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| EMSY links the BRCA2 pathway to sporadic breast and ovarian cancer L Hughes-Davies, D Huntsman, M Ruas, F Fuks, J Bye, SF Chin, J Milner, ... Cell 115 (5), 523-535, 2003 | 470 | 2003 |
| Differential expression of selected histone modifier genes in human solid cancers H Özdağ, AE Teschendorff, AA Ahmed, SJ Hyland, C Blenkiron, L Bobrow, ... BMC genomics 7 (1), 1-15, 2006 | 281 | 2006 |
| Human MLH1 deficiency predisposes to hematological maligancy and neurofibromatosis type 1 MD Ricciardone, T Özçelik, B Cevher, H Özdağ, M Tuncer, A Gürgey, ... Cancer Research 59 (2), 290-293, 1999 | 277 | 1999 |
| p300 regulates p53-dependent apoptosis after DNA damage in colorectal cancer cells by modulation of PUMA/p21 levels NG Iyer, SF Chin, H Ozdag, Y Daigo, DE Hu, M Cariati, K Brindle, ... Proceedings of the National Academy of Sciences 101 (19), 7386-7391, 2004 | 170 | 2004 |
| A 1 Mb minimal amplicon at 8p11–12 in breast cancer identifies new candidate oncogenes MJ Garcia, JCM Pole, SF Chin, A Teschendorff, A Naderi, H Ozdag, ... Oncogene 24 (33), 5235-5245, 2005 | 166 | 2005 |
| Disruption of ALX1 causes extreme microphthalmia and severe facial clefting: expanding the spectrum of autosomal-recessive ALX-related frontonasal dysplasia E Uz, Y Alanay, D Aktas, I Vargel, S Gucer, G Tuncbilek, F von Eggeling, ... The American Journal of Human Genetics 86 (5), 789-796, 2010 | 118 | 2010 |
| Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontia M Tekin, BÖ Hişmi, S Fitoz, H Özdağ, FB Cengiz, A Sırmacı, İ Aslan, ... The American Journal of Human Genetics 80 (2), 338-344, 2007 | 116 | 2007 |
| Screening of 38 genes identifies mutations in 62% of families with nonsyndromic deafness in Turkey D Duman, A Sirmaci, FB Cengiz, H Ozdag, M Tekin Genetic testing and molecular biomarkers 15 (1-2), 29-33, 2011 | 77 | 2011 |
| Mutation analysis of CBP and PCAF reveals rare inactivating mutations in cancer cell lines but not in primary tumours H Özdağ, SJ Batley, A Försti, NG Iyer, Y Daigo, J Boutell, MJ Arends, ... British journal of cancer 87 (10), 1162-1165, 2002 | 75 | 2002 |
| A truncating mutation in SERPINB6 is associated with autosomal-recessive nonsyndromic sensorineural hearing loss A Sırmacı, S Erbek, J Price, M Huang, D Duman, FB Cengiz, G Bademci, ... The American Journal of Human Genetics 86 (5), 797-804, 2010 | 57 | 2010 |
| Genome-wide transcriptional reorganization associated with senescence-to-immortality switch during human hepatocellular carcinogenesis G Yildiz, A Arslan-Ergul, S Bagislar, O Konu, H Yuzugullu, ... PloS one 8 (5), e64016, 2013 | 47 | 2013 |
| Mutations in TMC1 contribute significantly to nonsyndromic autosomal recessive sensorineural hearing loss: a report of five novel mutations A Sırmacı, D Duman, H Öztürkmen-Akay, S Erbek, A İncesulu, ... International journal of pediatric otorhinolaryngology 73 (5), 699-705, 2009 | 44 | 2009 |
| Possible causes of chromosome instability: comparison of chromosomal abnormalities in cancer cell lines with mutations in BRCA1, BRCA2, CHK2 and BUB1 M Grigorova, JM Staines, H Ozdag, C Caldas, PAW Edwards Cytogenetic and genome research 104 (1-4), 333-340, 2004 | 44 | 2004 |
| Recurrent and private MYO15A mutations are associated with deafness in the Turkish population FB Cengiz, D Duman, A Sırmacı, S Tokgöz-Yilmaz, S Erbek, ... Genetic testing and molecular biomarkers 14 (4), 543-550, 2010 | 42 | 2010 |
| Germ line< i> BRCA1</i> and< i> BRCA2</i> gene mutations in Turkish breast cancer patients H Özdag, M Tez, I Sayek, M Müslümanoglu, O Tarcan, F Içli, M Öztürk, ... European Journal of Cancer 36 (16), 2076-2082, 2000 | 29 | 2000 |
| A founder TMIE mutation is a frequent cause of hearing loss in southeastern Anatolia A Sırmacı, H Öztürkmen‐Akay, S Erbek, A Incesulu, D Duman, ... Clinical genetics 75 (6), 562-567, 2009 | 22 | 2009 |
| Behçet's: A Disease or a syndrome? answer from an expression profiling study AK Oğuz, ST Yılmaz, ÇŞ Oygür, T Candar, I Sayın, SS Kılıçoğlu, İ Ergün, ... PLoS One 11 (2), e0149052, 2016 | 16 | 2016 |
| From RNA isolation to microarray analysis: comparison of methods in FFPE tissues N Belder, Ö Coskun, BD Erdogan, O Ilk, B Savas, A Ensari, H Özdağ Pathology-Research and Practice 212 (8), 678-685, 2016 | 15 | 2016 |
| A Novel (δβ)°-Thalassemia due to a∼ 30-kb Deletion Observed in a Turkish Family R Öner, C Öner, G Erdem, H Balkan, H Özdağ, M Erkan, F Gümrük, ... Acta haematologica 96 (4), 232-236, 1996 | 13 | 1996 |
Mustafa TekinDivision of Clinical and Translational Genetics, Miller School of Medicine, University of MiamiEmail verificata su miami.edu
