Ahmad I - Search Results

1

[No authors listed] [No authors listed] PMID: 38095343

2

Homozygous frameshift variant in desmoglein 2 gene causes biventricular arrhythmogenic right ventricular cardiomyopathy.

Noor Ul Ayan H, Ali PS, Korejo AA, Thiele H, Nürnberg P, Tariq M, Jamal SZ, Erdmann J, Ahmad I. Noor Ul Ayan H, et al. Among authors: ahmad i. Clin Genet. 2023 Aug;104(2):266-268. doi: 10.1111/cge.14321. Epub 2023 Mar 12. Clin Genet. 2023. PMID: 36843528

3

Novel Variants in MPV17, PRX, GJB1, and SACS Cause Charcot-Marie-Tooth and Spastic Ataxia of Charlevoix-Saguenay Type Diseases.

Zaman Q, Khan MA, Sahar K, Rehman G, Khan H, Rehman M, Najumuddin, Ahmad I, Tariq M, Muthaffar OY, Abdulkareem AA, Bibi F, Naseer MI, Faisal MS, Wasif N, Jelani M. Zaman Q, et al. Among authors: ahmad i. Genes (Basel). 2023 Jan 27;14(2):328. doi: 10.3390/genes14020328. Genes (Basel). 2023. PMID: 36833258 Free PMC article.

4

The interleukin-11 receptor variant p.W307R results in craniosynostosis in humans.

Ahmad I, Lokau J, Kespohl B, Malik NA, Baig SM, Hartig R, Behme D, Schwab R, Altmüller J, Jameel M, Mucha S, Thiele H, Tariq M, Nürnberg P, Erdmann J, Garbers C. Ahmad I, et al. Sci Rep. 2023 Aug 18;13(1):13479. doi: 10.1038/s41598-023-39466-y. Sci Rep. 2023. PMID: 37596289 Free PMC article.

5

A novel MAP3K20 mutation causing centronuclear myopathy-6 with fiber-type disproportion in a Pakistani family.

Ahmad I, Khan A, Noor Ul Ayan H, Budde B, Altmüller J, Korejo AA, Nürnberg G, Thiele H, Tariq M, Nürnberg P, Erdmann J. Ahmad I, et al. J Hum Genet. 2023 Feb;68(2):107-109. doi: 10.1038/s10038-022-01085-2. Epub 2022 Oct 11. J Hum Genet. 2023. PMID: 36217027 Free PMC article. No abstract available.

6

A Novel Missense Mutation in TNNI3K Causes Recessively Inherited Cardiac Conduction Disease in a Consanguineous Pakistani Family.

Ramzan S, Tennstedt S, Tariq M, Khan S, Noor Ul Ayan H, Ali A, Munz M, Thiele H, Korejo AA, Mughal AR, Jamal SZ, Nürnberg P, Baig SM, Erdmann J, Ahmad I. Ramzan S, et al. Among authors: ahmad i. Genes (Basel). 2021 Aug 21;12(8):1282. doi: 10.3390/genes12081282. Genes (Basel). 2021. PMID: 34440456 Free PMC article.

7

NGS-driven molecular diagnosis of heterogeneous hereditary neurological disorders reveals novel and known variants in disease-causing genes.

Khan A, Tian S, Tariq M, Khan S, Safeer M, Ullah N, Akbar N, Javed I, Asif M, Ahmad I, Ullah S, Satti HS, Khan R, Naeem M, Ali M, Rendu J, Fauré J, Dieterich K, Latypova X, Baig SM, Malik NA, Zhang F, Khan TN, Liu C. Khan A, et al. Among authors: ahmad i. Mol Genet Genomics. 2022 Nov;297(6):1601-1613. doi: 10.1007/s00438-022-01945-8. Epub 2022 Aug 24. Mol Genet Genomics. 2022. PMID: 36002593

8

Meta-analysis of genome-wide association studies of aggressive and chronic periodontitis identifies two novel risk loci.

Munz M, Richter GM, Loos BG, Jepsen S, Divaris K, Offenbacher S, Teumer A, Holtfreter B, Kocher T, Bruckmann C, Jockel-Schneider Y, Graetz C, Ahmad I, Staufenbiel I, van der Velde N, Uitterlinden AG, de Groot LCPGM, Wellmann J, Berger K, Krone B, Hoffmann P, Laudes M, Lieb W, Franke A, Erdmann J, Dommisch H, Schaefer AS. Munz M, et al. Among authors: ahmad i. Eur J Hum Genet. 2019 Jan;27(1):102-113. doi: 10.1038/s41431-018-0265-5. Epub 2018 Sep 14. Eur J Hum Genet. 2019. PMID: 30218097 Free PMC article.

9

Report of Hermansky-Pudlak Syndrome in Two Families with Novel Variants in HPS3 and HPS4 Genes.

Zaman Q, Sadeeda, Anas M, Rehman G, Khan Q, Iftikhar A, Ahmad M, Owais M, Ahmad I, Muthaffar OY, Abdulkareem AA, Bibi F, Jelani M, Naseer MI. Zaman Q, et al. Among authors: ahmad i, ahmad m. Genes (Basel). 2023 Jan 5;14(1):145. doi: 10.3390/genes14010145. Genes (Basel). 2023. PMID: 36672886 Free PMC article.

10

Efficient detection of nitric oxide a biomarker associated with COVID19 via N, P co-doped C₆₀ fullerene: a computational study.

Khan AA, Ahmad R, Mehmood F, Ahmad I. Khan AA, et al. Among authors: ahmad i. J Mol Model. 2024 May 14;30(6):166. doi: 10.1007/s00894-024-05954-9. J Mol Model. 2024. PMID: 38744728

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