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
|