Genetic 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, Harbison, Madeleine D, Netchine, Irène
Published in Genetics in medicine (01.02.2018)
Published in Genetics in medicine (01.02.2018)
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Journal Article
SARS-CoV-2 Variants in Lebanon: Evolution and Current Situation
Fayad, Nancy, Abi Habib, Walid, Kandeil, Ahmed, El-Shesheny, Rabeh, Kamel, Mina Nabil, Mourad, Youmna, Mokhbat, Jacques, Kayali, Ghazi, Goldstein, Jimi, Abdallah, Jad
Published in Biology (Basel, Switzerland) (14.06.2021)
Published in Biology (Basel, Switzerland) (14.06.2021)
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Journal Article
Detection 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, Dhanasekaran, Vijaykrishna, Webby, Richard, Kayali, Ghazi
Published in Pathogens (Basel) (26.06.2023)
Published in Pathogens (Basel) (26.06.2023)
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Journal Article
BISCUIT: 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, Berman, Benjamin P, Triche, Timothy J, Shen, Hui
Published in Nucleic acids research (12.04.2024)
Published in Nucleic acids research (12.04.2024)
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Journal Article
Liver X Receptors differentially modulate central myelin gene mRNA levels in a region-, age- and isoform-specific manner
Shackleford, Ghjuvan’ Ghjacumu, Grenier, Julien, Abi Habib, Walid, Massaad, Charbel, Meffre, Delphine
Published in The Journal of steroid biochemistry and molecular biology (01.05.2017)
Published in The Journal of steroid biochemistry and molecular biology (01.05.2017)
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Journal Article
11p15 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, Bouc, Yves, Harbison, Madeleine D., Netchine, Irene
Published in Human mutation (01.01.2017)
Published in Human mutation (01.01.2017)
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Journal Article
Chromosome 14q32.2 Imprinted Region Disruption as an Alternative Molecular Diagnosis of Silver-Russell Syndrome
Geoffron, Sophie, Abi Habib, Walid, Chantot-Bastaraud, Sandra, Dubern, Béatrice, Steunou, Virginie, Azzi, Salah, Afenjar, Alexandra, Busa, Tiffanny, Pinheiro Canton, Ana, Chalouhi, Christel, Dufourg, Marie-Noëlle, Esteva, Blandine, Fradin, Mélanie, Geneviève, David, Heide, Solveig, Isidor, Bertrand, Linglart, Agnès, Morice Picard, Fanny, Naud-Saudreau, Catherine, Oliver Petit, Isabelle, Philip, Nicole, Pienkowski, Catherine, Rio, Marlène, Rossignol, Sylvie, Tauber, Maithé, Thevenon, Julien, Vu-Hong, Thuy-Ai, Harbison, Madeleine D, Salem, Jennifer, Brioude, Frédéric, Netchine, Irène, Giabicani, Eloïse
Published in The journal of clinical endocrinology and metabolism (01.07.2018)
Published in The journal of clinical endocrinology and metabolism (01.07.2018)
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Journal Article
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
Abi Habib, Walid, Azzi, Salah, Brioude, Frédéric, Steunou, Virginie, Thibaud, Nathalie, Das Neves, Cristina, Le Jule, Marilyne, Chantot-Bastaraud, Sandra, Keren, Boris, Lyonnet, Stanislas, Michot, Caroline, Rossi, Massimiliano, Pasquier, Laurent, Gicquel, Christine, Rossignol, Sylvie, Le Bouc, Yves, Netchine, Irène
Published in Human molecular genetics (01.11.2014)
Published in Human molecular genetics (01.11.2014)
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Journal Article
Increasing 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, Brachet, Cécile, Brischoux-Boucher, Elise, Caldagues, Emmanuelle, Coutant, Regis, Cuvelier, Marie-Laure, Gelwane, Georges, Guemas, Isabelle, Houang, Muriel, Isidor, Bertrand, Jeandel, Claire, Lespinasse, James, Naud-Saudreau, Catherine, Jesuran-Perelroizen, Monique, Perrin, Laurence, Piard, Juliette, Sechter, Claire, Souchon, Pierre-François, Storey, Caroline, Thomas, Domitille, Le Bouc, Yves, Rossignol, Sylvie, Netchine, Irène, Brioude, Frédéric
Published in Journal of medical genetics (01.03.2020)
Published in Journal of medical genetics (01.03.2020)
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Journal Article
Transcriptional 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, Netchine, Irène
Published in Science advances (01.02.2019)
Published in Science advances (01.02.2019)
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Journal Article
Exhaustive 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, Habib, Walid Abi, Blaise, Annick, Koudou, Yves, Busato, Florence, Le Bouc, Yves, Netchine, Irène
Published in Journal of medical genetics (01.01.2015)
Published in Journal of medical genetics (01.01.2015)
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Journal Article
Lebanese SARS-CoV-2 genomics: 24 months of the pandemic
Fayad, Nancy, Habib, Walid Abi, El-Shesheny, Rabeh, Kandeil, Ahmed, Mourad, Youmna, Mokhbat, Jacques, Kayali, Ghazi, Goldstein, Jimi, Abdallah, Jad
Published in Virus research (01.08.2022)
Published in Virus research (01.08.2022)
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Journal Article
Complex 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, Habib, Walid Abi, Thibaud, Nathalie, Neves, Cristina Das, Jule, Marilyne Le, Brachet, Cécile, Heinrichs, Claudine, Bouc, Yves Le, Netchine, Irène
Published in Human mutation (01.10.2014)
Published in Human mutation (01.10.2014)
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