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Variants in GLI3 Cause Greig Cephalopolysyndactyly Syndrome.

Abdullah, Yousaf M, Azeem Z, Bilal M, Liaqat K, Hussain S, Ahmad F, Ghous T, Ullah A, Ahmad W. Abdullah, et al. Among authors: azeem z. Genet Test Mol Biomarkers. 2019 Oct;23(10):744-750. doi: 10.1089/gtmb.2019.0071. Epub 2019 Oct 1. Genet Test Mol Biomarkers. 2019. PMID: 31573334

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Novel heterozygous sequence variant in the GLI1 underlies postaxial polydactyly.

Yousaf M, Ullah A, Azeem Z, Isani Majeed A, Memon MI, Ghous T, Basit S, Ahmad W. Yousaf M, et al. Among authors: azeem z. Congenit Anom (Kyoto). 2020 Jul;60(4):115-119. doi: 10.1111/cga.12361. Epub 2019 Oct 29. Congenit Anom (Kyoto). 2020. PMID: 31621941

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Identification of a Novel Homozygous Missense (c.443A>T:p.N148I) Mutation in BBS2 in a Kashmiri Family with Bardet-Biedl Syndrome.

Ali G, Sadia, Foo JN, Nasir A, Chang CH, Chew EG, Latif Z, Azeem Z, Ain-Ul-Batool S, Kazmi SAR, Awan NB, Khan AH, Rehman FU, Khalid M, Wali A, Sarwar S, Akhtar W, Ahmed Abbasi A, Nisar R. Ali G, et al. Among authors: azeem z. Biomed Res Int. 2021 Feb 23;2021:6626015. doi: 10.1155/2021/6626015. eCollection 2021. Biomed Res Int. 2021. PMID: 33688495 Free PMC article.

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4,5-Dioxo-imidazolinium Cation-Promoted α-Selective Dehydrative Glycosylation of 2-Deoxy- and 2,6-Dideoxy Sugars.

Javed, Tiwari A, Azeem Z, Mandal PK. Javed, et al. Among authors: azeem z. J Org Chem. 2022 Mar 4;87(5):3718-3729. doi: 10.1021/acs.joc.1c02650. Epub 2022 Jan 21. J Org Chem. 2022. PMID: 35060383

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Recent advances in palladium-catalyzed C(sp³)/C(sp²)-H bond functionalizations: access to C-branched glycosides.

Azeem Z, Mandal PK. Azeem Z, et al. Org Biomol Chem. 2022 Jan 5;20(2):264-281. doi: 10.1039/d1ob02142g. Org Biomol Chem. 2022. PMID: 34904995 Review.

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The Connotation of Variances in the Risk Predictors, Medications, Homocysteine, and Homocysteine Pathway Gene Polymorphisms with CVA/Stroke.

Masud R, Khan AUH, Anjum AF, Jawwad G, Azeem Z, Baqai HZ, Hashmi SN. Masud R, et al. Among authors: azeem z. Glob Med Genet. 2020 Dec;7(4):113-120. doi: 10.1055/s-0041-1722884. Epub 2021 Feb 9. Glob Med Genet. 2020. PMID: 33693444 Free PMC article.

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Sequence variants in four genes underlying Bardet-Biedl syndrome in consanguineous families.

Ullah A, Umair M, Yousaf M, Khan SA, Nazim-Ud-Din M, Shah K, Ahmad F, Azeem Z, Ali G, Alhaddad B, Rafique A, Jan A, Haack TB, Strom TM, Meitinger T, Ghous T, Ahmad W. Ullah A, et al. Among authors: azeem z. Mol Vis. 2017 Jul 21;23:482-494. eCollection 2017. Mol Vis. 2017. PMID: 28761321 Free PMC article.

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Novel candidate genes and variants underlying autosomal recessive neurodevelopmental disorders with intellectual disability.

Santos-Cortez RLP, Khan V, Khan FS, Mughal ZU, Chakchouk I, Lee K, Rasheed M, Hamza R, Acharya A, Ullah E, Saqib MAN, Abbe I, Ali G, Hassan MJ, Khan S, Azeem Z, Ullah I, Bamshad MJ, Nickerson DA, Schrauwen I, Ahmad W, Ansar M, Leal SM. Santos-Cortez RLP, et al. Among authors: azeem z. Hum Genet. 2018 Sep;137(9):735-752. doi: 10.1007/s00439-018-1928-6. Epub 2018 Aug 22. Hum Genet. 2018. PMID: 30167849 Free PMC article.

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Novel sequence variants in the LIPH and LPAR6 genes underlies autosomal recessive woolly hair/hypotrichosis in consanguineous families.

Ahmad F, Sharif S, Furqan Ubaid M, Shah K, Khan MN, Umair M, Azeem Z, Ahmad W. Ahmad F, et al. Among authors: azeem z. Congenit Anom (Kyoto). 2018 Jan;58(1):24-28. doi: 10.1111/cga.12226. Epub 2017 Jun 12. Congenit Anom (Kyoto). 2018. PMID: 28425126

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DFNB89, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 16q21-q23.2.

Basit S, Lee K, Habib R, Chen L, Umm-e-Kalsoom, Santos-Cortez RL, Azeem Z, Andrade P, Ansar M, Ahmad W, Leal SM. Basit S, et al. Among authors: azeem z. Hum Genet. 2011 Apr;129(4):379-85. doi: 10.1007/s00439-010-0934-0. Epub 2010 Dec 22. Hum Genet. 2011. PMID: 21181198 Free PMC article.

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