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

Year Number of Results
1952 1
1954 3
1955 1
1957 2
1962 1
1963 1
1964 1
1966 1
1967 1
1977 2
1978 1
1980 3
1981 1
1982 4
1983 3
1984 3
1985 2
1986 5
1987 3
1989 5
1990 10
1991 4
1992 6
1993 4
1994 4
1995 13
1996 11
1997 12
1998 3
1999 17
2000 16
2001 11
2002 10
2003 15
2004 16
2005 18
2006 11
2007 19
2008 13
2009 18
2010 17
2011 15
2012 15
2013 12
2014 8
2015 7
2016 5
2017 4
2018 2
2019 1
2020 2
2021 3
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344 results
Results by year
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Page 1
Duplications in the DMD gene.
White SJ, Aartsma-Rus A, Flanigan KM, Weiss RB, Kneppers AL, Lalic T, Janson AA, Ginjaar HB, Breuning MH, den Dunnen JT. White SJ, et al. Among authors: breuning mh. Hum Mutat. 2006 Sep;27(9):938-45. doi: 10.1002/humu.20367. Hum Mutat. 2006. PMID: 16917894
Unified criteria for ultrasonographic diagnosis of ADPKD.
Pei Y, Obaji J, Dupuis A, Paterson AD, Magistroni R, Dicks E, Parfrey P, Cramer B, Coto E, Torra R, San Millan JL, Gibson R, Breuning M, Peters D, Ravine D. Pei Y, et al. Among authors: breuning m. J Am Soc Nephrol. 2009 Jan;20(1):205-12. doi: 10.1681/ASN.2008050507. Epub 2008 Oct 22. J Am Soc Nephrol. 2009. PMID: 18945943 Free PMC article.
Diagnostic exome sequencing in 266 Dutch patients with visual impairment.
Haer-Wigman L, van Zelst-Stams WA, Pfundt R, van den Born LI, Klaver CC, Verheij JB, Hoyng CB, Breuning MH, Boon CJ, Kievit AJ, Verhoeven VJ, Pott JW, Sallevelt SC, van Hagen JM, Plomp AS, Kroes HY, Lelieveld SH, Hehir-Kwa JY, Castelein S, Nelen M, Scheffer H, Lugtenberg D, Cremers FP, Hoefsloot L, Yntema HG. Haer-Wigman L, et al. Among authors: breuning mh. Eur J Hum Genet. 2017 May;25(5):591-599. doi: 10.1038/ejhg.2017.9. Epub 2017 Feb 22. Eur J Hum Genet. 2017. PMID: 28224992 Free PMC article.
Coffin-Siris syndrome and the BAF complex: genotype-phenotype study in 63 patients.
Santen GW, Aten E, Vulto-van Silfhout AT, Pottinger C, van Bon BW, van Minderhout IJ, Snowdowne R, van der Lans CA, Boogaard M, Linssen MM, Vijfhuizen L, van der Wielen MJ, Vollebregt MJ; Coffin-Siris consortium, Breuning MH, Kriek M, van Haeringen A, den Dunnen JT, Hoischen A, Clayton-Smith J, de Vries BB, Hennekam RC, van Belzen MJ. Santen GW, et al. Among authors: breuning mh. Hum Mutat. 2013 Nov;34(11):1519-28. doi: 10.1002/humu.22394. Epub 2013 Aug 30. Hum Mutat. 2013. PMID: 23929686
[Maturity-onset diabetes of the young].
van der Tuin K, Hannema SE, Houdijk EC, Losekoot M, de Koning EJ, Breuning MH. van der Tuin K, et al. Among authors: breuning mh. Ned Tijdschr Geneeskd. 2015;159:A9247. Ned Tijdschr Geneeskd. 2015. PMID: 26374728 Review. Dutch.
Overgrowth syndromes:from classical to new.
Visser R, Kant SG, Wit JM, Breuning MH. Visser R, et al. Among authors: breuning mh. Pediatr Endocrinol Rev. 2009 Mar;6(3):375-94. Pediatr Endocrinol Rev. 2009. PMID: 19396024 Review.
Incipient CADASIL.
Lesnik Oberstein SA, van den Boom R, Middelkoop HA, Ferrari MD, Knaap YM, van Houwelingen HC, Breuning MH, van Buchem MA, Haan J. Lesnik Oberstein SA, et al. Among authors: breuning mh. Arch Neurol. 2003 May;60(5):707-12. doi: 10.1001/archneur.60.5.707. Arch Neurol. 2003. PMID: 12756134
Genetic analysis of short stature.
Kant SG, Wit JM, Breuning MH. Kant SG, et al. Among authors: breuning mh. Horm Res. 2003;60(4):157-65. doi: 10.1159/000073226. Horm Res. 2003. PMID: 14530602 Review.
Analysis of published PKD1 gene sequence variants.
Gout AM; ADPKD Gene Variant Consortium, Ravine D, Harris PC, Rossetti S, Peters D, Breuning M, Henske EP, Koizumi A, Inoue S, Shimizu Y, Thongnoppakhun W, Yenchitsomanus PT, Deltas C, Sandford R, Torra R, Turco AE, Jeffery S, Fontes M, Somlo S, Furu LM, Smulders YM, Mercier B, Ferec C, Burtey S, Pei Y, Kalaydjieva L, Bogdanova N, McCluskey M, Geon LJ, Wouters CH, Reiterova J, Stekrová J, San Millan JL, Aguiari G, Del Senno L. Gout AM, et al. Among authors: breuning m. Nat Genet. 2007 Apr;39(4):427-8. doi: 10.1038/ng0407-427. Nat Genet. 2007. PMID: 17392796 Review. No abstract available.
344 results
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