Barbara Schormair (B Schormair)

ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 12

Top Venues

Nature genetics

Movement disorders : official journal of the Movement Disorder Society

Sleep

Clinical genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Barbara Schormair, Chen Zhao, Steven Bell, Maria Didriksen, Muhammad S Nawaz, Nathalie Schandra, Ambra Stefani, Birgit Högl, Yves Dauvilliers, Cornelius G Bachmann, David Kemlink, Karel Sonka, 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 Wszolek, Abubaker Ibrahim, Melanie Bergmann, Volker Kittke, Philip Harrer, Joseph Dowsett, Sofiene Chenini, Sisse Rye Ostrowski, Erik Sørensen, Christian Erikstrup, Ole Birger Vesterager Pedersen, Mie Topholm Bruun, Kaspar R Nielsen, Adam S Butterworth, Nicole Soranzo, Willem Hendrik Ouwehand, David J Roberts, John Danesh, Brendan Burchell, Nicholas A Furlotte, Priyanka Nandakumar, null null, null null, Christopher J Earley, William G Ondo, Lan Xiong, Alex Desautels, Markus Perola, Pavel Vodicka, Christian Dina, Monika Stoll, Andre Franke, Wolfgang Lieb, Alexandre F R Stewart, Svati H Shah, Christian Gieger, Annette Peters, David B Rye, Guy A Rouleau, Klaus Berger, Hreinn Stefansson, Henrik Ullum, Kari Stefansson, David A Hinds, Emanuele Di Angelantonio, Konrad Oexle, Juliane Winkelmann
Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction. Nature genetics 56 (6) (2024)
Barbara Schormair, Chen Zhao, Steven Bell, Maria Didriksen, Muhammad S Nawaz, Nathalie Schandra, Ambra Stefani, Birgit Högl, Yves Dauvilliers, Cornelius G Bachmann, David Kemlink, Karel Sonka, 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 Wszolek, Abubaker Ibrahim, Melanie Bergmann, Volker Kittke, Philip Harrer, Joseph Dowsett, Sofiene Chenini, Sisse Rye Ostrowski, Erik Sørensen, Christian Erikstrup, Ole Birger Vesterager Pedersen, Mie Topholm Bruun, Kaspar R Nielsen, Adam S Butterworth, Nicole Soranzo, Willem Hendrik Ouwehand, David J Roberts, John Danesh, Brendan Burchell, Nicholas A Furlotte, Priyanka Nandakumar, null null, null null, Christopher J Earley, William G Ondo, Lan Xiong, Alex Desautels, Markus Perola, Pavel Vodicka, Christian Dina, Monika Stoll, Andre Franke, Wolfgang Lieb, Alexandre F R Stewart, Svati H Shah, Christian Gieger, Annette Peters, David B Rye, Guy A Rouleau, Klaus Berger, Hreinn Stefansson, Henrik Ullum, Kari Stefansson, David A Hinds, Emanuele Di Angelantonio, Konrad Oexle, Juliane Winkelmann
Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction. Nature genetics (2024)
Barbara Schormair, Chen Zhao, Steven Bell, Maria Didriksen, Muhammad S Nawaz, Nathalie Schandra, Ambra Stefani, Birgit Högl, Yves Dauvilliers, Cornelius G Bachmann, David Kemlink, Karel Sonka, 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 Wszolek, Abubaker Ibrahim, Melanie Bergmann, Volker Kittke, Philip Harrer, Joseph Dowsett, Sofiene Chenini, Sisse Rye Ostrowski, Erik Sørensen, Christian Erikstrup, Ole Birger Vesterager Pedersen, Mie Topholm Bruun, Kaspar R Nielsen, Adam S Butterworth, Nicole Soranzo, Willem Hendrik Ouwehand, David J Roberts, John Danesh, Brendan Burchell, Nicholas A Furlotte, Priyanka Nandakumar, null null, null null, Christopher J Earley, William G Ondo, Lan Xiong, Alex Desautels, Markus Perola, Pavel Vodicka, Christian Dina, Monika Stoll, Andre Franke, Wolfgang Lieb, Alexandre F R Stewart, Svati H Shah, Christian Gieger, Annette Peters, David B Rye, Guy A Rouleau, Klaus Berger, Hreinn Stefansson, Henrik Ullum, Kari Stefansson, David A Hinds, Emanuele Di Angelantonio, Konrad Oexle, Juliane Winkelmann
Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction. Nature genetics 56 (6) (2024)
Barbara Schormair, Chen Zhao, Steven Bell, Maria Didriksen, Muhammad S Nawaz, Nathalie Schandra, Ambra Stefani, Birgit Högl, Yves Dauvilliers, Cornelius G Bachmann, David Kemlink, Karel Sonka, 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 Wszolek, Abubaker Ibrahim, Melanie Bergmann, Volker Kittke, Philip Harrer, Joseph Dowsett, Sofiene Chenini, Sisse Rye Ostrowski, Erik Sørensen, Christian Erikstrup, Ole Birger Vesterager Pedersen, Mie Topholm Bruun, Kaspar R Nielsen, Adam S Butterworth, Nicole Soranzo, Willem Hendrik Ouwehand, David J Roberts, John Danesh, Brendan Burchell, Nicholas A Furlotte, Priyanka Nandakumar, null null, null null, Christopher J Earley, William G Ondo, Lan Xiong, Alex Desautels, Markus Perola, Pavel Vodicka, Christian Dina, Monika Stoll, Andre Franke, Wolfgang Lieb, Alexandre F R Stewart, Svati H Shah, Christian Gieger, Annette Peters, David B Rye, Guy A Rouleau, Klaus Berger, Hreinn Stefansson, Henrik Ullum, Kari Stefansson, David A Hinds, Emanuele Di Angelantonio, Konrad Oexle, Juliane Winkelmann
Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction. Nature genetics 56 (6) (2024)
Barbara Schormair, Chen Zhao, Steven Bell, Maria Didriksen, Muhammad S Nawaz, Nathalie Schandra, Ambra Stefani, Birgit Högl, Yves Dauvilliers, Cornelius G Bachmann, David Kemlink, Karel Sonka, 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 Wszolek, Abubaker Ibrahim, Melanie Bergmann, Volker Kittke, Philip Harrer, Joseph Dowsett, Sofiene Chenini, Sisse Rye Ostrowski, Erik Sørensen, Christian Erikstrup, Ole Birger Vesterager Pedersen, Mie Topholm Bruun, Kaspar R Nielsen, Adam S Butterworth, Nicole Soranzo, Willem Hendrik Ouwehand, David J Roberts, John Danesh, Brendan Burchell, Nicholas A Furlotte, Priyanka Nandakumar, null null, null null, Christopher J Earley, William G Ondo, Lan Xiong, Alex Desautels, Markus Perola, Pavel Vodicka, Christian Dina, Monika Stoll, Andre Franke, Wolfgang Lieb, Alexandre F R Stewart, Svati H Shah, Christian Gieger, Annette Peters, David B Rye, Guy A Rouleau, Klaus Berger, Hreinn Stefansson, Henrik Ullum, Kari Stefansson, David A Hinds, Emanuele Di Angelantonio, Konrad Oexle, Juliane Winkelmann
Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction. Nature genetics 56 (6) (2024)
Barbara Schormair, Chen Zhao, Steven Bell, Maria Didriksen, Muhammad S Nawaz, Nathalie Schandra, Ambra Stefani, Birgit Högl, Yves Dauvilliers, Cornelius G Bachmann, David Kemlink, Karel Sonka, 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 Wszolek, Abubaker Ibrahim, Melanie Bergmann, Volker Kittke, Philip Harrer, Joseph Dowsett, Sofiene Chenini, Sisse Rye Ostrowski, Erik Sørensen, Christian Erikstrup, Ole Birger Vesterager Pedersen, Mie Topholm Bruun, Kaspar R Nielsen, Adam S Butterworth, Nicole Soranzo, Willem Hendrik Ouwehand, David J Roberts, John Danesh, Brendan Burchell, Nicholas A Furlotte, Priyanka Nandakumar, null null, null null, Christopher J Earley, William G Ondo, Lan Xiong, Alex Desautels, Markus Perola, Pavel Vodicka, Christian Dina, Monika Stoll, Andre Franke, Wolfgang Lieb, Alexandre F R Stewart, Svati H Shah, Christian Gieger, Annette Peters, David B Rye, Guy A Rouleau, Klaus Berger, Hreinn Stefansson, Henrik Ullum, Kari Stefansson, David A Hinds, Emanuele Di Angelantonio, Konrad Oexle, Juliane Winkelmann
Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction. Nature genetics 56 (6) (2024)
Barbara Schormair, Chen Zhao, Steven Bell, Maria Didriksen, Muhammad S Nawaz, Nathalie Schandra, Ambra Stefani, Birgit Högl, Yves Dauvilliers, Cornelius G Bachmann, David Kemlink, Karel Sonka, 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 Wszolek, Abubaker Ibrahim, Melanie Bergmann, Volker Kittke, Philip Harrer, Joseph Dowsett, Sofiene Chenini, Sisse Rye Ostrowski, Erik Sørensen, Christian Erikstrup, Ole Birger Vesterager Pedersen, Mie Topholm Bruun, Kaspar R Nielsen, Adam S Butterworth, Nicole Soranzo, Willem Hendrik Ouwehand, David J Roberts, John Danesh, Brendan Burchell, Nicholas A Furlotte, Priyanka Nandakumar, null null, null null, Christopher J Earley, William G Ondo, Lan Xiong, Alex Desautels, Markus Perola, Pavel Vodicka, Christian Dina, Monika Stoll, Andre Franke, Wolfgang Lieb, Alexandre F R Stewart, Svati H Shah, Christian Gieger, Annette Peters, David B Rye, Guy A Rouleau, Klaus Berger, Hreinn Stefansson, Henrik Ullum, Kari Stefansson, David A Hinds, Emanuele Di Angelantonio, Konrad Oexle, Juliane Winkelmann
Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction. Nature genetics 56 (6) (2024)
Björn-Hergen Laabs, Katja Lohmann, Eva-Juliane Vollstedt, Tobias Reinberger, Lisa-Marie Nuxoll, Gamze Kilic-Berkmen, Joel S Perlmutter, Sebastian Loens, Cruchaga Carlos, Andre Franke, Valerija Dobricic, Frauke Hinrichs, Anne Grözinger, Eckart Altenmüller, Steven Bellows, Sylvia Boesch, Susan B Bressman, Kevin R Duque, Alberto J Espay, Andreas Ferbert, Jeanne S Feuerstein, Samuel Frank, Thomas Gasser, Bernhard Haslinger, Robert Jech, Frank Kaiser, Christoph Kamm, Katja Kollewe, Andrea A Kühn, Mark S LeDoux, Ebba Lohmann, Abhimanyu Mahajan, Alexander Münchau, Trisha Multhaupt-Buell, Alexander Y Pantelyat, Sarah E Pirio Richardson, Deborah Raymond, Stephen G Reich, Rachel Saunders-Pullman, Barbara Schormair, Nutan Sharma, Azadeh Hamzehei Sichani, Kristina Simonyan, Jens Volkmann, Aparna Wagle Shukla, Juliane Winkelmann, Laura J Wright, Michael Zech, Kirsten E Zeuner, Simone Zittel, Meike Kasten, Yan V Sun, Tobias Bäumer, Norbert Brüggemann, Laurie J Ozelius, Hyder A Jinnah, Christine Klein, Inke R König
Genetic Risk Factors in Isolated Dystonia Escape Genome-Wide Association Studies. Movement disorders : official journal of the Movement Disorder Society (2024)
Philip Harrer, Nazanin Mirza-Schreiber, Vanessa Mandel, Sigrun Roeber, Ambra Stefani, Shamsun Naher, Matias Wagner, Christian Gieger, Melanie Waldenberger, Annette Peters, Birgit Högl, Jochen Herms, Barbara Schormair, Chen Zhao, Juliane Winkelmann, Konrad Oexle
Epigenetic Association Analyses and Risk Prediction of RLS. Movement disorders : official journal of the Movement Disorder Society (2023)
Barbara Schormair, Chen Zhao, Aaro V Salminen, Konrad Oexle, Juliane Winkelmann, null null
Reassessment of candidate gene studies for idiopathic restless legs syndrome in a large genome-wide association study dataset of European ancestry. Sleep 45 (8) (2022)
Franziska Hopfner, Stefanie H Mueller, Silke Szymczak, Olaf Junge, Lukas Tittmann, Sandra May, Katja Lohmann, Harald Grallert, Wolfgang Lieb, Konstantin Strauch, Martina Müller-Nurasyid, Klaus Berger, Barbara Schormair, Juliane Winkelmann, Brit Mollenhauer, Claudia Trenkwalder, Walter Maetzler, Daniela Berg, Meike Kasten, Christine Klein, Günter U Höglinger, Thomas Gasser, Guenther Deuschl, André Franke, Michael Krawczak, Astrid Dempfle, Gregor Kuhlenbäumer
Rare Variants in Specific Lysosomal Genes Are Associated With Parkinson's Disease. Movement disorders : official journal of the Movement Disorder Society 35 (7) (2020)
Barbara Schormair, David Kemlink, B Mollenhauer, O Fiala, G Machetanz, Jan Roth, R Berutti, T M Strom, B Haslinger, C Trenkwalder, D Zahorakova, P Martasek, Evžen Růžička, J Winkelmann
Diagnostic exome sequencing in early-onset Parkinson's disease confirms VPS13C as a rare cause of autosomal-recessive Parkinson's disease. Clinical genetics 93 (3) (2018)

Barbara Schormair.css-eqlu8i{font-size:small;padding-left:4px;} (B Schormair)

Publication Activity (10 Years)

Top Topics

Top Venues

Barbara Schormair (B Schormair)