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

Year Number of Results
1984 3
1985 2
1986 3
1987 4
1988 3
1989 1
1991 2
1993 1
1995 1
1996 1
1997 2
1999 1
2000 2
2001 4
2002 4
2003 3
2004 5
2005 8
2006 10
2007 8
2008 13
2009 19
2010 13
2011 17
2012 21
2013 13
2014 15
2015 19
2016 21
2017 41
2018 30
2019 26
2020 43
2021 49
2022 39
2023 46
2024 42
2025 57
2026 12

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Search Results

529 results

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Page 1
Racism in healthcare: a scoping review.
Hamed S, Bradby H, Ahlberg BM, Thapar-Björkert S. Hamed S, et al. BMC Public Health. 2022 May 16;22(1):988. doi: 10.1186/s12889-022-13122-y. BMC Public Health. 2022. PMID: 35578322 Free PMC article.
High-Dimensional Single-Cell Analysis Identifies Organ-Specific Signatures and Conserved NK Cell Subsets in Humans and Mice.
Crinier A, Milpied P, Escalière B, Piperoglou C, Galluso J, Balsamo A, Spinelli L, Cervera-Marzal I, Ebbo M, Girard-Madoux M, Jaeger S, Bollon E, Hamed S, Hardwigsen J, Ugolini S, Vély F, Narni-Mancinelli E, Vivier E. Crinier A, et al. Among authors: hamed s. Immunity. 2018 Nov 20;49(5):971-986.e5. doi: 10.1016/j.immuni.2018.09.009. Epub 2018 Nov 6. Immunity. 2018. PMID: 30413361 Free PMC article.
Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes.
Cortese A, Zhu Y, Rebelo AP, Negri S, Courel S, Abreu L, Bacon CJ, Bai Y, Bis-Brewer DM, Bugiardini E, Buglo E, Danzi MC, Feely SME, Athanasiou-Fragkouli A, Haridy NA; Inherited Neuropathy Consortium; Isasi R, Khan A, Laurà M, Magri S, Pipis M, Pisciotta C, Powell E, Rossor AM, Saveri P, Sowden JE, Tozza S, Vandrovcova J, Dallman J, Grignani E, Marchioni E, Scherer SS, Tang B, Lin Z, Al-Ajmi A, Schüle R, Synofzik M, Maisonobe T, Stojkovic T, Auer-Grumbach M, Abdelhamed MA, Hamed SA, Zhang R, Manganelli F, Santoro L, Taroni F, Pareyson D, Houlden H, Herrmann DN, Reilly MM, Shy ME, Zhai RG, Zuchner S. Cortese A, et al. Among authors: hamed sa. Nat Genet. 2020 May;52(5):473-481. doi: 10.1038/s41588-020-0615-4. Epub 2020 May 4. Nat Genet. 2020. PMID: 32367058 Free PMC article.
Genotype and phenotype spectrum of Charcot-Marie-Tooth disease due to mutations in SORD.
Cortese A, Dohrn MF, Curro R, Negri S, Lassuthova P, Pisciotta C, Tozza S, Al-Ajmi A, Feng C, Tomaselli PJ, Fernandez-Eulate G, Haddad S, Laurà M, Rossor AM, Vegezzi E, Facchini S, Sleigh JN, Rebelo A, Beijer D, Raposo J, Saporta M, Lauerova B, Pernice HF, Achenbach P, Schöne U, Alon T, Deschauer M, Cordts I, Obermaier CD, Winter N, Creigh PD, Sowden JE, Rehbein T, Magri S, Bertini A, Saveri P, Ripellino P, Huang J, Nadaj-Pakleza A, Ross A, Holt JKL, Brennan KM, Sukenik-Halevy R, Bizaoui V, Parman Y, Battaloglu E, Cakar A, Alrohaif H, Hammans S, Kumar KR, Kennerson ML, Kayserili H, Amado DA, Hahn K, Valentino P, Cavalcanti F, Gaetano C, Taroni F, Braathen GJ, Houlden H, Stojkovic T, Peric S, Bolino A, Previtali SC, Yi-Chung L, Başak AN, Hamed SA, Rojas-Garcia R, Claeys KG, Marques W, Sevilla T, Schlotter-Weigel B, Manganelli F, Zhang R, Herrmann DN, Scherer SS, Seeman P, Pareyson D, Reilly MM, Shy ME, Züchner S. Cortese A, et al. Among authors: hamed sa. Brain. 2025 Oct 3;148(10):3737-3747. doi: 10.1093/brain/awaf021. Brain. 2025. PMID: 39938083 Free PMC article.
US Food and Drug Administration Approval Summary: Elacestrant for Estrogen Receptor-Positive, Human Epidermal Growth Factor Receptor 2-Negative, ESR1-Mutated Advanced or Metastatic Breast Cancer.
Shah M, Lingam H, Gao X, Gittleman H, Fiero MH, Krol D, Biel N, Ricks TK, Fu W, Hamed S, Li F, Sun JJ, Fan J, Schuck R, Grimstein M, Tang L, Kalavar S, Abukhdeir A, Pathak A, Ghosh S, Bulatao I, Tilley A, Pierce WF, Mixter BD, Tang S, Pazdur R, Kluetz P, Amiri-Kordestani L. Shah M, et al. Among authors: hamed s. J Clin Oncol. 2024 Apr 1;42(10):1193-1201. doi: 10.1200/JCO.23.02112. Epub 2024 Feb 21. J Clin Oncol. 2024. PMID: 38381994 Free PMC article. Clinical Trial.
Biallelic variants in ARHGAP19 cause a progressive inherited motor-predominant neuropathy.
Dominik N, Efthymiou S, Record CJ, Miao X, Lin RQ, Parmar JM, Scardamaglia A, Maroofian R, Lowe SA, Aughey GN, Wilson AD, Curro R, Schnekenberg RP, Alavi S, Leclaire L, He Y, Zhelcheska K, Bellaïche Y, Gaugué I, Skorupinska M, Van de Vondel L, Da'as SI, Turchetti V, Güngör S, Monahan GV, Ghayoor Karimiani E, Jamshidi Y, Lamont PJ, Armirola-Ricaurte C, Topaloglu H, Jordanova A, Zaman M, Banu SH, Marques W, Tomaselli PJ, Aynekin B, Cansu A, Per H, Güleç A, Alvi JR, Sultan T, Khan A, Zifarelli G, Ibrahim S, Mancini GMS, Motazacker MM, Brusse E, Lupo V, Sevilla T, Başak AN, Tekgul S, Palvadeau RJ, Baets J, Parman Y, Çakar A, Horvath R, Haack TB, Stahl JH, Grundmann-Hauser K, Park J, Zuchner S, Laing NG, Wilson LA, Rossor AM, Polke J, Figueiredo FB, Pessoa A, Kok F, Coimbra-Neto AR, Franca MC Jr, Ravenscroft G, Hamed SA, Chung WK, Pittman AM, Osborn DP, Hanna M, Cortese A, Reilly MM, Jepson JE, Lamarche-Vane N, Houlden H. Dominik N, et al. Among authors: hamed sa. J Clin Invest. 2025 Oct 14;135(23):e184474. doi: 10.1172/JCI184474. eCollection 2025 Dec 1. J Clin Invest. 2025. PMID: 41086021 Free PMC article.
529 results