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

Year Number of Results
2002 1
2005 1
2006 2
2007 1
2008 2
2009 2
2010 5
2011 4
2012 3
2013 6
2014 1
2015 3
2016 6
2017 4
2018 1
2019 1
2020 3
2021 3
2022 0
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Search Results

43 results
Results by year
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Page 1
Characterizing the Genetic Architecture of Parkinson's Disease in Latinos.
Loesch DP, Horimoto ARVR, Heilbron K, Sarihan EI, Inca-Martinez M, Mason E, Cornejo-Olivas M, Torres L, Mazzetti P, Cosentino C, Sarapura-Castro E, Rivera-Valdivia A, Medina AC, Dieguez E, Raggio V, Lescano A, Tumas V, Borges V, Ferraz HB, Rieder CR, Schumacher-Schuh A, Santos-Lobato BL, Velez-Pardo C, Jimenez-Del-Rio M, Lopera F, Moreno S, Chana-Cuevas P, Fernandez W, Arboleda G, Arboleda H, Arboleda-Bustos CE, Yearout D, Zabetian CP; 23andMe Research Team, Cannon P, Thornton TA, O'Connor TD, Mata IF; Latin American Research Consortium on the Genetics of Parkinson's Disease (LARGE-PD). Loesch DP, et al. Among authors: yearout d. Ann Neurol. 2021 Sep;90(3):353-365. doi: 10.1002/ana.26153. Epub 2021 Jul 22. Ann Neurol. 2021. PMID: 34227697
Concerns and Needs of Patients With Head and Neck Cancer in the COVID-19 Era.
Yan F, Rauscher E, Hollinger A, Caputo MA, Ready J, Nguyen SA, Fakhry C, Nathan CO, Leonardis C, Yearout D, Day TA, Moore MG. Yan F, et al. Among authors: yearout d. OTO Open. 2021 Sep 30;5(3):2473974X211047794. doi: 10.1177/2473974X211047794. eCollection 2021 Jul-Sep. OTO Open. 2021. PMID: 34616997 Free PMC article.
Genome-Wide Analysis of Copy Number Variation in Latin American Parkinson's Disease Patients.
Sarihan EI, Pérez-Palma E, Niestroj LM, Loesch D, Inca-Martinez M, Horimoto ARVR, Cornejo-Olivas M, Torres L, Mazzetti P, Cosentino C, Sarapura-Castro E, Rivera-Valdivia A, Dieguez E, Raggio V, Lescano A, Tumas V, Borges V, Ferraz HB, Rieder CR, Schumacher-Schuh AF, Santos-Lobato BL, Velez-Pardo C, Jimenez-Del-Rio M, Lopera F, Moreno S, Chana-Cuevas P, Fernandez W, Arboleda G, Arboleda H, Arboleda-Bustos CE, Yearout D, Zabetian CP, Thornton TA, O'Connor TD, Lal D, Mata IF; Latin American Research Consortium on the Genetics of Parkinson's Disease (LARGE-PD)‡. Sarihan EI, et al. Among authors: yearout d. Mov Disord. 2021 Feb;36(2):434-441. doi: 10.1002/mds.28353. Epub 2020 Nov 5. Mov Disord. 2021. PMID: 33150996 Free PMC article.
Human PON1, a biomarker of risk of disease and exposure.
Furlong CE, Suzuki SM, Stevens RC, Marsillach J, Richter RJ, Jarvik GP, Checkoway H, Samii A, Costa LG, Griffith A, Roberts JW, Yearout D, Zabetian CP. Furlong CE, et al. Among authors: yearout d. Chem Biol Interact. 2010 Sep 6;187(1-3):355-61. doi: 10.1016/j.cbi.2010.03.033. Epub 2010 Mar 23. Chem Biol Interact. 2010. PMID: 20338154 Free PMC article. Review.
Not classical homeopathy.
Drosdovech M, Neumann S, Evans D, Blake S, Peck LS, Yearout DR, Ulbrich B, Facinelli J, Delgado R, Hoberg L, Harman J, Sthamann M, Lindsay M, Kwong H, Lampru A, Lamb J, Stagmeier K, Doyle JL, Elliot J, Siemon L. Drosdovech M, et al. Among authors: yearout dr. Can Vet J. 2002 Dec;43(12):908-9; author reply 910-1. Can Vet J. 2002. PMID: 12561681 Free PMC article. No abstract available.
Large-scale exploratory genetic analysis of cognitive impairment in Parkinson's disease.
Mata IF, Johnson CO, Leverenz JB, Weintraub D, Trojanowski JQ, Van Deerlin VM, Ritz B, Rausch R, Factor SA, Wood-Siverio C, Quinn JF, Chung KA, Peterson-Hiller AL, Espay AJ, Revilla FJ, Devoto J, Yearout D, Hu SC, Cholerton BA, Montine TJ, Edwards KL, Zabetian CP. Mata IF, et al. Among authors: yearout d. Neurobiol Aging. 2017 Aug;56:211.e1-211.e7. doi: 10.1016/j.neurobiolaging.2017.04.009. Epub 2017 Apr 20. Neurobiol Aging. 2017. PMID: 28526295 Free PMC article.
Novel compound heterozygous FBXO7 mutations in a family with early onset Parkinson's disease.
Lorenzo-Betancor O, Lin YH, Samii A, Jayadev S, Kim HM, Longfellow K, Distad BJ, Yearout D, Mata IF, Zabetian CP. Lorenzo-Betancor O, et al. Among authors: yearout d. Parkinsonism Relat Disord. 2020 Nov;80:142-147. doi: 10.1016/j.parkreldis.2020.09.035. Epub 2020 Sep 22. Parkinsonism Relat Disord. 2020. PMID: 33002721 Free PMC article.
The RAB39B p.G192R mutation causes X-linked dominant Parkinson's disease.
Mata IF, Jang Y, Kim CH, Hanna DS, Dorschner MO, Samii A, Agarwal P, Roberts JW, Klepitskaya O, Shprecher DR, Chung KA, Factor SA, Espay AJ, Revilla FJ, Higgins DS, Litvan I, Leverenz JB, Yearout D, Inca-Martinez M, Martinez E, Thompson TR, Cholerton BA, Hu SC, Edwards KL, Kim KS, Zabetian CP. Mata IF, et al. Among authors: yearout d. Mol Neurodegener. 2015 Sep 24;10:50. doi: 10.1186/s13024-015-0045-4. Mol Neurodegener. 2015. PMID: 26399558 Free PMC article.
43 results