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Eine Ebene höherGruppiert nach: Dokumententyp |
Veröffentlichungsdatum
Anzahl der Publikationen: 20
2024
Kittke, Volker 
ORCID: https://orcid.org/0000-0001-8866-1388; Zhao, Chen; Lam, Daniel D.; Harrer, Philip; Krezel, Wojciech; Schormair, Barbara ORCID: https://orcid.org/0000-0003-0942-5243; Oexle, Konrad ORCID: https://orcid.org/0000-0001-7447-2252 und Winkelmann, Juliane ORCID: https://orcid.org/0000-0002-3074-599X
(2024):
RLS-associated MEIS transcription factors control distinct processes in human neural stem cells.
In: Scientific Reports, Bd. 14, 28986
[PDF, 3MB]
ORCID: https://orcid.org/0000-0001-8866-1388; Zhao, Chen; Lam, Daniel D.; Harrer, Philip; Krezel, Wojciech; Schormair, Barbara ORCID: https://orcid.org/0000-0003-0942-5243; Oexle, Konrad ORCID: https://orcid.org/0000-0001-7447-2252 und Winkelmann, Juliane ORCID: https://orcid.org/0000-0002-3074-599X
(2024):
RLS-associated MEIS transcription factors control distinct processes in human neural stem cells.
In: Scientific Reports, Bd. 14, 28986
[PDF, 3MB]
Schormair, Barbara ORCID: https://orcid.org/0000-0003-0942-5243; Zhao, Chen; Bell, Steven ORCID: https://orcid.org/0000-0001-6774-3149; Didriksen, Maria ORCID: https://orcid.org/0000-0002-4856-496X; Nawaz, Muhammad S.; Schandra, Nathalie; Stefani, Ambra ORCID: https://orcid.org/0000-0003-4259-8824; Högl, Birgit; Dauvilliers, Yves; Bachmann, Cornelius G.; Kemlink, David; Sonka, Karel; Paulus, Walter; Trenkwalder, Claudia; Oertel, Wolfgang H.; Hornyak, Magdolna; Teder-Laving, Maris; Metspalu, Andres; Hadjigeorgiou, Georgios M. ORCID: https://orcid.org/0000-0001-5386-4273; Polo, Olli; Fietze, Ingo; Ross, Owen A. ORCID: https://orcid.org/0000-0003-4813-756X; Wszolek, Zbigniew K. ORCID: https://orcid.org/0000-0001-5487-1053; Ibrahim, Abubaker; Bergmann, Melanie; Kittke, Volker ORCID: https://orcid.org/0000-0001-8866-1388; Harrer, Philip; Dowsett, Joseph ORCID: https://orcid.org/0000-0001-5381-2633; Chenini, Sofiene; Ostrowski, Sisse Rye ORCID: https://orcid.org/0000-0001-5288-3851; Sørensen, Erik; Erikstrup, Christian ORCID: https://orcid.org/0000-0001-6551-6647; Pedersen, Ole B. ORCID: https://orcid.org/0000-0003-2312-5976; Topholm Bruun, Mie ORCID: https://orcid.org/0000-0002-8819-5388; Nielsen, Kaspar R.; Butterworth, Adam S. ORCID: https://orcid.org/0000-0002-6915-9015; Soranzo, Nicole ORCID: https://orcid.org/0000-0003-1095-3852; Ouwehand, Willem H. ORCID: https://orcid.org/0000-0002-7744-1790; Roberts, David J.; Danesh, John; Burchell, Brendan; Furlotte, Nicholas A.; Nandakumar, Priyanka; Bonnefond, Amélie; Potier, Louis; Earley, Christopher J.; Ondo, William G.; Xiong, Lan; Desautels, Alex; Perola, Markus; Vodicka, Pavel; Dina, Christian ORCID: https://orcid.org/0000-0002-7722-7348; Stoll, Monika ORCID: https://orcid.org/0000-0002-2711-4281; Franke, Andre ORCID: https://orcid.org/0000-0003-1530-5811; Lieb, Wolfgang ORCID: https://orcid.org/0000-0003-2544-4460; Stewart, Alexandre F. R. ORCID: https://orcid.org/0000-0003-2673-9164; Shah, Svati H.; Gieger, Christian ORCID: https://orcid.org/0000-0001-6986-9554; Peters, Annette ORCID: https://orcid.org/0000-0001-6645-0985; Rye, David B.; Rouleau, Guy A.; Berger, Klaus; Stefansson, Hreinn; Ullum, Henrik; Stefansson, Kari; Hinds, David A. ORCID: https://orcid.org/0000-0002-4911-803X; Di Angelantonio, Emanuele; Oexle, Konrad ORCID: https://orcid.org/0000-0001-7447-2252 und Winkelmann, Juliane ORCID: https://orcid.org/0000-0002-3074-599X
(2024):
Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction.
In: Nature Genetics, Bd. 56, Nr. 6: S. 1090-1099
[PDF, 3MB]
ORCID: https://orcid.org/0000-0003-0942-5243; Zhao, Chen; Bell, Steven ORCID: https://orcid.org/0000-0001-6774-3149; Didriksen, Maria ORCID: https://orcid.org/0000-0002-4856-496X; Nawaz, Muhammad S.; Schandra, Nathalie; Stefani, Ambra ORCID: https://orcid.org/0000-0003-4259-8824; Högl, Birgit; Dauvilliers, Yves; Bachmann, Cornelius G.; Kemlink, David; Sonka, Karel; Paulus, Walter; Trenkwalder, Claudia; Oertel, Wolfgang H.; Hornyak, Magdolna; Teder-Laving, Maris; Metspalu, Andres; Hadjigeorgiou, Georgios M. ORCID: https://orcid.org/0000-0001-5386-4273; Polo, Olli; Fietze, Ingo; Ross, Owen A. ORCID: https://orcid.org/0000-0003-4813-756X; Wszolek, Zbigniew K. ORCID: https://orcid.org/0000-0001-5487-1053; Ibrahim, Abubaker; Bergmann, Melanie; Kittke, Volker ORCID: https://orcid.org/0000-0001-8866-1388; Harrer, Philip; Dowsett, Joseph ORCID: https://orcid.org/0000-0001-5381-2633; Chenini, Sofiene; Ostrowski, Sisse Rye ORCID: https://orcid.org/0000-0001-5288-3851; Sørensen, Erik; Erikstrup, Christian ORCID: https://orcid.org/0000-0001-6551-6647; Pedersen, Ole B. ORCID: https://orcid.org/0000-0003-2312-5976; Topholm Bruun, Mie ORCID: https://orcid.org/0000-0002-8819-5388; Nielsen, Kaspar R.; Butterworth, Adam S. ORCID: https://orcid.org/0000-0002-6915-9015; Soranzo, Nicole ORCID: https://orcid.org/0000-0003-1095-3852; Ouwehand, Willem H. ORCID: https://orcid.org/0000-0002-7744-1790; Roberts, David J.; Danesh, John; Burchell, Brendan; Furlotte, Nicholas A.; Nandakumar, Priyanka; Bonnefond, Amélie; Potier, Louis; Earley, Christopher J.; Ondo, William G.; Xiong, Lan; Desautels, Alex; Perola, Markus; Vodicka, Pavel; Dina, Christian ORCID: https://orcid.org/0000-0002-7722-7348; Stoll, Monika ORCID: https://orcid.org/0000-0002-2711-4281; Franke, Andre ORCID: https://orcid.org/0000-0003-1530-5811; Lieb, Wolfgang ORCID: https://orcid.org/0000-0003-2544-4460; Stewart, Alexandre F. R. ORCID: https://orcid.org/0000-0003-2673-9164; Shah, Svati H.; Gieger, Christian ORCID: https://orcid.org/0000-0001-6986-9554; Peters, Annette ORCID: https://orcid.org/0000-0001-6645-0985; Rye, David B.; Rouleau, Guy A.; Berger, Klaus; Stefansson, Hreinn; Ullum, Henrik; Stefansson, Kari; Hinds, David A. ORCID: https://orcid.org/0000-0002-4911-803X; Di Angelantonio, Emanuele; Oexle, Konrad ORCID: https://orcid.org/0000-0001-7447-2252 und Winkelmann, Juliane ORCID: https://orcid.org/0000-0002-3074-599X
(2024):
Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction.
In: Nature Genetics, Bd. 56, Nr. 6: S. 1090-1099
[PDF, 3MB]
Harrer, Philip; Inderhees, Julica ORCID: https://orcid.org/0000-0003-4523-3652; Zhao, Chen; Schormair, Barbara; Tilch, Erik; Gieger, Christian; Peters, Annette ORCID: https://orcid.org/0000-0001-6645-0985; Jöhren, Olaf ORCID: https://orcid.org/0000-0002-0532-5133; Fleming, Thomas; Nawroth, Peter P.; Berger, Klaus; Hermesdorf, Marco ORCID: https://orcid.org/0000-0003-3541-7212; Winkelmann, Juliane; Schwaninger, Markus und Oexle, Konrad ORCID: https://orcid.org/0000-0001-7447-2252
(2024):
Phenotypic and genome-wide studies on dicarbonyls: major associations to glomerular filtration rate and gamma-glutamyltransferase activity.
In: eBioMedicine, Bd. 101, 105007
[PDF, 1MB]
ORCID: https://orcid.org/0000-0003-4523-3652; Zhao, Chen; Schormair, Barbara; Tilch, Erik; Gieger, Christian; Peters, Annette ORCID: https://orcid.org/0000-0001-6645-0985; Jöhren, Olaf ORCID: https://orcid.org/0000-0002-0532-5133; Fleming, Thomas; Nawroth, Peter P.; Berger, Klaus; Hermesdorf, Marco ORCID: https://orcid.org/0000-0003-3541-7212; Winkelmann, Juliane; Schwaninger, Markus und Oexle, Konrad ORCID: https://orcid.org/0000-0001-7447-2252
(2024):
Phenotypic and genome-wide studies on dicarbonyls: major associations to glomerular filtration rate and gamma-glutamyltransferase activity.
In: eBioMedicine, Bd. 101, 105007
[PDF, 1MB]
2023
Harrer, Philip; Mirza‐Schreiber, Nazanin; Mandel, Vanessa; Roeber, Sigrun; Stefani, Ambra ORCID: https://orcid.org/0000-0003-4259-8824; Naher, Shamsun; Wagner, Matias ORCID: https://orcid.org/0000-0002-4454-8823; Gieger, Christian; Waldenberger, Melanie; Peters, Annette ORCID: https://orcid.org/0000-0001-6645-0985; Högl, Birgit; Herms, Jochen; Schormair, Barbara ORCID: https://orcid.org/0000-0003-0942-5243; Zhao, Chen; Winkelmann, Juliane und Oexle, Konrad ORCID: https://orcid.org/0000-0001-7447-2252
(2023):
Epigenetic Association Analyses and Risk Prediction of RLS.
In: Movement Disorders, Bd. 38, Nr. 8: S. 1410-1418
[PDF, 685kB]
ORCID: https://orcid.org/0000-0003-4259-8824; Naher, Shamsun; Wagner, Matias ORCID: https://orcid.org/0000-0002-4454-8823; Gieger, Christian; Waldenberger, Melanie; Peters, Annette ORCID: https://orcid.org/0000-0001-6645-0985; Högl, Birgit; Herms, Jochen; Schormair, Barbara ORCID: https://orcid.org/0000-0003-0942-5243; Zhao, Chen; Winkelmann, Juliane und Oexle, Konrad ORCID: https://orcid.org/0000-0001-7447-2252
(2023):
Epigenetic Association Analyses and Risk Prediction of RLS.
In: Movement Disorders, Bd. 38, Nr. 8: S. 1410-1418
[PDF, 685kB]
2022
Zhang, Xu; Shu, Xin; Zhou, Xiaolin; Zhou, Cheng; Yang, Pu; Diao, Muhe; Hu, Haiyang; Gan, Xinyu; Zhao, Chen und Fan, Chunzhen
(2022):
Magnetic reed biochar materials as adsorbents for aqueous copper and phenol removal.
In: Environmental Science and Pollution Research, Bd. 30, Nr. 2: S. 3659-3667
Witzel, Simon; Wagner, Matias; Zhao, Chen; Kandler, Katharina; Graf, Elisabeth; Berutti, Riccardo; Oexle, Konrad; Brenner, David; Winkelmann, Juliane und Ludolph, Albert C.
(2022):
Fast versus slow disease progression in amyotrophic lateral sclerosis-clinical and genetic factors at the edges of the survival spectrum.
In: Neurobiology of Aging, Bd. 119: S. 117-126
Lam, Daniel D.; Nikolic, Ana Antic; Zhao, Chen; Mirza-Schreiber, Nazanin; Krezel, Wojciech; Oexle, Konrad und Winkelmann, Juliane
(2022):
Intronic elements associated with insomnia and restless legs syndrome exhibit cell-type-specific epigenetic features contributing to MEIS1 regulation.
In: Human Molecular Genetics, Bd. 31, Nr. 11: S. 1733-1746
[PDF, 1MB]
Schormair, Barbara; Zhao, Chen; Salminen, Aaro; Oexle, Konrad und Winkelmann, Juliane
(2022):
Reassessment of candidate gene studies for idiopathic restless legs syndrome in a large genome-wide association study dataset of European ancestry.
In: Sleep, Bd. 45, Nr. 8
[PDF, 5MB]
Zhao, Chen; Enriquez, Paloma; Izadifar, Morteza; Poeppel, Ernst; Bao, Yan und Zabotkina, Vera
(2022):
Complementarity of mental content and logistic algorithms in a taxonomy of cognitive functions.
In: Psych Journal, Bd. 11, Nr. 6: S. 973-979
Mu, Nan; Zhang, Dongxue und Zhao, Chen
(2022):
Temporal reproduction: A paradigm indicating a 3-s time window.
In: Psych Journal, Bd. 12, Nr. 4: S. 535-536
Bao, Yan; Zhang, Dongxue; Zhao, Chen; Poeppel, Ernst und Zabotkina, Vera
(2022):
An Aesthetic Frame for Three Modes of Knowing.
In: Psych Journal, Bd. 11, Nr. 5: S. 636-644
Tilch, Erik; Schormair, Barbara ORCID: https://orcid.org/0000-0003-0942-5243; Zhao, Chen; Högl, Birgit; Stefani, Ambra; Berger, Klaus; Trenkwalder, Claudia; Bachmann, Cornelius G.; Hornyak, Magdolna; Fietze, Ingo; Müller-Nurasyid, Martina ORCID: https://orcid.org/0000-0003-3793-5910; Peters, Annette; Herms, Stefan; Nöthen, Markus M.; Müller-Myhsok, Bertram; Oexle, Konrad und Winkelmann, Juliane
(2022):
ExomeChip-based rare variant association study in restless legs syndrome.
In: Sleep Medicine, Bd. 94: S. 26-30
[PDF, 598kB]
ORCID: https://orcid.org/0000-0003-0942-5243; Zhao, Chen; Högl, Birgit; Stefani, Ambra; Berger, Klaus; Trenkwalder, Claudia; Bachmann, Cornelius G.; Hornyak, Magdolna; Fietze, Ingo; Müller-Nurasyid, Martina ORCID: https://orcid.org/0000-0003-3793-5910; Peters, Annette; Herms, Stefan; Nöthen, Markus M.; Müller-Myhsok, Bertram; Oexle, Konrad und Winkelmann, Juliane
(2022):
ExomeChip-based rare variant association study in restless legs syndrome.
In: Sleep Medicine, Bd. 94: S. 26-30
[PDF, 598kB]
2021
Wagner, Matias; Lorenz, Georg; Volk, Alexander E.; Brunet, Theresa; Edbauer, Dieter; Berutti, Riccardo; Zhao, Chen; Anderl-Straub, Sarah; Bertram, Lars; Danek, Adrian ORCID: https://orcid.org/0000-0001-8857-5383; Deschauer, Marcus; Dill, Veronika; Fassbender, Klaus; Fliessbach, Klaus; Goetze, Katharina S.; Jahn, Holger; Kornhuber, Johannes; Landwehrmeyer, Bernhard; Lauer, Martin; Obrig, Hellmuth; Prudlo, Johannes; Schneider, Anja; Schroeter, Matthias L.; Uttner, Ingo; Vukovich, Ruth; Wiltfang, Jens; Winkler, Andrea S.; Zhou, Qihui; Ludolph, Albert C.; Oexle, Konrad; Otto, Markus; Diehl-Schmid, Janine und Winkelmann, Juliane
(2021):
Clinico-genetic findings in 509 frontotemporal dementia patients.
In: Molecular Psychiatry, Bd. 26, Nr. 10: S. 5824-5832
[PDF, 1MB]
ORCID: https://orcid.org/0000-0001-8857-5383; Deschauer, Marcus; Dill, Veronika; Fassbender, Klaus; Fliessbach, Klaus; Goetze, Katharina S.; Jahn, Holger; Kornhuber, Johannes; Landwehrmeyer, Bernhard; Lauer, Martin; Obrig, Hellmuth; Prudlo, Johannes; Schneider, Anja; Schroeter, Matthias L.; Uttner, Ingo; Vukovich, Ruth; Wiltfang, Jens; Winkler, Andrea S.; Zhou, Qihui; Ludolph, Albert C.; Oexle, Konrad; Otto, Markus; Diehl-Schmid, Janine und Winkelmann, Juliane
(2021):
Clinico-genetic findings in 509 frontotemporal dementia patients.
In: Molecular Psychiatry, Bd. 26, Nr. 10: S. 5824-5832
[PDF, 1MB]
Dzinovic, Ivana; Skorvanek, Matej; Pavelekova, Petra; Zhao, Chen; Keren, Boris; Whalen, Sandra; Bakhtiari, Somayeh; Chih Jin, Sheng; Kruer, Michael C.; Jech, Robert; Winkelmann, Juliane und Zech, Michael
(2021):
Variant recurrence confirms the existence of a FBXO31-related spastic-dystonic cerebral palsy syndrome.
In: Annals of Clinical and Translational Neurology, Bd. 8, Nr. 4: S. 951-955
[PDF, 248kB]
2020
Zech, Michael; Jech, Robert; Boesch, Sylvia; Skorvanek, Matej; Weber, Sandrina; Wagner, Matias; Zhao, Chen; Jochim, Angela; Necpal, Jan; Dincer, Yasemin; Vill, Katharina; Distelmaier, Felix; Stoklosa, Malgorzata; Krenn, Martin; Grunwald, Stephan; Bock-Bierbaum, Tobias; Fecikova, Anna; Havrankova, Petra; Roth, Jan; Prihodova, Iva; Adamovicova, Miriam; Ulmanova, Olga; Bechyne, Karel; Danhofer, Pavlina; Vesely, Branislav; Han, Vladimir; Pavelekova, Petra; Gdovinova, Zuzana; Mantel, Tobias; Meindl, Tobias; Sitzberger, Alexandra; Schroeder, Sebastian; Blaschek, Astrid; Roser, Timo; Bonfert, Michaefa; Haberlandt, Edda; Plecko, Barbara; Leineweber, Birgit; Berweck, Steffen; Herberhold, Thomas; Langguth, Berthold; Svantnerova, Jana; Minar, Michal; Ramos-Rivera, Gonzalo Alonso; Wojcik, Monica H.; Pajusalu, Sander; Ounap, Katrin; Schatz, Ulrich A.; Poelsler, Laura; Milenkovic, Ivan; Laccone, Franco; Pilhofer, Veronika; Colombo, Roberto; Patzer, Steffi; Iuso, Arcangela; Vera, Julia; Troncoso, Monica; Fang, Fang; Prokisch, Holger; Wilbert, Friederike; Eckenweiler, Matthias; Graf, Elisabeth; Westphal, Dominik S.; Riedhammer, Korbinian M.; Brunet, Theresa; Alhaddad, Bader; Berutti, Riccardo; Strom, Tim M.; Hecht, Martin; Baumann, Matthias; Wolf, Marc; Telegrafi, Aida; Person, Richard E.; Zamora, Francisca Milian; Henderson, Lindsay B.; Weise, David; Musacchio, Thomas; Volkmann, Jens; Szuto, Anna; Becker, Jessica; Cremer, Kirsten; Sycha, Thomas; Zimprich, Fritz; Kraus, Verena; Makowski, Christine; Gonzalez-Alegre, Pedro; Bardakjian, Tanya M.; Ozelius, Laurie J.; Vetro, Annafisa; Guerrini, Renzo; Maier, Esther; Borggraefe, Ingo; Kuster, Alice; Wortmann, Saskia B.; Hackenberg, Annette; Steinfeld, Robert; Assmann, Birgit; Staufner, Christian; Opladen, Thomas; Ruzicka, Evzen; Cohn, Ronald D.; Dyment, David; Chung, Wendy K.; Engels, Hartmut; Ceballos-Baumann, Andres; Ploski, Rafai; Daumke, Ofiver; Haslinger, Bernhard; Mall, Volker; Oexle, Konrad und Winkehnann, Juliane
(2020):
Monogenic variants in dystonia: an exome-wide sequencing study.
In: Lancet Neurology, Bd. 19, Nr. 11: S. 908-918
[PDF, 1MB]
Tilch, Erik; Schormair, Barbara; Zhao, Chen; Salminen, Aaro; Nikolic, Ana Antic; Holzknecht, Evi; Hoegl, Birgit; Poewe, Werner; Bachmann, Cornelius G.; Paulus, Walter; Trenkwalder, Claudia; Oertel, Wolfgang H.; Hornyak, Magdolna; Fietze, Ingo; Berger, Klaus; Lichtner, Peter; Gieger, Christian; Peters, Annette; Mueller-Myhsok, Bertram; Hoischen, Alexander; Winkelmann, Juliane und Oexle, Konrad
(2020):
Identification of Restless Legs Syndrome Genes by Mutational Load Analysis.
In: Annals of Neurology, Bd. 87, Nr. 2: S. 184-193
[PDF, 285kB]
Steel, Dora; Zech, Michael; Zhao, Chen; Barwick, Katy E. S.; Burke, Derek; Demailly, Diane; Kumar, Kishore R.; Zorzi, Giovanna; Nardocci, Nardo; Kaiyrzhanov, Rauan; Wagner, Matias; Iuso, Arcangela; Berutti, Riccardo; Skorvanek, Matej; Necpal, Jan; Davis, Ryan; Wiethoff, Sarah; Mankad, Kshitij; Sudhakar, Sniya; Ferrini, Arianna; Sharma, Suvasini; Kamsteeg, Erik-Jan; Tijssen, Marina A.; Verschuuren, Corien; Egmond, Martje E. van; Flowers, Joanna M.; McEntagart, Meriel; Tucci, Arianna; Coubes, Philippe; Bustos, Bernabe I.; Gonzalez-Latapi, Paulina; Tisch, Stephen; Darveniza, Paul; Gorman, Kathleen M.; Peall, Kathryn J.; Bötzel, Kai; Koch, Jan C.; Kmiec, Tomasz; Plecko, Barbara; Boesch, Sylvia; Haslinger, Bernhard; Jech, Robert; Garavaglia, Barbara; Wood, Nick; Houlden, Henry; Gissen, Paul; Lubbe, Steven J.; Sue, Carolyn M.; Cif, Laura; Mencacci, Niccolo E.; Anderson, Glenn; Kurian, Manju A. und Winkelmann, Juliane
(2020):
Loss-of-Function Variants in HOPS Complex Genes VPS16 and VPS41 Cause Early Onset Dystonia Associated with Lysosomal Abnormalities.
In: Annals of Neurology, Bd. 88, Nr. 5: S. 867-877
[PDF, 20MB]
Zech, Michael; Jech, Robert; Boesch, Sylvia; Skorvanek, Matej; Weber, Sandrina; Wagner, Matias; Zhao, Chen; Jochim, Angela; Necpal, Jan; Dincer, Yasemin; Vill, Katharina; Disteimaier, Felix; Stoklosa, Malgorzata; Krenn, Martin; Grunwald, Stephan; Bock-Bierbaum, Tobias; Fecikova, Anna; Havrankova, Petra; Roth, Jan; Prihodova, Iva; Adamovicova, Miriam; Ulmanova, Olga; Bechyne, Karel; Danhofer, Pavlina; Vesely, Branislav; Han, Vladimir; Pavelekova, Petra; Gdovinova, Zuzana; Mantel, Tobias; Meindl, Tobias; Sitzberger, Alexandra; Schröder, Sebastian; Blaschek, Astrid; Roser, Timo; Bonfert, Michaela V.; Haberlandt, Edda; Plecko, Barbara; Leineweber, Birgit; Berweck, Steffen; Herberhold, Thomas; Langguth, Berthold; Svantnerova, Jana; Minar, Michal; Ramos-Rivera, Gonzalo Alonso; Wojcik, Monica H.; Pajusalu, Sander; Ounap, Katrin; Schatz, Ulrich A.; Pölsler, Laura; Milenkovic, Ivan; Laccone, Franco; Pilhofer, Veronika; Colombo, Roberto; Patzer, Steffi; Iuso, Arcangela; Vera, Julia; Troncoso, Monica; Fang, Fang; Prokisch, Holger; Wilbert, Friederike; Eckenweiler, Matthias; Graf, Elisabeth; Westphal, Dominik S.; Riedhammer, Korbinian M.; Brunet, Theresa; Alhaddad, Bader; Berutti, Riccardo; Strom, Tim M.; Hecht, Martin; Baumann, Matthias; Wolf, Marc; Telegrafi, Aida; Person, Richard E.; Zamora, Francisca Milian; Henderson, Lindsay B.; Weise, David; Musacchio, Thomas; Volkmann, Jens; Szuto, Anna; Becker, Jessica; Cremer, Kirsten; Sycha, Thomas; Zimprich, Fritz; Kraus, Verena; Makowski, Christine; Gonzalez-Alegre, Pedro; Bardakjian, Tanya M.; Ozelius, Laurie J.; Vetro, Annafisa; Guerrini, Renzo; Maier, Esther; Borggraefe, Ingo; Kuster, Alice; Wortmann, Saskia B.; Hackenberg, Annette; Steinfeld, Robert; Assmann, Birgit; Staufner, Christian; Opladen, Thomas; Ruzicka, Evzen; Cohn, Ronald D.; Dyment, David; Chung, Wendy K.; Engels, Hartmut; Ceballos-Baumann, Andres; Ploski, Rafai; Daumke, Ofiver; Haslinger, Bernhard; Mall, Volker; Oexle, Konrad und Winkehnann, Juliane
(2020):
Monogenic variants in dystonia: an exome-wide sequencing study.
In: Lancet Neurology, Bd. 19, Nr. 11: S. 908-918
2019
Lane, Jacqueline M.; Jones, Samuel E.; Dashti, Hassan S.; Wood, Andrew R.; Aragam, Krishna G.; Hees, Vincent T. van; 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, Richa; Martinsen, Amy E.; Skogholt, Anne H.; Sivertsen, Borge; Bragantini, Daniela; Kallestad, Havard; Janszky, Imre; Guzey, Ismail C.; Nilsen, Kristian B.; Fritsche, Lars; Pedersen, Linda M.; Gabrielsen, Maiken E.; Johnsen, Marianne B.; Lie, Marie U.; Engstrom, Morten; Sand, Trond und Zhou, Wei
(2019):
Biological and clinical insights from genetics of insomnia symptoms.
In: Nature Genetics, Bd. 51, Nr. 3:
387-+
[PDF, 538kB]
2018
Zhao, Chen; Zhang, Dongxue und Bao, Yan
(2018):
A time window of 3 s in the aesthetic appreciation of poems.
In: Psych Journal, Bd. 7, Nr. 1: S. 51-52