Trends in scientific publishing: does quantity compromises quality in life sciences and medicine? von El Shamieh, Said, Chebly, Alain

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Spotlight on borderline-IGHV mutational status in chronic lymphocytic leukemia von Rammal, Souraya, Semaan, Warde, Aprahamian, Natalia, Moussallem, Romy, Chebly, Alain

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A novel nonsense variant in POGZ expanding the spectrum of White-Sutton syndrome: A case report von Chebly, Alain, Salem, Nabiha, Moussallem, Romy, Moukarzel, Adib

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Complex karyotypes in hematologic disorders: a 12-year single-center study from Lebanon von Rammal, Souraya, Abou Abdallah, Farid, Attieh, Charbel, El Mounajjed, Zeinab, Semaan, Warde, Chebly, Alain

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Exploring hTERT promoter methylation in cutaneous T‐cell lymphomas von Chebly, Alain, Ropio, Joana, Peloponese, Jean‐Marie, Poglio, Sandrine, Prochazkova‐Carlotti, Martina, Cherrier, Floriane, Ferrer, Jacky, Idrissi, Yamina, Segal‐Bendirdjian, Evelyne, Chouery, Eliane, Farra, Chantal, Pham‐Ledard, Anne, Beylot‐Barry, Marie, Merlio, Jean‐Philippe, Tomb, Roland, Chevret, Edith

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Targeting Epigenetic Modifiers Can Reduce the Clonogenic Capacities of Sézary Cells von Chebly, Alain, Prochazkova-Carlotti, Martina, Idrissi, Yamina, Bresson-Bepoldin, Laurence, Poglio, Sandrine, Farra, Chantal, Beylot-Barry, Marie, Merlio, Jean-Philippe, Tomb, Roland, Chevret, Edith

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hMZF-2 , the Elusive Transcription Factor von Chebly, Alain, Peloponese, Jean-Marie, Ségal-Bendirdjian, Evelyne, Merlio, Jean-Philippe, Tomb, Roland, Chevret, Edith

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An unusual case of chronic lymphocytic leukemia with trisomy 12 and t(14;18) and a favorable response to ibrutinib von Haddad, Fady Gh, Chebly, Alain, El Sett, Antoine, Kourie, Hampig Raphael, Farra, Chantal

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Genome Engineering as a Therapeutic Approach in Cancer Therapy: A Comprehensive Review von Gemayel, Jack, Chebly, Alain, Kourie, Hampig, Hanna, Colette, Mheidly, Kayane, Mhanna, Melissa, Karam, Farah, Ghoussaini, Daniel, Najjar, Paula El, Khalil, Charbel

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Reliable blood cancer cells' telomere length evaluation by qPCR von Ropio, Joana, Chebly, Alain, Ferrer, Jacky, Prochazkova‐Carlotti, Martina, Idrissi, Yamina, Azzi‐Martin, Lamia, Cappellen, David, Pham‐Ledard, Anne, Soares, Paula, Merlio, Jean‐Philippe, Chevret, Edith

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First molecular study in Lebanese patients with Cockayne syndrome and report of a novel mutation in ERCC8 gene von Chebly, Alain, Corbani, Sandra, Abou Ghoch, Joelle, Mehawej, Cybel, Megarbane, André, Chouery, Eliane

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Pediatric M5 acute myeloid leukemia with MLL-SEPT6 fusion and a favorable outcome von Chebly, Alain, Djambas Khayat, Claudia, Yammine, Tony, Korban, Rima, Semaan, Warde, Bou Zeid, Jessica, Farra, Chantal

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Chromosomal instability in cancers of unknown primary von Chebly, Alain, Yammine, Tony, Boussios, Stergios, Pavlidis, Nicholas, Rassy, Elie

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A rare case of acute myeloid leukemia with t(12;19)(q13;q13) von Chebly, Alain, Haddad, Fady Gh, Bassil, Josiane, Yammine, Tony, Korban, Rima, Semaan, Warde, El Karak, Fady, Kourie, Hampig Raphael, Farra, Chantal

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T-cell lymphocytes’ aging clock: telomeres, telomerase and aging von Chebly, Alain, Khalil, Charbel, Kuzyk, Alexandra, Beylot-Barry, Marie, Chevret, Edith

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The impact of mosaic loss of the Y chromosome (mLOY) in men of advanced age von Abou Abdallah, Farid, Abdel Massih, Christine, Attieh, Charbel, Chebly, Alain

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A homozygous missense variant in PTPN2 with early-onset Crohn’s disease, growth failure and dysmorphic features in an infant: a case report von AWWAD, JOHNNY, SOUAID, MIRNA, YAMMINE, TONY, CHEBLY, ALAIN, SALEM, NABIHA, ESBER, RITA, FARRA, CHANTAL

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Delving into the Metabolism of Sézary Cells: A Brief Review von Cherfan, Carel, Chebly, Alain, Rezvani, Hamid Reza, Beylot-Barry, Marie, Chevret, Edith

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Mesenchymal stem cells-derived secretome and extracellular vesicles: perspective and challenges in cancer therapy and clinical applications von Gemayel, Jack, Chaker, Diana, El Hachem, Georges, Mhanna, Melissa, Salemeh, Rawad, Hanna, Colette, Harb, Frederic, Ibrahim, Ahmad, Chebly, Alain, Khalil, Charbel

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Surviving the storm: A 6-year journey with bowel perforations and aneurysms in vascular Ehlers-Danlos syndrome — A case report von Habib, Farid Abi, Osseis, Michael, Chebly, Alain, El Feghali, Elie, Noun, Roger

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