Binnaz Yalcin - Wellcome Trust Ctr Human Genet, Univ Oxford

基本信息

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职业迁徙

个人简介

Binnaz Yalcin currently works at the Centre for Translational and Molecular medicine Inserm Unit 1231 in Dijon. Binnaz does research at the intersection of neuroscience and genetics. The current project of her team is 'Mouse neuromorphogenesis'.

研究兴趣

论文共 69 篇作者统计合作学者相似作者

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Biallellic Variants in SNAPIN Are Associated with a Novel Foetal Neuroanatomical Phenotype

Maayke de Koning,Hammad Yousaf,Kelly Gilmore,Mariette Hoffer,Georgios Kellaris,Phebe Adama van Scheltema,Monique Haak,Cacha Peeters-Scholte,Delphine Heron,Boris Keren,Karen El Akouri,Sophie Lanone,Maylis Dagouassat,Binnaz Yalcin,Neeta Vora,Manon Suerink,Erica Davis,Gijs Santen

EUROPEAN JOURNAL OF HUMAN GENETICS (2024): 42-42

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Bi-allelic Variants in WDR47 Cause a Complex Neurodevelopmental Syndrome

Efil Bayam,Peggy Tilly,Stephan C Collins,José Rivera Alvarez,Meghna Kannan, Lucile Tonneau, Elena Brivio,Bruno Rinaldi, Romain Lecat,Noémie Schwaller,Ludovica Cotellessa,Sateesh Maddirevula,Fabiola Monteiro, Carlos M Guardia,João Paulo Kitajima,Fernando Kok,Mitsuhiro Kato, A,Mustafa A Salih,Saeed Al Tala,Mais O Hashem,Hiroko Tada,Hirotomo Saitsu, Mariano Stabile, Paolo Giacobini,Sylvie Friant,Zafer Yüksel,Mitsuko Nakashima,Fowzan S Alkuraya,Binnaz Yalcin,Juliette D Godin

EMBO molecular medicineno. 1 (2024): 129-168

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Automatic Segmentation of Histological Images of Mouse Brains

Juan Cisneros,Alain Lalande,Binnaz Yalcin,Fabrice Meriaudeau,Stephan Collins

DIGITAL AND COMPUTATIONAL PATHOLOGY, MEDICAL IMAGING 2024（2024）

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Exploring the Pathological Mechanisms Underlying Cohen Syndrome

Fabrizio Vacca,Binnaz Yalcin,Muhammad Ansar

Frontiers in neuroscience (2024): 1431400-1431400

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Automatic Segmentation of Histogical Images of the Brain of Mice

Juan Cisneros,Alain Lalande,Binnaz Yalcin,Fabrice Meriaudeau,Stephan Collins

Medical Imaging 2024 Digital and Computational Pathology (2024)

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De Novo Variants Found in Three Distinct Schizophrenia Populations Hit a Common Core Gene Network Related to Microtubule and Actin Cytoskeleton Gene Ontology Classes

Yann Loe-Mie,Christine Plancon,Caroline Dubertret,Takeo Yoshikawa,Binnaz Yalcin,Stephan C. Collins,Anne Boland,Jean-Francois Deleuze,Philip Gorwood,Dalila Benmessaoud,Michel Simonneau,Aude-Marie Lepagnol-Bestel

Lifeno. 2 (2024): 244-244

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Clinical, Genetic and Molecular Delineation of KPTNrelated Disorder in Humans and Mice Identifies Mtor Inhibition As a Candidate Therapeutic Approach

EUROPEAN JOURNAL OF HUMAN GENETICS (2024): 59-60

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Variant-specific Pathophysiological Mechanisms of AFF3 Differently Influence Transcriptome Profiles

Sissy Bassani,Jacqueline Chrast,Giovanna Ambrosini,Norine Voisin,Frédéric Schütz,Alfredo Brusco,Fabio Sirchia, Lydia Turban,Susanna Schubert,Rami Abou Jamra,Jan-Ulrich Schlump,Desiree DeMille,Pinar Bayrak-Toydemir,Gary Rex Nelson, Kristen Nicole Wong,Laura Duncan,Mackenzie Mosera,Christian Gilissen,Lisenka E. L. M. Vissers,Rolph Pfundt,Rogier Kersseboom,Hilde Yttervik,Geir Åsmund Myge Hansen,Marie Falkenberg Smeland,Kameryn M. Butler,Michael J. Lyons,Claudia M. B. Carvalho,Chaofan Zhang,James R. Lupski,Lorraine Potocki, Leticia Flores-Gallegos, Rodrigo Morales-Toquero,Florence Petit,Binnaz Yalcin, Annabelle Tuttle,Houda Zghal Elloumi, Lane McCormick,Mary Kukolich,Oliver Klaas,Judit Horvath,Marcello Scala,Michele Iacomino,Francesca Operto,Federico Zara,Karin Writzl,Aleš Maver,Maria K. Haanpää,Pia Pohjola, Harri Arikka,Anneke J. A. Kievit, Camilla Calandrini,Christian Iseli,Nicolas Guex,Alexandre Reymond

GENOME MEDICINE（2024）

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