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

Year Number of Results
1994 1
1997 1
1998 1
1999 4
2000 2
2001 1
2002 3
2003 4
2004 2
2006 3
2007 3
2008 5
2009 5
2010 4
2011 3
2012 4
2013 3
2014 8
2015 7
2016 5
2017 7
2018 8
2019 11
2020 14
2021 7
2022 8
2023 5
2024 1

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116 results

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Page 1
A Winning New Combination? Toward Clinical Application in Oncology.
Maqsood Q, Sumrin A, Iqbal M, Hussain N, Mahnoor M, Zafar Saleem M, Perveen R. Maqsood Q, et al. Among authors: perveen r. Cancer Control. 2023 Jan-Dec;30:10732748231175240. doi: 10.1177/10732748231175240. Cancer Control. 2023. PMID: 37166227 Free PMC article. Review.
Biallelic TMEM260 variants cause truncus arteriosus, with or without renal defects.
Pagnamenta AT, Jackson A, Perveen R, Beaman G, Petts G, Gupta A, Hyder Z, Chung BH, Kan AS, Cheung KW, Kerstjens-Frederikse WS, Abbott KM; Genomics England Research Consortium; Elpeleg O, Taylor JC, Banka S, Ta-Shma A. Pagnamenta AT, et al. Among authors: perveen r. Clin Genet. 2022 Jan;101(1):127-133. doi: 10.1111/cge.14071. Epub 2021 Oct 11. Clin Genet. 2022. PMID: 34612517
Factors Responsible for Prehospital Delay in Patients with Acute Coronary Syndrome in Bangladesh.
Khaled MFI, Adhikary DK, Islam MM, Alam MM, Rahman MW, Chowdhury MT, Perveen R, Ahmed S, Ashab E, Shakil SS, Ansari S, Das BC, Mohammad N, Ehsan MA, Jamil ABM, Mostafa Z, Abedin Z, Banerjee SK. Khaled MFI, et al. Among authors: perveen r. Medicina (Kaunas). 2022 Sep 2;58(9):1206. doi: 10.3390/medicina58091206. Medicina (Kaunas). 2022. PMID: 36143884 Free PMC article.
HSPA8 Single-Nucleotide Polymorphism Is Associated with Serum HSC70 Concentration and Carotid Artery Atherosclerosis in Nonalcoholic Fatty Liver Disease.
Zhao W, Mori H, Tomiga Y, Tanaka K, Perveen R, Mine K, Inadomi C, Yoshioka W, Kubotsu Y, Isoda H, Kuwashiro T, Oeda S, Akiyama T, Zhao Y, Ozaki I, Nagafuchi S, Kawaguchi A, Aishima S, Anzai K, Takahashi H. Zhao W, et al. Among authors: perveen r. Genes (Basel). 2022 Jul 16;13(7):1265. doi: 10.3390/genes13071265. Genes (Basel). 2022. PMID: 35886046 Free PMC article.
Further delineation of the KAT6B molecular and phenotypic spectrum.
Gannon T, Perveen R, Schlecht H, Ramsden S, Anderson B, Kerr B, Day R, Banka S, Suri M, Berland S, Gabbett M, Ma A, Lyonnet S, Cormier-Daire V, Yilmaz R, Borck G, Wieczorek D, Anderlid BM, Smithson S, Vogt J, Moore-Barton H, Simsek-Kiper PO, Maystadt I, Destrée A, Bucher J, Angle B, Mohammed S, Wakeling E, Price S, Singer A, Sznajer Y, Toutain A, Haye D, Newbury-Ecob R, Fradin M, McGaughran J, Tuysuz B, Tein M, Bouman K, Dabir T, Van den Ende J, Luk HM, Pilz DT, Eason J, Davies S, Reardon W, Garavelli L, Zuffardi O, Devriendt K, Armstrong R, Johnson D, Doco-Fenzy M, Bijlsma E, Unger S, Veenstra-Knol HE, Kohlhase J, Lo IF; DDD study; Smith J, Clayton-Smith J. Gannon T, et al. Among authors: perveen r. Eur J Hum Genet. 2015 Sep;23(9):1165-70. doi: 10.1038/ejhg.2014.248. Epub 2014 Nov 26. Eur J Hum Genet. 2015. PMID: 25424711 Free PMC article.
116 results