Naveed Wasif - Search Results

Year	Number of Results
2007	1
2008	2
2009	1
2010	4
2011	2
2012	2
2013	2
2014	1
2015	1
2019	5
2020	3
2021	2
2022	2
2023	7
2024	2

1

Molecular insight into CREBBP and TANGO2 variants causing intellectual disability.

Hussain SI, Muhammad N, Khan N, Khan M, Fardous F, Tahir R, Yasin M, Khan SA, Saleha S, Muhammad N, Wasif N, Khan S. Hussain SI, et al. Among authors: wasif n. J Gene Med. 2024 Jan;26(1):e3591. doi: 10.1002/jgm.3591. Epub 2023 Sep 18. J Gene Med. 2024. PMID: 37721116

2

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: wasif n. Genes (Basel). 2023 Jan 27;14(2):328. doi: 10.3390/genes14020328. Genes (Basel). 2023. PMID: 36833258 Free PMC article.

3

Variants in KIAA0825 underlie autosomal recessive postaxial polydactyly.

Ullah I, Kakar N, Schrauwen I, Hussain S, Chakchouk I, Liaqat K, Acharya A, Wasif N, Santos-Cortez RLP, Khan S, Aziz A, Lee K, Couthouis J, Horn D, Kragesteen BK, Spielmann M, Thiele H, Nickerson DA, Bamshad MJ, Gitler AD, Ahmad J, Ansar M, Borck G, Ahmad W, Leal SM. Ullah I, et al. Among authors: wasif n. Hum Genet. 2019 Jun;138(6):593-600. doi: 10.1007/s00439-019-02000-0. Epub 2019 Apr 13. Hum Genet. 2019. PMID: 30982135 Free PMC article.

4

A novel frameshift variant in UBA2 causing split-hand/foot malformations in a Pakistani family.

Parveen A, Tariq M, Khan SA, Kakar N, Arif A, Wasif N. Parveen A, et al. Among authors: wasif n. Hum Genome Var. 2023 May 23;10(1):16. doi: 10.1038/s41439-023-00242-z. Hum Genome Var. 2023. PMID: 37221169 Free PMC article.

5

A novel homozygous splice site variant in CERS3 causes autosomal recessive congenital ichthyosis.

Jan H, Wasif N, Naqvi SK, Ullah I, Ahmad W. Jan H, et al. Among authors: wasif n. Congenit Anom (Kyoto). 2023 Jul;63(4):127-128. doi: 10.1111/cga.12518. Epub 2023 May 1. Congenit Anom (Kyoto). 2023. PMID: 37128664 No abstract available.

6

The Expansion of the Spectrum in Stuttering Disorders to a Novel ARMC Gene Family (ARMC3).

Rehman AU, Hamid M, Khan SA, Eisa M, Ullah W, Rehman ZU, Khan MA, Basit S, Muhammad N, Khan S, Wasif N. Rehman AU, et al. Among authors: wasif n. Genes (Basel). 2022 Dec 6;13(12):2299. doi: 10.3390/genes13122299. Genes (Basel). 2022. PMID: 36553564 Free PMC article.

7

The First Report of a Missense Variant in RFX2 Causing Non-Syndromic Tooth Agenesis in a Consanguineous Pakistani Family.

Khan SA, Khan S, Muhammad N, Rehman ZU, Khan MA, Nasir A, Kalsoom UE, Khan AK, Khan H, Wasif N. Khan SA, et al. Among authors: wasif n. Front Genet. 2022 Jan 25;12:782653. doi: 10.3389/fgene.2021.782653. eCollection 2021. Front Genet. 2022. PMID: 35145545 Free PMC article.

8

Structural and functional implications of SLC13A3 and SLC9A6 mutations: an in silico approach to understanding intellectual disability.

Hussain SI, Muhammad N, Shah SUD, Fardous F, Khan SA, Khan N, Rehman AU, Siddique M, Wasan SA, Niaz R, Ullah H, Khan N, Muhammad N, Mirza MU, Wasif N, Khan S. Hussain SI, et al. Among authors: wasif n. BMC Neurol. 2023 Oct 4;23(1):353. doi: 10.1186/s12883-023-03397-y. BMC Neurol. 2023. PMID: 37794328 Free PMC article.

9

Whole Exome Sequencing Confirms Molecular Diagnostics of Three Pakhtun Families With Autosomal Recessive Epidermolysis Bullosa.

Fozia F, Nazli R, Bibi N, Khan SA, Muhammad N, Shakeeb N, Khan S, Jelani M, Wasif N. Fozia F, et al. Among authors: wasif n. Front Pediatr. 2021 Aug 3;9:727288. doi: 10.3389/fped.2021.727288. eCollection 2021. Front Pediatr. 2021. PMID: 34414147 Free PMC article.

10

Autosomal recessive variants c.953A>C and c.97-1G>C in NSUN2 causing intellectual disability: a molecular dynamics simulation study of loss-of-function mechanisms.

Muhammad N, Hussain SI, Rehman ZU, Khan SA, Jan S, Khan N, Muzammal M, Abbasi SW, Kakar N, Rehman ZU, Khan MA, Mirza MU, Muhammad N, Khan S, Wasif N. Muhammad N, et al. Among authors: wasif n. Front Neurol. 2023 May 25;14:1168307. doi: 10.3389/fneur.2023.1168307. eCollection 2023. Front Neurol. 2023. PMID: 37305761 Free PMC article.

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