Skip to content

Miss Annie Godwin

Research Associate

  1. 2021
  2. Published

    Biallelic variants in COPB1 cause a novel, severe intellectual disability syndrome with cataracts and variable microcephaly

    William L. Macken, Miss Annie Louise Godwin, Gabrielle Wheway, Karen Stals, Liliya Nazlamova, Sian Ellard, Ahmed Alfares, Taghrid Aloraini, Lamia AlSubaie, Majid Alfadhel & 7 others, Sulaiman Alajaji, Htoo A. Wai, Jay Self, Andrew G.L. Douglas, Alexander P. Kao, Professor Matt Guille & Diana Baralle, 25 Feb 2021, In: Genome Medicine. 13, 1, p. 1-19 19 p., 34.

    Research output: Contribution to journalArticlepeer-review

  3. 2020
  4. Published

    Opposite modulation of RAC1 by mutations in TRIO is associated with distinct, domain specific neurodevelopmental disorders

    Sónia Barbosa, Stephanie Greville-Heygate, Maxime Bonnet, Miss Annie Louise Godwin, Christine Fagotto-Kaufmann, Andrey V. Kajava, Damien Laouteouet, Rebecca Mawby, Htoo Aung Wai, Alexander Dingemans & 28 others, Bert De Vries, Marjorlaine Willems, Yline Capri, Sarju G. Mehta, Helen Cox, David Goudie, Fleur Vansenne, Peter Turnpenny, Marie Vincent, Gaëtan Lesca, Jozef Hertecant, Diana Rodriguez, Gérard Marion, Audrey Putoux, Keri Ramsey, Vincent Cantagrel, Siddharth Banka, Ajoy Sarkar, Marcie Steeves, Michael Parker, Emma Clement, Sébastien Moutton, Frédéric Tran-Mau-Them, Amélie Piton, Professor Matt Guille, Anne Debant, Susanne Schmidt & Diana Baralle, 5 Mar 2020, In: American Journal of Human Genetics. 106, 3, p. 338-355 18 p.

    Research output: Contribution to journalArticlepeer-review

ID: 4685811