Robinson PN - Search Results

1

A systematic, large-scale comparison of transcription factor binding site models.

Hombach D, Schwarz JM, Robinson PN, Schuelke M, Seelow D. Hombach D, et al. Among authors: robinson pn. BMC Genomics. 2016 May 21;17:388. doi: 10.1186/s12864-016-2729-8. BMC Genomics. 2016. PMID: 27209209 Free PMC article.

2

The Human Phenotype Ontology: a tool for annotating and analyzing human hereditary disease.

Robinson PN, Köhler S, Bauer S, Seelow D, Horn D, Mundlos S. Robinson PN, et al. Am J Hum Genet. 2008 Nov;83(5):610-5. doi: 10.1016/j.ajhg.2008.09.017. Epub 2008 Oct 23. Am J Hum Genet. 2008. PMID: 18950739 Free PMC article.

3

Short ultraconserved promoter regions delineate a class of preferentially expressed alternatively spliced transcripts.

Rödelsperger C, Köhler S, Schulz MH, Manke T, Bauer S, Robinson PN. Rödelsperger C, et al. Among authors: robinson pn. Genomics. 2009 Nov;94(5):308-16. doi: 10.1016/j.ygeno.2009.07.005. Epub 2009 Aug 4. Genomics. 2009. PMID: 19660540 Free article.

4

Composite transcriptome assembly of RNA-seq data in a sheep model for delayed bone healing.

Jäger M, Ott CE, Grünhagen J, Hecht J, Schell H, Mundlos S, Duda GN, Robinson PN, Lienau J. Jäger M, et al. Among authors: robinson pn. BMC Genomics. 2011 Mar 24;12:158. doi: 10.1186/1471-2164-12-158. BMC Genomics. 2011. PMID: 21435219 Free PMC article.

5

Improved exome prioritization of disease genes through cross-species phenotype comparison.

Robinson PN, Köhler S, Oellrich A; Sanger Mouse Genetics Project; Wang K, Mungall CJ, Lewis SE, Washington N, Bauer S, Seelow D, Krawitz P, Gilissen C, Haendel M, Smedley D. Robinson PN, et al. Genome Res. 2014 Feb;24(2):340-8. doi: 10.1101/gr.160325.113. Epub 2013 Oct 25. Genome Res. 2014. PMID: 24162188 Free PMC article.

6

Saturation analysis of ChIP-seq data for reproducible identification of binding peaks.

Hansen P, Hecht J, Ibrahim DM, Krannich A, Truss M, Robinson PN. Hansen P, et al. Among authors: robinson pn. Genome Res. 2015 Sep;25(9):1391-400. doi: 10.1101/gr.189894.115. Epub 2015 Jul 10. Genome Res. 2015. PMID: 26163319 Free PMC article.

7

Crowdsourced direct-to-consumer genomic analysis of a family quartet.

Corpas M, Valdivia-Granda W, Torres N, Greshake B, Coletta A, Knaus A, Harrison AP, Cariaso M, Moran F, Nielsen F, Swan D, Weiss Solís DY, Krawitz P, Schacherer F, Schols P, Yang H, Borry P, Glusman G, Robinson PN. Corpas M, et al. Among authors: robinson pn. BMC Genomics. 2015 Nov 7;16:910. doi: 10.1186/s12864-015-1973-7. BMC Genomics. 2015. PMID: 26547235 Free PMC article.

8

Erratum to: A systematic, large-scale comparison of transcription factor binding site models.

Hombach D, Schwarz JM, Robinson PN, Schuelke M, Seelow D. Hombach D, et al. Among authors: robinson pn. BMC Genomics. 2016 Jul 20;17(1):502. doi: 10.1186/s12864-016-2818-8. BMC Genomics. 2016. PMID: 27440159 Free PMC article. No abstract available.

9

Q-nexus: a comprehensive and efficient analysis pipeline designed for ChIP-nexus.

Hansen P, Hecht J, Ibn-Salem J, Menkuec BS, Roskosch S, Truss M, Robinson PN. Hansen P, et al. Among authors: robinson pn. BMC Genomics. 2016 Nov 4;17(1):873. doi: 10.1186/s12864-016-3164-6. BMC Genomics. 2016. PMID: 27814676 Free PMC article.

10

Harmonising phenomics information for a better interoperability in the rare disease field.

Maiella S, Olry A, Hanauer M, Lanneau V, Lourghi H, Donadille B, Rodwell C, Köhler S, Seelow D, Jupp S, Parkinson H, Groza T, Brudno M, Robinson PN, Rath A. Maiella S, et al. Among authors: robinson pn. Eur J Med Genet. 2018 Nov;61(11):706-714. doi: 10.1016/j.ejmg.2018.01.013. Epub 2018 Feb 7. Eur J Med Genet. 2018. PMID: 29425702 Review.

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