Hussain HMJ - Search Results

1

Whole exome sequencing identified a novel missense alteration in CC2D2A causing Joubert syndrome 9 in a Pakhtun family.

Khan MI, Latif M, Saif M, Ahmad H, Khan AU, Naseer MI, Hussain HMJ, Jelani M. Khan MI, et al. Among authors: hussain hmj. J Gene Med. 2021 Jan;23(1):e3279. doi: 10.1002/jgm.3279. Epub 2020 Oct 27. J Gene Med. 2021. PMID: 32989887

2

Whole exome sequencing identifies a novel dominant missense mutation underlying leukonychia in a Pakistani family.

Khan T, Khan M, Yousaf A, Khan S, Naeem M, Shah A, Murtaza G, Ali A, Jabeen N, Hussain HMJ, Ma H, Zhang Y, Zubair M, Jiang X, Zhang H. Khan T, et al. Among authors: hussain hmj. J Hum Genet. 2018 Oct;63(10):1071-1076. doi: 10.1038/s10038-018-0491-2. Epub 2018 Jul 23. J Hum Genet. 2018. PMID: 30033443 Clinical Trial.

3

Whole Exome Sequencing Revealed a Novel Nonsense Variant in the GNRHR Gene Causing Normosmic Hypogonadotropic Hypogonadism in a Pakistani Family.

Hussain HMJ, Murtaza G, Jiang X, Khan R, Khan M, Kakakhel MBS, Khan T, Wahab F, Zhang H, Zhang Y, Khan MB, Ahmed P, Ma H, Xu Z. Hussain HMJ, et al. Horm Res Paediatr. 2019;91(1):9-16. doi: 10.1159/000497114. Epub 2019 Apr 4. Horm Res Paediatr. 2019. PMID: 30947225 Clinical Trial.

4

Clinical and genetic analysis of lipoprotein glomerulopathy patients caused by APOE mutations.

Yang M, Weng Q, Pan X, Hussain HMJ, Yu S, Xu J, Yu X, Liu Y, Jin Y, Zhang C, Li X, Ren H, Chen N, Xie J. Yang M, et al. Among authors: hussain hmj. Mol Genet Genomic Med. 2020 Aug;8(8):e1281. doi: 10.1002/mgg3.1281. Epub 2020 May 22. Mol Genet Genomic Med. 2020. PMID: 32441489 Free PMC article.

5

Next-Generation Sequencing Identifies Pathogenic Variants in HGF, POU3F4, TECTA, and MYO7A in Consanguineous Pakistani Deaf Families.

Mei X, Zhou Y, Amjad M, Yang W, Zhu R, Asif M, Hussain HMJ, Yang T, Iqbal F, Hu H. Mei X, et al. Among authors: hussain hmj. Neural Plast. 2021 Apr 22;2021:5528434. doi: 10.1155/2021/5528434. eCollection 2021. Neural Plast. 2021. PMID: 33976695 Free PMC article.

6

Novel Pathogenic Mutations Identified from Whole-Genome Sequencing in Unsolved Cases of Patients Affected with Inherited Retinal Diseases.

Hussain HMJ, Wang M, Huang A, Schmidt R, Qian X, Yang P, Marra M, Li Y, Pennesi ME, Chen R. Hussain HMJ, et al. Genes (Basel). 2023 Feb 9;14(2):447. doi: 10.3390/genes14020447. Genes (Basel). 2023. PMID: 36833373 Free PMC article.

7

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: hussain hmj. 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.

8

The evolutionarily conserved genes: Tex37, Ccdc73, Prss55 and Nxt2 are dispensable for fertility in mice.

Khan M, Jabeen N, Khan T, Hussain HMJ, Ali A, Khan R, Jiang L, Li T, Tao Q, Zhang X, Yin H, Yu C, Jiang X, Shi Q. Khan M, et al. Among authors: hussain hmj. Sci Rep. 2018 Mar 21;8(1):4975. doi: 10.1038/s41598-018-23176-x. Sci Rep. 2018. PMID: 29563520 Free PMC article.

9

The deubiquitinating gene Usp29 is dispensable for fertility in male mice.

Huang Z, Khan M, Xu J, Khan T, Ma H, Khan R, Hussain HMJ, Jiang X, Shi Q. Huang Z, et al. Among authors: hussain hmj. Sci China Life Sci. 2019 Apr;62(4):544-552. doi: 10.1007/s11427-018-9469-4. Epub 2019 Mar 22. Sci China Life Sci. 2019. PMID: 30919279

10

The testis-specifically expressed Dpep3 is not essential for male fertility in mice.

Xie Y, Khan R, Wahab F, Hussain HMJ, Ali A, Ma H, Jiang H, Xu J, Zaman Q, Khan M, Jiang X, Shi Q. Xie Y, et al. Among authors: hussain hmj. Gene. 2019 Aug 30;711:143925. doi: 10.1016/j.gene.2019.06.015. Epub 2019 Jun 15. Gene. 2019. PMID: 31212048

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