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

Year Number of Results
2000 1
2001 2
2002 1
2004 2
2005 5
2006 6
2007 4
2008 1
2009 3
2010 5
2011 7
2012 7
2013 7
2014 6
2015 6
2016 8
2017 2
2018 5
2019 2
2020 2
2021 5
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78 results
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Page 1
Truncating mutations in APP cause a distinct neurological phenotype.
Klein S, Goldman A, Lee H, Ghahremani S, Bhakta V; UCLA Clinical Genomics Center, Nelson SF, Martinez-Agosto JA. Klein S, et al. Among authors: bhakta v. Ann Neurol. 2016 Sep;80(3):456-60. doi: 10.1002/ana.24727. Epub 2016 Aug 4. Ann Neurol. 2016. PMID: 27422356 Free PMC article.
Molecular analysis of precursor lesions in familial pancreatic cancer.
Crnogorac-Jurcevic T, Chelala C, Barry S, Harada T, Bhakta V, Lattimore S, Jurcevic S, Bronner M, Lemoine NR, Brentnall TA. Crnogorac-Jurcevic T, et al. Among authors: bhakta v. PLoS One. 2013;8(1):e54830. doi: 10.1371/journal.pone.0054830. Epub 2013 Jan 23. PLoS One. 2013. PMID: 23372777 Free PMC article.
78 results
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