Alison J Coffey

ORCID

Publication Activity (10 Years)

Years Active: 2022-2024
Publications (10 Years): 11

Top Venues

European journal of human genetics : EJHG

Human mutation

This page only lists publications with an associated author ORCID identifier.

Publications

Carolyn M Brown, Laura M Amendola, Anjana Chandrasekhar, R Tanner Hagelstrom, Gillian Halter, Akanchha Kesari, Erin Thorpe, Denise L Perry, Ryan J Taft, Alison J Coffey
A framework for the evaluation and reporting of incidental findings in clinical genomic testing. European journal of human genetics : EJHG 32 (6) (2024)
Samin A Sajan, Ralph Gradisch, Florian D Vogel, Alison J Coffey, Daria Salyakina, Diana Soler, Parul Jayakar, Anuj Jayakar, Simona E Bianconi, Annina H Cooper, Shuxi Liu, Nancy William, Ira Benkel-Herrenbrück, Robert Maiwald, Corina Heller, Saskia Biskup, Steffen Leiz, Dominik Sebastian Westphal, Matias Wagner, Amy Clarke, Thomas Stockner, Margot Ernst, Akanchha Kesari, Martin Krenn
De novo variants in GABRA4 are associated with a neurological phenotype including developmental delay, behavioral abnormalities and epilepsy. European journal of human genetics : EJHG 32 (8) (2024)
Samin A Sajan, Ralph Gradisch, Florian D Vogel, Alison J Coffey, Daria Salyakina, Diana Soler, Parul Jayakar, Anuj Jayakar, Simona E Bianconi, Annina H Cooper, Shuxi Liu, Nancy William, Ira Benkel-Herrenbrück, Robert Maiwald, Corina Heller, Saskia Biskup, Steffen Leiz, Dominik Sebastian Westphal, Matias Wagner, Amy Clarke, Thomas Stockner, Margot Ernst, Akanchha Kesari, Martin Krenn
De novo variants in GABRA4 are associated with a neurological phenotype including developmental delay, behavioral abnormalities and epilepsy. European journal of human genetics : EJHG 32 (8) (2024)
Samin A Sajan, Ralph Gradisch, Florian D Vogel, Alison J Coffey, Daria Salyakina, Diana Soler, Parul Jayakar, Anuj Jayakar, Simona E Bianconi, Annina H Cooper, Shuxi Liu, Nancy William, Ira Benkel-Herrenbrück, Robert Maiwald, Corina Heller, Saskia Biskup, Steffen Leiz, Dominik Sebastian Westphal, Matias Wagner, Amy Clarke, Thomas Stockner, Margot Ernst, Akanchha Kesari, Martin Krenn
De novo variants in GABRA4 are associated with a neurological phenotype including developmental delay, behavioral abnormalities and epilepsy. European journal of human genetics : EJHG 32 (8) (2024)
Carolyn M Brown, Laura M Amendola, Anjana Chandrasekhar, R Tanner Hagelstrom, Gillian Halter, Akanchha Kesari, Erin Thorpe, Denise L Perry, Ryan J Taft, Alison J Coffey
A framework for the evaluation and reporting of incidental findings in clinical genomic testing. European journal of human genetics : EJHG (2024)
Samin A Sajan, Ralph Gradisch, Florian D Vogel, Alison J Coffey, Daria Salyakina, Diana Soler, Parul Jayakar, Anuj Jayakar, Simona E Bianconi, Annina H Cooper, Shuxi Liu, Nancy William, Ira Benkel-Herrenbrück, Robert Maiwald, Corina Heller, Saskia Biskup, Steffen Leiz, Dominik Sebastian Westphal, Matias Wagner, Amy Clarke, Thomas Stockner, Margot Ernst, Akanchha Kesari, Martin Krenn
De novo variants in GABRA4 are associated with a neurological phenotype including developmental delay, behavioral abnormalities and epilepsy. European journal of human genetics : EJHG (2024)
Carolyn M Brown, Laura M Amendola, Anjana Chandrasekhar, R Tanner Hagelstrom, Gillian Halter, Akanchha Kesari, Erin Thorpe, Denise L Perry, Ryan J Taft, Alison J Coffey
A framework for the evaluation and reporting of incidental findings in clinical genomic testing. European journal of human genetics : EJHG 32 (6) (2024)
Samin A Sajan, Ralph Gradisch, Florian D Vogel, Alison J Coffey, Daria Salyakina, Diana Soler, Parul Jayakar, Anuj Jayakar, Simona E Bianconi, Annina H Cooper, Shuxi Liu, Nancy William, Ira Benkel-Herrenbrück, Robert Maiwald, Corina Heller, Saskia Biskup, Steffen Leiz, Dominik Sebastian Westphal, Matias Wagner, Amy Clarke, Thomas Stockner, Margot Ernst, Akanchha Kesari, Martin Krenn
De novo variants in GABRA4 are associated with a neurological phenotype including developmental delay, behavioral abnormalities and epilepsy. European journal of human genetics : EJHG 32 (8) (2024)
Samin A Sajan, Ralph Gradisch, Florian D Vogel, Alison J Coffey, Daria Salyakina, Diana Soler, Parul Jayakar, Anuj Jayakar, Simona E Bianconi, Annina H Cooper, Shuxi Liu, Nancy William, Ira Benkel-Herrenbrück, Robert Maiwald, Corina Heller, Saskia Biskup, Steffen Leiz, Dominik Sebastian Westphal, Matias Wagner, Amy Clarke, Thomas Stockner, Margot Ernst, Akanchha Kesari, Martin Krenn
De novo variants in GABRA4 are associated with a neurological phenotype including developmental delay, behavioral abnormalities and epilepsy. European journal of human genetics : EJHG (2024)
Carolyn M Brown, Laura M Amendola, Anjana Chandrasekhar, R Tanner Hagelstrom, Gillian Halter, Akanchha Kesari, Erin Thorpe, Denise L Perry, Ryan J Taft, Alison J Coffey
A framework for the evaluation and reporting of incidental findings in clinical genomic testing. European journal of human genetics : EJHG 32 (6) (2024)
Julie P Taylor, Alka Malhotra, Nicole J Burns, Amanda R Clause, Carolyn M Brown, Brendan T Burns, Anjana Chandrasekhar, Zinayida Schlachetzki, Maren Bennett, Erin Thorpe, Ryan J Taft, Denise L Perry, Alison J Coffey
A clinical laboratory's experience using GeneMatcher-Building stronger gene-disease relationships. Human mutation 43 (6) (2022)

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Publication Activity (10 Years)

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Alison J Coffey