A. Nazlı Başak

Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion

Onur Emre Onat, Süleyman Gülsüner, Kaya Bilgüvar et al. · European Journal of Human Genetics · 2012 · 136 citations · Full text

Cerebellar Atrophy, Quadrupedal Locomotion, Molecular Physiology +11

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 et al. · Genome Research · 2011 · 87 citations · Full text

The genetic structure of the Turkish population reveals high levels of variation and admixture

Meltem Ece Kars, A. Nazlı Başak, Onur Emre Onat et al. · Proceedings of the National Academy of Sciences · 2021 · 84 citations · Full text

Association of Variants in the <i>SPTLC1</i> Gene With Juvenile Amyotrophic Lateral Sclerosis

Janel O. Johnson, Ruth Chia, Danny E. Miller et al. · JAMA Neurology · 2021 · 78 citations · Full text

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 et al. · Annals of Neurology · 2020 · 73 citations · Full text