List of works - Hilal Özdag

A 1 Mb minimal amplicon at 8p11-12 in breast cancer identifies new candidate oncogenes

scientific article

A founder TMIE mutation is a frequent cause of hearing loss in southeastern Anatolia

scientific article published on 5 May 2009

A novel approach for small sample size family-based association studies: sequential tests ⬇️

scientific article published on March 23, 2011

Behçet's: A Disease or a Syndrome? Answer from an Expression Profiling Study

scientific article published on 18 February 2016

Biologic tumor behavior in pilocytic astrocytomas

scientific article published on 14 January 2012

C-type lectin domain family 12, member A: A common denominator in Behçet's syndrome and acute gouty arthritis

scientific article published on 02 May 2015

EMSY links the BRCA2 pathway to sporadic breast and ovarian cancer

scientific article (publication date: 26 November 2003)

From RNA isolation to microarray analysis: Comparison of methods in FFPE tissues

scientific article published on 12 February 2016

Functionally conserved effects of rapamycin exposure on zebrafish.

scientific article published on 28 March 2016

Genome Sequence of the Boron-Tolerant and -Requiring Bacterium Bacillus boroniphilus.

scientific article published on 2 January 2014

Genome-wide transcriptional reorganization associated with senescence-to-immortality switch during human hepatocellular carcinogenesis

scientific article

H2AX gene does not have a modifier effect on ataxia-telangiectasia phenotype

article

Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontia

scientific article

Isotopic biomarker discovery and application in translational medicine.

scientific article published on 28 December 2009

Mutations in TMC1 contribute significantly to nonsyndromic autosomal recessive sensorineural hearing loss: a report of five novel mutations.

scientific article published in February 2009

Novel plasminogen gene mutations in Turkish patients with type I plasminogen deficiency

scientific article published on 01 September 2016

Optimization of gene expression microarray protocol for formalin-fixed paraffin-embedded tissues

scientific article published on 6 February 2016

Protocol for qRT-PCR analysis from formalin fixed paraffin embedded tissue sections from diffuse large b-cell lymphoma: Validation of the six-gene predictor score.

scientific article

Recurrent and private MYO15A mutations are associated with deafness in the Turkish population.

scientific article published in August 2010

Screening of 38 genes identifies mutations in 62% of families with nonsyndromic deafness in Turkey

scientific article published on 30 November 2010

The effect of biological heterogeneity on R-CHOP treatment outcome in diffuse large B-cell lymphoma across five international regions

scientific article published on 10 October 2016

p300 regulates p53-dependent apoptosis after DNA damage in colorectal cancer cells by modulation of PUMA/p21 levels

scientific article

List of works by Hilal Özdag

A 1 Mb minimal amplicon at 8p11-12 in breast cancer identifies new candidate oncogenes

A founder TMIE mutation is a frequent cause of hearing loss in southeastern Anatolia

A novel approach for small sample size family-based association studies: sequential tests ⬇️

Behçet's: A Disease or a Syndrome? Answer from an Expression Profiling Study

Biologic tumor behavior in pilocytic astrocytomas

C-type lectin domain family 12, member A: A common denominator in Behçet's syndrome and acute gouty arthritis

EMSY links the BRCA2 pathway to sporadic breast and ovarian cancer

From RNA isolation to microarray analysis: Comparison of methods in FFPE tissues

Functionally conserved effects of rapamycin exposure on zebrafish.

Genome Sequence of the Boron-Tolerant and -Requiring Bacterium Bacillus boroniphilus.

Genome-wide transcriptional reorganization associated with senescence-to-immortality switch during human hepatocellular carcinogenesis

H2AX gene does not have a modifier effect on ataxia-telangiectasia phenotype

Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontia

Isotopic biomarker discovery and application in translational medicine.

Mutations in TMC1 contribute significantly to nonsyndromic autosomal recessive sensorineural hearing loss: a report of five novel mutations.

Novel plasminogen gene mutations in Turkish patients with type I plasminogen deficiency

Optimization of gene expression microarray protocol for formalin-fixed paraffin-embedded tissues

Protocol for qRT-PCR analysis from formalin fixed paraffin embedded tissue sections from diffuse large b-cell lymphoma: Validation of the six-gene predictor score.

Recurrent and private MYO15A mutations are associated with deafness in the Turkish population.

Screening of 38 genes identifies mutations in 62% of families with nonsyndromic deafness in Turkey

The effect of biological heterogeneity on R-CHOP treatment outcome in diffuse large B-cell lymphoma across five international regions

p300 regulates p53-dependent apoptosis after DNA damage in colorectal cancer cells by modulation of PUMA/p21 levels