Ayse Nazli Basak (Ayşe Nazlı Başak, Nazli A Başak, Nazlı A Başak, A Nazli Basak, A Nazlı Başak, A Nazlı Başak, Ayşe Nazli Başak)

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 24

Top Topics

Amyotrophic Lateral Sclerosis

Top Venues

Movement disorders : official journal of the Movement Disorder Society

Annals of clinical and translational neurology

medRxiv : the preprint server for health sciences

The Australasian journal of dermatology

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

Publications

Alessandra Scaravilli, Davide Negroni, Claudio Senatore, Lorenzo Ugga, Mirco Cosottini, Ivana Ricca, Benjamin Bender, Andreas Traschütz, Ayse Nazli Basak, Atay Vural, Bart P van de Warrenburg, Alexandra Durr, Roberta La Piana, Dagmar Timmann, null null, Rebecca Schüle, Matthis Synofzik, Filippo Maria Santorelli, Sirio Cocozza
MRI-ARSACS: An Imaging Index for Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) Identification Based on the Multicenter PROSPAX Study. Movement disorders : official journal of the Movement Disorder Society (2024)
Nazmiye Selin Salici, Adil Ozcanli, Gunel Rasulova, Ayse Nazli Basak, Seyma Tekgul, Seçil Vural
Successful infliximab treatment in siblings with Netherton syndrome: Unveiling a novel SPINK5 gene variant and literature review. The Australasian journal of dermatology 65 (3) (2024)
Francesca Magrinelli, Christelle Tesson, Plamena R Angelova, Ainara Salazar-Villacorta, Jose A Rodriguez, Annarita Scardamaglia, Brian Hon-Yin Chung, Matthew Jaconelli, Barbara Vona, Noemí Esteras, Anna Ka-Yee Kwong, Thomas Courtin, Reza Maroofian, Shahryar Alavi, Raja S Nirujogi, Mariasavina Severino, Patrick A Lewis, Stephanie Efthymiou, Benjamin J O'Callaghan, Rebecca Buchert, Linda Sofan, Pawel Lis, Chloé Pinon, Guido J Breedveld, Martin Man Chun Chui, David P Murphy, Vanessa Pitz, Mary B Makarious, Marlene Cassar, Bassem A Hassan, Sana Iftikhar, Clarissa Rocca, Peter Bauer, Michele Tinazzi, Marina Svetel, Bedia Samanci, Hasmet A Hanagasi, Basar Bilgiç, Jose A Obeso, Mónica M Kurtis, Guillaume Cogan, Ayse Nazli Basak, Güneş Kiziltan, Tuğçe Gül, Gül Yalçın Çakmaklı, Bülent Elibol, Nina Barisic, Earny Wei-Sen Ng, Sze-Shing Fan, Tova Hershkovitz, Karin Weiss, Javeria Raza Alvi, Tipu Sultan, Issam Azmi Alkhawaja, Tawfiq Froukh, Hadeel Abdollah E Alrukban, Christine Fauth, Ulrich A Schatz, Thomas Zöggeler, Michael Zech, Karen L Stals, Vinod C Varghese, Sonia Gandhi, Cornelis Blauwendraat, John A Hardy, Suzanne Lesage, Vincenzo Bonifati, Tobias B Haack, Aida Maria Bertoli-Avella, Robert Steinfeld, Dario R Alessi, Hermann Steller, Alexis Brice, Andrey Y Abramov, Kailash P Bhatia, Henry Houlden
PSMF1 variants cause a phenotypic spectrum from early-onset Parkinson's disease to perinatal lethality by disrupting mitochondrial pathways. medRxiv : the preprint server for health sciences (2024)
Francesca Magrinelli, Christelle Tesson, Plamena R Angelova, Ainara Salazar-Villacorta, Jose A Rodriguez, Annarita Scardamaglia, Brian Hon-Yin Chung, Matthew Jaconelli, Barbara Vona, Noemí Esteras, Anna Ka-Yee Kwong, Thomas Courtin, Reza Maroofian, Shahryar Alavi, Raja S Nirujogi, Mariasavina Severino, Patrick A Lewis, Stephanie Efthymiou, Benjamin J O'Callaghan, Rebecca Buchert, Linda Sofan, Pawel Lis, Chloé Pinon, Guido J Breedveld, Martin Man Chun Chui, David P Murphy, Vanessa Pitz, Mary B Makarious, Marlene Cassar, Bassem A Hassan, Sana Iftikhar, Clarissa Rocca, Peter Bauer, Michele Tinazzi, Marina Svetel, Bedia Samanci, Hasmet A Hanagasi, Basar Bilgiç, Jose A Obeso, Mónica M Kurtis, Guillaume Cogan, Ayse Nazli Basak, Güneş Kiziltan, Tuğçe Gül, Gül Yalçın Çakmaklı, Bülent Elibol, Nina Barisic, Earny Wei-Sen Ng, Sze-Shing Fan, Tova Hershkovitz, Karin Weiss, Javeria Raza Alvi, Tipu Sultan, Issam Azmi Alkhawaja, Tawfiq Froukh, Hadeel Abdollah E Alrukban, Christine Fauth, Ulrich A Schatz, Thomas Zöggeler, Michael Zech, Karen L Stals, Vinod C Varghese, Sonia Gandhi, Cornelis Blauwendraat, John A Hardy, Suzanne Lesage, Vincenzo Bonifati, Tobias B Haack, Aida Maria Bertoli-Avella, Robert Steinfeld, Dario R Alessi, Hermann Steller, Alexis Brice, Andrey Y Abramov, Kailash P Bhatia, Henry Houlden
PSMF1 variants cause a phenotypic spectrum from early-onset Parkinson's disease to perinatal lethality by disrupting mitochondrial pathways. medRxiv : the preprint server for health sciences (2024)
Alessandra Scaravilli, Davide Negroni, Claudio Senatore, Lorenzo Ugga, Mirco Cosottini, Ivana Ricca, Benjamin Bender, Andreas Traschütz, Ayse Nazli Basak, Atay Vural, Bart P van de Warrenburg, Alexandra Durr, Roberta La Piana, Dagmar Timmann, null null, Rebecca Schüle, Matthis Synofzik, Filippo Maria Santorelli, Sirio Cocozza
MRI-ARSACS: An Imaging Index for Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) Identification Based on the Multicenter PROSPAX Study. Movement disorders : official journal of the Movement Disorder Society 39 (8) (2024)
Heather Marriott, Thomas P Spargo, Ahmad Al Khleifat, Peter M Andersen, Ayse Nazli Basak, Johnathan Cooper-Knock, Philippe Corcia, Philippe Couratier, Mamede de Carvalho, Vivian Drory, Marc Gotkine, John E Landers, Russell McLaughlin, Jesús S Mora Pardina, Karen E Morrison, Susana Pinto, Christopher E Shaw, Pamela J Shaw, Vincenzo Silani, Nicola Ticozzi, Philip Van Damme, Leonard H van den Berg, Patrick Vourc'h, Markus Weber, Jan H Veldink, null null, Richard J Dobson, Patrick Schwab, Ammar Al Chalabi, Alfredo Iacoangeli
Mutations in the tail and rod domains of the neurofilament heavy-chain gene increase the risk of ALS. Annals of clinical and translational neurology 11 (7) (2024)
Francesca Magrinelli, Christelle Tesson, Plamena R Angelova, Ainara Salazar-Villacorta, Jose A Rodriguez, Annarita Scardamaglia, Brian Hon-Yin Chung, Matthew Jaconelli, Barbara Vona, Noemí Esteras, Anna Ka-Yee Kwong, Thomas Courtin, Reza Maroofian, Shahryar Alavi, Raja S Nirujogi, Mariasavina Severino, Patrick A Lewis, Stephanie Efthymiou, Benjamin J O'Callaghan, Rebecca Buchert, Linda Sofan, Pawel Lis, Chloé Pinon, Guido J Breedveld, Martin Man Chun Chui, David P Murphy, Vanessa Pitz, Mary B Makarious, Marlene Cassar, Bassem A Hassan, Sana Iftikhar, Clarissa Rocca, Peter Bauer, Michele Tinazzi, Marina Svetel, Bedia Samanci, Hasmet A Hanagasi, Basar Bilgiç, Jose A Obeso, Mónica M Kurtis, Guillaume Cogan, Ayse Nazli Basak, Güneş Kiziltan, Tuğçe Gül, Gül Yalçın Çakmaklı, Bülent Elibol, Nina Barisic, Earny Wei-Sen Ng, Sze-Shing Fan, Tova Hershkovitz, Karin Weiss, Javeria Raza Alvi, Tipu Sultan, Issam Azmi Alkhawaja, Tawfiq Froukh, Hadeel Abdollah E Alrukban, Christine Fauth, Ulrich A Schatz, Thomas Zöggeler, Michael Zech, Karen L Stals, Vinod C Varghese, Sonia Gandhi, Cornelis Blauwendraat, John A Hardy, Suzanne Lesage, Vincenzo Bonifati, Tobias B Haack, Aida Maria Bertoli-Avella, Robert Steinfeld, Dario R Alessi, Hermann Steller, Alexis Brice, Andrey Y Abramov, Kailash P Bhatia, Henry Houlden
PSMF1 variants cause a phenotypic spectrum from early-onset Parkinson's disease to perinatal lethality by disrupting mitochondrial pathways. medRxiv : the preprint server for health sciences (2024)
Heather Marriott, Thomas P Spargo, Ahmad Al Khleifat, Peter M Andersen, Ayse Nazli Basak, Johnathan Cooper-Knock, Philippe Corcia, Philippe Couratier, Mamede de Carvalho, Vivian Drory, Marc Gotkine, John E Landers, Russell McLaughlin, Jesús S Mora Pardina, Karen E Morrison, Susana Pinto, Christopher E Shaw, Pamela J Shaw, Vincenzo Silani, Nicola Ticozzi, Philip Van Damme, Leonard H van den Berg, Patrick Vourc'h, Markus Weber, Jan H Veldink, null null, Richard J Dobson, Patrick Schwab, Ammar Al Chalabi, Alfredo Iacoangeli
Mutations in the tail and rod domains of the neurofilament heavy-chain gene increase the risk of ALS. Annals of clinical and translational neurology 11 (7) (2024)
Lukas Beichert, Winfried Ilg, Christoph Kessler, Andreas Traschütz, Selina Reich, Filippo M Santorelli, Ayse Nazli Basak, Cynthia Gagnon, null null, Rebecca Schüle, Matthis Synofzik
Digital Gait Outcomes for Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS): Discriminative, Convergent, and Ecological Validity in a Multicenter Study (PROSPAX). Movement disorders : official journal of the Movement Disorder Society (2024)
Nazmiye Selin Salici, Adil Ozcanli, Gunel Rasulova, Ayse Nazli Basak, Seyma Tekgul, Seçil Vural
Successful infliximab treatment in siblings with Netherton syndrome: Unveiling a novel SPINK5 gene variant and literature review. The Australasian journal of dermatology 65 (3) (2024)
Nazmiye Selin Salici, Adil Ozcanli, Gunel Rasulova, Ayse Nazli Basak, Seyma Tekgul, Seçil Vural
Successful infliximab treatment in siblings with Netherton syndrome: Unveiling a novel SPINK5 gene variant and literature review. The Australasian journal of dermatology (2024)
Heather Marriott, Thomas P Spargo, Ahmad Al Khleifat, Peter M Andersen, Ayse Nazli Basak, Johnathan Cooper-Knock, Philippe Corcia, Philippe Couratier, Mamede de Carvalho, Vivian Drory, Marc Gotkine, John E Landers, Russell McLaughlin, Jesús S Mora Pardina, Karen E Morrison, Susana Pinto, Christopher E Shaw, Pamela J Shaw, Vincenzo Silani, Nicola Ticozzi, Philip Van Damme, Leonard H van den Berg, Patrick Vourc'h, Markus Weber, Jan H Veldink, null null, Richard J Dobson, Patrick Schwab, Ammar Al Chalabi, Alfredo Iacoangeli
Mutations in the tail and rod domains of the neurofilament heavy-chain gene increase the risk of ALS. Annals of clinical and translational neurology (2024)
Heather Marriott, Thomas P Spargo, Ahmad Al Khleifat, Peter M Andersen, Ayse Nazli Basak, Johnathan Cooper-Knock, Philippe Corcia, Philippe Couratier, Mamede de Carvalho, Vivian Drory, Marc Gotkine, John E Landers, Russell McLaughlin, Jesús S Mora Pardina, Karen E Morrison, Susana Pinto, Christopher E Shaw, Pamela J Shaw, Vincenzo Silani, Nicola Ticozzi, Philip Van Damme, Leonard H van den Berg, Patrick Vourc'h, Markus Weber, Jan H Veldink, null null, Richard J Dobson, Patrick Schwab, Ammar Al Chalabi, Alfredo Iacoangeli
Mutations in the tail and rod domains of the neurofilament heavy-chain gene increase the risk of ALS. Annals of clinical and translational neurology 11 (7) (2024)
David Pellerin, Pablo Iruzubieta, Şeyma Tekgül, Matt C Danzi, Catherine Ashton, Marie-Josée Dicaire, Marion Wandzel, Virginie Roth, Phillipa J Lamont, Céline Bonnet, Mathilde Renaud, Matthis Synofzik, Stephan Zuchner, Bernard Brais, Ayse Nazli Basak, Henry Houlden
Non-GAA Repeat Expansions in FGF14 Are Likely Not Pathogenic-Reply to: "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 38 (8) (2023)
Maike F Dohrn, Danique Beijer, Museer A Lone, Elif Bayraktar, Piraye Oflazer, Rotem Orbach, Sandra Donkervoort, A Reghan Foley, Aubrey Rose, Michael Lyons, Raymond J Louie, Kenneth Gable, Teresa Dunn, Sitong Chen, Matt C Danzi, Matthis Synofzik, Carsten G Bönnemann, Ayse Nazli Basak, Thorsten Hornemann, Stephan Zuchner
Recurrent de-novo gain-of-function mutation in SPTLC2 confirms dysregulated sphingolipid production to cause juvenile amyotrophic lateral sclerosis. Journal of neurology, neurosurgery, and psychiatry (2023)
Paul J Hop, Ramona A J Zwamborn, Eilis J Hannon, Gemma L Shireby, Marta F Nabais, Emma M Walker, Wouter Van Rheenen, Joke J F A van Vugt, Annelot M Dekker, Henk-Jan Westeneng, Gijs H P Tazelaar, Kristel R van Eijk, Matthieu Moisse, Denis Baird, Ahmad Al Khleifat, Alfredo Iacoangeli, Nicola Ticozzi, Antonia Ratti, Johnathan Cooper-Knock, Karen E Morrison, Dame Pamela J Shaw, Ayse Nazli Basak, Adriano Chio, Andrea Calvo, Cristina Moglia, Antonio Canosa, Maura Brunetti, Maurizio Grassano, Marc Gotkine, Yossef Lerner, Michal Zabari, Patrick Vourc'h, Philippe Corcia, Philippe Couratier, Jesus S Mora, Teresa Salas, Patrick Dion, Jay P Ross, Robert David Henderson, Susan Mathers, Pamela A McCombe, Merrilee Needham, Garth Nicholson, Dominic B Rowe, Roger Pamphlett, Karen A Mather, Perminder Singh Sachdev, Sarah Furlong, Fleur C Garton, Anjali K Henders, Tian Lin, Shyuan T Ngo, Frederik J Steyn, Leanne Wallace, Kelly Louise Williams, null null, null null, Miguel Mitne Neto, Ruben J Cauchi, Ian P Blair, Matthew C Kiernan, Vivian Drory, Monica Povedano, Mamede de Carvalho, Susana Pinto, Markus Weber, Guy A Rouleau, Vincenzo Silani, John E Landers, Christopher E Shaw, Peter Munch Andersen, Allan F McRae, Michael A van Es, R Jeroen Pasterkamp, Naomi R Wray, Russell Lewis McLaughlin, Orla Hardiman, Kevin P Kenna, Ellen A Tsai, Heiko Runz, Ammar Al Chalabi, Leonard H van den Berg, Philip Van Damme, Jonathan S Mill, Jan Herman Veldink
Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALS. Science translational medicine 14 (633) (2022)
Duygu Aydemir, Selcuk Surucu, Ayse Nazli Basak, Nuriye Nuray Ulusu
Evaluation of the Hematological and Serum Biochemistry Parameters in the Pre-Symptomatic and Symptomatic Stages of ALS Disease to Support Early Diagnosis and Prognosis. Cells 11 (22) (2022)
Belgin Sever, Halilibrahim Çiftçi, Hasan DeMirci, Hilal Sever, Firdevs Ocak, Burak Yulug, Hiroshi Tateishi, Takahisa Tateishi, Masami Otsuka, Mikako Fujita, Ayse Nazli Basak
Comprehensive Research on Past and Future Therapeutic Strategies Devoted to Treatment of Amyotrophic Lateral Sclerosis. International journal of molecular sciences 23 (5) (2022)
Liedewei Van de Vondel, Jonathan De Winter, Danique Beijer, Giulia Coarelli, Melanie Wayand, Robin Palvadeau, Martje G Pauly, Katrin Klein, Maren Rautenberg, Léna Guillot-Noël, Tine Deconinck, Atay Vural, Sibel Ertan, Okan Dogu, HIlmi Uysal, Vesna Brankovic, Rebecca Herzog, Alexis Brice, Alexandra Durr, Stephan Klebe, Friedrich Stock, Almut Turid Bischoff, Tim W Rattay, María-Jesús Sobrido, Giovanna De Michele, Peter De Jonghe, Thomas Klopstock, Katja Lohmann, Ginevra Zanni, Filippo M Santorelli, Vincent Timmerman, Tobias B Haack, Stephan Züchner, null null, Rebecca Schüle, Giovanni Stevanin, Matthis Synofzik, Ayse Nazli Basak, Jonathan Baets
De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia. Movement disorders : official journal of the Movement Disorder Society 37 (6) (2022)
Meltem Ece Kars, Ayse Nazli Basak, Onur Emre Onat, Kaya Bilguvar, Jungmin Choi, Yuval Itan, Caner Çağlar, Robin Palvadeau, Jean Laurent Casanova, David N Cooper, Peter D Stenson, Alper Yavuz, Hakan Buluş, Murat Günel, Jeffrey M Friedman, Tayfun Özçelik
The genetic structure of the Turkish population reveals high levels of variation and admixture. Proceedings of the National Academy of Sciences of the United States of America 118 (36) (2022)
Matthieu Moisse, Ramona A J Zwamborn, Joke J F A van Vugt, Rick A A van der Spek, Wouter Van Rheenen, Brendan Kenna, Kristel Van Eijk, Kevin Kenna, Philippe Corcia, Philippe Couratier, Patrick Vourc'h, Orla Hardiman, Russell Lewis McLaughlin, Marc Gotkine, Vivian Drory, Nicola Ticozzi, Vincenzo Silani, Mamede de Carvalho, Jesus S Mora, Monica Povedano, Peter Munch Andersen, Markus Weber, Ayse Nazli Basak, Xiao Chen, Michael A Eberle, Ammar Al Chalabi, Chris Shaw, Dame Pamela J Shaw, Karen E Morrison, John E Landers, Jonathan D Glass, Wim Robberecht, Michael A Van Es, Leonard H Van Den Berg, Jan Herman Veldink, Philip Van Damme, null null
The Effect of SMN Gene Dosage on ALS Risk and Disease Severity. Annals of neurology 89 (4) (2021)
Süleyman Güler, Tuğçe Gül, Şükran Güler, Maja C Haerle, Ayse Nazli Basak
Early-Onset Parkinson's Disease: A Novel Deletion Comprising the DJ-1 and TNFRSF9 Genes. Movement disorders : official journal of the Movement Disorder Society (2021)
Ayse Nazli Basak
Reply to letter to the editor by De Michele et al. Neurogenetics 21 (2) (2020)
Ceren Tunca, Tuncay Şeker, Fulya Akcimen, Cemre Coşkun, Elif Bayraktar, Robin Palvadeau, Seyit Zor, Cemile Kocoglu, Ece Kartal, Nesli Ece Şen, Hamid Hamzeiy, Aslıhan Özoğuz Erimiş, Utku Norman, Oğuzhan Karakahya, Gülden Olgun, Tahsin Akgün, Hacer Durmuş, Erdi Şahin, Arman Çakar, Esra Başar Gürsoy, Gülsen Babacan Yıldız, Barış İşak, Kayıhan Uluç, Haşmet Hanağası, Başar Bilgiç, Nilda Turgut, Fikret Aysal, Mustafa Ertaş, Cavit Boz, Dilcan Kotan, Halil İdrisoğlu, Aysun Soysal, Nurten Uzun Adatepe, Mehmet Ali Akalın, Filiz Koç, Ersin Tan, Piraye Oflazer, Feza Deymeer, Öznur Taştan, A Ercüment Çiçek, Erşen Kavak, Yeşim Parman, Ayse Nazli Basak
Revisiting the complex architecture of ALS in Turkey: Expanding genotypes, shared phenotypes, molecular networks, and a public variant database. Human mutation 41 (8) (2020)