Gholami M - Search Results

1

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

Ghafouri-Fard S, Fardaei M, Gholami M, Miryounesi M. Ghafouri-Fard S, et al. Among authors: gholami m. Gene. 2015 Oct 15;571(1):149-50. doi: 10.1016/j.gene.2015.07.058. Epub 2015 Jul 18. Gene. 2015. PMID: 26192461

2

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

Gholami M, Esfandiary A, Vatanparast M, Mirfakhraie R, Hosseini MM, Ghafouri-Fard S. Gholami M, et al. Cell Biochem Funct. 2016 Apr;34(3):158-62. doi: 10.1002/cbf.3174. Epub 2016 Feb 29. Cell Biochem Funct. 2016. PMID: 26931655

3

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

Torkamandi S, Rezaei S, Mirfakhraei R, Askari M, Piltan S, Gholami M. Torkamandi S, et al. Among authors: gholami m. Gene. 2020 Feb 15;727:144228. doi: 10.1016/j.gene.2019.144228. Epub 2019 Oct 26. Gene. 2020. PMID: 31669637

4

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

Torkamandi S, Rezaei S, Mirfakhraie R, Golmohamadi S, Gholami M. Torkamandi S, et al. Among authors: gholami m. Mol Biol Rep. 2020 May;47(5):4021-4027. doi: 10.1007/s11033-020-05424-4. Epub 2020 Apr 12. Mol Biol Rep. 2020. PMID: 32281057

5

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

Torkamandi S, Rezaei S, Mirfakhraie R, Bayat S, Piltan S, Gholami M. Torkamandi S, et al. Among authors: gholami m. J Clin Lab Anal. 2020 Aug;34(8):e23358. doi: 10.1002/jcla.23358. Epub 2020 May 17. J Clin Lab Anal. 2020. PMID: 32419160 Free PMC article.

6

A Novel Splicesite Mutation in the EDAR Gene Causes Severe Autosomal Recessive Hypohydrotic (Anhidrotic) Ectodermal Dysplasia in an Iranian Family.

Torkamandi S, Gholami M, Mohammadi-Asl J, Rezaie S, Zaimy MA, Omrani MD. Torkamandi S, et al. Among authors: gholami m. Int J Mol Cell Med. 2016 Fall;5(4):260-263. Epub 2016 Oct 23. Int J Mol Cell Med. 2016. PMID: 28357203 Free PMC article.

7

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

Rostampour D, Zolfaghari MR, Gholami M. Rostampour D, et al. Among authors: gholami m. J Clin Lab Anal. 2022 Mar;36(3):e24253. doi: 10.1002/jcla.24253. Epub 2022 Jan 29. J Clin Lab Anal. 2022. PMID: 35092705 Free PMC article.

8

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

Amin-Beidokhti M, Gholami M, Abedin-Do A, Pirjani R, Sadeghi H, Karamoddin F, Yassaee VR, Mirfakhraie R. Amin-Beidokhti M, et al. Among authors: gholami m. Clin Exp Hypertens. 2019;41(8):697-701. doi: 10.1080/10641963.2018.1539097. Epub 2018 Nov 8. Clin Exp Hypertens. 2019. PMID: 30409050 Free article.

9

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

Gholami M, Mirfakhraie R, Pirjani R, Taheripanah R, Bayat S, Daryabari SA, Noori M, Ghaderian SMH. Gholami M, et al. Clin Exp Hypertens. 2018;40(7):613-616. doi: 10.1080/10641963.2017.1411500. Epub 2017 Dec 5. Clin Exp Hypertens. 2018. PMID: 29206055 Free article.

10

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

Kamaliyan Z, Pouriamanesh S, Soosanabadi M, Gholami M, Mirfakhraie R. Kamaliyan Z, et al. Among authors: gholami m. Sci Rep. 2018 Jan 9;8(1):142. doi: 10.1038/s41598-017-17518-4. Sci Rep. 2018. PMID: 29317647 Free PMC article.

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