| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A case–control study of single-nucleotide variants in microRNA biogenesis genes (AGO1 and GEMIN4) in people with primary immune thrombocytopenia
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Mohamed, Haydi Sayed
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24 |
1 |
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artikel
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| 2 |
A computational analysis reveals eight novel high-risk single nucleotide variants of human tumor suppressor LHPP gene
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Feroz, Tasmiah
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24 |
1 |
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artikel
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| 3 |
A glance on Immunogenetics Laboratory: from the origins to the future
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Madalese, Donato
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24 |
1 |
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artikel
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| 4 |
Allelic variation in TUSC1 gene: rs1462218557 is associated with male infertility and azoospermia
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Vahidi Emami, Zahra
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24 |
1 |
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artikel
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| 5 |
A meta-analysis and review on genetic mapping of type 2 diabetes mellitus in Iraq
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Musafer, Karar N. J.
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24 |
1 |
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artikel
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| 6 |
An exploratory pharmacogenetic screening of SLC22A6, SLC22A8, ABCC4 and ABCC10 genes in a cohort of Ghanaian HBV patients
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Thomford, Nicholas Ekow
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24 |
1 |
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artikel
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| 7 |
A novel missense mutation in PLEKHG5 gene causing an intermediate form of autosomal-recessive Charcot–Marie–Tooth disease in an Iraqi family
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Neissi, Mostafa
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24 |
1 |
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artikel
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| 8 |
A novel mutation in the SOX5 gene c.1627del; p.(Tyr543IlefsTer14) is associated to Lamb–Shaffer syndrome: a case report
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Cuenca Alcocel, Jose
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24 |
1 |
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artikel
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| 9 |
A novel pathogenic splice-site variant in the PTCH1 gene c.3549+1G>T, associated with Gorlin syndrome: a case report
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Conde-Rubio, Paula
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24 |
1 |
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artikel
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| 10 |
Association between leukocyte telomere length and COVID-19 severity
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Mahmoodpoor, Ata
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24 |
1 |
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artikel
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| 11 |
Association between miR-138-5p, miR-132-3p, SIRT1, STAT3, and CD36 and atherogenic indices in blood mononuclear cells from patients with atherosclerosis
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Ehsani, Samira
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24 |
1 |
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artikel
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| 12 |
Association between MTHFR C677T variant and risk for congenital heart defects in Egyptian children: a case–control study including meta-analysis based on 147 cases and 143 controls
|
Esmaiel, Nora N.
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24 |
1 |
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artikel
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| 13 |
Association between the single-nucleotide polymorphism (rs1030868) variant in matrix metallopeptidase 2 gene and the development of lymphedema
|
Shakra, Mohammed Youssef
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24 |
1 |
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artikel
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| 14 |
Association of ABCA1 gene with Coronary Artery Disease (CAD): an overview
|
Yadav, Tanu
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24 |
1 |
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artikel
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| 15 |
Association of ADAM33 gene with COPD pathophysiology: a case–control study
|
Soomro, Tahmina
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24 |
1 |
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artikel
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| 16 |
Association of angiotensin-converting enzyme I/D polymorphism and apolipoprotein B with cardiometabolic abnormalities among young adults: a pilot study from Delhi
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Suokhrie, Seyielenuo
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24 |
1 |
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artikel
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| 17 |
Association of CYP1A2 and GST gene variants with asthma in cases presenting with allergic chronic rhinosinusitis
|
Jangala, Madhavi
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24 |
1 |
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artikel
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| 18 |
Association of IL-1β rs16944 and IL-1RN rs2234663 gene polymorphisms with graft function in renal transplant recipients
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Issac, Marianne Samir Makboul
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24 |
1 |
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artikel
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| 19 |
Association of maternal genetic polymorphisms with fetal growth restriction syndrome in Russian pregnant women from Rostov region
|
Alset, Dema
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24 |
1 |
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artikel
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| 20 |
Association of MTHFR C677T polymorphism with risk of preterm birth in Indian mothers: a case–control study
|
Rathod, Pratibha
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24 |
1 |
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artikel
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| 21 |
Association of OXTR polymorphism (rs53576) with depression: a meta-analysis
|
Eid, Moez
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24 |
1 |
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artikel
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| 22 |
Association of serum miR-375, miR-155 and miR-146b levels with distinguish of papillary thyroid cancer from benign thyroid masses among Iranian patients
|
Mobini, Gholam-Reza
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24 |
1 |
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artikel
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| 23 |
Association study between rs1571801 and rs16260 with prostate adenocarcinoma predisposition in Iranian population
|
Rahimi, Abbas
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24 |
1 |
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artikel
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| 24 |
B-lymphocyte-activating factor is a potential biomarker associated with susceptibility to Graves’ disease in Iraqi women
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Ibrahim, Hiba Y.
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24 |
1 |
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artikel
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| 25 |
Characterization of blaTEM and blaCTX-M beta-lactam resistance genes in chronic rhinosinusitis
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Arian Nejad, Mojdeh
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24 |
1 |
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artikel
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| 26 |
Circulating expression patterns of TL1A and FFAR2 in patients with stable and unstable angina
|
Kamel, Amira A.
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24 |
1 |
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artikel
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| 27 |
Cognitive impairment in beta thalassemia major and intermedia pediatric patients: a cross-sectional study
|
Elderini, Esraa Elmorsi Abdelaziz
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24 |
1 |
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artikel
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| 28 |
Comments on: rs3761548 (C/A) and rs5902434 (del/ATT) polymorphisms of Foxp3 gene in Iranian patients with migraine
|
Saadat, Mostafa
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24 |
1 |
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artikel
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| 29 |
Comparative evaluation of ZMYND-8 and RARβ2 genes promoters’ methylation changes in tumor and tumor margin tissues of patients with lung cancer
|
Pourasghariazar, Mahdieh
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24 |
1 |
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artikel
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| 30 |
Congenital hypothyroidism: a case report of an Egyptian child with congenital heart disease, pelvic kidney and cavernous transformation of portal vein
|
Elsedfy, Heba
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24 |
1 |
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artikel
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| 31 |
Correction: Relationship between expression levels of TDRD7 and CRYBB3 and development of age-related cortico-nuclear cataracts
|
Yildiz, Saliha Handan
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24 |
1 |
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artikel
|
| 32 |
Description of a patient with developmental delay and dysmorphic features caused by a novel SHANK2 deletion
|
Molina Herranz, David
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24 |
1 |
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artikel
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| 33 |
Detection of a de novo heterozygous ANK2 variant in a child with autism spectrum disorder and epilepsy: a case report
|
Morais, Catarina Granjo
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24 |
1 |
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artikel
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| 34 |
Early diagnosis of congenital muscular pathologies using next-generation sequencing: experiences from a tertiary center in Morocco
|
El Kadiri, Youssef
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24 |
1 |
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artikel
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| 35 |
Effect of Dioscorea extract on Bax and Bcl-2 gene expression in MCF-7 and HFF cell lines
|
Bojar Doulaby, Fatemeh
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24 |
1 |
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artikel
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| 36 |
Effect of hydroxyurea on SP1, LIN28B, IGF2BP3, COL4A5, BCL2, gamma globin genes expression: an in vitro study
|
Fashami, Akram Agha-Amini
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24 |
1 |
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artikel
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| 37 |
Effect of oxidative stress-related genetic variants: “Explicating the role of reactive oxygen species influenced antioxidant gene polymorphism,” a risk stratification of type 2 diabetes mellitus-associated nephropathy: a systematic review
|
Begum, Farhana
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24 |
1 |
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artikel
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| 38 |
Effects of ABCG2 C421A and ABCG2 G34A genetic polymorphisms on clinical outcome and response to imatinib mesylate, in Iranian chronic myeloid leukemia patients
|
Nouri, Negar
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24 |
1 |
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artikel
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| 39 |
Evaluation of the expression of the long non-coding RNAs, LOWEG and MINCR, and their clinical significance in human gastric cancer
|
Ghasemzadeh, Tooraj
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24 |
1 |
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artikel
|
| 40 |
Evaluation of the HOXA9 and MEIS1 genes as a potential biomarker in adult acute myeloid leukemia
|
Abdelrahman, Amira M. N.
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24 |
1 |
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artikel
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| 41 |
Evaluation of therapeutic potentials of some bioactive compounds in selected African plants targeting main protease (Mpro) in SARS-CoV-2: a molecular docking study
|
Akinwumi, Ishola Abeeb
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24 |
1 |
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artikel
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| 42 |
Expanding the genotype–phenotype correlations in Alport syndrome: novel mutations, digenic inheritance, and genetic modifiers
|
Sahin, Ibrahim
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24 |
1 |
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artikel
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| 43 |
FAM72D in plasma cell myeloma: a friend or enemy
|
Ahmed, Riham Ahmed Ramadan
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24 |
1 |
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artikel
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| 44 |
First application of next-generation sequencing in four families with Wilson disease in Morocco
|
Sahli, Maryem
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24 |
1 |
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artikel
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| 45 |
Genetic and metabolic aspects of non-alcoholic fatty liver disease (NAFLD) pathogenicity
|
Samarasinghe, Saumya Madushani
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24 |
1 |
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artikel
|
| 46 |
Genetic association analysis of rs662799 ( − 1131A > G) polymorphism of APOA5 gene with morphometric and physio-metric traits using multiplex PCR
|
Fatma, Rafat
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24 |
1 |
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artikel
|
| 47 |
Genetic diversity of Mycobacterium tuberculosis isolates from northwest of Iran during COVID-19 era
|
Kashi, Peyvand
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24 |
1 |
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artikel
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| 48 |
Genetic polymorphism of organic cation transporter 2 (OCT2) and its effects on the pharmacokinetics and pharmacodynamics of Metformin: a narrative review
|
Borra, Swathi Swaroopa
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24 |
1 |
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artikel
|
| 49 |
Genetic testing and family screening in idiopathic pediatric cardiomyopathy: a prospective observational study from a tertiary care center in North India
|
Bhatt, Dheeraj D.
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|
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24 |
1 |
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artikel
|
| 50 |
Genetic tool used to diagnose achromatopsia: first case report from India
|
Pritti, Kumari
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24 |
1 |
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artikel
|
| 51 |
Genome-wide landscape of RNA-binding protein (RBP) networks as potential molecular regulators of psychiatric co-morbidities: a computational analysis
|
Nishanth, M. J.
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24 |
1 |
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artikel
|
| 52 |
Germline rad 50 mutation in a case with synchronous breast and kidney cancer: a rare case
|
Ilangovan, Bhargavi
|
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24 |
1 |
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artikel
|
| 53 |
Higher incidence of co-expression of BCR-ABL fusion transcripts in an Eastern Indian population
|
Kumar, Ajeet
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24 |
1 |
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artikel
|
| 54 |
HLA alleles associated with COVID-19 susceptibility and severity in different populations: a systematic review
|
Fakhkhari, Meryem
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24 |
1 |
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artikel
|
| 55 |
Identification of the cuproptosis-related ceRNA network and risk model in acute ischemic stroke by integrated bioinformatics analysis
|
Jia, Fang
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24 |
1 |
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artikel
|
| 56 |
Identification of two Iranian siblings with cerebrotendinous xanthomatosis: a case report
|
Beyzaei, Zahra
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24 |
1 |
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artikel
|
| 57 |
In silico analysis of missense SNPs in GABRA1, GABRB1, and GABRB3 genes associated with some diseases in neurodevelopmental disorders
|
Manaz, Mehmet
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24 |
1 |
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artikel
|
| 58 |
In silico identification of prospective virulence factors associated with candidiasis in Meyerozyma guilliermondii strain SO from genome dataset
|
Zainudin, Robiatul Azilah
|
|
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24 |
1 |
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artikel
|
| 59 |
Integrated structure model-based virtual screening approaches identified anti-cancer agents against prostate cancer by targeting MAOB protein
|
Molla, Mohammad Habibur Rahman
|
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24 |
1 |
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artikel
|
| 60 |
Integrative bioinformatics analysis of miRNA and mRNA expression profiles identified some potential biomarkers for breast cancer
|
Rezaeijo, Seyed Masoud
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24 |
1 |
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artikel
|
| 61 |
Investigating the importance of EGFR (− 216G/T), Exo1 (K589E) and LEP (− 2548G/A) gene polymorphisms with risk of lung cancer as potential diagnostic biomarker in Iranian population
|
Pezeshki, Milad
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24 |
1 |
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artikel
|
| 62 |
Investigation of HER2 I655V and PHB 3′UTR C > T polymorphisms in azoospermic infertile males
|
Yildiz, Irem
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24 |
1 |
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artikel
|
| 63 |
In vitro anticancer activity of hydatid cyst fluid on colon cancer cell line (C26)
|
Motavallihaghi, Seyedmousa
|
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24 |
1 |
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artikel
|
| 64 |
Knowledge of genetics of hearing and genetic counseling among practicing audiologists
|
Madhu, Harini
|
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24 |
1 |
|
artikel
|
| 65 |
Mendelian susceptibility to mycobacterial disease: an overview
|
Errami, Abderrahmane
|
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24 |
1 |
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artikel
|
| 66 |
Metformin reduces the cellular DNA repair capacity and enhances the effect of curcumin on the induction of apoptosis in AGS gastric cancer cells
|
Zarei, Ehsan
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24 |
1 |
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artikel
|
| 67 |
Molecular profiling of BRCA1 and BRCA2 genes in Turkish patients with early-onset breast cancer
|
Karakaya, Taner
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24 |
1 |
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artikel
|
| 68 |
Mutational spectrum of the AP3B1 gene in an Iraqi family affected with Hermansky–Pudlak syndrome type 2
|
Neissi, Mostafa
|
|
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24 |
1 |
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artikel
|
| 69 |
Mutual interaction of lncRNAs and epigenetics: focusing on cancer
|
Ranjbar, Maryam
|
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24 |
1 |
|
artikel
|
| 70 |
Novel MTO1 mutations associated with an intrafamilial phenotypic variability
|
Almeida, Catarina Maria
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24 |
1 |
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artikel
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| 71 |
Novel PPP1R21 mutation in a family with autosomal recessive neurodevelopmental disorder: results of genomics and molecular analysis
|
Ghazi-Nader, Donya
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24 |
1 |
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artikel
|
| 72 |
Novel pyrroline-5-carboxylate reductase 2 (PYCR2) mutation in an Iranian patient with hypomyelinating leukodystrophy: findings of molecular and in silico investigations
|
Akbari, Maryam
|
|
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24 |
1 |
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artikel
|
| 73 |
Prevalence of TP53 gene Pro72Arg (rs1042522) single nucleotide polymorphism among Egyptian breast cancer patients
|
Ahmed, Shaza
|
|
|
24 |
1 |
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artikel
|
| 74 |
Relationship between expression levels of TDRD7 and CRYBB3 and development of age-related cortico-nuclear cataracts
|
Yildiz, Saliha Handan
|
|
|
24 |
1 |
|
artikel
|
| 75 |
rs3761548 (C/A) and rs5902434 (del/ATT) polymorphisms of Foxp3 gene in Iranian patients with migraine
|
Faraji, Fardin
|
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|
24 |
1 |
|
artikel
|
| 76 |
STAT3 gene polymorphisms and susceptibility to breast cancer in the Moroccan population
|
Ighid, Nassima
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24 |
1 |
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artikel
|
| 77 |
The contribution of FTO rs9939609 and RETN rs1862513 polymorphisms in predisposing resettled indigenous (Orang Asli) Temiar to metabolic syndrome
|
Harun, Nur Sakinah
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24 |
1 |
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artikel
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| 78 |
The expression level of ARF and p53 in AML patients, and their relation to patients' outcome
|
Nabil, Reem
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24 |
1 |
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artikel
|
| 79 |
The importance of personalized medicine in chronic myeloid leukemia management: a narrative review
|
Zaker, Erfan
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24 |
1 |
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artikel
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| 80 |
The role of HLA genotypes in understanding the pathogenesis of severe COVID-19
|
Arab, Fatemeh
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24 |
1 |
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artikel
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| 81 |
The role of miRNA20a and miRNA320 in Iraqi patients with COVID-19: a case–control study
|
Abed, Reema Mohammed
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24 |
1 |
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artikel
|
| 82 |
The role of miRNA-29b1, MMP-2, MMP-9 mRNAs, and proteins in early diagnosis of HCC
|
Abdel-Tawab, Marwa Sayed
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24 |
1 |
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artikel
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| 83 |
The role of miRNAs in the diagnosis and treatment of male infertility: a review study
|
Sinaei, Roya
|
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24 |
1 |
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artikel
|
| 84 |
The study of long noncoding RNA TUG 1 and ZEB2-AS1 expression in newly diagnosed Egyptian adult acute myeloid leukemia patients
|
Abdelrahman, Amira Mohamed Noureldin
|
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24 |
1 |
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artikel
|
| 85 |
The study of the impact of additional chromosomal aberrations and c-MYC and BCR::ABL1 genes amplification on CML patient’s characteristics: relation to haematological parameters and patient outcome
|
Attia, Hend
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24 |
1 |
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artikel
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| 86 |
Understanding polycystic ovary syndrome in light of associated key genes
|
Bhimwal, Tanisha
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24 |
1 |
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artikel
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| 87 |
Understanding the role of adipokines and adipogenesis family in hepatocellular carcinoma
|
Singh, Prithvi
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24 |
1 |
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artikel
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