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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 | 540 | 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, 1-15, 2006 | 327 | 2006 |
| Human mlh1 deficiency predisposes to hematological maligancy and neurofibromatosis type MD Ricciardone, T Ozçelik, B Cevher, H Ozdag, M Tuncer, A Gürgey, ... Cancer research 59 (2), 290-293, 1999 | 322 | 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 | 192 | 2004 |
| A 1 Mb minimal amplicon at 8p11–12 in breast cancer identifies new candidate oncogenes MJ Garcia, J Pole, SF Chin, A Teschendorff, A Naderi, H Ozdag, M Vias, ... Oncogene 24 (33), 5235-5245, 2005 | 177 | 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 | 165 | 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, I Aslan, ... The American Journal of Human Genetics 80 (2), 338-344, 2007 | 150 | 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 | 105 | 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 | 78 | 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 | 71 | 2010 |
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| 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 | 65 | 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 | 56 | 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 | 54 | 2010 |
| 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 | 36 | 2009 |
| 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 | 33 | 2000 |
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| 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 | 28 | 2016 |
| SLCO1B1 polymorphisms are associated with drug intolerance in childhood leukemia maintenance therapy I Eldem, D Yavuz, Ö Cumaoğullari, T Ileri, EÜ İnce, M Ertem, BD Erdoğan, ... Journal of Pediatric Hematology/Oncology 40 (5), e289-e294, 2018 | 23 | 2018 |
Carlos CaldasUniversity of CambridgeEmail yang diverifikasi di cruk.cam.ac.uk
