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

Year Number of Results
1980 1
1988 2
1989 5
1990 1
1991 2
1992 4
1993 1
1995 1
1996 2
1997 2
1999 3
2001 1
2003 1
2005 2
2006 1
2007 1
2008 4
2009 4
2010 2
2011 4
2012 7
2013 5
2014 6
2015 5
2016 4
2017 2
2018 1
2022 0
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69 results
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Page 1
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways.
Cirulli ET, Lasseigne BN, Petrovski S, Sapp PC, Dion PA, Leblond CS, Couthouis J, Lu YF, Wang Q, Krueger BJ, Ren Z, Keebler J, Han Y, Levy SE, Boone BE, Wimbish JR, Waite LL, Jones AL, Carulli JP, Day-Williams AG, Staropoli JF, Xin WW, Chesi A, Raphael AR, McKenna-Yasek D, Cady J, Vianney de Jong JM, Kenna KP, Smith BN, Topp S, Miller J, Gkazi A; FALS Sequencing Consortium, Al-Chalabi A, van den Berg LH, Veldink J, Silani V, Ticozzi N, Shaw CE, Baloh RH, Appel S, Simpson E, Lagier-Tourenne C, Pulst SM, Gibson S, Trojanowski JQ, Elman L, McCluskey L, Grossman M, Shneider NA, Chung WK, Ravits JM, Glass JD, Sims KB, Van Deerlin VM, Maniatis T, Hayes SD, Ordureau A, Swarup S, Landers J, Baas F, Allen AS, Bedlack RS, Harper JW, Gitler AD, Rouleau GA, Brown R, Harms MB, Cooper GM, Harris T, Myers RM, Goldstein DB. Cirulli ET, et al. Among authors: sims kb. Science. 2015 Mar 27;347(6229):1436-41. doi: 10.1126/science.aaa3650. Epub 2015 Feb 19. Science. 2015. PMID: 25700176 Free PMC article.
Von Hippel-Lindau disease: gene to bedside.
Sims KB. Sims KB. Curr Opin Neurol. 2001 Dec;14(6):695-703. doi: 10.1097/00019052-200112000-00004. Curr Opin Neurol. 2001. PMID: 11723376 Review.
Strikingly different clinicopathological phenotypes determined by progranulin-mutation dosage.
Smith KR, Damiano J, Franceschetti S, Carpenter S, Canafoglia L, Morbin M, Rossi G, Pareyson D, Mole SE, Staropoli JF, Sims KB, Lewis J, Lin WL, Dickson DW, Dahl HH, Bahlo M, Berkovic SF. Smith KR, et al. Among authors: sims kb. Am J Hum Genet. 2012 Jun 8;90(6):1102-7. doi: 10.1016/j.ajhg.2012.04.021. Epub 2012 May 17. Am J Hum Genet. 2012. PMID: 22608501 Free PMC article.
Mutations in the Norrie disease gene.
Schuback DE, Chen ZY, Craig IW, Breakefield XO, Sims KB. Schuback DE, et al. Among authors: sims kb. Hum Mutat. 1995;5(4):285-92. doi: 10.1002/humu.1380050403. Hum Mutat. 1995. PMID: 7627181
69 results