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Alal Eran, Ph.D.

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Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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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. Dinstein I, Arazi A, Golan HM, Koller J, Elliott E, Gozes I, Shulman C, Shifman S, Raz R, Davidovitch N, Gev T, Aran A, Stolar O, Ben-Itzchak E, Snir IM, Israel-Yaacov S, Bauminger-Zviely N, Bonneh YS, Gal E, Shamay-Tsoory S, Zait AZ, Hadad BS, Gross R, Faroy M, Bachmat E, Eran A, Uzefovsky F, Flusser H, Michaelovski A, Levine SZ, Kodesh A, Gothelf D, Marom D, Feldman HB, Yosef DB, Bloch AM, Sadaka Y, Schtaierman C, Davidovitch M, Begin M, Gabis LV, Zachor D, Menashe I, Golan O, Meiri G. The National Autism Database of Israel: a Resource for Studying Autism Risk Factors, Biomarkers, Outcome Measures, and Treatment Efficacy. J Mol Neurosci. 2020 09; 70(9):1303-1312. PMID: 32720227.
    Citations:    
  2. Luo Y, Eran A, Palmer N, Avillach P, Levy-Moonshine A, Szolovits P, Kohane IS. A multidimensional precision medicine approach identifies an autism subtype characterized by dyslipidemia. Nat Med. 2020 Sep; 26(9):1375-1379. PMID: 32778826.
    Citations:    
  3. Tal Y, Adini A, Eran A, Adini I. Racial disparity in Covid-19 mortality rates - A plausible explanation. Clin Immunol. 2020 08; 217:108481. PMID: 32473354.
    Citations:    
  4. Mao C, Eran A, Luo Y. Efficient Genomic Interval Queries Using Augmented Range Trees. Sci Rep. 2019 03 25; 9(1):5059. PMID: 30911095.
    Citations:    
  5. Palmer N, Beam A, Agniel D, Eran A, Manrai A, Spettell C, Steinberg G, Mandl K, Fox K, Nelson SF, Kohane I. Association of Sex With Recurrence of Autism Spectrum Disorder Among Siblings. JAMA Pediatr. 2017 11 01; 171(11):1107-1112. PMID: 28973142.
    Citations: 2     Fields:    Translation:Humans
  6. Murphy SN, Avillach P, Bellazzi R, Phillips L, Gabetta M, Eran A, McDuffie MT, Kohane IS. Combining clinical and genomics queries using i2b2 - Three methods. PLoS One. 2017; 12(4):e0172187. PMID: 28388645.
    Citations: 1     Fields:    Translation:Humans
  7. Somekh J, Peleg M, Eran A, Koren I, Feiglin A, Demishtein A, Shiloh R, Heiner M, Kong SW, Elazar Z, Kohane I. A model-driven methodology for exploring complex disease comorbidities applied to autism spectrum disorder and inflammatory bowel disease. J Biomed Inform. 2016 10; 63:366-378. PMID: 27522000.
    Citations: 1     Fields:    Translation:Humans
  8. Vieira NM, Elvers I, Alexander MS, Moreira YB, Eran A, Gomes JP, Marshall JL, Karlsson EK, Verjovski-Almeida S, Lindblad-Toh K, Kunkel LM, Zatz M. Jagged 1 Rescues the Duchenne Muscular Dystrophy Phenotype. Cell. 2015 Nov 19; 163(5):1204-1213. PMID: 26582133.
    Citations: 29     Fields:    Translation:AnimalsCells
  9. Kawahara G, Gasperini MJ, Myers JA, Widrick JJ, Eran A, Serafini PR, Alexander MS, Pletcher MT, Morris CA, Kunkel LM. Dystrophic muscle improvement in zebrafish via increased heme oxygenase signaling. Hum Mol Genet. 2015 Aug 01; 24(15):4480-1. PMID: 26034133.
    Citations: 2     Fields:    
  10. Kawahara G, Gasperini MJ, Myers JA, Widrick JJ, Eran A, Serafini PR, Alexander MS, Pletcher MT, Morris CA, Kunkel LM. Dystrophic muscle improvement in zebrafish via increased heme oxygenase signaling. Hum Mol Genet. 2014 Apr 01; 23(7):1869-78. PMID: 24234649.
    Citations: 10     Fields:    Translation:AnimalsCells
  11. Kohane IS, Eran A. Can we measure autism? Sci Transl Med. 2013 Oct 30; 5(209):209ed18. PMID: 24174324.
    Citations: 2     Fields:    Translation:Humans
  12. Vardarajan BN, Eran A, Jung JY, Kunkel LM, Wall DP. Haplotype structure enables prioritization of common markers and candidate genes in autism spectrum disorder. Transl Psychiatry. 2013 May 28; 3:e262. PMID: 23715297.
    Citations: 9     Fields:    Translation:HumansCells
  13. Kong SW, Collins CD, Shimizu-Motohashi Y, Holm IA, Campbell MG, Lee IH, Brewster SJ, Hanson E, Harris HK, Lowe KR, Saada A, Mora A, Madison K, Hundley R, Egan J, McCarthy J, Eran A, Galdzicki M, Rappaport L, Kunkel LM, Kohane IS. Characteristics and predictive value of blood transcriptome signature in males with autism spectrum disorders. PLoS One. 2012; 7(12):e49475. PMID: 23227143.
    Citations: 35     Fields:    Translation:HumansCells
  14. Eran A, Li JB, Vatalaro K, McCarthy J, Rahimov F, Collins C, Markianos K, Margulies DM, Brown EN, Calvo SE, Kohane IS, Kunkel LM. Comparative RNA editing in autistic and neurotypical cerebella. Mol Psychiatry. 2013 Sep; 18(9):1041-8. PMID: 22869036.
    Citations: 17     Fields:    Translation:HumansCells
  15. Fisher T, Shamay-Tsoory SG, Eran A, Aharon-Peretz J. Characterization of recovery and neuropsychological consequences of orbitofrontal lesion: A case study. Neurocase. 2011 Jun; 17(3):285-93. PMID: 21667397.
    Citations:    
  16. Eran A, Graham KR, Vatalaro K, McCarthy J, Collins C, Peters H, Brewster SJ, Hanson E, Hundley R, Rappaport L, Holm IA, Kohane IS, Kunkel LM. Comment on "Autistic-like phenotypes in Cadps2-knockout mice and aberrant CADPS2 splicing in autistic patients". J Clin Invest. 2009 Apr; 119(4):679-80; author reply 680-1. PMID: 19339759.
    Citations: 5     Fields:    Translation:HumansAnimalsCells
  17. Eisenberg I, Eran A, Nishino I, Moggio M, Lamperti C, Amato AA, Lidov HG, Kang PB, North KN, Mitrani-Rosenbaum S, Flanigan KM, Neely LA, Whitney D, Beggs AH, Kohane IS, Kunkel LM. Distinctive patterns of microRNA expression in primary muscular disorders. Proc Natl Acad Sci U S A. 2007 Oct 23; 104(43):17016-21. PMID: 17942673.
    Citations: 190     Fields:    Translation:HumansCells
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.