Similar articles for PMID: 18989397

Year	Number of Results
1999	1
2000	1
2002	2
2003	3
2004	4
2005	5
2006	3
2007	3
2008	3
2009	3
2010	5
2011	4
2012	3
2013	6
2014	4
2015	6
2016	4
2017	8
2018	2
2019	9
2020	3
2021	3
2024	0

1

Genome-wide analysis of human disease alleles reveals that their locations are correlated in paralogous proteins.

Yandell M, Moore B, Salas F, Mungall C, MacBride A, White C, Reese MG. Yandell M, et al. PLoS Comput Biol. 2008 Nov;4(11):e1000218. doi: 10.1371/journal.pcbi.1000218. Epub 2008 Nov 7. PLoS Comput Biol. 2008. PMID: 18989397 Free PMC article.

2

SNP-VISTA: an interactive SNP visualization tool.

Shah N, Teplitsky MV, Minovitsky S, Pennacchio LA, Hugenholtz P, Hamann B, Dubchak IL. Shah N, et al. BMC Bioinformatics. 2005 Dec 8;6:292. doi: 10.1186/1471-2105-6-292. BMC Bioinformatics. 2005. PMID: 16336665 Free PMC article.

3

Functional and Structural Consequence of Rare Exonic Single Nucleotide Polymorphisms: One Story, Two Tales.

Gu W, Gurguis CI, Zhou JJ, Zhu Y, Ko EA, Ko JH, Wang T, Zhou T. Gu W, et al. Genome Biol Evol. 2015 Oct 9;7(10):2929-40. doi: 10.1093/gbe/evv191. Genome Biol Evol. 2015. PMID: 26454016 Free PMC article.

4

MAPPIN: a method for annotating, predicting pathogenicity and mode of inheritance for nonsynonymous variants.

Gosalia N, Economides AN, Dewey FE, Balasubramanian S. Gosalia N, et al. Nucleic Acids Res. 2017 Oct 13;45(18):10393-10402. doi: 10.1093/nar/gkx730. Nucleic Acids Res. 2017. PMID: 28977528 Free PMC article.

5

Cataloging coding sequence variations in human genome databases.

Won HH, Kim HJ, Lee KA, Kim JW. Won HH, et al. PLoS One. 2008;3(10):e3575. doi: 10.1371/journal.pone.0003575. Epub 2008 Oct 30. PLoS One. 2008. PMID: 18974781 Free PMC article.

6

Pathway networks generated from human disease phenome.

Cirincione AG, Clark KL, Kann MG. Cirincione AG, et al. BMC Med Genomics. 2018 Sep 14;11(Suppl 3):75. doi: 10.1186/s12920-018-0386-2. BMC Med Genomics. 2018. PMID: 30255817 Free PMC article.

7

Variants in Nebulin (NEB) Are Linked to the Development of Familial Primary Angle Closure Glaucoma in Basset Hounds.

Ahram DF, Grozdanic SD, Kecova H, Henkes A, Collin RW, Kuehn MH. Ahram DF, et al. PLoS One. 2015 May 4;10(5):e0126660. doi: 10.1371/journal.pone.0126660. eCollection 2015. PLoS One. 2015. PMID: 25938837 Free PMC article.

8

QTL mapping using high-throughput sequencing.

Jamann TM, Balint-Kurti PJ, Holland JB. Jamann TM, et al. Methods Mol Biol. 2015;1284:257-85. doi: 10.1007/978-1-4939-2444-8_13. Methods Mol Biol. 2015. PMID: 25757777 Review.

9

A visual and curatorial approach to clinical variant prioritization and disease gene discovery in genome-wide diagnostics.

James RA, Campbell IM, Chen ES, Boone PM, Rao MA, Bainbridge MN, Lupski JR, Yang Y, Eng CM, Posey JE, Shaw CA. James RA, et al. Genome Med. 2016 Feb 2;8(1):13. doi: 10.1186/s13073-016-0261-8. Genome Med. 2016. PMID: 26838676 Free PMC article.

10

Towards prediction and prioritization of disease genes by the modularity of human phenome-genome assembled network.

Jiang JQ, Dress AW, Chen M. Jiang JQ, et al. J Integr Bioinform. 2010 Nov 22;7(2). doi: 10.2390/biecoll-jib-2010-149. J Integr Bioinform. 2010. PMID: 21098881 Retracted.

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