Dr. Ihtisham  Bukhari

Dr. Ihtisham Bukhari

Assistant Professor
King Saud University, Saudi Arabia


Highest Degree
Ph.D. in Genetics from University of Science and Technology, China

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Area of Interest:

Biomedical Sciences
100%
Reproductive Biology
62%
Cytogenetics
90%
Embryology
75%
Infertility
55%

Selected Publications

  1. Ren, F., Q. Zhao, M. Zhao, S. Zhu and B. Liu et al. 2021. Immune Infiltration Profiling in Gastric Cancer and their Clinical Implications. Cancer Sci. 10.1111/cas.15057.
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  2. Yakout, S.M., N.M. Al-Daghri, I. Bukhari, M.N.K. Khattak and S. Sabico et al., 2020. Vitamin D level and its relation to muscle and fat mass in adult male Arabs. Saudi J. Bio. Sci., 27: 2452-2456.
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  3. Qazi, T.J., Q. Wu, A. Aierken, D. Lu and I. Bukhari et al., 2020. Whole-exome sequencing identifies a novel mutation in spermine synthase gene (SMS) associated with snyder-robinson syndrome. BMC Med. Genet., 10.1186/s12881-020-01095-x.
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  4. Jiao, Y., S. Fan, N. Jabeen, H. Zhang and R. Khan et al., 2020. A top6bl mutation abolishes meiotic DNA double-strand break formation and causes human infertility. Sci. Bull., 65: 2120-2129.
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  5. Ain, N.U., N. Muhammad, M. Dianatpour, M. Baroncelli and M. Iqbal et al. 2020. Biallelic TMEM251 Variants in Patients with Severe Skeletal Dysplasia and Extreme Short Stature. Hum. Mutat. 42: 89-101.
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  6. Abdi, S., I. Bukhari, M.G.A. Ansari, R.A. BinBaz and A.K. Mohammed et al., 2020. Association of polymorphisms in rank and rankl genes with osteopenia in arab postmenopausal women. Dis. Markers, 10.1155/2020/1285216.
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  7. Khan, R., A. Aftab, S. Tabassum, H.M.J. Hussain and A. Hameed et al., 2019. Identification of CDKN2A variants in breast cancer patients in Pakistan. Genes Genet. Syst., 94: 117-122.
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  8. Khan, R., 2019. Association of MTHFR C677T with idiopathic recurrent pregnancy loss in anhui province of China. Int. J. Human Genetics, 10.31901/24566330.2019/19.04.728.
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  9. Khan, M.R., I. Bukhari, R. Khan, H.M.J. Hussain and M. Wu et al., 2019. TP53LNC-DB, the database of lncRNAs in the P53 signalling network. Database, 10.1093/database/bay136.
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  10. Al-Daghri, N.M., A.K. Mohammed, I. Bukhari, M. Rikli and S. Abdi et al., 2019. Efficacy of vitamin D supplementation according to vitamin D-binding protein polymorphisms. Nutrition, 63-64: 148-154.
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  11. Yin, H., H. Ma, S. Hussain, H. Zhang and X. Xie et al., 2018. Correction: a homozygous fancm frameshift pathogenic variant causes male infertility. Genet. Med., 21: 266-266.
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  12. Krishnaswamy, S., I. Bukhari, A.K. Mohammed, O.E. Amer, G. Tripathi, M.S. Alokail and N.M. Al-Daghri, 2018. Identification of the splice variants of recepteur d’origine nantais (RON) in lung cancer cell lines. Gene, 679: 335-340.
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  13. Al-Daghri, N.M., I. Bukhari, S.M. Yakout, S. Sabico, M.N.K. Khattak, I. Aziz and M.S. Alokail, 2018. Associations of serum nitric oxide with vitamin d and other metabolic factors in apparently healthy adolescents. BioMed. Res. Int., 10.1155/2018/1489132.
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  14. Liu, H., H. Liu, J. Tang, Q. Lin and Y. Sun et al., 2017. Whole exome sequencing identifies a novel mutation in the PITX3 gene, causing autosomal dominant congenital cataracts in a Chinese family. Ann. Clin. Lab. Sci., 47: 92-95.
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  15. Imtiaz, A., I.A. Belyantseva, A.J. Beirl, C. Fenollar-Ferrer and R. Bashir et al., 2017. CDC14A phosphatase is essential for hearing and male fertility in mouse and human. Hum. Mol. Genet., 27: 780-798.
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  16. Bukhari, I., G. Li, L. Wang, F. Iqbal and H. Zhang et al., 2017. Effects of androgen receptor mutation on testicular histopathology of patient having complete androgen insensitivity. J. Mol. Histol., 48: 159-167.
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  17. Al-Daghri1, N., S. Yakout, I. Bukhari, M. Khattak and Y. AlSaleh et al., 2017. Parathyroid hormone in relation to various vitamin d metabolites in adult females. Medicine, Vol. 96. 10.1097/MD.0000000000008071.
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  18. Zhu, J., H. Liu, J. Tang, M.R. Khan and B. Wang, et al ., 2016. Identification of minor chromosomal defects causing abnormal fetus and spontaneous abortions Br. J. Biomed. Sci., 73: 67-73.
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  19. Wu, C., L. Wang, F. Iqbal, X. Jiang and I. Bukhari, et al ., 2016. Preferential Y-Y pairing and synapsis and abnormal meiotic recombination in a 47,XYY man with non obstructive azoospermia. Mol. Cytogenet, 9: 1-9.
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  20. Tang, J., G. Feng, Y. Sun, C. Wang and M.R. Khan, et al ., 2016. Genetic screening of neonates for 20 most common mutations in deafness associated genes in anhui province of china. Pak. J. Zool., 48: 1573-1577.
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  21. Naz, S., Imtiaz A, Mujtaba G, Maqsood A and Bashir R et al ., 2016. Genetic causes of moderate to severe hearing loss point to modifiers. Clin Genet. 10.1111/cge.12856.
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  22. Zhu, J., H. Liu, Y. Wang, M.R. Khan and I. Bukhari et al ., 2015. Genetic and clinical features of triploid fetus: a case report in han chinese population. Pak. J. Zool., 47: 595-598.
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  23. Yang, Q., N. Zhang, F. Zhao, W. Zha and S. Dai, et al ., 2015. Processing of semen by density gradient centrifugation selects spermatozoa with longer telomeres for assisted reproduction techniques. Reprod. Biomed. Online., 31: 44-50.
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  24. Wang, L., Z. Xu, F. Iqbal, L. Zhong and Y. Zhang, et al ., 2015. Decreased XY recombination and disturbed meiotic prophase I progression in an infertile 48, XYY, +sSMC man. Chromosome Res., 23: 267-276.
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  25. Wang, L., F. Iqbal, G. Li, X. Jiang and I. Bukhari, et al ., 2015. Abnormal meiotic recombination with complex chromosomal rearrangement in an azoospermic man. Reprod Biomed Online, 30: 651-658.
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  26. Jiang, X., T. Ma, Y. Zhang, H. Zhang and S. Yin, et al ., 2015. Specific deletion of Cdh2 in Sertoli cells leads to altered meiotic progression and subfertility of mice. Biol Reprod, 92: 79-79.
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  27. Bukhari, I., N. Muhammad, F. Gul, S. Ahmad and Z. Anwar, et al ., 2015. Frequency of anencephaly in hazara division of Pakistan. Am. J. Drug Delivery Ther., 2: 39-43.
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  28. Bukhari, I., G. Li, L. Wang, X. Jiang and F. Iqbal, et al ., 2015. Mutation p. Y572C in androgen receptor gene is associated with Sertoli cell only phenotype in a patient with complete androgen insensitivity. Hum. Genet. Embryol., 6: 1-45.
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  29. Wang, Z., H. Yin, Y. Zhang, Y. Feng and Z. Yan, et al ., 2014. MiR-214- mediated downregulation of RNF8 induces chromosomal instability in ovarian cancer cells. Cell Cycle, 13: 3519-3528.
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  30. Wang, Z., H. Yin, L. Lv, Y. Feng and S. Chen, et al ., 2014. Unrepaired DNA damage facilitates elimination of uniparental chromosomes in interspecific hybrid cells. Cell Cycle, 13: 1345-1356.
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  31. Jiang, XH., I. Bukhari, W. Zheng, S. Yin and Z.Wang, et al ., 2014. Blood-testis barrier and spermatogenesis: lessons from genetically-modified mice. Asian. J. Androl., 16: 572-580.
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  32. Jiang, X., H. Zhang, S. Yin, Y. Zhang and W. Yang et al ., 2014. Specific deficiency of Plzf paralog, Zbtb20, in Sertoli cells does not affect spermatogenesis and fertility in mice. Sci. Rep., 10.1038/srep07062.
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  33. Bukhari, I., G. Mujtaba and S. Naz, 2013. Contribution of GJB2 mutations to the deafness in Hazara Pakistan. Biochem. Genet., 51: 524-529.
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  34. Mujtaba, G., I. Bukhari, A. fatmia and S. Naz, 2012. A p.C343S Missense Mutation in PJVK causes Progressive Hearing Loss Gene. Gene, 504: 98-101.
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  35. Bukhari, I., M. Hassan, F.M. Abassi, Y. Shakir and A. Khan, et al ., 2012. Antibacterial spectrum of traditionally used medicinal plant of Hazara, Pakistan. Afri. J. Biotechnol., 11: 8404-8406.
  36. Bukhari, I., M. Hassan, F.M. Abassi, G. Mujtaba and N. Mahmood et al ., 2011. Study on comparative pharmacological efficacy of berberis lysium and penicillin G. Afri. J. Microbiol. Res., 5: 725-728.
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  37. Abbasi, F.M., S.H. Shah, A. Gul, A. Majid and M. Afzal, et al ., 2010. Localizing introgression on the chromosome of rise by genomic in situ hybridization (GISH). Afri. J. Biotechnol., 9: 4851-4854.
  38. Abbasi, F.M., A.H. Shah, R. Masood, R. Mujadad and F. Nawaz, et al ., 2010. Production and molecular characterization of wide cross derivatives in rice. Afri. J. Biotechnol., 9: 3732-3735.