Candace Myers - University of Washington Seattle

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论文共 57 篇作者统计合作学者相似作者

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Solving the Etiology of Developmental and Epileptic Encephalopathy with Spike-Wave Activation in Sleep (D/EE-SWAS)

ANNALS OF NEUROLOGYno. 5 (2024): 932-943

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P596: Diagnostic Challenges and Phenotypic Variations in Chimeric Genome-Wide Maternal and Paternal Uniparental Disomy: A Prenatal and Postnatal Perspective

Candace Myers,Whitney Neufeld-Kaiser,Iya Znoyko, Cindy Johnson,Edith Cheng, Joseph Jwang,Anita Beck,Daynna Wolff,Yajuan Liu

Genetics in Medicine Open (2024): 101502

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Role of CACNG2 Variants in Human Pathology

Sara Cabet, Atul Maheshwari,Jeffrey Noebels,Alica Goldman, Mark Farrant, Stuart Cull-Candy,Ian Coombs,Cecile Bats,Julien Courchet,Dorota Studniarczyk, Margot Vallen,Sylvia Stockler, David Koehn,Kristal Louie,Candace Myers,Heather Jaspan, Jennifer Cech, Jason Lockrow, Elizabeth Gerard,Gemma Louise Carvill,Marwan Shinawi,Aida Telegrafi,Lance Rodan,Yuri Zarate,Jillian G. Buchan, Kenzie Pulsifer, Ebba Alkhunaizi,Vanda McNiven, Samantha Olson,Jennifer Morrison,Patricia Wheeler,Kirsty McWalter,Kristin Monaghan,Carrie Costin,Jill A. Rosenfeld,Almuth Caliebe,Nadine Hornig, Hadil Alrohaif,Reem M. Elshafie,Jonathan Levy,Anne-Claude Tabet, Vincent Trebossen, Clothilde Boulay,Gabrielle Rudolf,Bertrand Isidor, Benjamin Cogne,Damien Sanlaville,Gaetan Lesca

EUROPEAN JOURNAL OF HUMAN GENETICS (2024): 496-496

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Somatic Activating BRAF Variants Cause Isolated Lymphatic Malformations

Kaitlyn Zenner,Dana M. Jensen,Victoria Dmyterko,Giridhar M. Shivaram,Candace T. Myers,Cate R. Paschal,Erin R. Rudzinski, Minh-Hang M. Pham, V. Chi Cheng,Scott C. Manning,Randall A. Bly,Sheila Ganti,Jonathan A. Perkins,James T. Bennett

Human Genetics and Genomics Advances（2022）

引用3浏览0WOS引用

Intestinal Pathology in Patients with Pathogenic ACTG2-Variant Visceral Myopathy: 16 Patients from 12 Families and Review of the Literature

Raj P. Kapur,Allan M. Goldstein,Deborah S. Loeff,Candace T. Myers,Cate Paschal

Pediatric and developmental pathology（2022）

引用2浏览0引用

32. Genetic Testing for Individuals with Non-Syndromic Differences in Sex Development (DSD): Collaborative Approach Yields Results

Cate Randall Paschal,Candace T. Myers,Madelyn Gillentine,Darci L. Sternen,Audrey Squire,Patricia Fechner,Anne-Marie Amies Oelschlager,Margarett Shnorhavorian,Margaret Adam

Cancer Genetics (2022): 11

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Severe speech impairment is a distinguishing feature of FOXP1-related disorder

Ruth O. Braden,David J. Amor,Simon E. Fisher,Cristina Mei,Candace T. Myers,Heather Mefford,Deepak Gill,Siddharth Srivastava,Lindsay C. Swanson,Himanshu Goel,Ingrid E. Scheffer,Angela T. Morgan

DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY（2021）

引用18浏览0WOS引用

The Co‐occurrence of Wilson Disease and X‐linked Agammaglobulinemia in One Family Highlights the Promising Diagnostic Potential of Proteolytic Analysis

Sheri A. Poskanzer,Jenny Thies,Christopher J. Collins,Candace T. Myers,Remwilyn Dayuha,Phi Duong,Fan Yi,Irene J. Chang,Hans D. Ochs,Troy R. Torgerson,Si Houn Hahn

Molecular Genetics & Genomic Medicine（2020）

引用4浏览0WOS引用

Damaging De Novo Missense Variants in EEF1A2 Lead to a Developmental and Degenerative Epileptic‐dyskinetic Encephalopathy

HUMAN MUTATION（2020）

引用15浏览0WOS引用

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