Shahzad S - Search Results

1

Plant beneficial endophytic bacteria: Mechanisms, diversity, host range and genetic determinants.

Afzal I, Shinwari ZK, Sikandar S, Shahzad S. Afzal I, et al. Among authors: shahzad s. Microbiol Res. 2019 Apr;221:36-49. doi: 10.1016/j.micres.2019.02.001. Epub 2019 Feb 4. Microbiol Res. 2019. PMID: 30825940 Free article. Review.

2

Updated strategies for the management, pathogenesis and molecular genetics of different forms of ichthyosis syndromes with prominent hair abnormalities.

Rasheed M, Shahzad S, Zaeem A, Afzal I, Gul A, Khalid S. Rasheed M, et al. Among authors: shahzad s. Arch Dermatol Res. 2017 Dec;309(10):773-785. doi: 10.1007/s00403-017-1780-x. Epub 2017 Sep 14. Arch Dermatol Res. 2017. PMID: 28913623 Review.

3

Characterization and applications of glutaminase free L-asparaginase from indigenous Bacillus halotolerans ASN9.

Shafqat I, Shahzad S, Yasmin A, Chaudhry MT, Ahmed S, Javed A, Afzal I, Bibi M. Shafqat I, et al. Among authors: shahzad s. PLoS One. 2023 Nov 28;18(11):e0288620. doi: 10.1371/journal.pone.0288620. eCollection 2023. PLoS One. 2023. PMID: 38015853 Free PMC article.

4

Homozygous variants in the HEXB and MBOAT7 genes underlie neurological diseases in consanguineous families.

Khan S, Rawlins LE, Harlalka GV, Umair M, Ullah A, Shahzad S, Javed M, Baple EL, Crosby AH, Ahmad W, Gul A. Khan S, et al. Among authors: shahzad s. BMC Med Genet. 2019 Dec 18;20(1):199. doi: 10.1186/s12881-019-0907-7. BMC Med Genet. 2019. PMID: 31852446 Free PMC article.

5

An intrafamilial phenotypic variability in Ellis-Van Creveld syndrome due to a novel 27 bps deletion mutation.

Zaka A, Shahzad S, Rao HZ, Kanwal S, Gul A, Basit S. Zaka A, et al. Among authors: shahzad s. Am J Med Genet A. 2021 Oct;185(10):2888-2894. doi: 10.1002/ajmg.a.62360. Epub 2021 May 26. Am J Med Genet A. 2021. PMID: 34037314

6

A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family.

Ahmad F, Ahmed I, Nasir A, Umair M, Shahzad S, Muhammad D, Santos-Cortez RLP, Leal SM, Ahmad W. Ahmad F, et al. Among authors: shahzad s. Eur J Dermatol. 2018 Apr 1;28(2):209-216. doi: 10.1684/ejd.2017.3210. Eur J Dermatol. 2018. PMID: 29611532 Free PMC article.

7

Sequence variants in nine different genes underlying rare skin disorders in 10 consanguineous families.

Shah K, Mehmood S, Jan A, Abbe I, Hussain Ali R, Khan A, Chishti MS, Lee K, Ahmad F, Ansar M; University of Washington Center for Mendelian Genomics; Shahzad S, Nickerson DA, Bamshad MJ, Coucke PJ, Santos-Cortez RLP, Spritz RA, Leal SM, Ahmad W. Shah K, et al. Among authors: shahzad s. Int J Dermatol. 2017 Dec;56(12):1406-1413. doi: 10.1111/ijd.13778. Int J Dermatol. 2017. PMID: 29130490 Free PMC article.

8

Exome sequencing revealed a novel nonsense variant in ALX3 gene underlying frontorhiny.

Ullah A, Umair M, E-Kalsoom U, Shahzad S, Basit S, Ahmad W. Ullah A, et al. Among authors: shahzad s. J Hum Genet. 2018 Jan;63(1):97-100. doi: 10.1038/s10038-017-0358-y. Epub 2017 Nov 16. J Hum Genet. 2018. PMID: 29215096 Clinical Trial.

9

CDKN2A/P16INK4A variants association with breast cancer and their in-silico analysis.

Aftab A, Shahzad S, Hussain HMJ, Khan R, Irum S, Tabassum S. Aftab A, et al. Among authors: shahzad s. Breast Cancer. 2019 Jan;26(1):11-28. doi: 10.1007/s12282-018-0894-0. Epub 2018 Jul 23. Breast Cancer. 2019. PMID: 30039340 Review.

10

Autosomal-Recessive Hearing Impairment Due to Rare Missense Variants within S1PR2.

Santos-Cortez RL, Faridi R, Rehman AU, Lee K, Ansar M, Wang X, Morell RJ, Isaacson R, Belyantseva IA, Dai H, Acharya A, Qaiser TA, Muhammad D, Ali RA, Shams S, Hassan MJ, Shahzad S, Raza SI, Bashir ZE, Smith JD, Nickerson DA, Bamshad MJ; University of Washington Center for Mendelian Genomics; Riazuddin S, Ahmad W, Friedman TB, Leal SM. Santos-Cortez RL, et al. Among authors: shahzad s. Am J Hum Genet. 2016 Feb 4;98(2):331-8. doi: 10.1016/j.ajhg.2015.12.004. Epub 2016 Jan 21. Am J Hum Genet. 2016. PMID: 26805784 Free PMC article.

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