Publications
2021
Theresa
Paulus,
Tobias
Bäumer,
Julius
Verrel,
Anne
Weissbach,
Veit
Roessner,
Christian
Beste, and
Alexander
Münchau,
Pandemic Tic-like Behaviors Following Social Media Consumption, Mov Disord , vol. 36, no. 12, pp. 2932–2935, 2021.
Pandemic Tic-like Behaviors Following Social Media Consumption, Mov Disord , vol. 36, no. 12, pp. 2932–2935, 2021.
| DOI: | 10.1002/mds.28800 |
Giovanni
Defazio,
Hyder A.
Jinnah,
Alfredo
Berardelli,
Joel S.
Perlmutter,
Gamze Kilic
Berkmen,
Brian D.
Berman,
Joseph
Jankovic,
Tobias
Bäumer,
Cynthia
Comella,
Adam C.
Cotton,
Tommaso
Ercoli,
Gina
Ferrazzano,
Susan
Fox,
Han-Joon
Kim,
Emile Sami
Moukheiber,
Sarah Pirio
Richardson,
Anne
Weissbach,
Laura J.
Wrigth, and
Mark
Hallett,
Diagnostic criteria for blepharospasm: A multicenter international study, Parkinsonism Relat Disord , vol. 91, pp. 109–114, 2021.
Diagnostic criteria for blepharospasm: A multicenter international study, Parkinsonism Relat Disord , vol. 91, pp. 109–114, 2021.
| DOI: | 10.1016/j.parkreldis.2021.09.004 |
Lina
Schubert,
Julius
Verrel,
Amelie
Behm,
Tobias
Bäumer,
Christian
Beste, and
Alexander
Münchau,
Inter-individual differences in urge-tic associations in Tourette syndrome, Cortex , vol. 143, pp. 80–91, 2021.
Inter-individual differences in urge-tic associations in Tourette syndrome, Cortex , vol. 143, pp. 80–91, 2021.
| DOI: | 10.1016/j.cortex.2021.06.017 |
Elodie M.
Richard,
Somayeh
Bakhtiari,
Ashley P. L.
Marsh,
Rauan
Kaiyrzhanov,
Matias
Wagner,
Sheetal
Shetty,
Alex
Pagnozzi,
Sandra M.
Nordlie,
Brandon S.
Guida,
Patricia
Cornejo,
Helen
Magee,
James
Liu,
Bethany Y.
Norton,
Richard I.
Webster,
Lisa
Worgan,
Hakon
Hakonarson,
Jiankang
Li,
Yiran
Guo,
Mahim
Jain,
Alyssa
Blesson,
Lance H.
Rodan,
Mary-Alice
Abbott,
Anne
Comi,
Julie S.
Cohen,
Bader
Alhaddad,
Thomas
Meitinger,
Dominic
Lenz,
Andreas
Ziegler,
Urania
Kotzaeridou,
Theresa
Brunet,
Anna
Chassevent,
Constance
Smith-Hicks,
Joseph
Ekstein,
Tzvi
Weiden,
Andreas
Hahn,
Nazira
Zharkinbekova,
Peter
Turnpenny,
Arianna
Tucci,
Melissa
Yelton,
Rita
Horvath,
Serdal
Gungor,
Semra
Hiz,
Yavuz
Oktay,
Hanns
Lochmuller,
Marcella
Zollino,
Manuela
Morleo,
Giuseppe
Marangi,
Vincenzo
Nigro,
Annalaura
Torella,
Michele
Pinelli,
Simona
Amenta,
Ralf A.
Husain,
Benita
Grossmann,
Marion
Rapp,
Claudia
Steen,
Iris
Marquardt,
Mona
Grimmel,
Ute
Grasshoff,
G. Christoph
Korenke,
Marta
Owczarek-Lipska,
John
Neidhardt,
Francesca Clementina
Radio,
Cecilia
Mancini,
Dianela Judith
Claps Sepulveda,
Kirsty
McWalter,
Amber
Begtrup,
Amy
Crunk,
Maria J.
Guillen Sacoto,
Richard
Person,
Rhonda E.
Schnur,
Maria Margherita
Mancardi,
Florian
Kreuder,
Pasquale
Striano,
Federico
Zara,
Wendy K.
Chung,
Warren A.
Marks,
Clare L.
van Eyk,
Dani L.
Webber,
Mark A.
Corbett,
Kelly
Harper,
Jesia G.
Berry,
Alastair H.
MacLennan,
Jozef
Gecz,
Marco
Tartaglia,
Vincenzo
Salpietro,
John
Christodoulou,
Jan
Kaslin,
Sergio
Padilla-Lopez,
Kaya
Bilguvar,
Alexander
Münchau,
Zubair M.
Ahmed,
Robert B.
Hufnagel,
Michael C.
Fahey,
Reza
Maroofian,
Henry
Houlden,
Heinrich
Sticht,
Shrikant M.
Mane,
Aboulfazl
Rad,
Barbara
Vona,
Sheng Chih
Jin,
Tobias B.
Haack,
Christine
Makowski,
Yoel
Hirsch,
Saima
Riazuddin, and
Michael C.
Kruer,
Bi-allelic variants in SPATA5L1 lead to intellectual disability, spastic-dystonic cerebral palsy, epilepsy, and hearing loss, Am J Hum Genet , vol. 108, no. 10, pp. 2006–2016, 2021.
Bi-allelic variants in SPATA5L1 lead to intellectual disability, spastic-dystonic cerebral palsy, epilepsy, and hearing loss, Am J Hum Genet , vol. 108, no. 10, pp. 2006–2016, 2021.
| DOI: | 10.1016/j.ajhg.2021.08.003 |
Mohamed
Abdulkadir,
Dongmei
Yu,
Lisa
Osiecki,
Robert A.
King,
Thomas V.
Fernandez,
Lawrence W.
Brown,
Keun-Ah
Cheon,
Barbara J.
Coffey,
Blanca
Garcia-Delgar,
Donald L.
Gilbert,
Dorothy E.
Grice,
Julie
Hagstrøm,
Tammy
Hedderly,
Isobel
Heyman,
Hyun Ju
Hong,
Chaim
Huyser,
Laura
Ibanez-Gomez,
Young Key
Kim,
Young-Shin
Kim,
Yun-Joo
Koh,
Sodahm
Kook,
Samuel
Kuperman,
Bennett
Leventhal,
Marcos
Madruga-Garrido,
Athanasios
Maras,
Pablo
Mir,
Astrid
Morer,
Alexander
Münchau,
Kerstin J.
Plessen,
Veit
Roessner,
Eun-Young
Shin,
Dong-Ho
Song,
Jungeun
Song,
Frank
Visscher,
Samuel H.
Zinner,
Carol A.
Mathews,
Jeremiah M.
Scharf,
Jay A.
Tischfield,
Gary A.
Heiman,
Andrea
Dietrich, and
Pieter J.
Hoekstra,
Investigation of gene-environment interactions in relation to tic severity, J Neural Transm (Vienna) , vol. 128, no. 11, pp. 1757–1765, 2021.
Investigation of gene-environment interactions in relation to tic severity, J Neural Transm (Vienna) , vol. 128, no. 11, pp. 1757–1765, 2021.
| DOI: | 10.1007/s00702-021-02396-y |
Daniela
Choukair,
Fabian
Hauck,
Markus
Bettendorf,
Heiko
Krude,
Christoph
Klein,
Tobias
Bäumer,
Reinhard
Berner,
Min Ae
Lee-Kirsch,
Corinna
Grasemann,
Peter
Burgard, and
Georg F.
Hoffmann,
An Integrated clinical pathway for diagnosis, treatment and care of rare diseases: model, operating procedures, and results of the project TRANSLATE-NAMSE funded by the German Federal Joint Committee, Orphanet J Rare Dis , vol. 16, no. 1, pp. 474, 2021.
An Integrated clinical pathway for diagnosis, treatment and care of rare diseases: model, operating procedures, and results of the project TRANSLATE-NAMSE funded by the German Federal Joint Committee, Orphanet J Rare Dis , vol. 16, no. 1, pp. 474, 2021.
| DOI: | 10.1186/s13023-021-02092-w |
Meng
Wang,
Tolulope
Sajobi,
Francesca
Morgante,
Charles
Adler,
Pinky
Agarwal,
Tobias
Bäumer,
Alfredo
Berardelli,
Brian D.
Berman,
Joel
Blumin,
Max
Borsche,
Allison
Brashear,
Andres
Deik,
Kevin
Duque,
Alberto J.
Espay,
Gina
Ferrazzano,
Jeanne
Feuerstein,
Susan
Fox,
Samuel
Frank,
Mark
Hallett,
Joseph
Jankovic,
Mark S.
LeDoux,
Julie
Leegwater-Kim,
Abhimanyu
Mahajan,
Irene A.
Malaty,
William
Ondo,
Alexander
Pantelyat,
Sarah
Pirio-Richardson,
Emmanuel
Roze,
Rachel
Saunders-Pullman,
Oksana
Suchowersky,
Daniel
Truong,
Marie
Vidailhet,
Aparna Wagle
Shukla,
Joel S.
Perlmutter,
Hyder A.
Jinnah, and
Davide
Martino,
Predictive modeling of spread in adult-onset isolated dystonia: Key properties and effect of tremor inclusion, Eur J Neurol , vol. 28, no. 12, pp. 3999–4009, 2021.
Predictive modeling of spread in adult-onset isolated dystonia: Key properties and effect of tremor inclusion, Eur J Neurol , vol. 28, no. 12, pp. 3999–4009, 2021.
| DOI: | 10.1111/ene.15031 |
Nico
Adelhöfer,
Theresa
Paulus,
Moritz
Mückschel,
Tobias
Bäumer,
Annet
Bluschke,
Adam
Takacs,
Eszter
Tóth-Fáber,
Zsanett
Tarnok,
Veit
Roessner,
Anne
Weissbach,
Alexander
Münchau, and
Christian
Beste,
Increased scale-free and aperiodic neural activity during sensorimotor integration-a novel facet in Tourette syndrome, Brain Commun , vol. 3, no. 4, pp. fcab250, 2021.
Increased scale-free and aperiodic neural activity during sensorimotor integration-a novel facet in Tourette syndrome, Brain Commun , vol. 3, no. 4, pp. fcab250, 2021.
| DOI: | 10.1093/braincomms/fcab250 |
Tobias
Bäumer, and
Max
Borsche,
Behandlung der Zervikalen Dystonie mit Botulinumtoxin – Schritt für Schritt, Neurol up2date , vol. 04, no. 03, pp. 227–234, 2021. Georg Thieme Verlag KG.
Behandlung der Zervikalen Dystonie mit Botulinumtoxin – Schritt für Schritt, Neurol up2date , vol. 04, no. 03, pp. 227–234, 2021. Georg Thieme Verlag KG.
| DOI: | 10.1055/a-1319-3333 |
Xiaolong
Cao,
Yeting
Zhang,
Mohamed
Abdulkadir,
Li
Deng,
Thomas V.
Fernandez,
Blanca
Garcia-Delgar,
Julie
Hagstrøm,
Pieter J.
Hoekstra,
Robert A.
King,
Justin
Koesterich,
Samuel
Kuperman,
Astrid
Morer,
Cara
Nasello,
Kerstin J.
Plessen,
Joshua K.
Thackray,
Lisheng
Zhou,
[GROUP]
Tourette International Collaborative Genetics Study (TIC Genetics),
Andrea
Dietrich,
Jay A.
Tischfield,
Gary A.
Heiman, and
Jinchuan
Xing,
Whole-exome sequencing identifies genes associated with Tourette’s disorder in multiplex families, Mol Psychiatry , vol. 26, no. 11, pp. 6937–6951, 2021.
Whole-exome sequencing identifies genes associated with Tourette’s disorder in multiplex families, Mol Psychiatry , vol. 26, no. 11, pp. 6937–6951, 2021.
| DOI: | 10.1038/s41380-021-01094-1 |
Emilia M.
Gatto,
Ruth H.
Walker,
Claudio
Gonzalez,
Martin
Cesarini,
Giovanni
Cossu,
Christopher D.
Stephen,
Bettina
Balint,
Mayela
Rodríguez-Violante,
Joseph
Jankovic,
Francesca
Morgante,
Hyder A.
Jinnah, and
[GROUP]
Rare Movement Disorders Study Group of the International Parkinson Disease, Movement Disorders Society,
Worldwide barriers to genetic testing for movement disorders, Eur J Neurol , vol. 28, no. 6, pp. 1901–1909, 2021.
Worldwide barriers to genetic testing for movement disorders, Eur J Neurol , vol. 28, no. 6, pp. 1901–1909, 2021.
| DOI: | 10.1111/ene.14826 |
Matthew
Halvorsen,
Jin
Szatkiewicz,
Poorva
Mudgal,
Dongmei
Yu,
[GROUP]
Psychiatric Genomics Consortium TS/OCD Working Group,
Ashley E.
Nordsletten,
David
Mataix-Cols,
Carol A.
Mathews,
Jeremiah M.
Scharf,
Manuel
Mattheisen,
Mary M.
Robertson,
Andrew
McQuillin, and
James J.
Crowley,
Elevated common variant genetic risk for tourette syndrome in a densely-affected pedigree, Mol Psychiatry , vol. 26, no. 12, pp. 7522–7529, 2021.
Elevated common variant genetic risk for tourette syndrome in a densely-affected pedigree, Mol Psychiatry , vol. 26, no. 12, pp. 7522–7529, 2021.
| DOI: | 10.1038/s41380-021-01277-w |
C.W.
Ip,
Tobias
Bäumer,
A.
Ceballos-Baumann,
C.
Klein,
J.
Müller,
M.
Naumann,
V.
Tronnier, and
J.
Volkmann,
Dystonie, S1-Leitlinie, AWMF Online , 2021.
Dystonie, S1-Leitlinie, AWMF Online , 2021.

