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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 1
2023 0

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141 results

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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.
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.
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.
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.
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.
The origin of the RB1 imprint.
Kanber D, Buiting K, Roos C, Gromoll J, Kaya S, Horsthemke B, Lohmann D. Kanber D, et al. Among authors: buiting k. PLoS One. 2013 Nov 25;8(11):e81502. doi: 10.1371/journal.pone.0081502. eCollection 2013. PLoS One. 2013. PMID: 24282601 Free PMC article.
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.
141 results