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

Year Number of Results
1976 1
2009 3
2010 2
2011 1
2012 6
2013 3
2014 7
2015 7
2016 10
2017 6
2018 5
2019 3
2020 7
2021 7
2022 3
2023 0
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60 results
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Page 1
PIGF deficiency causes a phenotype overlapping with DOORS syndrome.
Salian S, Benkerroum H, Nguyen TTM, Nampoothiri S, Kinoshita T, Félix TM, Stewart F, Sisodiya SM, Murakami Y, Campeau PM. Salian S, et al. Hum Genet. 2021 Jun;140(6):879-884. doi: 10.1007/s00439-020-02251-2. Epub 2021 Jan 2. Hum Genet. 2021. PMID: 33386993
MED27, SLC6A7, and MPPE1 Variants in a Complex Neurodevelopmental Disorder with Severe Dystonia.
Reid KM, Spaull R, Salian S, Barwick K, Meyer E, Zhen J, Hirata H, Sheipouri D, Benkerroum H, Gorman KM, Papandreou A, Simpson MA, Hirano Y, Farabella I, Topf M, Grozeva D, Carss K, Smith M, Pall H, Lunt P, De Gressi S, Kamsteeg EJ, Haack TB, Carr L, Guerreiro R, Bras J, Maher ER, Scott RH, Vandenberg RJ, Raymond FL, Chong WK, Sudhakar S, Mankad K, Reith ME, Campeau PM, Harvey RJ, Kurian MA. Reid KM, et al. Among authors: salian s. Mov Disord. 2022 Oct;37(10):2139-2146. doi: 10.1002/mds.29147. Epub 2022 Jul 25. Mov Disord. 2022. PMID: 35876425 Free PMC article.
Familial 7q11.23 duplication with variable phenotype.
Patil SJ, Salian S, Bhat V, Girisha KM, Shrivastava Y, Vs K, Sapare A. Patil SJ, et al. Among authors: salian s. Am J Med Genet A. 2015 Nov;167A(11):2727-30. doi: 10.1002/ajmg.a.37226. Epub 2015 Jun 24. Am J Med Genet A. 2015. PMID: 26109321
Age-Net: An MRI-Based Iterative Framework for Brain Biological Age Estimation.
Armanious K, Abdulatif S, Shi W, Salian S, Kustner T, Weiskopf D, Hepp T, Gatidis S, Yang B. Armanious K, et al. Among authors: salian s. IEEE Trans Med Imaging. 2021 Jul;40(7):1778-1791. doi: 10.1109/TMI.2021.3066857. Epub 2021 Jun 30. IEEE Trans Med Imaging. 2021. PMID: 33729932
Short-Term Hypothermic Holding of Mouse Immature Testicular Tissue Does Not Alter the Expression of DNA Methyltransferases and Global DNA Methylation Level, Post-Organotypic Culture.
Pandya RK, Uppangala S, Salian SR, Gupta S, Kalthur G, Schlatt S, Adiga SK. Pandya RK, et al. Among authors: salian sr. Front Endocrinol (Lausanne). 2022 Mar 23;13:854297. doi: 10.3389/fendo.2022.854297. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 35399926 Free PMC article.
Expanding the Phenotypic Spectrum of GPI Anchoring Deficiency Due to Biallelic Variants in GPAA1.
Castle AMR, Salian S, Bassan H, Sofrin-Drucker E, Cusmai R, Herman KC, Heron D, Keren B, Johnstone DL, Mears W, Morlot S, Nguyen TTM, Rock R, Stolerman E, Russo J, Burns WB, Jones JR, Serpieri V, Wallaschek H, Zanni G, Dyment DA, Campeau PM. Castle AMR, et al. Among authors: salian s. Neurol Genet. 2021 Oct 21;7(6):e631. doi: 10.1212/NXG.0000000000000631. eCollection 2021 Dec. Neurol Genet. 2021. PMID: 34703884 Free PMC article.
60 results