Andreoletti G - Search Results

1

Identification of Variants in Genes Associated with Single-gene Inflammatory Bowel Disease by Whole-exome Sequencing.

Ashton JJ, Andreoletti G, Coelho T, Haggarty R, Batra A, Afzal NA, Beattie RM, Ennis S. Ashton JJ, et al. Among authors: andreoletti g. Inflamm Bowel Dis. 2016 Oct;22(10):2317-27. doi: 10.1097/MIB.0000000000000890. Inflamm Bowel Dis. 2016. PMID: 27537055

2

Immuno-genomic profiling of patients with inflammatory bowel disease: a systematic review of genetic and functional in vivo studies of implicated genes.

Coelho T, Andreoletti G, Ashton JJ, Pengelly RJ, Gao Y, RamaKrishnan A, Batra A, Beattie RM, Williams AP, Ennis S. Coelho T, et al. Among authors: andreoletti g. Inflamm Bowel Dis. 2014 Oct;20(10):1813-9. doi: 10.1097/MIB.0000000000000174. Inflamm Bowel Dis. 2014. PMID: 25171511 Review.

3

Exome analysis of patients with concurrent pediatric inflammatory bowel disease and autoimmune disease.

Andreoletti G, Ashton JJ, Coelho T, Willis C, Haggarty R, Gibson J, Holloway J, Batra A, Afzal NA, Beattie RM, Ennis S. Andreoletti G, et al. Inflamm Bowel Dis. 2015 Jun;21(6):1229-36. doi: 10.1097/MIB.0000000000000381. Inflamm Bowel Dis. 2015. PMID: 25895113 Free PMC article.

4

Genes implicated in thiopurine-induced toxicity: Comparing TPMT enzyme activity with clinical phenotype and exome data in a paediatric IBD cohort.

Coelho T, Andreoletti G, Ashton JJ, Batra A, Afzal NA, Gao Y, Williams AP, Beattie RM, Ennis S. Coelho T, et al. Among authors: andreoletti g. Sci Rep. 2016 Oct 5;6:34658. doi: 10.1038/srep34658. Sci Rep. 2016. PMID: 27703193 Free PMC article. Clinical Trial.

5

De novo and rare mutations in the HSPA1L heat shock gene associated with inflammatory bowel disease.

Takahashi S, Andreoletti G, Chen R, Munehira Y, Batra A, Afzal NA, Beattie RM, Bernstein JA, Ennis S, Snyder M. Takahashi S, et al. Among authors: andreoletti g. Genome Med. 2017 Jan 26;9(1):8. doi: 10.1186/s13073-016-0394-9. Genome Med. 2017. PMID: 28126021 Free PMC article.

6

Exome Analysis of Rare and Common Variants within the NOD Signaling Pathway.

Andreoletti G, Shakhnovich V, Christenson K, Coelho T, Haggarty R, Afzal NA, Batra A, Petersen BS, Mort M, Beattie RM, Ennis S. Andreoletti G, et al. Sci Rep. 2017 Apr 19;7:46454. doi: 10.1038/srep46454. Sci Rep. 2017. PMID: 28422189 Free PMC article.

7

Familial Ebstein Anomaly: Whole Exome Sequencing Identifies Novel Phenotype Associated With FLNA.

Mercer CL, Andreoletti G, Carroll A, Salmon AP, Temple IK, Ennis S. Mercer CL, et al. Among authors: andreoletti g. Circ Cardiovasc Genet. 2017 Dec;10(6):e001683. doi: 10.1161/CIRCGENETICS.116.001683. Circ Cardiovasc Genet. 2017. PMID: 29237676

8

A SNP profiling panel for sample tracking in whole-exome sequencing studies.

Pengelly RJ, Gibson J, Andreoletti G, Collins A, Mattocks CJ, Ennis S. Pengelly RJ, et al. Among authors: andreoletti g. Genome Med. 2013 Sep 27;5(9):89. doi: 10.1186/gm492. eCollection 2013. Genome Med. 2013. PMID: 24070238 Free PMC article.

9

AMMECR1: a single point mutation causes developmental delay, midface hypoplasia and elliptocytosis.

Andreoletti G, Seaby EG, Dewing JM, O'Kelly I, Lachlan K, Gilbert RD, Ennis S. Andreoletti G, et al. J Med Genet. 2017 Apr;54(4):269-277. doi: 10.1136/jmedgenet-2016-104100. Epub 2016 Nov 3. J Med Genet. 2017. PMID: 27811305 Free PMC article.

10

Erratum to: a SNP profiling panel for sample tracking in whole-exome sequencing studies.

Pengelly RJ, Gibson J, Andreoletti G, Collins A, Mattocks CJ, Ennis S. Pengelly RJ, et al. Among authors: andreoletti g. Genome Med. 2015 May 7;7(1):44. doi: 10.1186/s13073-015-0163-1. eCollection 2015. Genome Med. 2015. PMID: 25949530 Free PMC article.

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