Ana Westenberger

ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 31

Top Venues

Movement disorders : official journal of the Movement Disorder Society

Movement disorders clinical practice

Annals of neurology

Clinical genetics

University of Luebeck

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

Affiliation History

University of Luebeck Jan 01 2002

Germany

Group leader :: Institute of Neurogenetics

Publications

Andona Milovanović, Ana Westenberger, Iva Stanković, Olivera Tamaš, Marija Branković, Ana Marjanović, Björn-Hergen Laabs, Max Brand, Rajasumi Rajalingam, Connie Marras, Katja Lohmann, Vesna Branković, Ivana Novaković, Igor Petrović, Marina Svetel, Christine Klein, Vladimir S Kostić, Natasa Dragašević-Mišković
ANO10-Related Spinocerebellar Ataxia: MDSGene Systematic Literature Review and a Romani Case Series. Movement disorders : official journal of the Movement Disorder Society 39 (5) (2024)
Ana Westenberger, Volha Skrahina, Tatiana Usnich, Christian Beetz, Eva-Juliane Vollstedt, Björn-Hergen Laabs, Jefri J Paul, Filipa Curado, Snezana Skobalj, Hanaa Gaber, Maria Olmedillas, Xenia Bogdanovic, Najim Ameziane, Nathalie Schell, Jan Olav Aasly, Mitra Afshari, Pinky Agarwal, Jason Aldred, Fernando Alonso-Frech, Roderick Anderson, Rui Araújo, David Arkadir, Micol Avenali, Mehmet Balal, Sandra Benizri, Sagari Bette, Perminder Bhatia, Michael Bonello, Pedro Braga-Neto, Sarah Brauneis, Francisco Eduardo Costa Cardoso, Francesco Cavallieri, Joseph Classen, Lisa Cohen, Della Coletta, David Crosiers, Paskal Cullufi, Khashayar Dashtipour, Meltem Demirkiran, Patricia de Carvalho Aguiar, Anna De Rosa, Ruth Djaldetti, Okan Dogu, Maria Gabriela Dos Santos Ghilardi, Carsten Eggers, Bulent Elibol, Aaron Ellenbogen, Sibel Ertan, Giorgio Fabiani, Björn H Falkenburger, Simon Farrow, Tsviya Fay-Karmon, Gerald J Ferencz, Erich Talamoni Fonoff, Yara Dadalti Fragoso, Gençer Genç, Arantza Gorospe, Francisco Grandas, Doreen Gruber, Mark Gudesblatt, Tanya Gurevich, Johann Hagenah, Hasmet A Hanagasi, Sharon Hassin-Baer, Robert A Hauser, Jorge Hernández-Vara, Birgit Herting, Vanessa K Hinson, Elliot Hogg, Michele Tao-Ming Hu, Eduardo Hummelgen, Kelly Hussey, Jon Infante, Stuart H Isaacson, Serge Jauma, Natalia Koleva-Alazeh, Gregor Kuhlenbäumer, Andrea Kühn, Irene Litvan, Lydia López-Manzanares, McKenzie Luxmore, Sujeena Manandhar, Veronique Marcaud, Katerina Markopoulou, Connie Marras, Mark McKenzie, Michele Matarazzo, Marcelo Merello, Brit Mollenhauer, John C Morgan, Stephen Mullin, Thomas Musacchio, Bennett Myers, Anna Negrotti, Anette Nieves, Zeev Nitsan, Nader Oskooilar, Özgür Öztop-Çakmak, Gian Pal, Nicola Pavese, Antonio Percesepe, Tommaso Piccoli, Carolina Pinto de Souza, Tino Prell, Mark Pulera, Jason Raw, Kathrin Reetz, Johnathan Reiner, David Rosenberg, Marta Ruiz-Lopez, Javier Ruiz Martinez, Esther Sammler, Bruno Lopes Dos Santos-Lobato, Rachel Saunders-Pullman, Ilana Schlesinger, Christine M Schofield, Artur F Schumacher-Schuh, Burton Scott, Ángel Sesar, Stuart J Shafer, Ray Sheridan, Monty Silverdale, Rani Sophia, Mariana Spitz, Pantelis Stathis, Fabrizio Stocchi, Michele Tagliati, Yen F Tai, Annelies Terwecoren, Sven Thonke, Lars Tönges, Giulia Toschi, Vitor Tumas, Peter Paul Urban, Laura Vacca, Wim Vandenberghe, Enza Maria Valente, Franco Valzania, Lydia Vela-Desojo, Caroline Weill, David Weise, Joanne Wojcieszek, Martin Wolz, Gilad Yahalom, Gul Yalcin-Cakmakli, Simone Zittel, Yair Zlotnik, Krishna K Kandaswamy, Alexander Balck, Henrike Hanssen, Max Borsche, Lara M Lange, Ilona Csoti, Katja Lohmann, Meike Kasten, Norbert Brüggemann, Arndt Rolfs, Christine Klein, Peter Bauer
Relevance of genetic testing in the gene-targeted trial era: the Rostock Parkinson's disease study. Brain : a journal of neurology 147 (8) (2024)
Andona Milovanović, Nataša Dragaševic-Mišković, Mirja Thomsen, Max Borsche, Frauke Hinrichs, Ana Westenberger, Christine Klein, Norbert Brüggemann, Marija Branković, Ana Marjanović, Marina Svetel, Vladimir S Kostić, Katja Lohmann
RFC1 and FGF14 Repeat Expansions in Serbian Patients with Cerebellar Ataxia. Movement disorders clinical practice 11 (6) (2024)
Ana Westenberger, Volha Skrahina, Tatiana Usnich, Christian Beetz, Eva-Juliane Vollstedt, Björn-Hergen Laabs, Jefri J Paul, Filipa Curado, Snezana Skobalj, Hanaa Gaber, Maria Olmedillas, Xenia Bogdanovic, Najim Ameziane, Nathalie Schell, Jan Olav Aasly, Mitra Afshari, Pinky Agarwal, Jason Aldred, Fernando Alonso-Frech, Roderick Anderson, Rui Araújo, David Arkadir, Micol Avenali, Mehmet Balal, Sandra Benizri, Sagari Bette, Perminder Bhatia, Michael Bonello, Pedro Braga-Neto, Sarah Brauneis, Francisco Eduardo Costa Cardoso, Francesco Cavallieri, Joseph Classen, Lisa Cohen, Della Coletta, David Crosiers, Paskal Cullufi, Khashayar Dashtipour, Meltem Demirkiran, Patricia de Carvalho Aguiar, Anna De Rosa, Ruth Djaldetti, Okan Dogu, Maria Gabriela Dos Santos Ghilardi, Carsten Eggers, Bulent Elibol, Aaron Ellenbogen, Sibel Ertan, Giorgio Fabiani, Björn H Falkenburger, Simon Farrow, Tsviya Fay-Karmon, Gerald J Ferencz, Erich Talamoni Fonoff, Yara Dadalti Fragoso, Gençer Genç, Arantza Gorospe, Francisco Grandas, Doreen Gruber, Mark Gudesblatt, Tanya Gurevich, Johann Hagenah, Hasmet A Hanagasi, Sharon Hassin-Baer, Robert A Hauser, Jorge Hernández-Vara, Birgit Herting, Vanessa K Hinson, Elliot Hogg, Michele Tao-Ming Hu, Eduardo Hummelgen, Kelly Hussey, Jon Infante, Stuart H Isaacson, Serge Jauma, Natalia Koleva-Alazeh, Gregor Kuhlenbäumer, Andrea Kühn, Irene Litvan, Lydia López-Manzanares, McKenzie Luxmore, Sujeena Manandhar, Veronique Marcaud, Katerina Markopoulou, Connie Marras, Mark McKenzie, Michele Matarazzo, Marcelo Merello, Brit Mollenhauer, John C Morgan, Stephen Mullin, Thomas Musacchio, Bennett Myers, Anna Negrotti, Anette Nieves, Zeev Nitsan, Nader Oskooilar, Özgür Öztop-Çakmak, Gian Pal, Nicola Pavese, Antonio Percesepe, Tommaso Piccoli, Carolina Pinto de Souza, Tino Prell, Mark Pulera, Jason Raw, Kathrin Reetz, Johnathan Reiner, David Rosenberg, Marta Ruiz-Lopez, Javier Ruiz Martinez, Esther Sammler, Bruno Lopes Dos Santos-Lobato, Rachel Saunders-Pullman, Ilana Schlesinger, Christine M Schofield, Artur F Schumacher-Schuh, Burton Scott, Ángel Sesar, Stuart J Shafer, Ray Sheridan, Monty Silverdale, Rani Sophia, Mariana Spitz, Pantelis Stathis, Fabrizio Stocchi, Michele Tagliati, Yen F Tai, Annelies Terwecoren, Sven Thonke, Lars Tönges, Giulia Toschi, Vitor Tumas, Peter Paul Urban, Laura Vacca, Wim Vandenberghe, Enza Maria Valente, Franco Valzania, Lydia Vela-Desojo, Caroline Weill, David Weise, Joanne Wojcieszek, Martin Wolz, Gilad Yahalom, Gul Yalcin-Cakmakli, Simone Zittel, Yair Zlotnik, Krishna K Kandaswamy, Alexander Balck, Henrike Hanssen, Max Borsche, Lara M Lange, Ilona Csoti, Katja Lohmann, Meike Kasten, Norbert Brüggemann, Arndt Rolfs, Christine Klein, Peter Bauer
Relevance of genetic testing in the gene-targeted trial era: the Rostock Parkinson's disease study. Brain : a journal of neurology 147 (8) (2024)
Andona Milovanović, Ana Westenberger, Iva Stanković, Olivera Tamaš, Marija Branković, Ana Marjanović, Björn-Hergen Laabs, Max Brand, Rajasumi Rajalingam, Connie Marras, Katja Lohmann, Vesna Branković, Ivana Novaković, Igor Petrović, Marina Svetel, Christine Klein, Vladimir S Kostić, Natasa Dragašević-Mišković
ANO10-Related Spinocerebellar Ataxia: MDSGene Systematic Literature Review and a Romani Case Series. Movement disorders : official journal of the Movement Disorder Society (2024)
Andona Milovanović, Nataša Dragaševic-Mišković, Mirja Thomsen, Max Borsche, Frauke Hinrichs, Ana Westenberger, Christine Klein, Norbert Brüggemann, Marija Branković, Ana Marjanović, Marina Svetel, Vladimir S Kostić, Katja Lohmann
RFC1 and FGF14 Repeat Expansions in Serbian Patients with Cerebellar Ataxia. Movement disorders clinical practice (2024)
Andona Milovanović, Nataša Dragaševic-Mišković, Mirja Thomsen, Max Borsche, Frauke Hinrichs, Ana Westenberger, Christine Klein, Norbert Brüggemann, Marija Branković, Ana Marjanović, Marina Svetel, Vladimir S Kostić, Katja Lohmann
RFC1 and FGF14 Repeat Expansions in Serbian Patients with Cerebellar Ataxia. Movement disorders clinical practice 11 (6) (2024)
Andona Milovanović, Nataša Dragaševic-Mišković, Mirja Thomsen, Max Borsche, Frauke Hinrichs, Ana Westenberger, Christine Klein, Norbert Brüggemann, Marija Branković, Ana Marjanović, Marina Svetel, Vladimir S Kostić, Katja Lohmann
RFC1 and FGF14 Repeat Expansions in Serbian Patients with Cerebellar Ataxia. Movement disorders clinical practice 11 (6) (2024)
Andona Milovanović, Ana Westenberger, Iva Stanković, Olivera Tamaš, Marija Branković, Ana Marjanović, Björn-Hergen Laabs, Max Brand, Rajasumi Rajalingam, Connie Marras, Katja Lohmann, Vesna Branković, Ivana Novaković, Igor Petrović, Marina Svetel, Christine Klein, Vladimir S Kostić, Natasa Dragašević-Mišković
ANO10-Related Spinocerebellar Ataxia: MDSGene Systematic Literature Review and a Romani Case Series. Movement disorders : official journal of the Movement Disorder Society 39 (5) (2024)
Andona Milovanović, Nataša Dragaševic-Mišković, Mirja Thomsen, Max Borsche, Frauke Hinrichs, Ana Westenberger, Christine Klein, Norbert Brüggemann, Marija Branković, Ana Marjanović, Marina Svetel, Vladimir S Kostić, Katja Lohmann
RFC1 and FGF14 Repeat Expansions in Serbian Patients with Cerebellar Ataxia. Movement disorders clinical practice 11 (6) (2024)
Renana Mertin, Cid Diesta, Norbert Brüggemann, Raymond L Rosales, Henrike Hanssen, Ana Westenberger, Julia Steinhardt, Marcus Heldmann, Hans T S Manalo, Jean Q Oropilla, Christine Klein, Christoph Helmchen, Andreas Sprenger
Oculomotor abnormalities indicate early executive dysfunction in prodromal X-linked dystonia-parkinsonism (XDP). Journal of neurology (2023)
Henrike Hanssen, Cid C E Diesta, Marcus Heldmann, Jackson Dy, Jeffrey Tantianpact, Julia Steinhardt, Rosanna Sauza, Hans T S Manalo, Andreas Sprenger, Charles Jordan Reyes, Raphael Tucazon, Björn-Hergen Laabs, Aloysius Domingo, Raymond L Rosales, Christine Klein, Thomas F Münte, Ana Westenberger, Jean Q Oropilla, Norbert Brüggemann
Basal Ganglia Atrophy as a Marker for Prodromal X-linked Dystonia-Parkinsonism. Annals of neurology (2023)
Ana Westenberger, Adriana Ruiz-Herrera, Sevcan Bozdoğan, Atil Bisgin, Mohammed Almuqbil, Amal Alhashem, Talal Alanzi, Antonio Romito, Arndt Rolfs, Patricia Dias, Raquel Gouveia Silva, Aida Maria Bertoli-Avella, Peter Bauer, Christian Beetz
Spectrum of FAR1 (Fatty Acyl-CoA Reductase 1) Variants and Related Neurological Conditions. Movement disorders : official journal of the Movement Disorder Society 38 (3) (2023)
Ana Westenberger, Adriana Ruiz-Herrera, Sevcan Bozdoğan, Atil Bisgin, Mohammed Almuqbil, Amal Alhashem, Talal Alanzi, Antonio Romito, Arndt Rolfs, Patricia Dias, Raquel Gouveia Silva, Aida Maria Bertoli-Avella, Peter Bauer, Christian Beetz
Spectrum of FAR1 (Fatty Acyl-CoA Reductase 1) Variants and Related Neurological Conditions. Movement disorders : official journal of the Movement Disorder Society 38 (3) (2023)
Martin Niethammer, Chris C Tang, Roland Dominic G Jamora, An Vo, Nha Nguyen, Yilong Ma, Shichun Peng, Jeff L Waugh, Ana Westenberger, David Eidelberg
A network imaging biomarker of X-linked dystonia-parkinsonism. Annals of neurology (2023)
Paula Saffie-Awad, Katja Lohmann, Yasmin Hirmas, Frauke Hinrichs, Mirja Thomsen, Marcelo Kauffman, Theresa Lüth, Joanne Trinh, Ana Westenberger, Pedro Chaná-Cuevas, Christine Klein
Shaking Up Ataxia: FGF14 and RFC1 Repeat Expansions in Affected and Unaffected Members of a Chilean Family. Movement disorders : official journal of the Movement Disorder Society (2023)
Henrike Hanssen, Cid C E Diesta, Marcus Heldmann, Jackson Dy, Jeffrey Tantianpact, Julia Steinhardt, Rosanna Sauza, Hans T S Manalo, Andreas Sprenger, Charles Jourdan Reyes, Raphael Tuazon, Björn-Hergen Laabs, Aloysius Domingo, Raymond L Rosales, Christine Klein, Thomas F Münte, Ana Westenberger, Jean Q Oropilla, Norbert Brüggemann
Basal Ganglia Atrophy as a Marker for Prodromal X-Linked Dystonia-Parkinsonism. Annals of neurology (2023)
Ana Westenberger, Adriana Ruiz-Herrera, Sevcan Bozdoğan, Atil Bisgin, Mohammed Almuqbil, Amal Alhashem, Talal Alanzi, Antonio Romito, Arndt Rolfs, Patricia Dias, Raquel Gouveia Silva, Aida Maria Bertoli-Avella, Peter Bauer, Christian Beetz
Spectrum of FAR1 (Fatty Acyl-CoA Reductase 1) Variants and Related Neurological Conditions. Movement disorders : official journal of the Movement Disorder Society (2023)
Salem Alawbathani, Suliman Khan, Ana Westenberger, Christian Beetz, Lokesh Lingappa
A novel biallelic nonsense variant in SLC38A3 causing epileptic encephalopathy in an Indian family. Clinical genetics (2022)
Angela Rosenbohm, Hendrik Pott, Mirja Thomsen, Haloom Rafehi, Sabine Kaya, Silke Szymczak, Alexander E Volk, Kathrin Mueller, Isabel Silveira, Jochen H Weishaupt, Holger Tönnies, Philip Seibler, Katja Zschiedrich, Susen Schaake, Ana Westenberger, Christine Zühlke, Christel Depienne, Joanne Trinh, Albert C Ludolph, Christine Klein, Melanie Bahlo, Katja Lohmann
Familial Cerebellar Ataxia and Amyotrophic Lateral Sclerosis/Frontotemporal Dementia with DAB1 and C9ORF72 Repeat Expansions: An 18-Year Study. Movement disorders : official journal of the Movement Disorder Society (2022)
Alonso G Zea Vera, Adrienne Bruce, Travis R Larsh, Zachary Jordan, Norbert Brüggemann, Ana Westenberger, Alberto J Espay, Donald L Gilbert, Steve W Wu
Spectrum of Pediatric to Early Adulthood POLR3A -Associated Movement Disorders. Movement disorders clinical practice 10 (2) (2022)
Alonso G Zea Vera, Adrienne Bruce, Travis R Larsh, Zachary Jordan, Norbert Brüggemann, Ana Westenberger, Alberto J Espay, Donald L Gilbert, Steve W Wu
Spectrum of Pediatric to Early Adulthood POLR3A -Associated Movement Disorders. Movement disorders clinical practice 10 (2) (2022)
Shela Marie Algodon, Tanja Fischer, Raymond Rosales, Roland Dominic Go Jamora, Cid Czarina Diesta, Gerard Saranza, Norbert Brüggemann, Christine Klein, Ana Westenberger
Low Frequency of p.S510G in PIAS1 Challenges its Relevance for Modifying Repeat Expansion Disorders. Movement disorders : official journal of the Movement Disorder Society 37 (10) (2022)
Björn-Hergen Laabs, Christine Klein, Jelena Pozojevic, Aloysius Domingo, Norbert Brüggemann, Karen Grütz, Raymond L Rosales, Roland Dominic Go Jamora, Gerard Saranza, Cid Czarina E Diesta, Michael Wittig, Susen Schaake, Marija Dulovic-Mahlow, Jana Quismundo, Pia Otto, Patrick Acuna, Criscely Go, Nutan Sharma, Trisha Multhaupt-Buell, Ulrich Müller, Henrike Hanssen, Fabian Kilpert, Andre Franke, Arndt Rolfs, Peter Bauer, Valerija Dobričić, Katja Lohmann, Laurie J Ozelius, Frank J Kaiser, Inke Regina König, Ana Westenberger
Identifying genetic modifiers of age-associated penetrance in X-linked dystonia-parkinsonism. Nature communications 12 (1) (2021)
Charles Jourdan Reyes, Björn-Hergen Laabs, Susen Schaake, Theresa Lüth, Raphaela Ardicoglu, Aleksandar Rakovic, Karen Grütz, Daniel Alvarez-Fischer, Roland Dominic Jamora, Raymond L Rosales, Imke Weyers, Inke Regina König, Norbert Brüggemann, Christine Klein, Valerija Dobricic, Ana Westenberger, Joanne Trinh
Brain Regional Differences in Hexanucleotide Repeat Length in X-Linked Dystonia-Parkinsonism Using Nanopore Sequencing. Neurology. Genetics 7 (4) (2021)
Lia Abbasi-Moheb, Ana Westenberger, Maha Alotaibi, Malak Ali AlGhamdi, Jozef L Hertecant, Amir Ariamand, Christian Beetz, Arndt Rolfs, Aida Maria Bertoli-Avella, Peter Bauer
Biallelic loss-of-function HACD1 variants are a bona fide cause of congenital myopathy. Clinical genetics 99 (4) (2021)
Salem Alawbathani, Ana Westenberger, Natalia Ordonez-Herrera, Mariam Al-Hilali, Homoud Al Hebby, Fahad Alabbas, Amal M Alhashem, Ghaleb Elyamany, Andre Megarbane, Melis Kose, Nadia Alhashmi, Nashat Al Sukaiti, Mohammed Al-Raqad, Samah Al-Tawalbeh, Omar Abu Adas Blanco, Fadiah Alkhattabi, Danielle Sng, Ruslan Al-Ali, Suliman Khan, Hasan Tawamie, Kornelia Tripolszki, Vasiliki Karageorgou, Roberta Trunzo, Fuad Al Mutairi, Bruno Reversade, Peter Bauer, Aida Maria Bertoli-Avella
Biallelic ZNFX1 variants are associated with a spectrum of immuno-hematological abnormalities. Clinical genetics (2021)
Jelena Pozojevic, Christian Beetz, Ana Westenberger
The importance of genetic testing for dystonia patients and translational research. Journal of neural transmission (Vienna, Austria : 1996) 128 (4) (2021)
Christian Beetz, Ana Westenberger, Ruslan Al-Ali, Najim Ameziane, Nadia Alhashmi, Rose-Mary Boustany, Fuad Al Mutairi, Majid Alfadhel, Zuhair Al-Hassnan, Moenaldeen AlSayed, Krishna K Kandaswamy, Omid Paknia, Volha Skrahina, Arndt Rolfs, Peter Bauer
LRRK2 Loss-of-Function Variants in Patients with Rare Diseases: No Evidence for a Phenotypic Impact. Movement disorders : official journal of the Movement Disorder Society 36 (4) (2021)
Paskal Cullufi, Mirela Tabaku, Virtut Velmishi, Agim Gjikopulli, Sonila Tomori, Ermira Dervishi, Aferdita Tako, Anika Leubauer, Ana Westenberger, Claudia Cozma, Christian Beetz, Peter Bauer, Stefan Wirth, Arndt Rolfs
Genetic characterization of the Albanian Gaucher disease patient population. JIMD reports 57 (1) (2020)
Ana Westenberger, Charles Jourdan Reyes, Gerard Saranza, Valerija Dobricic, Henrike Hanssen, Aloysius Domingo, Björn-Hergen Laabs, Susen Schaake, Jelena Pozojevic, Aleksandar Rakovic, Karen Grütz, Kimberly Begemann, Uwe Walter, Dirk Dressler, Peter Bauer, Arndt Rolfs, Alexander Münchau, Frank J Kaiser, Laurie J Ozelius, Roland Dominic Jamora, Raymond L Rosales, Cid Czarina E Diesta, Katja Lohmann, Inke Regina König, Norbert Brüggemann, Christine Klein
A hexanucleotide repeat modifies expressivity of X-linked dystonia parkinsonism. Annals of neurology 85 (6) (2019)

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Publication Activity (10 Years)

Top Topics

Top Venues

Ana Westenberger