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Results by year

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

Year Number of Results
1983 2
1984 5
1985 1
1987 1
1988 1
1991 3
1992 8
1993 9
1994 7
1995 8
1996 4
1997 12
1998 6
1999 11
2000 12
2001 11
2002 12
2003 8
2004 8
2005 11
2006 6
2007 10
2008 4
2009 6
2010 11
2011 11
2012 13
2013 6
2014 8
2015 8
2016 7
2017 9
2018 5
2019 3
2020 9
2021 14
2022 4
2023 3
2024 1

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Search Results

259 results

Results by year

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Page 1
FOXP1 Syndrome.
Rappold G, Siper P, Kostic A, Braden R, Morgan A, Koene S, Kolevzon A. Rappold G, et al. 2023 Sep 21. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2023 Sep 21. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 37733892 Free Books & Documents. Review.
SHOX Deficiency Disorders.
Binder G, Rappold GA. Binder G, et al. Among authors: rappold ga. 2005 Dec 12 [updated 2024 May 23]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2005 Dec 12 [updated 2024 May 23]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301394 Free Books & Documents. Review.
The serotonin receptor 3E variant is a risk factor for female IBS-D.
Fritz N, Berens S, Dong Y, Martínez C, Schmitteckert S, Houghton LA, Goebel-Stengel M, Wahl V, Kabisch M, Götze D, D'Amato M, Zheng T, Röth R, Mönnikes H, Tesarz J, Engel F, Gauss A, Raithel M, Andresen V, Keller J, Frieling T, Pehl C, Stein-Thöringer C, Clarke G, Kennedy PJ, Cryan JF, Dinan TG, Quigley EMM, Spiller R, Beltrán C, Madrid AM, Torres V, Mayer EA, Sayuk G, Gazouli M, Karamanolis G, Bustamante M, Estivil X, Rabionet R, Hoffmann P, Nöthen MM, Heilmann-Heimbach S, Schmidt B, Franke A, Lieb W, Herzog W, Boeckxstaens G, Wouters MM, Simrén M, Rappold GA, Vicario M, Santos J, Schaefert R, Lorenzo-Bermejo J, Niesler B. Fritz N, et al. Among authors: rappold ga. J Mol Med (Berl). 2022 Nov;100(11):1617-1627. doi: 10.1007/s00109-022-02244-w. Epub 2022 Sep 19. J Mol Med (Berl). 2022. PMID: 36121467 Free PMC article.
Protect minorities in genetic research.
Lipphardt V, Rappold GA, Surdu M. Lipphardt V, et al. Among authors: rappold ga. Science. 2021 Sep 24;373(6562):1452. doi: 10.1126/science.abm2270. Epub 2021 Sep 23. Science. 2021. PMID: 34554779 No abstract available.
The human SHOX mutation database.
Niesler B, Fischer C, Rappold GA. Niesler B, et al. Among authors: rappold ga. Hum Mutat. 2002 Nov;20(5):338-41. doi: 10.1002/humu.10125. Hum Mutat. 2002. PMID: 12402330
SHOX: growth, Léri-Weill and Turner syndromes.
Blaschke RJ, Rappold GA. Blaschke RJ, et al. Among authors: rappold ga. Trends Endocrinol Metab. 2000 Aug;11(6):227-30. doi: 10.1016/s1043-2760(00)00262-9. Trends Endocrinol Metab. 2000. PMID: 10878753 Review.
All shook up by SHOX deficiency.
Rappold GA, Shanske A, Saenger P. Rappold GA, et al. J Pediatr. 2005 Oct;147(4):422-4. doi: 10.1016/j.jpeds.2005.06.048. J Pediatr. 2005. PMID: 16227022 No abstract available.
259 results