Prof Ahmad Settin CV

CURRICULUM VITAE

AHMAD ABD AL SALAM SETTIN

MBBCh MS MD





Personal Details:

· Name : Ahmad Abd-Al-Salam Setteen

· Date of Birth : October 13, 1955

· Place of Birth : Mansoura, Egypt

· Mailing Address : Genetics Unit, Mansoura University Children Hospital, Egypt Tel. (Home) : +20 502214343

· Fax : +20502324092

· Mobile : +20109430440

· Current Address : College of Medicine, Quassim University, BO 6040,

· Buraydah 51432, Saudi Arabia

· Mobile : +966556040530

· E-Mail: Settin@qumed.edu.sa

· Settin@mans.edu.eg

· Settin60@gmail.com

Settin60@yahoo.co.uk

Settin60@hotmail.com

· Home page : http://sites.google.com/site/profahmadSettincvsite/

· Marital Status : Married, Wife is a doctor.



Current Position:

· Professor of Pediatrics, College of Medicine, Quassim University, Buraydah 51432 BO 6655, Saudi Arabia-- Nov. 2005

· Professor, Pediatrics and Genetics, Faculty of Medicine, Mansoura University, Egypt-- Nov. 2005



Major Research Interests:

· Genetics (Genetic Counselling, Molecular Genetics, Cytogenetics)

· Flow cytometry

· Medical Statistics


Degrees And Specialty Certifications:

· Doctorate Degree (M.D.), General Pediatrics and Genetics, Faculty of Medicine, Mansoura University, Egypt. Nov. 1986

· Master’s Degree (M.S.), General Pediatrics Faculty of Medicine, Mansoura University. Nov. 1983

· Bachelor Degree (M.B.B.Ch), General Medicine and Surgery Faculty of Medicine, Mansoura University Nov. 1979

Registration With Medical Bodies And Societies:

· European Society of Human Genetics

· Eastern Mediterranean Association of Medical Editors

· Egyptian Pediatric Genetics Society

· Egyptian Pediatric Association

· Egyptian Medical Syndicate, Registration No. 46632.



General Education

· Primary School(6 years), Mansoura, Egypt (1961-1967)

· Preparatory School (3 years),Mansoura, Egypt (1967-1970)

· Secondary School (3 year), Cairo, Egypt (1970-1973)

· Egyptian General Certificate of Education 1973 (Honored for the highest score in whole Egypt)


University Education

· Basic Science :Faculty of Science, Mansoura University, Egypt (1974)

· Medicine and Surgery, Faculty of Medicine, Mansoura University, Egypt (1975 – 1979). Final Grading Excellent Degree with Honor.


Postgraduate Education :

· MS “First Part” : General Science and Genetics (Nov. 1981 to Nov. 1982)

· MS “Second Part” : General Pediatrics (Nov. 1982 to Nov. 1983)

· Doctorate Degree (MD) in Pediatrics (Nov 1983 to November 1986)

Faculty of Medicine, Mansoura University, Egypt



Professional Experience:

· Resident House Officer, Mansoura University Hospitals, Egypt: general surgery, urology, anesthesia, emergency, general medicine, pediatrics and obstetrics and gynecology (March 1980 - February 1981).

· Resident training program of Pediatrics in the Pediatric Department in Mansoura University Hospital (March 1981 - February 1884).

· Assistant Lecturer of Pediatrics, Department of Pediatrics, Mansoura University. Worked in the Pediatric Hematology Oncology Unit (February 1984 - February 1987)

· Assistant Professor of Pediatrics & Genetics, Genetics Unit, Faculty of Medicine, Mansoura University. Attended Endocrinology and Genetics Units practiced Clinical Genetics in addition to Genetic counselling activities (February1987 - March 1992)

· Associate Professor, Pediatrics and Genetics, Genetics Unit, Ped. Dept., Fac. of Medicine, Mansoura University, Egypt. One of the teaching staff of the Faculty teaching General Pediatrics and Genetics both for undergraduates and postgraduate students and supervising the running researches in the Genetics Unit. (March 1992 - Feb 1998).

· Professor, Pediatrics and Genetics, Genetics Unit, Ped. Dept., Fac. of Medicine, Mansoura University, Egypt. One of the teaching staff of the Faculty teaching General Pediatrics and Genetics both for undergraduates and postgraduate students and supervising the running researches in the Genetics Unit. (Feb 1998 till now)




(European School of Medical Genetics, 1990)



Postgraduate Experience and Research Activities


· Fellowship for research and training in the field of Molecular Genetics, United Nation Industrial and Development Organization/ International Center of Genetic Engineering and Biotechnology (UNIDO/ICGEB) , Institute of Cell Biology, CNR, ROME, Italy (June 1991-June 1992, 1 year)

· The Third Course of European School of Medical Genetics. Sestri Levanti, Genoa, Italy (April, 1990, 10 days)

· Medical Ethics related to Scientific Reseach Online Course (University of Pittsburgh School of Medicine, Western Psychiatric Institute Pennsylvania University, USA, 2009)

· Genetic counselling training under supervision of Prof Marina Frontali, Institute of Medical Research, Rome, italy ( 3 months starting from April, 1993)

· Trainining in Diagnostic Cyotogenetics and molecular cytogenetics (FISH), Medical Genetics Center, Munich, Germany (Feb, 2004, 3 months)

· Trainining in molecular cytogenetics (FISH) Genetics Institute Martin Luther University, Halle/saale Germany, (June, 2000, 10 days)

· Trainining in innunocytometric analysis using FACSCalibur Flowcytometer Becton Dickenson, BD, Heidelberg, Germany, (Feb, 2000, 10 days)

· British Council Seminar 9580 “Advances in Medical Genetics”Institute of Medical Genetics, University of Wales, Cardiff, UK (March 1996, 7 days)

· Workshop on “Chochrane Authorship”, Ain Shams University, Cairo, 4-5 December 2013

· Workshop on “Using lectures in a student-directed learning programme” and on “Practicing the principles of effective feedback” Qassim and Maastricht Universities, February 2012.

· Workshop on "Prevention and Control of Chronic Diseases" conducted at Qassim University in collaboration with Stanford Prevention Research Center (Stanford School of Medicine, USA) (16-20 Oct. 2010).

· The 24th meeting of the Saudi Biological Society « Biotechnology Reality and Applications » Madina, Saudi Arabia, 9 April 2009

· National conference on Recent Advances and Future Trends in Diabetic Care, Qassim University, College of Medicine, 24 May 2007

· Workshops for Human Development Programmes in Mansoura and Qassim University, Egypt and Saudi Arabia

· Workshops for Medical Education Programmes in Mansoura and Qassim University, Egypt and Saudi Arabia

· Annual Meetings of the Egyptian Medical Genetics Associations

· Annual Meetings of the Pediatric Departments all over the Egyptian Universities

· University CME programmes : Giving training and research talks in the Scientific Seminars on Genetics, Pediatrics and Immunology

· TOT (training of trainers) programs held at Mansoura University for human development of University staff.





(Institute of Genetics, Wales University, 1996)

Supervisor of Scientific Works and Projects:

· Editor : International Health Sciences Jouranl

· Editor : World Journal of Experimental Medicine

· Reviewer : Various International Scientific Journals

· Member : Eastern Mediterranean Association of Medical Editors

Supervisor of Scientific Projects and Medical Theses


· Genetic analysis of schizophrenia among Egyptian families (collaboration with Vishwajit L. Nimgaonkar, Department of Psychiatry, University of Pittsburgh School of Medicine, Western Psychiatric Institute Pennsylvania University, USA) (2005-till now)

· Genetic background and molecular analysis of dermatology related disorders as lishmaniasis and vitiligo in Qassim Region, Saudi Arabia (2010 till now)

· Genetic analyses of polymorphic genetic markers among Saudi subjects from Qassim region including genes with potential association to hypertension, obesity, cardiovascular disorders, diabetes and dermatologic inflammatory disorders (2010 till now).

· Cytokine gene polymorphisms among Egyptian Cases of rheumatic fever, bronchial asthma, rheumatoid arthritis, diabetes type 1, leprosy and psoriasis (2006-2007)

· Frequency of factor V Leiden mutations among Egyptian cases with Myocardial infarction, Deep vein thrombosis and recurrent abortions (2006-2007)

· Molecular characterization (mutational analysis) of cases of familial Mediterranean fever (2005)

· Characterization of hemochromatosis and alpha one antitrypsin gene mutation among cases with liver cirrhosis (2005)

· Fibroblast growth factor 3 mutation (pro250arg) in craniosynostosis patients (2007)

· Diagnostic utility of PCR in giardiasis (2002)

· DNA ploidy and apoptosis of primary malignant brain tumours as a diagnostic and prognostic marker (2002)

· Biochemical analysis and fish for prenatal diagnosis of ch 21 and sex ch disorders (2002)

· Prenatal diagnosis of beta thalassemia using revesed dot blot technique (2001)

· DNA ploidy, c-myc and p35 in families with acute leukemias (2001)

· Y chromosome deletions in male children with genital malformations (2001)

· Use of DNA fingerprinting as a marker for paternity testing in mansoura district (2001)

· Diagnosis of minimal residual disease of childhood leukemias uning DNA ploidy (1999)

· Molecular characterization of fragile X syndrome (1999)

· Genetic markers of childhood leukemias (1999)

· Cytogenetic characterization of mentally retarded children from Damietta (1999)

· Genetic disorders of the urogenital system (1998)

· Molecular genetic characterization of g6pd deficiency in patients with acute haemolytic anaemia(1999)

· Pitutary adrenal axis and sex hormone in obese children and adolescents (1999)

· Biochemical characterization of g6pd deficiency in patients with acute haemolytic anaemia (1998)

· Genetic studies of rheumatic fever in relation to blood groups and secretor locus phenotypes (1996)

· Deletional dystrophin gene mutations in muscular dystrophy in Egypt (1992)

· Splenectomy in Egyptian thalassemics, correlative study of different phenotypes with their genotype (1992)

· Study of some aspects of nocturnal enuresis (1992)

· Screening for cystic fibrosis among the Egyptian population (1990)

· Screening umbilical cord blood for abnormal haemoglobin (1990)

· Role of salivary immunoglobulins in the suscep-tibility to rheumatic fever in multiplexfamilies (1990)

· 10 year retrospective evaluation of skeletal dysplasia in Mansoura Pediatric Genetics Unit (1989)



Publications: 
http://www.ncbi.nlm.nih.gov/pubmed/?term=settin

https://scholar.google.com/citations?hl=en&user=9A3N3eIAAAAJ&view_op=list_works&sortby=pubdate
  1. Tarabay M, Elshazli R, Settin A. African vs. Caucasian and Asian difference for the association of interleukin-10 promotor polymorphisms with type 2 diabetes mellitus (a meta-analysis study). Meta Gene. 2016 Mar 4;9:10-7. doi: 10.1016/j.mgene.2016.02.006. eCollection 2016 Sep. PubMed PMID: 27114918; PubMed Central PMCID: PMC4833051.

    2.          Nasef N, Shabaan A, Mohammed S, Kandel S, Settin A, Zedan M, Fouda A. Factors influencing parental consent for participation in clinical research involving their children in Egypt. East Mediterr Health J. 2014 Apr 3;20(3):162-8. PubMed PMID: 24950073.

    3.          Alzolibani AA, Al Robaee A, Al-Shobaili H, Al-Saif F, Al-Mekhadab E, SettinAA. Association of CYP2C9 Genetic Variants with Vitiligo. Ann Dermatol. 2014Jun;26(3):343-8. doi: 10.5021/ad.2014.26.3.343. Epub 2014 Jun 12. PubMed PMID:24966634; PubMed Central PMCID: PMC4069645.

    4.          Settin A, Salama A, Elshazli R. Signal transducer and activator oftranscription 4 (STAT4) G>T gene polymorphism in Egyptian cases with rheumatoidarthritis. Hum Immunol. 2014 Aug;75(8):863-6. doi: 10.1016/j.humimm.2014.06.013. Epub 2014 Jun 28. PubMed PMID: 24979672.

    5.          Elshazli R, Settin A, Salama A. Cytotoxic T lymphocyte associated antigen-4(CTLA-4) +49 A>G gene polymorphism in Egyptian cases with rheumatoid arthritis.Gene. 2015 Mar 1;558(1):103-7. doi: 10.1016/j.gene.2014.12.046. Epub 2014 Dec 24.PubMed PMID: 25542810.

    6.          Alzolibani AA, Al Robaee AA, Al Shobaili HA, Bin Saif G, Al-Saif F, Ali A,Settin A. Interleukin-4 -590 T>C and interleukin-4 receptor Q551R A>G genepolymorphisms in Saudi cases with alopecia areata. J Egypt Public Health Assoc.2015 Mar;90(1):20-3. doi: 10.1097/01.EPX.0000461326.05328.d3. PubMed PMID: 25853541.

    7.          Alzolibani AA, Settin A, Ahmed AA, Ismail H, Elhefni N, Al Robaee AA. Genetic polymorphisms of NFκB1 -94 del/ins ATTG, NFκB1A 2758 A>G and SUMO rs237025 G>A inpsoriasis. Int J Health Sci (Qassim). 2015 Jan;9(1):25-33. PubMed PMID: 25901130;PubMed Central PMCID: PMC4394936.

    8.          Elbaz R, Dawood N, Mostafa H, Zaki S, Wafa A, Settin A. Leptin genetetranucleotide repeat polymorphism in obese individuals in Egypt. Int J HealthSci (Qassim). 2015 Jan;9(1):63-71. PubMed PMID: 25901134; PubMed Central PMCID:PMC4394940.

    9.          Elshazli R, Settin A. Association of PTPN22 rs2476601 and STAT4 rs7574865polymorphisms with rheumatoid arthritis: A meta-analysis update. Immunobiology.2015 Aug;220(8):1012-24. doi: 10.1016/j.imbio.2015.04.003. Epub 2015 Apr 28. PubMed PMID: 25963842.

    10.     Salama A, Elshazli R, Elsaid A, Settin A. Protein tyrosine phosphatase non-receptor type 22 (PTPN22) +1858 C>T gene polymorphism in Egyptian cases with rheumatoid arthritis. Cell Immunol. 2014 Jul;290(1):62-5. doi:10.1016/j.cellimm.2014.05.003. Epub 2014 May 17. PubMed PMID: 24880676.

    11.     Nasef N, Shabaan A, Mohammed S, Kandel S, Settin A, Zedan M, Fouda A. Factors influencing parental consent for participation in clinical research involving their children in Egypt. East Mediterr Health J. 2014 Apr 3;20(3):162-8. PubMed PMID: 24950073.

    12.     Alzolibani AA, Al Robaee A, Al-Shobaili H, Al-Saif F, Al-Mekhadab E, Settin AA. Association of CYP2C9 Genetic Variants with Vitiligo. Ann Dermatol. 2014 Jun;26(3):343-8. doi: 10.5021/ad.2014.26.3.343. Epub 2014 Jun 12. PubMed PMID: 24966634; PubMed Central PMCID: PMC4069645.

    13.     Settin A, Salama A, Elshazli R. Signal transducer and activator of transcription 4 (STAT4) G>T gene polymorphism in Egyptian cases with rheumatoid arthritis. Hum Immunol. 2014 Aug;75(8):863-6. doi: 10.1016/j.humimm.2014.06.013. Epub 2014 Jun 28. PubMed PMID: 24979672.

    14.     Settin A, Abdalla AF, Al-Hussaini AS, El-Baz R, Galal A. Cure rate of Helicobacter pylori infection in Egyptian children related to CYP2C19 gene polymorphism. Indian J Gastroenterol. 2014 Mar 8. [Epub ahead of print] PubMed PMID: 24610583.

    15.     Settin A, El-Baz R, Ismaeel A, Tolba W, Allah WA. Association of ACE and MTHFR genetic polymorphisms with type 2 diabetes mellitus: Susceptibility and complications. J Renin Angiotensin Aldosterone Syst. 2014 Jan 22. [Epub ahead of print] PubMed PMID: 24452036.

    16.     Alsaid A, El-Missiry M, Hatata el-S, Tarabay M, Settin A. Association of IL-4-590 C>T and IL-13-1112 C>T gene polymorphisms with the susceptibility to type 2 diabetes mellitus. Dis Markers. 2013;35(4):243-7. doi: 10.1155/2013/107470. Epub 2013 Sep 9. PubMed PMID: 24167373; PubMed Central PMCID: PMC3782814.

    17.     Al-Shobaili HA, Settin AA, Alzolibani AA, Al Robaee A, Salem TA, Al-Saif F, Al-Mekhadab E. Interleukin-4 (-590 C>T) and Interleukin-4 Receptor (Q551R A>G) gene polymorphisms in Saudi patients with vitiligo. Eur J Dermatol. 2013 Jun 17. [Epub ahead of print] PubMed PMID: 23774696.

    18.     Alghasham A, Settin AA, Ali A, Dowaidar M, Ismail H. Association of MTHFR C677T and A1298C gene polymorphisms with hypertension. Int J Health Sci (Qassim). 2012 Jan;6(1):3-11. PubMed PMID: 23267299; PubMed Central PMCID: PMC3523778.

    19.      Ali A, Alghasham A, Ismail H, Dowaidar M, Settin A. ACE I/D and eNOS E298D gene polymorphisms in Saudi subjects with hypertension. J Renin Angiotensin Aldosterone Syst. 2012 Oct 5. [Epub ahead of print] PubMed PMID: 23042814.

    20.     Al-Shobaili HA, Salem TA, Alzolibani AA, Robaee AA, Settin AA. Tumor necrosis factor-α -308 G/A and interleukin 10 -1082 A/G gene polymorphisms in patients with acne vulgaris. J Dermatol Sci. 2012 Oct;68(1):52-5. Epub 2012 Jul 16. PubMed PMID: 22835835.

    21.     Settin A; Alghasham A; Ali A; Dowaidar M; Ismail H. Frequency of thrombophilic genetic polymorphisms among Saudi subjects compared with other populations Hematology, Volume 17, Number 3, May 2012 , pp. 176-182(7).

    22.     Alghasham A, Ali A, Ismail H, Dowaidar M, Settin AA. CYP2J2 -50 G/T and ADRB2 G46A gene polymorphisms in Saudi subjects with hypertension. Genet Test Mol Biomarkers. 2012 Sep;16(9):1027-31. doi: 10.1089/gtmb.2012.0006. Epub 2012 Jun 25. PubMed PMID: 22731644.

    23.     Al Robaee AA, AlZolibani A, Al Shobaili H, Settin A. Association of interleukin 4 (-590 T/C) and interleukin 4 receptor (Q551R A/G) gene polymorphisms with acne vulgaris. Ann Saudi Med. 2012 Jul-Aug;32(4):349-54. PubMed PMID: 22705603.

    24.     El-Baz R, Settin A, Ismaeel A, Khaleel AA, Abbas T, Tolba W, Abd Allah W, Sobh MA. MTHFR C677T, A1298C and ACE I/D polymorphisms as risk factors for diabetic nephropathy among type 2 diabetic patients. J Renin Angiotensin Aldosterone Syst. 2012 May 3. [Epub ahead of print] PubMed PMID: 22554825.

    25.     Settin A, Alkasem R, Ali E, ElBaz R, Mashaley AM. Factor V Leiden and prothrombin gene mutations in Egyptian cases with unexplained recurrent pregnancy loss. Hematology. 2011 Jan;16(1):59-63. PubMed PMID: 21269570.

    26.     Settin A, Elshazli R, Salama A, Elbaz R. Methylenetetrahydrofolate Reductase Gene Polymorphisms in Egyptian Women with Unexplained Recurrent Pregnancy Loss. Genet Test Mol Biomarkers. 2011 Aug 4. [Epub ahead of print] PubMed PMID:21815801.

    27.      Settin AA, Hassan HA, El-Baz RA, Hassan TA. Association of cytokine gene polymorphisms with psoriasis in cases from the nile delta of egypt. Indian J Dermatol. 2011 May;56(3):272-7. PubMed PMID: 21772586; PubMed Central PMCID: PMC3132902.

    28.     Aljarallah B, Ali A, Dowaidar M, Settin A. Prevalence of α-1-antitrypsin gene mutations in Saudi Arabia. Saudi J Gastroenterol. 2011 Jul-Aug;17(4):256-60. PubMed PMID: 21727732; PubMed Central PMCID: PMC3133983.

    29.     Zedan M, Settin A, El-Chennawi F, El-Desouky T, Nasef N, Fouda A. Eosinophilic cationic protein: is it useful in assessing control of childhood asthma? East Mediterr Health J. 2010 Oct;16(10):1045-9. PubMed PMID: 21222420.

    30.     Zedan M, Gamil N, El-Assmy M, Fayez E, Nasef N, Fouda A, Settin A. Montelukast as an episodic modifier for acute viral bronchiolitis: a randomized trial. Allergy Asthma Proc. 2010 Mar;31(2):147-53. PubMed PMID: 20406596.

    31.     Dowaidar M, Settin A. Risk of myocardial infarction related to factor V Leiden mutation: a meta-analysis. Genet Test Mol Biomarkers. 2010 Aug;14(4):493-8. PubMed PMID: 20642359.

    32.     Saadia Z, Alzolibani AA, Al Robaee A, Al Shobaili HA, Settin AA. Cutaneous Manifestations of Hypothyroidism amongst Gynecological consultations. Int J Health Sci (Qassim). 2010 Nov;4(2):168-77. PubMed PMID: 21475555; PubMed Central PMCID: PMC3068831.

    33.     Alshobaili HA, Shahzad M, Al-Marshood A, Khalil A, Settin A, Barrimah.Genetic background of psoriasis. Int J Health Sci (Qassim). 2010 Jan;4(1):23-9. PubMed PMID: 21475522; PubMed Central PMCID: PMC3068801.

    34.     Settin AA, El-Bestar SF, Gouida MS, El-Sherif MA, El-Leithy MA, Girgis NJ. Flow cytometry for cell cycle parameters in healthcare workers potentially exposed to ionizing radiation. J Egypt Public Health Assoc. 2009;84(5-6):443-56. PubMed PMID: 20673564.

    35.     Settin AA, Algasham A, Dowaidar M, Ismail H. Methylene tetrahydrofolate reductase and angiotensin converting enzyme gene polymorphisms related to overweight/obesity among Saudi subjects from Qassim Region. Dis Markers.2009;27(2):97-102. PubMed PMID: 19893205.

    36.     Algasham A, Ismail H, Dewaidar M, Settin AA. Methylene tetrahydrofolate reductase and angiotensin-converting enzyme gene polymorphisms among Saudipopulation from Qassim region. Genet Test Mol Biomarkers. 2009 Dec;13(6):817-20. PubMed PMID: 19810824.

    37.     Settin A, Hassan H, El-Baz R, Hassan T. Association of cytokine gene polymorphisms with psoriasis in cases from the Nile Delta of Egypt. Acta Dermatovenerol Alp Panonica Adriat. 2009 Sep;18(3):105-12. PubMed PMID: 19784523.

    38.     Badr El-Din NK, Settin A, Ali N, Abdel-Hady el-SK, Salem FK. Cytokine gene polymorphisms in Egyptian cases with brain tumors. J Egypt Natl Canc Inst. 2009 Jun;21(2):101-6. PubMed PMID: 21057561.

    39.     Settin A, Elbaz R, Abbas A, Abd-Al-Samad A, Noaman A. Angiotensin-converting enzyme gene insertion/deletion polymorphism in Egyptian patients with myocardial infarction.J Renin Angiotensin Aldosterone Syst. 2009 Jun;10(2):96-100.PMID: 19502257 

    40.     Settin A, Ismail A, El-Magd MA, El-Baz R, Kazamel A. Gene polymorphisms of TNF-alpha-308 (G/A), IL-10(-1082) (G/A), IL-6(-174) (G/C) and IL-1Ra (VNTR) in Egyptian cases with type 1 diabetes mellitus. Autoimmunity. 2009 Jan;42(1):50-5. PubMed PMID: 19127455.

    41.     Magdy Zedan, Ahmed Settin, Mohamed Farag, Mohamed EL-Bayoumi, Mohamed Ezz-Elregal, Alaa Abd-Elkader, Engy Osman, Ashraf Fouda. HOW DO EGYPTIAN CHILDREN DESCRIBE ASTHMA SYMPTOMS? Egyptian Journal of Bronchology, Vol 3, No 1, June, 2009

    42.     Settin A, Ali N, Salem FK. Cytokine gene polymorphisms in Egyptian cases with brain tumors. Egypt J Immunol. 2008;15(2):15-23. PubMed PMID: 20306684.

    43.     Settin A, Zedan M, Farag M, El Regal ME, Osman E. Gene polymorphisms of IL-6(-174) G/C and IL-1Ra VNTR in Egyptian asthmatic children. Indian J Pediatr. 2008 Sep 22. [Epub ahead of print] PMID: 18810365.

    44.     Settin A, Dowaidar M, El-Baz R, Abd-Al-Samad A, El-Sayed I, Nasr M. Frequency of factor V Leiden mutation in Egyptian cases with myocardial infarction. Hematology. 2008 Jun;13(3):170-4. PMID: 18702875.

    45.     Zedan M, Settin A, Farag MK, El-Bayoumi M, El Regal ME, El Baz R, Osman E.Gene polymorphisms of tumor necrosis factor alpha-308 and interleukin-10-1082 among asthmatic Egyptian children. Allergy Asthma Proc. 2008 May-Jun;29(3):268-73. PMID: 18534084.

    46.     Settin A, Elsobky E, Hammad A, Al-Erany A. Rapid sex determination using PCR technique compared to classic cytogenetics. Int J Health Sci (Qassim). 2008 Jan;2(1):49-52. PubMed PMID: 21475471.

    47.     Al-Robaee AA, Al-Zolibani AA, Al-Shobili HA, Kazamel A, Settin A. IL-10 implications in psoriasis. Int J Health Sci (Qassim). 2008 Jan;2(1):53-8. PubMed PMID: 21475472.

    48.     Settin A, Almarsafawy H, Alhussieny A, Dowaidar M. Dysmorphic Features, Consanguinity and Cytogenetic Pattern of Congenital Heart Diseases: a pilot study from Mansoura Locality, Egypt. Int J Health Sci (Qassim). 2008 Jul;2(2):101-11. PubMed PMID: 21475491.

    49.     Settin A, Badr El-Din N, Ali N, Abdel-Hady El, Salem FK: Histopathologic Diagnosis, Cell Cycle Parameters and Clinical Behavior of 90 Egyptian Brain Tumor Cases. The Internet Journal of Neurology. 2008. Volume 9 Number 1

    50.     Settin A, Abdel-Hady H, El-Baz R, Saber I. Gene polymorphisms of TNF-alpha(-308), IL-10(-1082), IL-6(-174), and IL-1Ra(VNTR) related to susceptibility and severity of rheumatic heart disease. Pediatr Cardiol. 2007 Sep-Oct;28(5):363-71. Epub 2007 Jun 29. PMID: 17607501.

    51.     Settin A, Abu-Saif IS, El-Baz R, Dowaidar M, Kasim RA, Shabana S. Diagnosis of Sex Chromosome Disorders and Prenatal Diagnosis of Down Syndrome using Interphase Fluorescent In-Situ Hyperidization Technique. Int J Health Sci (Qassim). 2007 Jul;1(2):203-9. PubMed PMID: 21475429.

    52.     Settin A, El-Baz R, Abd Rasool M, El-Khalegy H, El-Sayed O, El-Bendary M, Al-Nagar AS. Clinical and molecular diagnosis of Familial Mediterranean Fever in Egyptian children. J Gastrointestin Liver Dis. 2007 Jun;16(2):141-5. PMID: 17592559 [PubMed - indexed for MEDLINE]

    53.     Settin A, Al Haggar M, Al Dosoky T, Al Baz R, Abdelrazik N, Fouda M, Aref S, Al-Tonbary Y. Prognostic cytogenetic markers in childhood acute lymphoblastic leukemia: cases from Mansoura Egypt. Hematology. 2007 Apr;12(2):103-11. PMID: 17454190 [PubMed - indexed for MEDLINE]

    54.     Settin A, Al Haggar M, Al Dosoky T, Al Baz R, Abdelrazik N, Fouda M, Aref S, Al-Tonbary Y. Prognostic cytogenetic markers in childhood acute lymphoblastic leukemia. Indian J Pediatr. 2007 Mar;74(3):255-63. PMID: 17401264 [PubMed - indexed for MEDLINE]

    55.     Settin A, Nassar S, Abdel-Latif A, Elbaz R, El-Mongy S, Hassan A, Hassan A. Association of cytokine gene polymorphism with susceptibility and clinical types of leprosy. Int J Health Sci (Qassim). 2007 Jan;1(1):25-33. PubMed PMID: 21475449.

    56.     Settin A, Attallah AG, Abo-Sekina M M, Ali E M, Gawish G E-H. Lymphocytes DNA Content, P53, C-Myc And Bcl-2 As Predictive Markers In Childhood With Acute Lymphoblastic Leukemia. Egyptian Journal of Biochemistry and Molecular Biology Vol. 25 (2) 2007: pp. 192-211

    57.     Settin A, Al Haggar M, Al Dosoky T, Al Baz R, Abdelrazik N, Fouda M, Aref S, Al-Tonbary Y. Prognostic cytogenetic markers in childhood acute lymphoblastic leukemia: cases from Mansoura, Egypt. Hematology. 2006 Oct;11(5):341-9. PubMed PMID: 17607584.

    58.     Settin A, El-Bendary M, Abo-Al-Kassem R, El Baz R. Molecular analysis of A1AT (S and Z) and HFE (C282Y and H63D) gene mutations in Egyptian cases with HCV liver cirrhosis. J Gastrointestin Liver Dis. 2006 Jun;15(2):131-5. PMID: 16802007 [PubMed - indexed for MEDLINE]

    59.     Settin A, Abu Seif M, Al Shahat M, El-Baz R, Abou El-Kheir E. Gene Polymorphisms of TNF-α-308(G/A), IL-10-1082(G/A), IL6-174(G/C) and IL1Ra(VNTR) in Egyptian Cases with Adult and Early Onset Periodontitis. The Internet Journal of Dental Science. 2006. Volume 4 Number 1.

    60.     Settin A, Al-Haggar M, El Marsafawy H, Abd Alkader A, El Baz R, Mansour A et al., Genetic Analysis of Rheumatic Fever Among Egyptian Families, Consanguinity Pattern, Segregation Analysis and Blood Group Association. J.Med.Sci., 6(3); 415-422, 2006

    61.     Settin A, Al-Haggar M, Neamatallah M, Al- Said A, Hafez M. Detection of beta-thalassaemia mutations using primer-specific amplification compared to reversed dot blot hybridization technique in Egyptian cases. Haema 2006; 9(3): 401-409

    62.     Settin A, Al Haggar M, Gouida M, ElBaz R, AbuAlKasem R, AlMorsy Z. Diagnostic Significance of Flow Cytometric Analysis of DNA Ploidy and Apoptosis in Children with Lymphadenopathy Haema 2006; 9(2): 240-24.

    63.     Settin, Al-Haggar M, Al-Baz R, Yousof H, Osman N. Screening for G6PD Mediterranean mutation among Egyptian neonates with high or prolonged jaundice. Haema 2006; 9(1): 83-90

    64.     Al Haggar M, Settin A, Ragab M, Al Shahat M, Abdel-Hadi H, Toson E et al.,. Segregation Analysis of P53, c-myc and DNA Ploidy Using Flow Cytometry Among Egyptian Families with Childhood Leukemia. J. M. Sci., 6(6): 906-914, 2006

    65.     Settin A, Al-Dosokey T, Al-Haggar M, El-Bendary M, Ezz M, El Baz R,et al.,. C282Y and H63D Haemochromatosis Alleles in Egyptian Patients with Cirrhosis. Arab J Gastroenterol 2006; 7(2):59-63

    66.     Settin A, Al-Dosokey T, Al-Haggar M, Al-Bendary M, Ezz M, El Baz R, et al., Increased Risk of Liver Cirrhosis Among Egyptian Carriers of S and/or Z Mutant Alleles of Alpha1-Antitrypsin Gene. Arab J Gastroenterol 2006; 7(1):

    67.     Abdelrazik N, Settin A, Al-Haggar M, Al-Dosoky T, Al-Baz R, Fouda M, Aref S, Al-Tonbary Y. Prognostic Cytogenetic Markers in Childhood Acute Lymphoblastic Leukemia : Cases from Mansoura, Egypt. Turkish Journal of Haematology 2005, Volume 22, Number 3 (Supplement

    68.     Settin A, Al-Haggar M, Al-Baz R, Al-Aiouty M, Hafez M. Screening of Mentally Handicapped Egyptian Children For Fragile X Syndrome Using Clinical, Cytogenetic And Molecular Approaches. J Pediatr Neurol 2005; 3(4):217-225

    69.     Hassan AM, Settin A , Nassar S, , Elbaz R, Hassan AA. TNF-a, IL-10, IL-6 and IL-1RA Gene Polymorphism in Leprosy in an Egyptian Locality. Egyptian Journal of Medical Human Genetics. Vol 6, No. 1 May 2005

    70.     Nassar, S; Abdel-Latif, A; EL-Mongy, S; Hassan, A; Baz, R EL; Settin, A. TNF-[alpha], IL10, IL6 and IL1RA Gene Polymorphism in Leprosy in an Egyptian locality. Journal of Investigative Dermatology. 123(2):A41, August 2004.

    71.     Settin A, Fayed H, Youssef H, Al Baz R, Fathi M, El Missiry A et al.,. Frequency of AZF Gene Microdeletions among Infertile Men with Idiopathic Oligozoospermia and Azoospermia in Nile Delta Region of Egypt. Egypt.J.Derm. & Androl Bound Vol. 24. No (1,2,3,4) 2004

    72.     Mohamed E, Seham A Gad El-Hak, Settin A, Amal A Ibrahim, Rizk A El-Baz, Doaa A A El-Morsi. Assessment of the role of blood group systems and three DNA loci (ALU TPA-25, HUMFES/FPS and HUMF13A1) in paternity testing in a sample of Egyptian population. Mansoura J. Forensic Med. Clin. Toxicol. Vol.XII No.2, July 2004

    73.     Hatem NL, Settin Hatem, Marzouk I M, Omar TEI, Okasha AG. Clinical and Genetic Study for identification of the Fragile X syndrome. European Journal of Pediatric Neurology, Vol 7, 5, 2003.

    74.     Settin A, Fayed H, Soliman Y, Younis M. Cytogenetic pattern, Y- Chromosome Deletion and Sperm Morphology, Motility and DNA Ploidy in Male Partners of Cases of Recurrent Abortion. Egypt.J.Derm. & Androl. Bound Vol. 23. No (1,2,3,4) 2003.

    75.     Hassan Abdel-Raheim Fayed, Rizk A. El Baz, Ahmed Abdel Khalek, Ahmed A Settin, Is Flow Cytometry an Important Complementary to Semen Analysis? Significance of Haploid Sperm Count. Egypt. J.Derm. & Androl. Bound Vol. 23. No (1,2,3,4) 2003

    76.     M. Hafez, M. EL-Ziny, S. Hawas, Z. EL-Morsy, A. Settin, M. Shokeir, A. R. EL-Hadidy, M. M. Hafez, R. EL-Baz and B. EL-Deek. Implications of TNF-alpha, sFas and Apoptosis in Insulin Dependent Diabetes Mellitus J. Med. Sci., 2 (3): 95-102 May - June, 2002

    77.     M Hafez, A Settin, Z El-Morsi, Y Al-Tonbary, R El-Baz, T El-Desoky, M El-Haggar, M Shokeir, A Shaltout, A Mansour, N Abdel Razik, H Al Marsafawy and M Lotfy. Gene Mutations of Glucose-6-Phosphate Dehydrogenase in Egypt. The Egyptian Journal of Paediatrics Vol. 17, No.4, 651-671, 2000

    78.     Hafez, S. Hawas, M. F. El-Battoty, Z. El Morsi, A Shaltout, A. Settin, M Shokeir, M El-Haggar, H Al Marsafawy, MM Ali, G Attia and B El Deek. Gene Expression And Circulating Cytokines In Juvenile Rheumatoid Arthritis. The Egyptian Journal of Paediatrics Vol. 17, No.4, 627-650, 2000.

    79.     Essam M Karawya, Camelia A Abdel Malak, Ahmad A Settin And Abdou G El-Sharaway. Chromosomal Abnormalities In Mentally Handicapped Children From Damietta Covernorate. Egypt. J. Med. Sci. 21(I) June, 2000: 237-246

    80.     M. Hafez, A. El-Beshlawy, A. Settin, et al. Beta-Globin Gene Clusters Haplotypes Associated with Sickle Cell Mutation Among Egyptian Patients. The Egyptian Journal of Pediatrics Vol. 16, No. 4, 1999 : 669-681.

    81.     A Settin, Z. El Morsi, M El Zayat, N Al Mousa. Title Newborn Screening For Hemoglobinopathies in Dakahlia, Egypt. Benha Medical Journal, Vol 14 No 1 Jan 1997 Letter to the Editor BMJ-ME, January, 1997

    82.     A Settin, A. Al-Gilany. Carrier And Gene Frequency Of Beta Thalassemia Depicted From Consanguinity Data Of Family Cases And Controls. The Egyptian Journal of Paediatrics Vol. 17, No1-2, 1997: 129-136.

    83.     Abd Alhady Algilany, A. Settein. Standardized Indicators Of Breastfeeding In Rural Dakahlia, Egypt. The Egyptian Journal of Paediatrics Vol. 14, No. 1-2, 1997:117-128.

    84.     Aref, L. A. Mahmoud, M. Hafez, O. S. Salama, A. Settin. Prevalence of iron deficiency and iron deficiency anaemia among the Egyptian population. Letter to the editor, BMJ, October, 1997

    85.     M Hafez, M Awadall, A Settin, Sohier Abu Ela, A Shaltout, M Shokeir, R. Al Baz, M Tawfik. Molecular Characterization Of Duchenne Muscular Dystrophy Gene Deletions Using PCR Technique. The Egyptian Journal of Paediatrics Vol. 14, No. 1-2, 1997 : 177-187.

    86.     Settin, A. Al-Gilany. Consanguinity Related to b-thalassemia and Offspring Mortality in Dakahlia , Egypt. Letter to the Editor BMJ-ME, December 1996

    87.     A Settein. Abd Alhady Algilany, M Zahran, H Foad and Gomaa Z . Presumble Frequency of Hyperlipidemia and Familial Hypercholesterolemia among Adolescent Students, Possible Influencing Socio-Demographic and Mental Health Factors on their Lipoprotein Profile. Benha Medical Journal, Vol 13 No 3 Sept 1996.

    88.     M. Hafez, F. El-Battoty, S. Hawas, A. El-Ghawit, A. Shaishaa, A. Settin, A. Mansour, A. Shaltout, W. El-Tarshoubi, F. El-kenawy. The Genetic Susceptibility for Autoantiboy Production in Rheumatoid Arthritis. The Egyptian Journal of immunology vol.3, No.1, 1996 : 69-75.

    89.     Hafez M, el-Fiky A, Bassiouny MR, el-Hafez SA, el-Morsy A, Khaled A, el-Ziny M, al-Tonbary Y, Settein A. Clinico-immunogenetic study on Egyptian multicase tuberculous families. Dis Markers. 1992 May-Jun;10(3):143-9. PMID: 1294359 [PubMed - indexed for MEDLINE]

    90.     M. Hafez., F. EL-Shennawy., M.Montaser., A.Sheishaa., A.Settein., M.Abou EL Kheir. M.Bassiouny., I. Saied., M.Hazem., S.Sallam., F.Gaballa, and M.Nagaty. Immunoneurogenetic Aspects Of Idiopathic Epilepsy In Multicase Families. The new Egyptian Journal of Medicine vol. 6, No. 5, 1992 : 1644-1652.

    91.     M. Hafez., Y. EL-Tonbary., S.Shama, A. Settein., A.Sheishaa., A. Shaltout A. Mansour., N.EL-Kholy., S. Sallam., A.EL-Hadidy., S.Hawas and H. Nageeb. The value of chromasomal studies in diagnosis, prognosis and DNA. characterization in lymphomas. The new Egyptian Journal of Medicine vol. 7, No. 6, 1992 : 1292-1298.

    92.     L. Felicetti L, G. Deidda , A. Novelletto ,L. Terrenato, , A. Settin And Hafez M. Application Of DNA Recominant Techniques To The Diagnosis And Prevention Of Human Inherited Diseases: Molecular Basis Of Beta-Thalassemia In Egypt, A Pioneer Project Of Italian-Egyptian Cooperation. Proceedings of The First Egyptian-Italian Symposium on Biotechnology, Assuit, Egypt (Nov. 21-23, 1992).

    93.     Settin A., Deidda G., Al-Tonbary A, Aref Kh, Novelletto A., Terrenato- L., Felicetti L., Habbosha M, and Hafez M. Molecular Analysis of b- thalassemia Mutations in the Mediterranean Coast and Nile Delta of Egypt. Proceedings of The First Egyptian-Italian Symposium on Biotechnology, Assuit, Egypt (Nov. 21-23, 1992).

    94.     Hafez M, el-Battoty MF, Hawas S, el-Ziny M, Sheashaa A, Settin A, Bassiouny MR, Hawas SA. Susceptibility to and severity of rheumatoid arthritis in multicase families. Br J Rheumatol. 1991 Jun;30(3):181-5. PMID: 2049577 [PubMed - indexed for MEDLINE]

    95.     A. Settin And A. Abd El-Kader. “Blood Groups And Thalassemia, Family Studies” The New Egyptian Journal of Medicine Vol 5, No 4, 1991 : 436-440.

    96.     Hafez M, Abdalla A, el-Shennawy F, al-Tonbary Y, Sheaishaa A, el-Morsi Z, Tawfik S, Settien A, Abou el-Khair M. Immunogenetic study of the response to streptococcal carbohydrate antigen of the cell wall in rheumatic fever. Ann Rheum Dis. 1990 Sep;49(9):708-14. PMID: 2241288 [PubMed - indexed for MEDLINE]

    97.     Novelletto A, Hafez M, Deidda G, Di Rienzo A, Felicetti L, el-Tahan H, el Morsi Z, el-Ziny M, al-Tonbary Y, Sittien A, et al. Molecular characterization of beta-thalassemia mutations in Egypt. Hum Genet. 1990 Aug;85(3):272-4. PMID: 1975554 [PubMed - indexed for MEDLINE]

    98.     Settin A Clinico-Pathological Study of Childhood Lyphadenopathy. M.D. Thesis, Faculty of Medicine, Mansoura University, Egypt 1985.

    99.     Settin A Clinico-Epidemiological Study of Some Childhood Malignancies MS Thesis, Faculty of Medicine, Mansoura University, Egypt 1983. 

     


Presentations National and International Conferences and Meetings

· “Genetic Testing, what is the benefit?” Second international conference of experts on disability and rehabilitation change with modern vision Onaizah , Saudi Arabia 4-5/3/2014

· First conference for experts on disability and rehabilitation, Oniza, Qassim, Saudi Arabia, 14-16 May 2012.

· International conference of biomarkers, Riadh, Saudi Arabia, 4-6 May, 2010

· 3th Annual Medical Research Meeting, Qassim University, 27 June, 2010

· 4th Annual Medical Research Meeting, Qassim University, 1 June, 2011

· 6th Annual Medical Research Meeting, Qassim University, 16-17 April 2012

· Methylene tetrahydrofolate reductase and angiotensin converting enzyme gene polymorphisms related to overweight/obesity among Saudi subjects from Qassim Region The 4th International Conference of Biomarkers in Chronic Diseases (2010) Riyadh, Saudi Arabia

· Vitamin D Receptor Gene Polymorphism in Relation to Cancer” Qassim University, April, 2010
· Methylenetetrahydrofolate Reductase (MTHFR) and Angiotensin Converting Enzyme (ACE) Gene Polymorphisms among Saudi Population from Qassim Region The 24th Meeting of Saudi biological society, Biotechnology: Reality and Application, Madinah Almunawwarah, at Taibah University, 12-14 Rabia Althani, 1430 H (7-9 April, 2009).

· Genetic Counselling in Diabetes Millitus. National Conference of Diabetes Qassim University May 2008

· Characterization of b thalassemia mutations in the northeastern provinces of Egypt using reverse dot blot hybridization Y. Al-Tonbary, M. Settin, A. El-Gharib, M. Abdel-Razik, M. Shaat Mansoura University, MANSOURA, Egypt. Haematologica 2007; 92[suppl.2]:504. Abstract 1405. 12th Congress of the European Hematology Association, June 7-10, 2007

· Cancer Risk in Families of Childhood Leukemia Suggested by Flowcytometric Analysis of p53, c-myc and DNA Ploidy Ahmad A Settin, Mohammad S Al Haggar, May Al Shahat, Mona A Samy, Rizk A El Baz.. Poster presentation, 1st international Onco-Epidemiology congress, Aida Hotel – North Coast 1-3/9/2005

· Flow Cytometric Nuclear DNA Content Analysis Of Lymphadenopathy In Children: Diagnostic Significance Of Nuclear DNA Ploidy And Apoptosis. Ahmad A Settin, Seham A AlMansy, Mona S Gouida, Tarek A Atia, Rizk A ElBaz, Rabab A Ali, Zakaria I AlMorsy. Presented to the meeting of the Egyptian Society of Histological and Cytological research, December 2004

· Clinical and Genetic Study for identification of the Fragile X syndrome, NL Hatem, AA Settin, I M Marzouk, TEI Omar, AG Okasha.; The 5th International Congress of the European Pediatric Neurology Society (Taormina, Italy, 22-25 October, 2003).

· Prevalence of iron deficiency and iron deficiency anaemia among the Egyptian population. Aref, L. A. Mahmoud, M. Hafez, O. S. Salama, A. Settin. The XIV meeting of the Inernational Society of Haematology. Stockholm, Sweden AUG 30-SEPT 4. 1997.

· Egyptian-Italian Workshop on "Recent advances in approaching genetic disorders" Fac. Med. Mansoura Univ. Mansoura Egypt, April, 1993.

· Presumptive Evidence For Inherited Deficiency Of Secretory Iga In Rheumatic Families. M.Hafez, A. Settin, S. Hawas, A. Shaishaa, M. Abul Khair Conference of the Arab Union of Pediatric Societies Cairo Dec., 1990. and the 12th Annual Pediatric conference Mansoura University, May 30-31 1991

· TNF-[alpha], IL10, IL6 and IL1RA Gene Polymorphism in Leprosy in an Egyptian locality. Nassar, S; Abdel-Latif, A; EL-Mongy, S; Hassan, A; Baz, R EL; Settin, A. Poster Presentations to the 34th meeting of the European Society of Dermatological Research 2004).

· Von Willibrand Factor and Plasminogen Activator Inhibitor in Children with IDDM M A El-Ziny, OS Salama, AA Sittin, T El-Desoky, MA Kishta.,Abstract book of Conference on Child Health and the 9th Conference of Union of Arab Pediatric Societies Jeddah, November 6-8, 2001

· xiv meeting of the Inernational Society of Haematology, Stockholm, Sweden AUG 30-SEPT 4. 1997. Sh. El-Sallab, Y. Al-Tonbary, S. Hawwas, M. R. Bassiony, M. El-Ayyouty,

· Deletional Mutation in Duchenne Muscular Dystrophy. M Hafez, A Settin, S Abu Ela, A Shaltout, M Shokeir, M El-Haggar and M Tawfik.. Presented in the Annual Conference of Mansoura Faculty of Medicine, October 24-25, 1996.

· PCR Diagnosis of -thalassemia.A Settin. Presented in the Annual Conference of Mansoura Faculty of Medicine, October 24-25, 1996.

· M Hafez, A Settin, M Sheir., L Terrenato et . Gene mutations and clinical presentations in relation to splenectomy in -thalassemia. The 5th International Conference on Thalassaemias and the Haemoglobinopathies. Nicosia-Cyprus 29th March - 3rd April, 1993.

· M Hafez, M El-Ziny, Y El-Tonbary, A Settin, A Sheishaa, A Shaltout et al. Chromosomal Analysis in Lymphomas. Presented in the First National Conference of the Egyptian Pediatric Genetic Society April,1993.

· Settin A., Deidda G., Al-Tonbary A, Aref Kh, Novelletto A., Terrenato- L., Felicetti L., Habbosha M, and Hafez M. Molecular Analysis Of  Thalassemia Mutations In The Mediterranean Coast And Nile Delta Of Egypt. 1st International Conference of Environmental Mutagenesis in Egypt (19-25 January 1992, Mariot Hotel, Cairo) and 1st national conference of the Egyptian Pediatric Genetic Society April,1993

· Hafez, L. A. Mahmoud, O. S. Salama, L. Terrenato, L. Felicetti, A. Settin , A. Novelletto, S. Aref, - Thalassemia Carrier And Gene Frequency Among Egyptian Population. Presentation First National Conference of the Egyptian Pediatric Genetic Society April,1993.

· A. Settin, M. Hafez. Genetic Aspects Of Extrahepatic Biliary Atresia. First National Conference of the Egyptian Pediatric Genetic Society April,1993.

· The Genetic Susceptibility for Autoantibody Production in Rheumatoid Arthritis. M. Hafez, F. El-Battoty, S. Hawas, A. El-Ghawit, A. Shaishaa, A. Settin, A. Mansour, A. Shaltout, W. El-Tarshoubi, F. El-kenawy. Presented at the First National Conference of the Egyptian Pediatric Genetic Society April,1993.

· M. Hafez, M. AL-Battoty, S. Hawas, Y. AL-Tonbary, A. Sarhan, A. Sheishaa, A. Settin, M. Abou AL-Kheir. and B. EL-Kady. Disease severity and immunogenetic regulation in Juvenile rheumatoid arthritis Presented at the 11th Annual Pediatric conference Mansoura University, May 24th 1990..

· A Settin and M.Hafez. Inbreeding Among The Egyptian Population And Its Effect On Genetic Disorders. The 11th Pediatric Conference, Mansoura University, 1990.

· M Hafez, G El- Wehedy, N El-Kholy, Y Al-Tonbary, A Settin , S Shamaa, N Nagib. Genetic Markers in Hodgkin’s Lymphoma. The Conference of the Egyptian Society of Tumor Marker Oncology (Nov. 1989).

· A Settin, M. Farag, A. Sheishaa, M. Kashaba. Some Prevalence Data Of Statural Deviation, Obesity And Goiter In Egyptian Children. Presented at the 11th Pediatric Conference, May 1989, Mansoura University.






(With Professor Hafez, Prof Terranato, II Univer Rome, Prof Marina Frontali and Prof Felicetti, CNR, Rome)



Honors and Awards:



· Honored as the best staff in Pediatric Department, Qassim University, 2010

· Honored as the best instructor for E-learning activities in the College of Medicine, Qassim University, 2009

· Honored as the first in the last year of medical study in the Faculty of Medicine Mansoura University 1979 with a final grading “Excellent with Honor".

· Honored as the University Ideal Student 1977 and awarded a visit to Germany.

· Honored as the headmost for the highest grade in whole Egypt among candidates for the general certificate of education 1973 (Final Score 99.3%) and awarded a travel to some European countries




With Stanford Prevention Research Center team, Qassim University, 2010

Referees



· Prof Vishwajit L. Nimgaonkar, Department of Psychiatry, University of Pittsburgh School of Medicine, Western Psychiatric Institute Pennsylvania University, USA

· Prof. Dr. Abd Alfattah Attallah. National Institute of Health USA (Biotechnology Center, New Damietta, Egypt)

· Prof. Dr. Ezzat Elsubki, Prof of Pediatrics and Genetics, Ain Shams University, and Head of Medical Genetics Center, Cairo, Egypt.

· Luciano Felicetti. Ex. Director of Research, Biology Department, Institute of Cell Biology, CNR, Rome Italy

· Prof. Dr. Luciano Terrenato. Prof. of Population Genetics, Biology Department II University of Rome, Rome, Italy

· Prof. Dr. Hansmann. Head of Institute of Genetics, Martin Luther University, Haale/Saale Germany

· Prof Dr Holiniski Feder. Director of Medical Genetics Center, Munich, Germany

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