W. Devine

发表

Early patterning and specification of cardiac progenitors in gastrulating mesoderm

Joshua D. Wythe, B. Bruneau, K. Koshiba-Takeuchi, 2014, eLife.

De novo heterozygous variants in SLC30A7 are a candidate cause for Joubert syndrome

J. Lupski, J. Posey, Z. Coban-Akdemir, 2022, American journal of medical genetics. Part A.

Homologous Recombination Deficiency and Ovarian Cancer Treatment Decisions: Practical Implications for Pathologists for Tumor Typing and Reporting.

J. Rabban, W. Devine, Lee-may Chen, 2022, Surgical pathology clinics.

Tumor and Constitutional Sequencing for Neurofibromatosis Type 1

J. Shieh, W. Devine, Schuyler Tong, 2022, JCO precision oncology.

A Mesp1-dependent developmental breakpoint in transcriptional and epigenomic specification of early cardiac precursors

B. Bruneau, D. Srivastava, Sanjeev S. Ranade, 2022, bioRxiv.

ALK Immunoexpression is Specific for Inflammatory Myofibroblastic Tumor Among Vulvovaginal Mesenchymal Neoplasms

A. Sangoi, A. Horvai, J. Rabban, 2022, International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists.

Hydra: A mixture modeling framework for subtyping pediatric cancer cohorts using multimodal gene expression signatures

David Haussler, Holly C Beale, Lauren M Sanders, 2020, PLoS Comput. Biol..

A TBX5 dosage-sensitive gene regulatory network for human congenital heart disease

Joshua M. Stuart, J. Seidman, B. Bruneau, 2019, bioRxiv.

EMILIN1 deficiency causes arterial tortuosity with osteopenia and connects impaired elastogenesis with defective collagen fibrillogenesis.

Takako Sasaki, S. Ellard, Stacey L. Cole, 2022, American journal of human genetics.

ETS factors regulate Vegf-dependent arterial specification.

Joshua D. Wythe, B. Bruneau, P. Oettgen, 2013, Developmental cell.

NTRK fusion cervical sarcoma: a report of three cases, emphasising morphological and immunohistochemical distinction from other uterine sarcomas, including adenosarcoma

Jessica L. Davis, A. Sangoi, G. Bean, 2020, Histopathology.

Targeted Therapy and Checkpoint Immunotherapy in Lung Cancer.

R. Ruiz-Cordero, W. Devine, R. Ruiz‐Cordero, 2020, Surgical pathology clinics.

Modeling Human TBX5 Haploinsufficiency Predicts Regulatory Networks for Congenital Heart Disease.

Joshua M. Stuart, J. Seidman, B. Bruneau, 2019, Developmental cell.

Identification of high-risk human papillomavirus and Rb/E2F pathway genomic alterations in mutually exclusive subsets of colorectal neuroendocrine carcinoma

W Patrick Devine, Kuang-Yu Jen, Kirk Jones, 2018, Modern Pathology.

Next-Generation Sequencing of Retinoblastoma Identifies Pathogenic Alterations beyond RB1 Inactivation That Correlate with Aggressive Histopathologic Features.

A. Olshen, C. Onodera, B. Bastian, 2019, Ophthalmology.

Practical roles for molecular diagnostic testing in ovarian adult granulosa cell tumour, Sertoli–Leydig cell tumour, microcystic stromal tumour and their mimics

A. Karnezis, J. Rabban, W. Devine, 2020, Histopathology.

New cases that expand the genotypic and phenotypic spectrum of Congenital NAD Deficiency Disorder

Shannon Rego, S. Dunwoodie, P. Shannon, 2021, Human mutation.

Requirement for chitin biosynthesis in epithelial tube morphogenesis.

M. Krasnow, L. Messina, S. Luschnig, 2005, Proceedings of the National Academy of Sciences of the United States of America.

Exome sequencing versus targeted gene panels for the evaluation of nonimmune hydrops fetalis.

U. Hodoğlugil, T. Sparks, M. Norton, 2021, American journal of obstetrics and gynecology.

Expanding the phenotype of males with OFD1 pathogenic variants-a case report and literature review.

A. Slavotinek, W. Devine, Balram Gangaram, 2022, European journal of medical genetics.

Cytoplasmic Pattern p53 Immunoexpression in Pelvic and Endometrial Carcinomas With TP53 Mutation Involving Nuclear Localization Domains

K. Garg, J. Rabban, C. Zaloudek, 2021, The American journal of surgical pathology.

Cortical Neurons Require Otx1 for the Refinement of Exuberant Axonal Projections to Subcortical Targets

S. Mcconnell, J. Weimann, P. Brûlet, 1999, Neuron.

Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population

P. Kwok, M. Kvale, U. Hodoğlugil, 2023, NPJ genomic medicine.

Diagnostic Yield of Exome Sequencing in a Diverse Pediatric and Prenatal Population is not Associated with Genetic Ancestry

P. Kwok, M. Kvale, U. Hodoğlugil, 2023, medRxiv.

A novel reporter allele for monitoring Dll4 expression within the embryonic and adult mouse

Alexander M. Rhyner, Joshua D. Wythe, Alexander M. Herman, 2017, Biology Open.

EML4::ALK fusions in complex lymphatic malformations

Matthew A. Zapala, E. Hsiao, N. Gupta, 2023, Pediatric blood & cancer.

Author response: Early patterning and specification of cardiac progenitors in gastrulating mesoderm

Joshua D. Wythe, B. Bruneau, K. Koshiba-Takeuchi, 2014 .

Genetic and Immunohistochemical Profiling of Mammary Hidradenoma and Comparison to Mucoepidermoid Carcinoma.

M. Troxell, Yunni-Yi Chen, G. Bean, 2023, Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc.

Modeling Human TBX5 Haploinsufficiency Predicts Regulatory Networks for Congenital Heart Disease.

Joshua M. Stuart, J. Seidman, B. Bruneau, 2020, Developmental cell.