A. Nazlı Başak

2.8k citations

56 papers · 864 indexed · h-index 17

Neurology top 5%
- Amyotrophic Lateral Sclerosis Research 16
- Neurological diseases and metabolism 11
- Parkinson's Disease Mechanisms and Treatments 9
Genetics top 10%
- Neurogenetic and Muscular Disorders Research 15
- Hemoglobinopathies and Related Disorders 5
Neurology top 10%
- Amyotrophic Lateral Sclerosis Research 16
- Neurological diseases and metabolism 11
- Parkinson's Disease Mechanisms and Treatments 9
Cellular and Molecular Neuroscience top 10%
- Genetic Neurodegenerative Diseases 13
- Hereditary Neurological Disorders 7
Cell Biology
Molecular Biology
- Mitochondrial Function and Pathology 8

Co-authors: Mehmet Ozansoy Kaya Bilgüvar Murat Günel Ghazi Omar Tadmouri Onur Emre Onat Tayfun Özçelık Haluk Topaloğlu Üner Tan
Cited by: Neurology Genetics
Journals: Proceedings of the National Academy of Sciences (1 paper)PLoS ONE (4 papers)Annals of Neurology (1 paper)
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

The 25 scholars most cited alongside A. Nazlı Başak, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with A. Nazlı Başak Line = papers co-authored together A. Nazlı Başak links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Exosome Proteomics of SOD1 ^D90A Mutation Suggest Early Disease Mechanisms, and FN1 as a Biomarker Annals of Clinical and Translational Neurology ·Mukesh Gautam,Ali Laith,Aslıhan Günel,Melda Yardimoğlu Yilmaz,A. Nazlı Başak,Halil Atilla Idrısoğlu,P. Hande Özdi̇nler	2025	1
2	Successful infliximab treatment in siblings with Netherton syndrome: Unveiling a novel SPINK5 gene variant and literature review Australasian Journal of Dermatology ·Nazmiye Selin Salıcı,Adil Özcanlı,Günel Rasulova,A. Nazlı Başak,Şeyma Tekgül,Seçil Vural	2024	2
3	MRI‐ARSACS: An Imaging Index for Autosomal Recessive Spastic Ataxia of Charlevoix‐Saguenay (ARSACS) Identification Based on the Multicenter PROSPAX Study Movement Disorders ·Alessandra Scaravilli,Davide Negroni,C. Senatore,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	2024	2
4	Phenotypical spectrum of SACS variants: Neuromuscular perspective of a complex neurodegenerative disorder Acta Neurologica Scandinavica ·Arman Çakar,Meltem İnci,Ayşe Nur Özdağ Acarlı,Sinan Çomu,Ayşe Candayan,Esra Battaloğlu,Şeyma Tekgül,A. Nazlı Başak,Hacer Durmuş,Yeşim Parman	2022	2
5	Comprehensive Research on Past and Future Therapeutic Strategies Devoted to Treatment of Amyotrophic Lateral Sclerosis International Journal of Molecular Sciences ·Belgin Sever,Halil I. Ciftci,Hasan DeMi̇rci̇,Hilal Sever,Firdevs Ocak,Burak Yuluğ,Hiroshi Tateishi,Takahisa Tateishi,Masami Otsuka,Mikako Fujita,A. Nazlı Başak	2022	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? Neurogenetics ·Sevim Türay,Recep Eröz,A. Nazlı Başak	2021	8
7	The genetic structure of the Turkish population reveals high levels of variation and admixture Proceedings of the National Academy of Sciences ·Meltem Ece Kars,A. Nazlı Başak,Onur Emre Onat,Kaya Bilgüvar,Jungmin Choi,Yuval Itan,Caner Çağlar,Robin Palvadeau,Jean‐Laurent Casanova,D.N. Cooper,Peter D. Stenson,Alper Yavuz,Hakan Buluş,Murat Günel,Jeffrey M. Friedman,Tayfun Özçelık	2021	47
8	Cerebellar ataxia, neuropathy and vestibular areflexia syndrome (canvas): an important cause of late-onset ataxia with unique clinical features Acta Neurologica Belgica ·Arman Çakar,Erdi Şahin,Seden Tezel,Ayşe Candayan,Bedia Samancı,Esra Battaloğlu,A. Nazlı Başak,Başar Bılgıç,Haşmet Hanağası,Hacer Durmuş,Yeşim Parman	2021	2
9	A novel PNPLA6 mutation in a Turkish family with intractable Holmes tremor and spastic ataxia Neurological Sciences ·Ahmed Serkan Emekli,Bedia Samancı,Gülşah Şimşir,Haşmet Hanağası,Hakan Gürvıt,Başar Bılgıç,A. Nazlı Başak	2020	11
10	The first biallelic missense mutation in the FXN gene in a consanguineous Turkish family with Charcot-Marie-Tooth-like phenotype Neurogenetics ·Ayşe Candayan,Gulshan Yunisova,Arman Çakar,Hacer Durmuş,A. Nazlı Başak,Yeşim Parman,Esra Battaloğlu	2019	17
11	Cerebellar cognitive-affective syndrome preceding ataxia associated with complex extrapyramidal features in a Turkish SCA48 family Neurogenetics ·Robin Palvadeau,Zeynep Ece Kaya Güleç,Gülşah Şimşir,Atay Vural,Özgür Öztop Çakmak,Gençer Genç,Murat Serhat Aygün,Okan Falay,A. Nazlı Başak,Sibel Ertan	2019	20
12	A novel homozygous FBXO38 variant causes an early-onset distal hereditary motor neuronopathy type IID Journal of Human Genetics ·Fulya Akçimen,Atay Vural,Hacer Durmuş,Arman Çakar,Henry Houlden,Yeşim Parman,A. Nazlı Başak	2019	9
13	Clinical and molecular characterization and response to acitretin in three families with Sjögren‐Larsson syndrome International Journal of Dermatology ·Seçil Vural,Atay Vural,Fulya Akçimen,Işın Sinem Bağcı,Ceren Tunca,Aslı Gündoğdu Eken,Thomas Ruzicka,A. Nazlı Başak	2018	6
14	Characterization of the c9orf72 GC-rich low complexity sequence in two cohorts of Italian and Turkish ALS cases Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration ·Lucia Corrado,Cinzia Tiloca,Clarissa Locci,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	2018	2
15	Assessment of the corticospinal fiber integrity in mirror movement disorder Journal of Clinical Neuroscience ·Bilgehan Solmaz,Mustafa Görkem Özyurt,Demir Berk Ata,Fulya Akçimen,Mohammed Shabsog,Kemal S. Türker,Hakkı Dalçık,Oktay Algın,A. Nazlı Başak,Merve Özgür,Safiye Çavdar	2018	3
16	ERLIN1 mutations cause teenage-onset slowly progressive ALS in a large Turkish pedigree European Journal of Human Genetics ·Ceren Tunca,Fulya Akçimen,Cemre Coşkun,Aslı Gündoğdu-Eken,Cemile Koçoğlu,Betül Çevik,Can Ebru Bekircan‐Kurt,Ersin Tan,A. Nazlı Başak	2018	24
17	Search for SCA2 blood RNA biomarkers highlights Ataxin-2 as strong modifier of the mitochondrial factor PINK1 levels Neurobiology of Disease ·Nesli Ece Şen,Jessica Drost,Suzana Gispert,Sylvia Torres-Odio,Ewa Damrath,Michael Klinkenberg,Hamid Hamzeiy,Gülden Akdal,Halil Güllüoğlu,A. Nazlı Başak,Georg Auburger	2016	29
18	Both Ubiquitin Ligases FBXW8 and PARK2 Are Sequestrated into Insolubility by ATXN2 PolyQ Expansions, but Only FBXW8 Expression Is Dysregulated PLoS ONE ·Melanie V. Halbach,Tanja Stehning,Ewa Damrath,Marina Jendrach,Nesli Ece Şen,A. Nazlı Başak,Georg Auburger	2015	23
19	Homozygosity mapping and targeted genomic sequencing reveal the gene responsible for cerebellar hypoplasia and quadrupedal locomotion in a consanguineous kindred Genome Research ·Süleyman Gülsüner,Ayşe B. Tekinay,Katja Doerschner,Hüseyin Boyacı,Kaya Bilgüvar,Hilal Ünal,Aslihan Ors,Onur Emre Onat,Ergin Atalar,A. Nazlı Başak,Haluk Topaloğlu,Tülay Kansu,Meli̇ha Tan,Üner Tan,Murat Günel,Tayfun Özçelık	2011	51
20	Genetic Predisposition to β-Thalassemia and Sickle Cell Anemia in Turkey: A Molecular Diagnostic Approach Methods in molecular biology ·A. Nazlı Başak,Şükrü Tüzmen	2010	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), Genetic Neurodegenerative Diseases (13 papers), Neurological diseases and metabolism (11 papers), Parkinson's Disease Mechanisms and Treatments (9 papers), Mitochondrial Function and Pathology (8 papers), Hereditary Neurological Disorders (7 papers) and Hemoglobinopathies and Related Disorders (5 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.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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