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

Year Number of Results
1977 1
1987 1
1988 4
1989 3
1990 5
1991 7
1992 6
1993 2
1994 1
1995 1
1996 2
1997 3
1998 3
1999 2
2000 4
2001 3
2002 3
2003 1
2004 4
2005 6
2006 6
2007 5
2008 5
2009 4
2010 6
2011 9
2012 6
2013 3
2014 6
2015 6
2016 2
2017 1
2018 2
2019 5
2020 3
2022 1
2023 3
2024 1

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125 results

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Page 1
Novel germ line DDX41 mutations define families with a lower age of MDS/AML onset and lymphoid malignancies.
Lewinsohn M, Brown AL, Weinel LM, Phung C, Rafidi G, Lee MK, Schreiber AW, Feng J, Babic M, Chong CE, Lee Y, Yong A, Suthers GK, Poplawski N, Altree M, Phillips K, Jaensch L, Fine M, D'Andrea RJ, Lewis ID, Medeiros BC, Pollyea DA, King MC, Walsh T, Keel S, Shimamura A, Godley LA, Hahn CN, Churpek JE, Scott HS. Lewinsohn M, et al. Among authors: suthers gk. Blood. 2016 Feb 25;127(8):1017-23. doi: 10.1182/blood-2015-10-676098. Epub 2015 Dec 28. Blood. 2016. PMID: 26712909 Free PMC article.
Fronto-facio-nasal dysplasia.
Suthers G, David D, Clark B. Suthers G, et al. Clin Dysmorphol. 1997 Jul;6(3):245-9. doi: 10.1097/00019605-199707000-00008. Clin Dysmorphol. 1997. PMID: 9220195 Review.
Pharmacogenetics of statin intolerance.
Suthers G, Somogyi AA. Suthers G, et al. Intern Med J. 2020 Apr;50(4):506-507. doi: 10.1111/imj.14788. Intern Med J. 2020. PMID: 32270606 No abstract available.
The psychosocial impact of prostate cancer screening for BRCA1 and BRCA2 carriers.
Bancroft EK, Page EC, Brook MN, Pope J, Thomas S, Myhill K, Helfand BT, Talaty P, Ong KR, Douglas E, Cook J, Rosario DJ, Salinas M, Buys SS, Anson J, Davidson R, Longmuir M, Side L, Eccles DM, Tischkowitz M, Taylor A, Cruellas M, Ballestero EP, Cleaver R, Varughese M, Barwell J, LeButt M, Greenhalgh L, Hart R, Azzabi A, Jobson I, Cogley L, Evans DG, Rothwell J, Taylor N, Hogben M, Saya S; IMPACT Study Steering Committee; IMPACT Collaborators; Eeles RA, Aaronson NK. Bancroft EK, et al. BJU Int. 2024 Sep;134(3):484-500. doi: 10.1111/bju.16432. Epub 2024 Jun 5. BJU Int. 2024. PMID: 38839570
Phenotypic heterogeneity and the single gene.
Suthers GK, Davies KE. Suthers GK, et al. Am J Hum Genet. 1992 May;50(5):887-91. Am J Hum Genet. 1992. PMID: 1570841 Free PMC article. No abstract available.
Mutations, malformations and mortality.
Suthers G. Suthers G. J Paediatr Child Health. 1996 Feb;32(1):10-5. doi: 10.1111/j.1440-1754.1996.tb01532.x. J Paediatr Child Health. 1996. PMID: 8652204 Review.
Carrier screening "within the panel".
Suthers G, Mina K. Suthers G, et al. Genet Med. 2019 May;21(5):1257. doi: 10.1038/s41436-018-0317-9. Epub 2018 Oct 16. Genet Med. 2019. PMID: 30327542 Free article. No abstract available.
125 results