Khan I - Search Results

1

A DNAH17 missense variant causes flagella destabilization and asthenozoospermia.

Zhang B, Ma H, Khan T, Ma A, Li T, Zhang H, Gao J, Zhou J, Li Y, Yu C, Bao J, Ali A, Murtaza G, Yin H, Gao Q, Jiang X, Zhang F, Liu C, Khan I, Zubair M, Hussain HMJ, Khan R, Yousaf A, Yuan L, Lu Y, Xu X, Wang Y, Tao Q, Hao Q, Fang H, Cheng H, Zhang Y, Shi Q. Zhang B, et al. Among authors: khan r, khan t, khan i. J Exp Med. 2020 Feb 3;217(2):e20182365. doi: 10.1084/jem.20182365. J Exp Med. 2020. PMID: 31658987 Free PMC article.

2

Novel loss-of-function variants in DNAH17 cause multiple morphological abnormalities of the sperm flagella in humans and mice.

Zhang B, Khan I, Liu C, Ma A, Khan A, Zhang Y, Zhang H, Kakakhel MBS, Zhou J, Zhang W, Li Y, Ali A, Jiang X, Murtaza G, Khan R, Zubair M, Yuan L, Khan M, Wang L, Zhang F, Wang X, Ma H, Shi Q. Zhang B, et al. Among authors: khan r, khan a, khan m, khan i. Clin Genet. 2021 Jan;99(1):176-186. doi: 10.1111/cge.13866. Epub 2020 Nov 2. Clin Genet. 2021. PMID: 33070343

3

Normal spermatogenesis and fertility in Ddi1 (DNA damage inducible 1) mutant mice.

Yousaf A, Wu Y, Khan R, Shah W, Khan I, Shi Q, Jiang X. Yousaf A, et al. Among authors: khan r, khan i. Reprod Biol. 2020 Dec;20(4):520-524. doi: 10.1016/j.repbio.2020.08.006. Epub 2020 Oct 19. Reprod Biol. 2020. PMID: 33092996

4

Novel biallelic loss-of-function mutations in CFAP43 cause multiple morphological abnormalities of the sperm flagellum in Pakistani families.

Khan I, Shah B, Dil S, Ullah N, Zhou JT, Zhao DR, Zhang YW, Jiang XH, Khan R, Khan A, Ali H, Zubair M, Shah W, Zhang H, Shi QH. Khan I, et al. Among authors: khan r, khan a. Asian J Androl. 2021 Nov-Dec;23(6):627-632. doi: 10.4103/aja.aja_26_21. Asian J Androl. 2021. PMID: 34100391 Free PMC article.

5

Novel frameshift mutation in STK33 is associated with asthenozoospermia and multiple morphological abnormalities of the flagella.

Ma H, Zhang B, Khan A, Zhao D, Ma A, Zhou J, Khan I, Khan K, Zhang H, Zhang Y, Jiang X, Dil S, Zeb A, Rahim F, Shi Q. Ma H, et al. Among authors: khan a, khan k, khan i. Hum Mol Genet. 2021 Oct 13;30(21):1977-1984. doi: 10.1093/hmg/ddab165. Hum Mol Genet. 2021. PMID: 34155512

6

A novel stop-gain mutation in ARMC2 is associated with multiple morphological abnormalities of the sperm flagella.

Khan I, Dil S, Zhang H, Zhang B, Khan T, Zeb A, Zhou J, Nawaz S, Zubair M, Khan K, Ma H, Shi Q. Khan I, et al. Among authors: khan t, khan k. Reprod Biomed Online. 2021 Nov;43(5):913-919. doi: 10.1016/j.rbmo.2021.07.021. Epub 2021 Aug 8. Reprod Biomed Online. 2021. PMID: 34493464

7

Identification and Functional Investigation of Novel Heterozygous HELQ Mutations in Patients with Sertoli Cell-only Syndrome.

Murtaza G, Yang L, Khan I, Unar A, Khan M, Huan Z, Khan R, Shi Q. Murtaza G, et al. Among authors: khan r, khan m, khan i. Genet Test Mol Biomarkers. 2021 Oct;25(10):654-659. doi: 10.1089/gtmb.2021.0104. Genet Test Mol Biomarkers. 2021. PMID: 34672775

8

Biallelic Variants in CFAP61 Cause Multiple Morphological Abnormalities of the Flagella and Male Infertility.

Ma A, Zeb A, Ali I, Zhao D, Khan A, Zhang B, Zhou J, Khan R, Zhang H, Zhang Y, Khan I, Shah W, Ali H, Javed AR, Ma H, Shi Q. Ma A, et al. Among authors: khan r, khan a, khan i. Front Cell Dev Biol. 2022 Jan 31;9:803818. doi: 10.3389/fcell.2021.803818. eCollection 2021. Front Cell Dev Biol. 2022. PMID: 35174165 Free PMC article.

9

A recurrent homozygous missense mutation in CCDC103 causes asthenoteratozoospermia due to disorganized dynein arms.

Zubair M, Khan R, Ma A, Hameed U, Khan M, Abbas T, Ahmad R, Zhou JT, Shah W, Hussain A, Ahmed N, Khan I, Khan K, Zhang YW, Zhang H, Wu LM, Shi QH. Zubair M, et al. Among authors: khan r, khan k, khan m, khan i. Asian J Androl. 2022 May-Jun;24(3):255-259. doi: 10.4103/aja2021122. Asian J Androl. 2022. PMID: 35259782 Free PMC article.

10

In silico analysis of a novel pathogenic variant c.7G > A in C14orf39 gene identified by WES in a Pakistani family with azoospermia.

Ali H, Unar A, Zubair M, Dil S, Ullah F, Khan I, Hussain A, Shi Q. Ali H, et al. Among authors: khan i. Mol Genet Genomics. 2022 May;297(3):719-730. doi: 10.1007/s00438-022-01876-4. Epub 2022 Mar 19. Mol Genet Genomics. 2022. PMID: 35305148

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