A. Nazli Basak, PhD - Publications

Affiliations: 
1987- Molecular Biology and Genetics Bogazici University, Istanbul, Turkey 

22 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2015 Iskender C, Kartal E, Akcimen F, Kocoglu C, Ozoguz A, Kotan D, Eraksoy M, Parman YG, Basak AN. Turkish families with juvenile motor neuron disease broaden the phenotypic spectrum of SPG11. Neurology. Genetics. 1: e25. PMID 27066562 DOI: 10.1212/NXG.0000000000000025  0.64
2015 Erol AM, Kilic AK, Celik A, Celik C, Basak AN. Brait-Fahn-Schwarz disease: Parkinson's disease and amyotrophic lateral sclerosis complex. Acta Neurologica Belgica. PMID 26319125 DOI: 10.1007/s13760-015-0531-z  0.88
2014 Lahut S, Vadasz D, Depboylu C, Ries V, Krenzer M, Stiasny-Kolster K, Basak AN, Oertel WH, Auburger G. The PD-associated alpha-synuclein promoter Rep1 allele 2 shows diminished frequency in restless legs syndrome. Neurogenetics. 15: 189-92. PMID 24863655 DOI: 10.1007/s10048-014-0407-z  0.88
2013 Agim ZS, Esendal M, Briollais L, Uyan O, Meschian M, Martinez LA, Ding Y, Basak AN, Ozcelik H. Discovery, validation and characterization of Erbb4 and Nrg1 haplotypes using data from three genome-wide association studies of schizophrenia. Plos One. 8: e53042. PMID 23301017 DOI: 10.1371/journal.pone.0053042  0.88
2012 Synofzik M, Ronchi D, Keskin I, Basak AN, Wilhelm C, Gobbi C, Birve A, Biskup S, Zecca C, Fernández-Santiago R, Kaugesaar T, Schöls L, Marklund SL, Andersen PM. Mutant superoxide dismutase-1 indistinguishable from wild-type causes ALS. Human Molecular Genetics. 21: 3568-74. PMID 22595972 DOI: 10.1093/hmg/dds188  0.88
2011 Enunlu I, Ozansoy M, Basak AN. Alfa-class prefoldin protein UXT is a novel interacting partner of Amyotrophic Lateral Sclerosis 2 (Als2) protein. Biochemical and Biophysical Research Communications. 413: 471-5. PMID 21907703 DOI: 10.1016/j.bbrc.2011.08.121  0.88
2011 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, et al. Homozygosity mapping and targeted genomic sequencing reveal the gene responsible for cerebellar hypoplasia and quadrupedal locomotion in a consanguineous kindred. Genome Research. 21: 1995-2003. PMID 21885617 DOI: 10.1101/gr.126110.111  0.88
2011 Giardine B, Borg J, Higgs DR, Peterson KR, Philipsen S, Maglott D, Singleton BK, Anstee DJ, Basak AN, Clark B, Costa FC, Faustino P, Fedosyuk H, Felice AE, Francina A, et al. Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach. Nature Genetics. 43: 295-301. PMID 21423179 DOI: 10.1038/ng.785  0.88
2011 Basak AN, Tuzmen S. Genetic predisposition to β-thalassemia and sickle cell anemia in Turkey: a molecular diagnostic approach. Methods in Molecular Biology (Clifton, N.J.). 700: 291-307. PMID 21204041 DOI: 10.1007/978-1-61737-954-3_19  0.88
2010 Lesage S, Patin E, Condroyer C, Leutenegger AL, Lohmann E, Giladi N, Bar-Shira A, Belarbi S, Hecham N, Pollak P, Ouvrard-Hernandez AM, Bardien S, Carr J, Benhassine T, Tomiyama H, ... ... Basak AN, et al. Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans. Human Molecular Genetics. 19: 1998-2004. PMID 20197411 DOI: 10.1093/hmg/ddq081  0.88
2010 Kurt S, Karaer H, Kaplan Y, Akat I, Battaloglu E, Eruslu D, Basak AN. Combination of myotonic dystrophy and hereditary motor and sensory neuropathy. Journal of the Neurological Sciences. 288: 197-9. PMID 19846120 DOI: 10.1016/j.jns.2009.09.028  0.88
2009 Haghi M, Feizi AA, Feizi MA, Pouladi N, Basak AN. Is the frameshift codons 8/9 (+G) [FSC 8/9 (+G)] beta-thalassemia mutation, detected by the polymerase chain reaction-amplification refractory mutation system, really FSC 8/9 (+G)? Hemoglobin. 33: 279-82. PMID 19657845 DOI: 10.1080/03630260903081075  0.88
2009 Lederer CW, Basak AN, Aydinok Y, Christou S, El-Beshlawy A, Eleftheriou A, Fattoum S, Felice AE, Fibach E, Galanello R, Gambari R, Gavrila L, Giordano PC, Grosveld F, Hassapopoulou H, et al. An electronic infrastructure for research and treatment of the thalassemias and other hemoglobinopathies: the Euro-mediterranean ITHANET project. Hemoglobin. 33: 163-76. PMID 19657830 DOI: 10.1080/03630260903089177  0.88
2009 Barut S, Karaer H, Oksuz E, Eken AG, Basak AN. Bell's palsy and choreiform movements during peginterferon alpha and ribavirin therapy. World Journal of Gastroenterology : Wjg. 15: 3694-6. PMID 19653353 DOI: 10.3748/wjg.15.3694  0.88
2009 Taskapilioglu O, Seferoglu M, Akkaya C, Hakyemez B, Yusufoglu C, Basak AN, Gundogdu A, Bora I. Delayed diagnosis of a neuroBehçet patient with only brainstem and cerebellar atrophy: literature review. Journal of the Neurological Sciences. 277: 160-3. PMID 19000937 DOI: 10.1016/j.jns.2008.10.003  0.88
2008 Selcuk Duru N, Celkan T, Civilibal M, Ozbek NO, Basak AN, Elevli M. Coinheritance of sickle cell anemia and hereditary spherocytosis. Pediatric Blood & Cancer. 51: 560-3. PMID 18561176 DOI: 10.1002/pbc.21642  0.88
2006 Metzger S, Bauer P, Tomiuk J, Laccone F, Didonato S, Gellera C, Mariotti C, Lange HW, Weirich-Schwaiger H, Wenning GK, Seppi K, Melegh B, Havasi V, Balikó L, Wieczorek S, ... ... Basak AN, et al. Genetic analysis of candidate genes modifying the age-at-onset in Huntington's disease. Human Genetics. 120: 285-92. PMID 16847693 DOI: 10.1007/s00439-006-0221-2  0.88
2006 Metzger S, Bauer P, Tomiuk J, Laccone F, Didonato S, Gellera C, Soliveri P, Lange HW, Weirich-Schwaiger H, Wenning GK, Melegh B, Havasi V, Balikó L, Wieczorek S, Arning L, ... ... Basak AN, et al. The S18Y polymorphism in the UCHL1 gene is a genetic modifier in Huntington's disease. Neurogenetics. 7: 27-30. PMID 16369839 DOI: 10.1007/s10048-005-0023-z  0.88
2002 Bilenoglu O, Basak AN, Russell JE. A 3'UTR mutation affects beta-globin expression without altering the stability of its fully processed mRNA. British Journal of Haematology. 119: 1106-14. PMID 12472595 DOI: 10.1046/j.1365-2141.2002.03989.x  0.88
1997 Tüzmen S, Basak AN, Baysal E. Rare beta-thalassemia mutation IVS-II-848 (C-A) first reported in a Turkish Cypriot family. American Journal of Hematology. 54: 338-9. PMID 9092695 DOI: 10.1002/(SICI)1096-8652(199704)54:4<338::AID-AJH16>3.0.CO;2-7  0.88
1996 Altay C, Gürgey A, Basak AN, Tadmouri GO, Schroeder-Kurt T. Fanconi aplastic anemia associated with beta-thalassemia trait. American Journal of Hematology. 52: 239-40. PMID 8756104 DOI: 10.1002/(SICI)1096-8652(199607)52:3<239::AID-AJH26>3.0.CO;2-9  0.48
1990 Mink M, Basak AN, Küntzel H. Restoration of the yeast LEU2 gene by transcriptionally controlled recombination between tandem repeats. Molecular & General Genetics : Mgg. 223: 107-13. PMID 2259332 DOI: 10.1007/BF00315802  0.88
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