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Page 1
Molecular diagnostic assays for COVID-19: an overview.
Habibzadeh P, Mofatteh M, Silawi M, Ghavami S, Faghihi MA. Habibzadeh P, et al. Among authors: silawi m. Crit Rev Clin Lab Sci. 2021 Sep;58(6):385-398. doi: 10.1080/10408363.2021.1884640. Epub 2021 Feb 17. Crit Rev Clin Lab Sci. 2021. PMID: 33595397 Free PMC article. Review.
Expanding the molecular and clinical phenotypes of FUT8-CDG.
Ng BG, Dastsooz H, Silawi M, Habibzadeh P, Jahan SB, Fard MAF, Halliday BJ, Raymond K, Ruzhnikov MRZ, Tabatabaei Z, Taghipour-Sheshdeh A, Brimble E, Robertson SP, Faghihi MA, Freeze HH. Ng BG, et al. Among authors: silawi m. J Inherit Metab Dis. 2020 Jul;43(4):871-879. doi: 10.1002/jimd.12221. Epub 2020 Feb 23. J Inherit Metab Dis. 2020. PMID: 32049367 Free PMC article.
Identification of Candidate Genes for Pigmentation in Camels Using Genotyping-by-Sequencing.
Bitaraf Sani M, Zare Harofte J, Banabazi MH, Faraz A, Esmaeilkhanian S, Naderi AS, Salim N, Teimoori A, Bitaraf A, Zadehrahmani M, Burger PA, Asadzadeh N, Silawi M, Taghipour Sheshdeh A, Mohammad Nazari B, Faghihi MA, Roudbari Z. Bitaraf Sani M, et al. Among authors: silawi m. Animals (Basel). 2022 Apr 23;12(9):1095. doi: 10.3390/ani12091095. Animals (Basel). 2022. PMID: 35565522 Free PMC article.
Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia.
Farazi Fard MA, Rebelo AP, Buglo E, Nemati H, Dastsooz H, Gehweiler I, Reich S, Reichbauer J, Quintáns B, Ordóñez-Ugalde A, Cortese A, Courel S, Abreu L, Powell E, Danzi MC, Martuscelli NB, Bis-Brewer DM, Tao F, Zarei F, Habibzadeh P, Yavarian M, Modarresi F, Silawi M, Tabatabaei Z, Yousefi M, Farpour HR, Kessler C, Mangold E, Kobeleva X, Tournev I, Chamova T, Mueller AJ, Haack TB, Tarnopolsky M, Gan-Or Z, Rouleau GA, Synofzik M, Sobrido MJ, Jordanova A, Schüle R, Zuchner S, Faghihi MA. Farazi Fard MA, et al. Among authors: silawi m. Am J Hum Genet. 2019 Apr 4;104(4):767-773. doi: 10.1016/j.ajhg.2019.03.001. Epub 2019 Mar 28. Am J Hum Genet. 2019. PMID: 30929741 Free PMC article.
Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia.
Farazi Fard MA, Rebelo AP, Buglo E, Nemati H, Dastsooz H, Gehweiler I, Reich S, Reichbauer J, Quintáns B, Ordóñez-Ugalde A, Cortese A, Courel S, Abreu L, Powell E, Danzi MC, Martuscelli NB, Bis-Brewer DM, Tao F, Zarei F, Habibzadeh P, Yavarian M, Modarresi F, Silawi M, Tabatabaei Z, Yousefi M, Farpour HR, Kessler C, Mangold E, Kobeleva X, Tournev I, Chamova T, Mueller AJ, Haack TB, Tarnopolsky M, Gan-Or Z, Rouleau GA, Synofzik M, Sobrido MJ, Jordanova A, Schüle R, Zuchner S, Faghihi MA. Farazi Fard MA, et al. Among authors: silawi m. Am J Hum Genet. 2019 Jun 6;104(6):1251. doi: 10.1016/j.ajhg.2019.05.009. Am J Hum Genet. 2019. PMID: 31173719 Free PMC article. No abstract available.
Biallelic variants in TMEM222 cause a new autosomal recessive neurodevelopmental disorder.
Polla DL, Farazi Fard MA, Tabatabaei Z, Habibzadeh P, Levchenko OA, Nikuei P, Makrythanasis P, Hussain M, von Hardenberg S, Zeinali S, Fallah MS, Schuurs-Hoeijmakers JHM, Shahzad M, Fatima F, Fatima N, Kaat LD, Bruggenwirth HT, Fleming LR, Condie J, Ploski R, Pollak A, Pilch J, Demina NA, Chukhrova AL, Sergeeva VS, Venselaar H, Masri AT, Hamamy H, Santoni FA, Linda K, Ahmed ZM, Nadif Kasri N, de Brouwer APM, Bergmann AK, Hethey S, Yavarian M, Ansar M, Riazuddin S, Riazuddin S, Silawi M, Ruggeri G, Pirozzi F, Eftekhar E, Taghipour Sheshdeh A, Bahramjahan S, Mirzaa GM, Lavrov AV, Antonarakis SE, Faghihi MA, van Bokhoven H. Polla DL, et al. Among authors: silawi m. Genet Med. 2021 Jul;23(7):1246-1254. doi: 10.1038/s41436-021-01133-w. Epub 2021 Apr 6. Genet Med. 2021. PMID: 33824500 Free PMC article.
Genomic prediction for growth using a low-density SNP panel in dromedary camels.
Bitaraf Sani M, Zare Harofte J, Banabazi MH, Esmaeilkhanian S, Shafei Naderi A, Salim N, Teimoori A, Bitaraf A, Zadehrahmani M, Burger PA, Landi V, Silawi M, Taghipour Sheshdeh A, Faghihi MA. Bitaraf Sani M, et al. Among authors: silawi m. Sci Rep. 2021 Apr 7;11(1):7675. doi: 10.1038/s41598-021-87296-7. Sci Rep. 2021. PMID: 33828208 Free PMC article.
16 results