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Works (7)

NTRK‐fusion spindle cell tumour in the breast: expanding the differential of challenging spindle cell lesions on core biopsy

Histopathology
2025-01-30 | Journal article
Contributors: Christopher J Schwartz; Julia Ye; W. Patrick Devine; Yunn‐Yi Chen
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Cell-Type Specificity of Mosaic Chromosome 1q Gain Resolved by snRNA-seq in a Case of Epilepsy With Hyaline Protoplasmic Astrocytopathy

Neurology Genetics
2024-04 | Journal article
Contributors: Kun Leng; Cathryn R. Cadwell; Walter P. Devine; Tarik Tihan; Zhongxia Qi; Nilika S. Singhal; Orit A. Glenn; Sherry Kamiya; Arun P. Wiita; Amy C. Berger et al.
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Genetic ancestry and diagnostic yield of exome sequencing in a diverse population

npj Genomic Medicine
2024-01-03 | Journal article
Contributors: Yusuph Mavura; Nuriye Sahin-Hodoglugil; Ugur Hodoglugil; Mark Kvale; Pierre-Marie Martin; Jessica Van Ziffle; W. Patrick Devine; Sara L. Ackerman; Barbara A. Koenig; Pui-Yan Kwok et al.
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Tumor and Constitutional Sequencing for Neurofibromatosis Type 1

JCO Precision Oncology
2022-05 | Journal article
Contributors: Schuyler Tong; W. Patrick Devine; Joseph T. Shieh
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Exome sequencing vs targeted gene panels for the evaluation of nonimmune hydrops fetalis

American Journal of Obstetrics and Gynecology
2022-01 | Journal article
Contributors: Mary E. Norton; Jessica Van Ziffle; Billie R. Lianoglou; Ugur Hodoglugil; W. Patrick Devine; Teresa N. Sparks
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New cases that expand the genotypic and phenotypic spectrum of Congenital NAD Deficiency Disorder

Human Mutation
2021-07-16 | Journal article
Contributors: Justin O. Szot; Anne Slavotinek; Karen Chong; Oliver Brandau; Marjan Nezarati; Anna M. Cueto‐González; Millan S. Patel; Walter P. Devine; Shannon Rego; Alicia P. Acyinena et al.
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Modeling human TBX5 haploinsufficiency predicts regulatory networks for congenital heart disease

2019-11-08 | Other
Contributors: Irfan S. Kathiriya; Kavitha S. Rao; Giovanni Iacono; W. Patrick Devine; Andrew P. Blair; Swetansu K. Hota; Michael H. Lai; Bayardo I. Garay; Reuben Thomas; Henry Z. Gong et al.
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Peer review (2 reviews for 1 publication/grant)

Review activity for npj genomic medicine. (2)