Ahmad W - Search Results

1

Sequence variants in DLX5, HOXD13 and 445 kb-microduplication surrounding BTRC cause split-hand/foot malformation in three different families.

Abdullah, Hussain S, Ji W, Khan H, Mis EK, Mushtaq R, Chodhary M, Raza MH, Jan A, Ullah I, Khokha MK, Lakhani SA, Ahmad W. Abdullah, et al. Among authors: ahmad w. Clin Genet. 2024 Jan;105(1):109-111. doi: 10.1111/cge.14430. Epub 2023 Sep 30. Clin Genet. 2024. PMID: 37776184 No abstract available.

2

Novel mutations in the EXT1 gene in two consanguineous families affected with multiple hereditary exostoses (familial osteochondromatosis).

Faiyaz-Ul-Haque M, Ahmad W, Zaidi SH, Hussain S, Haque S, Ahmad M, Cohn DH, Tsui LC. Faiyaz-Ul-Haque M, et al. Among authors: ahmad w, ahmad m. Clin Genet. 2004 Aug;66(2):144-51. doi: 10.1111/j.1399-0004.2004.00275.x. Clin Genet. 2004. PMID: 15253765

3

Digenic inheritance of an autosomal recessive hypotrichosis in two consanguineous pedigrees.

Basit S, Wali A, Aziz A, Muhammad N, Jelani M, Ahmad W. Basit S, et al. Among authors: ahmad w. Clin Genet. 2011 Mar;79(3):273-81. doi: 10.1111/j.1399-0004.2010.01455.x. Clin Genet. 2011. PMID: 20528890

4

A novel homozygous missense mutation in WNT10B in familial split-hand/foot malformation.

Khan S, Basit S, Zimri FK, Ali N, Ali G, Ansar M, Ahmad W. Khan S, et al. Among authors: ahmad w. Clin Genet. 2012 Jul;82(1):48-55. doi: 10.1111/j.1399-0004.2011.01698.x. Epub 2011 May 27. Clin Genet. 2012. PMID: 21554266

5

Novel homozygous mutations in the genes ARL6 and BBS10 underlying Bardet-Biedl syndrome.

Khan S, Ullah I, Irfanullah, Touseef M, Basit S, Khan MN, Ahmad W. Khan S, et al. Among authors: ahmad w. Gene. 2013 Feb 15;515(1):84-8. doi: 10.1016/j.gene.2012.11.023. Epub 2012 Dec 6. Gene. 2013. PMID: 23219996

6

Mutations in the lipase-H gene causing autosomal recessive hypotrichosis and woolly hair.

Mehmood S, Jan A, Muhammad D, Ahmad F, Mir H, Younus M, Ali G, Ayub M, Ansar M, Ahmad W. Mehmood S, et al. Among authors: ahmad w, ahmad f. Australas J Dermatol. 2015 Aug;56(3):e66-70. doi: 10.1111/ajd.12157. Epub 2014 Mar 13. Australas J Dermatol. 2015. PMID: 24628704

7

In silico analysis of missense mutations in LPAR6 reveals abnormal phospholipid signaling pathway leading to hypotrichosis.

Raza SI, Muhammad D, Jan A, Ali RH, Hassan M, Ahmad W, Rashid S. Raza SI, et al. Among authors: ahmad w. PLoS One. 2014 Aug 13;9(8):e104756. doi: 10.1371/journal.pone.0104756. eCollection 2014. PLoS One. 2014. PMID: 25119526 Free PMC article.

8

A novel deletion mutation in the DSG4 gene underlies autosomal recessive hypotrichosis with variable phenotype in two unrelated consanguineous families.

Ullah A, Raza SI, Ali RH, Naveed AK, Jan A, Rizvi SD, Satti R, Ahmad W. Ullah A, et al. Among authors: ahmad w. Clin Exp Dermatol. 2015 Jan;40(1):78-84. doi: 10.1111/ced.12457. Epub 2014 Sep 23. Clin Exp Dermatol. 2015. PMID: 25251037

9

Genetics of human isolated hereditary hair loss disorders.

Basit S, Khan S, Ahmad W. Basit S, et al. Among authors: ahmad w. Clin Genet. 2015 Sep;88(3):203-12. doi: 10.1111/cge.12531. Epub 2014 Nov 22. Clin Genet. 2015. PMID: 25350920 Review.

10

Challenges and solutions for gene identification in the presence of familial locus heterogeneity.

Rehman AU, Santos-Cortez RL, Drummond MC, Shahzad M, Lee K, Morell RJ, Ansar M, Jan A, Wang X, Aziz A, Riazuddin S, Smith JD, Wang GT, Ahmed ZM, Gul K, Shearer AE, Smith RJ, Shendure J, Bamshad MJ, Nickerson DA; University of Washington Center for Mendelian Genomics; Hinnant J, Khan SN, Fisher RA, Ahmad W, Friderici KH, Riazuddin S, Friedman TB, Wilch ES, Leal SM. Rehman AU, et al. Among authors: ahmad w. Eur J Hum Genet. 2015 Sep;23(9):1207-15. doi: 10.1038/ejhg.2014.266. Epub 2014 Dec 10. Eur J Hum Genet. 2015. PMID: 25491636 Free PMC article.

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