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
1946 1
1949 1
1951 2
1952 1
1953 1
1985 3
1990 1
1992 1
1993 1
1994 1
1995 1
2000 1
2003 1
2005 1
2006 1
2007 2
2008 1
2009 4
2010 3
2011 1
2013 5
2014 1
2015 1
2016 4
2017 1
2019 2
2020 1
2021 4
2022 4
Text availability
Article attribute
Article type
Publication date

Search Results

46 results
Results by year
Filters applied: . Clear all
Page 1
The Axenfeld-Rieger Syndrome Gene FOXC1 Contributes to Left-Right Patterning.
Chrystal PW, French CR, Jean F, Havrylov S, van Baarle S, Peturson AM, Xu P, Crump JG, Pilgrim DB, Lehmann OJ, Waskiewicz AJ. Chrystal PW, et al. Among authors: french cr. Genes (Basel). 2021 Jan 26;12(2):170. doi: 10.3390/genes12020170. Genes (Basel). 2021. PMID: 33530637 Free PMC article.
Routine polysomnography in an epilepsy monitoring unit.
Phillips MC, Costello CA, White EJ, Smit M, Carino J, Strawhorn A, Jackson B, Kwan P, French CR, Yerra SR, Tan KM, O'Brien TJ, Goldin J. Phillips MC, et al. Among authors: french cr. Epilepsy Res. 2013 Aug;105(3):401-4. doi: 10.1016/j.eplepsyres.2013.02.015. Epub 2013 Mar 25. Epilepsy Res. 2013. PMID: 23535035
foxc1 is required for embryonic head vascular smooth muscle differentiation in zebrafish.
Whitesell TR, Chrystal PW, Ryu JR, Munsie N, Grosse A, French CR, Workentine ML, Li R, Zhu LJ, Waskiewicz A, Lehmann OJ, Lawson ND, Childs SJ. Whitesell TR, et al. Among authors: french cr. Dev Biol. 2019 Sep 1;453(1):34-47. doi: 10.1016/j.ydbio.2019.06.005. Epub 2019 Jun 11. Dev Biol. 2019. PMID: 31199900 Free article.
Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease.
French CR, Seshadri S, Destefano AL, Fornage M, Arnold CR, Gage PJ, Skarie JM, Dobyns WB, Millen KJ, Liu T, Dietz W, Kume T, Hofker M, Emery DJ, Childs SJ, Waskiewicz AJ, Lehmann OJ. French CR, et al. J Clin Invest. 2014 Nov;124(11):4877-81. doi: 10.1172/JCI75109. Epub 2014 Sep 24. J Clin Invest. 2014. PMID: 25250569 Free PMC article.
A pathogenic deletion in Forkhead Box L1 (FOXL1) identifies the first otosclerosis (OTSC) gene.
Abdelfatah N, Mostafa AA, French CR, Doucette LP, Penney C, Lucas MB, Griffin A, Booth V, Rowley C, Besaw JE, Tranebjærg L, Rendtorff ND, Hodgkinson KA, Little LA, Agrawal S, Parnes L, Batten T, Moore S, Hu P, Pater JA, Houston J, Galutira D, Benteau T, MacDonald C, French D, O'Rielly DD, Stanton SG, Young TL. Abdelfatah N, et al. Among authors: french cr. Hum Genet. 2022 Apr;141(3-4):965-979. doi: 10.1007/s00439-021-02381-1. Epub 2021 Oct 11. Hum Genet. 2022. PMID: 34633540 Free PMC article.
46 results