Ece Gül - ProZ.com

Ece Gül
Address : Türkiye - İstanbul - Şişli - Osmanbey
Home Telephone : 90 (212) 230 32 21
Cell Phone : 90 (543) 237 12 07
E-Mail : ortavalide@gmail.com
Personal Information
Total experience : 8 Years
Employment status : Freelancer
Educational Status : Master's Degree (Graduate)
Marital status : Single
Nationality : Turkey
Date of Birth : 22.02.1982
Place of birth : Turkey - İzmir
Driver's license : B (2001)
Education Information
University (Master's Degree) Istanbul University
10.2009- 02.2013 Institute Of Health Sciences, Genetik A.B.D.
University (Bachelor's Degree) Ege University
09.2000- 06.2004 Science Faculty, Biology
High School 60. Year Anatolian High School
05.2000
Foreign language
Reading Writing Speech
English Advanced Advanced Advanced
German Good Intermediate Intermediate
Job Experience
11.2011 - 01.2012
Department of Neurosurgery, Program on Neurogenetics (Gunel Lab), Yale
School of Medicine, New Haven USA
Visiting fellowship
Exome seqeunecing and data analysis
03.2010 - 02.2013
Istanbul University Cerrahpaşa Medical Faculty, Department of Pediatric
Genetics, Turkey
Graduate Assistant
DNA banking
Project assistant
Blood and tissue culture, pre- and postnatal karyotype analysis, FISH
SNP array
10.2009 - 03.2011
Istanbul University, Institute of Experimental Medical Research
Trainee
DNA and RNA extraction from blood, tissue and cell line
PCR, Real time quantitative PCR
11.2005 - 01.2009
CSA Global Publishing
Biologist
Translating, editing, and proof-reading of medical publications, books and education materials
Working with the technical team for the final checkout
Producing content and briefs for marketing and sales department
Cooperating with customers, editors, and marketing and sales department
08.2005 - 09.2005 Prolab
Biologist/Intern
Biochemical and microbiological analysis
07.2003 - 09.2003 İzsu İzmir Çiğli Wastewater Treatment Facility İzmir
Biologist/Intern
Determination of inorganic and organic matter in wastewater and sludge
Bacteriological analysis of wastewater
Enhanced biological phosphorus removal
Computer skills microsoft office (word, excel, powerpoint) and DNA analysis programs
Certificate Information ZD ( Zertifikat Deutsch )
GOETHE- INSTITUT - 24.06.2004
Seminars and Courses
4. DETAE DAYS
Istanbul University, Institute of Experimental Medical Research 12.11.2012 - 15.11.2012 (24
Hours)
Western Blot Training
Istanbul Technical University 08.09.2012 - 09.09.2012 (16 Hours)
Neurometabolic Dysmorphology Symposium
Istanbul University 25.02.2011 - 26.02.2011 (16 Hours)
Annual Symposium of the Society of Inborn Errors of Metabolism
Society of Inborn Errors of Metabolism 31.08.2010 - 03.09.2010 (32 Hours)
Effective Speaking and Diction
Bilgi University Ece Okay Işıldar 03.12.2007 - 21.01.2008 (20 Hours)
Team Development Seminar
Baltaş-Baltaş 27.04.2007 - 28.04.2007 (16 Hours)
Translation 1 (English)
Yıldız Teknik University 02.12.2005 - 04.02.2006 (32 Hours)
Neurobiology Winter School
Ege University (EBILTEM) 17.02.2003 - 23.02.2003 (32 Hours)
Research Methods in Biological Sciences
Ege University ( EBILTEM ) 26.08.2002 - 01.09.2002 (32 Hours)
Publications
Beyhan Tüysüz, Saliha Yılmaz, Ece Gül, Luis Kolb, Kaya Bilguvar, Olcay Evliyaoğlu, Murat Günel. Expanding The
Clinical Phenotype of Spondyloepimethaphyseal Dyslasia Pakistani Type Caused By PAPSS2 Deficiency in a
Large Turkish Family. American Journal of Human Genetics. In press 2013.
Nilay Güneş, Sibel, Filiz Basak Cengiz, Duygu Duman, Ece Gül, Mustafa Tekin, Beyhan Tüysüz. (2013) Branchiooculofacial syndrome (BOFS) in a newborn caused by a novel mutation of TFAP2A gene. (Manuscript submitted
for publication).
Beyhan Tüysüz, Kaya Bilguvar, Cengiz Yalçınkaya, Naci Koçer, Okay Çağlayan, Ece Gül, Sinan Çomu, Murat
Günel. Autosomal recessive spastic quadriplegia with severe mental retardation and specific MRI findings caused
by homozygous AP4M1 and AP4B1 gene mutation. (Manuscript submitted for publication).
Reports
B Tüysüz, S Yılmaz, K Bilguvar, O Kasapçopur, E Gül, M Günel. Autosomal-recessive primary hypertrophic
osteoarthropathy caused by homozygous deletion in HPGD gene: Neonatal findings and long-term follow-up.
American Society of Human Genetics Annual Meeting, P 252.3132F, November 2012, San Francisco, USA
E Gül, S Yılmaz, K Bilguvar, Ö Kasapçopur, M Günel, B Tüysüz. Eleven patients with Camptodactyly-Arthropathy
syndrome in a kindred Turkish family caused by a novel 1 bp homozygous deletion in PRG4 gene. European
Journal of Human Genetics. Volume 20 Suppl. 1 P02.051, June 2012, Nürnberg, Germany
E Gül, A Payaş, S Yılmaz, A Aydın, B Tüysüz. Replacement Therapy in 10 Patients with Mps Type-6. Journal of
Inherited Metabolic Disease. Volume 33 Suppl.1 S148.475-P, August 2010, İstanbul, Turkey.
References
Beyhan Tüysüz
Istanbul University Cerrahpaşa Medical Faculty,
Department of Pediatric Genetics - Professor Doctor
Tel : 05325077863 | E-Mail : beyhan@istanbul.edu.tr
Sibel Aylin Uğur İşeri
Istanbul University, Institute of Experimental Medical
Research - Lecturer Doctor
Tel : 05334630562 | E-Mail : ugursibel@yahoo.com
Sevgi Beyazova
The GADA Group - Senior Product Manager
Tel : 05307638066 | E-Mail : sevgibey@gmail.com
Çiğdem Ergül Kahraman
Siemens Healthcare - Business Manager
Tel : 05308747392
Hobbies : Short film making, Scuba Diving (CMAS 1*), swimming, trekking, traveling
Smoking : I don't smoke