Devina Ung - INSERM, Univ Tours | 人才画像

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Bio

Devina C. Ung worked at the Seaver Autism Center for Research and treatment, ICAHN School of Medicine at Mount Sinai, in New York. Devina does research in Molecular Biology, Genetics and Neuroscience. Their most recent publication as first author is 'Ptchd1 deficiency induces excitatory synaptic and cognitive dysfunctions in mouse.'

Research Interests

Papers共 12 篇Author StatisticsCo-AuthorSimilar Experts

By YearBy Citation主题筛选期刊级别筛选合作者筛选合作机构筛选

GRID1/GluD1 Homozygous Variants Linked to Intellectual Disability and Spastic Paraplegia Impair Mglu1/5 Receptor Signaling and Excitatory Synapses

Dévina C. Ung,Nicolas Pietrancosta, Elena Baz Badillo, Brigitt Raux,Daniel Tapken, Andjela Zlatanovic, Adrien Doridant,Ben Pode-Shakked,Annick Raas-Rothschild,Orly Elpeleg,Bassam Abu-Libdeh,Nasrin Hamed,Marie-Amélie Papon,Sylviane Marouillat,Rose-Anne Thépault, Giovanni Stevanin,Jonathan Elegheert,Mathieu Letellier,Michael Hollmann,Bertrand Lambolez,Ludovic Tricoire,Annick Toutain,Régine Hepp,Frédéric Laumonnier

MOLECULAR PSYCHIATRY（2024）

Cited0Views0WOSBibtex

Study of Ubiquitin Pathway Genes in a French Population with Amyotrophic Lateral Sclerosis: Focus on HECW1 Encoding the E3 Ligase NEDL1

Shanez Haouari,Christian Robert Andres,Debora Lanznaster,Sylviane Marouillat,Celine Brulard,Audrey Dangoumau,Devina Ung,Charlotte Veyrat-Durebex,Frederic Laumonnier,Helene Blasco,Philippe Couratier,Philippe Corcia,Patrick Vourc'h

International Journal of Molecular Sciences（2023）

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Contribution of the Dihydropyrimidinase-Like Proteins Family in Synaptic Physiology and in Neurodevelopmental Disorders

Florence Desprez,Dévina C. Ung,Patrick Vourc’h,Médéric Jeanne,Frédéric Laumonnier

Frontiers in Neuroscience（2023）

Cited3Views0Bibtex

Developmental and Behavioral Phenotypes in a Mouse Model of DDX3X Syndrome

Andrea Boitnott,Marta Garcia-Forn,Devina C. Ung,Kristi Niblo,Danielle Mendonca, Yeaji Park, Michael Flores, Sylvia Maxwell,Jacob Ellegood,Lily R. Qiu,Dorothy E. Grice,Jason P. Lerch,Mladen-Roko Rasin,Joseph D. Buxbaum,Elodie Drapeau,Silvia De Rubeis

BIOLOGICAL PSYCHIATRY（2021）

Cited11Views0WOSBibtex

Deciphering DDX3X Syndrome to Capture Determinants of Intellectual Disability

Devina Ung,Andrea Boitnott,Danielle Mendonca,Kristi Niblo,Ricardo Soto-Rifo,Elodie Drapeau,Joseph D. Buxbaum, Roko-Mladen Rasin,Silvia De Rubeis

Biological Psychiatry（2020）

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Exploring the Neurodevelopmental Bases of DDX3X Syndrome

Dévina C. Ung

INSAR 2019 Annual Meeting (2019)

Cited0Views0Bibtex

Whole Genome Sequencing Identifies a De Novo 2.1 Mb Balanced Paracentric Inversion Disrupting FOXP1 and Leading to Severe Intellectual Disability

M-L Vuillaume,B Cogné,M Jeanne,A Boland,D-C Ung,D Quinquis,T Besnard,J-F Deleuze,R Redon,S Bézieau,F Laumonnier,A Toutain

Clinica chimica acta international journal of clinical chemistry（2018）

Cited9Views0WOSBibtex

Supplementary information Ptchd 1 deficiency induces exciatory synaptic and cognitive dysfunctions in mouse

Dévina C Ung,Giovanni Iacono,Hamid Méziane, Emmanuelle Blanchard,Marie-Amélie Papon,Martijn Selten,Jon-Ruben van Rhijn,Rodrick Montjean,Julien Rucci, Stéphane Martin, Andrew Fleet,Marie-Christine Birling,Sylviane Marouillat, Ronald Roepman,Mohammed Selloum,Aline Lux,Rose-Anne Thépault, Paul Hamel,Kirti Mittal, John B Vincent,Olivier Dorseuil,Henk G Stunnenberg,Pierre Billuart,Nael Nadif Kasri,Yann Hérault,Frédéric Laumonnier

semanticscholar（2017）

Cited0Views0Bibtex

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