Abbas S - Search Results

1

Biallelic Missense Mutation in the ECEL1 Underlies Distal Arthrogryposis Type 5 (DA5D).

Umair M, Khan A, Hayat A, Abbas S, Asiri A, Younus M, Amin W, Nawaz S, Khan S, Malik E, Alfadhel M, Ahmad F. Umair M, et al. Among authors: abbas s. Front Pediatr. 2019 Aug 28;7:343. doi: 10.3389/fped.2019.00343. eCollection 2019. Front Pediatr. 2019. PMID: 31555621 Free PMC article.

2

Knowledge of Medicinal Plants for Children Diseases in the Environs of District Bannu, Khyber Pakhtoonkhwa (KPK).

Shaheen S, Abbas S, Hussain J, Mabood F, Umair M, Ali M, Ahmad M, Zafar M, Farooq U, Khan A. Shaheen S, et al. Among authors: abbas s. Front Pharmacol. 2017 Jul 17;8:430. doi: 10.3389/fphar.2017.00430. eCollection 2017. Front Pharmacol. 2017. PMID: 28769789 Free PMC article.

3

First direct evidence of involvement of a homozygous loss-of-function variant in the EPS15L1 gene underlying split-hand/split-foot malformation.

Umair M, Ullah A, Abbas S, Ahmad F, Basit S, Ahmad W. Umair M, et al. Among authors: abbas s. Clin Genet. 2018 Mar;93(3):699-702. doi: 10.1111/cge.13152. Epub 2018 Jan 25. Clin Genet. 2018. PMID: 29023680

4

Long non-coding RNAs as molecular players in plant defense against pathogens.

Zaynab M, Fatima M, Abbas S, Umair M, Sharif Y, Raza MA. Zaynab M, et al. Among authors: abbas s. Microb Pathog. 2018 Aug;121:277-282. doi: 10.1016/j.micpath.2018.05.050. Epub 2018 May 31. Microb Pathog. 2018. PMID: 29859899 Review.

5

Role of secondary metabolites in plant defense against pathogens.

Zaynab M, Fatima M, Abbas S, Sharif Y, Umair M, Zafar MH, Bahadar K. Zaynab M, et al. Among authors: abbas s. Microb Pathog. 2018 Nov;124:198-202. doi: 10.1016/j.micpath.2018.08.034. Epub 2018 Aug 23. Microb Pathog. 2018. PMID: 30145251 Review.

6

SGCD Homozygous Nonsense Mutation (p.Arg97^∗) Causing Limb-Girdle Muscular Dystrophy Type 2F (LGMD2F) in a Consanguineous Family, a Case Report.

Younus M, Ahmad F, Malik E, Bilal M, Kausar M, Abbas S, Shaheen S, Kakar MU, Alfadhel M, Umair M. Younus M, et al. Among authors: abbas s. Front Genet. 2019 Jan 23;9:727. doi: 10.3389/fgene.2018.00727. eCollection 2018. Front Genet. 2019. PMID: 30733730 Free PMC article.

7

Homozygous missense variant in the TTN gene causing autosomal recessive limb-girdle muscular dystrophy type 10.

Khan A, Wang R, Han S, Umair M, Abbas S, Khan MI, Alshabeeb MA, Alfadhel M, Zhang X. Khan A, et al. Among authors: abbas s. BMC Med Genet. 2019 Oct 29;20(1):166. doi: 10.1186/s12881-019-0895-7. BMC Med Genet. 2019. PMID: 31664938 Free PMC article.

8

Correction to: Homozygous missense variant in the TTN gene causing autosomal recessive limb-girdle muscular dystrophy type 10.

Khan A, Wang R, Han S, Umair M, Abbas S, Khan MI, Alshabeeb MA, Alfadheland M, Zhang X. Khan A, et al. Among authors: abbas s. BMC Med Genet. 2019 Dec 12;20(1):195. doi: 10.1186/s12881-019-0929-1. BMC Med Genet. 2019. PMID: 31830914 Free PMC article.

9

Identification of a novel biallelic missense variant in the KIAA0825 underlies postaxial polydactyly type A.

Hayat A, Umair M, Abbas S, Rauf A, Ahmad F, Ullah S, Ahmad W, Khan B. Hayat A, et al. Among authors: abbas s. Genomics. 2020 Jul;112(4):2729-2733. doi: 10.1016/j.ygeno.2020.03.006. Epub 2020 Mar 5. Genomics. 2020. PMID: 32147526 Free article.

10

Biallelic variants in four genes underlying recessive osteogenesis imperfecta.

Hayat A, Hussain S, Bilal M, Kausar M, Almuzzaini B, Abbas S, Tanveer A, Khan A, Siddiqi S, Foo JN, Ahmad F, Khan F, Khan B, Anees M, Mäkitie O, Alfadhel M, Ahmad W, Umair M. Hayat A, et al. Among authors: abbas s. Eur J Med Genet. 2020 Aug;63(8):103954. doi: 10.1016/j.ejmg.2020.103954. Epub 2020 May 13. Eur J Med Genet. 2020. PMID: 32413570

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