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

Year Number of Results
2002 4
2003 3
2004 7
2005 5
2007 2
2008 1
2009 4
2010 1
2011 2
2012 5
2013 4
2014 5
2015 5
2016 3
2017 3
2018 3
2019 2
2020 3
2021 5
2022 1
2023 2
2024 0

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66 results

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Page 1
AXIN1 bi-allelic variants disrupting the C-terminal DIX domain cause craniometadiaphyseal osteosclerosis with hip dysplasia.
Terhal P, Venhuizen AJ, Lessel D, Tan WH, Alswaid A, Grün R, Alzaidan HI, von Kroge S, Ragab N, Hempel M, Kubisch C, Novais E, Cristobal A, Tripolszki K, Bauer P, Fischer-Zirnsak B, Nievelstein RAJ, van Dijk A, Nikkels P, Oheim R, Hahn H, Bertoli-Avella A, Maurice MM, Kornak U. Terhal P, et al. Among authors: hahn h. Am J Hum Genet. 2023 Sep 7;110(9):1470-1481. doi: 10.1016/j.ajhg.2023.07.011. Epub 2023 Aug 14. Am J Hum Genet. 2023. PMID: 37582359 Free PMC article.
Insights into pediatric rhabdomyosarcoma research: Challenges and goals.
Yohe ME, Heske CM, Stewart E, Adamson PC, Ahmed N, Antonescu CR, Chen E, Collins N, Ehrlich A, Galindo RL, Gryder BE, Hahn H, Hammond S, Hatley ME, Hawkins DS, Hayes MN, Hayes-Jordan A, Helman LJ, Hettmer S, Ignatius MS, Keller C, Khan J, Kirsch DG, Linardic CM, Lupo PJ, Rota R, Shern JF, Shipley J, Sindiri S, Tapscott SJ, Vakoc CR, Wexler LH, Langenau DM. Yohe ME, et al. Among authors: hahn h. Pediatr Blood Cancer. 2019 Oct;66(10):e27869. doi: 10.1002/pbc.27869. Epub 2019 Jun 21. Pediatr Blood Cancer. 2019. PMID: 31222885 Free PMC article. Review.
Tumor suppressive functions of WNT5A in rhabdomyosarcoma.
Ragab N, Bauer J, Uhmann A, Marx A, Hahn H, Simon-Keller K. Ragab N, et al. Among authors: hahn h. Int J Oncol. 2022 Sep;61(3):102. doi: 10.3892/ijo.2022.5392. Epub 2022 Jul 7. Int J Oncol. 2022. PMID: 35796028 Free PMC article.
Mechanochemical control of epidermal stem cell divisions by B-plexins.
Jiang C, Javed A, Kaiser L, Nava MM, Xu R, Brandt DT, Zhao D, Mayer B, Fernández-Baldovinos J, Zhou L, Höß C, Sawmynaden K, Oleksy A, Matthews D, Weinstein LS, Hahn H, Gröne HJ, Graumann PL, Niessen CM, Offermanns S, Wickström SA, Worzfeld T. Jiang C, et al. Among authors: hahn h. Nat Commun. 2021 Feb 26;12(1):1308. doi: 10.1038/s41467-021-21513-9. Nat Commun. 2021. PMID: 33637728 Free PMC article.
Heterozygous truncating variants in SUFU cause congenital ocular motor apraxia.
Schröder S, Li Y, Yigit G, Altmüller J, Bader I, Bevot A, Biskup S, Dreha-Kulaczewski S, Christoph Korenke G, Kottke R, Mayr JA, Preisel M, Toelle SP, Wente-Schulz S, Wortmann SB, Hahn H, Boltshauser E, Uhmann A, Wollnik B, Brockmann K. Schröder S, et al. Among authors: hahn h. Genet Med. 2021 Feb;23(2):341-351. doi: 10.1038/s41436-020-00979-w. Epub 2020 Oct 7. Genet Med. 2021. PMID: 33024317 Free PMC article.
Context-dependent modulation of aggressiveness of pediatric tumors by individual oncogenic RAS isoforms.
Bauer J, Cuvelier N, Ragab N, Simon-Keller K, Nitzki F, Geyer N, Botermann DS, Elmer DP, Rosenberger A, Rando TA, Biressi S, Fagin JA, Saur D, Dullin C, Schildhaus HU, Schulz-Schaeffer W, Aberger F, Uhmann A, Hahn H. Bauer J, et al. Among authors: hahn h. Oncogene. 2021 Aug;40(31):4955-4966. doi: 10.1038/s41388-021-01904-4. Epub 2021 Jun 25. Oncogene. 2021. PMID: 34172934 Free PMC article.
Canonical WNT/β-Catenin Signaling Plays a Subordinate Role in Rhabdomyosarcomas.
Ragab N, Viehweger F, Bauer J, Geyer N, Yang M, Seils A, Belharazem D, Brembeck FH, Schildhaus HU, Marx A, Hahn H, Simon-Keller K. Ragab N, et al. Among authors: hahn h. Front Pediatr. 2018 Dec 5;6:378. doi: 10.3389/fped.2018.00378. eCollection 2018. Front Pediatr. 2018. PMID: 30568936 Free PMC article.
66 results