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

Year Number of Results
1987 1
1988 1
1996 1
2001 1
2005 1
2008 1
2009 5
2010 3
2011 2
2012 6
2013 5
2014 4
2015 5
2016 3
2017 1
2018 2
2019 5
2020 3
2021 3
2022 2
2023 4
2024 2

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52 results

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Page 1
A mutation update on the LDS-associated genes TGFB2/3 and SMAD2/3.
Schepers D, Tortora G, Morisaki H, MacCarrick G, Lindsay M, Liang D, Mehta SG, Hague J, Verhagen J, van de Laar I, Wessels M, Detisch Y, van Haelst M, Baas A, Lichtenbelt K, Braun K, van der Linde D, Roos-Hesselink J, McGillivray G, Meester J, Maystadt I, Coucke P, El-Khoury E, Parkash S, Diness B, Risom L, Scurr I, Hilhorst-Hofstee Y, Morisaki T, Richer J, Désir J, Kempers M, Rideout AL, Horne G, Bennett C, Rahikkala E, Vandeweyer G, Alaerts M, Verstraeten A, Dietz H, Van Laer L, Loeys B. Schepers D, et al. Among authors: rideout al. Hum Mutat. 2018 May;39(5):621-634. doi: 10.1002/humu.23407. Epub 2018 Mar 6. Hum Mutat. 2018. PMID: 29392890 Free PMC article.
Genetics and Precision Medicine: Heritable Thoracic Aortic Disease.
Demo E, Rigelsky C, Rideout AL, Graf M, Pariani M, Regalado E, MacCarrick G. Demo E, et al. Among authors: rideout al. Med Clin North Am. 2019 Nov;103(6):1005-1019. doi: 10.1016/j.mcna.2019.08.001. Epub 2019 Aug 31. Med Clin North Am. 2019. PMID: 31582001 Review.
Genetics: schizophrenia.
Rideout AL, Carroll JC, Blaine SM, Cremin C, Dorman H, Gibbons CA, Honeywell C, Meschino WS, Permaul J, Allanson J. Rideout AL, et al. Can Fam Physician. 2009 Dec;55(12):1207. Can Fam Physician. 2009. PMID: 20008600 Free PMC article. No abstract available.
Germline mutations in MAP3K6 are associated with familial gastric cancer.
Gaston D, Hansford S, Oliveira C, Nightingale M, Pinheiro H, Macgillivray C, Kaurah P, Rideout AL, Steele P, Soares G, Huang WY, Whitehouse S, Blowers S, LeBlanc MA, Jiang H, Greer W, Samuels ME, Orr A, Fernandez CV, Majewski J, Ludman M, Dyack S, Penney LS, McMaster CR, Huntsman D, Bedard K. Gaston D, et al. Among authors: rideout al. PLoS Genet. 2014 Oct 23;10(10):e1004669. doi: 10.1371/journal.pgen.1004669. eCollection 2014 Oct. PLoS Genet. 2014. PMID: 25340522 Free PMC article.
Automated detection of low ejection fraction from a one-lead electrocardiogram: application of an AI algorithm to an electrocardiogram-enabled Digital Stethoscope.
Attia ZI, Dugan J, Rideout A, Maidens JN, Venkatraman S, Guo L, Noseworthy PA, Pellikka PA, Pham SL, Kapa S, Friedman PA, Lopez-Jimenez F. Attia ZI, et al. Among authors: rideout a. Eur Heart J Digit Health. 2022 May 23;3(3):373-379. doi: 10.1093/ehjdh/ztac030. eCollection 2022 Sep. Eur Heart J Digit Health. 2022. PMID: 36712160 Free PMC article.
Grange syndrome due to homozygous YY1AP1 missense rare variants.
Ciuffetelli Alamo IV, Kwartler CS, Regalado ER, Afifi RO, Parkash S, Rideout A, Guo DC, Milewicz DM. Ciuffetelli Alamo IV, et al. Among authors: rideout a. Am J Med Genet A. 2019 Dec;179(12):2500-2505. doi: 10.1002/ajmg.a.61379. Epub 2019 Oct 21. Am J Med Genet A. 2019. PMID: 31633303
52 results