Christine Moore - Division of Medical Genetics, Northwell Health

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Papers共 5 篇Author StatisticsCo-AuthorSimilar Experts

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Author Correction: CHD3 Helicase Domain Mutations Cause a Neurodevelopmental Syndrome with Macrocephaly and Impaired Speech and Language

Lot Snijders Blok,Justine Rousseau,Joanna Twist,Sophie Ehresmann,Motoki Takaku,Hanka Venselaar,Lance H. Rodan,Catherine B. Nowak,Jessica Douglas,Kathryn J. Swoboda,Marcie A. Steeves,Inderneel Sahai,Connie T. R. M. Stumpel,Alexander P. A. Stegmann,Patricia Wheeler,Marcia Willing,Elise Fiala,Aaina Kochhar,William T. Gibson,Ana S. A. Cohen,Ruky Agbahovbe,A. Micheil Innes,P. Y. Billie Au,Julia Rankin,Ilse J. Anderson,Steven A. Skinner,Raymond J. Louie,Hannah E. Warren,Alexandra Afenjar,Boris Keren,Caroline Nava,Julien Buratti,Arnaud Isapof,Diana Rodriguez,Raymond Lewandowski,Jennifer Propst,Ton van Essen,Murim Choi,Sangmoon Lee,Jong H. Chae,Susan Price,Rhonda E. Schnur,Ganka Douglas,Ingrid M. Wentzensen,Christiane Zweier,André Reis,Martin G. Bialer,Christine Moore,Marije Koopmans,Eva H. Brilstra,Glen R. Monroe,Koen L. I. van Gassen,Ellen van Binsbergen,Ruth Newbury-Ecob,Lucy Bownass,Ingrid Bader,Johannes A. Mayr,Saskia B. Wortmann,Kathy J. Jakielski,Edythe A. Strand,Katja Kloth,Tatjana Bierhals,Jeremy F. McRae,John D. Roberts,Robert M. Petrovich,Shinichi Machida,Hitoshi Kurumizaka,Stefan Lelieveld,Rolph Pfundt,Sandra Jansen,Pelagia Deriziotis,Laurence Faivre,Julien Thevenon,Mirna Assoum,Lawrence Shriberg,Tjitske Kleefstra,Han G. Brunner,Paul A. Wade,Simon E. Fisher,Philippe M. Campeau

Nature Communications（2019）

Cited84Views0WOSNATUREBibtex

Author Correction : CHD3 Helicase Domain Mutations Cause a Neurodevelopmental Syndrome with Macrocephaly and Impaired Speech and Language (nature Communications, (2018), 9, 1, (4619), 10.1038/S41467-018-06014-6)

semanticscholar（2019）

Cited23Views0Bibtex

A Cryptic Cause of Cardiac Arrest

Tanya Mokhateb-Rafii,Martin Bialer,Shaun Rodgers,Christine Moore,Todd Sweberg

Journal of Emergency Medicine（2018）

Cited3Views0WOSBibtex

Germline De Novo Mutations in GNB1 Cause Severe Neurodevelopmental Disability, Hypotonia, and Seizures

The American Journal of Human Geneticsno. 5 (2016): 1001-1010

Cited105Views0WOSBibtex

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