| Year |
Citation |
Score |
| 2020 |
Akar OS, Gunes S, Abur U, Altundag E, Asci R, Onat OE, Ozcelik T, Ogur G. Multiscale analysis of SRY-positive 46,XX testicular disorder of sex development: Presentation of nine cases. Andrologia. e13739. PMID 32882067 DOI: 10.1111/And.13739 |
0.381 |
|
| 2018 |
Demirayak P, Onat OE, Gevrekci AÖ, Gülsüner S, Uysal H, Bilgen RS, Doerschner K, Özçelik TS, Boyacı H. Abnormal subcortical activity in congenital mirror movement disorder with RAD51 mutation. Diagnostic and Interventional Radiology (Ankara, Turkey). 24: 392-401. PMID 30406765 DOI: 10.5152/Dir.2018.18096 |
0.591 |
|
| 2018 |
Urgen BM, Topac Y, Ustun FS, Demirayak P, Oguz KK, Kansu T, Saygi S, Ozcelik T, Boyaci H, Doerschner K. Homozygous LAMC3 mutation links to structural and functional changes in visual attention networks. Neuroimage. PMID 29626609 DOI: 10.1016/J.Neuroimage.2018.03.077 |
0.3 |
|
| 2018 |
Demirayak P, Sen M, Ustun S, Gungor M, Topaloglu H, Celik ND, Akbostanci MC, Ozcelik T, Tekinay AB, Oguz KK. Morphometric and Microstructural Alterations Differ with Age of Onset in Patients with Essential Tremor Journal of Neurological Disorders. 6. DOI: 10.4172/2329-6895.1000373 |
0.333 |
|
| 2016 |
Özçelik T, Onat OE. Genomic landscape of the Greater Middle East. Nature Genetics. 48: 978-9. PMID 27573686 DOI: 10.1038/Ng.3652 |
0.323 |
|
| 2016 |
Kanaan SB, Onat OE, Balandraud N, Martin GV, Nelson JL, Azzouz DF, Auger I, Arnoux F, Martin M, Roudier J, Ozcelik T, Lambert NC. Evaluation of X Chromosome Inactivation with Respect to HLA Genetic Susceptibility in Rheumatoid Arthritis and Systemic Sclerosis. Plos One. 11: e0158550. PMID 27355582 DOI: 10.1371/Journal.Pone.0158550 |
0.314 |
|
| 2015 |
Doldur-Balli F, Ozel MN, Gulsuner S, Tekinay AB, Ozcelik T, Konu O, Adams MM. Characterization of a novel zebrafish (Danio rerio) gene, wdr81, associated with cerebellar ataxia, mental retardation and dysequilibrium syndrome (CAMRQ). Bmc Neuroscience. 16: 96. PMID 27390838 DOI: 10.1186/S12868-015-0229-4 |
0.67 |
|
| 2015 |
Unal Gulsuner H, Gulsuner S, Mercan FN, Onat OE, Walsh T, Shahin H, Lee MK, Dogu O, Kansu T, Topaloglu H, Elibol B, Akbostanci C, King MC, Ozcelik T, Tekinay AB. Reply to Tzoulis et al.: Genetic and clinical heterogeneity of essential tremor. Proceedings of the National Academy of Sciences of the United States of America. 112: E2269. PMID 25825780 DOI: 10.1073/Pnas.1503756112 |
0.687 |
|
| 2015 |
Doldur-Balli F, Ozel MN, Gulsuner S, Tekinay AB, Ozcelik T, Konu O, Adams MM. Characterization of a novel zebrafish (Danio rerio) gene, wdr81, associated with cerebellar ataxia, mental retardation and dysequilibrium syndrome (CAMRQ) Bmc Neuroscience. 16. DOI: 10.1186/s12868-015-0229-4 |
0.636 |
|
| 2014 |
Unal Gulsuner H, Gulsuner S, Mercan FN, Onat OE, Walsh T, Shahin H, Lee MK, Dogu O, Kansu T, Topaloglu H, Elibol B, Akbostanci C, King MC, Ozcelik T, Tekinay AB. Mitochondrial serine protease HTRA2 p.G399S in a kindred with essential tremor and Parkinson disease. Proceedings of the National Academy of Sciences of the United States of America. 111: 18285-90. PMID 25422467 DOI: 10.1073/Pnas.1419581111 |
0.679 |
|
| 2014 |
Dal GM, Ergüner B, Sa??ro?lu MS, Yüksel B, Onat OE, Alkan C, Özçelik T. Early postzygotic mutations contribute to de novo variation in a healthy monozygotic twin pair. Journal of Medical Genetics. 51: 455-9. PMID 24764354 DOI: 10.1136/Jmedgenet-2013-102197 |
0.333 |
|
| 2013 |
Ozçelik T. 2012 William Allan Award introduction: Uta Francke. American Journal of Human Genetics. 92: 323-4. PMID 23472753 DOI: 10.1016/J.Ajhg.2012.12.018 |
0.392 |
|
| 2013 |
Okten G, Gunes S, Onat OE, Tukun A, Ozcelik T, Kocak I. Disruption of HDX gene in premature ovarian failure. Systems Biology in Reproductive Medicine. 59: 218-22. PMID 23441923 DOI: 10.3109/19396368.2013.769028 |
0.376 |
|
| 2013 |
Gunes S, Asci R, Okten G, Atac F, Onat OE, Ogur G, Aydin O, Ozcelik T, Bagci H. Two males with SRY-positive 46,XX testicular disorder of sex development. Systems Biology in Reproductive Medicine. 59: 42-7. PMID 23110663 DOI: 10.3109/19396368.2012.731624 |
0.372 |
|
| 2013 |
Onat OE, Gulsuner S, Bilguvar K, Nazli Basak A, Topaloglu H, Tan M, Tan U, Gunel M, Ozcelik T. Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion. European Journal of Human Genetics : Ejhg. 21: 281-5. PMID 22892528 DOI: 10.1038/Ejhg.2012.170 |
0.701 |
|
| 2012 |
Sarac O, Gulsuner S, Yildiz-Tasci Y, Ozcelik T, Kansu T. Neuro-ophthalmologic findings in humans with quadrupedal locomotion. Ophthalmic Genetics. 33: 249-52. PMID 22686558 DOI: 10.3109/13816810.2012.689412 |
0.665 |
|
| 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, ... Ozcelik T, 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 |
0.69 |
|
| 2011 |
Barak T, Kwan KY, Louvi A, Demirbilek V, Sayg? S, Tüysüz B, Choi M, Boyac? H, Doerschner K, Zhu Y, Kaymakçalan H, Y?lmaz S, Bak?rc?o?lu M, Ca?layan AO, Oztürk AK, et al. Recessive LAMC3 mutations cause malformations of occipital cortical development. Nature Genetics. 43: 590-4. PMID 21572413 DOI: 10.1038/Ng.836 |
0.371 |
|
| 2011 |
Azzouz DF, Onat OE, Balandraud N, Kanaan SB, Roudier J, Ozcelik T, Lambert NC. Skewed X chromosome inactivation in rheumatoid arthritis women Annals of the Rheumatic Diseases. 70: A88-A88. DOI: 10.1136/Ard.2010.149021.16 |
0.312 |
|
| 2010 |
Kolb LE, Arlier Z, Yalcinkaya C, Ozturk AK, Moliterno JA, Erturk O, Bayrakli F, Korkmaz B, DiLuna ML, Yasuno K, Bilguvar K, Ozcelik T, Tuysuz B, State MW, Gunel M. Novel VLDLR microdeletion identified in two Turkish siblings with pachygyria and pontocerebellar atrophy. Neurogenetics. 11: 319-25. PMID 20082205 DOI: 10.1007/S10048-009-0232-Y |
0.431 |
|
| 2009 |
Uz E, Mustafa C, Topaloglu R, Bilginer Y, Dursun A, Kasapcopur O, Ozen S, Bakkaloglu A, Ozcelik T. Increased frequency of extremely skewed X chromosome inactivation in juvenile idiopathic arthritis. Arthritis and Rheumatism. 60: 3410-2. PMID 19877028 DOI: 10.1002/Art.24956 |
0.35 |
|
| 2009 |
Chabchoub G, Uz E, Maalej A, Mustafa CA, Rebai A, Mnif M, Bahloul Z, Farid NR, Ozcelik T, Ayadi H. Analysis of skewed X-chromosome inactivation in females with rheumatoid arthritis and autoimmune thyroid diseases. Arthritis Research & Therapy. 11: R106. PMID 19589151 DOI: 10.1186/Ar2759 |
0.312 |
|
| 2008 |
Plagnol V, Uz E, Wallace C, Stevens H, Clayton D, Ozcelik T, Todd JA. Extreme clonality in lymphoblastoid cell lines with implications for allele specific expression analyses. Plos One. 3: e2966. PMID 18698422 DOI: 10.1371/Journal.Pone.0002966 |
0.307 |
|
| 2008 |
Ozcelik T, Akarsu N, Uz E, Caglayan S, Gulsuner S, Onat OE, Tan M, Tan U. Reply to Herz et al. and Humphrey et al.: Genetic heterogeneity of cerebellar hypoplasia with quadrupedal locomotion. Proceedings of the National Academy of Sciences of the United States of America. 105: E32-3. PMID 18544652 DOI: 10.1073/Pnas.0804078105 |
0.649 |
|
| 2008 |
Ozcelik T, Akarsu N, Uz E, Caglayan S, Gulsuner S, Onat OE, Tan M, Tan U. Mutations in the very low-density lipoprotein receptor VLDLR cause cerebellar hypoplasia and quadrupedal locomotion in humans. Proceedings of the National Academy of Sciences of the United States of America. 105: 4232-6. PMID 18326629 DOI: 10.1073/Pnas.0710010105 |
0.699 |
|
| 2008 |
Uz E, Loubiere LS, Gadi VK, Ozbalkan Z, Stewart J, Nelson JL, Ozcelik T. Skewed X-chromosome inactivation in scleroderma. Clinical Reviews in Allergy & Immunology. 34: 352-5. PMID 18157513 DOI: 10.1007/S12016-007-8044-Z |
0.356 |
|
| 2008 |
Ozcelik T. X chromosome inactivation and female predisposition to autoimmunity. Clinical Reviews in Allergy & Immunology. 34: 348-51. PMID 18097773 DOI: 10.1007/S12016-007-8051-0 |
0.374 |
|
| 2008 |
Kaplan Y, Vargel I, Kansu T, Akin B, Rohmann E, Kamaci S, Uz E, Ozcelik T, Wollnik B, Akarsu NA. Skewed X inactivation in an X linked nystagmus family resulted from a novel, p.R229G, missense mutation in the FRMD7 gene. The British Journal of Ophthalmology. 92: 135-41. PMID 17962394 DOI: 10.1136/Bjo.2007.128157 |
0.363 |
|
| 2007 |
Hatirnaz O, Ure U, Ar C, Akyerli C, Soysal T, Ferhano?lu B, Ozçelik T, Ozbek U. The SOCS-1 gene methylation in chronic myeloid leukemia patients. American Journal of Hematology. 82: 729-30. PMID 17315216 DOI: 10.1002/Ajh.20886 |
0.332 |
|
| 2007 |
Uz E, Dolen I, Al AR, Ozcelik T. Extremely skewed X-chromosome inactivation is increased in pre-eclampsia. Human Genetics. 121: 101-5. PMID 17115188 DOI: 10.1007/S00439-006-0281-3 |
0.349 |
|
| 2006 |
Onat OE, Tez M, Ozçelik T, Törüner GA. MDM2 T309G polymorphism is associated with bladder cancer. Anticancer Research. 26: 3473-5. PMID 17094469 |
0.587 |
|
| 2006 |
Bagislar S, Ustuner I, Cengiz B, Soylemez F, Akyerli CB, Ceylaner S, Ceylaner G, Acar A, Ozcelik T. Extremely skewed X-chromosome inactivation patterns in women with recurrent spontaneous abortion. The Australian & New Zealand Journal of Obstetrics & Gynaecology. 46: 384-7. PMID 16953851 DOI: 10.1111/J.1479-828X.2006.00622.X |
0.313 |
|
| 2006 |
Ozcelik T, Uz E, Akyerli CB, Bagislar S, Mustafa CA, Gursoy A, Akarsu N, Toruner G, Kamel N, Gullu S. Evidence from autoimmune thyroiditis of skewed X-chromosome inactivation in female predisposition to autoimmunity. European Journal of Human Genetics : Ejhg. 14: 791-7. PMID 16596118 DOI: 10.1038/Sj.Ejhg.5201614 |
0.633 |
|
| 2005 |
Ozbalkan Z, Bagi?lar S, Kiraz S, Akyerli CB, Ozer HT, Yavuz S, Birlik AM, Calgüneri M, Ozçelik T. Skewed X chromosome inactivation in blood cells of women with scleroderma. Arthritis and Rheumatism. 52: 1564-70. PMID 15880831 DOI: 10.1002/Art.21026 |
0.346 |
|
| 2004 |
Ozcelik T, Vakil V, Smith E, Braunstein M, Maroney J, Klueppelberg U, Bagislar S, Akyerli C, Batuman O. Evidence for Clonality in Circulating Endothelial Progenitor Cells in Multiple Myeloma. Blood. 104: 2357-2357. DOI: 10.1182/Blood.V104.11.2357.2357 |
0.335 |
|
| 2002 |
Ozçelik T. Uncovering the complex mysteries of mosaicism. Nature. 417: 588. PMID 12050634 DOI: 10.1038/417588A |
0.41 |
|
| 2002 |
Topçu M, Akyerli C, Sayi A, Törüner GA, Koço?lu SR, Cimbi? M, Ozçelik T. Somatic mosaicism for a MECP2 mutation associated with classic Rett syndrome in a boy. European Journal of Human Genetics : Ejhg. 10: 77-81. PMID 11896459 DOI: 10.1038/Sj.Ejhg.5200745 |
0.671 |
|
| 2002 |
Sullivan A, Yuille M, Repellin C, Reddy A, Reelfs O, Bell A, Dunne B, Gusterson BA, Osin P, Farrell PJ, Yulug I, Evans A, Ozcelik T, Gasco M, Crook T. Concomitant inactivation of p53 and Chk2 in breast cancer. Oncogene. 21: 1316-24. PMID 11857075 DOI: 10.1038/Sj.Onc.1205207 |
0.319 |
|
| 2001 |
Törüner GA, Uçar A, Tez M, Cetinkaya M, Ozen H, Ozçelik T. P53 codon 72 polymorphism in bladder cancer--no evidence of association with increased risk or invasiveness. Urological Research. 29: 393-5. PMID 11828992 DOI: 10.1007/S002400100218 |
0.614 |
|
| 2001 |
Törüner GA, Akyerli C, Uçar A, Aki T, Atsu N, Ozen H, Tez M, Cetinkaya M, Ozçelik T. Polymorphisms of glutathione S-transferase genes (GSTM1, GSTP1 and GSTT1) and bladder cancer susceptibility in the Turkish population. Archives of Toxicology. 75: 459-64. PMID 11757669 DOI: 10.1007/S002040100268 |
0.6 |
|
| 2001 |
Topaloglu R, Akierli C, Bakkaloglu A, Aydintug O, Ozen S, Besbas N, Ozcelik T. Survey of factor V Leiden and prothrombin gene mutations in systemic lupus erythematosus Clinical Rheumatology. 20: 259-261. PMID 11529632 DOI: 10.1007/S100670170040 |
0.348 |
|
| 2000 |
Ozdag H, Tez M, Sayek I, Müslümanoglu M, Tarcan O, Içli F, Oztürk M, Ozçelik T. Germ line BRCA1 and BRCA2 gene mutations in Turkish breast cancer patients. European Journal of Cancer (Oxford, England : 1990). 36: 2076-82. PMID 11044644 DOI: 10.1016/S0959-8049(00)00277-X |
0.352 |
|
| 2000 |
Mazoyer S, Leary J, Kirk J, Fleischmann E, Wagner T, Claes K, Messiaen L, Foulkes W, Desrochers M, Simard J, Phelan CM, Kwan E, Narod SA, Vahteristo P, Nevanlinna H, et al. The exon 13 duplication in the BRCA1 gene is a founder mutation present in geographicaly diverse populations American Journal of Human Genetics. 67: 207-212. PMID 10827109 DOI: 10.1086/302974 |
0.363 |
|
| 1999 |
Gul A, Aslantas AB, Tekinay T, Konice M, Ozcelik T. Procoagulant mutations and venous thrombosis in Behcet's disease [4] Rheumatology. 38: 1298-1299. PMID 10587567 DOI: 10.1093/Rheumatology/38.12.1298 |
0.315 |
|
| 1996 |
Gül A, Ozbek U, Oztürk C, Inanç M, Koniçe M, Ozçelik T. Coagulation factor V gene mutation increases the risk of venous thrombosis in behçet's disease. British Journal of Rheumatology. 35: 1178-80. PMID 8948311 DOI: 10.1093/Rheumatology/35.11.1178 |
0.381 |
|
| 1993 |
Rivera H, Lindgren V, Bryke CR, Ozcelik T, Yang-Feng TL, Francke U. Remarks on constitutional 5q deletions [3] American Journal of Human Genetics. 53: 532-534. PMID 8328466 |
0.4 |
|
| 1993 |
Andres DA, Milatovich A, Ozçelik T, Wenzlau JM, Brown MS, Goldstein JL, Francke U. cDNA cloning of the two subunits of human CAAX farnesyltransferase and chromosomal mapping of FNTA and FNTB loci and related sequences. Genomics. 18: 105-12. PMID 8276393 DOI: 10.1006/Geno.1993.1432 |
0.455 |
|
| 1993 |
Ibraghimov-Beskrovnaya O, Milatovich A, Ozcelik T, Yang B, Koepnick K, Francke U, Campbell KP. Human dystroglycan: skeletal muscle cDNA, genomic structure, origin of tissue specific isoforms and chromosomal localization. Human Molecular Genetics. 2: 1651-7. PMID 8268918 DOI: 10.1093/Hmg/2.10.1651 |
0.504 |
|
| 1992 |
Suter U, Welcher AA, Ozcelik T, Snipes GJ, Kosaras B, Francke U, Billings-Gagliardi S, Sidman RL, Shooter EM. Trembler mouse carries a point mutation in a myelin gene. Nature. 356: 241-4. PMID 1552943 DOI: 10.1038/356241A0 |
0.559 |
|
| 1992 |
Berkemeier LR, Ozçelik T, Francke U, Rosenthal A. Human chromosome 19 contains the neurotrophin-5 gene locus and three related genes that may encode novel acidic neurotrophins. Somatic Cell and Molecular Genetics. 18: 233-45. PMID 1496419 DOI: 10.1007/Bf01233860 |
0.532 |
|
| 1992 |
Murphy PM, Ozçelik T, Kenney RT, Tiffany HL, McDermott D, Francke U. A structural homologue of the N-formyl peptide receptor. Characterization and chromosome mapping of a peptide chemoattractant receptor family. The Journal of Biological Chemistry. 267: 7637-43. PMID 1373134 |
0.4 |
|
| 1992 |
Davidson JJ, Ozçelik T, Hamacher C, Willems PJ, Francke U, Kilimann MW. cDNA cloning of a liver isoform of the phosphorylase kinase alpha subunit and mapping of the gene to Xp22.2-p22.1, the region of human X-linked liver glycogenosis. Proceedings of the National Academy of Sciences of the United States of America. 89: 2096-100. PMID 1372435 DOI: 10.1073/Pnas.89.6.2096 |
0.516 |
|
| 1992 |
Lindgren V, Bryke CR, Ozcelik T, Yang-Feng TL, Francke U. Phenotypic, cytogenetic, and molecular studies of three patients with constitutional deletions of chromosome 5 in the region of the gene for familial adenomatous polyposis. American Journal of Human Genetics. 50: 988-97. PMID 1315124 |
0.502 |
|
| 1992 |
Leff SE, Brannan CI, Reed ML, Ozçelik T, Francke U, Copeland NG, Jenkins NA. Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region. Nature Genetics. 2: 259-64. PMID 1303276 DOI: 10.1038/Ng1292-259 |
0.56 |
|
| 1992 |
Ahuja SK, Ozçelik T, Milatovitch A, Francke U, Murphy PM. Molecular evolution of the human interleukin-8 receptor gene cluster. Nature Genetics. 2: 31-6. PMID 1303245 DOI: 10.1038/Ng0992-31 |
0.491 |
|
| 1991 |
Ozçelik T, Rosenthal A, Francke U. Chromosomal mapping of brain-derived neurotrophic factor and neurotrophin-3 genes in man and mouse. Genomics. 10: 569-75. PMID 1889807 DOI: 10.1016/0888-7543(91)90437-J |
0.533 |
|
| 1991 |
Perin MS, Johnston PA, Ozcelik T, Jahn R, Francke U, Südhof TC. Structural and functional conservation of synaptotagmin (p65) in Drosophila and humans. The Journal of Biological Chemistry. 266: 615-22. PMID 1840599 |
0.438 |
|
| 1991 |
Archidiacono N, Lerone M, Rocchi M, Anvret M, Ozcelik T, Francke U, Romeo G. Rett syndrome: exclusion mapping following the hypothesis of germinal mosaicism for new X-linked mutations. Human Genetics. 86: 604-6. PMID 1673961 DOI: 10.1007/Bf00201549 |
0.553 |
|
| 1990 |
Archer BT, Ozçelik T, Jahn R, Francke U, Südhof TC. Structures and chromosomal localizations of two human genes encoding synaptobrevins 1 and 2. The Journal of Biological Chemistry. 265: 17267-73. PMID 1976629 |
0.487 |
|
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