Christopher Fincher - Publications

Affiliations: 
Biology Massachusetts Institute of Technology, Cambridge, MA, United States 

3/9 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Scimone ML, Atabay KD, Fincher CT, Bonneau AR, Li DJ, Reddien PW. Muscle and neuronal guidepost-like cells facilitate planarian visual system regeneration. Science (New York, N.Y.). 368. PMID 32586989 DOI: 10.1126/science.aba3203  0.88
2018 Scimone ML, Wurtzel O, Malecek K, Fincher CT, Oderberg IM, Kravarik KM, Reddien PW. foxF-1 Controls Specification of Non-body Wall Muscle and Phagocytic Cells in Planarians. Current Biology : Cb. 28: 3787-3801.e6. PMID 30471994 DOI: 10.1016/j.cub.2018.10.030  0.88
2018 Fincher CT, Wurtzel O, de Hoog T, Kravarik KM, Reddien PW. Cell type transcriptome atlas for the planarian . Science (New York, N.Y.). PMID 29674431 DOI: 10.1126/science.aaq1736  0.88
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2015 Paré AC, Vichas A, Fincher CT, Mirman Z, Farrell DL, Mainieri A, Zallen JA. Erratum: A positional Toll receptor code directs convergent extension in Drosophila. Nature. PMID 26444242 DOI: 10.1038/nature15719  0.01
2014 Paré AC, Vichas A, Fincher CT, Mirman Z, Farrell DL, Mainieri A, Zallen JA. A positional Toll receptor code directs convergent extension in Drosophila. Nature. 515: 523-7. PMID 25363762 DOI: 10.1038/nature13953  0.01
2014 Kaiser FJ, Ansari M, Braunholz D, Concepción Gil-Rodríguez M, Decroos C, Wilde JJ, Fincher CT, Kaur M, Bando M, Amor DJ, Atwal PS, Bahlo M, Bowman CM, Bradley JJ, Brunner HG, et al. Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance. Human Molecular Genetics. 23: 2888-900. PMID 24403048 DOI: 10.1093/hmg/ddu002  0.01
2012 Izumi K, Conlin LK, Berrodin D, Fincher C, Wilkens A, Haldeman-Englert C, Saitta SC, Zackai EH, Spinner NB, Krantz ID. Duplication 12p and Pallister-Killian syndrome: a case report and review of the literature toward defining a Pallister-Killian syndrome minimal critical region. American Journal of Medical Genetics. Part A. 158: 3033-45. PMID 23169682 DOI: 10.1002/ajmg.a.35500  0.01
2012 Braunholz D, Hullings M, Gil-Rodríguez MC, Fincher CT, Mallozzi MB, Loy E, Albrecht M, Kaur M, Limon J, Rampuria A, Clark D, Kline A, Dalski A, Eckhold J, Tzschach A, et al. Isolated NIBPL missense mutations that cause Cornelia de Lange syndrome alter MAU2 interaction. European Journal of Human Genetics : Ejhg. 20: 271-6. PMID 21934712 DOI: 10.1038/ejhg.2011.175  0.01
2012 Braunholz D, Hullings M, Gil-Rodríguez MC, Fincher CT, Mallozzi MB, Loy E, Albrecht M, Kaur M, Limon J, Rampuria A, Clark D, Kline A, Dalski A, Eckhold J, Tzschach A, et al. Erratum: Isolated NIPBL missense mutations that cause Cornelia de Lange syndrome alter MAU2 interaction European Journal of Human Genetics. 20: 366-366. DOI: 10.1038/ejhg.2011.209  0.01
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