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A multi-omics dataset for the analysis of frontotemporal dementia genetic subtypes.
Sci Data. 2023 Dec 1;10(1):849. doi: 10.1038/s41597-023-02598-x.
Sci Data. 2023.
PMID: 38040703
Free PMC article.
HPCA confirmed as a genetic cause of DYT2-like dystonia phenotype.
Atasu B, Hanagasi H, Bilgic B, Pak M, Erginel-Unaltuna N, Hauser AK, Guven G, Simón-Sánchez J, Heutink P, Gasser T, Lohmann E.
Atasu B, et al.
Mov Disord. 2018 Aug;33(8):1354-1358. doi: 10.1002/mds.27442. Epub 2018 Aug 25.
Mov Disord. 2018.
PMID: 30145809
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Role of LRRK2 and SNCA in autosomal dominant Parkinson's disease in Turkey.
Kessler C, Atasu B, Hanagasi H, Simón-Sánchez J, Hauser AK, Pak M, Bilgic B, Erginel-Unaltuna N, Gurvit H, Gasser T, Lohmann E.
Kessler C, et al. Among authors: atasu b.
Parkinsonism Relat Disord. 2018 Mar;48:34-39. doi: 10.1016/j.parkreldis.2017.12.007. Epub 2017 Dec 9.
Parkinsonism Relat Disord. 2018.
PMID: 29248340
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Biallelic variants in TSPOAP1, encoding the active-zone protein RIMBP1, cause autosomal recessive dystonia.
Mencacci NE, Brockmann MM, Dai J, Pajusalu S, Atasu B, Campos J, Pino G, Gonzalez-Latapi P, Patzke C, Schwake M, Tucci A, Pittman A, Simon-Sanchez J, Carvill GL, Balint B, Wiethoff S, Warner TT, Papandreou A, Soo A, Rein R, Kadastik-Eerme L, Puusepp S, Reinson K, Tomberg T, Hanagasi H, Gasser T, Bhatia KP, Kurian MA, Lohmann E, Õunap K, Rosenmund C, Südhof TC, Wood NW, Krainc D, Acuna C.
Mencacci NE, et al. Among authors: atasu b.
J Clin Invest. 2021 Apr 1;131(7):e140625. doi: 10.1172/JCI140625.
J Clin Invest. 2021.
PMID: 33539324
Free PMC article.
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Genotype-Phenotype correlations of SCARB2 associated clinical presentation: a case report and in-depth literature review.
Atasu B, Acarlı ANO, Bilgic B, Baykan B, Demir E, Ozluk Y, Turkmen A, Hauser AK, Guven G, Hanagasi H, Gurvit H, Emre M, Gasser T, Lohmann E.
Atasu B, et al.
BMC Neurol. 2022 Mar 28;22(1):122. doi: 10.1186/s12883-022-02628-y.
BMC Neurol. 2022.
PMID: 35346091
Free PMC article.
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Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia.
Minnerop M, Kurzwelly D, Wagner H, Soehn AS, Reichbauer J, Tao F, Rattay TW, Peitz M, Rehbach K, Giorgetti A, Pyle A, Thiele H, Altmüller J, Timmann D, Karaca I, Lennarz M, Baets J, Hengel H, Synofzik M, Atasu B, Feely S, Kennerson M, Stendel C, Lindig T, Gonzalez MA, Stirnberg R, Sturm M, Roeske S, Jung J, Bauer P, Lohmann E, Herms S, Heilmann-Heimbach S, Nicholson G, Mahanjah M, Sharkia R, Carloni P, Brüstle O, Klopstock T, Mathews KD, Shy ME, de Jonghe P, Chinnery PF, Horvath R, Kohlhase J, Schmitt I, Wolf M, Greschus S, Amunts K, Maier W, Schöls L, Nürnberg P, Zuchner S, Klockgether T, Ramirez A, Schüle R.
Minnerop M, et al. Among authors: atasu b.
Brain. 2017 Jun 1;140(6):1561-1578. doi: 10.1093/brain/awx095.
Brain. 2017.
PMID: 28459997
Free PMC article.
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Dissecting genetic architecture of rare dystonia: genetic, molecular and clinical insights.
Atasu B, Simón-Sánchez J, Hanagasi H, Bilgic B, Hauser AK, Guven G, Heutink P, Gasser T, Lohmann E.
Atasu B, et al.
J Med Genet. 2024 Apr 19;61(5):443-451. doi: 10.1136/jmg-2022-109099.
J Med Genet. 2024.
PMID: 38458754
Free PMC article.
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Pallidal Deep Brain Stimulation Improves HPCA-Linked (DYT 2) Dystonia.
Samanci B, Şahin E, Samanci Y, Bilgiç B, Atasu B, Lohmann E, Peker S, Hanağası HA.
Samanci B, et al. Among authors: atasu b.
Mov Disord Clin Pract. 2024 Feb;11(2):184-187. doi: 10.1002/mdc3.13947. Epub 2023 Dec 20.
Mov Disord Clin Pract. 2024.
PMID: 38386491
No abstract available.
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