ZEB2 haploinsufficient Mowat-Wilson syndrome induced pluripotent stem cells show disrupted GABAergic transcriptional regulation and function
Schuster, Jens, Klar, Joakim, Khalfallah, Ayda, Laan, Loora, Hoeber, Jan, Fatima, Ambrin, Sequeira, Velin Marita, Jin, Zhe, Korol, Sergiy V., Huss, Mikael, Nordgren, Ann, Anderlid, Britt Marie, Gallant, Caroline, Birnir, Bryndis, Dahl, Niklas
Published in Frontiers in molecular neuroscience (24.10.2022)
Published in Frontiers in molecular neuroscience (24.10.2022)
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Mowat-Wilson syndrome: Generation of two human iPS cell lines (UUIGPi004A and UUIGPi005A) from siblings with a truncating ZEB2 gene variant
Schuster, Jens, Sobol, Maria, Fatima, Ambrin, Khalfallah, Ayda, Laan, Loora, Anderlid, Britt-Marie, Nordgren, Ann, Dahl, Niklas
Published in Stem cell research (01.08.2019)
Published in Stem cell research (01.08.2019)
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COL1A1 association and otosclerosis: A meta-analysis
Schrauwen, Isabelle, Khalfallah, Ayda, Ealy, Megan, Fransen, Erik, Claes, Charlotte, Huber, Alex, Murillo, Laura Rodriguez, Masmoudi, Saber, Smith, Richard J.H., Van Camp, Guy
Published in American journal of medical genetics. Part A (01.05.2012)
Published in American journal of medical genetics. Part A (01.05.2012)
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Recurrent GATA1 mutations in Diamond‐Blackfan anaemia
Klar, Joakim, Khalfallah, Ayda, Arzoo, Pakeeza Shaiq, Gazda, Hanna T., Dahl, Niklas
Published in British journal of haematology (01.09.2014)
Published in British journal of haematology (01.09.2014)
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Methods of Reprogramming to Induced Pluripotent Stem Cell Associated with Chromosomal Integrity and Delineation of a Chromosome 5q Candidate Region for Growth Advantage
Sobol, Maria, Raykova, Doroteya, Cavelier, Lucia, Khalfallah, Ayda, Schuster, Jens, Dahl, Niklas
Published in Stem cells and development (01.09.2015)
Published in Stem cells and development (01.09.2015)
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Recurrent GATA 1 mutations in D iamond‐ B lackfan anaemia
Klar, Joakim, Khalfallah, Ayda, Arzoo, Pakeeza Shaiq, Gazda, Hanna T., Dahl, Niklas
Published in British journal of haematology (01.09.2014)
Published in British journal of haematology (01.09.2014)
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Association of COL1A1 and TGFB1 Polymorphisms with Otosclerosis in a Tunisian Population
Khalfallah, Ayda, Schrauwen, Isabelle, Mnejja, Malek, HadjKacem, Hassen, Dhouib, Leila, Mosrati, Mohamed Ali, Hakim, Bochra, Lahmar, Imed, Charfeddine, Ilhem, Driss, Nabil, Ayadi, Hammadi, Ghorbel, Abdelmonem, Van Camp, Guy, Masmoudi, Saber
Published in Annals of human genetics (01.09.2011)
Published in Annals of human genetics (01.09.2011)
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A novel missense mutation in the ESRRB gene causes DFNB35 hearing loss in a Tunisian family
Ben Saïd, Mariem, Ayedi, Leila, Mnejja, Melek, Hakim, Bochra, Khalfallah, Ayda, Charfeddine, Ilhem, Khifagi, Chamseddine, Turki, Khalil, Ayadi, Hammadi, BenZina, Zeineb, Ghorbel, Abdelmonem, Castillo, Ignacio del, Masmoudi, Saber, Aifa, Mounira Hmani
Published in European journal of medical genetics (01.11.2011)
Published in European journal of medical genetics (01.11.2011)
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Genetic variants in RELN are associated with otosclerosis in a non‐European population from Tunisia
Khalfallah, Ayda, Schrauwen, Isabelle, Mnaja, Malek, Fransen, Erik, Lahmar, Imed, Ealy, Megan, Dhouib, Leila, Ayadi, Hammadi, Charfedine, Ilhem, Driss, Nabil, Ghorbel, Abdelmonem, Smith, Richard J.H., Masmoudi, Saber, Van Camp, Guy
Published in Annals of human genetics (01.09.2010)
Published in Annals of human genetics (01.09.2010)
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Association of COL1A1 and TGFB1 Polymorphisms with Otosclerosis in a Tunisian Population: COL1A1 & TGFB1 variants and otosclerosis
Khalfallah, Ayda, Schrauwen, Isabelle, Mnejja, Malek, HadjKacem, Hassen, Dhouib, Leila, Mosrati, Mohamed Ali, Hakim, Bochra, Lahmar, Imed, Charfeddine, Ilhem, Driss, Nabil, Ayadi, Hammadi, Ghorbel, Abdelmonem, Van Camp, Guy, Masmoudi, Saber
Published in Annals of human genetics (01.09.2011)
Published in Annals of human genetics (01.09.2011)
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