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W. Devine · SciRah

Researcher profile · Semantic Scholar

W. Devine

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W. Devine — researcher profile on SciRah

h-index: 13
Works: 32
Citations: 1,285

Most-cited papers

Targeted Therapy and Checkpoint Immunotherapy in Lung Cancer.
R. Ruiz-Cordero, W. Devine
2020Surgical Pathology Clinics406 citations
Semantic Scholar
Cortical neurons require Otx1 for the refinement of exuberant axonal projections to subcortical targets.
J. Weimann, Y.Alex Zhang, M. E. Levin, W. Devine +2 more
1999Neuron210 citations Open access
Semantic Scholar
Requirement for chitin biosynthesis in epithelial tube morphogenesis.
W. Devine, B. Lubarsky, K. Shaw, S. Luschnig +2 more
2005Proceedings of the National Academy of Sciences of the United States of America162 citations Open access
Semantic Scholar
ETS factors regulate Vegf-dependent arterial specification
Joshua D. Wythe, Lan T. H. Dang, W. Devine, Emilie Boudreau +8 more
2013Developmental Cell140 citations Open access
Semantic Scholar
Modeling human TBX5 haploinsufficiency predicts regulatory networks for congenital heart disease
Irfan S. Kathiriya, Kavitha S. Rao, G. Iacono, W. Devine +23 more
2020Developmental Cell90 citations Open access
Semantic Scholar
Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population
A. Slavotinek, Shannon Rego, Nuriye N Sahin-Hodoglugil, M. Kvale +34 more
2023npj Genomic Medicine45 citations Open access
Semantic Scholar
Cytoplasmic Pattern p53 Immunoexpression in Pelvic and Endometrial Carcinomas With TP53 Mutation Involving Nuclear Localization Domains
J. Rabban, Karuna Garg, Nicholas R Ladwig, C. Zaloudek +1 more
2021American Journal of Surgical Pathology35 citations
Semantic Scholar
Novel SOX10 indel mutations drive schwannomas through impaired transactivation of myelination gene programs
Erik A. Williams, A. Ravindranathan, Rohit Gupta, Nicholas O. Stevers +37 more
2023Neuro-Oncology29 citations Open access
Semantic Scholar
New Cases that Expand the Genotypic and Phenotypic Spectrum of Congenital NAD Deficiency Disorder
J. Szot, A. Slavotinek, K. Chong, O. Brandau +24 more
2021Human Mutation27 citations Open access
Semantic Scholar
Exome sequencing versus targeted gene panels for the evaluation of nonimmune hydrops fetalis
M. Norton, J. Van Ziffle, B. Lianoglou, U. Hodoglugil +2 more
2021American Journal of Obstetrics and Gynecology27 citations Open access
Semantic Scholar
Genetic ancestry and diagnostic yield of exome sequencing in a diverse population
Y. Mavura, Nuriye N Sahin-Hodoglugil, U. Hodoglugil, M. Kvale +9 more
2024npj Genomic Medicine22 citations Open access
Semantic Scholar
EMILIN1 deficiency causes arterial tortuosity with osteopenia and connects impaired elastogenesis with defective collagen fibrillogenesis.
Christin S. Adamo, A. Beyens, A. Schiavinato, D. Keene +36 more
2022American Journal of Human Genetics20 citations Open access
Semantic Scholar
A Mesp1-dependent developmental breakpoint in transcriptional and epigenomic specification of early cardiac precursors
A. Krup, Sarah Winchester, Sanjeev S Ranade, Ayushi Agrawal +8 more
2023Development17 citations Open access
Semantic Scholar
Genetic and Immunohistochemical Profiling of Mammary Hidradenoma and Comparison to Mucoepidermoid Carcinoma.
M. Black, N. Neumann, G. Krings, S. Najjar +8 more
2023Modern Pathology13 citations
Semantic Scholar
ALK Immunoexpression is Specific for Inflammatory Myofibroblastic Tumor Among Vulvovaginal Mesenchymal Neoplasms
Christopher J. Bowman, F. Medeiros, O. Fadare, Ankur R. Sangoi +4 more
2022International Journal of Gynecological Pathology10 citations
Semantic Scholar
EML4::ALK fusions in complex lymphatic malformations
Beth Apsel Winger, W. Devine, Edward C. Hsiao, Matthew A. Zapala +4 more
2023Pediatric Blood & Cancer7 citations Open access
Semantic Scholar
De novo heterozygous variants in SLC30A7 are a candidate cause for Joubert syndrome
Monica Penon-Portmann, M. Eldomery, L. Potocki, D. Marafi +10 more
2022American Journal of Medical Genetics. Part A7 citations Open access
Semantic Scholar
Tumor and Constitutional Sequencing for Neurofibromatosis Type 1
Schuyler Tong, W. Devine, Joseph T. C. Shieh
2022JCO Precision Oncology6 citations Open access
Semantic Scholar
Expanding the phenotype of males with OFD1 pathogenic variants-a case report and literature review
Balram Gangaram, W. Devine, A. Slavotinek
2022European Journal of Medical Genetics4 citations Open access
Semantic Scholar
PATH-02. NOVEL SOX10 INDEL MUTATIONS DRIVE SCHWANNOMAS THROUGH IMPAIRED TRANSACTIVATION OF MYELINATION GENE PROGRAMS
Erik A. Williams, Ajay Ravindranathan, Rohit Gupta, Nicholas O. Stevers +37 more
2023Neuro-Oncology3 citations Open access
Semantic Scholar
Homologous Recombination Deficiency and Ovarian Cancer Treatment Decisions: Practical Implications for Pathologists for Tumor Typing and Reporting.
J. Rabban, Lee-may Chen, W. Devine
2022Surgical Pathology Clinics3 citations
Semantic Scholar
A TBX5 dosage-sensitive gene regulatory network for human congenital heart disease
Irfan S. Kathiriya, Kavitha S. Rao, G. Iacono, W. Devine +20 more
2019bioRxiv2 citations Open access
Semantic Scholar
Author response: Early patterning and specification of cardiac progenitors in gastrulating mesoderm
W. Devine, Joshua D. Wythe, Matthew George, Kazuko Koshiba-Takeuchi +1 more
20142 citations Open access
Semantic Scholar
Diagnostic Yield of Exome Sequencing in a Diverse Pediatric and Prenatal Population is not Associated with Genetic Ancestry
Y. Mavura, Nuriye N Sahin-Hodoglugil, U. Hodoglugil, M. Kvale +9 more
2023medRxiv1 citations Open access
Semantic Scholar
Author Correction: Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population
A. Slavotinek, Shannon Rego, Nuriye N Sahin-Hodoglugil, M. Kvale +34 more
2023npj Genomic Medicine0 citations Open access
Semantic Scholar
IDENTIFICATION OF GENOMIC BIOMARKERS OF DISEASE PROGRESSION AND SURVIVAL IN NEWLY‐DIAGNOSED PRIMARY CNS LYMPHOMA
S. Mo, H. Geng, A. Ballapuram, L. Chen +5 more
2023Hematological Oncology0 citations Open access
Semantic Scholar
P535: Validation and real-life experience of a comprehensive, targeted next-generation sequencing panel for hereditary cancer predisposition
A. Pinard, A. Chua, U. Hodoglugil, Pièrre-Marie Martin +6 more
2023Genetics in Medicine Open0 citations Open access
Semantic Scholar
O41: Genes associated with disease in fetuses compared to children: Exome sequencing in a large pediatric and prenatal cohort
T. Sparks, B. Lianoglou, Nuriye Sahin-Holodlugil, M. Kvale +10 more
2023Genetics in Medicine Open0 citations Open access
Semantic Scholar
O40: Clinical utility of prenatal exome sequencing in a diverse cohort*
Mary Norton, B. Lianoglou, Matthew A. Shear, Sara L. Ackerman +11 more
2023Genetics in Medicine Open0 citations Open access
Semantic Scholar
P5 Germline testing for endometrial cancer in the age of next generation sequencing
Amie M. Blanco, J. Rabban, W. Devine, Lauren Rehbein
2022Gynecologic Oncology0 citations
Semantic Scholar
Pilot experience using tumor-based next generation sequencing increases compliance and reduces barriers for ovarian cancer genetic testing
Lee-may Chen, W. Devine, J. Chapman, J. Mak +1 more
2021Gynecologic Oncology0 citations
Semantic Scholar
Abstract 10914: Refining Genotype-Phenotype Correlations for Post-Mortem Genetic Testing of Sudden Cardiac Death: From the POST SCD Study
C. Cheung, Julianne Wojciak, Meghan Tanel, A. Connolly +3 more
2021Circulation0 citations
Semantic Scholar

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