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NG Iyer, H Özdag, C Caldas
Oncogene 23 (24), 4225-4231, 2004
|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
|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), 90, 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
|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
|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
|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
|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
|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
|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
|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
|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
|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
|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
|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
|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
|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
|Behçet's: A disease or a syndrome? Answer from an expression profiling study|
AK Oğuz, ST Yılmaz, ÇŞ Oygür, T Çandar, I Sayın, SS Kılıçoğlu, İ Ergün, ...
PloS one 11 (2), e0149052, 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
|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