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

Year Number of Results
1988 1
1990 1
1992 3
1993 5
1994 3
1995 1
1996 6
1997 8
1998 5
1999 7
2000 6
2001 7
2003 5
2004 5
2005 1
2006 3
2007 6
2008 10
2009 6
2010 10
2011 4
2012 6
2013 7
2014 10
2015 9
2016 8
2017 3
2018 6
2019 3
2020 1
2021 1
2022 0
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Search Results

140 results
Results by year
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Page 1
Multilocus methylation defects in imprinting disorders.
Mackay DJ, Eggermann T, Buiting K, Garin I, Netchine I, Linglart A, de Nanclares GP. Mackay DJ, et al. Among authors: buiting k. Biomol Concepts. 2015 Mar;6(1):47-57. doi: 10.1515/bmc-2014-0037. Biomol Concepts. 2015. PMID: 25581766 Free article. Review.
Mosaicism and uniparental disomy in prenatal diagnosis.
Eggermann T, Soellner L, Buiting K, Kotzot D. Eggermann T, et al. Among authors: buiting k. Trends Mol Med. 2015 Feb;21(2):77-87. doi: 10.1016/j.molmed.2014.11.010. Epub 2014 Dec 2. Trends Mol Med. 2015. PMID: 25547535 Review.
Prader-Willi syndrome and Angelman syndrome.
Buiting K. Buiting K. Am J Med Genet C Semin Med Genet. 2010 Aug 15;154C(3):365-76. doi: 10.1002/ajmg.c.30273. Am J Med Genet C Semin Med Genet. 2010. PMID: 20803659 Review.
Imprinting defects on human chromosome 15.
Horsthemke B, Buiting K. Horsthemke B, et al. Among authors: buiting k. Cytogenet Genome Res. 2006;113(1-4):292-9. doi: 10.1159/000090844. Cytogenet Genome Res. 2006. PMID: 16575192 Review.
Genomic imprinting and imprinting defects in humans.
Horsthemke B, Buiting K. Horsthemke B, et al. Among authors: buiting k. Adv Genet. 2008;61:225-46. doi: 10.1016/S0065-2660(07)00008-9. Adv Genet. 2008. PMID: 18282508 Review.
Recommendations for a nomenclature system for reporting methylation aberrations in imprinted domains.
Monk D, Morales J, den Dunnen JT, Russo S, Court F, Prawitt D, Eggermann T, Beygo J, Buiting K, Tümer Z; Nomenclature group of the European Network for Human Congenital Imprinting Disorders. Monk D, et al. Among authors: buiting k. Epigenetics. 2018;13(2):117-121. doi: 10.1080/15592294.2016.1264561. Epub 2018 Jan 25. Epigenetics. 2018. PMID: 27911167 Free PMC article. Review.
Imprinting mutations on human chromosome 15.
Horsthemke B, Dittrich B, Buiting K. Horsthemke B, et al. Among authors: buiting k. Hum Mutat. 1997;10(5):329-37. doi: 10.1002/(SICI)1098-1004(1997)10:5<329::AID-HUMU1>3.0.CO;2-A. Hum Mutat. 1997. PMID: 9375847 Review.
Beckwith-Wiedemann syndrome: Clinical, histopathological and molecular study of two Tunisian patients and review of literature.
Sassi H, Elaribi Y, Jilani H, Rejeb I, Hizem S, Sebai M, Kasdallah N, Bouthour H, Hannachi S, Beygo J, Saad A, Buiting K, H'mida Ben-Brahim D, BenJemaa L. Sassi H, et al. Among authors: buiting k. Mol Genet Genomic Med. 2021 Oct;9(10):e1796. doi: 10.1002/mgg3.1796. Epub 2021 Sep 12. Mol Genet Genomic Med. 2021. PMID: 34510813 Free PMC article. Review.
Imprinting of RB1 (the new kid on the block).
Buiting K, Kanber D, Horsthemke B, Lohmann D. Buiting K, et al. Brief Funct Genomics. 2010 Jul;9(4):347-53. doi: 10.1093/bfgp/elq014. Epub 2010 Jun 15. Brief Funct Genomics. 2010. PMID: 20551090 Review.
140 results