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Year Number of Results
2000 1
2001 2
2002 1
2003 2
2005 2
2008 1
2009 1
2012 1
2015 3
2016 1
2017 2
2018 8
2019 6
2020 13
2021 13
2022 12
2023 8
2024 12
2025 20

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104 results

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Page 1
Single-cell multiregion dissection of Alzheimer's disease.
Mathys H, Boix CA, Akay LA, Xia Z, Davila-Velderrain J, Ng AP, Jiang X, Abdelhady G, Galani K, Mantero J, Band N, James BT, Babu S, Galiana-Melendez F, Louderback K, Prokopenko D, Tanzi RE, Bennett DA, Tsai LH, Kellis M. Mathys H, et al. Among authors: prokopenko d. Nature. 2024 Aug;632(8026):858-868. doi: 10.1038/s41586-024-07606-7. Epub 2024 Jul 24. Nature. 2024. PMID: 39048816 Free PMC article.
Blood-based Transcriptomic and Proteomic Biomarkers of Emphysema.
Suryadevara R, Gregory A, Lu R, Xu Z, Masoomi A, Lutz SM, Berman S, Yun JH, Saferali A, Ryu MH, Moll M, Sin DD, Hersh CP, Silverman EK, Dy J, Pratte KA, Bowler RP, Castaldi PJ, Boueiz A; COPDGene investigators. Suryadevara R, et al. Am J Respir Crit Care Med. 2024 Feb 1;209(3):273-287. doi: 10.1164/rccm.202301-0067OC. Am J Respir Crit Care Med. 2024. PMID: 37917913 Free PMC article.
Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations.
Sakornsakolpat P, Prokopenko D, Lamontagne M, Reeve NF, Guyatt AL, Jackson VE, Shrine N, Qiao D, Bartz TM, Kim DK, Lee MK, Latourelle JC, Li X, Morrow JD, Obeidat M, Wyss AB, Bakke P, Barr RG, Beaty TH, Belinsky SA, Brusselle GG, Crapo JD, de Jong K, DeMeo DL, Fingerlin TE, Gharib SA, Gulsvik A, Hall IP, Hokanson JE, Kim WJ, Lomas DA, London SJ, Meyers DA, O'Connor GT, Rennard SI, Schwartz DA, Sliwinski P, Sparrow D, Strachan DP, Tal-Singer R, Tesfaigzi Y, Vestbo J, Vonk JM, Yim JJ, Zhou X, Bossé Y, Manichaikul A, Lahousse L, Silverman EK, Boezen HM, Wain LV, Tobin MD, Hobbs BD, Cho MH; SpiroMeta Consortium; International COPD Genetics Consortium. Sakornsakolpat P, et al. Among authors: prokopenko d. Nat Genet. 2019 Mar;51(3):494-505. doi: 10.1038/s41588-018-0342-2. Epub 2019 Feb 25. Nat Genet. 2019. PMID: 30804561 Free PMC article.
New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries.
Shrine N, Guyatt AL, Erzurumluoglu AM, Jackson VE, Hobbs BD, Melbourne CA, Batini C, Fawcett KA, Song K, Sakornsakolpat P, Li X, Boxall R, Reeve NF, Obeidat M, Zhao JH, Wielscher M, Weiss S, Kentistou KA, Cook JP, Sun BB, Zhou J, Hui J, Karrasch S, Imboden M, Harris SE, Marten J, Enroth S, Kerr SM, Surakka I, Vitart V, Lehtimäki T, Allen RJ, Bakke PS, Beaty TH, Bleecker ER, Bossé Y, Brandsma CA, Chen Z, Crapo JD, Danesh J, DeMeo DL, Dudbridge F, Ewert R, Gieger C, Gulsvik A, Hansell AL, Hao K, Hoffman JD, Hokanson JE, Homuth G, Joshi PK, Joubert P, Langenberg C, Li X, Li L, Lin K, Lind L, Locantore N, Luan J, Mahajan A, Maranville JC, Murray A, Nickle DC, Packer R, Parker MM, Paynton ML, Porteous DJ, Prokopenko D, Qiao D, Rawal R, Runz H, Sayers I, Sin DD, Smith BH, Soler Artigas M, Sparrow D, Tal-Singer R, Timmers PRHJ, Van den Berge M, Whittaker JC, Woodruff PG, Yerges-Armstrong LM, Troyanskaya OG, Raitakari OT, Kähönen M, Polašek O, Gyllensten U, Rudan I, Deary IJ, Probst-Hensch NM, Schulz H, James AL, Wilson JF, Stubbe B, Zeggini E, Jarvelin MR, Wareham N, Silverman EK, Hayward C, Morris AP, Butterworth AS, Scott RA, Walters RG, Meyers DA, Cho MH, Strachan DP, Hall IP, … See abstract for full author list ➔ Shrine N, et al. Among authors: prokopenko d. Nat Genet. 2019 Mar;51(3):481-493. doi: 10.1038/s41588-018-0321-7. Epub 2019 Feb 25. Nat Genet. 2019. PMID: 30804560 Free PMC article.
Longitudinal Changes in Airway Mucus Plugs and FEV1 in COPD.
Mettler SK, Nardelli P, Campo MI, San José Estépar R, Manapragada PP, Abozeed M, Aziz MU, Zahid M, Grumley S, Nath HP, Yen A, Sonavane S, Clarenbach CF, Wang W, Pistenmaa CL, Washko GR, Estépar RSJ, Cho MH, Diaz AA; COPDGene Investigators; COPDGene site investigators. Mettler SK, et al. N Engl J Med. 2025 May 15;392(19):1973-1975. doi: 10.1056/NEJMc2502456. N Engl J Med. 2025. PMID: 40367384 Free PMC article. No abstract available.
The gain-of-function TREM2-T96K mutation increases risk for Alzheimer's disease by impairing microglial function.
Pilat DJ, Le H, Prokopenko D, Lin CJ, Eimer WA, Quinti L, Gavrilles EP, Garcia SN, Heitman SN; Alzheimer’s Disease Neuroimaging Initiative (ADNI); McGinty D, Cetinbas M, Sadreyev RI, Tanzi RE, Griciuc A. Pilat DJ, et al. Among authors: prokopenko d. Neuron. 2025 Oct 17:S0896-6273(25)00745-7. doi: 10.1016/j.neuron.2025.09.032. Online ahead of print. Neuron. 2025. PMID: 41109213 Free article.
104 results