Instructor's Portfolio

Dr. CRISTINA SKRYPNYK


Assistant Professor

College of Medicine and Medical Sciences
Work Tel No: 17237315 Work Fax No: 17246022
cristinas@agu.edu.bh



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Qualifications

Qualifications

- University of Medicine "G. T. Popa",Iasi,Romania/Medical Doctor/1990-1996
- Ministry of Health, Office of Professional Qualification Recognition Romania/ Specialist Physician in Medical Genetics/2004
- University of Medicine "G. T. Popa"Iasi, Romania,Human Genetics Unit/PhD title in Medical Sciences/2007
- Ministry of Health, Office of Professional Qualification Recognition Romania/Consultant Physician in Medical Genetics/2009
- Ministry of Education and Research, Ministry of Labor Romania/Project Manager/2009

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Work Experience

Experience

- Assistant Professor/Arabian Gulf University, College of Medical Sciences, Manama,Bahrain/since 09.2010
- Consultant Medical Genetics/University Medical Center, King Abdulla Medical City, since 2016
- Consultant Medical Genetics/Al Jawhara Center for Molecular Medicine, Manama, Bahrain/since 09.2010-2016

-Assistant Professor/University of Oradea, Faculty of Medicine,Genetics Department
- Consultant Medical Genetics/Clinical Municipal Hospital „Dr.G.Curteanu",Genetics Depart.,Oradea,Romania/10.2009-09.2010
- Specialist Medical Genetics/Clinical Municipal Hospital"Dr. G. Curteanu" Genetics Depart.,Oradea,Romania/03.2004–09.2009
- Resident physician in Medical Genetics/County Health Office,Oradea, Romania/04.1999-04.2004

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Scientific Production

Publication

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Teaching Courses

Teaching Courses

College of Medicine and Medical Sciences
- Chair of Unit IX
- PBL Tutor to Year 2, 3 ,4 students, Unit II- Unit IX
- Resource faculty for Year 2, 3, 4, 5 students Unit II- Unit IX
- Ethics and professionalism workshop, Year 4
- PhD program in Molecular Medicine, courses B1,B8,C5
- Master program- Personalized Medicine, courses 502, 602, 604
- Master program- Laboratory Medicine, module II resources, Basic Concepts in
Human Genetics

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Academic Supervision

Supervised the following theses

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Committees

 

Attendance in most important committees within the university

- ACCM accreditation- phase 2 subcommittee
- Graduate study committee 2015-2016
- Academic committee PhD in Molecular Medicine
- BSc Exam committee
- Advisory committees- academic adviser for Year 3
- NCAAA accreditation- faculty group responsible for participating in community services; Standard 11.

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Memberships

 

- American Society of Human Genetics
- European Society of Human Genetics
- European Cytogeneticists Association
- Asia Pacific Society of Human Genetics
- Romanian Society of Medical Genetics
- Bahrain Medical Society
- Bahrain Higher Education Council, Ministry of Education, Health Sector Task
Force
- Bahrain Higher Education Council, Ministry of Education, Research Sector Task
Force
- International Federation of University Women
- International Conferences for Rare Diseases and Orphan Drugs
- Central and Eastern European Genetic Network
- Information Center for Rare Disorders Romania
- European Organization of Rare Disorders EURORDIS
- EuroGentest
- Rare Chromosomal Disorders Support Group
- Assistant editor of “Romanian Journal of Rare Diseases”
- Editorial committee member of Romanian medical review-“Stetoscop”
- Scientific referee of Romanian Medical Publishing Antaeus
- Scientific referee Romanian Review of Laboratory Medicine RRLM
- Scientific referee Journal of Translational Medicine
- Scientific referee Arab Gulf Journal of Scientific Research
- International Judge for the ESHG/ ASHG DNA-Day International Essay contest

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Community Service

 

-International Rare Disease, Bahrain Public Campaign, 10-28 February 2018 organizing committee chair and volunteer.
-International Rare Disease, Bahrain Public Campaign, 25 February 2017 City Center Mall, organizing committee chair and volunteer.
-International Rare Disease, Bahrain Public Campaign, 13-29 February 2016, Ramli Mall, Bahrain International Mall, City Center Mall, organizing committee chair and volunteer.
-Open evening for patients and their families, Al Jawhara Center, 29 of February 2016
-Rare diseases awareness national public campaign, 28 of February 2015, City Center, Manama, Bahrain
-Exhibition of Special need services, Special Families Support Group, 6 of February 2015, Amwaj Bahrain- volunteer representative of Al Jawhara Center
-British School work placement students program- AJC guide and professional assistance, June 2014
-From gene to disease- seminar for patients and their families- 28 of March 2014
- Rare Disease Public Campaign Bahrain, 28 February 2014, City Center Mall, organizing committee member and volunteer
- Rare Disease Public Campaign Bahrain, 29 February 2013, Seef Mall, organizing committee member and volunteer
- Ministry of Education, Visits of high schools students, 11-12 December 2012; 23- 24, 29- 30 April 2013- Lecture “The meaning of medical genetics and its contribution to the people health”.
- RIA Center Manama, Bahrain- 2013- volunteer
- EUROPLAN project 2010
- EURORDIS- Orphan drug task force-2009
- International Day of Rare disorders 2009, 2010- Romania campaign
- European Day of Rare Disorders 2008- Romania campaign
- EUROGENTEST Network of Excellence- 2007
- Central East European Trust, National Alliance for Rare Diseases, Zalau, Romania, 2007-2008
- EUROGENE project- European reference portal for Genetic Medicine-2007
-Romanian Prader Willi / Williams / Down/ PKU/ Werdnig Hoffmann/ Associations 2006
-Romanian National Association of Rare Disorders- scientifically board-2006


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Research Interests

 

- genomic disorders
- rare disorders
- genomics ethics

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Lectures/Seminars/Workshops

 

Training courses and workshops:

2018
- “Advanced tutorial skills”- Maastricht University Netherlands in collaboration with AGU, ManamaBahrain 7-8 January 2018
- “PBL case construction” Maastricht University Netherlands in collaboration with AGU, Manama Bahrain 5-6 January 2018
2017
- BLC course, NHRA, Manama Bahrain, 4 December 2017
- „Identifying Minimal Competence A priori for setting cut points”, Workshop oAGU, College of Medicine and Medical Sciences, 8 November 2017
- „Assessments- from Basic Principles to OSCE examining” workshop, University of Manchester School of Medical Sciences, Division of Medical Education, AGU Bahrain, 24-25 April 2017
-Developing as a Clinical tutor-key learning and teaching skills workshop- University of Manchester School of Medical Sciences, Division of Medical Education, AGU Bahrain, 22-23 April 2017
Rare diseases registries and national plans, international specialized workshop, 7-8 April 2017, Al Jawhara Center Bahrain
-5D workshop: drug discovery, desgin, development and delivery, Al Jawhara Center 23 March 2017
2016
- „Post examination analysis &standard setting workshop”, Faculty Development Program, Arabian Gulf University, Manama, Bahrain, 12-14 November 2016
-„Problems as Instructional Tool in PBL: how to construct a problem?”, Faculty Development Program, Arabian Gulf University, Manama, Bahrain, 9 November 2016
- "Standard setting in summative examination”, workshop. Medical Education Unit & WHO Collaborating Center for Health Professionals Educational Development, Faculty Development Program, Arabian Gulf University. Manama, Bahrain, 18 May 2016.
- „Construction of Learning Outcomes and Objectives”, workshop. Medical Education Unit & WHO Collaborating Center for Health Professionals Educational Development, Faculty Development Program,Arabian Gulf University, Manama, Bahrain 27 April 2016
- Medical Education Colloquium, Arabian Gulf University, Manama, Bahrain, 11 April 2016.
- “Professionalism and Ethics workshop”- facilitator, 7-8 February 2016, Arabian Gulf University, Bahrain
- “Construction of cluster MCQs” Student Assessment Workshop 1, Arabian Gulf University Bahrain Feb 3, 2016
2015
- „Creating an Endowment Policy and Research Fund Structure for Bahrain”, 4th October 2015, MENA Center for Investment, Higher Education Council, Bahrain
- „Multiple sclerosis workshop, Bahrain Neuroassociation, 28 of May 20015, Al jawhara Center for Molecular Medicine
-“Implementing the National Research Strategy”, MENA centre for Investment, Higher Education Council, Ministry of Education, 14 May 2015
-“Scientific writing: Focus on Health Policy and Systems Research/ health Services Research”, 1-2 March 2015, Alliance for Health Policy and Systems Research, Arabian Gulf University, Bahrain.
-“Professionalism and Ethics workshop”- facilitator, 7-8 February 2015, Arabian Gulf University, Bahrain
-“Latest and essential knowledge of translational research and clinical trial”, 12 January 2015, Ministry of Health, Directorate of Training, Bahrain
2014
- “Literature Review Made Easy for Researcher" RCTD workshop, 7-8 November, HD Video Conferencing
- “Music therapy for patients with developmental delay”, workshop, Affinity associates meeting,25th of October 2014, Affinity Consultancy Bahrain.
-“Nodal Institution to support the conduct and use of implementation and health policy & systems research in policy and programme planning, implementation and scale up”, NationalStakeholders Meeting, 8-9 April 2014, Arabian Gulf University
- “Nodal Institution to support the conduct and use of implementation and health policy & systems research in policy and programme planning, implementation and scale up”,Workshop on “ Capacity Building on Implementation Research/Health Policy Systems Research” 21-22 May 2014, Arabian Gulf University
2013
- “Evidenced based medicine “workshop, WHO Collaborating Centre for Educational
Development, College of Medicine and Medical Sciences, Arabian Gulf University, 19-20 April2013, Manama, Bahrain.
2012
- “2nd Course in Bioinformatics” – Arabian Gulf University, Biotechnology program, 11- 22 March 2012 , Manama, Bahrain.
- Cochrane Library Seminar, June 2012, Al Jawhara Center, Bahrain
“How to get yourself published in an academic journal”- workshop, RCSI, May 2012, Bahrain,
-“Course and program specifications and reports”-workshop, 15-16 November, Arabian Gulf University, Manama, Bahrain
2011
- “Course and program Specifications And Reports”, The Quality Assurance
Office and the Saudi National Council for Academic Accreditation and Assessment, Arabian Gulf University, Kingdom of Bahrain,15-16 November 2011
-„Tutoring skills” training program, Arabian Gulf University, College of Medicine and Medical Sciences,, Kingdom of Bahrain 15 and 25 January 2011
2010
- Course „ Project manager”, Ministry of Work, Ministry of Education, Research and Youth, S.C.Romarketing SRL, April 2010 Romania
2009
- Course „ Project manager”, Ministry of Work, Ministry of Education, Research and Youth, S.C.Idas Group SRL, June 2009. Romania


Lecturer

- "Best Practice in Medical Genetics:genetic testing and ethical issues"- workshop,1st Gulf Medical Administration Forum, 6 June 2013, Manama, Bahrain
- "“Ethics and professionalism workshop”, Introduction to problem based learning, year II, College of Medicine, Arabian Gulf University, 6th September 2012,4 September 2013
-"Medical ethics workshop” Year IV, College of Medicine, Arabian Gulf University, 26 March 2013

Postgraduates training course in genetics:

2017
- Diagnostic Challenges: Review and Discussion of Unique Cases, American Colle of Medical Genetics and genomics,19 October 2017 , Orlando, Florida, USA at the Annual Meeting of the American Society of Human Genetics, 17-21 October 2017
2016
- Tackling the genetics of neuromuscular disorders, International practical teaching course, Institute of Myology France, AL Jawhara Center Bahrain, 21-23 March 2016
-Genetic counselling course, Pan Arab Human Genetic Conference, Dubai, 23 January 2016.
2015
- 28th Course in Medical Genetics, 17-21 May, European Genetics Foundation European School of Genetic Medicine, Bologna, Italy- webcasted Remote Training Center Al Jawhara Institute, Manama, Bahrain.
-4th Course in Next Generation Sequencing , 13-16 May, European Genetics Foundation European School of Genetic Medicine, Bologna, Italy- webcasted Remote Training Center Al Jawhara Institute, Manama, Bahrain.
-“LSD Masterclass 2015, The Mucopolysaccharidoses”, 13-14 of March 2015, Dubai, Dubai, United Arab Emirates
2014
- 3rd Course in Next Generation Sequencing , 7-10 May, European Genetics Foundation European School of Genetic Medicine, Bologna, Italy- webcasted Remote Training Center Al JawharaInstitute, Manama, Bahrain.
-27th Course in Medical Genetics, 11-15 May, European Genetics Foundation European School of Genetic Medicine, Bologna, Italy- webcasted Remote Training Center Al Jawhara Institute,
2013
-“Best practice in Medical Genetics:genetic testing and ethical issues", 6 June 1st Gulf Medical Administration Forum, Manama, Bahrain
- 26th Course in Medical Genetics, 12-16 May, European Genetics Foundation European School of Genetic Medicine, Bologna, Italy- webcasted Remote Training Center Al Jawhara Institute, Manama, Bahrain.
2012
- “Cardiovascular genetics- genetic counseling”, online course, Division of Human Genetics, The Heart Institute at Cincinnati Children’s Medical Center, May 2012. USA.
2010
- Course “ Genetics practical applications in endocrinology- from classical cytogenetics to Molecular genetics techniques”, 19-21May 2010, Tg. Mures, Romania
2009
2nd Course “The integration of cytogenetics, microarrays and massive sequencing in biomedical and clinical research”- 18-22 October 2009, European Genetics Foundation European School of Genetic Medicine, Bologna, Italy.
2008
- 3rd Course in Clinical Cytogenetics, August 30th- September 4th, Goldrain, South Tirol, Italy.
-„Molecular Cytogenetics techniques using in situ hybridisation”- practical course of molecular cytogenetics, 21-23 May 2008, Timisoara, Romania.
-The 5th German- Romanian Genetics Course, 14-17 April, Oradea, Baile Felix, Romania
2007
- Course „Actualities in Pediatrics”, Oradea, Romania 7- 11 May 2007
2006
- 7th Course , Genetic Counselling in Practice, Bologna University Residential Center Bertinoro di Romagna, 9-14 November, 2006, Italy.
2005
-The 4th German- Romanian Genetics Course, 21-24 April, Oradea, Romania
- Course „Actualities in Pediatrics”, Oradea, Romania 3-8 May 2005
2004
-Cardiac Morphology 3, 3 December, Gottsegen Hungarian Institute of Cardiology,Pediatric Cardiac, Budapest, Hungary.
-Course „Actualities in Pediatrics”, Oradea, Romania 26-30 April 2004
2003
- Course „Actualities in Pediatrics”, Oradea, Romania 31 March – 4 April 2003
2002
-The 24th Syndromclub, April 27, Institut of Clinical Genetics, Dresden University of Technology, Germany.
-The 3rd German- Romanian Genetics Course, September 6-7, Oradea,Romania
2001
- The 14th Course in Medical Genetics of European School of Genetic Medicine, March 25-31, La Nunziata Centre, Sestri Levante,Genoa-Italy
-The 22nd Saxonian Thuringian Syndrome Club, 21 October, Charite Champus Virchow Klinicum, Berlin, Germany
2000
- The 2nd German- Romanian Genetics Course, 6-7 March, Oradea-Arad, Romania


Oral presentations:

- "From human genes to disorders", Seminar for patients and their families, Al Jawhara Center Bahrain, 28 March 2014
- "ECARUCA - the online database for rare chromosome disorders", 5th Pan Arab Human Genetics Conference, Dubai, United Arab Emirates, 17-19 November 2013.
- "Prenatal genetic diagnosis", SMC Obstetrics and Gynecology Department, Continuing Education Program, 20 of June,2013
- "Rare Diseases impact into societies worldwide", Rare Disease Day Symposium 2013 Bahrain, 26 of February, Al Jawhara Center, Manama, Bahrain.
-" The meaning of medical genetics and its contribution to the people health", Highschool students visits to Al Jawhara Center, 9, 12 December 2012.
"Medical Genetics today", American Mission Hospital, The Continuing Medical Education Program- 4 July 2011, Manama, Bahrain
-"Genetics data bases-a guide for proper and sharp diagnosis",AlJawhara Center Journal Club, 2nd of June 2011
-"Rare genomic disorders", Journal Club, Anatomy Department, College of Medicine and Medical Sciences, Arabian Gulf University, 24 January 2011
-"Genomic disorders",Al Jawhara Center Journal Club,11 November 2010
-"Breast cancer- background and molecular diagnostic methods",Al-Jawhara Center Journal Club,7 October 2010
- “Genetics data base used in medical practice”. National Medical Genetics Conference, 24-26 Septembrie 2009, Sibiu, Romania
-"„The role of medical geneticist in the management team of rare disorders”,Balkan Congress for Rare Diseases Romania, 26-28 June 2009, Cluj Napoca, Romania.
- „Mechanisms and assays for rare genomic disorders”,Balkan Congress for Rare Diseases Romania, 26-28 June 2009, Cluj Napoca, Romania.
-“Genotype-phenotype correlation in Prader Willi syndrome- an overview of the literature”, 1st Eastern European Conference on PWS „Review Multidisciplinary approach in the management of PWS”, Timisoara, 24-25 April 2009.
- “Importance of an early and correct diagnosis for a correct genetic counseling", Diagnosis, treatment and management of rare diseases patients workshop, National Alliance for Rare Diseases, National Center for Family Medicine Studies, Bucharest, 28 February 2009.
- Diagnosis and therapy in Down Syndrome”, Oradea, 3 December 2008.
- International Pediatric Cardiology Symposium, 9-12 October 2008, Tg Mures, Romania
-"Early diagnosis of rare diseases”. Trust of trust- Hope and trust for rare disease patients", 24 September 2008, Cluj, Romania
- The 5th German-Romanian Genetics Course, 14-17 April 2008, Oradea, Romania
-“Beeckwith Wiedemann syndrome”, First Rare Disease European Day Symposium , Faculty of medicine and Pharmacy, 28 February 2008,Oradea, Romania
- „Light and shadows; diagnosing rare genetics disorders”, Rare disorders- finding the needs and establishing the priorities,Zal?u, 2-3 November, Romania
- „Diagnosis of microdeletion and microduplications syndromes, from karyotype to molecular genetics tests”,The 6th National Congress of Laboratory Medicine", 11-13 October, 2007, Sibiu, Romania
- „Importance of the minor criteria for a positive clinical diagnosis of Prader Willi syndrome patients", 6th International Prader-Willi Syndrome Scientific Conference, 1st Romanian Prader-Willi Syndrome and Rare Diseases Conference, 21-24 June 2007, Cluj-Napoca, Romania.
-"Genetics test across borders”, 6th International Prader-Willi Syndrome Scientific Conference, 1st Romanian Prader-Willi Syndrome and Rare Diseases Conference, 21-24 June 2007, Cluj-Napoca, Romania.
- “Molecular genetics contributions in the diagnosis of microdeletion and microduplication syndromes”. Romanian Society of Medical Genetics Conference, 25-27 May 2007, Moeciu de Sus, Brasov, Romania .
- „Beckwith Wiedemann syndrome-paternal UPD 11”. The 2nd Romanian Congress of Medical Genetics, 20-23 September 2006, Cluj, Romania

Posters:

-" Rare genetic diseases- Genetic counselling challenges". Cristina Skrypnyk. 10th Asia-Pacific Conference on Human Genetics 5th - 8th December 2012, Kuala Lumpur, Malaysia.
-„Cardiovascular spectrum in Williams Beuren syndrome”. C. Skrypnyk, M. Bembea, C. Jurca, C. Liveratou, D. Smeets. European Human Genetics Conference 23-26 May 2009, Vienna, Austria. In European Journal of Human genetics, Vol 17, Supplement 2, May 2009, pg 141.
-„From phenotype to mosaic paternal UPD11p15 in Beckwith Wiedeman Syndrome” C Skrypnyk, M. Bembea,V Bica, C. Rusu, C. Jurca, W. Kress, A. Baumer. European Human Genetics Conference 31 May-3 June 2008, Barcelona, Spain. In European Journal of Human genetics, Vol16, Supplement 2, p 133.
-„Screening for subtelomeric rearrangements by multiplex ligation-dependent probe amplification (MLPA) in 30 patients with mental retardation.” C. Skrypnyk, M. Bembea, C. Jurca, E. Neagu, D. Iancu, L. Barbarii, C. Rusu. Genomic Disorders 2008, Wellcome Trust Conference Centre, Hinxton, Cambridge, UK, 17-20 march 2008.
-“MLPA for the detection of cryptic subtelomeric rearrangements in mental retardation patients- cases report “. C. Skrypnyk, M. Bembea, C. Jurca, E. Neagu, D. Iancu, L. Barbarii, C. Rusu. 6th European Cytogenetics Conference, 7-10 July 2007, Istanbul, Turkey.
-„Williams Syndrome - observing the phenotype and understanding the genotype”. C. Skrypnyk, M. Bembea, C. Rusu, M. Volosciuc, M. Gramescu, M. Covic, D. Smeets, O. Bartsch. Genomic Disorders 2007, 21-24 March 2007, Wellcome Trust Genome Campus, Hinxton, Cambridge, UK.
-„ Genetic counselling in microdeletions syndromes”. C. Skrypnyk, M. Bembea, V. Belengeanu, E. Tomescu, P. Grigorescu Sido, M. Covic. The 7th Course Genetic Counselling in Practice, European School of Genetic Medicine, November 9-14 2006, Bertinoro, Italy.
-„Prader-Willi Syndrome: clinical and molecular particular aspects” C. Skrypnyk, M. Bembea, O. Bartsch, C. Aulehla-Scholz, W. Kress . Second Eastern European Confererence on Rare Diseases and Orphan Drugs. Fostering Research on Rare Diseases in Eastern European Countries, 8-9 Septembrie 2006, Plovdiv, Bulgaria- in extenso, Conference proceedings ISBN978-954-91025-3-6, pg 179-180.
-„A particular case of syndromatic ichtyosis”. C. Skrypnyk, O. Bartsch, M. Bembea, V. Filip, I. I. Vancsik. European Conference of Human Genetics, Amsterdam, 6-9 May, 2006.
-„Hereditary multiple exostoses disease- clinical and genetical aspects”. C. Skrypnyk, M. Bembea, O. Vancsik, M. Barbu, C. Barbu. -European Conference of Human Genetics, Prague, 9-11 May, 2005.
-„Singular and syndromatic ano-rectal malformations“. C. Skrypnyk , M. Bembea, R. Spineanu, F. Galos, O. Vancsik, , C. Todor, D. Lerintiu- “The 10th International Congress of Human Genetics”:15-19 May 2001, Vienna, Austria.

Conferences attended:
2017
- First conference on Computational Biology and Medicine, November 16, Manama, Bahrain
- 8th International Arab Neonatal Congress, Manama Bahrain 18-20 May 2017
-The 5th Ethical Symposium, Controversies on the use of stem cells, 25 May 2017, King Hamad University Hospital, Bahrain
- The 4th CMMS Research Day- 15 May, 2017 Arabian Gulf University, Bahrain
- Pearl Pediatric Conference, 23-25 February 2017, Manama, Bahrain
- Update on genetic myopathies Seminar , &th February 2017, Al Jawhara Center
2016
- KHUH RCSI International Research Conference, 16-17 November 2016, Bahrain
- 13th Middle East Metabolic Group Meeting”, Amman, Jordan, 28-30 October 2016
- „Bahrain National Sickle Cell disease Symposium”, 29 September 2016, Manama, Bahrain
- “Detection of trisomies and deletion syndromes in fetuses- NIFTY test and a new era”, Al Jawhara Center,Hereditary diseases Group, Bahrain, 25 September 2016
- The 3rd CMMS Research Day- 9 May, 2016, Arabian Gulf University, Bahrain
- XIII International Congress of Middle East Africa Council of Ophthalmology 4-8 May 2016, Manama, Bahrain
- The fourth Ethical Symposium, 5 May 2016, King Hamad University Hospital, Bahrain
- 13th International Congress of Human Genetics, Kyoto, Japan, 3-7 April 2016.
- “Stem cells –promises and controversies”- 8th regional conference, American University of Beirut, The Halim El Hoss Bioethics and Professionalism Program, Arabian Gulf University, Manama Bahrain, 26-27 March 2016 .
- RCSI’s Oncology symposium, 30 January 3016, Manama, Bahrain.
- 6th Pan Arab Congress of Human Genetics, Dubai, 21-23 January 2016.
2015
- Functional Genomics Symposium, Sidra Medical and Research Center, Qatar Foundation, Doha Qatar, 13-14 December 2015
- “Towards Bahrain genome project, building on international experiences” Al Jawhara Center 9th Scientific Conference, 28-29 November 2015, Bahrain.
- 35 Years of Visionary Achievements, 11th Forum, “New frontiers in Medical Sciences: Personalized Medicine”, 9 November 2015, Arabian Gulf University, Bahrain.
- 12th Middle East Metabolic Group Meeting”, Muscat, Oman, 29th October-1st November 2015
- The 2nd CMMS Research Day- 18 May, 2015, Arabian Gulf University, Bahrain
-“The third Ethical Symposium” 7 May 2015, King Hamad University Hospital, Bahrain
-" Al Kindi 1st International Pediatric Conference, 25 of April, Gulf Hotel, Bahrain
-“1st International Congress on Clinical Genetics and Genetic Counseling in Rare Diseases”, Seville, April 16-17 2015, Spain.
2014
- Second Ethical Symposium 2014, Thursday 16 October 2014, King Hamad University Hospital, Bahrain
- Advances In Neurogenetics Research "A collaborative Symposium" 21-22 March 2014, Doha, Qatar.
-A walk through Forensic Medicine- 20-21 March 2014, Arabian Gulf University, Manama, Bahrain
-“BMJ meeting”, Ministry of Health, Public Health Department, 24 April 2014, Al Jawhara Center Bahrain
- 4th Bahrain Heart Association (BHA) Congress, 26-28 February 2014, Manama, Bahrain.
2013
- 9th GCC Medical Education Conference”, 23-25 November 2013, Arabian Gulf University
- 5th Pan Arab Human Genetics Conference &Golden Helix Symposium, 17-19 Nov, Dubai
-European Cytogenetic Association Conference, 28 June-2 July, Dublin, Ireland
- 1st Gulf Forum for Medical Administration “Code of Ethics”, 4-6 June, Manama, Bahrain
- 3rd GCC Symposium in Clinical Nutrition, 10-11 April, University Medical Center, Bahrain
- First International Rheumatology Conference, 9th of March, King Hamad Hospital,, Bahrain
- Dementia Symposium, 5th of March, 2013, Al Jawhara Center, Manama, Bahrain
- First International Diabetes Symposium, 2-3 March 2013, Arabian Gulf University, Baharain
- Rare Disease Day Symposium Bahrain 2013, 26th of February 2013, Al Jawhara Center Bahrain
2012
-10th Asia Pacific Conference in Human Genetics, 5-8 December 2012, Kuala Lumpur Malaysia
-IUPS Physiology teaching Conferences and workshop, 31 March- 1April 2012, Arabian Gulf, University, Manama, Bahrain
2011
-8th International Conference, HH Princess Al Jawhara Centre, 28-29 November 2011, Manama, Bahrain
- European Human Genetics Conference, 28-31 May 2011, Amsterdam, Holland
- Symposium „Array in daily practice: promises and pitfalls”, 27 May 20011, Amsterdam
2010
- EUROPLAN Conference European Project of Rare Diseases National Plans Development 18-19 June 2010, Romanian Parliament, Bucharest, Romania.
- National Congress for Breast Cancer-, Baile Felix 12-15 May 2010, Romania.
2009
- “OI in motion” Rehabilitation and Physiotherapy in Osteogenesis Imperfecta, 20-22.11.2009, Rheinsberg, Germany.
- National Conference of Medical Genetics, 24-26 September 2009, Sibiu, Romania.
- Balkan Congress for Rare Diseases Romania, 26-28 June 2009, Cluj Napoca, Romania.
- European Human Genetics Conference 25-26 May, 2009, Vienna, Austria.
- 1st Eastern European Conference on PWS „Review Multidisciplinary approach in the management of PWS”, Timisoara, 24-25 April 2009.
- "How to diagnose, to treat and to manage the patients with rare disorders"- National Alliance for Rare Disorder, National Center for Family Medicine, Bucharest, 28 February 2009.
- National Conference of Medical Genetics, 25-27 May 2009, Moeciu de Sus, Romania.
2008
- „Diagnosis and therapy in Down syndrome”, 3 December 2008, Oradea, Romania.
- “National Strategies and Action Plans for Rare Diseases in Europe”, “State of the art and sharing experiences: towards EU Recommendations”, 18 November 2008, Salle Laroque French Ministry of Health, Paris, France,
-„EURORDIS- Conference of National Aliances”, 17 November, Rare Diseases Platform, Paris
- The third international symposium of Pediatric Cardiology , 9-12 October 2008, Tg Mures,
-„Trust of Trust- hope and trust for patients with rare disorders”, 24 September 2008, Cluj Napoca, Romania.
-European Human Genetics Conference 2008, 31May- 3 June, Barcelona, Spain
-Genomic Disorders 2008, 17-20 March,Wellcome Trust Genome,Cambridge
-„First European Day of Rare Disorders”- Symposium, 28 February 2008, Faculty of Medicine and Pharmacy,Oradea, Romania
2007
- “Rare disorders- from needs to priorities”2-3 November 2007, Zalau, Romania
-Building Towards Profesional Competence and Patient Confidence, EuroGentest, October 27-28, 2007, Milan, Italy.
- The 6th National Congress with international participation of Laboratory Medicine, the 2nd symposium of Immunopathology, 11-13 October 2007, Sibiu, Romania.
- 6th European Cytogenetics Conference, 7-10 July 2007, Istanbul, Turkey.
- 6th International Prader-Willi Syndrome Scientific Conference, 1st Romanian Prader Willi Syndrome and Rare Diseases Conference, 21-24 June 2007, Cluj, Romania.
- Genomic Disorders 2007, 21-23 March, Wellcome Trust Genome,Cambridge, UK.
2006
- European Human Genetics Conference 2005, 6-9 May, Amsterdam, The Nederland.
- Second Eastern European Conference on Rare Diseases and Orphan Drugs, 8-9 September, Plovdiv, Bulgaria
- 2nd Romanian Congress of Medical Genetics, 20-23 Septembrie 2006, Cluj Napoca, Romania.
- Save PKU kids”, 29-30 September, Oradea, Romania.
2005
- European Human Genetics Conference 2005, 7-10 May, Prague, Czech Republic.
-1st National Conference of Bioethics, Iasi, Romania.
2004
-The 3rd National Symposium of genetics disorders, endocrine amd metabolic disorders in children ”12 June 2004, Cluj Napoca, Romania
2003
-The International Congress of Mucoviscidosis, May 7-9 , Timisoara, Romania.
- International Congress of Perinatal Medicine, October 1-4, Cluj Napoca, Romania
2002
-1st National Congress of Medical Genetics, 19-22 September Oradea, Romania
2001
-The 10th International Congress of Human Genetics,May 15-19, Vienna
-100 Jahre Nobelpreis an Emil von Behring: 20 Oktober, 2001, Berlin, Germany
-International Symposium in Bioethics- 2nd edition :22-24 of June 2001, Oradea, Romania
-Scientific meeting Romania-Sweden: 23-24 February 2001, Oradea, Romania
2000
-The 4th National Conference of Neonatolgy: 28-30 September 2000 Oradea, Romania
-The 1st Congress of The Anatomy Departments, The Medical Union of Balkans and Black Sea Region Countries:2-4 June 2000 Oradea, Romania
1999
-National Conference of Medical Genetics, 7-10 October 1999, Constanta, Romania
-The 3rd National Congress of Social Pediatrics, 30 September- 2 October 1999, Romania
-Balkan Medical Days: 28-30 April 1999 Iasi, Romania

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Publications prior to joining AGU

 


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Others

 

Expertise:
Genetic diseases- evaluation, diagnosis, testing, management
Genetic counseling
Cytogenetics and Molecular Cytogenetics, Molecular Genetics

Cytogenetics and molecular genetics trainings:
- Genome Wide Array diagnostic technique: Division of Genome Diagnostics, Human Genetics Department, Radboud University Medical Center, Nijmegen, Holland,2013
-RT PCR, FISH techniques: GeneticLab, Bucharest, Romania, Molecular Department, 2008
-FISH technique: University of Medicine and Pharmacy Timisoara, Romania, 2008
-PCR technique: GeneticLab, Bucharest, Romania, Molecular Department, 2005
-PCR,Southern Blot techniques,DNA sequencing: Molecular Department, Institute of Human Genetics, University of Wuerzburg, Germany, 2004
- Cancer Cytogenetics: Clinical Institute of Pediatrics, Hematology Center, Cytogenetics and Molecular Cytogenetics Department, Debrecen, Hungary, 2002
- FISH, PCR techniques, DNA sequencing: Molecular Cytogenetics and Molecular Laboratories, Institute of Clinical Genetics, Dresden, Germany,2001 and 2002


• Professional books- coauthor:
- Coordinator Maria Puiu: „Medical Awarness in rare genetics disorders/ Alerta medicala in bolile genetice rare” ISBN 978-606-8054-39-1 pg.466. Cristina Skrypnyk: pg. 50-81, 268, 384-385,439. Editura Victor Babes, Timisoara, 2011
-Coordinators Mircea Covic, Dragos Stefanescu, Ionel Sandovici: „Medical Genetics- second edition / Genetica Medicala- editia a II-a/”- ISBN 978-973-46-1960-3, pg 713. Chapter 9: Genetics disorders and genomic medicine- authors: M. Covic, G. Tauser, C. Skrypnyk, I. Sandovici, pp.319-344; Chapter 11: Chromosomal disorders- authors: V. Gorduza, C. Popovici, C. Scrypnyk, M. Covic, V. Belengeanu, D. Stoicanescu, M. Panzaru, L. Butnariu, pp.384-416. Editura Polirom Iasi, 2011
-Coordinator Marius Bembea „Izolate genetice din Bihor/ Genetics isolates in Bihor”, ISBN 978-973-759-999-5 pg.181. Colaborators- Kinga Kozma, Claudia Jurca, Cristina Skrypnyk, Serban Bembea, Oana Iuhas, Radu Harbuz, Corina Nagy. Editura Universitatii din Oradea, 2009
-Coordinator Maria Puiu, Cristina Skrypnyk „Mic ghid de diagnostic al bolilor genetice/ Small guide of rare diseases diagnosis”., ISBN 978-606-92022-0-3 pg.183pg. Cristina Skrypnyk: pg. 15-16, 17, 21-22, 73-74, 141-142, 173. Editura Victor Babes, Timisoara, 2009
-Coordinator Cristina Rusu „Metode de screening si diagnostic a bolilor genetice/ Methods for screening and diagnosis of genetics disorders.” Cristina Skrypnyk: pg 113-121, 141-154, 215-223. ISBN 978-973-7682-31-4; 266pg;.Editura Gr. T. Popa U.M.F. Iasi, 2007
-Coordinator Maria Puiu. „Esentialul in 101 boli genetice rare/ Essential in 101 rare genetics disorders”. Cristina Skrypnyk :pg. 66, 67-72, 80-82, 470-472. ISBN 978-973-638-327-4, 511 pg; Editura Orizonturi Universitare, Timisoara, 2007
-Valeria Filip, Cristina Skrypnyk. „ Malformatii de tub neural/ Neural tube defects”. - ISBN (10) 973-87960-1-6, ISBN (13) 978-973-87960- 1-0, 175 pg, Editura Universitatii Agora, Oradea, 2006
-Valeria Filip, Laura Lele, Cristina Skrypnyk „ Nou nascutul la termen/ New born at term”. ISBN (10) 973-87960-0-8, ISBN (13) 978- 973- 87960-0-3, 87 pg Editura Universitatii Agora, Oradea, 2006

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Contact Information

 

Work Tel No: 17237315 Work Fax No: 17246022
cristinas@agu.edu.bh

 

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