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

Year Number of Results
2000 3
2001 5
2002 3
2003 4
2004 1
2005 1
2006 1
2008 1
2010 1
2011 2
2012 3
2013 1
2014 1
2016 1
2017 1
2018 3
2019 1
2020 1
2022 0
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30 results
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Page 1
Advances in neuroimaging.
Rodie ME, Forbes KP, Muir K. Rodie ME, et al. Among authors: forbes kp. Endocr Dev. 2014;27:63-75. doi: 10.1159/000363628. Epub 2014 Sep 9. Endocr Dev. 2014. PMID: 25247645 Review.
ErCas12a CRISPR-MAD7 for Model Generation in Human Cells, Mice, and Rats.
Liu Z, Schiel JA, Maksimova E, Strezoska Ž, Zhao G, Anderson EM, Wu Y, Warren J, Bartels A, van Brabant Smith A, Lowe CE, Forbes KP. Liu Z, et al. Among authors: forbes kp. CRISPR J. 2020 Apr;3(2):97-108. doi: 10.1089/crispr.2019.0068. CRISPR J. 2020. PMID: 32315227 Free PMC article.
Multishot diffusion-weighted FSE using PROPELLER MRI.
Pipe JG, Farthing VG, Forbes KP. Pipe JG, et al. Among authors: forbes kp. Magn Reson Med. 2002 Jan;47(1):42-52. doi: 10.1002/mrm.10014. Magn Reson Med. 2002. PMID: 11754441 Free article.
Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated with Craniofacial, Neurological, Cardiovascular, and Skeletal Features.
Turnpenny PD, Wright MJ, Sloman M, Caswell R, van Essen AJ, Gerkes E, Pfundt R, White SM, Shaul-Lotan N, Carpenter L, Schaefer GB, Fryer A, Innes AM, Forbes KP, Chung WK, McLaughlin H, Henderson LB, Roberts AE, Heath KE, Paumard-Hernández B, Gener B; DDD study, Fawcett KA, Gjergja-Juraški R, Pilz DT, Fry AE. Turnpenny PD, et al. Among authors: forbes kp. Am J Hum Genet. 2018 Nov 1;103(5):786-793. doi: 10.1016/j.ajhg.2018.09.012. Epub 2018 Oct 18. Am J Hum Genet. 2018. PMID: 30343942 Free PMC article.
Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated with Craniofacial, Neurological, Cardiovascular, and Skeletal Features.
Turnpenny PD, Wright MJ, Sloman M, Caswell R, van Essen AJ, Gerkes E, Pfundt R, White SM, Shaul-Lotan N, Carpenter L, Schaefer GB, Fryer A, Innes AM, Forbes KP, Chung WK, McLaughlin H, Henderson LB, Roberts AE, Heath KE, Paumard-Hernández B, Gener B; DDD study, Fawcett KA, Gjergja-Juraški R, Pilz DT, Fry AE. Turnpenny PD, et al. Among authors: forbes kp. Am J Hum Genet. 2018 Dec 6;103(6):1054-1055. doi: 10.1016/j.ajhg.2018.11.009. Am J Hum Genet. 2018. PMID: 30526864 Free PMC article. No abstract available.
30 results