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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 8
2017 2
2018 5
2019 3
2020 7
2021 3
2022 4
2023 2
2024 1

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291 results

Results by year

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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.
Systematic analysis and prediction of genes associated with monogenic disorders on human chromosome X.
Leitão E, Schröder C, Parenti I, Dalle C, Rastetter A, Kühnel T, Kuechler A, Kaya S, Gérard B, Schaefer E, Nava C, Drouot N, Engel C, Piard J, Duban-Bedu B, Villard L, Stegmann APA, Vanhoutte EK, Verdonschot JAJ, Kaiser FJ, Tran Mau-Them F, Scala M, Striano P, Frints SGM, Argilli E, Sherr EH, Elder F, Buratti J, Keren B, Mignot C, Héron D, Mandel JL, Gecz J, Kalscheuer VM, Horsthemke B, Piton A, Depienne C. Leitão E, et al. Among authors: horsthemke b. Nat Commun. 2022 Nov 2;13(1):6570. doi: 10.1038/s41467-022-34264-y. Nat Commun. 2022. PMID: 36323681 Free PMC article.
Early-set POMC methylation variability is accompanied by increased risk for obesity and is addressable by MC4R agonist treatment.
Lechner L, Opitz R, Silver MJ, Krabusch PM, Prentice AM, Field MS, Stachelscheid H, Leitão E, Schröder C, Fernandez Vallone V, Horsthemke B, Jöckel KH, Schmidt B, Nöthen MM, Hoffmann P, Herms S, Kleyn PW, Megges M, Blume-Peytavi U, Weiss K, Mai K, Blankenstein O, Obermayer B, Wiegand S, Kühnen P. Lechner L, et al. Among authors: horsthemke b. Sci Transl Med. 2023 Jul 19;15(705):eadg1659. doi: 10.1126/scitranslmed.adg1659. Epub 2023 Jul 19. Sci Transl Med. 2023. PMID: 37467315
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.
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.
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 defects on human chromosome 15.
Horsthemke B, Buiting K. Horsthemke B, et al. Cytogenet Genome Res. 2006;113(1-4):292-9. doi: 10.1159/000090844. Cytogenet Genome Res. 2006. PMID: 16575192 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.
291 results