A. Nazlı Başak - Concepedia

Author

A. Nazlı Başak

Also Known As

A Başak, A Nazli Basak, A Nazlı Başak, A. NAZLI BAŞAK, A. Nazli Basak, A. Nazli Başak, A. Nazlı Başak, A.N. Başak, A.Nazlı Başak, AYSE Nazli Basak

141

Publications

2.7K

Citations

H-Index

Concepts

All Affiliations

Boğaziçi University Koç University Istanbul University Inserm Cukurova University

About

A. Nazlı Başak is an author at Boğaziçi University specializing in medicine, genetics, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	12	429
2	Public Health	3	3	92
3	Cell Biology	3	3	85
4	Natural Sciences	2	2	44
5	Health Sciences	1	1	136

A. Nazlı Başak

Publications

1.2K

Citations

H-Index

Page 1

	Year	Citations
Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion Onur Emre Onat, Süleyman Gülsüner, Kaya Bilgüvar, European Journal of Human Genetics Cerebellar AtrophyQuadrupedal LocomotionMolecular PhysiologyMitochondrial FunctionGenetics	2012	136
Homozygosity mapping and targeted genomic sequencing reveal the gene responsible for cerebellar hypoplasia and quadrupedal locomotion in a consanguineous kindred Süleyman Gülsüner, Ayşe B. Tekinay, Katja Doerschner, Genome Research	2011	87
The genetic structure of the Turkish population reveals high levels of variation and admixture Meltem Ece Kars, A. Nazlı Başak, Onur Emre Onat, Proceedings of the National Academy of Sciences	2021	84
Association of Variants in the <i>SPTLC1</i> Gene With Juvenile Amyotrophic Lateral Sclerosis Janel O. Johnson, Ruth Chia, Danny E. Miller, JAMA Neurology	2021	78
Clinico‐Genetic, Imaging and Molecular Delineation of <scp><i>COQ8A</i></scp>‐Ataxia: A Multicenter Study of 59 Patients Andreas Traschütz, Tommaso Schirinzi, Lucia Laugwitz, Annals of Neurology	2020	73
Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans Suzanne Lesage, Étienne Patin, Christel Condroyer, Human Molecular Genetics	2010	61
Human genetics and neuropathology suggest a link between miR-218 and amyotrophic lateral sclerosis pathophysiology Irit Reichenstein, Chen Eitan, Sandra Díaz-García, Science Translational Medicine	2019	59
ATXN2 and Its Neighbouring Gene SH2B3 Are Associated with Increased ALS Risk in the Turkish Population Suna Lahut, Özgür Ömür, Özgün Uyan, PLoS ONE	2012	58
Discovery, Validation and Characterization of Erbb4 and Nrg1 Haplotypes Using Data from Three Genome-Wide Association Studies of Schizophrenia Zeynep Sena Ağım, Melda Esendal, Laurent Briollais, PLoS ONE GeneticsGenetic EpidemiologyGenome-wide Association StudyPsychiatric GeneticsEnvironmental Factors	2013	53
Bi-allelic variants in HOPS complex subunit VPS41 cause cerebellar ataxia and abnormal membrane trafficking Leslie E. Sanderson, Kristina Lanko, Maysoon Alsagob, Brain	2021	50

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