Walid Abi Habib

Genetic disruption of the oncogenic HMGA2–PLAG1–IGF2 pathway causes fetal growth restriction

Walid Abi Habib, Frédéric Brioude, Thomas Édouard et al. · Genetics in Medicine · 2017 · 137 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Extensive investigation of the IGF2/H19 imprinting control region reveals novel OCT4/SOX2 binding site defects associated with specific methylation patterns in Beckwith-Wiedemann syndrome

Walid Abi Habib, Salah Azzi, Frédéric Brioude et al. · Human Molecular Genetics · 2014 · 72 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Chromosome 14q32.2 Imprinted Region Disruption as an Alternative Molecular Diagnosis of Silver-Russell Syndrome

Sophie Geoffron, Walid Abi Habib, Sandra Chantot‐Bastaraud et al. · The Journal of Clinical Endocrinology & Metabolism · 2018 · 60 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Transcriptional profiling at the <i>DLK1/MEG3</i> domain explains clinical overlap between imprinting disorders

Walid Abi Habib, Frédéric Brioude, Salah Azzi et al. · Science Advances · 2019 · 51 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

BISCUIT: an efficient, standards-compliant tool suite for simultaneous genetic and epigenetic inference in bulk and single-cell studies

Wanding Zhou, Benjamin K. Johnson, Jacob Morrison et al. · Nucleic Acids Research · 2024 · 44 citations · Full text

Life Sciences, Bioinformatics, Genetics +17