Ilyas M - Search Results

1

Spastic paraplegia preceding PSEN1-related familial Alzheimer's disease.

Chelban V, Breza M, Szaruga M, Vandrovcova J, Murphy D, Lee CJ, Alikhwan S, Bourinaris T, Vavougios G, Ilyas M, Halim SA, Al-Harrasi A, Kartanou C, Ronald C, Blumcke I, Alexoudi A, Gatzonis S, Stefanis L, Karadima G, Wood NW, Chávez-Gutiérrez L, Hardy J, Houlden H, Koutsis G. Chelban V, et al. Among authors: ilyas m. Alzheimers Dement (Amst). 2021 May 2;13(1):e12186. doi: 10.1002/dad2.12186. eCollection 2021. Alzheimers Dement (Amst). 2021. PMID: 33969176 Free PMC article.

2

Identification of common genetic markers of paroxysmal neurological disorders using a network analysis approach.

Ilyas M, Salpietro V, Efthymiou S, Bourinaris T, Tariq A, Imdad M, Ahmad A, Ahmad H, Houlden H. Ilyas M, et al. Neurol Sci. 2020 Apr;41(4):851-857. doi: 10.1007/s10072-019-04113-w. Epub 2019 Dec 6. Neurol Sci. 2020. PMID: 31808001

3

A novel variant in the DSE gene leads to Ehlers-Danlos musculocontractural type 2 in a Pakistani family.

Ullah I, Aamir M, Ilyas M, Ahmed A, Jelani M, Ullah W, Abbas M, Ishfaq M, Ali F, Yip J, Efthymiou S, Ahmed H, Houlden H. Ullah I, et al. Among authors: ilyas m. Congenit Anom (Kyoto). 2021 Sep;61(5):177-182. doi: 10.1111/cga.12436. Epub 2021 Jul 13. Congenit Anom (Kyoto). 2021. PMID: 34184791

4

Novel variants underlying autosomal recessive intellectual disability in Pakistani consanguineous families.

Ilyas M, Efthymiou S, Salpietro V, Noureen N, Zafar F, Rauf S, Mir A, Houlden H. Ilyas M, et al. BMC Med Genet. 2020 Mar 24;21(1):59. doi: 10.1186/s12881-020-00998-z. BMC Med Genet. 2020. PMID: 32209057 Free PMC article.

5

In silico identification of novel IL-1β inhibitors to target protein-protein interfaces.

Halim SA, Jawad M, Ilyas M, Mir Z, Mirza AA, Husnain T. Halim SA, et al. Among authors: ilyas m. Comput Biol Chem. 2015 Oct;58:158-66. doi: 10.1016/j.compbiolchem.2015.06.004. Epub 2015 Jun 30. Comput Biol Chem. 2015. PMID: 26253030

6

Author Correction: Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia.

Cortese A, Simone R, Sullivan R, Vandrovcova J, Tariq H, Yau WY, Humphrey J, Jaunmuktane Z, Sivakumar P, Polke J, Ilyas M, Tribollet E, Tomaselli PJ, Devigili G, Callegari I, Versino M, Salpietro V, Efthymiou S, Kaski D, Wood NW, Andrade NS, Buglo E, Rebelo A, Rossor AM, Bronstein A, Fratta P, Marques WJ, Züchner S, Reilly MM, Houlden H. Cortese A, et al. Among authors: ilyas m. Nat Genet. 2019 May;51(5):920. doi: 10.1038/s41588-019-0422-y. Nat Genet. 2019. PMID: 31028356 Free PMC article.

7

The Islamic perspective of organ donation in Pakistan.

Ilyas M, Alam M, Ahmad H. Ilyas M, et al. Saudi J Kidney Dis Transpl. 2009 Jan;20(1):154-6. Saudi J Kidney Dis Transpl. 2009. PMID: 19112239 No abstract available.

8

Population genetic structure of domain I of apical membrane antigen-1 in Plasmodium falciparum isolates from Hazara division of Pakistan.

Afridi SG, Irfan M, Ahmad H, Aslam M, Nawaz M, Ilyas M, Khan A. Afridi SG, et al. Among authors: ilyas m. Malar J. 2018 Oct 26;17(1):389. doi: 10.1186/s12936-018-2539-3. Malar J. 2018. PMID: 30367656 Free PMC article.

9

A comprehensive Y-STR portrait of Yousafzai's population.

Tabassum S, Ilyas M, Ullah I, Israr M, Ahmad H. Tabassum S, et al. Among authors: ilyas m. Int J Legal Med. 2017 Sep;131(5):1241-1242. doi: 10.1007/s00414-017-1550-5. Epub 2017 Feb 16. Int J Legal Med. 2017. PMID: 28210813

10

Mitochondrial DNA diversity in the Khattak and Kheshgi of the Peshawar Valley, Pakistan.

Zubair M, Hemphill BE, Schurr TG, Tariq M, Ilyas M, Ahmad H. Zubair M, et al. Among authors: ilyas m. Genetica. 2020 Aug;148(3-4):195-206. doi: 10.1007/s10709-020-00095-2. Epub 2020 Jun 30. Genetica. 2020. PMID: 32607672

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