Başak AN - Search Results

1

The distinct genetic pattern of ALS in Turkey and novel mutations.

Özoğuz A, Uyan Ö, Birdal G, Iskender C, Kartal E, Lahut S, Ömür Ö, Agim ZS, Eken AG, Sen NE, Kavak P, Saygı C, Sapp PC, Keagle P, Parman Y, Tan E, Koç F, Deymeer F, Oflazer P, Hanağası H, Gürvit H, Bilgiç B, Durmuş H, Ertaş M, Kotan D, Akalın MA, Güllüoğlu H, Zarifoğlu M, Aysal F, Döşoğlu N, Bilguvar K, Günel M, Keskin Ö, Akgün T, Özçelik H, Landers JE, Brown RH, Başak AN. Özoğuz A, et al. Among authors: basak an. Neurobiol Aging. 2015 Apr;36(4):1764.e9-1764.e18. doi: 10.1016/j.neurobiolaging.2014.12.032. Epub 2015 Jan 10. Neurobiol Aging. 2015. PMID: 25681989 Free PMC article.

2

Two young sisters with spinocerebellar ataxia type 2 showing different clinical progression of disease.

Yiş U, Dirik E, Kurul SH, Eken AG, Başak AN. Yiş U, et al. Among authors: basak an. Cerebellum. 2009 Jun;8(2):127-9. doi: 10.1007/s12311-008-0080-6. Epub 2008 Nov 21. Cerebellum. 2009. PMID: 19023636

3

Bell's palsy and choreiform movements during peginterferon alpha and ribavirin therapy.

Barut S, Karaer H, Oksuz E, Eken AG, Basak AN. Barut S, et al. Among authors: basak an. World J Gastroenterol. 2009 Aug 7;15(29):3694-6. doi: 10.3748/wjg.15.3694. World J Gastroenterol. 2009. PMID: 19653353 Free PMC article.

4

Homozygosity mapping and targeted genomic sequencing reveal the gene responsible for cerebellar hypoplasia and quadrupedal locomotion in a consanguineous kindred.

Gulsuner S, Tekinay AB, Doerschner K, Boyaci H, Bilguvar K, Unal H, Ors A, Onat OE, Atalar E, Basak AN, Topaloglu H, Kansu T, Tan M, Tan U, Gunel M, Ozcelik T. Gulsuner S, et al. Among authors: basak an. Genome Res. 2011 Dec;21(12):1995-2003. doi: 10.1101/gr.126110.111. Epub 2011 Sep 1. Genome Res. 2011. PMID: 21885617 Free PMC article. Clinical Trial.

5

ATXN2 and its neighbouring gene SH2B3 are associated with increased ALS risk in the Turkish population.

Lahut S, Ömür Ö, Uyan Ö, Ağım ZS, Özoğuz A, Parman Y, Deymeer F, Oflazer P, Koç F, Özçelik H, Auburger G, Başak AN. Lahut S, et al. Among authors: basak an. PLoS One. 2012;7(8):e42956. doi: 10.1371/journal.pone.0042956. Epub 2012 Aug 20. PLoS One. 2012. PMID: 22916186 Free PMC article.

6

Discovery, validation and characterization of Erbb4 and Nrg1 haplotypes using data from three genome-wide association studies of schizophrenia.

Agim ZS, Esendal M, Briollais L, Uyan O, Meschian M, Martinez LA, Ding Y, Basak AN, Ozcelik H. Agim ZS, et al. Among authors: basak an. PLoS One. 2013;8(1):e53042. doi: 10.1371/journal.pone.0053042. Epub 2013 Jan 3. PLoS One. 2013. PMID: 23301017 Free PMC article.

7

Genome-wide copy number variation in sporadic amyotrophic lateral sclerosis in the Turkish population: deletion of EPHA3 is a possible protective factor.

Uyan Ö, Ömür Ö, Ağım ZS, Özoğuz A, Li H, Parman Y, Deymeer F, Oflazer P, Koç F, Tan E, Özçelik H, Başak AN. Uyan Ö, et al. Among authors: basak an. PLoS One. 2013 Aug 26;8(8):e72381. doi: 10.1371/journal.pone.0072381. eCollection 2013. PLoS One. 2013. PMID: 23991104 Free PMC article.

8

FBXO7-R498X mutation: phenotypic variability from chorea to early onset parkinsonism within a family.

Gündüz A, Eken AG, Bilgiç B, Hanagasi HA, Bilgüvar K, Günel M, Başak AN, Ertan S. Gündüz A, et al. Among authors: basak an. Parkinsonism Relat Disord. 2014 Nov;20(11):1253-6. doi: 10.1016/j.parkreldis.2014.07.016. Epub 2014 Aug 14. Parkinsonism Relat Disord. 2014. PMID: 25169713

9

Both ubiquitin ligases FBXW8 and PARK2 are sequestrated into insolubility by ATXN2 PolyQ expansions, but only FBXW8 expression is dysregulated.

Halbach MV, Stehning T, Damrath E, Jendrach M, Şen NE, Başak AN, Auburger G. Halbach MV, et al. Among authors: basak an. PLoS One. 2015 Mar 19;10(3):e0121089. doi: 10.1371/journal.pone.0121089. eCollection 2015. PLoS One. 2015. PMID: 25790475 Free PMC article.

10

Turkish families with juvenile motor neuron disease broaden the phenotypic spectrum of SPG11.

Iskender C, Kartal E, Akcimen F, Kocoglu C, Ozoguz A, Kotan D, Eraksoy M, Parman YG, Basak AN. Iskender C, et al. Among authors: basak an. Neurol Genet. 2015 Oct 8;1(3):e25. doi: 10.1212/NXG.0000000000000025. eCollection 2015 Oct. Neurol Genet. 2015. PMID: 27066562 Free PMC article.

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