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

Year Number of Results
1990 5
1991 29
1992 12
1993 7
1994 6
1995 7
1996 14
1997 13
1998 17
1999 3
2000 4
2001 5
2002 1
2003 1
2004 2
2005 1
2008 5
2009 4
2015 1
2019 1
2020 6
2021 10
2022 7
2023 4
2024 4

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161 results

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Page 1
Mutation in the alpha-synuclein gene identified in families with Parkinson's disease.
Polymeropoulos MH, Lavedan C, Leroy E, Ide SE, Dehejia A, Dutra A, Pike B, Root H, Rubenstein J, Boyer R, Stenroos ES, Chandrasekharappa S, Athanassiadou A, Papapetropoulos T, Johnson WG, Lazzarini AM, Duvoisin RC, Di Iorio G, Golbe LI, Nussbaum RL. Polymeropoulos MH, et al. Science. 1997 Jun 27;276(5321):2045-7. doi: 10.1126/science.276.5321.2045. Science. 1997. PMID: 9197268
Genetics of Parkinson's disease.
Polymeropoulos MH. Polymeropoulos MH. Ann N Y Acad Sci. 2000;920:28-32. doi: 10.1111/j.1749-6632.2000.tb06901.x. Ann N Y Acad Sci. 2000. PMID: 11193165 Review.
Genetics of Parkinson's disease.
Nussbaum RL, Polymeropoulos MH. Nussbaum RL, et al. Among authors: polymeropoulos mh. Hum Mol Genet. 1997;6(10):1687-91. doi: 10.1093/hmg/6.10.1687. Hum Mol Genet. 1997. PMID: 9300660 Review.
A gene map of the human genome.
Schuler GD, Boguski MS, Stewart EA, Stein LD, Gyapay G, Rice K, White RE, Rodriguez-Tomé P, Aggarwal A, Bajorek E, Bentolila S, Birren BB, Butler A, Castle AB, Chiannilkulchai N, Chu A, Clee C, Cowles S, Day PJ, Dibling T, Drouot N, Dunham I, Duprat S, East C, Edwards C, Fan JB, Fang N, Fizames C, Garrett C, Green L, Hadley D, Harris M, Harrison P, Brady S, Hicks A, Holloway E, Hui L, Hussain S, Louis-Dit-Sully C, Ma J, MacGilvery A, Mader C, Maratukulam A, Matise TC, McKusick KB, Morissette J, Mungall A, Muselet D, Nusbaum HC, Page DC, Peck A, Perkins S, Piercy M, Qin F, Quackenbush J, Ranby S, Reif T, Rozen S, Sanders C, She X, Silva J, Slonim DK, Soderlund C, Sun WL, Tabar P, Thangarajah T, Vega-Czarny N, Vollrath D, Voyticky S, Wilmer T, Wu X, Adams MD, Auffray C, Walter NA, Brandon R, Dehejia A, Goodfellow PN, Houlgatte R, Hudson JR Jr, Ide SE, Iorio KR, Lee WY, Seki N, Nagase T, Ishikawa K, Nomura N, Phillips C, Polymeropoulos MH, Sandusky M, Schmitt K, Berry R, Swanson K, Torres R, Venter JC, Sikela JM, Beckmann JS, Weissenbach J, Myers RM, Cox DR, James MR, Bentley D, Deloukas P, Lander ES, Hudson TJ. Schuler GD, et al. Among authors: polymeropoulos mh. Science. 1996 Oct 25;274(5287):540-6. Science. 1996. PMID: 8849440 Review.
Enrichment of Motilin Receptor Loss-of-Function Variants in Gastroparesis.
Smieszek SP, Carlin JL, Xiao C, Birznieks G, Polymeropoulos CM, Polymeropoulos MH. Smieszek SP, et al. Among authors: polymeropoulos mh. Clin Transl Gastroenterol. 2022 Apr 1;13(4):e00474. doi: 10.14309/ctg.0000000000000474. Clin Transl Gastroenterol. 2022. PMID: 35297797 Free PMC article.
Elevated plasma levels of CXCL16 in severe COVID-19 patients.
Smieszek SP, Polymeropoulos VM, Polymeropoulos CM, Przychodzen BP, Birznieks G, Polymeropoulos MH. Smieszek SP, et al. Among authors: polymeropoulos mh. Cytokine. 2022 Apr;152:155810. doi: 10.1016/j.cyto.2022.155810. Epub 2022 Jan 31. Cytokine. 2022. PMID: 35121493 Free PMC article. Clinical Trial.
Loss-of-function mutations in IFNAR2 in COVID-19 severe infection susceptibility.
Smieszek SP, Polymeropoulos VM, Xiao C, Polymeropoulos CM, Polymeropoulos MH. Smieszek SP, et al. Among authors: polymeropoulos mh. J Glob Antimicrob Resist. 2021 Sep;26:239-240. doi: 10.1016/j.jgar.2021.06.005. Epub 2021 Jul 15. J Glob Antimicrob Resist. 2021. PMID: 34273592 Free PMC article.
161 results