Lucy Raymond

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Her research aims to identify and understand the genetic causes of intellectual disability. Her research group conducts detailed analysis of the whole DNA genome in affected families, and this has allowed them to identify novel genes that contribute to this disease. A vital new part of this is their participation in a collaborative UK initiative to analyse the genomes of 10,000 patients in unprecedented detail.

Research Interests

Papers共 263 篇Author StatisticsCo-AuthorSimilar Experts

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The ClinGen Syndromic Disorders Gene Curation Expert Panel: Assessing the Clinical Validity of 111 Gene-Disease Relationships

Eleanor C Broeren, Vanessa N Gitau,Alicia B Byrne, Pamela Ajuyah,Marie B Balzotti,Jonathan S Berg,Krista Bluske, B Monica Bowen, Matthew P Brown, Amanda Buchanan, Brendan T Burns,Nicole J Burns,Anjana Chandrasekhar,Aditi Chawla,Jessica X Chong,Maya Chopra,Amanda R Clause,Marina T DiStefano,Stephanie DiTroia,Marwa A Elnagheeb, Amanda N Girod,Himanshu Goel,Katie L Golden-Grant,Thuong Ha,Ada Hamosh, Jennifer M Huang, Madeline Y Hughes,Saumya S Jamuar,Sylvia Kam,Akanchha Kesari,Ai Ling Koh, Rhonda N T Lassiter,Sarah E Leigh,Gabrielle Lemire,Jiin Ying Lim,Alka Malhotra,Hannah R McCurry,Becky Milewski,Shahida Moosa, Stephen A Murray,Emma H Owens,Elizabeth E Palmer, Brooke C Palus,Mayher J Patel,Revathi Rajkumar, Julie C Ratliff,F Lucy Raymond, Bruno Della Ripa Rodrigues Assis, Samin A Sajan,Zinayida Schlachetzki,Sarah A Schmidt,Zornitza Stark,Samuel P Strom,Julie P Taylor,Courtney Thaxton,Devon L Thrush,Sabrina Toro, Kezang C Tshering,Nicole A Vasilevsky,Bess Wayburn, Ryan F Webb,Anne O'Donnell-Luria,Alison J Coffey

Genetics in medicine open (2025): 103429-103429

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Exome and Genome Sequencing to Diagnose the Genetic Basis of Neonatal Hypotonia

Sarah U. Morton,Gregory Costain,Courtney E. French,Emma Wakeling,Anna Szuto,John Christodoulou,Ronald Cohn, Basil T. Darras, Monica H. Wojcik,Alissa M. D'Gama, James J. Dowling, Sebastian Lunke,Francesco Muntoni,Lucy Raymond,David Rowitch, Alan H. Beggs, Zornitza Stark, Pankaj B. Agrawal

Neurologyno. 1 (2025)

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Congenital Titinopathy: Comprehensive Characterization of the Most Severe End of the Disease Spectrum

Sandra Coppens,Nicolas Deconinck,Patricia Sullivan,Andrei Smolnikov,Joshua S. Clayton, Kaitlyn R. Griffin,Kristi J. Jones,Catheline N. Vilain,Hazim Kadhim,Samantha J. Bryen,Fathimath Faiz,Leigh B. Waddell,Frances J. Evesson,Madhura Bakshi,Jason R. Pinner,Amanda Charlton,Susan Brammah,Nicole S. Graf,Michael Krivanek,Chee Geap Tay,Nicola C. Foulds,Marjorie A. Illingworth, Neil H. Thomas,Sian Ellard, Ingrid Mazanti,Soo-Mi Park,Courtney E. French, Jennifer Brewster, Gusztav Belteki, Shazia Hoodbhoy, Kieren Allinson,Deepa Krishnakumar,Gareth Baynam, Bradley M. Wood, Michelle Ward,Kayal Vijayakumar, Amber Syed, Archana Murugan,Anirban Majumdar,Ingrid J. Scurr, Miranda P. Splitt, Corina Moldovan,Deepthi C. de Silva, Kumudu Senanayake,Thatjana Gardeitchik,Yvonne Arens,Sandra T. Cooper,Nigel G. Laing,F. Lucy Raymond,Heinz Jungbluth,Erik-Jan Kamsteeg,Adnan Manzur,Susan M. Corley,Gianina Ravenscroft, Marc R. Wilkins,Mark J. Cowley, Mark Pinese,Rahul Phadke,Mark R. Davis,Francesco Muntoni,Emily C. Oates

ANNALS OF NEUROLOGY (2025)

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Exome and Genome Sequencing to Diagnose the Genetic Basis of Neonatal Hypotonia: an International Consortium Study

Sarah U Morton,Gregory Costain,Courtney E French,Emma Wakeling,Anna Szuto,John Christodoulou,Ronald Cohn,Basil T Darras,Monica H Wojcik,Alissa M D'Gama,James J Dowling, Sebastian Lunke,Francesco Muntoni,Lucy Raymond,David Rowitch,Alan H Beggs, Zornitza Stark,Pankaj B Agrawal

Neurologyno. 1 (2024): e210106-e210106

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Population Screening Requires Robust Evidence-Genomics is No Exception

Clare Turnbull,Helen Firth,Andrew O. M. Wilkie,William Newman,F. Lucy Raymond,Ian Tomlinson,Robin Lachmann,Caroline F. Wright,Sarah Wordsworth,Angela George,Margaret Mccartney,Anneke Lucassen

The Lancetno. 10426 (2024): 583-586

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Abrogation of MAP4K4 Protein Function Causes Congenital Anomalies in Humans and Zebrafish

SCIENCE ADVANCESno. 17 (2023)

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Genome Sequencing and Comprehensive Rare Variant Analysis of 465 Families with Neurodevelopmental Disorders

AMERICAN JOURNAL OF HUMAN GENETICSno. 8 (2023): 1343-1355

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Identifying the Neurodevelopmental and Psychiatric Signatures of Genomic Disorders Associated with Intellectual Disability: a Machine Learning Approach

Nicholas Donnelly,Adam Cunningham, Sergio Marco Salas,Matthew Bracher-Smith,Samuel Chawner,Jan Stochl,Tamsin Ford,F. Lucy Raymond,Valentina Escott-Price,Marianne B. M. van den Bree

Molecular Autism（2023）

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Emeritus Professor

Papers共 263 篇Author StatisticsCo-AuthorSimilar Experts