Time trends in the regional distribution of physicians, nurses and midwives in Europe
Winkelmann, Juliane, Muench, Ulrike, Maier, Claudia B
Published in BMC health services research (12.10.2020)
Published in BMC health services research (12.10.2020)
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Treatment of restless legs syndrome: Evidence‐based review and implications for clinical practice (Revised 2017)
Winkelmann, Juliane, Allen, Richard P., Högl, Birgit, Inoue, Yuichi, Oertel, Wolfgang, Salminen, Aaro V., Winkelman, John W., Trenkwalder, Claudia, Sampaio, Cristina
Published in Movement disorders (01.07.2018)
Published in Movement disorders (01.07.2018)
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Biological and clinical insights from genetics of insomnia symptoms
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
Published in Nature genetics (01.03.2019)
Published in Nature genetics (01.03.2019)
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Mutant Adenosine Deaminase 2 in a Polyarteritis Nodosa Vasculopathy
Navon Elkan, Paulina, Pierce, Sarah B, Segel, Reeval, Walsh, Tom, Barash, Judith, Padeh, Shai, Zlotogorski, Abraham, Berkun, Yackov, Press, Joseph J, Mukamel, Masha, Voth, Isabel, Hashkes, Philip J, Harel, Liora, Hoffer, Vered, Ling, Eduard, Yalcinkaya, Fatos, Kasapcopur, Ozgur, Lee, Ming K, Klevit, Rachel E, Renbaum, Paul, Weinberg-Shukron, Ariella, Sener, Elif F, Schormair, Barbara, Zeligson, Sharon, Marek-Yagel, Dina, Strom, Tim M, Shohat, Mordechai, Singer, Amihood, Rubinow, Alan, Pras, Elon, Winkelmann, Juliane, Tekin, Mustafa, Anikster, Yair, King, Mary-Claire, Levy-Lahad, Ephrat
Published in The New England journal of medicine (06.03.2014)
Published in The New England journal of medicine (06.03.2014)
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Clinico-genetic findings in 509 frontotemporal dementia patients
Wagner, Matias, Lorenz, Georg, Volk, Alexander E., Brunet, Theresa, Edbauer, Dieter, Berutti, Riccardo, Zhao, Chen, Anderl-Straub, Sarah, Bertram, Lars, Danek, Adrian, Deschauer, Marcus, Dill, Veronika, Fassbender, Klaus, Fliessbach, Klaus, Götze, 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, Winkelmann, Juliane
Published in Molecular psychiatry (01.10.2021)
Published in Molecular psychiatry (01.10.2021)
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Journal Article
The role of patient navigators in ambulatory care: overview of systematic reviews
Budde, Hannah, Williams, Gemma A, Winkelmann, Juliane, Pfirter, Laura, Maier, Claudia B
Published in BMC health services research (28.10.2021)
Published in BMC health services research (28.10.2021)
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Journal Article
Haploinsufficiency of KMT2B, Encoding the Lysine-Specific Histone Methyltransferase 2B, Results in Early-Onset Generalized Dystonia
Zech, Michael, Boesch, Sylvia, Maier, Esther M., Borggraefe, Ingo, Vill, Katharina, Laccone, Franco, Pilshofer, Veronika, Ceballos-Baumann, Andres, Alhaddad, Bader, Berutti, Riccardo, Poewe, Werner, Haack, Tobias B., Haslinger, Bernhard, Strom, Tim M., Winkelmann, Juliane
Published in American journal of human genetics (01.12.2016)
Published in American journal of human genetics (01.12.2016)
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Journal Article
A Mutation in VPS35, Encoding a Subunit of the Retromer Complex, Causes Late-Onset Parkinson Disease
Zimprich, Alexander, Benet-Pagès, Anna, Struhal, Walter, Graf, Elisabeth, Eck, Sebastian H., Offman, Marc N., Haubenberger, Dietrich, Spielberger, Sabine, Schulte, Eva C., Lichtner, Peter, Rossle, Shaila C., Klopp, Norman, Wolf, Elisabeth, Seppi, Klaus, Pirker, Walter, Presslauer, Stefan, Mollenhauer, Brit, Katzenschlager, Regina, Foki, Thomas, Hotzy, Christoph, Reinthaler, Eva, Harutyunyan, Ashot, Kralovics, Robert, Peters, Annette, Zimprich, Fritz, Brücke, Thomas, Poewe, Werner, Auff, Eduard, Trenkwalder, Claudia, Rost, Burkhard, Ransmayr, Gerhard, Winkelmann, Juliane, Meitinger, Thomas, Strom, Tim M.
Published in American journal of human genetics (15.07.2011)
Published in American journal of human genetics (15.07.2011)
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Clinical exome sequencing in early‐onset generalized dystonia and large‐scale resequencing follow‐up
Zech, Michael, Boesch, Sylvia, Jochim, Angela, Weber, Sandrina, Meindl, Tobias, Schormair, Barbara, Wieland, Thomas, Lunetta, Christian, Sansone, Valeria, Messner, Michael, Mueller, Joerg, Ceballos‐Baumann, Andres, Strom, Tim M., Colombo, Roberto, Poewe, Werner, Haslinger, Bernhard, Winkelmann, Juliane
Published in Movement disorders (01.04.2017)
Published in Movement disorders (01.04.2017)
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Trisomy X syndrome with dystonia and a pathogenic SATB1 variant
Necpál, Ján, Zech, Michael, Winkelmann, Juliane, Jech, Robert
Published in Neurological sciences (01.09.2021)
Published in Neurological sciences (01.09.2021)
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De novo variants in neurodevelopmental disorders—experiences from a tertiary care center
Brunet, Theresa, Jech, Robert, Brugger, Melanie, Kovacs, Reka, Alhaddad, Bader, Leszinski, Gloria, Riedhammer, Korbinian M., Westphal, Dominik S., Mahle, Isabella, Mayerhanser, Katharina, Skorvanek, Matej, Weber, Sandrina, Graf, Elisabeth, Berutti, Riccardo, Necpál, Ján, Havránková, Petra, Pavelekova, Petra, Hempel, Maja, Kotzaeridou, Urania, Hoffmann, Georg F., Leiz, Steffen, Makowski, Christine, Roser, Timo, Schroeder, Sebastian A., Steinfeld, Robert, Strobl‐Wildemann, Gertrud, Hoefele, Julia, Borggraefe, Ingo, Distelmaier, Felix, Strom, Tim M., Winkelmann, Juliane, Meitinger, Thomas, Zech, Michael, Wagner, Matias
Published in Clinical genetics (01.07.2021)
Published in Clinical genetics (01.07.2021)
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Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy
WINKELMANN, Juliane, LING LIN, POLI, Francesca, GRUBERT, Fabian, WIELAND, Thomas, GRAF, Elisabeth, HALLMAYER, Joachim, STROM, Tim M, MIGNOT, Emmanuel, SCHORMAIR, Barbara, KORNUM, Birgitte R, FARACO, Juliette, PLAZZI, Giuseppe, MELBERG, Atle, CORNELIO, Ferdinando, URBAN, Alexander E, PIZZA, Fabio
Published in Human molecular genetics (15.05.2012)
Published in Human molecular genetics (15.05.2012)
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Spinal poly-GA inclusions in a C9orf72 mouse model trigger motor deficits and inflammation without neuron loss
Schludi, Martin H., Becker, Lore, Garrett, Lillian, Gendron, Tania F., Zhou, Qihui, Schreiber, Franziska, Popper, Bastian, Dimou, Leda, Strom, Tim M., Winkelmann, Juliane, von Thaden, Anne, Rentzsch, Kristin, May, Stephanie, Michaelsen, Meike, Schwenk, Benjamin M., Tan, Jing, Schoser, Benedikt, Dieterich, Marianne, Petrucelli, Leonard, Hölter, Sabine M., Wurst, Wolfgang, Fuchs, Helmut, Gailus-Durner, Valerie, de Angelis, Martin Hrabe, Klopstock, Thomas, Arzberger, Thomas, Edbauer, Dieter
Published in Acta neuropathologica (01.08.2017)
Published in Acta neuropathologica (01.08.2017)
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Prolonged release oxycodone–naloxone for treatment of severe restless legs syndrome after failure of previous treatment: a double-blind, randomised, placebo-controlled trial with an open-label extension
Trenkwalder, Claudia, Prof, Beneš, Heike, MD, Grote, Ludger, MD, García-Borreguero, Diego, MD, Högl, Birgit, MD, Hopp, Michael, MD, Bosse, Björn, Dipl Stat, Oksche, Alexander, MD, Reimer, Karen, Prof, Winkelmann, Juliane, Prof, Allen, Richard P, PhD, Kohnen, Ralf, PhD
Published in Lancet neurology (01.12.2013)
Published in Lancet neurology (01.12.2013)
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Opposite microglial activation stages upon loss of PGRN or TREM2 result in reduced cerebral glucose metabolism
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
Published in EMBO molecular medicine (01.06.2019)
Published in EMBO molecular medicine (01.06.2019)
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Journal Article
Skill-Mix Changes Targeting Health Promotion and Prevention Interventions and Effects on Outcomes in all Settings (Except Hospitals): Overview of Reviews
Maier, Claudia Bettina, Winkelmann, Juliane, Pfirter, Laura, Williams, Gemma A
Published in International journal of public health (09.05.2023)
Published in International journal of public health (09.05.2023)
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ImmunoChip study implicates antigen presentation to T cells in narcolepsy
Faraco, Juliette, Lin, Ling, Kornum, Birgitte Rahbek, Kenny, Eimear E, Trynka, Gosia, Einen, Mali, Rico, Tom J, Lichtner, Peter, Dauvilliers, Yves, Arnulf, Isabelle, Lecendreux, Michel, Javidi, Sirous, Geisler, Peter, Mayer, Geert, Pizza, Fabio, Poli, Francesca, Plazzi, Giuseppe, Overeem, Sebastiaan, Lammers, Gert Jan, Kemlink, David, Sonka, Karel, Nevsimalova, Sona, Rouleau, Guy, Desautels, Alex, Montplaisir, Jacques, Frauscher, Birgit, Ehrmann, Laura, Högl, Birgit, Jennum, Poul, Bourgin, Patrice, Peraita-Adrados, Rosa, Iranzo, Alex, Bassetti, Claudio, Chen, Wei-Min, Concannon, Patrick, Thompson, Susan D, Damotte, Vincent, Fontaine, Bertrand, Breban, Maxime, Gieger, Christian, Klopp, Norman, Deloukas, Panos, Wijmenga, Cisca, Hallmayer, Joachim, Onengut-Gumuscu, Suna, Rich, Stephen S, Winkelmann, Juliane, Mignot, Emmanuel
Published in PLoS genetics (01.02.2013)
Published in PLoS genetics (01.02.2013)
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Journal Article
Bi-allelic variants in RNF170 are associated with hereditary spastic paraplegia
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, Zuchner, Stephan, Kruer, Michael C., Winkelmann, Juliane, Jamshidi, Yalda, Schüle, Rebecca
Published in Nature communications (21.10.2019)
Published in Nature communications (21.10.2019)
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Journal Article
KMT2B rare missense variants in generalized dystonia
Zech, Michael, Jech, Robert, Havránková, Petra, Fečíková, Anna, Berutti, Riccardo, Urgošík, Dušan, Kemlink, David, Strom, Tim M., Roth, Jan, Růžička, Evžen, Winkelmann, Juliane
Published in Movement disorders (01.07.2017)
Published in Movement disorders (01.07.2017)
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Generation of two human iPSC lines, HMGUi004-A and FINCBi004-A, from fibroblasts of MPAN patients carrying pathogenic recessive mutations in the gene C19orf12
Zanuttigh, Enrica, Rusha, Ejona, Peron, Camille, Brunetti, Dario, Zorzi, Giovanna, Pertek, Anna, Nteli, Polyxeni, Winkelmann, Juliane, Tiranti, Valeria, Iuso, Arcangela
Published in Stem cell research (01.10.2023)
Published in Stem cell research (01.10.2023)
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