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

Year Number of Results
1942 1
1945 1
1975 2
1976 1
1977 3
1978 1
1980 1
1981 3
1982 2
1983 1
1985 2
1986 5
1987 3
1988 7
1989 7
1990 5
1991 9
1992 7
1993 9
1994 10
1995 10
1996 5
1997 3
1998 6
1999 3
2000 6
2001 3
2003 3
2004 3
2005 6
2006 9
2007 9
2008 10
2009 12
2010 8
2011 10
2012 12
2013 14
2014 13
2015 12
2016 7
2017 2
2018 8
2019 6
2020 2
2021 2
2022 2
2023 4
2024 2

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257 results

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Page 1
Marinus van den Ende.
van den Ende J. van den Ende J. S Afr Med J. 2009 Jan;99(1):29-32. S Afr Med J. 2009. PMID: 19374083
DNA Diagnostics of Hereditary Hearing Loss: A Targeted Resequencing Approach Combined with a Mutation Classification System.
Sommen M, Schrauwen I, Vandeweyer G, Boeckx N, Corneveaux JJ, van den Ende J, Boudewyns A, De Leenheer E, Janssens S, Claes K, Verstreken M, Strenzke N, Predöhl F, Wuyts W, Mortier G, Bitner-Glindzicz M, Moser T, Coucke P, Huentelman MJ, Van Camp G. Sommen M, et al. Among authors: van den ende j. Hum Mutat. 2016 Aug;37(8):812-9. doi: 10.1002/humu.22999. Epub 2016 May 6. Hum Mutat. 2016. PMID: 27068579
Obituary.
van den Ende JE. van den Ende JE. In Silico Biol. 2011-2012;11(3-4):95. doi: 10.3233/ISB-2012-0450. In Silico Biol. 2011. PMID: 22935963 No abstract available.
Import infectious diseases in Belgium.
Van Gompel A, Van den Ende J. Van Gompel A, et al. Among authors: van den ende j. Acta Clin Belg. 1998 Aug;53(4):245-50. doi: 10.1080/17843286.1998.11754169. Acta Clin Belg. 1998. PMID: 9795443 No abstract available.
Myhre syndrome in adulthood: clinical variability and emerging genotype-phenotype correlations.
Vanbelleghem E, Van Damme T, Beyens A, Symoens S, Claes K, De Backer J, Meerschaut I, Vanommeslaeghe F, Delanghe SE, van den Ende J, Beyltjens T, Scimone ER, Lindsay ME, Schimmenti LA, Hinze AM, Dunn E, Gomez-Ospina N, Vandernoot I, Delguste T, Coppens S, Cormier-Daire V, Tartaglia M, Garavelli L, Shieh J, Demir Ş, Arslan Ateş E, Zenker M, Rohanizadegan M, Rivera-Cruz G, Douzgou S; Myhre Syndrome Foundation; Lin AE, Callewaert B. Vanbelleghem E, et al. Among authors: van den ende j. Eur J Hum Genet. 2024 Sep;32(9):1086-1094. doi: 10.1038/s41431-024-01664-1. Epub 2024 Jul 12. Eur J Hum Genet. 2024. PMID: 38997468
Rapid diagnostic tests for malaria.
Bisoffi Z, Gobbi F, Van den Ende J. Bisoffi Z, et al. Among authors: van den ende j. BMJ. 2014 Jun 19;348:g3846. doi: 10.1136/bmj.g3846. BMJ. 2014. PMID: 24948696 No abstract available.
Multi-omics approach dissects cis-regulatory mechanisms underlying North Carolina macular dystrophy, a retinal enhanceropathy.
Van de Sompele S, Small KW, Cicekdal MB, Soriano VL, D'haene E, Shaya FS, Agemy S, Van der Snickt T, Rey AD, Rosseel T, Van Heetvelde M, Vergult S, Balikova I, Bergen AA, Boon CJF, De Zaeytijd J, Inglehearn CF, Kousal B, Leroy BP, Rivolta C, Vaclavik V, van den Ende J, van Schooneveld MJ, Gómez-Skarmeta JL, Tena JJ, Martinez-Morales JR, Liskova P, Vleminckx K, De Baere E. Van de Sompele S, et al. Among authors: van den ende j. Am J Hum Genet. 2022 Nov 3;109(11):2029-2048. doi: 10.1016/j.ajhg.2022.09.013. Epub 2022 Oct 14. Am J Hum Genet. 2022. PMID: 36243009 Free PMC article.
The threshold model revisited.
Djulbegovic B, Hozo I, Mayrhofer T, van den Ende J, Guyatt G. Djulbegovic B, et al. Among authors: van den ende j. J Eval Clin Pract. 2019 Apr;25(2):186-195. doi: 10.1111/jep.13091. Epub 2018 Dec 21. J Eval Clin Pract. 2019. PMID: 30575227 Free PMC article.
257 results