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Scientific Secretary
MAIN TOPICS
- Evolution of Human Genetics
- Cancer Genetics
- Multifactorial Disorders
- Chromosomal Disorders ( Flow Charts in Diagnostic Approach; new Technologies in diagnosis)
- Neurogenetics and Neurobiology
- Prenatal Diagnosis and PGD
- Genetic Counselling
- Planning of Genetic Research
- Biochemical Genetics
- Pharmacogenetics
- Quality Standardization in Laboratories and Patenting
- Ethics and Law
- Course : How to clone a gene?
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MAY 5th, 2008, Monday
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MAY 6th, 2008, Tuesday
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MAY 7th, 2008, Wednesday
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MAY 8th, 2008, Thursday
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MAY 9th, 2008, Friday
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| MAY 5th, 2008, Monday |
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HAll A |
HAll B |
16:00-17:30
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Education session: 1
Genetic counselling
Genetic counselling for complex familial cases (interactive)
Adnan YÜKSEL / Gönül OGUR /
Tahsin YAKUT
Genetic counselling in patological ultrasonographic findings and fetal pathology (interactive)
Ferda PERÇİN / Serdar CEYLANER / Beyhan TÜYSÜZ |
| 18:00-20:00 |
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Education session: 2
Dysmorphology
Minor anomalies leading to diagnosis in dsymorphology (interactive)
Hülya KAYSERİLİ / Memnune YÜKSEL APAK / Ferda PERÇİN
The syndromes that medical geneticist has to know? Consensus for diagnostic criteria / follow-up protocols
Özgür ÇOĞULLU / Sevim BALCI |
| 21:00-22:30 |
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Education session (discussion)
How to organize laboratory tests for rare disorders?
Nursel ELÇİOĞLU / Hülya KAYSERİLİ
How to plan research at a clinical setting?
Fusun DÜZCAN / Ferda ÖZKINAY
How to plan educational courses /workshops?
Ajlan TÜKÜN / Feride ŞAHİN /
Ahmet DURSUN / Uğur ÖZBEK
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| MAY 6th, 2008, Tuesday |
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Hall A |
Hall B |
09:00- 13:00
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Registration |
Education session: 3
Mitochondrial diseases
Mitochondrial DNA and its pathology
Sıtkı ÖZTAŞ
Mitochondrial diseases: case discussions
Mine ÇALIŞKAN
Education session: 4
Neurologic / Muscular disorders
Neurologic examination; how does it support the diagnosis?
Adnan YÜKSEL
Genetic approach to muscular diseases
Piraye SERDAROĞLU |
| 13:00-14:00 |
LUNCH |
| 14:00-15:30 |
Course: How to clone a disease causing gene? (Session 1)
Nurten AKARSU / Tayfun ÖZÇELİK |
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| 15:30-16:00 |
COFFEE BREAK |
| 16:00-17:30 |
Course: How to clone a disease causing gene? (Session 2)
Nurten AKARSU / Tayfun ÖZÇELİK |
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| 18:00-18:30 |
OPENING CEREMONY
Chaired by : Güven LÜLECİ |
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| 18:30-19:30 |
CONFERENCE
A genomic view of human history
Mary-Claire KING
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| 19:30-21:30 |
Welcome Reception |
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| MAY 7th, 2008, Wednesday |
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Hall A |
Hall B |
| 09:00-09:45 |
Ergül Tunçbilek Session
CONFERENCE
Fragile X syndrome: from diagnostic applications to pathomechanisms
Jean Louis MANDEL |
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| 09:45-10:30 |
CONFERENCE
Cellular plasticity in the Drosophila nervous system
Angela GIANGRANDE |
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| 10:30-11:00 |
COFFEE BREAK |
| 11:00-12:30 |
Şükran Taçoy Session:
Approach to etiopathogenesis of MR/MCA cases
Differential diagnosis of non syndromic mental retardation
Koray BODUROĞLU
Algorthyms leading to the definite diagnosis of sendromic mental retardation
Derya ERÇAL
The molecular karyotyping technology and its application in the diagnosis of patients with mental retardation and other congenital malformation conditions
Joris VELTMAN |
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| 12:30-13:15 |
LUNCH |
| 13:15-14:00 |
SATELLITE SYMPOSIUM (Roche Diagnostics) |
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| 14:00-16:00 |
Session: The role of cytogenetic and molecular cytogenetics methods in diagnosis
Genomic variation: a continuum from SNPs to chromosome aneuploidy
Orsetta ZUFFARDI
MLPA analysis and subtelomeric FISH methodology for cryptic subtelomeric regions
Beyhan DURAK
Evaluation of marker chromosomes
Birsen KARAMAN
Neocentric marker chromosomes and their effects on the phenotype
Dilek AKTAŞ
Oral presentations: Cytogenetics/ molecular cytogenetics |
Session: Immunogenetics
T cell signaling and immune system pathologies
Batu ERMAN
The role of host genetics in respiratory system diseases for different pathogens
Ferda ÖZKINAY
Model for a complex genetic disorder: Behcet’s Disease
Ahmet GÜL
Transcriptional regulation of MHC genes and autoimmune diseases
Zeynep SERCAN
Oral presantations: Immunogenetics |
| 16:00-19:00 |
Social program/Site visits
Tour 1 - Çanakkale martyrdom
Tour 2 – Troy / Assos ( ancient sites)
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| MAY 8th, 2008, Thursday |
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Hall A |
Hall B |
08:10-08:50
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Meet the experts
Problems arising in molecular diagnostic testing
Engin YILMAZ / Serpil ERASLAN |
Meet the experts
Diagnostic approaches for the cases with ambiguous genitalia
Gönül OĞUR / Abdullah BEREKET |
| 09:00-09:45 |
CONFERENCE
The beginnings of medical genetics: Lessons from the past for the future
Peter S. HARPER |
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| 09:50-10:30 |
Session: Genetics of complex disorders
High resolution genome analysis and psychosis
Nurten AKARSU
Genetics of idiopathic epilepsy
Uğur ÖZBEK
Genetics and autism
Betül BAKKALOĞLU |
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| 10:30-11:00 |
COFFEE BREAK |
| 11:00-12:30 |
Oral presentations : Cancer genetics |
Oral presentations : Clinical genetics |
| 12:30-13:15 |
LUNCH |
| 13:15-14:00 |
Satellite symposium (Affymetrix) |
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| 14:00-15:30 |
CONFERENCE
Genomic analysis of inherited breast and ovarian cancer
Mary-Claire KING
CONFERENCE
Management of familial cancers
Daniela TURCHETTI |
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| 15:30-16:00 |
COFFEE BREAK |
| 16:00-17:30 |
Session: Molecular biology of cancer
Genes effected by BRCA1 expression and gene expression profiles in breast cancer tumours
Işık YULUĞ
Epigenetic disregulation mechanisms leading to DNA hypomethylation in cancer
Ali GÜRE
Gene patenting and licensing: beyond the Myriad case
Gert MATHIJS
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Session: Therapeutic approaches to cancer in the genome era
High throughput analysis for the identification of molecular markers in cancer research
Hilal ÖZDAĞ
Targeting chromosomal translocation products in cancer therapy
Aykut ÜREN
Personalized / individualized treatment modalities and follow-up of cancer patients
Ahmet DEMİRKAZIK
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| 17:30-
18:00 |
Retirement Ceremony |
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| 19:30 |
GALA DINNER |
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| MAY 9th, 2008, Friday |
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Hall A |
Hall B |
08:10-08:50
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Meet the experts
Problems encountered in diagnostic cytogenetic testing
Sevilhan ARTAN / Sibel KARAÜZÜM
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Meet the experts
Diagnostic pitfalls in skeletal dysplasias
Beyhan TÜYSÜZ / Yasemin ALANAY |
| 09:00-09:45 |
CONFERENCE
Genetic services: the challenge of disseminating the appropriate
information
Ségolène AYMÉ |
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| 09:50-10:30 |
CONFERENCE
Congenital Disorders of Glycosylation: a rapidly expanding group of inborn errors of metabolism
Gert MATHIJS |
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| 10:30-11:00 |
COFFEE BREAK |
| 11:00-12:30 |
Sesssion: Gene cloning strategies in rare diseases
The genetic basis of distal arthrogryposes
Reha TOLUN
Mutations in LRP2, encoding the multiligand receptor megalin, cause Donnai-Barrow syndrome
Sibel KANTARCI
Clinical and genetic approaches to neuronal migration anomalies
Gökhan UYANIK |
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| 12:30-13:15 |
LUNCH |
| 13:15-14:00 |
SATELLITE MEETING |
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| 14:00-15:00 |
Session: Biochemical Genetics
Diagnosis, algorthyms and high resolution technologies in metabolic disorders
Ali DURSUN
Biochemical analysis of lysosomal diseases during prenatal and postnatal periods
Alan COOPER |
Session: Prenatal diagnosis / Preimplantation Genetics
Role of biochemical screening tests in prenatal diagnosis
Seher BAŞARAN
Alternative methods in diagnosis of chromosomal aneuploidies: interphase FISH / QF-PCR
Hüseyin ONAY
PGD: Update of clinical modalities
Muhterem BAHÇE |
| 15:00-16:00 |
Oral presentations:
Molecular and biochemical pathology of diseases |
Oral presentations :
Prenatal diagnosis / Preimplantation genetic diagnosis (PGD) |
| 16:00-16:30 |
COFFEE BREAK |
| 16:30-17:30 |
CONFERENCE
Expanding the phenotypic and molecular spectrum of limb malformation syndromes
Bernd WOLLNIK
Awards ceremony
Closing remarks |
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