Gaia Andreoletti

InstitutionDepartment of Pediatrics
AddressSan Francisco
California
United States
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    Publication Timeline
    COVID-19 publications
    Bar chart showing 1 Covid-19 publications, with a maximum of 1 publications in June 2021
    All Publications
    Bar chart showing 14 publications over 6 distinct years, with a maximum of 6 publications in 2017
    These graphs show COVID-19 publications by month since August 2019 and all publications written by authors of COVID-19 publications over the past 30 years.

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    Publication Field Summary
    This graph shows the number and percent of publications by field. Fields are based on how the National Library of Medicine (NLM) classifies the publications' journals and might not represent the specific topics of the publications. Note that an individual publication can be assigned to more than one field. As a result, the publication counts in this graph might add up to more than the number of publications the person has written. To see the data as text, click here.
    Publication List
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications.
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    PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Le BL, Andreoletti G, Oskotsky T, Vallejo-Gracia A, Rosales R, Yu K, Kosti I, Leon KE, Bunis DG, Li C, Kumar GR, White KM, GarcĂ­a-Sastre A, Ott M, Sirota M. Transcriptomics-based drug repositioning pipeline identifies therapeutic candidates for COVID-19. Sci Rep. 2021 06 10; 11(1):12310. PMID: 34112877.
      Citations: 4     Fields:    Translation:HumansCells
    2. Mercer CL, Andreoletti G, Carroll A, Salmon AP, Temple IK, Ennis S. Familial Ebstein Anomaly: Whole Exome Sequencing Identifies Novel Phenotype Associated With FLNA. Circ Cardiovasc Genet. 2017 Dec; 10(6). PMID: 29237676.
      Citations: 4     Fields:    Translation:HumansCells
    3. Hoskins RA, Repo S, Barsky D, Andreoletti G, Moult J, Brenner SE. Reports from CAGI: The Critical Assessment of Genome Interpretation. Hum Mutat. 2017 09; 38(9):1039-1041. PMID: 28817245.
      Citations: 19     Fields:    Translation:Humans
    4. Seaby EG, Gilbert RD, Andreoletti G, Pengelly RJ, Mercer C, Hunt D, Ennis S. Unexpected Findings in a Child with Atypical Hemolytic Uremic Syndrome: An Example of How Genomics Is Changing the Clinical Diagnostic Paradigm. Front Pediatr. 2017; 5:113. PMID: 28589114.
      Citations:    
    5. Andreoletti G, Shakhnovich V, Christenson K, Coelho T, Haggarty R, Afzal NA, Batra A, Petersen BS, Mort M, Beattie RM, Ennis S. Exome Analysis of Rare and Common Variants within the NOD Signaling Pathway. Sci Rep. 2017 04 19; 7:46454. PMID: 28422189.
      Citations: 5     Fields:    Translation:HumansCells
    6. Douglas AG, Andreoletti G, Talbot K, Hammans SR, Singh J, Whitney A, Ennis S, Foulds NC. ADCY5-related dyskinesia presenting as familial myoclonus-dystonia. Neurogenetics. 2017 Apr; 18(2):111-117. PMID: 28229249.
      Citations: 10     Fields:    Translation:Humans
    7. Takahashi S, Andreoletti G, Chen R, Munehira Y, Batra A, Afzal NA, Beattie RM, Bernstein JA, Ennis S, Snyder M. De novo and rare mutations in the HSPA1L heat shock gene associated with inflammatory bowel disease. Genome Med. 2017 01 26; 9(1):8. PMID: 28126021.
      Citations: 8     Fields:    Translation:HumansCells
    8. Andreoletti G, Seaby EG, Dewing JM, O'Kelly I, Lachlan K, Gilbert RD, Ennis S. AMMECR1: a single point mutation causes developmental delay, midface hypoplasia and elliptocytosis. J Med Genet. 2017 04; 54(4):269-277. PMID: 27811305.
      Citations: 5     Fields:    Translation:HumansCells
    9. Coelho T, Andreoletti G, Ashton JJ, Batra A, Afzal NA, Gao Y, Williams AP, Beattie RM, Ennis S. Genes implicated in thiopurine-induced toxicity: Comparing TPMT enzyme activity with clinical phenotype and exome data in a paediatric IBD cohort. Sci Rep. 2016 10 05; 6:34658. PMID: 27703193.
      Citations: 10     Fields:    Translation:HumansCTClinical Trials
    10. Ashton JJ, Andreoletti G, Coelho T, Haggarty R, Batra A, Afzal NA, Beattie RM, Ennis S. Identification of Variants in Genes Associated with Single-gene Inflammatory Bowel Disease by Whole-exome Sequencing. Inflamm Bowel Dis. 2016 10; 22(10):2317-27. PMID: 27537055.
      Citations: 11     Fields:    Translation:Humans
    11. Seaby EG, Gilbert RD, Pengelly RJ, Andreoletti G, Clarke A, Ennis S. Progressive myoclonic epilepsy with Fanconi syndrome. JRSM Open. 2016 Jun; 7(6):2054270415623145. PMID: 27293772.
      Citations:    
    12. Pengelly RJ, Gibson J, Andreoletti G, Collins A, Mattocks CJ, Ennis S. Erratum to: a SNP profiling panel for sample tracking in whole-exome sequencing studies. Genome Med. 2015; 7(1):44. PMID: 25949530.
      Citations: 3     Fields:    
    13. Coelho T, Andreoletti G, Ashton JJ, Pengelly RJ, Gao Y, RamaKrishnan A, Batra A, Beattie RM, Williams AP, Ennis S. Immuno-genomic profiling of patients with inflammatory bowel disease: a systematic review of genetic and functional in vivo studies of implicated genes. Inflamm Bowel Dis. 2014 Oct; 20(10):1813-9. PMID: 25171511.
      Citations: 3     Fields:    Translation:Humans
    14. Pengelly RJ, Gibson J, Andreoletti G, Collins A, Mattocks CJ, Ennis S. A SNP profiling panel for sample tracking in whole-exome sequencing studies. Genome Med. 2013; 5(9):89. PMID: 24070238.
      Citations: 26     Fields: