Medecine and Health

in-vitro Transcription in-vitro Diagnostics; Genomic Imprinting; DNA methylations; ingle cell NGS

Beckwith–Wiedemann Russell–Silver Syndromes: from new molecular insights to the comprehension of imprinting regulationAzzi, Salah; Abi Habib, Walid; Netchine, Irene; ;Current Opinion in Endocrinology, Diabetes and ObesityExtensive investigation of the IGF2/H19 imprinting control region reveals novel OCT4/SOX2 binding site defects associated with specific methylation patterns in Beckwith-Wiedemann syndrome;Abi Habib, Walid; Azzi, Salah; Brioude, Frédéric; Steunou, Virginie; Thibaud, Nathalie; Neves, Cristina Das; Le Jule, Marilyne; Chantot-Bastaraud, Sandra; Keren, Boris; Lyonnet, Stanislas; ;Human molecular geneticsComplex Tissue‐Specific Epigenotypes in Russell–Silver Syndrome Associated with 11p15 ICR1 Hypomethylation;Azzi, Salah; Blaise, Annick; Steunou, Virginie; Harbison, Madeleine D; Salem, Jennifer; Brioude, Frédéric; Rossignol, Sylvie; Abi Habib, Walid; Thibaud, Nathalie; Neves, Cristina Das; ;Human mutationExhaustive methylation analysis revealed uneven profiles of methylation at IGF2/ICR1/H19 11p15 loci in Russell Silver syndrome;Azzi, Salah; Steunou, Virginie; Tost, Jörg; Rossignol, Sylvie; Thibaud, Nathalie; Neves, Cristina Das; Le Jule, Marilyne; Abi Habib, Walid; Blaise, Annick; Koudou, Yves; ;Journal of medical geneticsLiver X Receptors differentially modulate central myelin gene mRNA levels in a region-, age-and isoform-specific manner;Grenier, Julien; Abi Habib, Walid; Massaad, Charbel; Meffre, Delphine; ;The Journal of steroid biochemistry and molecular biology11p15 ICR1 partial deletions associated with IGF2/H19 DMR hypomethylation and Silver–Russell syndrome;Abi Habib, Walid; Brioude, Frederic; Azzi, Salah; Salem, Jennifer; Das Neves, Cristina; Personnier, Claire; Chantot‐Bastaraud, Sandra; Keren, Boris; Le Bouc, Yves; Harbison, Madeleine D; ;Human MutationGenetic disruption of the oncogenic HMGA2-PLAG1-IGF2 pathway causes fetal growth restriction.;Abi Habib, Walid; Brioude, Frédéric; Edouard, Thomas; Bennett, James T; Lienhardt-Roussie, Anne; Tixier, Frédérique; Salem, Jennifer; Yuen, Tony; Azzi, Salah; Le Bouc, Yves; ;Genetics in medicine: official journal of the American College of Medical GeneticsChromosome 14q32. 2 imprinted region disruption as an alternative molecular diagnosis of Silver-Russell syndrome;Geoffron, Sophie; Abi Habib, Walid; Chantot-Bastaraud, Sandra; Dubern, Beatrice; Steunou, Virginie; Azzi, Salah; Afenjar, Alexandra; Busa, Tiffanny; Pinheiro Canton, Ana; Chalouhi, Christel; ;The Journal of Clinical Endocrinology & MetabolismDiagnosis of silver-russell syndrome in patients with chromosome 14q32. 2 imprinted region disruption: phenotypic and molecular analysis;Geoffron, Sophie; Habib, Walid Abi; Chantot-Bastaraud, Sandra; Harbison, Madeleine; Salem, Jenifer; Brioude, Frederic; Netchine, Irene; Giabicani, Eloise; ;HORMONE RESEARCH IN PAEDIATRICSTranscriptional profiling at the DLK1/MEG3 domain explains clinical overlap between imprinting disorders;Abi Habib, Walid; Brioude, Frédéric; Azzi, Salah; Rossignol, Sylvie; Linglart, Agnès; Sobrier, Marie-Laure; Giabicani, Éloïse; Steunou, Virginie; Harbison, Madeleine D; Le Bouc, Yves; ;Science AdvancesNormal Growth despite Combined Pituitary Hormone Deficiency;El Kholy, Mohamed; Elsedfy, Heba; Perin, Laurence; Abi Habib, Walid; Thibaud, Nathalie; Bozzola, Mauro; Rossignol, Sylvie; Leneuve, Patricia; Godeau, François; Chantot-Bastaraud, Sandra; ;Hormone research in paediatricsIncreasing knowledge in IGF1R defects: lessons from 35 new patients;Giabicani, Eloïse; Willems, Marjolaine; Steunou, Virginie; Chantot-Bastaraud, Sandra; Thibaud, Nathalie; Abi Habib, Walid; Azzi, Salah; Lam, Bich; Bérard, Laurence; Bony-Trifunovic, Hélène; ;Journal of medical geneticsLebanese SARS-CoV-2 genomics: 24 months of the pandemic;Fayad, Nancy; Abi Habib, Walid; El-Shesheny, Rabeh; Kandeil, Ahmed; Mourad, Youmna; Mokhbat, Jacques; Kayali, Ghazi; Goldstein, Jimi; Abdallah, Jad; ;Virus ResearchDetection of Coronaviruses in Bats in Lebanon during 2020;Kandeil, Ahmed; Abi-Said, Mounir; Badra, Rebecca; El-Shesheny, Rabeh; Al-Karmalawy, Ahmed A; Alnajjar, Radwan; Khalid, Zumama; Kamel, Mina Nabil; Abi Habib, Walid; Abdallah, Jad; ;PathogensBISCUIT: an efficient, standards-compliant tool suite for simultaneous genetic and epigenetic inference in bulk and single-cell studies;Zhou, Wanding; Johnson, Benjamin K; Morrison, Jacob; Beddows, Ian; Eapen, James; Katsman, Efrat; Semwal, Ayush; Habib, Walid Abi; Heo, Lyong; Laird, Peter W; ;Nucleic Acids ResearchHigh-coverage allele-resolved single-cell DNA methylation profiling by scDEEP-mC reveals cell lineage, X-inactivation state, and replication dynamics;Spix, Nathan J; Habib, Walid Abi; Zhang, Zhouwei; Eugster, Emily; Milliron, Hsiao-yun; Sokol, David; Lee, Kwang-Ho; Nolte, Paula A; Endicott, Jamie L; Krzyzanowski, Kelly F; ;bioRxiv