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ResearcherID: W-2037-2018
Scopus Author ID: 55759634300

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Education and qualifications (1)

Department of biochemistry and genetics, faculty of medicine, arak university of medical sciences, arak, iran.: Arak, Markazei, IR

2015-01-01 to present | PhD (medical genetics)
Education
Source: Self-asserted source
Milad Gholami

Works (29)

Exploring the Genetic Landscape of Knobloch Syndrome: Novel Variant Identification and Literature Review

OBM Genetics
2025-04-14 | Journal article
DOI: 10.21926/obm.genet.2502291
Contributors: Mohammad-Reza Ghasemi; Maryam Mirahmadi; Hadi Bayat; Morteza Sheikhi Nooshabadi; Sanaz Jamshidi; Shadab Salehpour; Reza Mirfakhraie; Fatemeh Fazeli; Mohammad Miryounesi; Milad Gholami
Source: check_circle
Crossref

Association Study of rs1421085 and rs9939609 in FTO Gene with Gestational Diabetes in the Arak City

Journal of Arak University of Medical Sciences
2024-03-01 | Journal article
DOI: 10.61186/jams.27.1.46
Contributors: Parnian Hekmatpou; Maryam Maryam Ghanbari; Milad Gholami
Source: check_circle
Crossref

The effect of Ccnb1ip1 insulator on monoclonal antibody expression in Chinese hamster ovary cells

Molecular Biology Reports
2022-05 | Journal article
DOI: 10.1007/s11033-022-07182-x
Contributors: Azam Rahimpour; Es’hagh Pourmaleki; Forough Shams; Zahra Payandeh; Navid Pourzardosht; Mojtaba Didehdar; Milad Gholami
Source: check_circle
Crossref

Novel insertion mutation in the PLA2G6 gene in an Iranian family with infantile neuroaxonal dystrophy

Journal of Clinical Laboratory Analysis
2022-01-29 | Journal article
DOI: 10.1002/jcla.24253
Part of ISSN: 0887-8013
Part of ISSN: 1098-2825
Source: Self-asserted source
Milad Gholami
grade
Preferred source (of 2)‎

Whole exome sequencing identified a novel homozygous ARV1 mutation in an Iranian family with developmental and epileptic encephalopathy-38

Meta Gene
2021-12 | Journal article
DOI: 10.1016/j.mgene.2021.100953
Part of ISSN: 2214-5400
Source: Self-asserted source
Milad Gholami

Differential expression of <i>Hsa-miR-517a/b</i> in placental tissue may contribute to the pathogenesis of preeclampsia

Journal of the Turkish-German Gynecological Association
2021-12-01 | Journal article
DOI: 10.4274/jtgga.galenos.2021.2021.0062
Contributors: Mona Amin-Beidokhti; Hossein Sadeghi; Reihaneh Pirjani; Latif Gachkar; Milad Gholami; Reza Mirfakhraie
Source: check_circle
Crossref

Targeted sequencing of CDH23 and GJB2 genes in an Iranian pedigree with Usher syndrome and non-syndromic hearing loss

Gene Reports
2021-06 | Journal article
DOI: 10.1016/j.genrep.2021.101149
Part of ISSN: 2452-0144
Source: Self-asserted source
Milad Gholami

CREB-binding protein (CREBBP) and preeclampsia: a new promising target gene

Molecular Biology Reports
2021-03-24 | Journal article
DOI: 10.1007/s11033-021-06215-1
Contributors: Hossein Sadeghi; Sahra Esmkhani; Reihaneh Pirjani; Mona Amin-Beidokhti; Milad Gholami; Ghasem Azizi Tabesh; Mohammad Reza Ghasemi; Latif Gachkar; Reza Mirfakhraie
Source: check_circle
Crossref

Mutational screening of RTK-BRAF genes in de novo adult acute myeloid leukemia

Gene Reports
2020-10 | Journal article
DOI: 10.1016/j.genrep.2020.100904
Part of ISSN: 2452-0144
Source: Self-asserted source
Milad Gholami

CYP24A1 expression analysis in uterine leiomyoma regarding MED12 mutation profile

Archives of Gynecology and Obstetrics
2020-10-06 | Journal article
DOI: 10.1007/s00404-020-05825-7
Part of ISSN: 0932-0067
Part of ISSN: 1432-0711
Source: Self-asserted source
Milad Gholami

A homozygous missense mutation of WFS1 gene causes Wolfram's syndrome without hearing loss in an Iranian family (a report of clinical heterogeneity).

Journal of clinical laboratory analysis
2020-05-17 | Journal article
DOI: 10.1002/jcla.23358
PMID: 32419160
PMC: PMC7439424
Source: Self-asserted source
Milad Gholami

The novel homozygous p.Asn197_Ser201del mutation in BTD gene is associated with profound biotinidase deficiency in an Iranian consanguineous family.

Molecular biology reports
2020-04-12 | Journal article
DOI: 10.1007/s11033-020-05424-4
PMID: 32281057
Source: Self-asserted source
Milad Gholami

Silibinin treatment results in reducing OPA1&MFN1 genes expression in a rat model hepatic ischemia-reperfusion.

Molecular biology reports
2020-04-05 | Journal article
DOI: 10.1007/s11033-020-05383-w
PMID: 32249375
Source: Self-asserted source
Milad Gholami

Investigation of CEBPA and CEBPA-AS genes expression in acute myeloid leukemia

Reports of Biochemistry and Molecular Biology
2019 | Journal article
EID:

2-s2.0-85060536169
Contributors: Gholami, M.; Bayat, S.; Manoochehrabadi, S.; Pashaiefar, H.; Omrani, M.D.; Jalaeikhoo, H.; Yassaee, V.R.; Ebrahimpour, M.R.; Behjati, F.; Mirfakhraie, R.
Source: Self-asserted source
Milad Gholami via Scopus - Elsevier

Ectopic expression of CYP24A1 circular RNA hsa_circ_0060927 in uterine leiomyomas.

Journal of clinical laboratory analysis
2019-11-20 | Journal article
DOI: 10.1002/jcla.23114
PMID: 31746073
PMC: PMC7171336
Source: Self-asserted source
Milad Gholami

Whole exome sequencing identified two homozygous ALMS1 mutations in an Iranian family with Alström syndrome.

Gene
2019-10-26 | Journal article
DOI: 10.1016/j.gene.2019.144228
PMID: 31669637
Source: Self-asserted source
Milad Gholami

ACE gene rs4343 polymorphism elevates the risk of preeclampsia in pregnant women

Journal of Human Hypertension
2018 | Journal article
DOI: 10.1038/s41371-018-0096-4
EID:

2-s2.0-85052596684
Contributors: Abedin Do, A.; Esmaeilzadeh, E.; Amin-Beidokhti, M.; Pirjani, R.; Gholami, M.; Mirfakhraie, R.
Source: Self-asserted source
Milad Gholami via Scopus - Elsevier

An intron variant in the FLT1 gene increases the risk of preeclampsia in Iranian women

Clinical and Experimental Hypertension
2018 | Journal article
DOI: 10.1080/10641963.2018.1539097
EID:

2-s2.0-85057344561
Contributors: Amin-Beidokhti, M.; Gholami, M.; Abedin-Do, A.; Pirjani, R.; Sadeghi, H.; Karamoddin, F.; Yassaee, V.R.; Mirfakhraie, R.
Source: Self-asserted source
Milad Gholami via Scopus - Elsevier

Association study of FOXP3 gene and the risk of 0020 pre-eclampsia

Clinical and Experimental Hypertension
2018 | Journal article
DOI: 10.1080/10641963.2017.1411500
EID:

2-s2.0-85036610453
Contributors: Gholami, M.; Mirfakhraie, R.; Pirjani, R.; Taheripanah, R.; Bayat, S.; Daryabari, S.A.; Noori, M.; Ghaderian, S.M.H.
Source: Self-asserted source
Milad Gholami via Scopus - Elsevier

Investigation of piwi-interacting RNA pathway genes role in idiopathic non-obstructive azoospermia

Scientific Reports
2018 | Journal article
DOI: 10.1038/s41598-017-17518-4
EID:

2-s2.0-85040520726
Contributors: Kamaliyan, Z.; Pouriamanesh, S.; Soosanabadi, M.; Gholami, M.; Mirfakhraie, R.
Source: Self-asserted source
Milad Gholami via Scopus - Elsevier

The rs4846049 polymorphism in the 3&rsquo;UTR region of the <em>MTHFR</em> gene increases the migraine susceptibility in an Iranian population

Journal of Pain Research
2018-01 | Journal article
DOI: 10.2147/JPR.S152930
Contributors: Mohaddeseh Salehi; Mona Amin-Beidokhti; Behnam Safarpour Lima; Milad Gholami; Gholamreza Javadi; Reza Mirfakhraie
Source: check_circle
Crossref
grade
Preferred source (of 2)‎

Functional genetic variants of FOXP3 and risk of multiple sclerosis

Iranian Red Crescent Medical Journal
2017 | Journal article
DOI: 10.5812/ircmj.34597
EID:

2-s2.0-85011888143
Contributors: Gholami, M.; Darvish, H.; Ahmadi, H.; Rahimi-Aliabadi, S.; Emamalizadeh, B.; Amirabadi, M.R.E.; Jamshidi, J.; Movafagh, A.
Source: Self-asserted source
Milad Gholami via Scopus - Elsevier

A novel splicesite mutation in the EDAR gene causes severe autosomal recessive hypohydrotic (anhidrotic) ectodermal dysplasia in an Iranian family

International Journal of Molecular and Cellular Medicine
2016 | Journal article
DOI: 10.22088/acadpub.BUMS.5.4.260
EID:

2-s2.0-85021854454
Contributors: Torkamandi, S.; Gholami, M.; Mohammadi-asl, J.; Rezaie, S.; Zaimy, M.A.; Omrani, M.D.
Source: Self-asserted source
Milad Gholami via Scopus - Elsevier

Genetic variants and expression study of FOXP3 gene in acute coronary syndrome in Iranian patients

Cell Biochemistry and Function
2016 | Journal article
DOI: 10.1002/cbf.3174
EID:

2-s2.0-84959271441
Contributors: Gholami, M.; Esfandiary, A.; Vatanparast, M.; Mirfakhraie, R.; Hosseini, M.M.; Ghafouri-Fard, S.
Source: Self-asserted source
Milad Gholami via Scopus - Elsevier

A case report: Autosomal recessive microcephaly caused by a novel mutation in MCPH1 gene

Gene
2015 | Journal article
DOI: 10.1016/j.gene.2015.07.058
EID:

2-s2.0-84939271002
Contributors: Ghafouri-Fard, S.; Fardaei, M.; Gholami, M.; Miryounesi, M.
Source: Self-asserted source
Milad Gholami via Scopus - Elsevier

The expression analysis of LATS2 gene in de novo AML patients

Medical Oncology
2014 | Journal article
DOI: 10.1007/s12032-014-0961-0
EID:

2-s2.0-84957433935
Contributors: Gholami, M.; Mirfakhraie, R.; Movafagh, A.; Jalaeekhoo, H.; Kalahroodi, R.; Zare-Abdollahi, D.; Zare-Karizi, S.
Source: Self-asserted source
Milad Gholami via Scopus - Elsevier

Identification of homogeneously staining regions in leukemia patients

Journal of Research in Medical Sciences
2013 | Journal article
EID:

2-s2.0-84878783351
Contributors: Moghadam, M.H.; Movafagh, A.; Omrani, M.; Ghanati, K.; Hashemi, M.; Poursafavi, F.; Darvish, H.; Abdolahi, D.Z.; Gholami, M.; Rostamy, M.R.H. et al.
Source: Self-asserted source
Milad Gholami via Scopus - Elsevier

Mutational Analysis of FLT3 Internal Tandem Duplication and D835 in De novo Adult Acute Myeloid Leukemia

Journal of Advances in Medicine and Medical Research
Journal article
Source: Self-asserted source
Milad Gholami

The structure Biology and Application of Phytohemagglutinin (PHA) in Phytomedicine: With special up-to-date references to lectins

Archives of Advances in Biosciences
Journal article
Source: Self-asserted source
Milad Gholami
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