Ehsan Ghayoor Karimiani
Ehsan Ghayoor Karimiani
Consultant Medical Geneticist, Next Generation Genetic Poly Clinic
Verified email at manchester.ac.uk - Homepage
TitleCited byYear
Microdroplet Technology: Principles and Emerging Applications in Biology and Chemistry
P Day, Y Zhang, A Manz
Springer, 2012
362012
Expression of IL-17 and COX2 gene in peripheral blood leukocytes of vitiligo patients
B Esmaeili, SAR Rezaee, P Layegh, JT Afshari, P Dye, EG Karimiani, ...
Iranian Journal of Allergy, Asthma and Immunology, 81-89, 2011
322011
Association of the expression of IL-4 and IL-13 genes, IL-4 and IgE serum levels with allergic asthma
JT Afshari, RF Hosseini, SH Farahabadi, F Heydarian, MH Boskabady, ...
Iranian Journal of Allergy, Asthma and Immunology, 69-72, 2007
322007
Single-cell analysis of K562 cells: an imatinib-resistant subpopulation is adherent and has upregulated expression of BCR-ABL mRNA and protein
EG Karimiani, F Marriage, AJ Merritt, J Burthem, RJ Byers, PJR Day
Experimental hematology 42 (3), 183-191. e5, 2014
172014
Evaluation of Methylation of MGMT (O6-Methyl Guanine Methyltransferase) Gene Promoter in Sporadic Colorectal Cancer.
HA Mohammadreza Farzanehfar, Hasan Vossoughinia
DNA and Cell Biology, 2013
172013
Mathematical modelling of miRNA mediated BCR.ABL protein regulation in chronic myeloid leukaemia vis-a-vis therapeutic strategies
M Verma, EG Karimiani, R Byers, S Rehman, PJR Day
Integrative Biology, 2013
162013
PLK1 and YY1 interaction in follicular lymphoma is associated with unfavourable outcome
HE Sandison, S Usher, EG Karimiani, G Ashton, LP Menasce, JA Radford, ...
Journal of clinical pathology 66 (9), 764-767, 2013
152013
Respiratory symptoms and pulmonary function changes among carpet weavers in Iran
MH Boskabady, EG Karimiani, HA Vostacolaei
International journal of occupational and environmental health 13 (4), 369-375, 2007
132007
Biallelic variants in KIF14 cause intellectual disability with microcephaly
P Makrythanasis, R Maroofian, A Stray-Pedersen, D Musaev, MS Zaki, ...
European Journal of Human Genetics 26 (3), 330, 2018
112018
Homozygous Mutations in CSF1R Cause a Pediatric-Onset Leukoencephalopathy and Can Result in Congenital Absence of Microglia
N Oosterhof, IJ Chang, EG Karimiani, LE Kuil, DM Jensen, R Daza, ...
The American Journal of Human Genetics 104 (5), 936-947, 2019
102019
Biallelic mutations in ADPRHL2, encoding ADP-ribosylhydrolase 3, lead to a degenerative pediatric stress-induced epileptic ataxia syndrome
SG Ghosh, K Becker, H Huang, TD Salazar, G Chai, V Salpietro, ...
The American Journal of Human Genetics 103 (3), 431-439, 2018
92018
Trauma mortality: Using injury severity score (ISS) for survival prediction in East of Iran
MR Ehsaei, A Sarreshtedar, H Ashraf, EG Karimiani
Razavi Int J Med 2 (1), 15189, 2014
92014
Microfluidic channel-assisted screening of hematopoietic malignancies.
F Mughal, SJ Baldock, E Ghayoor Karimiani, P J R Day
Genes Chromosomes and Cancer, 2013
82013
SLC10A7 mutations cause a skeletal dysplasia with amelogenesis imperfecta mediated by GAG biosynthesis defects
J Dubail, C Huber, S Chantepie, S Sonntag, B Tüysüz, E Mihci, ...
Nature communications 9 (1), 3087, 2018
52018
The Efficacy of Glasgow Coma Scale (GCS) Score and Acute Physiology and Chronic Health Evaluation (APACHE) II for Predicting Hospital Mortality of ICU Patients with Acute …
A Nik, MSS Andalibi, MR Ehsaei, A Zarifian, EG Karimiani, ...
Bulletin of Emergency & Trauma 6 (2), 141, 2018
52018
Personalised treatment of haematological malignancies through systems medicine based on single molecules in single cells
PJR Day, EG Karimiani
Integr. Biol., 2013
52013
Chromosomal analysis and BRCA2* 617delT/88delTG and BRIP1 (c. 2392C> T) mutations of Fanconi anemia in Iranian family, and its correlation to breast cancer susceptibility
MM Kooshyar, M Nassiri, EG Karimiani, M Doosti, K Nasiri, Z Rodbari
J. Chem. Pharm. Res 7, 147-153, 2015
42015
Cardiomyopathy with lethal arrhythmias associated with inactivation of KLHL24
C Hedberg-Oldfors, A Abramsson, DPS Osborn, O Danielsson, ...
Human molecular genetics 28 (11), 1919-1929, 2019
32019
Common KRAS and NRAS gene mutations in sporadic colorectal cancer in Northeastern Iranian patients
L Hamzehzadeh, F Khadangi, EG Karimiani, A Pasdar, MA Kerachian
Current problems in cancer 42 (6), 572-581, 2018
32018
Targeted sequencing with expanded gene profile enables high diagnostic yield in non‐5q‐spinal muscular atrophies
M Karakaya, M Storbeck, EA Strathmann, A Delle Vedove, I Hölker, ...
Human mutation 39 (9), 1284-1298, 2018
32018
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