Tania Attie-Bitach (Tania Attié-Bitach)

Scopus Author ID ResearcherID Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 39

Top Venues

European journal of human genetics : EJHG

Birth defects research

Nature cell biology

Clinical genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Laura M Watts, Marta Bertoli, Tania Attie-Bitach, Natalie Roux, Antonio Rausell, Catherine Paschal, Jessica L Zambonin, Cynthia J Curry, Blanche Martin, Rebecca S Tooze, Lara Hawkes, Usha Kini, Stephen R F Twigg, Andrew O M Wilkie
The phenotype of MEGF8-related Carpenter syndrome (CRPT2) is refined through the identification of eight new patients. European journal of human genetics : EJHG 32 (7) (2024)
Laura M Watts, Marta Bertoli, Tania Attie-Bitach, Natalie Roux, Antonio Rausell, Catherine Paschal, Jessica L Zambonin, Cynthia J Curry, Blanche Martin, Rebecca S Tooze, Lara Hawkes, Usha Kini, Stephen R F Twigg, Andrew O M Wilkie
The phenotype of MEGF8-related Carpenter syndrome (CRPT2) is refined through the identification of eight new patients. European journal of human genetics : EJHG (2024)
Laure Coquand, Clarisse Brunet Avalos, Anne-Sophie Macé, Sarah Farcy, Amandine Di Cicco, Marusa Lampic, Ryszard Wimmer, Betina Bessières, Tania Attie-Bitach, Vincent Fraisier, Pierre Sens, Fabien Guimiot, Jean-Baptiste Brault, Alexandre D Baffet
A cell fate decision map reveals abundant direct neurogenesis bypassing intermediate progenitors in the human developing neocortex. Nature cell biology (2024)
Quentin Hennocq, Nicolas Garcelon, Thomas Bongibault, Thomas Bouygues, Sandrine Marlin, Jeanne Amiel, Lucile Boutaud, Maxime Douillet, Stanislas Lyonnet, Vèronique Pingault, Arnaud Picard, Marlèe Rio, Tania Attie-Bitach, Roman H Khonsari, Nathalie Roux
Artificial intelligence-based diagnosis in fetal pathology using external ear shapes. Prenatal diagnosis (2024)
Laura M Watts, Marta Bertoli, Tania Attie-Bitach, Natalie Roux, Antonio Rausell, Catherine Paschal, Jessica L Zambonin, Cynthia J Curry, Blanche Martin, Rebecca S Tooze, Lara Hawkes, Usha Kini, Stephen R F Twigg, Andrew O M Wilkie
The phenotype of MEGF8-related Carpenter syndrome (CRPT2) is refined through the identification of eight new patients. European journal of human genetics : EJHG 32 (7) (2024)
Laura M Watts, Marta Bertoli, Tania Attie-Bitach, Natalie Roux, Antonio Rausell, Catherine Paschal, Jessica L Zambonin, Cynthia J Curry, Blanche Martin, Rebecca S Tooze, Lara Hawkes, Usha Kini, Stephen R F Twigg, Andrew O M Wilkie
The phenotype of MEGF8-related Carpenter syndrome (CRPT2) is refined through the identification of eight new patients. European journal of human genetics : EJHG 32 (7) (2024)
Romain Nicolle, Lucile Boutaud, Laurence Loeuillet, Naima Talhi, Sarah Grotto, Nicolas Bourgon, Agnese Feresin, Aurélie Coussement, Mathilde Barrois, Marie-Paule Beaujard, Thomas Rambaud, Férechté Razavi, Tania Attie-Bitach
Expanding the phenotypic spectrum of LIG4 pathogenic variations: neuro-histopathological description of 4 fetuses with stenosis of the aqueduct. European journal of human genetics : EJHG 32 (5) (2024)
Romain Nicolle, Lucile Boutaud, Laurence Loeuillet, Naima Talhi, Sarah Grotto, Nicolas Bourgon, Agnese Feresin, Aurélie Coussement, Mathilde Barrois, Marie-Paule Beaujard, Thomas Rambaud, Férechté Razavi, Tania Attie-Bitach
Expanding the phenotypic spectrum of LIG4 pathogenic variations: neuro-histopathological description of 4 fetuses with stenosis of the aqueduct. European journal of human genetics : EJHG 32 (5) (2024)
Laure Coquand, Clarisse Brunet Avalos, Anne-Sophie Macé, Sarah Farcy, Amandine Di Cicco, Marusa Lampic, Ryszard Wimmer, Betina Bessières, Tania Attie-Bitach, Vincent Fraisier, Pierre Sens, Fabien Guimiot, Jean-Baptiste Brault, Alexandre D Baffet
A cell fate decision map reveals abundant direct neurogenesis bypassing intermediate progenitors in the human developing neocortex. Nature cell biology 26 (5) (2024)
Laure Coquand, Clarisse Brunet Avalos, Anne-Sophie Macé, Sarah Farcy, Amandine Di Cicco, Marusa Lampic, Ryszard Wimmer, Betina Bessières, Tania Attie-Bitach, Vincent Fraisier, Pierre Sens, Fabien Guimiot, Jean-Baptiste Brault, Alexandre D Baffet
A cell fate decision map reveals abundant direct neurogenesis bypassing intermediate progenitors in the human developing neocortex. Nature cell biology 26 (5) (2024)
Romain Nicolle, Lucile Boutaud, Laurence Loeuillet, Naima Talhi, Sarah Grotto, Nicolas Bourgon, Agnese Feresin, Aurélie Coussement, Mathilde Barrois, Marie-Paule Beaujard, Thomas Rambaud, Férechté Razavi, Tania Attie-Bitach
Expanding the phenotypic spectrum of LIG4 pathogenic variations: neuro-histopathological description of 4 fetuses with stenosis of the aqueduct. European journal of human genetics : EJHG (2024)
Romain Nicolle, Lucile Boutaud, Laurence Loeuillet, Naima Talhi, Sarah Grotto, Nicolas Bourgon, Agnese Feresin, Aurélie Coussement, Mathilde Barrois, Marie-Paule Beaujard, Thomas Rambaud, Férechté Razavi, Tania Attie-Bitach
Expanding the phenotypic spectrum of LIG4 pathogenic variations: neuro-histopathological description of 4 fetuses with stenosis of the aqueduct. European journal of human genetics : EJHG 32 (5) (2024)
Laure Coquand, Clarisse Brunet Avalos, Anne-Sophie Macé, Sarah Farcy, Amandine Di Cicco, Marusa Lampic, Ryszard Wimmer, Betina Bessières, Tania Attie-Bitach, Vincent Fraisier, Pierre Sens, Fabien Guimiot, Jean-Baptiste Brault, Alexandre D Baffet
A cell fate decision map reveals abundant direct neurogenesis bypassing intermediate progenitors in the human developing neocortex. Nature cell biology (2024)
Laure Coquand, Clarisse Brunet Avalos, Anne-Sophie Macé, Sarah Farcy, Amandine Di Cicco, Marusa Lampic, Ryszard Wimmer, Betina Bessières, Tania Attie-Bitach, Vincent Fraisier, Pierre Sens, Fabien Guimiot, Jean-Baptiste Brault, Alexandre D Baffet
A cell fate decision map reveals abundant direct neurogenesis bypassing intermediate progenitors in the human developing neocortex. Nature cell biology 26 (5) (2024)
Laura M Watts, Marta Bertoli, Tania Attie-Bitach, Natalie Roux, Antonio Rausell, Catherine Paschal, Jessica L Zambonin, Cynthia J Curry, Blanche Martin, Rebecca S Tooze, Lara Hawkes, Usha Kini, Stephen R F Twigg, Andrew O M Wilkie
The phenotype of MEGF8-related Carpenter syndrome (CRPT2) is refined through the identification of eight new patients. European journal of human genetics : EJHG 32 (7) (2024)
Laure Coquand, Clarisse Brunet Avalos, Anne-Sophie Macé, Sarah Farcy, Amandine Di Cicco, Marusa Lampic, Ryszard Wimmer, Betina Bessières, Tania Attie-Bitach, Vincent Fraisier, Pierre Sens, Fabien Guimiot, Jean-Baptiste Brault, Alexandre D Baffet
A cell fate decision map reveals abundant direct neurogenesis bypassing intermediate progenitors in the human developing neocortex. Nature cell biology (2024)
Romain Nicolle, Lucile Boutaud, Laurence Loeuillet, Naima Talhi, Sarah Grotto, Nicolas Bourgon, Agnese Feresin, Aurélie Coussement, Mathilde Barrois, Marie-Paule Beaujard, Thomas Rambaud, Férechté Razavi, Tania Attie-Bitach
Expanding the phenotypic spectrum of LIG4 pathogenic variations: neuro-histopathological description of 4 fetuses with stenosis of the aqueduct. European journal of human genetics : EJHG 32 (5) (2024)
Laure Coquand, Clarisse Brunet Avalos, Anne-Sophie Macé, Sarah Farcy, Amandine Di Cicco, Marusa Lampic, Ryszard Wimmer, Betina Bessières, Tania Attie-Bitach, Vincent Fraisier, Pierre Sens, Fabien Guimiot, Jean-Baptiste Brault, Alexandre D Baffet
A cell fate decision map reveals abundant direct neurogenesis bypassing intermediate progenitors in the human developing neocortex. Nature cell biology 26 (5) (2024)
Eva Kohaut, Flavie Ader, Caroline Rooryck, Fanny Pelluard, Maryse Bonnière, Gwenaelle André, Fanny Sauvestre, Philippe Roth, Diala Khraiche, Bettina Bessières, Tania Attie-Bitach, Pascale Richard
Morphological and genetic causes of fetal cardiomyopathies. Clinical genetics (2023)
Marion Aubert-Mucca, Caroline Janel, Valérie Porquet-Bordes, Olivier Patat, Renaud Touraine, Thomas Edouard, Caroline Michot, Aude Tessier, Valérie Cormier-Daire, Tania Attie-Bitach, Geneviève Baujat
Clinical heterogeneity of NADSYN1-associated VCRL syndrome. Clinical genetics (2023)
Yosra Lajmi, Laurence Loeuillet, Giulia Petrilli, Charles Egloff, Juliette Nectoux, Clémence Molac, Nathalie Roux, Emmanuelle Pannier, Amale Achaiaa, Zaina Ait Arkoub, Sophie Chuon, Aurélie Coussement, Jean Michel Dupont, Valérie Malan, Emmanuel Spaggiari, Ferechte Razavi, Jeanne Amiel, Bettina Bessières, Sarah Grotto, Tania Attie-Bitach
Two novel variations p.(Ser1275Thr) and p.(Ser1275Arg) in FLT4 causing prenatal hereditary lymphedema type 1. Birth defects research (2022)
Audrey Lamouroux, Coralie Dauge, Constance Wells, Eve Mousty, Lucile Pinson, Hélène Cavé, Yline Capri, Jean-Michel Faure, Frédéric Grosjean, Fanny Sauvestre, Tania Attie-Bitach, Fanny Pelluard, David Geneviève
Extending the prenatal Noonan's phenotype by review of ultrasound and autopsy data. Prenatal diagnosis 42 (5) (2022)
Yosra Lajmi, Laurence Loeuillet, Giulia Petrilli, Charles Egloff, Juliette Nectoux, Clémence Molac, Nathalie Roux, Emmanuelle Pannier, Amale Achaiaa, Zaina Ait Arkoub, Sophie Chuon, Aurélie Coussement, Jean Michel Dupont, Valérie Malan, Emmanuel Spaggiari, Ferechte Razavi, Jeanne Amiel, Bettina Bessières, Sarah Grotto, Tania Attie-Bitach
Two novel variations p.(Ser1275Thr) and p.(Ser1275Arg) in FLT4 causing prenatal hereditary lymphedema type 1. Birth defects research 115 (5) (2022)
Bertrand Chesneau, Marion Aubert-Mucca, Félix Fremont, Jacmine Pechmeja, Vincent Soler, Bertrand Isidor, Mathilde Nizon, Hélène Dollfus, Josseline Kaplan, Lucas Fares-Taie, Jean-Michel Rozet, Tiffany Busa, Didier Lacombe, Sophie Naudion, Jeanne Amiel, Marlène Rio, Tania Attie-Bitach, Cécile Lesage, Dominique Thouvenin, Sylvie Odent, Godelieve Morel, Catherine Vincent-Delorme, Odile Boute, Clemence Vanlerberghe, Anne Dieux, Simon Boussion, Laurence Faivre, Lucile Pinson, Fanny Laffargue, Gwenaël Le Guyader, Guylène Le Meur, Fabienne Prieur, Victor Lambert, Beatrice Laudier, Edouard Cottereau, Carmen Ayuso, Marta Corton-Pérez, Laurence Bouneau, Cédric Le Caignec, Véronique Gaston, Claire Jeanton-Scaramouche, Delphine Dupin-Deguine, Patrick Calvas, Nicolas Chassaing, Julie Plaisancié
First evidence of SOX2 mutations in Peters' anomaly: Lessons from molecular screening of 95 patients. Clinical genetics 101 (5-6) (2022)
Yosra Lajmi, Laurence Loeuillet, Giulia Petrilli, Charles Egloff, Juliette Nectoux, Clémence Molac, Nathalie Roux, Emmanuelle Pannier, Amale Achaiaa, Zaina Ait Arkoub, Sophie Chuon, Aurélie Coussement, Jean Michel Dupont, Valérie Malan, Emmanuel Spaggiari, Ferechte Razavi, Jeanne Amiel, Bettina Bessières, Sarah Grotto, Tania Attie-Bitach
Two novel variations p.(Ser1275Thr) and p.(Ser1275Arg) in FLT4 causing prenatal hereditary lymphedema type 1. Birth defects research 115 (5) (2022)
Lyse Ruaud, Nathalie Roux, Lucile Boutaud, Bettina Bessières, Faustine Ageorges, Amale Achaiaa, Christine Bole, Patrick Nitschke, Cécile Masson, Michel Vekemans, Alain Verloes, Tania Attie-Bitach
Biallelic THOC6 pathogenic variants: Prenatal phenotype and review of the literature. Birth defects research 114 (10) (2022)
Yosra Lajmi, Laurence Loeuillet, Giulia Petrilli, Charles Egloff, Juliette Nectoux, Clémence Molac, Nathalie Roux, Emmanuelle Pannier, Amale Achaiaa, Zaina Ait Arkoub, Sophie Chuon, Aurélie Coussement, Jean Michel Dupont, Valérie Malan, Emmanuel Spaggiari, Ferechte Razavi, Jeanne Amiel, Bettina Bessières, Sarah Grotto, Tania Attie-Bitach
Two novel variations p.(Ser1275Thr) and p.(Ser1275Arg) in FLT4 causing prenatal hereditary lymphedema type 1. Birth defects research 115 (5) (2022)
Suzanne Chartier, Lucile Boutaud, Edouard Le Guillou, Caroline Alby, Clarisse Billon, Anne-Élodie Millischer, Catherine Caillaud, Louise Galmiche, Charlotte Mechler, Pascale Sonigo, Nathalie Boddaert, Stanislas Lyonnet, Sophie Rondeau, Christine Bole-Feysot, Cecile Masson, Yves Ville, Philippe Roth, Isabelle Desguerre, Férechté Encha-Razavi, Tania Attie-Bitach
Prenatal-onset of congenital neuronal ceroid lipofuscinosis with a novel CTSD mutation. Birth defects research 113 (18) (2021)
Claude Darcha, Fanny Laffargue, Lucile Boutaud, Denis Gallot, Claire Dauphin, Jean Marc Garcier, Amale Achaiaa, Patrick Nitschke, Cécile Fourrage, Carole Goumy, Tania Attie-Bitach
Novel CDK10 variants with multicystic dysplastic kidney, left ventricular non-compaction, and a solitary median maxillary central incisor. Clinical genetics 100 (3) (2021)
Leila Ghesh, Marie Denis Musquer, Louise Devisme, Morgane Stichelbout, Lucile Boutaud, Nadia Elkhartoufi, Pascal Vaast, Odile Boute, Anne-Sophie Riteau, Claudine Le Vaillant, Norbert Winer, Madeleine Joubert, Stéphane Bezieau, Sophie Thomas, Tania Attie-Bitach, Claire Beneteau
The first two non-Finnish HYLS1 variants: Expanding the phenotypic spectrum of hydrolethalus syndrome. Clinical genetics 100 (4) (2021)
Emmanuelle Szenker-Ravi, Tim Ott, Muznah Khatoo, Anne Moreau de Bellaing, Wei Xuan Goh, Yan Ling Chong, Anja Beckers, Darshini Kannesan, Guillaume Louvel, Priyanka Anujan, Vydianathan Ravi, Carine Bonnard, Sebastien Moutton, Patric Schoen, Mélanie Fradin, Estelle Colin, Andre Megarbane, Linda Daou, Ghassan Chehab, Sylvie Di Filippo, Caroline Rooryck, Jean François Deleuze, Anne Boland-Auge, Nicolas Arribard, Rukiye Eker, Sumanty Tohari, Alvin Yu-Jin Ng, Marlène Rio, Chun Teck Lim, Birgit Eisenhaber, Frank Eisenhaber, Byrappa Venkatesh, Jeanne Amiel, Hugues Roest Crollius, Christopher T Gordon, Achim Gossler, Sudipto Roy, Tania Attie-Bitach, Martin Blum, Patrice Bouvagnet, Bruno Reversade
Discovery of a genetic module essential for assigning left-right asymmetry in humans and ancestral vertebrates. Nature genetics 54 (1) (2021)
Ahmed El Mouatani, Geraldine van Winckel, Khaoula Zaafrane-Khachnaoui, Sandra Whalen, Amale Achaiaa, Sophie Kaltenbach, Andrea Superti-Furga, Michel Vekemans, Heidi Fodstad, Fabienne Giuliano, Tania Attie-Bitach
Homozygous GLI3 variants observed in three unrelated patients presenting with syndromic polydactyly. American journal of medical genetics. Part A 185 (12) (2021)
Simon Boussion, Fabienne Escande, Anne-Sophie Jourdain, Thomas Smol, Perrine Brunelle, Céline Duhamel, Yves Alembik, Tania Attie-Bitach, Geneviève Baujat, Anne Bazin, Maryse Bonnière, Philippe Carassou, Dominique Carles, Louise Devisme, Cyril Goizet, Alice Goldenberg, Sarah Grotto, Agnès Guichet, Pierre-Simon Jouk, Laurence Loeuillet, Charlotte Mechler, Caroline Michot, Fanny Pelluard, Audrey Putoux, Sandra Whalen, Jamal Ghoumid, Sylvie Manouvrier-Hanu, Florence Petit
TAR syndrome: Clinical and molecular characterization of a cohort of 26 patients and description of novel noncoding variants of RBM8A. Human mutation 41 (7) (2020)
Huw B Thomas, Katherine A Wood, Weronika A Buczek, Christopher T Gordon, Véronique Pingault, Tania Attie-Bitach, Kathryn E Hentges, Vinod C Varghese, Jeanne Amiel, William G Newman, Raymond T O'Keefe
EFTUD2 missense variants disrupt protein function and splicing in mandibulofacial dysostosis Guion-Almeida type. Human mutation 41 (8) (2020)
Aude Tessier, Lucile Boutaud, Ange-Line Bruel, Christel Thauvin-Robinet, Philippe Roth, Valérie Malan, Marie-Paule Beaujard, Amale Achaiaa, Judite de Oliveira, Julie Steffann, Ferechte Encha-Razavi, Laurence Faivre, Bettina Bessières, Tania Attie-Bitach
Hydrothorax in fetal cases of Opitz G/BBB diagnosis: Extending the phenotype? Clinical genetics 98 (6) (2020)
Svetlana Gorokhova, Jeremie Mortreux, Alexandra Afenjar, Tania Attie-Bitach, Maud Blanluet, Valérie Cormier-Daire, Anne-Marie Guerrot, Anne-Sophie Lebre, Valérie Malan, Gaël Nicolas, Sophie Rondeau, Nicole Philip, Pascale Saugier-Veber, Catherine Badens, Chantal Missirian
Significant contribution of intragenic deletions to ARID1B mutation spectrum. Genetics in medicine : official journal of the American College of Medical Genetics 21 (11) (2019)
Séverine Bacrot, Charlotte Mechler, Naima Talhi, Dominique Martin-Coignard, Philippe Roth, Caroline Michot, Amale Ichkou, Olivier Alibeu, Patrick Nitschke, Sophie Thomas, Michel Vekemans, Férechté Razavi, Lucile Boutaud, Tania Attie-Bitach
Whole exome sequencing diagnoses the first fetal case of Bainbridge-Ropers syndrome presenting as pontocerebellar hypoplasia type 1. Birth defects research 110 (6) (2018)
Suzanne Chartier, Caroline Alby, Lucile Boutaud, Sophie Thomas, Nadia Elkhartoufi, Jelena Martinovic, Josseline Kaplan, Alexandra Benachi, Didier Lacombe, Pascale Sonigo, Séverine Drunat, Michel Vekemans, Joël Agenor, Férechté Encha Razavi, Tania Attie-Bitach
A neuropathological study of novel RTTN gene mutations causing a familial microcephaly with simplified gyral pattern. Birth defects research 110 (7) (2018)
Caroline Alby, Lucile Boutaud, Maryse Bonnière, Sophie Collardeau-Frachon, Laurent Guibaud, Estelle Lopez, Ange-Line Bruel, Bernard Aral, Pascale Sonigo, Philippe Roth, Claude Vibert-Guigue, Vanina Castaigne, Bruno Carbonne, Nicole Joyé, Laurence Faivre, Marie-Pierre Cordier, Antoinette Bernabe Gelot, Maurizio Clementi, Isabella Mammi, Michel Vekemans, Féréchté Razavi, Marie Gonzales, Christel Thauvin-Robinet, Tania Attie-Bitach
In utero ultrasound diagnosis of corpus callosum agenesis leading to the identification of orofaciodigital type 1 syndrome in female fetuses. Birth defects research 110 (4) (2017)

Tania Attie-Bitach.css-eqlu8i{font-size:small;padding-left:4px;} (Tania Attié-Bitach)

Publication Activity (10 Years)

Top Topics

Top Venues

Tania Attie-Bitach (Tania Attié-Bitach)