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

Year Number of Results
1972 10
1973 3
1982 1
1999 1
2005 1
2006 3
2007 2
2008 3
2009 1
2010 4
2011 2
2012 4
2013 2
2014 2
2015 10
2016 10
2017 3
2018 4
2019 8
2020 4
2021 3
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71 results
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Page 1
Insights into the genetic architecture of the human face.
White JD, Indencleef K, Naqvi S, Eller RJ, Hoskens H, Roosenboom J, Lee MK, Li J, Mohammed J, Richmond S, Quillen EE, Norton HL, Feingold E, Swigut T, Marazita ML, Peeters H, Hens G, Shaffer JR, Wysocka J, Walsh S, Weinberg SM, Shriver MD, Claes P. White JD, et al. Among authors: hens g. Nat Genet. 2021 Jan;53(1):45-53. doi: 10.1038/s41588-020-00741-7. Epub 2020 Dec 7. Nat Genet. 2021. PMID: 33288918 Free PMC article.
Non-Syndromic Cleft Lip with or without Cleft Palate: Genome-Wide Association Study in Europeans Identifies a Suggestive Risk Locus at 16p12.1 and Supports SH3PXD2A as a Clefting Susceptibility Gene.
van Rooij IA, Ludwig KU, Welzenbach J, Ishorst N, Thonissen M, Galesloot TE, Ongkosuwito E, Bergé SJ, Aldhorae K, Rojas-Martinez A, Kiemeney LA, Vermeesch JR, Brunner H, Roeleveld N, Devriendt K, Dormaar T, Hens G, Knapp M, Carels C, Mangold E. van Rooij IA, et al. Among authors: hens g. Genes (Basel). 2019 Dec 7;10(12):1023. doi: 10.3390/genes10121023. Genes (Basel). 2019. PMID: 31817908 Free PMC article. Clinical Trial.
Vestibular dysfunction is a manifestation of 22q11.2 deletion syndrome.
Willaert A, Van Eynde C, Verhaert N, Desloovere C, Vander Poorten V, Devriendt K, Swillen A, Hens G. Willaert A, et al. Among authors: hens g. Am J Med Genet A. 2019 Mar;179(3):448-454. doi: 10.1002/ajmg.a.7. Epub 2019 Jan 11. Am J Med Genet A. 2019. PMID: 30635960
Three-dimensional Morphing and Its Added Value in the Rhinoplasty Consult.
Lekakis G, Hens G, Claes P, Hellings PW. Lekakis G, et al. Among authors: hens g. Plast Reconstr Surg Glob Open. 2019 Jan 4;7(1):e2063. doi: 10.1097/GOX.0000000000002063. eCollection 2019 Jan. Plast Reconstr Surg Glob Open. 2019. PMID: 30859032 Free PMC article.
Deletions and loss-of-function variants in TP63 associated with orofacial clefting.
Khandelwal KD, van den Boogaard MH, Mehrem SL, Gebel J, Fagerberg C, van Beusekom E, van Binsbergen E, Topaloglu O, Steehouwer M, Gilissen C, Ishorst N, van Rooij IALM, Roeleveld N, Christensen K, Schoenaers J, Bergé S, Murray JC, Hens G, Devriendt K, Ludwig KU, Mangold E, Hoischen A, Zhou H, Dötsch V, Carels CEL, van Bokhoven H. Khandelwal KD, et al. Among authors: hens g. Eur J Hum Genet. 2019 Jul;27(7):1101-1112. doi: 10.1038/s41431-019-0370-0. Epub 2019 Mar 8. Eur J Hum Genet. 2019. PMID: 30850703 Free PMC article. Clinical Trial.
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