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

Year Number of Results
1980 1
1981 3
1982 1
1983 1
1984 3
1985 3
1986 1
1987 6
1988 3
1989 5
1990 14
1991 9
1992 15
1993 14
1994 11
1995 8
1996 9
1997 17
1998 9
1999 19
2000 7
2001 8
2002 1
2003 8
2004 4
2005 8
2006 7
2007 7
2008 11
2009 9
2010 11
2011 7
2012 6
2013 6
2014 13
2015 6
2016 9
2017 2
2018 5
2019 3
2020 7
2021 4
2022 5
2023 2
2024 2
2025 0

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294 results

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Page 1
Angelman syndrome - insights into a rare neurogenetic disorder.
Buiting K, Williams C, Horsthemke B. Buiting K, et al. Among authors: horsthemke b. Nat Rev Neurol. 2016 Oct;12(10):584-93. doi: 10.1038/nrneurol.2016.133. Epub 2016 Sep 12. Nat Rev Neurol. 2016. PMID: 27615419 Review.
A critical appraisal of clinical epigenetics.
Horsthemke B. Horsthemke B. Clin Epigenetics. 2022 Jul 28;14(1):95. doi: 10.1186/s13148-022-01315-6. Clin Epigenetics. 2022. PMID: 35902960 Free PMC article.
Epimutations in human disease.
Horsthemke B. Horsthemke B. Curr Top Microbiol Immunol. 2006;310:45-59. doi: 10.1007/3-540-31181-5_4. Curr Top Microbiol Immunol. 2006. PMID: 16909906 Review.
N6-adenosine methylation in MiRNAs.
Berulava T, Rahmann S, Rademacher K, Klein-Hitpass L, Horsthemke B. Berulava T, et al. Among authors: horsthemke b. PLoS One. 2015 Feb 27;10(2):e0118438. doi: 10.1371/journal.pone.0118438. eCollection 2015. PLoS One. 2015. PMID: 25723394 Free PMC article.
Assisted reproduction: the epigenetic perspective.
Horsthemke B, Ludwig M. Horsthemke B, et al. Hum Reprod Update. 2005 Sep-Oct;11(5):473-82. doi: 10.1093/humupd/dmi022. Epub 2005 Jul 1. Hum Reprod Update. 2005. PMID: 15994847 Review.
Evidence for correlations between BMI-associated SNPs and circRNAs.
Rajcsanyi LS, Diebels I, Pastoors L, Kanber D, Peters T, Volckmar AL, Zheng Y, Grosse M, Dieterich C, Hebebrand J, Kaiser FJ, Horsthemke B, Hinney A. Rajcsanyi LS, et al. Among authors: horsthemke b. Sci Rep. 2022 Jul 25;12(1):12643. doi: 10.1038/s41598-022-16495-7. Sci Rep. 2022. PMID: 35879369 Free PMC article.
Imprinting mutations on human chromosome 15.
Horsthemke B, Dittrich B, Buiting K. Horsthemke B, et al. 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.
The adult phenotype of Schaaf-Yang syndrome.
Marbach F, Elgizouli M, Rech M, Beygo J, Erger F, Velmans C, Stumpel CTRM, Stegmann APA, Beck-Wödl S, Gillessen-Kaesbach G, Horsthemke B, Schaaf CP, Kuechler A. Marbach F, et al. Among authors: horsthemke b. Orphanet J Rare Dis. 2020 Oct 19;15(1):294. doi: 10.1186/s13023-020-01557-8. Orphanet J Rare Dis. 2020. PMID: 33076953 Free PMC article.
Imprinting in Prader-Willi and Angelman syndromes.
Nicholls RD, Saitoh S, Horsthemke B. Nicholls RD, et al. Among authors: horsthemke b. Trends Genet. 1998 May;14(5):194-200. doi: 10.1016/s0168-9525(98)01432-2. Trends Genet. 1998. PMID: 9613204 Review.
294 results