong, Spieler Derek, Kaffe Maria, Zimprich Alexander, Kettunen Johannes, Perola Markus, Silander Kaisa, Cournu-Rebeix Isabelle, Francavilla Marcella, Fontenille Claire, Fontaine Bertrand, Vodicka Pavel, Prokisch Holger, Lichtner Peter, Peppard Paul, Faraco Juliette, Mignot Emmanuel, Gieger Christian, Illig Thomas, Wichmann H-Erich, Müller-Myhsok Bertram, Meitinger Thom |
Genome-wide association study of motor coordination problems in ADHD identifies genes for brain and muscle function.
The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry 2012 Mar 13 (3): 211-22. Fliers Ellen A, Vasquez Alejandro Arias, Poelmans Geert, Rommelse Nanda, Altink Marieke, Buschgens Cathelijne, Asherson Philip, Banaschewski Tobias, Ebstein Richard, Gill Michael, Miranda Ana, Mulas Fernando, Oades Robert D, Roeyers Herbert, Rothenberger Aribert, Sergeant Joseph, Sonuga-Barke Edmund, Steinhausen Hans-Christoph, Faraone Stephen V, Buitelaar Jan K, Franke Barba |
Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits.
Nature genetics 2017 Jun . Hammerschlag Anke R, Stringer Sven, de Leeuw Christiaan A, Sniekers Suzanne, Taskesen Erdogan, Watanabe Kyoko, Blanken Tessa F, Dekker Kim, Te Lindert Bart H W, Wassing Rick, Jonsdottir Ingileif, Thorleifsson Gudmar, Stefansson Hreinn, Gislason Thorarinn, Berger Klaus, Schormair Barbara, Wellmann Juergen, Winkelmann Juliane, Stefansson Kari, Oexle Konrad, Van Someren Eus J W, Posthuma Daniel |
Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis.
The Lancet. Neurology 2017 Nov 16 (11): 898-907. Schormair Barbara, Zhao Chen, Bell Steven, Tilch Erik, Salminen Aaro V, Pütz Benno, Dauvilliers Yves, Stefani Ambra, Högl Birgit, Poewe Werner, Kemlink David, Sonka Karel, Bachmann Cornelius G, Paulus Walter, Trenkwalder Claudia, Oertel Wolfgang H, Hornyak Magdolna, Teder-Laving Maris, Metspalu Andres, Hadjigeorgiou Georgios M, Polo Olli, Fietze Ingo, Ross Owen A, Wszolek Zbigniew, Butterworth Adam S, Soranzo Nicole, Ouwehand Willem H, Roberts David J, Danesh John, Allen Richard P, Earley Christopher J, Ondo William G, Xiong Lan, Montplaisir Jacques, Gan-Or Ziv, Perola Markus, Vodicka Pavel, Dina Christian, Franke Andre, Tittmann Lukas, Stewart Alexandre F R, Shah Svati H, Gieger Christian, Peters Annette, Rouleau Guy A, Berger Klaus, Oexle Konrad, Di Angelantonio Emanuele, Hinds David A, Müller-Myhsok Bertram, Winkelmann Juliane, , |
Genetic studies of accelerometer-based sleep measures yield new insights into human sleep behaviour.
Nature communications 2019 04 10 (1): 1585. Jones Samuel E, van Hees Vincent T, Mazzotti Diego R, Marques-Vidal Pedro, Sabia Séverine, van der Spek Ashley, Dashti Hassan S, Engmann Jorgen, Kocevska Desana, Tyrrell Jessica, Beaumont Robin N, Hillsdon Melvyn, Ruth Katherine S, Tuke Marcus A, Yaghootkar Hanieh, Sharp Seth A, Ji Yingjie, Harrison Jamie W, Freathy Rachel M, Murray Anna, Luik Annemarie I, Amin Najaf, Lane Jacqueline M, Saxena Richa, Rutter Martin K, Tiemeier Henning, Kutalik Zoltán, Kumari Meena, Frayling Timothy M, Weedon Michael N, Gehrman Philip R, Wood Andrew |
Biological and clinical insights from genetics of insomnia symptoms.
Nature genetics 2019 03 51 (3): 387-393. Lane Jacqueline M, Jones Samuel E, Dashti Hassan S, Wood Andrew R, Aragam Krishna G, van Hees Vincent T, Strand Linn B, Winsvold Bendik S, Wang Heming, Bowden Jack, Song Yanwei, Patel Krunal, Anderson Simon G, Beaumont Robin N, Bechtold David A, Cade Brian E, Haas Mary, Kathiresan Sekar, Little Max A, Luik Annemarie I, Loudon Andrew S, Purcell Shaun, Richmond Rebecca C, Scheer Frank A J L, Schormair Barbara, Tyrrell Jessica, Winkelman John W, Winkelmann Juliane, , Hveem Kristian, Zhao Chen, Nielsen Jonas B, Willer Cristen J, Redline Susan, Spiegelhalder Kai, Kyle Simon D, Ray David W, Zwart John-Anker, Brumpton Ben, Frayling Timothy M, Lawlor Deborah A, Rutter Martin K, Weedon Michael N, Saxena Ric |
Association of genetic variants in migraineurs with and without restless legs syndrome.
Annals of clinical and translational neurology 2020 Sep . Lin Guan-Yu, Lin Yu-Kai, Liang Chih-Sung, Lee Jiunn-Tay, Tsai Chia-Lin, Hung Kuo-Sheng, Luo Wen-Jie, Tsai Chia-Kuang, Hsu Yu-Wei, Ho Tsung-Han, Yang Fu-C |
Large genome-wide association study identifies three novel risk variants for restless legs syndrome.
Communications biology 2020 Nov 3 (1): 703. Didriksen Maria, Nawaz Muhammad Sulaman, Dowsett Joseph, Bell Steven, Erikstrup Christian, Pedersen Ole B, Sørensen Erik, Jennum Poul J, Burgdorf Kristoffer S, Burchell Brendan, Butterworth Adam S, Soranzo Nicole, Rye David B, Trotti Lynn Marie, Saini Prabhjyot, Stefansdottir Lilja, Magnusson Sigurdur H, Thorleifsson Gudmar, Sigmundsson Thordur, Sigurdsson Albert P, Van Den Hurk Katja, Quee Franke, Tanck Michael W T, Ouwehand Willem H, Roberts David J, Earley Eric J, Busch Michael P, Mast Alan E, Page Grier P, Danesh John, Di Angelantonio Emanuele, Stefansson Hreinn, Ullum Henrik, Stefansson Ka |
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- Page last updated:May 13, 2024
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