کنگره ژنتیک

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Row	Title	Presenting Author	Scientific Chapter	Affiliation
1	A Novel Missence Mutation in the Transglutaminase-1 Gene in an Autosomal Recessive Congenital Ichthyosis Patient	Ahmadi shadmehri Aazam	تازه هاي ژنتيک و اختلالات شايع ژنتيکي	Social Welfare Organization of South Khorasan Province, Birjand, Iran
2	Whole-exome sequencing (WES) provides the possibility of genome-wide preconception carrier screening	Alipour Olyaei Nasrin	تازه هاي ژنتيک و اختلالات شايع ژنتيکي	Genomic Research Center, Shahid Beheshti University of Medical Sciences, Taleghani Hospital, Aarabi St., Yaman Ave., Velenjak, Tehran-Iran
3	Genetic causes of premature ovarian failure	Almadani Seyed navid	تازه هاي ژنتيک و اختلالات شايع ژنتيکي	Department of Genetics,Reproductive Biomedicine Reserch Center ,Royan Institute for Reproductive Biomedicine , ACECR ,Tehran, Iran
4	Effects of familial hypercholesterolemia-associated genes on the phenotype of premature myocardial infarction.	Asadi Seyed ehsan	تازه هاي ژنتيک و اختلالات شايع ژنتيکي	phd of Nursing, Esfahan Medical University, Esfahan, Iran.
5	ازدواج فامیلی و اختلالات ژنتیکی	Asadpour Shaghayegh	تازه هاي ژنتيک و اختلالات شايع ژنتيکي	دانشگاه آزاد اسلامی بابل
6	The robust bioinformatics pipeline and comprehensive clinical review of patients with genetic disorders significantly improve overall diagnosis by exome sequencing	Bahreini Amir	تازه هاي ژنتيک و اختلالات شايع ژنتيکي	Karyogen, Isfahan, IRAN
7	Role of the clinical genetic databases in a better performance of genetic counseling	Falah Masoumeh	تازه هاي ژنتيک و اختلالات شايع ژنتيکي	ENT and Head & Neck Research Center and Department, The Five Senses Institute, Hazrat Rasool Akram Hospital, Iran University of Medical Sciences, Tehran, Islamic Republic of Iran;
8	DOCK8-related immunodeficiency syndrome (DIDS): novel deleterious mutations	Gharesouran Jalal	تازه هاي ژنتيک و اختلالات شايع ژنتيکي	Division of Medical Genetics, Tabriz Children's Hospital, Tabriz University of Medical Sciences, Tabriz, Iran.
9	SPINK5 and Netherton syndrome: novel deleterious mutation	Gharesouran Jalal	تازه هاي ژنتيک و اختلالات شايع ژنتيکي	Molecular Genetics Division, GMG center, Tabriz, Iran
10	Comparison and comparison of telomerase expression in healthy tissue and breast cancer	Igder Mohsen	تازه هاي ژنتيک و اختلالات شايع ژنتيکي	Tabriz university
11	Diagnosis of lethal or prenatal-onset or familial coinciding recessive disorders by parental exome sequencing	Jamali Payman	تازه هاي ژنتيک و اختلالات شايع ژنتيکي	Aliakbar genetic counseling center, Shahrood welfare office, Shahrood, Iran
12	Carrier detection of CAH, in a consanguineous family with a deseased affected child	Jazayeri Roshanak	تازه هاي ژنتيک و اختلالات شايع ژنتيکي	Department of Genetics, Faculty of Medicine, Alborz University of Medical Sciences, Karaj, Iran
13	New Phenotypes for Old Genes	Kariminejad Ariana	تازه هاي ژنتيک و اختلالات شايع ژنتيکي	Chief Genetic Counselor
14	The first world report of a homozygous mutation in Pseudouridine synthase-3 gene (PUS3) in two patients with intellectual disability in an Iranian family	Keshavarz Parvaneh	تازه هاي ژنتيک و اختلالات شايع ژنتيکي	Genetics Medical Laboratory of Dr Keshavarz, Rasht, Iran- School of Medicine (Department of Genetics), Guilan University of Medical Science, Rasht, Iran
15	Association of a genetic variant in Interleukin-10 gene with increased risk and inflammation associated with cervical cancer	Maftouh Mina	تازه هاي ژنتيک و اختلالات شايع ژنتيکي	Mashhad University of Medical Sciences
16	شناسایی موتاسیون جدید (c.1006C>T) در ژن SPG20 مرتبط با سندروم Troyer	Mahdavi Mohammad Reza	تازه هاي ژنتيک و اختلالات شايع ژنتيکي	دانشگاه علوم پزشکی مازندران
17	شناسایی موتاسیون جدید در ژن AIPL1 همبسته با بیماری Leber Congeital Amaurosis	Mahdavi Mohammad Reza	تازه هاي ژنتيک و اختلالات شايع ژنتيکي	دانشگاه علوم پزشکی مازندران
18	LAMA1 gene variant associated with intellectual disability and sever myopia - a case report	Moghbelinejad Sahar	تازه هاي ژنتيک و اختلالات شايع ژنتيکي	3Cellualr and molecular research center, Qazvin university of medical science, Qazvin, IRAN.
19	Genetic Approach to Recurrent Pregnancy Loss	Pooladi Arash	تازه هاي ژنتيک و اختلالات شايع ژنتيکي	1- Cellular and Molecular Research Center, Medical Genetics and Molecular Medicine Department, Kurdistan University of Medical Sciences, Sanandaj, Iran.
20	Characterization of human papillomavirus (HPV) genotypes among patients referred to gynecology clinic, Laleh hospital, Tehran, Iran.	Rezaei IMAN	تازه هاي ژنتيک و اختلالات شايع ژنتيکي	مركز ژنتيك بيمارستان لاله و پژوهشگاه بيماريهاي ويروسي، بخش تشخيص مولكولي
21	بررسی و مقایسه بیان آنزیم تلومراز در بافت سالم و بافت سرطانی پستان¬ها	Rezvani Zahra sadat	تازه هاي ژنتيک و اختلالات شايع ژنتيکي	دانشجوی کارشناسی ارشد رشته زیست شناسی، گرایش ژنتیک، دانشگاه آزاد اسلامی واحد علوم و تحقیقات آذربایجان شرقی
22	اختلالات متابولیسم ارثی	Shahzadeh fazeli Seyed abolhassan	تازه هاي ژنتيک و اختلالات شايع ژنتيکي	Department of Genetics, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran.
23	Two variants in exon and intron 9 of LDLR gene in Iranian familial hypercholesterolemia patients	Tajamolian Masoud	تازه هاي ژنتيک و اختلالات شايع ژنتيکي	Medical Genetic Research Center, Shahid Sadoughi University of Medical science, Yazd,Iran
24	آنالیز پیوستگی لوکوس در ناشنوایان DFNB77 و DFNB37 های غیر سندرومی با وراثت اتوزومال مغلوب در استان هرمزگان	Ahmadi Banafsheh	تازه هاي ژنتيک و اختلالات شايع ژنتيکي	Medical Biotechnology Resarch Center, Ashkezar Branch, Islamic Azad University, Ashkezar, Yazd
25	: شناسایی جهش A1298C ژن MTHFR در مردان نابارور	Darvishi Maryam	تازه هاي ژنتيک و اختلالات شايع ژنتيکي	دانشگاه آزاد اسلامی واحد دزفول
26	سندرم داون و آزمایشات قبل از تولد برای شناسایی آن	Fakeri Mahsa	تازه هاي ژنتيک و اختلالات شايع ژنتيکي	دانشگاه سراسری تبریز
27	Determine a mutation in a daughter suffer from hydrocephalus and developmental disorder	Ghavabesh Jassem	تازه هاي ژنتيک و اختلالات شايع ژنتيکي	Center of Geneics consulation of Ahwaz Behzisti
28	Investigation and Comparison of margin and tumor in breast cancer patient (lominal A) by proteomic approach	Khani Ramtin	تازه هاي ژنتيک و اختلالات شايع ژنتيکي	Young Researchers and Elite club, Azad Islamic University, Medical science branch, Tehran, Iran
29	Detection of a new pathogenic mutation on DMD gene associated with Duchene Muscular Dystrophy	Mohaddes Ardebili Seied Vahid	تازه هاي ژنتيک و اختلالات شايع ژنتيکي	Cytogenetics Division, Dr. Mohaddes Medical Genetics Laboratory (DMMGL), Tabriz, Iran
30	Association of A Novel Balanced Reciprocal Translocation and Recurrent Miscarriage: A Case Report	Mohaddes Ardebili Seied Vahid	تازه هاي ژنتيک و اختلالات شايع ژنتيکي	Cytogenetics Division, Dr. Mohaddes Medical Genetics Laboratory (DMMGL), Tabriz, Iran
31	A brief view on the role of genetic counseling in neuromuscular disease	Sadeghinia Farnaz	تازه هاي ژنتيک و اختلالات شايع ژنتيکي	Genetics research center, University of social welfare and rehabilitation sciences, Tehran, Iran
32	Case Report of Bardet Biedl Syndrome	Sorkhkooh Azari Noushin	تازه هاي ژنتيک و اختلالات شايع ژنتيکي	Allame Amini Genetic Consultant Center, Tabriz, Iran
33	Effects of N-acetyl-cysteine supplementation on sperm quality, chromatin integrity and level of oxidative stress in infertile men.	Asadi Seyed ehsan	ديس مورفولوژي	phd of Nursing, Esfahan Medical University, Esfahan, Iran.
34	Deletion 22q11.2 syndrome frequency in patients with cleft palate referred to Alzahra Hospital, Isfahan, Iran	Nejati Omid	ديس مورفولوژي	22 Bahman Hospital- Medical and Pathological laboratory - Islamic Azad University of Mashhad, Iran
35	A Case report of Expanding the clinical spectrum of Van Maldergem Syndrome in Hasti genetic counselling centre in south Khorasan	Rezazadeh Jamileh	ديس مورفولوژي	اداره کل بهزیستی خراسان جنوبی
36	اثربخشی آموزش مهارت‌های ارتباطی بر بهبود کیفیت زندگی افراد کم بینای آرپی	Mozafari HOSEIN	نابينايي	آموزش وپرورش استثنایی
37	Application of multi-gene panel in juvenile-onset glaucoma: report of 2 cases with dominant & recessive inheritance	Vahedi Afsaneh	نابينايي	Mana genetic counseling center, Shahrood, Iran.
38	Maternal circulating microRNAs as non-invasive biomarkers for prenatal diagnosis of congenital heart defects	Abtin Maryam	اختلالات قلبي – عروقي	Department of medical genetics, Faculty of medicine, Tabriz university of medical sciences,Tabriz, Iran
39	بررسی علل مرگ کودکان 59-1 ماهه ناشی از ناهنجاری مادرزادی در بخش خارج بیمارستانی دانشگاه علوم پزشکی تبریز ولزوم انجام مشاوره ژنتیک	Ansari Masoumeh	اختلالات قلبي – عروقي	معاونت بهداشت دانشگاه علوم پزشکی تبریز
40	Randomized, double-blind, placebo-controlled clinical trial of choline supplementation in school-aged children with fetal alcohol spectrum disorders.	Asadi Seyed ehsan	تراتولوژي	phd of Nursing, Esfahan Medical University, Esfahan, Iran.
41	تحلیل روابط "تنظیم هیجانی"،"بهزیستی روانشناختی" ،"ریسک فاکتورهای قلبی در بیماران مبتلا به سکته قلبی	Ghobadi Soroush	اختلالات قلبي – عروقي	سازمان بهزیستی
42	Association of a genetic variant in the angiopoietin-like protein 4 gene with metabolic syndrome.	Avan Amir	اختلالات قلبي – عروقي	Metabolic syndrome Research center, Mashhad University of Medical Sciences, Mashhad, Iran
43	Rare P376L variant in the SR-BI gene associates with HDL dysfunction and risk of cardiovascular disease	Avan Amir	اختلالات قلبي – عروقي	Metabolic syndrome Research center, Mashhad University of Medical Sciences, Mashhad, Iran
44	Bioinformatics study and genetic counseling contribute to the diagnosis of cardiovascular disorders	Mansouri Fatemeh	اختلالات قلبي – عروقي	Department of Genetics and Immunology, Faculty of Medicine, Urmia University of Medical Sciences, Urmia, Iran.
45	The study of KCNE1 gene mutations in Iranian LQTS patients	Norouzi Rambod	اختلالات قلبي – عروقي	1-Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, Iran 2- Department of Biology, Faculty of Basic Science, Kharazmi University, Tehran, Iran
46	A novel large exon deletion in GFAP gene, Adult Alexander disease in Iran; The first report in the world	Alizadeh Fatemeh	Other related topics	Genomic Psychiatry Department, Roozbeh Hospital, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
47	بررسی وضعیت موجود تشخیص ناهنجاریهای مادرزادی با انجام سونوگرافی دردانشگاه علوم پزشکی تبریز	Ansari Masoumeh	Other related topics	معاونت بهداشت دانشگاه علوم پزشکی تبریز
48	Effect of inorganic polyphosphate on microvascular endothelial permeability and its mechanism: focus on AMP kinase signaling pathway	Avan Amir	Other related topics	Metabolic syndrome Research center, Mashhad University of Medical Sciences, Mashhad, Iran
49	Genetic Consultation, Genomics Techniques and further in-vitro fertilization Strategies in families with a child involved with auto-immune hemolytic disorders	Banihashemi Kambiz	Other related topics	Academic member, ATU, MSRT, Tehran, Iran
50	preferencing 4p medicnes	Darsaneh Zahra	Other related topics	azad babol university
51	جنبه های بالینی تفسیر کلینیکال داده های WES در جمعیت ایرانی	Dastmalchi Romina	Other related topics	دانشگاه علوم پزشکی شهید بهشتی
52	Associated genes with early and late onset of symptoms in patients with Charcot–Marie–Tooth disease	Gharesouran Jalal	Other related topics	Division of Medical Genetics, Tabriz Children's Hospital, Tabriz University of Medical Sciences, Tabriz, Iran
53	مشاوره ویژه ژنتیک ناباروری در مردان آزواسپرمیک با اختلالات کروموزومی و حذف های جزئی در ناحیه AZF	Montazeri Somayeh	Other related topics	دانشجوی دکترای ژنتیک، مرکز تحقیقات ژنتیک تالاسمی،هموفیلی و تشخیص قبل از تولد، بیمارستان آیت الله شهید دستغیب دانشگاه علوم پزشکی شیراز،شیراز، ایران
54	The role of genetic counseling in the prevention of hearing loss in Iranian patients	Morovvati Saeid	Other related topics	Human Genetic Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran.
55	Association of heteromorphism of chromosome 9 and recurrent abortion (ultrasound diagnosed blighted ovum)	Nazarabadi Mohamad	Other related topics	MASSHAD University of Medical Science Department Of medical Genetic & polyclinic Genetics Of Nasle Omid
56	نتایج 381 مورد آمنیوسنتز	Reyhanifar Farahnaz	Other related topics	بیمارستان فوق تخصصی بهبود
57	بایدهاونبایدهای تست های غربالگری ئوران بارداری	Reyhanifar Farahnaz	Other related topics	سازمان بهزیستی
58	spinocerbellar ataxia	Sahebalzamani Afsaneh	Other related topics	kerman Welfare organization
59	Glioblastomas and Genetic Counseling	Salmani Tayyebali	Other related topics	Department of Medical Genetics, Shahid Beheshti University of Medical Sciences, Tehran, Iran
60	The gene association between obesity and type 2 diabetes	Sheikhpour Mojgan	Other related topics	Department of Mycobacteriology and Pulmonary Research, Pasteur Institute of Iran, Tehran, Iran.
61	Association between four novel miRNAs polymorphisms and susceptibility to idiopathic recurrent spontaneous abortion	Hosseinzadeh Asghar	Other related topics	Department of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran
62	Cytogenetic investigation and Clinical Phenotype of patients with primary amenorrhea in Kermanshah Province, west of Iran	Jalilian Nazanin	Other related topics	department of Clinical Biochemistry, School of Medicine, Kermanshah University of Medical Sciences
63	Expression of CAPN11 and UBQLN3 in non-obstructive azoospermia	Karimi Masoumeh	Other related topics	department of mesenchymal stem cell, academic center for education culture and researc, Qom, Iran.
64	AMP-kinase inhibitor dorsomorphin reduces the proliferation and migration behavior of colorectal cancer cells by targeting the AKT/mTOR Pathway	Maftouh Mina	Other related topics	Metabolic syndrome Research center, Mashhad University of Medical Sciences, Mashhad, Iran
65	Comparison of neonatal blood glucose of diabetic mothers who took hypoglycemic drug and diabetic mothers who did not take medication at Buali Hospital 2017 – 2018	Mohammadnuri Marjan	Other related topics	Pediatrician , Assistant professor , Pediatric Department ,Tehran Medical sciences Branch , Islamic Azad University , Tehran , Iran
66	Repot on a Second Case of Cockayne Syndrome in Zanjan Province due to a Missense Mutation in ERCC6 Gene	Nikfar Ali	Other related topics	Zanjan Metabolic Diseases Research Center, Zanjan University of Medical Sciences, Zanjan, Iran
67	The Impotance of The Genetic Counseling	Rahimi Maryam	Other related topics	The Genetic Research Center, The University of Social Welfare and Rehabilitation Sciences, Tehran, Iran
68	Phelan-McDermid syndrome presenting with developmental delays: a case reaport	Yousefipour Faride	Other related topics	مرکز مشاوره ژنتیک دولتی بهزیستی