Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2006 1
2008 1
2009 3
2010 2
2012 3
2013 2
2015 2
2017 1
2018 3
2019 4
2020 5
2021 5
2022 3
2023 4
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

35 results

Results by year

Filters applied: . Clear all
Page 1
A TMC8 splice variant causes epidermodysplasia verruciformis in a Pakistani family.
Xiong X, Uddin SA, Munir S, Cesarato N, Thiele H, Hassan N, Kumar S, Rehman FU, Naeem M, Wali A, Basit S, Basmanav FB, Ayub M, Betz RC. Xiong X, et al. Among authors: wali a. Clin Exp Dermatol. 2023 Mar 22;48(4):434-437. doi: 10.1093/ced/llad042. Clin Exp Dermatol. 2023. PMID: 36750324 No abstract available.
Contracting out health services in fragile states.
Palmer N, Strong L, Wali A, Sondorp E. Palmer N, et al. Among authors: wali a. BMJ. 2006 Mar 25;332(7543):718-21. doi: 10.1136/bmj.332.7543.718. BMJ. 2006. PMID: 16565130 Free PMC article. Review.
ADAMTS1, MPDZ, MVD, and SEZ6: candidate genes for autosomal recessive nonsyndromic hearing impairment.
Bharadwaj T, Schrauwen I, Rehman S, Liaqat K, Acharya A, Giese APJ, Nouel-Saied LM, Nasir A, Everard JL, Pollock LM, Zhu S, Bamshad MJ, Nickerson DA, Ali RH, Ullah A, Wali A, Ali G, Santos-Cortez RLP, Ahmed ZM, McDermott BM Jr, Ansar M, Riazuddin S, Ahmad W, Leal SM. Bharadwaj T, et al. Among authors: wali a. Eur J Hum Genet. 2022 Jan;30(1):22-33. doi: 10.1038/s41431-021-00913-x. Epub 2021 Jun 16. Eur J Hum Genet. 2022. PMID: 34135477 Free PMC article.
A Recurrent Nonsense Mutation in NECTIN4 Underlying Ectodermal Dysplasia-Syndactyly Syndrome with a Novel Phenotype in a Consanguineous Kashmiri Family.
Ali G, Sadia S, Ain-Ul-Batool S, Azeem Z, Awan NB, Kazmi SAR, Ur-Rehman Z, Anjum Z, Ur-Rehman F, Wali A, Khan K, Zaman N, Ayub M, Sajid M, Hassan N. Ali G, et al. Among authors: wali a. Genet Res (Camb). 2023 Oct 4;2023:9999660. doi: 10.1155/2023/9999660. eCollection 2023. Genet Res (Camb). 2023. PMID: 37829154 Free PMC article.
35 results