Univ.-Prof. Dr. med. Alexander Münchau
Universität zu Lübeck
Universitätsklinikum Schleswig-Holstein, Campus Lübeck
Ratzeburger Allee 160
23562 Lübeck
Gebäude CBBM (Haus 66),
Raum 012,2.OG
| Email: | alexander.muenchau(at)uni-luebeck.de |
| Phone: | 0451 3101 8215 |
| Fax: | 0451 3101 8225 |
Publikationen
2026
Julius
Verrel,
Ronja
Schappert,
Nele
Brügge,
Tina
Rawish,
Tobias
Bäumer,
Yifan
Hao,
Roland
Stenger,
Christian
Beste,
Sebastian
Fudickar,
Veit
Roessner, and
Alexander
Münchau,
Eye blinking abnormalities in Tourette syndrome: Blink more or blink differently?, Parkinsonism Relat Disord , vol. 142, pp. 108121, 2026.
Eye blinking abnormalities in Tourette syndrome: Blink more or blink differently?, Parkinsonism Relat Disord , vol. 142, pp. 108121, 2026.
| DOI: | 10.1016/j.parkreldis.2025.108121 |
2025
Nicolas D.
Münster,
Philip
Schmalbrock,
Christian
Beste,
Alexander
Münchau, and
Christian
Frings,
Adding meaningful distal action effects in feature binding, Atten Percept Psychophys , vol. 87, no. 5, pp. 1650–1664, 2025.
Adding meaningful distal action effects in feature binding, Atten Percept Psychophys , vol. 87, no. 5, pp. 1650–1664, 2025.
| DOI: | 10.3758/s13414-025-03092-9 |
Nicolas D.
Münster,
Philip
Schmalbrock,
Christian
Beste,
Alexander
Münchau, and
Christian
Frings,
Adding meaningful distal action effects in feature binding, Atten Percept Psychophys , vol. 87, no. 5, pp. 1650–1664, 2025.
Adding meaningful distal action effects in feature binding, Atten Percept Psychophys , vol. 87, no. 5, pp. 1650–1664, 2025.
| DOI: | 10.3758/s13414-025-03092-9 |
Axel
Schmidt,
Magdalena
Danyel,
Kathrin
Grundmann,
Theresa
Brunet,
Hannah
Klinkhammer,
Tzung-Chien
Hsieh,
Hartmut
Engels,
Sophia
Peters,
Alexej
Knaus,
Shahida
Moosa,
Luisa
Averdunk,
Felix
Boschann,
Henrike Lisa
Sczakiel,
Sarina
Schwartzmann,
Martin Atta
Mensah,
Jean Tori
Pantel,
Manuel
Holtgrewe,
Annemarie
Bösch,
Claudia
Weiß,
Natalie
Weinhold,
Aude-Annick
Suter,
Corinna
Stoltenburg,
Julia
Neugebauer,
Tillmann
Kallinich,
Angela M.
Kaindl,
Susanne
Holzhauer,
Christoph
Bührer,
Philip
Bufler,
Uwe
Kornak,
Claus-Eric
Ott,
Markus
Schülke,
Hoa Huu Phuc
Nguyen,
Sabine
Hoffjan,
Corinna
Grasemann,
Tobias
Rothoeft,
Folke
Brinkmann,
Nora
Matar,
Sugirthan
Sivalingam,
Claudia
Perne,
Elisabeth
Mangold,
Martina
Kreiss,
Kirsten
Cremer,
Regina C.
Betz,
Martin
Mücke,
Lorenz
Grigull,
Thomas
Klockgether,
Isabel
Spier,
André
Heimbach,
Tim
Bender,
Fabian
Brand,
Christiane
Stieber,
Alexandra Marzena
Morawiec,
Pantelis
Karakostas,
Valentin S.
Schäfer,
Sarah
Bernsen,
Patrick
Weydt,
Sergio
Castro-Gomez,
Ahmad
Aziz,
Marcus
Grobe-Einsler,
Okka
Kimmich,
Xenia
Kobeleva,
Demet
Önder,
Hellen
Lesmann,
Sheetal
Kumar,
Pawel
Tacik,
Meghna Ahuja
Bhasin,
Pietro
Incardona,
Min Ae
Lee-Kirsch,
Reinhard
Berner,
Catharina
Schuetz,
Julia
Körholz,
Tanita
Kretschmer,
Nataliya
Di Donato,
Evelin
Schröck,
André
Heinen,
Ulrike
Reuner,
Amalia-Mihaela
Hanßke,
Frank J.
Kaiser,
Eva
Manka,
Martin
Munteanu,
Alma
Kuechler,
Kiewert
Cordula,
Raphael
Hirtz,
Elena
Schlapakow,
Christian
Schlein,
Jasmin
Lisfeld,
Christian
Kubisch,
Theresia
Herget,
Maja
Hempel,
Christina
Weiler-Normann,
Kurt
Ullrich,
Christoph
Schramm,
Cornelia
Rudolph,
Franziska
Rillig,
Maximilian
Groffmann,
Ania
Muntau,
Alexandra
Tibelius,
Eva M. C.
Schwaibold,
Christian P.
Schaaf,
Michal
Zawada,
Lilian
Kaufmann,
Katrin
Hinderhofer,
Pamela M.
Okun,
Urania
Kotzaeridou,
Georg F.
Hoffmann,
Daniela
Choukair,
Markus
Bettendorf,
Malte
Spielmann,
Annekatrin
Ripke,
Martje G.
Pauly,
Alexander
Münchau,
Katja
Lohmann,
Irina
Hüning,
Britta
Hanker,
Tobias
Bäumer,
Rebecca
Herzog,
Yorck
Hellenbroich,
Dominik S.
Westphal,
Tim
Strom,
Reka
Kovacs,
Korbinian M.
Riedhammer,
Katharina
Mayerhanser,
Elisabeth
Graf,
Melanie
Brugger,
Julia
Hoefele,
Konrad
Oexle,
Nazanin
Mirza-Schreiber,
Riccardo
Berutti,
Ulrich
Schatz,
Martin
Krenn,
Christine
Makowski,
Heike
Weigand,
Sebastian
Schröder,
Meino
Rohlfs,
Katharina
Vill,
Fabian
Hauck,
Ingo
Borggraefe,
Wolfgang
Müller-Felber,
Ingo
Kurth,
Miriam
Elbracht,
Cordula
Knopp,
Matthias
Begemann,
Florian
Kraft,
Johannes R.
Lemke,
Julia
Hentschel,
Konrad
Platzer,
Vincent
Strehlow,
Rami
Abou Jamra,
Martin
Kehrer,
German
Demidov,
Stefanie
Beck-Wödl,
Holm
Graessner,
Marc
Sturm,
Lena
Zeltner,
Ludger J.
Schöls,
Janine
Magg,
Andrea
Bevot,
Christiane
Kehrer,
Nadja
Kaiser,
Ernest
Turro,
Denise
Horn,
Annette
Grüters-Kieslich,
Christoph
Klein,
Stefan
Mundlos,
Markus
Nöthen,
Olaf
Riess,
Thomas
Meitinger,
Heiko
Krude,
Peter M.
Krawitz,
Tobias
Haack,
Nadja
Ehmke, and
Matias
Wagner,
Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings, Nat Genet , vol. 57, no. 7, pp. 1790–1791, 2025.
Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings, Nat Genet , vol. 57, no. 7, pp. 1790–1791, 2025.
| DOI: | 10.1038/s41588-025-02271-6 |
Axel
Schmidt,
Magdalena
Danyel,
Kathrin
Grundmann,
Theresa
Brunet,
Hannah
Klinkhammer,
Tzung-Chien
Hsieh,
Hartmut
Engels,
Sophia
Peters,
Alexej
Knaus,
Shahida
Moosa,
Luisa
Averdunk,
Felix
Boschann,
Henrike Lisa
Sczakiel,
Sarina
Schwartzmann,
Martin Atta
Mensah,
Jean Tori
Pantel,
Manuel
Holtgrewe,
Annemarie
Bösch,
Claudia
Weiß,
Natalie
Weinhold,
Aude-Annick
Suter,
Corinna
Stoltenburg,
Julia
Neugebauer,
Tillmann
Kallinich,
Angela M.
Kaindl,
Susanne
Holzhauer,
Christoph
Bührer,
Philip
Bufler,
Uwe
Kornak,
Claus-Eric
Ott,
Markus
Schülke,
Hoa Huu Phuc
Nguyen,
Sabine
Hoffjan,
Corinna
Grasemann,
Tobias
Rothoeft,
Folke
Brinkmann,
Nora
Matar,
Sugirthan
Sivalingam,
Claudia
Perne,
Elisabeth
Mangold,
Martina
Kreiss,
Kirsten
Cremer,
Regina C.
Betz,
Martin
Mücke,
Lorenz
Grigull,
Thomas
Klockgether,
Isabel
Spier,
André
Heimbach,
Tim
Bender,
Fabian
Brand,
Christiane
Stieber,
Alexandra Marzena
Morawiec,
Pantelis
Karakostas,
Valentin S.
Schäfer,
Sarah
Bernsen,
Patrick
Weydt,
Sergio
Castro-Gomez,
Ahmad
Aziz,
Marcus
Grobe-Einsler,
Okka
Kimmich,
Xenia
Kobeleva,
Demet
Önder,
Hellen
Lesmann,
Sheetal
Kumar,
Pawel
Tacik,
Meghna Ahuja
Bhasin,
Pietro
Incardona,
Min Ae
Lee-Kirsch,
Reinhard
Berner,
Catharina
Schuetz,
Julia
Körholz,
Tanita
Kretschmer,
Nataliya
Di Donato,
Evelin
Schröck,
André
Heinen,
Ulrike
Reuner,
Amalia-Mihaela
Hanßke,
Frank J.
Kaiser,
Eva
Manka,
Martin
Munteanu,
Alma
Kuechler,
Kiewert
Cordula,
Raphael
Hirtz,
Elena
Schlapakow,
Christian
Schlein,
Jasmin
Lisfeld,
Christian
Kubisch,
Theresia
Herget,
Maja
Hempel,
Christina
Weiler-Normann,
Kurt
Ullrich,
Christoph
Schramm,
Cornelia
Rudolph,
Franziska
Rillig,
Maximilian
Groffmann,
Ania
Muntau,
Alexandra
Tibelius,
Eva M. C.
Schwaibold,
Christian P.
Schaaf,
Michal
Zawada,
Lilian
Kaufmann,
Katrin
Hinderhofer,
Pamela M.
Okun,
Urania
Kotzaeridou,
Georg F.
Hoffmann,
Daniela
Choukair,
Markus
Bettendorf,
Malte
Spielmann,
Annekatrin
Ripke,
Martje G.
Pauly,
Alexander
Münchau,
Katja
Lohmann,
Irina
Hüning,
Britta
Hanker,
Tobias
Bäumer,
Rebecca
Herzog,
Yorck
Hellenbroich,
Dominik S.
Westphal,
Tim
Strom,
Reka
Kovacs,
Korbinian M.
Riedhammer,
Katharina
Mayerhanser,
Elisabeth
Graf,
Melanie
Brugger,
Julia
Hoefele,
Konrad
Oexle,
Nazanin
Mirza-Schreiber,
Riccardo
Berutti,
Ulrich
Schatz,
Martin
Krenn,
Christine
Makowski,
Heike
Weigand,
Sebastian
Schröder,
Meino
Rohlfs,
Katharina
Vill,
Fabian
Hauck,
Ingo
Borggraefe,
Wolfgang
Müller-Felber,
Ingo
Kurth,
Miriam
Elbracht,
Cordula
Knopp,
Matthias
Begemann,
Florian
Kraft,
Johannes R.
Lemke,
Julia
Hentschel,
Konrad
Platzer,
Vincent
Strehlow,
Rami
Abou Jamra,
Martin
Kehrer,
German
Demidov,
Stefanie
Beck-Wödl,
Holm
Graessner,
Marc
Sturm,
Lena
Zeltner,
Ludger J.
Schöls,
Janine
Magg,
Andrea
Bevot,
Christiane
Kehrer,
Nadja
Kaiser,
Ernest
Turro,
Denise
Horn,
Annette
Grüters-Kieslich,
Christoph
Klein,
Stefan
Mundlos,
Markus
Nöthen,
Olaf
Riess,
Thomas
Meitinger,
Heiko
Krude,
Peter M.
Krawitz,
Tobias
Haack,
Nadja
Ehmke, and
Matias
Wagner,
Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings, Nat Genet , vol. 57, no. 7, pp. 1790–1791, 2025.
Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings, Nat Genet , vol. 57, no. 7, pp. 1790–1791, 2025.
| DOI: | 10.1038/s41588-025-02271-6 |
Keit Men
Wong,
Reza
Maroofian,
Kolja
Meier,
Susann
Diegmann,
Tinatin
Tkemaladze,
Javeria Raza
Alvi,
Behnoosh
Tasharrofi,
Stephanie
Efthymiou,
Alexander
Münchau,
G. Christoph
Korenke,
Naif
Almontashiri,
Wafaa
Eyaid,
Amna
Kashgari,
Modhi
Alotaibi,
Jutta
Gärtner,
Brenda
Huppke,
Mostafa
Asadollahi,
Gocha
Chikvinidze,
Mohammad
Keramatipour,
Tipu
Sultan,
Holger
Thiele,
Peter
Nürnberg,
Markus H.
Gräler,
Henry
Houlden, and
Peter
Huppke,
Biallelic ELOVL1 Variants Are Linked to Hypomyelinating Leukodystrophy, Movement Disorder, and Ichthyosis, Mov Disord , 2025.
Biallelic ELOVL1 Variants Are Linked to Hypomyelinating Leukodystrophy, Movement Disorder, and Ichthyosis, Mov Disord , 2025.
| DOI: | 10.1002/mds.30258 |
Keit Men
Wong,
Reza
Maroofian,
Kolja
Meier,
Susann
Diegmann,
Tinatin
Tkemaladze,
Javeria Raza
Alvi,
Behnoosh
Tasharrofi,
Stephanie
Efthymiou,
Alexander
Münchau,
G. Christoph
Korenke,
Naif
Almontashiri,
Wafaa
Eyaid,
Amna
Kashgari,
Modhi
Alotaibi,
Jutta
Gärtner,
Brenda
Huppke,
Mostafa
Asadollahi,
Gocha
Chikvinidze,
Mohammad
Keramatipour,
Tipu
Sultan,
Holger
Thiele,
Peter
Nürnberg,
Markus H.
Gräler,
Henry
Houlden, and
Peter
Huppke,
Biallelic ELOVL1 Variants Are Linked to Hypomyelinating Leukodystrophy, Movement Disorder, and Ichthyosis, Mov Disord , vol. 40, no. 9, pp. 1836–1850, 2025.
Biallelic ELOVL1 Variants Are Linked to Hypomyelinating Leukodystrophy, Movement Disorder, and Ichthyosis, Mov Disord , vol. 40, no. 9, pp. 1836–1850, 2025.
| DOI: | 10.1002/mds.30258 |
Lille
Kurvits,
Safiye
Tozdan,
Tina
Mainka,
Alexander
Münchau,
Kirsten R.
Müller-Vahl,
Andrea E.
Cavanna,
Peer
Briken, and
Christos
Ganos,
Compulsive sexual behavior and paraphilic interests in adults with chronic tic disorders and Tourette syndrome: a survey-based study, Int J Impot Res , vol. 37, no. 3, pp. 233–237, 2025.
Compulsive sexual behavior and paraphilic interests in adults with chronic tic disorders and Tourette syndrome: a survey-based study, Int J Impot Res , vol. 37, no. 3, pp. 233–237, 2025.
| DOI: | 10.1038/s41443-023-00729-x |
Lille
Kurvits,
Safiye
Tozdan,
Tina
Mainka,
Alexander
Münchau,
Kirsten R.
Müller-Vahl,
Andrea E.
Cavanna,
Peer
Briken, and
Christos
Ganos,
Compulsive sexual behavior and paraphilic interests in adults with chronic tic disorders and Tourette syndrome: a survey-based study, Int J Impot Res , vol. 37, no. 3, pp. 233–237, 2025.
Compulsive sexual behavior and paraphilic interests in adults with chronic tic disorders and Tourette syndrome: a survey-based study, Int J Impot Res , vol. 37, no. 3, pp. 233–237, 2025.
| DOI: | 10.1038/s41443-023-00729-x |
Astrid
Prochnow,
Annet
Bluschke,
Tina
Rawish,
Julia
Friedrich,
Yifan
Hao,
Christian
Frings,
Tobias
Bäumer,
Alexander
Münchau, and
Christian
Beste,
Differential modulation of neural oscillations in perception-action links in Tourette syndrome, Brain Commun , vol. 7, no. 3, pp. fcaf172, 2025.
Differential modulation of neural oscillations in perception-action links in Tourette syndrome, Brain Commun , vol. 7, no. 3, pp. fcaf172, 2025.
| DOI: | 10.1093/braincomms/fcaf172 |

