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Results by year

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

Year Number of Results
1988 1
1990 2
1991 1
1992 1
1993 2
1994 2
1995 1
1996 3
1997 3
1998 2
1999 5
2000 8
2001 9
2002 15
2003 20
2004 17
2005 17
2006 29
2007 31
2008 50
2009 51
2010 70
2011 44
2012 44
2013 53
2014 60
2015 50
2016 47
2017 51
2018 27
2019 29
2020 31
2021 25
2022 12
2023 13
2024 4

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PubMed for id: 650

732 results

Results by year

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Page 1
BMP2 rs1005464 is associated with mandibular condyle size variation.
Marañón-Vásquez GA, de Souza Araújo MT, de Oliveira Ruellas AC, Matsumoto MAN, Figueiredo M, Meyfarth SRS, Antunes LAA, Baratto-Filho F, Scariot R, Flores-Mir C, Kirschneck C, Santos Antunes L, Küchler EC. Marañón-Vásquez GA, et al. Sci Rep. 2024 Mar 12;14(1):5987. doi: 10.1038/s41598-024-56530-3. Sci Rep. 2024. PMID: 38472272 Free PMC article.
BMP2 is a potential causative gene for isolated dextrocardia situs solitus.
Yogi A, Iemura R, Nakatani H, Takasawa K, Gau M, Yamauchi T, Yoshida M, Moriyama K, Ishii T, Hosokawa S, Yamada M, Suzuki H, Kosaki K, Kashimada K, Morio T. Yogi A, et al. Eur J Med Genet. 2023 Sep;66(9):104820. doi: 10.1016/j.ejmg.2023.104820. Epub 2023 Aug 11. Eur J Med Genet. 2023. PMID: 37572998
Monoallelic loss-of-function BMP2 variants result in BMP2-related skeletal dysplasia spectrum.
Priestley JRC, Deshwar AR, Murthy H, D'Agostino MD, Dupuis L, Gangaram B, Gray C, Jobling R, Pannia E, Platzer K, Prescott K, Redman M, Rippert AL, Rosenfeld JA, Scott DA, Wang YW, Schmederer Z, Dalal A, Sarma AS, Skraban C, Dowling JJ, Mendoza-Londono R, Slavotinek A, Bhoj EJ. Priestley JRC, et al. Genet Med. 2023 Aug;25(8):100863. doi: 10.1016/j.gim.2023.100863. Epub 2023 Apr 28. Genet Med. 2023. PMID: 37125634
732 results