Götzl, Julia K;Brendel, Matthias;Werner, Georg;Parhizkar, Samira;Sebastian Monasor, Laura;Kleinberger, Gernot;Colombo, Alessio-Vittorio;Deussing, Maximilian;Wagner, Matias;Winkelmann, Juliane;Diehl-Schmid, Janine;Levin, Johannes;Fellerer, Katrin;Reifschneider, Anika;Bultmann, Sebastian;Bartenstein, Peter;Rominger, Axel;Tahirovic, Sabina;Smith, Scott T;Madore, Charlotte;Butovsky, Oleg;Capell, Anja;Haass, Christian
Opposite microglial activation stages upon loss of PGRN or TREM2 result in reduced cerebral glucose metabolism.
EMBO Mol Med
2019
11
6

Zech, Michael;Lam, Daniel D;Winkelmann, Juliane
Update on KMT2B-Related Dystonia.
Curr Neurol Neurosci Rep
2019
19
11

Salminen, Aaro V;Allen, Richard P;Högl, Birgit;Inoue, Yuichi;Oertel, Wolfgang;Winkelman, John W;Trenkwalder, Claudia;Sampaio, Cristina;Winkelmann, Juliane
Reply to: Safety of dopamine agonists for treating restless legs syndrome.
Mov Disord
2019
34
1
150-151

Salminen, Aaro V;Lam, Daniel D;Winkelmann, Juliane
Role of MEIS1 in restless legs syndrome: From GWAS to functional studies in mice.
Adv Pharmacol
2019
84
175-184

Zech, Michael;Wagner, Matias;Schormair, Barbara;Oexle, Konrad;Winkelmann, Juliane
[Exome diagnostics in neurology].
Nervenarzt
2019
90
2
131-137

Khan, Kamal;Zech, Michael;Morgan, Angela T;Amor, David J;Skorvanek, Matej;Khan, Tahir N;Hildebrand, Michael S;Jackson, Victoria E;Scerri, Thomas S;Coleman, Matthew;Rigbye, Kristin A;Scheffer, Ingrid E;Bahlo, Melanie;Wagner, Matias;Lam, Daniel D;Berutti, Riccardo;Havránková, Petra;Fečíková, Anna;Strom, Tim M;Han, Vladimir;Dosekova, Petra;Gdovinova, Zuzana;Laccone, Franco;Jameel, Muhammad;Mooney, Marie R;Baig, Shahid M;Jech, Robert;Davis, Erica E;Katsanis, Nicholas;Winkelmann, Juliane
Recessive variants in ZNF142 cause a complex neurodevelopmental disorder with intellectual disability, speech impairment, seizures, and dystonia.
Genet Med
2019
21
11
2532-2542

Salminen, Aaro V;Allen, Richard P;Högl, Birgit;Inoue, Yuichi;Oertel, Wolfgang;Winkelman, John W;Trenkwalder, Claudia;Sampaio, Cristina;Winkelmann, Juliane
Reply to: A note on rotigotine for restless legs syndrome after renal transplantation.
Mov Disord
2019
34
1
152-153

Rietschel, Marcella;Winkelmann, Juliane
[Genetics in neurology and psychiatry].
Nervenarzt
2019
90
2
97-98

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, Richa
Biological and clinical insights from genetics of insomnia symptoms.
Nat Genet
2019
51
3
387-393

Wagner, Matias;Osborn, Daniel P S;Gehweiler, Ina;Nagel, Maike;Ulmer, Ulrike;Bakhtiari, Somayeh;Amouri, Rim;Boostani, Reza;Hentati, Faycal;Hockley, Maryam M;Hölbling, Benedikt;Schwarzmayr, Thomas;Karimiani, Ehsan Ghayoor;Kernstock, Christoph;Maroofian, Reza;Müller-Felber, Wolfgang;Ozkan, Ege;Padilla-Lopez, Sergio;Reich, Selina;Reichbauer, Jennifer;Darvish, Hossein;Shahmohammadibeni, Neda;Tafakhori, Abbas;Vill, Katharina;Züchner, Stephan;Kruer, Michael C;Winkelmann, Juliane;Jamshidi, Yalda;Schüle, Rebecca
Bi-allelic variants in RNF170 are associated with hereditary spastic paraplegia.
Nat Commun
2019
10
1