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

Year Number of Results
1985 6
1986 6
1987 8
1988 4
1989 2
1990 2
1991 4
1992 6
1993 9
1994 3
1995 3
1996 4
1997 6
1998 7
1999 3
2000 4
2001 4
2002 7
2003 7
2004 2
2005 9
2006 3
2007 2
2008 2
2009 5
2010 5
2011 7
2012 8
2013 15
2014 4
2015 9
2016 4
2017 2
2018 8
2019 2
2020 1
2021 2
2022 1
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175 results
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Page 1
22q11.2 deletion syndrome.
McDonald-McGinn DM, Sullivan KE, Marino B, Philip N, Swillen A, Vorstman JA, Zackai EH, Emanuel BS, Vermeesch JR, Morrow BE, Scambler PJ, Bassett AS. McDonald-McGinn DM, et al. Among authors: scambler pj. Nat Rev Dis Primers. 2015 Nov 19;1:15071. doi: 10.1038/nrdp.2015.71. Nat Rev Dis Primers. 2015. PMID: 27189754 Free PMC article. Review.
Molecular genetics of 22q11.2 deletion syndrome.
Morrow BE, McDonald-McGinn DM, Emanuel BS, Vermeesch JR, Scambler PJ. Morrow BE, et al. Among authors: scambler pj. Am J Med Genet A. 2018 Oct;176(10):2070-2081. doi: 10.1002/ajmg.a.40504. Am J Med Genet A. 2018. PMID: 30380194 Free PMC article. Review.
TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum.
Davis EE, Zhang Q, Liu Q, Diplas BH, Davey LM, Hartley J, Stoetzel C, Szymanska K, Ramaswami G, Logan CV, Muzny DM, Young AC, Wheeler DA, Cruz P, Morgan M, Lewis LR, Cherukuri P, Maskeri B, Hansen NF, Mullikin JC, Blakesley RW, Bouffard GG; NISC Comparative Sequencing Program, Gyapay G, Rieger S, Tönshoff B, Kern I, Soliman NA, Neuhaus TJ, Swoboda KJ, Kayserili H, Gallagher TE, Lewis RA, Bergmann C, Otto EA, Saunier S, Scambler PJ, Beales PL, Gleeson JG, Maher ER, Attié-Bitach T, Dollfus H, Johnson CA, Green ED, Gibbs RA, Hildebrandt F, Pierce EA, Katsanis N. Davis EE, et al. Among authors: scambler pj. Nat Genet. 2011 Mar;43(3):189-96. doi: 10.1038/ng.756. Epub 2011 Jan 23. Nat Genet. 2011. PMID: 21258341 Free PMC article.
Distinct factors control histone variant H3.3 localization at specific genomic regions.
Goldberg AD, Banaszynski LA, Noh KM, Lewis PW, Elsaesser SJ, Stadler S, Dewell S, Law M, Guo X, Li X, Wen D, Chapgier A, DeKelver RC, Miller JC, Lee YL, Boydston EA, Holmes MC, Gregory PD, Greally JM, Rafii S, Yang C, Scambler PJ, Garrick D, Gibbons RJ, Higgs DR, Cristea IM, Urnov FD, Zheng D, Allis CD. Goldberg AD, et al. Among authors: scambler pj. Cell. 2010 Mar 5;140(5):678-91. doi: 10.1016/j.cell.2010.01.003. Cell. 2010. PMID: 20211137 Free PMC article.
Mechanisms and cell lineages in lymphatic vascular development.
Jafree DJ, Long DA, Scambler PJ, Ruhrberg C. Jafree DJ, et al. Among authors: scambler pj. Angiogenesis. 2021 May;24(2):271-288. doi: 10.1007/s10456-021-09784-8. Epub 2021 Apr 6. Angiogenesis. 2021. PMID: 33825109 Free PMC article. Review.
Clinical and molecular effects of CHD7 in the heart.
Corsten-Janssen N, Scambler PJ. Corsten-Janssen N, et al. Among authors: scambler pj. Am J Med Genet C Semin Med Genet. 2017 Dec;175(4):487-495. doi: 10.1002/ajmg.c.31590. Epub 2017 Oct 31. Am J Med Genet C Semin Med Genet. 2017. PMID: 29088513 Review.
Dual role for CXCL12 signaling in semilunar valve development.
Ridge LA, Kewbank D, Schütz D, Stumm R, Scambler PJ, Ivins S. Ridge LA, et al. Among authors: scambler pj. Cell Rep. 2021 Aug 24;36(8):109610. doi: 10.1016/j.celrep.2021.109610. Cell Rep. 2021. PMID: 34433040 Free PMC article.
The cystic fibrosis gene.
Scambler PJ. Scambler PJ. Arch Dis Child. 1989 Dec;64(12):1647-8. doi: 10.1136/adc.64.12.1647. Arch Dis Child. 1989. PMID: 2696430 Free PMC article. Review. No abstract available.
Human HOX gene mutations.
Goodman FR, Scambler PJ. Goodman FR, et al. Among authors: scambler pj. Clin Genet. 2001 Jan;59(1):1-11. doi: 10.1034/j.1399-0004.2001.590101.x. Clin Genet. 2001. PMID: 11206481 Review.
The 22q11 deletion syndromes.
Scambler PJ. Scambler PJ. Hum Mol Genet. 2000 Oct;9(16):2421-6. doi: 10.1093/hmg/9.16.2421. Hum Mol Genet. 2000. PMID: 11005797 Review.
175 results