A. Nazlı Başak

2.8k citations

56 papers · 864 indexed · h-index 17

Molecular Biology
Neurology top 5%
Cellular and Molecular Neuroscience top 10%
Genetics top 10%
Genetics

Co-authors: Mehmet Ozansoy Kaya Bilgüvar Murat Günel Ghazi Omar Tadmouri Onur Emre Onat Tayfun Özçelık Haluk Topaloğlu Üner Tan
Topics: Amyotrophic Lateral Sclerosis Research (16 papers)Neurogenetic and Muscular Disorders Research (15 papers)Genetic Neurodegenerative Diseases (13 papers)
Cited by: Neurology Genetics
Journals: Proceedings of the National Academy of Sciences PLoS ONE Annals of Neurology
Partner nations: Türkiye United States Germany

In The Last Decade

A. Nazlı Başak

53 papers receiving 844 citations

Peers

Countries citing papers authored by A. Nazlı Başak

Since Specialization

Citations

This map shows the geographic impact of A. Nazlı Başak's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by A. Nazlı Başak with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites A. Nazlı Başak more than expected).

Fields of papers citing papers by A. Nazlı Başak

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by A. Nazlı Başak. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by A. Nazlı Başak. The network helps show where A. Nazlı Başak may publish in the future.

Co-authorship network of co-authors of A. Nazlı Başak

This figure shows the co-authorship network connecting the top 25 collaborators of A. Nazlı Başak. A scholar is included among the top collaborators of A. Nazlı Başak based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with A. Nazlı Başak. A. Nazlı Başak is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Exosome Proteomics of SOD1 ^D90A Mutation Suggest Early Disease Mechanisms, and FN1 as a Biomarker 2025 ·Annals of Clinical and Translational Neurology ·Mukesh Gautam,(unknown),(unknown),(unknown),A. Nazlı Başak,Halil Atilla Idrısoğlu,P. Hande Özdi̇nler	1
2	Successful infliximab treatment in siblings with Netherton syndrome: Unveiling a novel SPINK5 gene variant and literature review 2024 ·Australasian Journal of Dermatology ·(unknown),(unknown),(unknown),A. Nazlı Başak,(unknown),Seçil Vural	2
3	MRI‐ARSACS: An Imaging Index for Autosomal Recessive Spastic Ataxia of Charlevoix‐Saguenay (ARSACS) Identification Based on the Multicenter PROSPAX Study 2024 ·Movement Disorders ·(unknown),(unknown),(unknown),Lorenzo Ugga,Mirco Cosottini,Ivana Ricca,Benjamin Bender,Andreas Traschütz,A. Nazlı Başak,Atay Vural,Bart P.C. van de Warrenburg,Alexandra Dürr,Roberta La Piana,Dagmar Timmann,Rebecca Schüle,Matthis Synofzik,Filippo M. Santorelli,Sirio Cocozza	2
4	Phenotypical spectrum of SACS variants: Neuromuscular perspective of a complex neurodegenerative disorder 2022 ·Acta Neurologica Scandinavica ·Arman Çakar,(unknown),(unknown),Sinan Çomu,(unknown),Esra Battaloğlu,(unknown),A. Nazlı Başak,(unknown),Yeşim Parman	2
5	Comprehensive Research on Past and Future Therapeutic Strategies Devoted to Treatment of Amyotrophic Lateral Sclerosis 2022 ·International Journal of Molecular Sciences ·Belgin Sever,Halil I. Ciftci,Hasan DeMi̇rci̇,(unknown),(unknown),Burak Yuluğ,Hiroshi Tateishi,Takahisa Tateishi,Masami Otsuka,Mikako Fujita,A. Nazlı Başak	49
6	A novel pathogenic variant in the 3ʹ end of the AGTPBP1 gene gives rise to neurodegeneration without cerebellar atrophy: an expansion of the disease phenotype? 2021 ·Neurogenetics ·(unknown),Recep Eröz,A. Nazlı Başak	8
7	The genetic structure of the Turkish population reveals high levels of variation and admixture 2021 ·Proceedings of the National Academy of Sciences ·(unknown),A. Nazlı Başak,Onur Emre Onat,Kaya Bilgüvar,Jungmin Choi,Yuval Itan,Caner Çağlar,(unknown),Jean‐Laurent Casanova,D.N. Cooper,Peter D. Stenson,Alper Yavuz,Hakan Buluş,Murat Günel,Jeffrey M. Friedman,Tayfun Özçelık	47
8	Cerebellar ataxia, neuropathy and vestibular areflexia syndrome (canvas): an important cause of late-onset ataxia with unique clinical features 2021 ·Acta Neurologica Belgica ·Arman Çakar,Erdi Şahin,(unknown),(unknown),Bedia Samancı,Esra Battaloğlu,A. Nazlı Başak,Başar Bılgıç,Haşmet Hanağası,(unknown),Yeşim Parman	2
9	A novel PNPLA6 mutation in a Turkish family with intractable Holmes tremor and spastic ataxia 2020 ·Neurological Sciences ·(unknown),Bedia Samancı,(unknown),Haşmet Hanağası,Hakan Gürvıt,Başar Bılgıç,A. Nazlı Başak	11
10	The first biallelic missense mutation in the FXN gene in a consanguineous Turkish family with Charcot-Marie-Tooth-like phenotype 2019 ·Neurogenetics ·(unknown),(unknown),Arman Çakar,Hacer Durmuş,A. Nazlı Başak,Yeşim Parman,Esra Battaloğlu	17
11	Cerebellar cognitive-affective syndrome preceding ataxia associated with complex extrapyramidal features in a Turkish SCA48 family 2019 ·Neurogenetics ·(unknown),(unknown),(unknown),Atay Vural,Özgür Öztop Çakmak,Gençer Genç,(unknown),(unknown),A. Nazlı Başak,Sibel Ertan	20
12	A novel homozygous FBXO38 variant causes an early-onset distal hereditary motor neuronopathy type IID 2019 ·Journal of Human Genetics ·Fulya Akçimen,Atay Vural,Hacer Durmuş,Arman Çakar,Henry Houlden,Yeşim Parman,A. Nazlı Başak	9
13	Clinical and molecular characterization and response to acitretin in three families with Sjögren‐Larsson syndrome 2018 ·International Journal of Dermatology ·Seçil Vural,Atay Vural,Fulya Akçimen,Işın Sinem Bağcı,Ceren Tunca,(unknown),Thomas Ruzicka,A. Nazlı Başak	6
14	Characterization of the c9orf72 GC-rich low complexity sequence in two cohorts of Italian and Turkish ALS cases 2018 ·Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration ·Lucia Corrado,Cinzia Tiloca,(unknown),Alessandra Bagarotti,Hamid Hamzeiy,Claudia Colombrita,Fabiola De Marchi,Nadia Barizzone,Diego Cotella,Nicola Ticozzi,Letizia Mazzini,A. Nazlı Başak,Antonia Ratti,Vincenzo Silani,Sandra D’Alfonso	2
15	Assessment of the corticospinal fiber integrity in mirror movement disorder 2018 ·Journal of Clinical Neuroscience ·(unknown),(unknown),(unknown),Fulya Akçimen,(unknown),Kemal S. Türker,Hakkı Dalçık,Oktay Algın,A. Nazlı Başak,(unknown),Safiye Çavdar	3
16	ERLIN1 mutations cause teenage-onset slowly progressive ALS in a large Turkish pedigree 2018 ·European Journal of Human Genetics ·Ceren Tunca,Fulya Akçimen,(unknown),Aslı Gündoğdu-Eken,(unknown),(unknown),Can Ebru Bekircan‐Kurt,Ersin Tan,A. Nazlı Başak	24
17	Search for SCA2 blood RNA biomarkers highlights Ataxin-2 as strong modifier of the mitochondrial factor PINK1 levels 2016 ·Neurobiology of Disease ·(unknown),(unknown),Suzana Gispert,Sylvia Torres-Odio,Ewa Damrath,Michael Klinkenberg,Hamid Hamzeiy,Gülden Akdal,(unknown),A. Nazlı Başak,Georg Auburger	29
18	Both Ubiquitin Ligases FBXW8 and PARK2 Are Sequestrated into Insolubility by ATXN2 PolyQ Expansions, but Only FBXW8 Expression Is Dysregulated 2015 ·PLoS ONE ·Melanie V. Halbach,(unknown),Ewa Damrath,Marina Jendrach,(unknown),A. Nazlı Başak,Georg Auburger	23
19	Homozygosity mapping and targeted genomic sequencing reveal the gene responsible for cerebellar hypoplasia and quadrupedal locomotion in a consanguineous kindred 2011 ·Genome Research ·Süleyman Gülsüner,Ayşe B. Tekinay,Katja Doerschner,Hüseyin Boyacı,Kaya Bilgüvar,(unknown),(unknown),Onur Emre Onat,Ergin Atalar,A. Nazlı Başak,Haluk Topaloğlu,Tülay Kansu,Meli̇ha Tan,Üner Tan,Murat Günel,Tayfun Özçelık	51
20	Genetic Predisposition to β-Thalassemia and Sickle Cell Anemia in Turkey: A Molecular Diagnostic Approach 2010 ·Methods in molecular biology ·A. Nazlı Başak,Şükrü Tüzmen	3

About A. Nazlı Başak

A. Nazlı Başak is a scholar working on Genetics, Neurology and Neurology, having authored 56 papers that have together received 864 indexed citations. Recurring topics across this work include Amyotrophic Lateral Sclerosis Research (16 papers), Neurogenetic and Muscular Disorders Research (15 papers) and Genetic Neurodegenerative Diseases (13 papers). The work is most often cited by research in Neurology (306 citations), Genetics (154 citations) and Neurology (112 citations). A. Nazlı Başak has collaborated with scholars based in Türkiye, United States and Germany. Frequent co-authors include Mehmet Ozansoy, Kaya Bilgüvar, Murat Günel, Ghazi Omar Tadmouri, Onur Emre Onat, Tayfun Özçelık, Haluk Topaloğlu, Üner Tan, Süleyman Gülsüner and Meli̇ha Tan. Their work appears in journals such as Proceedings of the National Academy of Sciences, PLoS ONE and Annals of Neurology.

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