Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Results by year

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

Year Number of Results
1970 1
1978 1
1980 1
1999 2
2002 3
2003 2
2004 2
2006 1
2007 2
2008 3
2009 2
2010 2
2011 6
2012 7
2013 10
2014 9
2015 7
2016 8
2017 4
2018 3
2019 3
2020 5
2021 5
2022 1
Text availability
Article attribute
Article type
Publication date

Search Results

74 results
Results by year
Filters applied: . Clear all
Page 1
Activins and cell migration.
Kang HY, Shyr CR. Kang HY, et al. Among authors: shyr cr. Vitam Horm. 2011;85:129-48. doi: 10.1016/B978-0-12-385961-7.00007-X. Vitam Horm. 2011. PMID: 21353879 Review.
Team-based care: A clinical pharmacist and family physicians.
Blain L, Flanagan PS, Shyr C. Blain L, et al. Among authors: shyr c. Can Pharm J (Ott). 2021 Jun 6;154(4):242-247. doi: 10.1177/17151635211017591. eCollection 2021 Jul-Aug. Can Pharm J (Ott). 2021. PMID: 34345316 Free PMC article. No abstract available.
Secondary biogenic amine deficiencies: genetic etiology, therapeutic interventions, and clinical effects.
van Karnebeek CD, Blydt-Hansen I, Matthews AM, Avramovic V, Price M, Drogemoller B, Shyr C, Lee J, Mwenifumbo J, Ghani A, Stockler S, Friedman JM, Lehman A; CAUSES Genomic Study, Ross CJ, Wasserman WW, Tarailo-Graovac M, Horvath GA. van Karnebeek CD, et al. Among authors: shyr c. Neurogenetics. 2021 Oct;22(4):251-262. doi: 10.1007/s10048-021-00652-7. Epub 2021 Jul 2. Neurogenetics. 2021. PMID: 34213677
Atypical cerebral palsy: genomics analysis enables precision medicine.
Matthews AM, Blydt-Hansen I, Al-Jabri B, Andersen J, Tarailo-Graovac M, Price M, Selby K, Demos M, Connolly M, Drögemoller B, Shyr C, Mwenifumbo J, Elliott AM, Lee J, Ghani A, Stöckler S, Salvarinova R, Vallance H, Sinclair G, Ross CJ, Wasserman WW, McKinnon ML, Horvath GA, Goez H, van Karnebeek CD; TIDE BC, United for Metabolic Diseases and the CAUSES Study. Matthews AM, et al. Among authors: shyr c. Genet Med. 2019 Jul;21(7):1621-1628. doi: 10.1038/s41436-018-0376-y. Epub 2018 Dec 13. Genet Med. 2019. PMID: 30542205 Free article.
Exome Sequencing and the Management of Neurometabolic Disorders.
Tarailo-Graovac M, Shyr C, Ross CJ, Horvath GA, Salvarinova R, Ye XC, Zhang LH, Bhavsar AP, Lee JJ, Drögemöller BI, Abdelsayed M, Alfadhel M, Armstrong L, Baumgartner MR, Burda P, Connolly MB, Cameron J, Demos M, Dewan T, Dionne J, Evans AM, Friedman JM, Garber I, Lewis S, Ling J, Mandal R, Mattman A, McKinnon M, Michoulas A, Metzger D, Ogunbayo OA, Rakic B, Rozmus J, Ruben P, Sayson B, Santra S, Schultz KR, Selby K, Shekel P, Sirrs S, Skrypnyk C, Superti-Furga A, Turvey SE, Van Allen MI, Wishart D, Wu J, Wu J, Zafeiriou D, Kluijtmans L, Wevers RA, Eydoux P, Lehman AM, Vallance H, Stockler-Ipsiroglu S, Sinclair G, Wasserman WW, van Karnebeek CD. Tarailo-Graovac M, et al. Among authors: shyr c. N Engl J Med. 2016 Jun 9;374(23):2246-55. doi: 10.1056/NEJMoa1515792. Epub 2016 May 25. N Engl J Med. 2016. PMID: 27276562 Free PMC article.
Correction to: FLAGS, frequently mutated genes in public exomes.
Shyr C, Tarailo-Graovac M, Gottlieb M, Lee JJ, van Karnebeek C, Wasserman WW. Shyr C, et al. BMC Med Genomics. 2017 Nov 29;10(1):69. doi: 10.1186/s12920-017-0309-7. BMC Med Genomics. 2017. PMID: 29187224 Free PMC article.
74 results