Juliane Winkelmann
Active 1999–2026
- 138
- Papers
- 23,610
- Citations
- 72
- h-index
- 127
- i10-index
Citations
Citation sources
Countries
Institutions
- Harvard University1.2%
- Inserm0.8%
- Broad Institute0.7%
- Massachusetts General Hospital0.7%
- University College London0.6%
- Brigham and Women's Hospital0.5%
- Other95.5%
Fields
- Medicine39.3%
- Biochemistry, Genetics and Molecular Biology35.6%
- Immunology and Microbiology10.6%
- Neuroscience8%
- Psychology2.7%
- Health Professions1%
- Other2.8%
Topics
- Inflammatory Bowel Disease4.6%
- Parkinson's Disease Mechanisms and Treatments4.6%
- Restless Legs Syndrome Research3%
- Sleep and Wakefulness Research2.9%
- Gut microbiota and health2.8%
- Sleep and related disorders2.5%
- Other79.6%
Coauthors
- Michael Zech30
- Claudia Trenkwalder29
- Barbara Schormair22
- Matias Wagner19
- Birgit Högl18
- Robert Jech16
- Riccardo Berutti15
- Matěj Škorvánek14
- Tim M. Strom14
- Sylvia Boesch13
- Wolfgang H. Oertel13
- Christian Gieger12
- Ján Necpál12
- Peter Lichtner12
- Walter Paulus11
- Bertram Müller‐Myhsok10
- David Kemlink10
- Konrad Oexle10
- Theresa Brunet10
- Holger Prokisch9
- Petra Havránková9
- Thomas Meitinger9
- Werner Poewe9
- Annette Peters8
All papers
- Host–microbe interactions have shaped the genetic architecture of inflammatory bowel disease
Authors: Luke Jostins, Stephan Ripke, Rinse K. Weersma, Richard H. Duerr, Dermot McGovern, Ken Hui, James Lee, L. Philip Schumm, Yashoda Sharma, Carl A. Anderson, Jonah Essers, Mitja Mitrovič, Kaida Ning, Isabelle Cleynen, Emilie Théâtre, Sarah L. Spain, Soumya Raychaudhuri, Philippe Goyette, Zhi Wei, Clara Abraham, Jean–Paul Achkar, Tariq Ahmad, Leila Amininejad, Ashwin N. Ananthakrishnan, Vibeke Andersen, Jane M. Andrews, Leonard Baidoo, Tobias Balschun, Peter A. Bampton, Alain Bitton, Gabrielle Boucher, Stephan Brand, Carsten Büning, Ariella Cohain, Sven Cichon, Mauro D’Amato, Dirk de Jong, Kathy L. Devaney, Marla C. Dubinsky, Cathryn Edwards, David Ellinghaus, Lynnette Ferguson, Denis Franchimont, Karin Fransén, Richard B. Gearry, Michel Georges, Christian Gieger, Jürgen Glas, Talin Haritunians, Ailsa Hart, Chris Hawkey, Matija Hedl, Xinli Hu, Tom H. Karlsen, Limas Kupčinskas, Subra Kugathasan, Anna Latiano, Debby Laukens, Ian C. Lawrance, Charlie W. Lees, Édouard Louis, Gillian Mahy, John Mansfield, Angharad R. Morgan, Craig Mowat, William G. Newman, Orazio Palmieri, Cyriel Y. Ponsioen, Uroš Potočnik, Natalie J. Prescott, Miguel Regueiro, Jerome I. Rotter, Richard K. Russell, Jeremy Sanderson, Miquel Sans, Jack Satsangi, Stefan Schreiber, Lisa A. Simms, Jurgita Šventoraitytė, Stephan R. Targan, Kent D. Taylor, Mark Tremelling, Hein W. Verspaget, Martine De Vos, Cisca Wijmenga, David C. Wilson, Juliane Winkelmann, Ramnik J. Xavier, Sebastian Zeißig, Bin Zhang, Hu Zhang, Hongyu Zhao, Mark S. Silverberg, Vito Annese, Håkon Håkonarson, Steven R. Brant, Graham Radford‐Smith, Christopher G. Mathew, John D. Rioux, Eric E. Schadt and 6 more - Nature 2012 cited by 4,917
- Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis
Authors: Athena Hadjixenofontos, Ashley Beecham, Jacob L. McCauley, Clara P. Manrique, Margaret A Pericak‐Vance, Ioanna Konidari, Nikolaos A Patsopoulos, Philip L. De Jager, Michelle Lee, Irene Y. Frohlich, Nikolaos A. Patsopoulos, Chris Spencer, Gavin Band, Céline Bellenguez, Alexander T Dilthey, Céline Bellenguez, Colin Freeman, Alexander Dilthey, Dionysia K. Xifara, Gavin Band, Peter Donnelly, Chris C. A. Spencer, Loukas Moutsianas, Amy Strange, Matti Pirinen, Gil McVean, Mary F. Davis, Nathalie Schnetz‐Boutaud, Jonathan L. Haines, Alastair Compston, Barnaby Fiddes, Stephen Sawcer, Anu Kemppinen, Maria Ban, Amie Baker, Robert Andrews, Chris Cotsapas, Hannah Blackburn, Cristin McCabe, Chris Cotsapas, David A. Hafler, Chris Cotsapas, Carl A. Anderson, Jeffrey C. Barrett, Sarah Hunt, Sarah Edkins, Panos Deloukas, Tejas Shah, Hannah Blackburn, Cordelia Langford, Robert Andrews, David J. Booth, Steve Vucic, Graeme J. Stewart, Leentje Cosemans, An Goris, Bénédicte Dubois, Annette Oturai, Per Soelberg Sørensen, Helle Bach Søndergaard, Finn Sellebjerg, Janna Saarela, Virpi Leppä, Isabelle Cournu‐Rebeix, Bertrand Fontaine, Vincent Damotte, Angela Jochim, Juliane Winkelmann, Muni Hoshi, Achim Berthele, Thomas Korn, Rebecca Selter, Viola Biberacher, Volker Siffrin, Verena Grummel, Helena Kronsbein, Dorothea Buck, Laura Bergamaschi, Lucia Corrado, Filippo Martinelli-Boneschi, Claes Martin, Volker Siffrin, Frauke Zipp, Felix Luessi, Giuseppe Liberatore, Christiane Graetz, Eva Zindler, Mariaemma Rodegher, Lucia Corrado, Sandra D’Alfonso, Elisabeth G Celius, Inger-Lise Mero, Lucia Corrado, Sandra D’Alfonso, Jan Hillert, Tomas Olsson, Melissa Sorosina, Paola Brambilla, Giuseppe Liberatore, Magdalena Lindén and 93 more - Nature Genetics 2013 cited by 1,442
- A Mutation in VPS35, Encoding a Subunit of the Retromer Complex, Causes Late-Onset Parkinson Disease
Authors: Alexander Zimprich, Anna Benet‐Pagès, Walter Struhal, Elisabeth Graf, Sebastian Eck, Marc N. Offman, Dietrich Haubenberger, Sabine Spielberger, Eva C. Schulte, Peter Lichtner, Shaila C. Rössle, Norman Klopp, Elisabeth Wolf, Klaus Seppi, Walter Pirker, Stefan Presslauer, Brit Mollenhauer, Regina Katzenschlager, Thomas Foki, Christoph Hotzy, Eva M. Reinthaler, Ashot S. Harutyunyan, Róbert Královics, Annette Peters, Fritz Zimprich, Thomas Brücke, Werner Poewe, Eduard Auff, Claudia Trenkwalder, Burkhard Rost, Gerhard Ransmayr, Juliane Winkelmann, Thomas Meitinger, Tim M. Strom - The American Journal of Human Genetics 2011 cited by 902
- Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity
Authors: Lam C. Tsoi, Sarah L. Spain, Jo Knight, Eva Ellinghaus, Philip E. Stuart, Francesca Capon, Jun Ding, Yanming Li, Trilokraj Tejasvi, Jóhann E. Guðjónsson, Hyun Min Kang, Michael H. Allen, Ross McManus, Giuseppe Novelli, Lena Samuelsson, Joost Schalkwijk, Mona Ståhle, A. David Burden, Catherine Smith, Michael J. Cork, Xavier Estivill, A. Bowcock, Gerald G. Krueger, Wolfgang Weger, Jane Worthington, Rachid Tazi‐Ahnini, Frank O. Nestlé, Adrian Hayday, Per Hoffmann, Juliane Winkelmann, Cisca Wijmenga, Cordelia Langford, Sarah Edkins, Robert Andrews, Hannah Blackburn, Amy Strange, Gavin Band, Richard D. Pearson, Damjan Vukcevic, Chris C. A. Spencer, Panos Deloukas, Ulrich Mrowietz, Stefan Schreiber, Stephan Weidinger, Sulev Kõks, Külli Kingo, Tõnu Esko, Andres Metspalu, Henry W. Lim, John J. Voorhees, Michael Weichenthal, H.‐Erich Wichmann, Vinod Chandran, Cheryl F. Rosen, Proton Rahman, Dafna D. Gladman, C.E.M. Griffiths, André Reis, Juha Kere, Rajan P. Nair, André Franke, Jonathan N W N Barker, Gonçalo R. Abecasis, James T Elder, Richard C. Trembath - Nature Genetics 2012 cited by 1,047
- Biological and clinical insights from genetics of insomnia symptoms
Authors: HUNT All In Sleep, Jacqueline M. Lane, Samuel E. Jones, Hassan S. Dashti, Andrew R. Wood, Krishna G. Aragam, Vincent T. van Hees, Linn Beate Strand, Bendik S. Winsvold, Heming Wang, Jack Bowden, Yanwei Song, Krunal Patel, Simon Anderson, Robin N. Beaumont, David A. Bechtold, Brian E. Cade, Mary E. Haas, Sekar Kathiresan, Max A. Little, Annemarie I. Luik, Andrew Loudon, Shaun Purcell, Rebecca C. Richmond, Frank A. J. L. Scheer, Barbara Schormair, Jessica Tyrrell, John W. Winkelman, Juliane Winkelmann, Kristian Hveem, Chen Zhao, Jonas B. Nielsen, Cristen J. Willer, Susan Redline, Kai Spiegelhalder, Simon D. Kyle, David Ray, John‐Anker Zwart, Ben Brumpton, Timothy M. Frayling, Debbie A. Lawlor, Martin K. Rutter, Michael N. Weedon, Richa Saxena - Nature Genetics 2019 cited by 418
- Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome
Authors: Margot A. Cousin, Blake A. Creighton, Keith A. Breau, Rebecca C. Spillmann, Erin Torti, Sruthi Dontu, Swarnendu Tripathi, Deepa Ajit, Reginald J. Edwards, Simone Afriyie, Julia Bay, Kathryn M. Harper, Alvaro A. Beltran, Lorena J. Munoz, Liset Falcon Rodriguez, Michael C. Stankewich, Richard Person, Yue Si, Elizabeth A. Normand, Amy Blevins, Alison S. May, Louise Bier, Vimla S. Aggarwal, Grazia M.S. Mancini, Marjon A. van Slegtenhorst, Kirsten Cremer, Jessica Becker, Hartmut Engels, Stefan Aretz, Jennifer MacKenzie, Eva H. Brilstra, Koen L.I. van Gassen, Richard H. van Jaarsveld, Renske Oegema, Gretchen Parsons, Paul R. Mark, Ingo Helbig, Sarah McKeown, Robert F. Stratton, Benjamin Cogné, Bertrand Isidor, Pilar Cacheiro, Damian Smedley, Helen V. Firth, Tatjana Bierhals, Katja Kloth, Deike Weiss, Cecilia Fairley, Joseph T.C. Shieh, Amy Kritzer, Parul Jayakar, Evangeline C. Kurtz‐Nelson, Raphael Bernier, Tianyun Wang, Evan E. Eichler, Ingrid M.B.H. van de Laar, Allyn McConkie‐Rosell, Marie McDonald, Jennifer L. Kemppainen, Brendan C. Lanpher, Laura Schultz‐Rogers, Lauren Gunderson, Pavel N. Pichurin, Grace Yoon, Michael Zech, Robert Jech, Juliane Winkelmann, Undiagnosed Diseases Network, Adriana S. Beltrán, Michael T. Zimmermann, Brenda Temple, Sheryl S. Moy, Eric W. Klee, Queenie K-G Tan, Damaris N. Lorenzo - Nature Genetics 2021 cited by 108
- Genome-wide Association Analysis of Psoriatic Arthritis and Cutaneous Psoriasis Reveals Differences in Their Genetic Architecture
Authors: Philip E. Stuart, Rajan P. Nair, Lam C. Tsoi, Trilokraj Tejasvi, Sayantan Das, Hyun Min Kang, Eva Ellinghaus, Vinod Chandran, Kristina Callis-Duffin, Robert W. Ike, Yanming Li, Xiaoquan Wen, Charlotta Enerbäck, Jóhann E. Guðjónsson, Sulev Kõks, Külli Kingo, Tõnu Esko, Ulrich Mrowietz, André Reis, Hans Wichmann, Christian Gieger, Per Hoffmann, Markus M. Nöthen, Juliane Winkelmann, Manfred Kunz, Elvia G. Moreta, Philip J. Mease, Christopher T. Ritchlin, A. Bowcock, Gerald G. Krueger, Henry W. Lim, Stephan Weidinger, Michael Weichenthal, John J. Voorhees, Proton Rahman, Peter K. Gregersen, André Franke, Dafna D. Gladman, Gonçalo R. Abecasis, James T. Elder - The American Journal of Human Genetics 2015 cited by 322
- European countries' responses in ensuring sufficient physical infrastructure and workforce capacity during the first COVID-19 wave
Authors: Juliane Winkelmann, Erin Webb, Gemma Williams, Cristina Hernández‐Quevedo, Claudia B. Maier, Димитра Пантели - Health Policy 2021 cited by 155
- Opposite microglial activation stages upon loss of PGRN or TREM2 result in reduced cerebral glucose metabolism
Authors: Julia K Götzl, Matthias Brendel, Georg Werner, Samira Parhizkar, Laura Sebastián Monasor, Gernot Kleinberger, Alessio-Vittorio Colombo, Maximilian Deußing, Matias Wagner, Juliane Winkelmann, Janine Diehl‐Schmid, Johannes Levin, Katrin Fellerer, Anika Reifschneider, Sebastian Bultmann, Peter Bartenstein, Axel Rominger, Sabina Tahirović, Scott T. Smith, Charlotte Madore, Oleg Butovsky, Anja Capell, Christian Haass - EMBO Molecular Medicine 2019 cited by 141
- Restless legs syndrome associated with major diseases
Authors: Claudia Trenkwalder, Richard P. Allen, Birgit Högl, Walter Paulus, Juliane Winkelmann - Neurology 2016 cited by 362
- Comorbidities, treatment, and pathophysiology in restless legs syndrome
Authors: Claudia Trenkwalder, Richard P. Allen, Birgit Högl, Stefan Clemens, Stephanie M. Patton, Barbara Schormair, Juliane Winkelmann - The Lancet Neurology 2018 cited by 266
- De novo variants in neurodevelopmental disorders—experiences from a tertiary care center
Authors: Theresa Brunet, Robert Jech, Melanie Brügger, Reka Kovacs, Bader Alhaddad, Gloria Leszinski, Korbinian M. Riedhammer, Dominik S. Westphal, Isabella Mahle, Katharina Mayerhanser, Matěj Škorvánek, Sandrina Weber, Elisabeth Graf, Riccardo Berutti, Ján Necpál, Petra Havránková, Petra Pavelekova, Maja Hempel, Urania Kotzaeridou, Georg F. Hoffmann, Steffen Leiz, Christine Makowski, Timo Roser, A. Sebastian Schroeder, Robert Steinfeld, Gertrud Strobl‐Wildemann, Julia Hoefele, Ingo Borggraefe, Felix Distelmaier, Tim M. Strom, Juliane Winkelmann, Thomas Meitinger, Michael Zech, Matias Wagner - Clinical Genetics 2021 cited by 119
- Mutant Adenosine Deaminase 2 in a Polyarteritis Nodosa Vasculopathy
Authors: Paulina Navon Elkan, Sarah B. Pierce, Reeval Segel, Tom Walsh, Judith Barash, Shai Padeh, Abraham Zlotogorski, Yackov Berkun, Joseph J. Press, M Mukamel, Isabel Voth, Philip J. Hashkes, Liora Harel, Vered Hoffer, Eduard Ling, Fatoş Yalçınkaya, Özgür Kasapçopur, Ming K. Lee, Rachel E. Klevit, Paul Renbaum, Ariella Weinberg‐Shukron, Elif Funda Şener, Barbara Schormair, Sharon Zeligson, Dina Marek‐Yagel, Tim M. Strom, Mordechai Shohat, Amihood Singer, Alan Rubinow, Elon Pras, Juliane Winkelmann, Mustafa Tekin, Yair Anikster, Mary‐Claire King, Ephrat Levy‐Lahad - New England Journal of Medicine 2014 cited by 706
- Guidelines for the first-line treatment of restless legs syndrome/Willis–Ekbom disease, prevention and treatment of dopaminergic augmentation: a combined task force of the IRLSSG, EURLSSG, and the RLS-foundation
Authors: Diego García‐Borreguero, Michael H. Silber, John W. Winkelman, Birgit Högl, Jacquelyn Bainbridge, Mark J. Buchfuhrer, Georgios M. Hadjigeorgiou, Yuichi Inoue, Mauro Manconi, Wolfgang H. Oertel, William G. Ondo, Juliane Winkelmann, Richard P. Allen - Sleep Medicine 2016 cited by 328
- Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits
Authors: Anke R. Hammerschlag, Sven Stringer, Christiaan de Leeuw, Suzanne Sniekers, Erdogan Taskesen, Kyoko Watanabe, Tessa F. Blanken, Kim Dekker, Bart H. W. Te Lindert, Rick Wassing, Ingileif Jónsdóttir, Guðmar Þorleifsson, Hreinn Stefánsson, Þórarinn Gíslason, Klaus Berger, Barbara Schormair, Juergen Wellmann, Juliane Winkelmann, Kāri Stefánsson, Konrad Oexle, Eus J.W. Van Someren, Daniëlle Posthuma - Nature Genetics 2017 cited by 311
- Loss‐of‐Function Variants in HOPS Complex Genes VPS16 and VPS41 Cause Early Onset Dystonia Associated with Lysosomal Abnormalities
Authors: Dora Steel, Michael Zech, Chen Zhao, Katy Barwick, Derek Burke, Diane Demailly, Kishore R. Kumar, Giovanna Zorzi, Nardo Nardocci, Rauan Kaiyrzhanov, Matias Wagner, Arcangela Iuso, Riccardo Berutti, Matěj Škorvánek, Ján Necpál, Ryan L. Davis, Sarah Wiethoff, Kshitij Mankad, Sniya Sudhakar, Arianna Ferrini, Suvasini Sharma, Erik‐Jan Kamsteeg, Marina A.J. Tijssen, Corien Verschuuren, Martje E. van Egmond, Joanna M. Flowers, Meriel McEntagart, Arianna Tucci, Philippe Coubes, Bernabé I. Bustos, Paulina González-Latapí, Stephen Tisch, Paul Darveniza, Kathleen M. Gorman, Kathryn J. Peall, Kai Bötzel, Jan Christoph Koch, Tomasz Kmieć, Barbara Plecko, Sylvia Boesch, Bernhard Haslinger, Robert Jech, Barbara Garavaglia, Nick Wood, Henry Houlden, Paul Gissen, Steven Lubbe, Carolyn M. Sue, Laura Cif, Niccolò E. Mencacci, Glenn Anderson, Manju A. Kurian, Juliane Winkelmann - Annals of Neurology 2020 cited by 110
- Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis
Authors: Jimmy Z. Liu, The International PSC Study Group, Johannes R. Hov, Trine Folseraas, Eva Ellinghaus, Simon Rushbrook, Nadezhda T. Doncheva, Ole A. Andreassen, Rinse K. Weersma, Tobias J. Weismüller, Bertus Eksteen, Pietro Invernizzi, Gideon M. Hirschfield, Daniel Gotthardt, Albert Parés, David Ellinghaus, Tejas Shah, Brian D. Juran, Piotr Milkiewicz, Christian Rust, Christoph Schramm, Tobias Müller, Brijesh Srivastava, Georgios Dalekos, Markus M. Nöthen, Stefan Herms, Juliane Winkelmann, Mitja Mitrovič, Felix Braun, Cyriel Y. Ponsioen, Peter J.P. Croucher, Martina Sterneck, Andreas Teufel, Andrew L. Mason, Janna Saarela, Virpi Leppä, Ruslan Dorfman, Domenico Alvaro, Annarosa Floreani, Suna Önengüt-Gümüşcü, Stephen S. Rich, Wesley K. Thompson, Andrew J. Schork, Sigrid Næss, Ingo Thomsen, Gabriele Mayr, Inke R. König, Kristian Hveem, Isabelle Cleynen, Javier Gutierrez‐Achury, Isis Ricaño-Ponce, David A. van Heel, Einar Björnsson, Richard Sandford, Peter R. Durie, Espen Melum, Morten H. Vatn, Mark S. Silverberg, Richard H. Duerr, Leonid Padyukov, Stephan Brand, Miquel Sans, Vito Annese, Jean–Paul Achkar, Kirsten Muri Boberg, Hanns–Ulrich Marschall, Olivier Chazouillères, Christopher L. Bowlus, Cisca Wijmenga, Erik Schrumpf, Séverine Vermeire, Mario Albrecht, John D. Rioux, Graeme Alexander, Annika Bergquist, Judy H. Cho, Stefan Schreiber, Michael P. Manns, Martti Färkkilâ, Anders M. Dale, Roger W. Chapman, Konstantinos N. Lazaridis, André Franke, Carl A. Anderson, Tom H. Karlsen - Nature Genetics 2013 cited by 398
- Relationship of serum beta‐synuclein with blood biomarkers and brain atrophy
Authors: Patrick Oeckl, Sarah Anderl‐Straub, Adrian Danek, Janine Diehl‐Schmid, Klaus Faßbender, Klaus Fließbach, Steffen Halbgebauer, Hans‐Jürgen Huppertz, Holger Jahn, Jan Kassubek, Johannes Kornhuber, G. Bernhard Landwehrmeyer, Martin Lauer, Johannes Prudlo, Anja Schneider, Matthias L. Schroeter, Petra Steinacker, Alexander E. Volk, Matias Wagner, Juliane Winkelmann, Jens Wiltfang, Albert C. Ludolph, Markus Otto - Alzheimer s & Dementia 2022 cited by 52
- Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis
Authors: Barbara Schormair, Chen Zhao, Steven Bell, Erik Tilch, Aaro V. Salminen, Benno Pütz, Yves Dauvilliers, Ambra Stefani, Birgit Högl, Werner Poewe, David Kemlink, Karel Šonka, Cornelius G. Bachmann, Walter Paulus, Claudia Trenkwalder, Wolfgang H. Oertel, Magdolna Hornyak, Maris Teder‐Laving, Andres Metspalu, Georgios M. Hadjigeorgiou, Olli Polo, Ingo Fietze, Owen A. Ross, Zbigniew K. Wszołek, Adam S. Butterworth, Nicole Soranzo, Willem H. Ouwehand, David J. Roberts, John Danesh, Richard P. Allen, Christopher J. Earley, William G. Ondo, Lan Xiong, Jacques Montplaisir, Ziv Gan‐Or, Markus Perola, Pavel Vodička, Christian Dina, André Franke, Lukas Tittmann, Alexandre F.R. Stewart, Svati H. Shah, Christian Gieger, Annette Peters, Guy A. Rouleau, Klaus Berger, Konrad Oexle, Emanuele Di Angelantonio, David A. Hinds, Bertram Müller‐Myhsok, Juliane Winkelmann, Beverley Balkau, Pierre Ducimetière, Eveline Eschwège, Fanny Rancière, François Alhenc‐Gelas, Yves Gallois, A Girault, Frédéric Fumeron, Michel Marre, Ronan Roussel, Fabrice Bonnet, Amélie Bonnefond, Stéphane Cauchi, Philippe Froguel, Joël Cogneau, C. Born, E Cacès, M. Cailleau, Olivier Lantieri, J.G. Moreau, F Rakotozafy, Jean Tichet, Sylviane Vol, Michelle Agee, Babak Alipanahi, Adam Auton, Robert K. Bell, Katarzyna Bryc, Sarah L. Elson, Pierre Fontanillas, Nicholas A. Furlotte, David A. Hinds, Bethann S. Hromatka, Karen E. Huber, Aaron Kleinman, Nadia K. Litterman, Matthew H. McIntyre, Joanna L. Mountain, Carrie A. M. Northover, Steven J. Pitts, J. Fah Sathirapongsasuti, Olga V. Sazonova, Janie F. Shelton, Suyash Shringarpure, Chao Tian, Joyce Y. Tung, Vladimir Vacic, Catherine H. Wilson - The Lancet Neurology 2017 cited by 240
- Oral Health Care in Europe: Financing, Access and Provision
Authors: Juliane Winkelmann, E van Ginneken, Jesús Gómez Rossi - European Journal of Public Health 2022 cited by 70
- Dense genotyping of immune-related loci in idiopathic inflammatory myopathies confirms HLA alleles as the strongest genetic risk factor and suggests different genetic background for major clinical subgroups
Authors: Simon Rothwell, Robert G. Cooper, Ingrid E. Lundberg, Frederick W. Miller, Peter K. Gregersen, John Bowes, Jiří Vencovský, Katalin Dankó, Vidya Limaye, Albert Selva-O’Callaghan, Michael G. Hanna, Pedro Machado, Lauren M. Pachman, Ann M. Reed, Lisa G. Rider, Joanna Cobb, Hazel Platt, Øyvind Molberg, Olivier Benvéniste, Pernille Mathiesen, Timothy Radstake, Andrea Doria, Jan De Bleecker, Boél De Paepe, Britta Maurer, William Ollier, Leonid Padyukov, Terrance P. OʼHanlon, Annette Lee, Christopher I. Amos, Christian Gieger, Thomas Meitinger, Juliane Winkelmann, Lucy R. Wedderburn, Hector Chinoy, Janine A. Lamb - Annals of the Rheumatic Diseases 2016 cited by 164
- Variants in Mitochondrial ATP Synthase Cause Variable Neurologic Phenotypes
Authors: Michael Zech, Robert Kopajtich, Katja Steinbrücker, Céline Bris, Naïg Guéguen, René G. Feichtinger, Melanie T. Achleitner, Neslihan Düzkale, Maximilien Périvier, Johannes Koch, Harald Engelhardt, Peter Freisinger, Matias Wagner, Theresa Brunet, Riccardo Berutti, Dmitrii Smirnov, Tharsini Navaratnarajah, Richard J. Rodenburg, Lynn Pais, Christina Austin‐Tse, Melanie O’Leary, Sylvia Boesch, Robert Jech, Somayeh Bakhtiari, Sheng Chih Jin, Friederike Wilbert, Michael C. Kruer, Saskia B. Wortmann, Matthias Eckenweiler, Johannes A. Mayr, Felix Distelmaier, Robert Steinfeld, Juliane Winkelmann, Holger Prokisch - Annals of Neurology 2021 cited by 41
- Clinico-genetic findings in 509 frontotemporal dementia patients
Authors: Matias Wagner, Georg Lorenz, Alexander E. Volk, Theresa Brunet, Dieter Edbauer, Riccardo Berutti, Chen Zhao, Sarah Anderl‐Straub, Lars Bertram, Adrian Danek, Marcus Deschauer, Veronika Dill, Klaus Faßbender, Klaus Fließbach, Katharina S. Götze, Holger Jahn, Johannes Kornhuber, G. Bernhard Landwehrmeyer, Martin Lauer, Hellmuth Obrig, Johannes Prudlo, Anja Schneider, Matthias L. Schroeter, Ingo Uttner, Ruth Vukovich, Jens Wiltfang, Andrea Sylvia Winkler, Qihui Zhou, Albert C. Ludolph, Konrad Oexle, Markus Otto, Janine Diehl‐Schmid, Juliane Winkelmann - Molecular Psychiatry 2021 cited by 54
- Treatment of restless legs syndrome: Evidence‐based review and implications for clinical practice (Revised 2017)§
Authors: Juliane Winkelmann, Richard P. Allen, Birgit Högl, Yuichi Inoue, Wolfgang H. Oertel, Aaro V. Salminen, John W. Winkelman, Claudia Trenkwalder, Cristina Sampaio - Movement Disorders 2018 cited by 170
