VPOT: A Customizable Variant Prioritization Ordering Tool for Annotated Variants by Eddie Ip, Gavin Chapman, David Winlaw, Sally L. Dunwoodie, Eleni Giannoulatou

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An image analysis protocol using CellProfiler for automated quantification of post-ischemic cardiac parameters by Alexander O. Ward, Vaibhao Janbandhu, Gavin Chapman, Sally L. Dunwoodie, Richard P. Harvey

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Myeloid-CITED2 Deficiency Exacerbates Diet-Induced Obesity and Pro-Inflammatory Macrophage Response by Atif Zafar, Hang Pong Ng, E. Ricky Chan, Sally L. Dunwoodie, Ganapati H. Mahabeleshwar

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Quantitative 3D analysis and visualization of cardiac fibrosis by microcomputed tomography by Vaibhao Janbandhu, Ella M.M.A. Martin, Gavin Chapman, Sally L. Dunwoodie, Richard P. Harvey

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Maternal heterozygosity of Slc6a19 causes metabolic perturbation and congenital NAD deficiency disorder in mice by Hartmut Cuny, Kayleigh Bozon, Rosemary B. Kirk, Delicia Z. Sheng, Stefan Bröer, Sally L. Dunwoodie

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ConanVarvar: a versatile tool for the detection of large syndromic copy number variation from whole-genome sequencing data by Mikhail Gudkov, Loïc Thibaut, Matloob Khushi, Gillian M. Blue, David S. Winlaw, Sally L. Dunwoodie, Eleni Giannoulatou

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Cited1 deficiency suppresses intestinal tumorigenesis. by Valérie Méniel, Fei Song, Toby Phesse, Madeleine Young, Oliver Poetz, Lee Parry, John R Jenkins, Geraint T Williams, Sally L Dunwoodie, Alastair Watson, Alan R Clarke

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Quantitative trait and transcriptome analysis of genetic complexity underpinning cardiac interatrial septation in mice using an advanced intercross line by Mahdi Moradi Marjaneh, Edwin P Kirk, Ralph Patrick, Dimuthu Alankarage, David T Humphreys, Gonzalo Del Monte-Nieto, Paola Cornejo-Paramo, Vaibhao Janbandhu, Tram B Doan, Sally L Dunwoodie, Emily S Wong, Chris Moran, Ian CA Martin, Peter C Thomson, Richard P Harvey

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NKX2-5 mutations causative for congenital heart disease retain functionality and are directed to hundreds of targets by Romaric Bouveret, Ashley J Waardenberg, Nicole Schonrock, Mirana Ramialison, Tram Doan, Danielle de Jong, Antoine Bondue, Gurpreet Kaur, Stephanie Mohamed, Hananeh Fonoudi, Chiann-mun Chen, Merridee A Wouters, Shoumo Bhattacharya, Nicolas Plachta, Sally L Dunwoodie, Gavin Chapman, Cédric Blanpain, Richard P Harvey

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A Genetics-First Approach Revealed Monogenic Disorders in Patients With ARM and VACTERL Anomalies by Romy van de Putte, Gabriel C. Dworschak, Gabriel C. Dworschak, Erwin Brosens, Erwin Brosens, Heiko M. Reutter, Heiko M. Reutter, Carlo L. M. Marcelis, Rocio Acuna-Hidalgo, Nehir E. Kurtas, Marloes Steehouwer, Sally L. Dunwoodie, Eberhard Schmiedeke, Stefanie Märzheuser, Nicole Schwarzer, Alice S. Brooks, Annelies de Klein, Cornelius E. J. Sloots, Dick Tibboel, Giulia Brisighelli, Giulia Brisighelli, Anna Morandi, Maria F. Bedeschi, Michael D. Bates, Michael D. Bates, Marc A. Levitt, Marc A. Levitt, Marc A. Levitt, Alberto Peña, Alberto Peña, Alberto Peña, Ivo de Blaauw, Nel Roeleveld, Han G. Brunner, Han G. Brunner, Iris A. L. M. van Rooij, Alexander Hoischen, Alexander Hoischen

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