Hassan Saei - Lab Hereditary Kidney Dis, Univ Paris Cite

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Bio

Hassan Saei is a PPU program Ph.D. fellow at the Imagine Institute of Genetic Diseases, in Paris, France. He is working on hereditary renal diseases and is interested in omics, data analysis, stem cell biology, and organoids. Email: hassan.saei@inserm.fr

Research Interests

Papers共 18 篇Author StatisticsCo-AuthorSimilar Experts

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Phenotypic Heterogeneity of ADTKD-MUC1 Diagnosed Using VNtyper, a Novel Genetic Technique

Jessica Kachmar,Hassan Saei,Vincent Morinière,Laurence Heidet,Bertrand Knebelmann,Olivier Gribouval,Manon Mautret-Godefroy,Stéphane Burtey,Vincent Vuiblet,Asma Alla, Axel Ibalanky,Olivier Moranne,Mathilde Nizon,Benjamin Savenkoff,Patrick Nitschké,Corinne Antignac,Guillaume Dorval

American Journal of Kidney Diseases (2025)

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Using VNtyper from Whole Exome Sequencing Data to Detect Pathogenic Variants in the MUC1 Gene

Hassan Saei,Cécile Masson,Vincent Morinière,Jessica Kachmar,Laurence Heidet,Olivier Gribouval,Corinne Antignac,Guillaume Dorval

Journal of the American Society of Nephrology JASNno. 2 (2024): 327-328

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#2606 Clinically Boosted Exome-Sequencing is Necessary for Accurate and Highly Sensitive Genetic Diagnosis of ADTKD-MUC1

Hassan Saei,Vincent Morinière,Laurence Heidet,Bertrand Knebelmann,Patrick Nitschke,Corinne Antignac,Guillaume Dorval

Nephrology Dialysis Transplantationno. Supplement_1 (2024)

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Clinically Boosted Exome-Sequencing is Necessary for Accurate and Highly Sensitive Genetic Diagnosis of ADTKD-MUC1

Hassan Saei,Vincent Moriniere,Laurence Heidet,Bertrand Knebelmann,Patrick Nitschke,Corinne Antignac,Guillaume Dorval

NEPHROLOGY DIALYSIS TRANSPLANTATION (2024)

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P135: X-linked Alport Syndrome: from Transcriptomic Diagnosis to Preclinical Assessment of Splice-Switching Oligonucleotide Therapy Using Patient-Derived Cells and Kidney Organoids*

Hassan Saei,Marie Boisson,Christelle Arrondel, Bruno Estebe,Nicolas Cagnard,Marc Bras,Vincent Morinière, Zaïna Aït Arkoub,Laurence Heidet,Olivier Gribouval,Patrick Nitschké,Corinne Antignac,Géraldine Mollet,Guillaume Dorval

Genetics in Medicine Open (2024): 101032

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#382 Unexpected Diagnoses of ADTKD-MUC1 with the Help of VNtyper

Jessica Kachmar,Hassan Saei,Vincent Morinière,Laurence Heidet,Olivier Gribouval,Manon Mautret-Godefroy,Bertrand Knebelmann,Stéphane Burtey,Vincent Vuiblet,Patrick Nitschké,Corinne Antignac,Guillaume Dorval

Nephrology Dialysis Transplantationno. Supplement_1 (2024)

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P168: MUC1 Gene Coding-Vntr Alignment-Free Genotyping Approach Augmented ADTKD Diagnosis in a Cohort of 3735 Patients with Hereditary Kidney Diseases

Hassan Saei,Jessica Kachmar,Vincent Morinière,Laurence Heidet,Olivier Gribouval,Said Lebbah,Frederic Tores,Manon Mautret-Godefroy,Bertrand Knebelmann,Stéphane Burtey,Vincent Vuiblet,Corinne Antignac,Patrick Nitschké,Guillaume Dorval

Genetics in Medicine Open (2024): 101065

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Unexpected Diagnoses of ADTKD-MUC1 with the Help of VNtyper

Jessica Kachmar,Hassan Saei,Vincent Moriniere,Laurence Heidet,Olivier Gribouval,Manon Mautret-Godefroy,Bertrand Knebelmann,Stephane Burtey,Vincent Vuiblet,Patrick Nitschke,Corinne Antignac,Guillaume Dorval

NEPHROLOGY DIALYSIS TRANSPLANTATION (2024)

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DEEP INTRONIC VARIANTS IN X-LINKED ALPORT SYNDROME: FROM DETECTION TO THERAPEUTIC HOPES

Jessica Kachmar,Hassan Saei,Marie Boisson,Christelle Arrondel,Nicolas Cagnard,Vincent Moriniere, Zaina Ait Arkoub,Laurence Heidet,Aurelie Hummel,Bertrand Knebelmann,Olivier Gribouval,Christine Bole-Feysot,Patrick Nitschke,Corinne Antignac,Guillaume Dorval

PEDIATRIC NEPHROLOGY (2023): S52-S52

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A Wave of Deep Intronic Mutations in X-linked Alport Syndrome

Marie Boisson,Christelle Arrondel,Nicolas Cagnard,Vincent Moriniere, Zaina Ait Arkoub,Hassan Saei,Laurence Heidet,Jessica Kachmar,Aurelie Hummel,Bertrand Knebelmann,Marie-Noelle Bonnet-Dupeyron,Bertrand Isidor, Hassane Izzedine,Eric Legrand, Philippe Couarch,Olivier Gribouval,Christine Bole-Feysot,Melanie Parisot,Patrick Nitschke,Corinne Antignac,Guillaume Dorval

KIDNEY INTERNATIONALno. 2 (2023): 367-377

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