| Row | Code | Title | Presenting Author | Affiliation | Reg. Status |
|
1
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1
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شناسایی موتاسیون جدید (c.1006C>T) در ژن SPG20 مرتبط با سندروم Troyer
|
Mahdavi
Mohammad Reza
|
دانشگاه علوم پزشکی مازندران
|
ثبت نام اولیه
|
|
2
|
28
|
The study of KCNE1 gene mutations in Iranian LQTS patients
|
Norouzi
Rambod
|
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
|
ثبت نام اولیه
|
|
3
|
35
|
SPINK5 and Netherton syndrome: novel deleterious mutation
|
Gharesouran
Jalal
|
Molecular Genetics Division, GMG center, Tabriz, Iran
|
ثبت نام قطعی
|
|
4
|
31
|
Maternal circulating microRNAs as non-invasive biomarkers for prenatal diagnosis of congenital heart defects
|
Abtin
Maryam
|
Department of medical genetics, Faculty of medicine, Tabriz university of medical sciences,Tabriz, Iran
|
ثبت نام قطعی
|
|
5
|
48
|
Bioinformatics study and genetic counseling contribute to the diagnosis of cardiovascular disorders
|
Mansouri
Fatemeh
|
Department of Genetics and Immunology, Faculty of Medicine, Urmia University of Medical Sciences, Urmia, Iran.
|
ثبت نام اولیه
|
|
6
|
69
|
Whole-exome sequencing (WES) provides the possibility of genome-wide preconception carrier screening
|
Alipour Olyaei
Nasrin
|
Genomic Research Center, Shahid Beheshti University of Medical Sciences, Taleghani Hospital, Aarabi St., Yaman Ave., Velenjak, Tehran-Iran
|
ثبت نام اولیه
|
|
7
|
29
|
نتایج 381 مورد آمنیوسنتز
|
Reyhanifar
Farahnaz
|
بیمارستان فوق تخصصی بهبود
|
ثبت نام قطعی
|
|
8
|
46
|
Association of a genetic variant in the angiopoietin-like protein 4 gene with metabolic syndrome.
|
Avan
Amir
|
Metabolic syndrome Research center, Mashhad University of Medical Sciences, Mashhad, Iran
|
ثبت نام قطعی
|
|
9
|
45
|
Effect of inorganic polyphosphate on microvascular endothelial permeability and its mechanism: focus on AMP kinase signaling pathway
|
Avan
Amir
|
Metabolic syndrome Research center, Mashhad University of Medical Sciences, Mashhad, Iran
|
ثبت نام قطعی
|
|
10
|
32
|
آنالیز پیوستگی لوکوس در ناشنوایان DFNB77 و DFNB37 های غیر سندرومی با وراثت اتوزومال مغلوب در استان هرمزگان
|
Ahmadi
Banafsheh
|
Medical Biotechnology Resarch Center, Ashkezar Branch, Islamic Azad University, Ashkezar, Yazd
|
ثبت نام اولیه
|
|
11
|
55
|
Phelan-McDermid syndrome presenting with developmental delays: a case reaport
|
Yousefipour
Faride
|
مرکز مشاوره ژنتیک دولتی بهزیستی
|
ثبت نام اولیه
|
|
12
|
51
|
Detection of a new pathogenic mutation on DMD gene associated with Duchene Muscular Dystrophy
|
Mohaddes Ardebili
Seied Vahid
|
Cytogenetics Division, Dr. Mohaddes Medical Genetics Laboratory (DMMGL), Tabriz, Iran
|
ثبت نام قطعی
|
|
13
|
52
|
اختلالات متابولیسم ارثی
|
Shahzadeh fazeli
Seyed abolhassan
|
Department of Genetics, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran.
|
ثبت نام اولیه
|
|
14
|
56
|
The Impotance of The Genetic Counseling
|
Rahimi
Maryam
|
The Genetic Research Center, The University of Social Welfare and Rehabilitation Sciences, Tehran, Iran
|
ثبت نام قطعی
|
|
15
|
36
|
تحلیل روابط "تنظیم هیجانی"،"بهزیستی روانشناختی" ،"ریسک فاکتورهای قلبی در بیماران مبتلا به سکته قلبی
|
Ghobadi
Soroush
|
سازمان بهزیستی
|
ثبت نام اولیه
|
|
16
|
38
|
Deletion 22q11.2 syndrome frequency in patients with cleft palate referred to Alzahra Hospital, Isfahan, Iran
|
Nejati
Omid
|
22 Bahman Hospital- Medical and Pathological laboratory - Islamic Azad University of Mashhad, Iran
|
ثبت نام قطعی
|
|
17
|
39
|
A Case report of Expanding the clinical spectrum of Van Maldergem Syndrome in Hasti genetic counselling centre in south Khorasan
|
Rezazadeh
Jamileh
|
اداره کل بهزیستی خراسان جنوبی
|
ثبت نام اولیه
|
|
18
|
42
|
Two variants in exon and intron 9 of LDLR gene in Iranian familial hypercholesterolemia patients
|
Tajamolian
Masoud
|
Medical Genetic Research Center, Shahid Sadoughi University of Medical science, Yazd,Iran
|
ثبت نام قطعی
|
|
19
|
49
|
سندرم داون و آزمایشات قبل از تولد برای شناسایی آن
|
Fakeri
Mahsa
|
دانشگاه سراسری تبریز
|
ثبت نام قطعی
|
|
20
|
37
|
Association between four novel miRNAs polymorphisms and susceptibility to idiopathic recurrent spontaneous abortion
|
Hosseinzadeh
Asghar
|
Department of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran
|
ثبت نام قطعی
|
|
21
|
40
|
Genetic Consultation, Genomics Techniques and further in-vitro fertilization Strategies in families with a child involved with auto-immune hemolytic disorders
|
Banihashemi
Kambiz
|
Academic member, ATU, MSRT, Tehran, Iran
|
ثبت نام قطعی
|
|
22
|
43
|
Association of a genetic variant in Interleukin-10 gene with increased risk and inflammation associated with cervical cancer
|
Maftouh
Mina
|
Mashhad University of Medical Sciences
|
ثبت نام قطعی
|
|
23
|
60
|
Glioblastomas and Genetic Counseling
|
Salmani
Tayyebali
|
Department of Medical Genetics, Shahid Beheshti University of Medical Sciences, Tehran, Iran
|
ثبت نام اولیه
|
|
24
|
64
|
: شناسایی جهش A1298C ژن MTHFR در مردان نابارور
|
Darvishi
Maryam
|
دانشگاه آزاد اسلامی واحد دزفول
|
ثبت نام اولیه
|
|
25
|
41
|
اثربخشی آموزش مهارت‌های ارتباطی بر بهبود کیفیت زندگی افراد کم بینای آرپی
|
Mozafari
HOSEIN
|
آموزش وپرورش استثنایی
|
ثبت نام قطعی
|
|
26
|
44
|
AMP-kinase inhibitor dorsomorphin reduces the proliferation and migration behavior of colorectal cancer cells by targeting the AKT/mTOR Pathway
|
Maftouh
Mina
|
Metabolic syndrome Research center, Mashhad University of Medical Sciences, Mashhad, Iran
|
ثبت نام قطعی
|
|
27
|
21
|
LAMA1 gene variant associated with intellectual disability and sever myopia - a case report
|
Moghbelinejad
Sahar
|
3Cellualr and molecular research center, Qazvin university of medical science, Qazvin, IRAN.
|
ثبت نام قطعی
|
|
28
|
50
|
Association of A Novel Balanced Reciprocal Translocation and Recurrent Miscarriage: A Case Report
|
Mohaddes Ardebili
Seied Vahid
|
Cytogenetics Division, Dr. Mohaddes Medical Genetics Laboratory (DMMGL), Tabriz, Iran
|
ثبت نام قطعی
|
|
29
|
53
|
Association of heteromorphism of chromosome 9 and recurrent abortion (ultrasound diagnosed blighted ovum)
|
Nazarabadi
Mohamad
|
MASSHAD University of Medical Science Department Of medical Genetic & polyclinic Genetics Of Nasle Omid
|
ثبت نام قطعی
|
|
30
|
54
|
A brief view on the role of genetic counseling in neuromuscular disease
|
Sadeghinia
Farnaz
|
Genetics research center, University of social welfare and rehabilitation sciences, Tehran, Iran
|
ثبت نام قطعی
|
|
31
|
16
|
Effects of N-acetyl-cysteine supplementation on sperm quality, chromatin integrity and level of oxidative stress in infertile men.
|
Asadi
Seyed ehsan
|
phd of Nursing, Esfahan Medical University, Esfahan, Iran.
|
ثبت نام اولیه
|
|
32
|
19
|
بایدهاونبایدهای تست های غربالگری ئوران بارداری
|
Reyhanifar
Farahnaz
|
سازمان بهزیستی
|
ثبت نام قطعی
|
|
33
|
20
|
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
|
Pediatrician , Assistant professor , Pediatric Department ,Tehran Medical sciences Branch , Islamic Azad University , Tehran , Iran
|
ثبت نام قطعی
|
|
34
|
22
|
A Novel Missence Mutation in the Transglutaminase-1 Gene in an Autosomal Recessive Congenital Ichthyosis Patient
|
Ahmadi shadmehri
Aazam
|
Social Welfare Organization of South Khorasan Province, Birjand, Iran
|
ثبت نام اولیه
|
|
35
|
65
|
A novel large exon deletion in GFAP gene, Adult Alexander disease in Iran; The first report in the world
|
Alizadeh
Fatemeh
|
Genomic Psychiatry Department, Roozbeh Hospital, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
|
ثبت نام قطعی
|
|
36
|
59
|
The role of genetic counseling in the prevention of hearing loss in Iranian patients
|
Morovvati
Saeid
|
Human Genetic Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran.
|
ثبت نام اولیه
|
|
37
|
66
|
جنبه های بالینی تفسیر کلینیکال داده های WES در جمعیت ایرانی
|
Dastmalchi
Romina
|
دانشگاه علوم پزشکی شهید بهشتی
|
ثبت نام قطعی
|
|
38
|
58
|
Genetic causes of premature ovarian failure
|
Almadani
Seyed navid
|
Department of Genetics,Reproductive Biomedicine Reserch Center ,Royan Institute for Reproductive Biomedicine , ACECR ,Tehran, Iran
|
ثبت نام اولیه
|
|
39
|
24
|
spinocerbellar ataxia
|
Sahebalzamani
Afsaneh
|
kerman Welfare organization
|
ثبت نام اولیه
|
|
40
|
25
|
بررسی وضعیت موجود تشخیص ناهنجاریهای مادرزادی با انجام سونوگرافی دردانشگاه علوم پزشکی تبریز
|
Ansari
Masoumeh
|
معاونت بهداشت دانشگاه علوم پزشکی تبریز
|
ثبت نام اولیه
|
|
41
|
27
|
Case Report of Bardet Biedl Syndrome
|
Sorkhkooh Azari
Noushin
|
Allame Amini Genetic Consultant Center, Tabriz, Iran
|
ثبت نام اولیه
|
|
42
|
67
|
preferencing 4p medicnes
|
Darsaneh
Zahra
|
azad babol university
|
ثبت نام قطعی
|
|
43
|
17
|
Randomized, double-blind, placebo-controlled clinical trial of choline supplementation in school-aged children with fetal alcohol spectrum disorders.
|
Asadi
Seyed ehsan
|
phd of Nursing, Esfahan Medical University, Esfahan, Iran.
|
ثبت نام اولیه
|
|
44
|
68
|
Repot on a Second Case of Cockayne Syndrome in Zanjan Province due to a Missense Mutation in ERCC6 Gene
|
Nikfar
Ali
|
Zanjan Metabolic Diseases Research Center, Zanjan University of Medical Sciences, Zanjan, Iran
|
ثبت نام اولیه
|
|
45
|
23
|
Application of multi-gene panel in juvenile-onset glaucoma: report of 2 cases with dominant & recessive inheritance
|
Vahedi
Afsaneh
|
Mana genetic counseling center, Shahrood, Iran.
|
ثبت نام اولیه
|
|
46
|
9
|
The gene association between obesity and type 2 diabetes
|
Sheikhpour
Mojgan
|
Department of Mycobacteriology and Pulmonary Research, Pasteur Institute of Iran, Tehran, Iran.
|
ثبت نام قطعی
|
|
47
|
4
|
Investigation and Comparison of margin and tumor in breast cancer patient (lominal A) by proteomic approach
|
Khani
Ramtin
|
Young Researchers and Elite club, Azad Islamic University, Medical science branch, Tehran, Iran
|
ثبت نام قطعی
|
|
48
|
6
|
Characterization of human papillomavirus (HPV) genotypes among patients referred to gynecology clinic, Laleh hospital, Tehran, Iran.
|
Rezaei
IMAN
|
مركز ژنتيك بيمارستان لاله و پژوهشگاه بيماريهاي ويروسي، بخش تشخيص مولكولي
|
ثبت نام اولیه
|
|
49
|
10
|
Determine a mutation in a daughter suffer from hydrocephalus and developmental disorder
|
Ghavabesh
Jassem
|
Center of Geneics consulation of Ahwaz Behzisti
|
ثبت نام اولیه
|
|
50
|
61
|
Comparison and comparison of telomerase expression in healthy tissue and breast cancer
|
Igder
Mohsen
|
Tabriz university
|
ثبت نام اولیه
|
|
51
|
5
|
ازدواج فامیلی و اختلالات ژنتیکی
|
Asadpour
Shaghayegh
|
دانشگاه آزاد اسلامی بابل
|
ثبت نام اولیه
|
|
52
|
3
|
Expression of CAPN11 and UBQLN3 in non-obstructive azoospermia
|
Karimi
Masoumeh
|
department of mesenchymal stem cell, academic center for education culture and researc, Qom, Iran.
|
ثبت نام قطعی
|
|
53
|
63
|
بررسی و مقایسه بیان آنزیم تلومراز در بافت سالم و بافت سرطانی پستان¬ها
|
Rezvani
Zahra sadat
|
دانشجوی کارشناسی ارشد رشته زیست شناسی، گرایش ژنتیک، دانشگاه آزاد اسلامی واحد علوم و تحقیقات آذربایجان شرقی
|
ثبت نام قطعی
|
|
54
|
7
|
Carrier detection of CAH, in a consanguineous family with a deseased affected child
|
Jazayeri
Roshanak
|
Department of Genetics, Faculty of Medicine, Alborz University of Medical Sciences, Karaj, Iran
|
ثبت نام قطعی
|
|
55
|
12
|
Genetic Approach to Recurrent Pregnancy Loss
|
Pooladi
Arash
|
1- Cellular and Molecular Research Center, Medical Genetics and Molecular Medicine Department, Kurdistan University of Medical Sciences, Sanandaj, Iran.
|
ثبت نام اولیه
|
|
56
|
2
|
شناسایی موتاسیون جدید در ژن AIPL1 همبسته با بیماری Leber Congeital Amaurosis
|
Mahdavi
Mohammad Reza
|
دانشگاه علوم پزشکی مازندران
|
ثبت نام اولیه
|
|
57
|
11
|
Cytogenetic investigation and Clinical Phenotype of patients with primary amenorrhea in Kermanshah Province, west of Iran
|
Jalilian
Nazanin
|
department of Clinical Biochemistry, School of Medicine, Kermanshah University of Medical Sciences
|
ثبت نام قطعی
|