Tania Attié-Bitach Imagine Institute, INSERM UMR 1163 Université de Paris Biography Publications Institution JoVE Articles Tania Attié-Bitach has not added a biography. If you are Tania Attié-Bitach and would like to personalize this page please email our Author Liaison for assistance. Publications Publisher Correction: Discovery of a Genetic Module Essential for Assigning Left-right Asymmetry in Humans and Ancestral Vertebrates Nature Genetics. Mar, 2022 | Pubmed ID: 35304595 Biallelic Pathogenic Variants in Roundabout Guidance Receptor 1 Associate with Syndromic Congenital Anomalies of the Kidney and Urinary Tract Kidney International. Feb, 2022 | Pubmed ID: 35227688 Targeted Next-generation Sequencing in a Large Series of Fetuses with Severe Renal Diseases Human Mutation. Mar, 2022 | Pubmed ID: 35005812 Discovery of a Genetic Module Essential for Assigning Left-right Asymmetry in Humans and Ancestral Vertebrates Nature Genetics. 01, 2022 | Pubmed ID: 34903892 GGCX-related Congenital Combined Vitamin K-dependent Clotting Factors Deficiency-1: Description of a Fetus with Chondrodysplasia Punctata American Journal of Medical Genetics. Part A. 01, 2022 | Pubmed ID: 34558179 Prenatal-onset of Congenital Neuronal Ceroid Lipofuscinosis with a Novel CTSD Mutation Birth Defects Research. 11, 2021 | Pubmed ID: 34491000 Homozygous GLI3 Variants Observed in Three Unrelated Patients Presenting with Syndromic Polydactyly American Journal of Medical Genetics. Part A. 12, 2021 | Pubmed ID: 34296525 Novel CDK10 Variants with Multicystic Dysplastic Kidney, Left Ventricular Non-compaction, and a Solitary Median Maxillary Central Incisor Clinical Genetics. 09, 2021 | Pubmed ID: 34114225 Loss-of-function and Missense Variants in NSD2 Cause Decreased Methylation Activity and Are Associated with a Distinct Developmental Phenotype Genetics in Medicine : Official Journal of the American College of Medical Genetics. 08, 2021 | Pubmed ID: 33941880 Phenotypic Spectrum and Genomics of Undiagnosed Arthrogryposis Multiplex Congenita Journal of Medical Genetics. Apr, 2021 | Pubmed ID: 33820833 Bi-allelic Pathogenic Variations in DNAJB11 Cause Ivemark II Syndrome, a Renal-hepatic-pancreatic Dysplasia Kidney International. 02, 2021 | Pubmed ID: 33129895 Hydrothorax in Fetal Cases of Opitz G/BBB Diagnosis: Extending the Phenotype? Clinical Genetics. 12, 2020 | Pubmed ID: 32926417 Fetal Megacystis-microcolon: Genetic Mutational Spectrum and Identification of PDCL3 As a Novel Candidate Gene Clinical Genetics. 09, 2020 | Pubmed ID: 32621347 Prenatal Exome Sequencing in 65 Fetuses with Abnormality of the Corpus Callosum: Contribution to Further Diagnostic Delineation Genetics in Medicine : Official Journal of the American College of Medical Genetics. 11, 2020 | Pubmed ID: 32565546 Bi-allelic Variations of SMO in Humans Cause a Broad Spectrum of Developmental Anomalies Due to Abnormal Hedgehog Signaling American Journal of Human Genetics. 06, 2020 | Pubmed ID: 32413283 Severe and Progressive Neuronal Loss in Myelomeningocele Begins Before 16 Weeks of Pregnancy American Journal of Obstetrics and Gynecology. 08, 2020 | Pubmed ID: 32283072 PAK3 Mutations Responsible for Severe Intellectual Disability and Callosal Agenesis Inhibit Cell Migration Neurobiology of Disease. 03, 2020 | Pubmed ID: 31843706 Clinical and Functional Characterization of the Recurrent TUBA1A P.(Arg2His) Mutation Brain Sciences. Aug, 2018 | Pubmed ID: 30087272 Fifteen Years of Research on Oral-facial-digital Syndromes: from 1 to 16 Causal Genes Journal of Medical Genetics. 06, 2017 | Pubmed ID: 28289185 [From Foetopathology to Disease-causing Gene] Annales De Pathologie. Nov, 2012 | Pubmed ID: 23127939 מודלים מבוססי תאי גזע פלוריפוטנטיים דו-ממדיים ותלת-ממדיים אנושיים לניתוח מעורבות סיליום ראשוני במהלך התפתחות ניאוקורטיקלית Lucile Boutaud*1, Marie Michael*1, Céline Banal2, Damelys Calderon1, Sarah Farcy1, Julie Pernelle1, Nicolas Goudin3, Camille Maillard1, Clémantine Dimartino1, Cécile Deleschaux1, Sébastien Dupichaud4, Corinne Lebreton1, Sophie Saunier1, Tania Attié-Bitach1,5, Nadia Bahi-Buisson1,6, Nathalie Lefort2, Sophie Thomas1 1Imagine Institute, INSERM UMR 1163, Université de Paris, 2Imagine Institute, iPSC Core Facility, INSERM UMR U1163, Université de Paris, 3Necker Bio-image Analysis platform of the SFR Necker, 4Imagine Institute, Cell Imaging Platform, INSERM-US24-CNRS UMS 3633 Structure Fédérative de Recherche Necker, INSERM UMR U1163, Université de Paris, 5Fédération de Génétique, Hôpital Necker-Enfants Malades, Assistance Publique Hôpitaux de Paris, 6Pediatric Neurology, APHP- Necker Enfants Malades Hospital JoVE 62667 Developmental Biology
מודלים מבוססי תאי גזע פלוריפוטנטיים דו-ממדיים ותלת-ממדיים אנושיים לניתוח מעורבות סיליום ראשוני במהלך התפתחות ניאוקורטיקלית Lucile Boutaud*1, Marie Michael*1, Céline Banal2, Damelys Calderon1, Sarah Farcy1, Julie Pernelle1, Nicolas Goudin3, Camille Maillard1, Clémantine Dimartino1, Cécile Deleschaux1, Sébastien Dupichaud4, Corinne Lebreton1, Sophie Saunier1, Tania Attié-Bitach1,5, Nadia Bahi-Buisson1,6, Nathalie Lefort2, Sophie Thomas1 1Imagine Institute, INSERM UMR 1163, Université de Paris, 2Imagine Institute, iPSC Core Facility, INSERM UMR U1163, Université de Paris, 3Necker Bio-image Analysis platform of the SFR Necker, 4Imagine Institute, Cell Imaging Platform, INSERM-US24-CNRS UMS 3633 Structure Fédérative de Recherche Necker, INSERM UMR U1163, Université de Paris, 5Fédération de Génétique, Hôpital Necker-Enfants Malades, Assistance Publique Hôpitaux de Paris, 6Pediatric Neurology, APHP- Necker Enfants Malades Hospital JoVE 62667 Developmental Biology