Publications by authors named "Christopher Fincher"

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A transcription factor atlas of stem cell fate in planarians.
Hunter O King, Kwadwo E Owusu-Boaitey, Christopher T Fincher, Peter W Reddien

Cell Rep· March 2024

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Co-Occurrence of Pallister-Killian Syndrome and Burkitt Lymphoma in a Patient with Near-Normal Neurocognitive Development.
Kosuke Izumi, Rebecca D Ganetzky, Gerald B W Wertheim, Cara M Skraban, Emma C Bedoukian, Christopher Fincher

Mol Syndromol· August 2023

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Muscle and neuronal guidepost-like cells facilitate planarian visual system regeneration.
M Lucila Scimone, Kutay D Atabay, Christopher T Fincher, Ashley R Bonneau, Dayan J Li

Science· June 2020

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foxF-1 Controls Specification of Non-body Wall Muscle and Phagocytic Cells in Planarians.
M Lucila Scimone, Omri Wurtzel, Kathryn Malecek, Christopher T Fincher, Isaac M Oderberg

Curr Biol· December 2018

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Cell type transcriptome atlas for the planarian .
Christopher T Fincher, Omri Wurtzel, Thom de Hoog, Kellie M Kravarik, Peter W Reddien

Science· May 2018

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Erratum: A positional Toll receptor code directs convergent extension in Drosophila.
Adam C Paré, Athea Vichas, Christopher T Fincher, Zachary Mirman, Dene L Farrell

Nature· November 2015

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A positional Toll receptor code directs convergent extension in Drosophila.
Adam C Paré, Athea Vichas, Christopher T Fincher, Zachary Mirman, Dene L Farrell

Nature· November 2014

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Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance.
Frank J Kaiser, Morad Ansari, Diana Braunholz, María Concepción Gil-Rodríguez, Christophe Decroos, Christopher T Fincher

Hum Mol Genet· June 2014

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Duplication 12p and Pallister-Killian syndrome: a case report and review of the literature toward defining a Pallister-Killian syndrome minimal critical region.
Kosuke Izumi, Laura K Conlin, Donna Berrodin, Christopher Fincher, Alisha Wilkens

Am J Med Genet A· December 2012

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Isolated NIBPL missense mutations that cause Cornelia de Lange syndrome alter MAU2 interaction.
Diana Braunholz, Melanie Hullings, María Concepcion Gil-Rodríguez, Christopher T Fincher, Mark B Mallozzi

Eur J Hum Genet· March 2012

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