Walter Patrick Devine, MD, PhD

Photo of Walter Patrick Devine, MD, PhD
Title(s)Associate Professor, Pathology
SchoolSchool of Medicine
Address513 Parnassus Avenue HSW, #450E
San Francisco CA 94143
ORCID ORCID Icon0000-0003-4634-8830 Additional info
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    Other Positions
    Title(s)Stuart Lindsay Endowed Professor in Experimental Pathology III


    Collapse Biography 
    Collapse education and training
    Stanford University, Stanford, CABS/MS06/1996Biology and Music
    Stanford Medical School, Stanford, CAPhD06/2004Biochemistry
    Stanford Medical School, Stanford, CAMD06/2006Medicine
    University of California, San Francisco, San Francisco, CAResidency06/2008Anatomic Pathology
    University of California, San Francisco, San Francisco, CAFellowship06/2018Molecular Genetic Pathology

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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
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    Altmetrics Details PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Prospective consecutive genomic profiling defines the distribution of meningioma molecular alterations across demographic groups. Neuro Oncol. 2026 Aug 19. Braman BC, Nguyen MP, Mirchia K, Morshed RA, Oberheim Bush NA, Arum Z, Villanueva-Meyer JE, Chen WC, Van Ziffle J, Rajkovic A, Chang SM, Devine WP, Perry A, Raleigh DR. PMID: 42616658.
      View in: PubMed   Mentions:
    2. Incremental yield of genome sequencing after exome sequencing for nonimmune hydrops fetalis spectrum. Am J Obstet Gynecol MFM. 2026 Sep; 8(9):102067. Boutin RCT, Lianoglou BR, Sahin Hodoglugil NN, Tick K, Santoli CMA, Hodoglugil U, Martin P, Van Ziffle J, Devine P, Risch N, Norton ME, Sparks TN. PMID: 42471198.
      View in: PubMed   Mentions:    Fields:    
    3. Mullerian Adenosarcomas with Extrauterine Involvement, Sarcomatous Overgrowth and MDM2 Amplification: A Diagnostic Challenge. Int J Surg Pathol. 2026 Jun 10; 10668969261457871. Kayraklioglu N, Sirohi D, Eilers G, Rabban J, Devine WP, Lu K, Horvai A, Gasper C. PMID: 42267461.
      View in: PubMed   Mentions:    Fields:    
    4. Prospective Genomic Profiling of Consecutive Meningiomas. JAMA Oncol. 2026 Jun 01; 12(6):660-662. Nguyen MP, Mirchia K, Braman BC, Morshed RA, Oberheim-Bush NA, Arum Z, Villanueva-Meyer JE, Chen WC, Van Ziffle J, Rajkovic A, Chang SM, Devine WP, Perry A, Raleigh DR. PMID: 41954897; PMCID: PMC13067134.
      View in: PubMed   Mentions:    Fields:    
    5. Ppm1d Clonal Hematopoiesis Does Not Promote Atherosclerosis in Murine Models. Arterioscler Thromb Vasc Biol. 2026 Jul; 46(7):e323733. De Jeronimo Diaz C, Liao H, Hardaway B, Li L, Gan AL, Liu M, Kim A, Qian G, Abramowicz S, Lam E, Tseng ZH, Devine WP, Tall AR, Yu Z, Miller PG, Ebert BL, Fidler TP. PMID: 42165150; PMCID: PMC13215213.
      View in: PubMed   Mentions:    Fields:    Translation:Animals
    6. Novel BRAF fusion in Erdheim-Chester disease with pulmonary manifestations: Importance of RNA-based testing and response to MEK inhibition. Histopathology. 2026 Sep; 89(3):558-561. Odintsov I, Tazelaar HD, Lee JC, Damon LE, Devine WP, Jones KD. PMID: 42082348; PMCID: PMC13441322.
      View in: PubMed   Mentions:    Fields:    
    7. Limited Availability of Short Tandem Repeat Genotype Testing in the United States for Diagnosis of Partial Hydatidiform Mole: A Dilemma for Practicing Precision Medicine. Am J Surg Pathol. 2026 Aug 01; 50(8):917-923. Warren L, Tafe LJ, Devine WP, Rabban JT. PMID: 42424170.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    8. Copy Number-low/TP53-mutated Endometrial Cancer With Wild-type p53 Immunoexpression: Implications for Risk Stratification and Management When Using Next-generation Sequencing for Molecular Classification. Mod Pathol. 2026 06; 39(6):101005. Rabban JT, Wolsky RJ, Kayraklioglu N, Davies KD, Aisner DL, Devine WP. PMID: 42025847.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    9. Genetic, Immunohistochemical and mRNA In Situ Hybridization Profiling of Condyloma with Concurrent Squamous Cell Carcinoma and High-Grade Squamous Intraepithelial Lesion. Mod Pathol. 2026 06; 39(6):100996. Samghabadi P, Ding C, Khorsandi N, Lu KL, Devine WP, Gasper C. PMID: 41936843.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    10. CGE26-139: Genomic Signatures of CNS and Systemic Relapse in Diffuse Large B-Cell Lymphoma (DLBCL) Patients Profiled With Next Generation Sequencing (NGS). J Natl Compr Canc Netw. 2026 Mar 31; 24(3.5). Bowers JT, Vijayanarayanan A, Gill N, Traglia M, Thomas R, Andreadis CB, Ai WZ, Ho C, Kaplan LD, Merrill MH, Seshadri MR, Randall MP, Rubenstein JL, Ganapathi K, Prakash S, Devine WP, Spinner MA. PMID: 41991041.
      View in: PubMed   Mentions:    Fields:    
    11. A Case of Encephalocraniocutaneous Lipomatosis (ECCL) With Atypical Clinical Presentation Diagnosed on Molecular Testing: FGFR1 ECCL Tumor Risk. Am J Med Genet A. 2026 Aug; 200(8):1862-1867. Thakral A, Santoli CMA, Idowu O, Dowd C, Vassar RL, Devine WP, Van Ziffle J, Frieden IJ, Tam A, Shieh JT. PMID: 41856681.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    12. TANC1::HTRA1 fusion in schwannomas. Brain Pathol. 2026 Sep; 36(5):e70084. Caliskan I, Mirchia K, Devine WP, Pekmezci M. PMID: 41685421; PMCID: PMC13429294.
      View in: PubMed   Mentions:    Fields:    
    13. A disrupted compartment boundary underlies abnormal cardiac patterning and congenital heart defects. Nat Cardiovasc Res. 2026 Jan; 5(1):67-83. Kathiriya IS, Dominguez MH, Rao KS, Muncie-Vasic JM, Devine WP, Hu KM, Hota SK, Garay BI, Quintero D, Goyal P, Matthews MN, Thomas R, Sukonnik T, Miguel-Perez D, Winchester S, Brower EF, Forjaz A, Wu PH, Wirtz D, Kiemen AL, Bruneau BG. PMID: 41461901; PMCID: PMC12811143.
      View in: PubMed   Mentions:    Fields:    Translation:Animals
    14. MultiSite Assembly of Gateway Induced Clones (MAGIC): a flexible cloning toolbox for use in vertebrate model systems. Development. 2025 11 15; 152(22). Gillespie WB, Zhang Y, Ruiz OE, Cerda J, Ortiz-Guzman J, Sherman M, Turner WD, Largoza G, Mosser LE, Fujimoto E, Chien CB, Kwan KM, Arenkiel BR, Devine WP, Wythe JD. PMID: 41230856; PMCID: PMC12669975.
      View in: PubMed   Mentions:    Fields:    Translation:HumansAnimalsCells
    15. Genomic Profiling of Intraocular Leiomyomas Reveals Recurrent Copy Number Alterations. Transl Vis Sci Technol. 2025 Nov 03; 14(11):25. Tang V, Chou Y, Demirkesen C, Bloomer MM, Crawford JB, Sarici AM, Shields C, Eagle RC, Iacob CE, Devine WP, Milman T, Pekmezci M. PMID: 41251529; PMCID: PMC12636993.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    16. Insights Into Congenital Lymphatic Anomalies Underlying Fetal Effusions. Prenat Diagn. 2026 01; 46(1):3-11. Vargo SG, Rogerson D, Devine P, Van Ziffle J, Sparks TN. PMID: 41185095; PMCID: PMC12744567.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    17. Genetic diseases underlying a spectrum of fetal effusions. Am J Obstet Gynecol. 2025 Oct; 233(4):333.e1-333.e11. Gulrajani NB, Lianoglou BR, Tick K, Sahin-Hodoglugil NN, Hodoglugil U, Devine P, Van Ziffle J, Norton ME, Sparks TN. PMID: 40348118; PMCID: PMC12370382.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    18. Identification of genomic biomarkers of disease progression and survival in primary CNS lymphoma. Blood Adv. 2025 Mar 11; 9(5):1117-1131. Geng H, Mo S, Chen L, Ballapuram A, Tsang M, Lu M, Rauschecker AM, Wen KW, Devine WP, Solomon DA, Rubenstein JL. PMID: 39536287; PMCID: PMC11914178.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    19. Clinical implementation of preemptive pharmacogenomics testing for personalized medicine at an academic medical center. J Am Med Inform Assoc. 2025 03 01; 32(3):566-571. Tamraz B, Shin J, Khanna R, Van Ziffle J, Knowles S, Stregowski S, Wan E, Kamath R, Collins C, Phunsur C, Tsai B, Kong P, Calanoc C, Pollard A, Sawhney R, Pleiman J, Devine WP, Croci R, Sashikanth A, Kroon L, Cucina R, Rajkovic A. PMID: 39665424; PMCID: PMC11833476.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    20. NTRK-fusion spindle cell tumour in the breast: expanding the differential of challenging spindle cell lesions on core biopsy. Histopathology. 2025 May; 86(6):1018-1021. Schwartz CJ, Ye J, Devine WP, Chen YY. PMID: 39888039.
      View in: PubMed   Mentions:    Fields:    
    21. Prenatal Exome Sequencing Identifies Dual Maternal-Fetal Diagnosis of HbF Mission Bay, a Novel HBG2 Variant Associated With Methemoglobinemia, Hypoxia and Hemolytic Anemia. Prenat Diagn. 2025 Jan 02. Shear MA, Lianoglou B, Hodoglugil U, Devine WP, Lal A, Gonzalez J, Sparks TN. PMID: 39746815.
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    22. Fetal Intracranial Hemorrhage due to Uniparental Disomy and Unmasked MPL-Related Congenital Amegakaryocytic Thrombocytopenia. Prenat Diagn. 2024 Dec 31. Gano D, Glenn OA, Rand L, Heraty K, Devine P, Norton ME, Sparks TN. PMID: 39739357.
      View in: PubMed   Mentions: 1     Fields:    
    23. Heritable Burden of Community Sudden Death by Autopsy and Molecular Phenotyping for Precision Genotype Correlation. JACC Clin Electrophysiol. 2025 03; 11(3):471-481. Tseng ZH, Salazar JW, Wojciak J, Devine WP, Kinkead BA, Yee M, Eik D, Feng J, Connolly AJ, Moffatt E. PMID: 39708038; PMCID: PMC12117619.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    24. TTN Variants, Dilated Cardiomyopathy, and Arrhythmic Causes by Autopsy Among Countywide Sudden Deaths. JACC Clin Electrophysiol. 2025 Jan; 11(1):213-216. Yee M, Salazar JW, Wojciak J, Devine WP, Moffatt E, Tseng ZH. PMID: 39641695; PMCID: PMC12077136.
      View in: PubMed   Mentions: 1     Fields:    
    25. Effective Use of ALK Inhibitors in EML4::ALK-Positive Lymphatic Malformations. Pediatr Blood Cancer. 2025 Feb; 72(2):e31441. Apsel Winger B, Dowd CF, Shimano KA, Devine WP, Mathes E, Frieden I, Schaefer C, Kothari A. PMID: 39529238.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    26. HER2 overexpression in urothelial carcinoma with GATA3 and PPARG copy number gains. Oncologist. 2024 08 05; 29(8):e1094-e1097. Zhu X, Chan E, Turski ML, Mendez CE, Hsu SC, Kumar V, Shipp C, Jindal T, Chang K, Onodera C, Devine WP, Grenert JP, Stohr BA, Ding CC, Stachler MD, Quigley DA, Feng FY, Chu CE, Porten SP, Chou J, Friedlander TW, Koshkin VS. PMID: 38908022; PMCID: PMC11299940.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    27. Neoadjuvant Osimertinib for the Treatment of Stage I-IIIA Epidermal Growth Factor Receptor-Mutated Non-Small Cell Lung Cancer: A Phase II Multicenter Study. J Clin Oncol. 2024 09 10; 42(26):3105-3114. Blakely CM, Urisman A, Gubens MA, Mulvey CK, Allen GM, Shiboski SC, Rotow JK, Chakrabarti T, Kerr DL, Aredo JV, Bacaltos B, Gee M, Tan L, Jones KD, Devine WP, Doebele RC, Aisner DL, Patil T, Schenk EL, Bivona TG, Riess JW, Coleman M, Kratz JR, Jablons DM. PMID: 39028931; PMCID: PMC11379363.
      View in: PubMed   Mentions: 40     Fields:    Translation:HumansCTClinical Trials
    28. Multisite Assembly of Gateway Induced Clones (MAGIC): a flexible cloning toolbox with diverse applications in vertebrate model systems. bioRxiv. 2024 Jul 13. Gillespie W, Zhang Y, Ruiz OE, Cerda J, Ortiz-Guzman J, Turner WD, Largoza G, Sherman M, Mosser LE, Fujimoto E, Chien CB, Kwan KM, Arenkiel BR, Devine WP, Wythe JD. PMID: 39026881; PMCID: PMC11257631.
      View in: PubMed   Mentions:
    29. Cell-Type Specificity of Mosaic Chromosome 1q Gain Resolved by snRNA-seq in a Case of Epilepsy With Hyaline Protoplasmic Astrocytopathy. Neurol Genet. 2024 Apr; 10(2):e200142. Leng K, Cadwell CR, Devine WP, Tihan T, Qi Z, Singhal NS, Glenn OA, Kamiya S, Wiita AP, Berger AC, Shieh JT, Titus EW, Paredes MF, Upadhyay V. PMID: 38586598; PMCID: PMC10997208.
      View in: PubMed   Mentions:
    30. A disrupted compartment boundary underlies abnormal cardiac patterning and congenital heart defects. bioRxiv. 2024 Mar 04. Kathiriya IS, Dominguez MH, Rao KS, Muncie-Vasic JM, Devine WP, Hu KM, Hota SK, Garay BI, Quintero D, Goyal P, Matthews MN, Thomas R, Sukonnik T, Miguel-Perez D, Winchester S, Brower EF, Forjaz A, Wu PH, Wirtz D, Kiemen AL, Bruneau BG. PMID: 38370632; PMCID: PMC10871243.
      View in: PubMed   Mentions: 1  
    31. Genetic ancestry and diagnostic yield of exome sequencing in a diverse population. NPJ Genom Med. 2024 Jan 03; 9(1):1. Mavura Y, Sahin-Hodoglugil N, Hodoglugil U, Kvale M, Martin PM, Van Ziffle J, Devine WP, Ackerman SL, Koenig BA, Kwok PY, Norton ME, Slavotinek A, Risch N. PMID: 38172272; PMCID: PMC10764913.
      View in: PubMed   Mentions: 8  
    32. Novel SOX10 indel mutations drive schwannomas through impaired transactivation of myelination gene programs. Neuro Oncol. 2023 12 08; 25(12):2221-2236. Williams EA, Ravindranathan A, Gupta R, Stevers NO, Suwala AK, Hong C, Kim S, Yuan JB, Wu J, Barreto J, Lucas CG, Chan E, Pekmezci M, LeBoit PE, Mully T, Perry A, Bollen A, Van Ziffle J, Devine WP, Reddy AT, Gupta N, Basnet KM, Macaulay RJB, Malafronte P, Lee H, Yong WH, Williams KJ, Juratli TA, Mata DA, Huang RSP, Hiemenz MC, Pavlick DC, Frampton GM, Janovitz T, Ross JS, Chang SM, Berger MS, Jacques L, Song JS, Costello JF, Solomon DA. PMID: 37436963; PMCID: PMC10708934.
      View in: PubMed   Mentions: 18     Fields:    Translation:Humans
    33. Author Correction: Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population. NPJ Genom Med. 2023 Oct 23; 8(1):34. Slavotinek A, Rego S, Sahin-Hodoglugil N, Kvale M, Lianoglou B, Yip T, Hoban H, Outram S, Anguiano B, Chen F, Michelson J, Cilio RM, Curry C, Gallagher RC, Gardner M, Kuperman R, Mendelsohn B, Sherr E, Shieh J, Strober J, Tam A, Tenney J, Weiss W, Whittle A, Chin G, Faubel A, Prasad H, Mavura Y, Van Ziffle J, Devine WP, Hodoglugil U, Martin PM, Sparks TN, Koenig B, Ackerman S, Risch N, Kwok PY, Norton ME. PMID: 37872195; PMCID: PMC10593851.
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    34. Genetic and Immunohistochemical Profiling of Mammary Hidradenoma and Comparison to Mucoepidermoid Carcinoma. Mod Pathol. 2023 10; 36(10):100270. Black MA, Neumann NM, Krings G, Najjar S, Troxell ML, Wang A, Devine WP, Vohra P, Gasper C, Chen YY, Cohen JN, Bean GR. PMID: 37422157.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    35. EML4::ALK fusions in complex lymphatic malformations. Pediatr Blood Cancer. 2023 Jun 28; e30516. Apsel Winger B, Devine WP, Hsiao EC, Zapala M, Van Ziffle J, Gupta N, Frieden IJ, Shimano KA. PMID: 37377128.
      View in: PubMed   Mentions: 2     Fields:    
    36. Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population. NPJ Genom Med. 2023 May 26; 8(1):10. Slavotinek A, Rego S, Sahin-Hodoglugil N, Kvale M, Lianoglou B, Yip T, Hoban H, Outram S, Anguiano B, Chen F, Michelson J, Cilio RM, Curry C, Gallagher RC, Gardner M, Kuperman R, Mendelsohn B, Sherr E, Shieh J, Strober J, Tam A, Tenney J, Weiss W, Whittle A, Chin G, Faubel A, Prasad H, Mavura Y, Van Ziffle J, Devine WP, Hodoglugil U, Martin PM, Sparks TN, Koenig B, Ackerman S, Risch N, Kwok PY, Norton ME. PMID: 37236975; PMCID: PMC10220040.
      View in: PubMed   Mentions: 23  
    37. TFG::ALK fusion in ALK positive large B-cell lymphoma: a case report and review of literature. Front Oncol. 2023; 13:1174606. Xiao A, Shahmarvand N, Nagy A, Kumar J, Van Ziffle J, Devine P, Huang F, Lezama L, Li P, Ohgami RS. PMID: 37305584; PMCID: PMC10248242.
      View in: PubMed   Mentions: 2  
    38. Diagnostic Yield of Exome Sequencing in a Diverse Pediatric and Prenatal Population is not Associated with Genetic Ancestry. medRxiv. 2023 May 24. Mavura Y, Sahin-Hodoglugil N, Hodoglugil U, Kvale M, Martin PM, Van Ziffle J, Devine WP, Ackerman SL, Koenig BA, Kwok PY, Norton ME, Slavotinek A, Risch N. PMID: 37293051; PMCID: PMC10246153.
      View in: PubMed   Mentions:
    39. A Mesp1-dependent developmental breakpoint in transcriptional and epigenomic specification of early cardiac precursors. Development. 2023 05 01; 150(9). Krup AL, Winchester SAB, Ranade SS, Agrawal A, Devine WP, Sinha T, Choudhary K, Dominguez MH, Thomas R, Black BL, Srivastava D, Bruneau BG. PMID: 36994838; PMCID: PMC10259516.
      View in: PubMed   Mentions: 7     Fields:    Translation:AnimalsCells
    40. Loss of p16 expression is a sensitive marker of CDKN2A homozygous deletion in malignant meningiomas. Acta Neuropathol. 2023 04; 145(4):497-500. Tang V, Lu R, Mirchia K, Van Ziffle J, Devine P, Lee J, Phillips JJ, Perry A, Raleigh DR, Lucas CG, Solomon DA. PMID: 36723772; PMCID: PMC10020299.
      View in: PubMed   Mentions: 15     Fields:    Translation:Humans
    41. EMILIN1 deficiency causes arterial tortuosity with osteopenia and connects impaired elastogenesis with defective collagen fibrillogenesis. Am J Hum Genet. 2022 12 01; 109(12):2230-2252. Adamo CS, Beyens A, Schiavinato A, Keene DR, Tufa SF, Mörgelin M, Brinckmann J, Sasaki T, Niehoff A, Dreiner M, Pottie L, Muiño-Mosquera L, Gulec EY, Gezdirici A, Braghetta P, Bonaldo P, Wagener R, Paulsson M, Bornaun H, De Rycke R, De Bruyne M, Baeke F, Devine WP, Gangaram B, Tam A, Balasubramanian M, Ellard S, Moore S, Symoens S, Shen J, Cole S, Schwarze U, Holmes KW, Hayflick SJ, Wiszniewski W, Nampoothiri S, Davis EC, Sakai LY, Sengle G, Callewaert B. PMID: 36351433; PMCID: PMC9748297.
      View in: PubMed   Mentions: 9     Fields:    Translation:HumansAnimals
    42. Targeted Next-Generation Sequencing Reveals Divergent Clonal Evolution in Components of Composite Pleomorphic Xanthoastrocytoma-Ganglioglioma. J Neuropathol Exp Neurol. 2022 07 19; 81(8):650-657. Lucas CG, Davidson CJ, Alashari M, Putnam AR, Whipple NS, Bruggers CS, Mendez JS, Cheshier SH, Walker JB, Ramani B, Cadwell CR, Sullivan DV, Lu R, Mirchia K, Van Ziffle J, Devine P, Goldschmidt E, Hervey-Jumper SL, Gupta N, Oberheim Bush NA, Raleigh DR, Bollen A, Tihan T, Pekmezci M, Solomon DA, Phillips JJ, Perry A. PMID: 35703914; PMCID: PMC9297094.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    43. The utility of pathologic examination and comprehensive phenotyping for accurate diagnosis with perinatal exome sequencing. Prenat Diagn. 2022 09; 42(10):1288-1294. Swanson K, Norton ME, Lianoglou BR, Jelin AC, Hodoglugil U, Van Ziffle J, Devine P, Sparks TN. PMID: 35723972; PMCID: PMC9531346.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    44. De novo heterozygous variants in SLC30A7 are a candidate cause for Joubert syndrome. Am J Med Genet A. 2022 08; 188(8):2360-2366. Penon-Portmann M, Eldomery MK, Potocki L, Marafi D, Posey JE, Coban-Akdemir Z, Harel T, Grochowski CM, Loucks H, Devine WP, Van Ziffle J, Doherty D, Lupski JR, Shieh JT. PMID: 35751429; PMCID: PMC9756141.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    45. Homologous Recombination Deficiency and Ovarian Cancer Treatment Decisions: Practical Implications for Pathologists for Tumor Typing and Reporting. Surg Pathol Clin. 2022 Jun; 15(2):219-234. Rabban JT, Chen LM, Devine WP. PMID: 35715159.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    46. Further description of two patients with biallelic variants in NADSYN1 in association with cardiac and vertebral anomalies. Am J Med Genet A. 2022 08; 188(8):2479-2484. Kortbawi H, Ames E, Pritchard A, Devine P, van Ziffle J, Slavotinek A. PMID: 35491967.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    47. Tumor and Constitutional Sequencing for Neurofibromatosis Type 1. JCO Precis Oncol. 2022 05; 6:e2100540. Tong S, Devine WP, Shieh JT. PMID: 35584348; PMCID: PMC9200388.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    48. Expanding the phenotype of males with OFD1 pathogenic variants-a case report and literature review. Eur J Med Genet. 2022 Jun; 65(6):104496. Gangaram B, Devine WP, Slavotinek A. PMID: 35398350; PMCID: PMC10369588.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    49. APOBEC Mutational Signature and Tumor Mutational Burden as Predictors of Clinical Outcomes and Treatment Response in Patients With Advanced Urothelial Cancer. Front Oncol. 2022; 12:816706. Natesan D, Zhang L, Martell HJ, Jindal T, Devine P, Stohr B, Espinosa-Mendez C, Grenert J, Van Ziffle J, Joseph N, Umetsu S, Onodera C, Turski M, Chan E, Desai A, Aggarwal R, Wong A, Porten S, Chou J, Friedlander T, Fong L, Small EJ, Sweet-Cordero A, Koshkin VS. PMID: 35321431; PMCID: PMC8935010.
      View in: PubMed   Mentions: 10  
    50. ALK Immunoexpression is Specific for Inflammatory Myofibroblastic Tumor Among Vulvovaginal Mesenchymal Neoplasms. Int J Gynecol Pathol. 2023 Jan 01; 42(1):1-10. Bowman CJ, Medeiros F, Fadare O, Sangoi AR, Horvai AE, Devine WP, McCluggage WG, Rabban JT. PMID: 35180768.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    51. Activating NTRK2 and ALK receptor tyrosine kinase fusions extend the molecular spectrum of pleomorphic xanthoastrocytomas of early childhood: a diagnostic overlap with infant-type hemispheric glioma. Acta Neuropathol. 2022 02; 143(2):283-286. Lucas CG, Abdullaev Z, Bruggers CS, Mirchia K, Whipple NS, Alashari MM, Lowichik A, Cheshier S, Phillips JJ, Devine P, Solomon DA, Quezado M, Aldape KD, Perry A. PMID: 34910220; PMCID: PMC8742815.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    52. Cytoplasmic Pattern p53 Immunoexpression in Pelvic and Endometrial Carcinomas With TP53 Mutation Involving Nuclear Localization Domains: An Uncommon But Potential Diagnostic Pitfall With Clinical Implications. Am J Surg Pathol. 2021 11 01; 45(11):1441-1451. Rabban JT, Garg K, Ladwig NR, Zaloudek CJ, Devine WP. PMID: 33899789.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansCells
    53. Exome sequencing vs targeted gene panels for the evaluation of nonimmune hydrops fetalis. Am J Obstet Gynecol. 2022 01; 226(1):128.e1-128.e11. Norton ME, Ziffle JV, Lianoglou BR, Hodoglugil U, Devine WP, Sparks TN. PMID: 34331894; PMCID: PMC8748274.
      View in: PubMed   Mentions: 17     Fields:    Translation:Humans
    54. New cases that expand the genotypic and phenotypic spectrum of Congenital NAD Deficiency Disorder. Hum Mutat. 2021 07; 42(7):862-876. Szot JO, Slavotinek A, Chong K, Brandau O, Nezarati M, Cueto-González AM, Patel MS, Devine WP, Rego S, Acyinena AP, Shannon P, Myles-Reid D, Blaser S, Mieghem TV, Yavuz-Kienle H, Skladny H, Miller K, Riera MDT, Martínez SA, Tizzano EF, Dupuis L, James Stavropoulos D, McNiven V, Mendoza-Londono R, Elliott AM, CAUSES Study, Phillips RS, Chapman G, Dunwoodie SL. PMID: 33942433; PMCID: PMC8238843.
      View in: PubMed   Mentions: 16     Fields:    Translation:HumansAnimals
    55. Segmental overgrowth and aneurysms due to mosaic PDGFRB p.(Tyr562Cys). Am J Med Genet A. 2021 05; 185(5):1430-1436. Chenbhanich J, Hu Y, Hetts S, Cooke D, Dowd C, Devine P, UCLA Clinical Genomics Center, Russell B, Kang SHL, Chang VY, Abla AA, Cornett P, Yeh I, Lee H, Martinez-Agosto JA, Frieden IJ, Shieh JT. PMID: 33683022.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    56. Modeling Human TBX5 Haploinsufficiency Predicts Regulatory Networks for Congenital Heart Disease. Dev Cell. 2021 02 08; 56(3):292-309.e9. Kathiriya IS, Rao KS, Iacono G, Devine WP, Blair AP, Hota SK, Lai MH, Garay BI, Thomas R, Gong HZ, Wasson LK, Goyal P, Sukonnik T, Hu KM, Akgun GA, Bernard LD, Akerberg BN, Gu F, Li K, Speir ML, Haeussler M, Pu WT, Stuart JM, Seidman CE, Seidman JG, Heyn H, Bruneau BG. PMID: 33321106; PMCID: PMC7878434.
      View in: PubMed   Mentions: 67     Fields:    Translation:HumansAnimalsCells
    57. De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathy. Genet Med. 2021 04; 23(4):653-660. Klöckner C, Sticht H, Zacher P, Popp B, Babcock HE, Bakker DP, Barwick K, Bonfert MV, Bönnemann CG, Brilstra EH, Care4Rare Canada Consortium, Chung WK, Clarke AJ, Devine P, Donkervoort S, Fraser JL, Friedman J, Gates A, Ghoumid J, Hobson E, Horvath G, Keller-Ramey J, Keren B, Kurian MA, Lee V, Leppig KA, Lundgren J, McDonald MT, McLaughlin HM, McTague A, Mefford HC, Mignot C, Mikati MA, Nava C, Raymond FL, Sampson JR, Sanchis-Juan A, Shashi V, Shieh JTC, Shinawi M, Slavotinek A, Stödberg T, Stong N, Sullivan JA, Taylor AC, Toler TL, van den Boogaard MJ, van der Crabben SN, van Gassen KLI, van Jaarsveld RH, Van Ziffle J, Wadley AF, Wagner M, Wigby K, Wigby K, Wortmann SB, Zarate YA, Møller RS, Lemke JR, Platzer K. PMID: 33299146.
      View in: PubMed   Mentions: 23     Fields:    Translation:Humans
    58. Exome Sequencing for Prenatal Diagnosis in Nonimmune Hydrops Fetalis. N Engl J Med. 2020 10 29; 383(18):1746-1756. Sparks TN, Lianoglou BR, Adami RR, Pluym ID, Holliman K, Duffy J, Downum SL, Patel S, Faubel A, Boe NM, Field NT, Murphy A, Laurent LC, Jolley J, Uy C, Slavotinek AM, Devine P, Hodoglugil U, Van Ziffle J, Sanders SJ, MacKenzie TC, Norton ME, University of California Fetal–Maternal Consortium, University of California, San Francisco Center for Maternal–Fetal Precision Medicine. PMID: 33027564; PMCID: PMC7650529.
      View in: PubMed   Mentions: 81     Fields:    Translation:Humans
    59. NTRK fusion cervical sarcoma: a report of three cases, emphasising morphological and immunohistochemical distinction from other uterine sarcomas, including adenosarcoma. Histopathology. 2020 Jul; 77(1):100-111. Rabban JT, Devine WP, Sangoi AR, Poder L, Alvarez E, Davis JL, Rudzinski E, Garg K, Bean GR. PMID: 31971278.
      View in: PubMed   Mentions: 30     Fields:    Translation:Humans
    60. Pediatric bithalamic gliomas have a distinct epigenetic signature and frequent EGFR exon 20 insertions resulting in potential sensitivity to targeted kinase inhibition. Acta Neuropathol. 2020 06; 139(6):1071-1088. Mondal G, Lee JC, Ravindranathan A, Villanueva-Meyer JE, Tran QT, Allen SJ, Barreto J, Gupta R, Doo P, Van Ziffle J, Onodera C, Devine P, Grenert JP, Samuel D, Li R, Metrock LK, Jin LW, Antony R, Alashari M, Cheshier S, Whipple NS, Bruggers C, Raffel C, Gupta N, Kline CN, Reddy A, Banerjee A, Hall MD, Mehta MP, Khatib Z, Maher OM, Brathwaite C, Pekmezci M, Phillips JJ, Bollen AW, Tihan T, Lucas JT, Broniscer A, Berger MS, Perry A, Orr BA, Solomon DA. PMID: 32303840; PMCID: PMC7792550.
      View in: PubMed   Mentions: 50     Fields:    Translation:Humans
    61. Hydra: A mixture modeling framework for subtyping pediatric cancer cohorts using multimodal gene expression signatures. PLoS Comput Biol. 2020 04; 16(4):e1007753. Pfeil J, Sanders LM, Anastopoulos I, Lyle AG, Weinstein AS, Xue Y, Blair A, Beale HC, Lee A, Leung SG, Dinh PT, Shah AT, Breese MR, Devine WP, Bjork I, Salama SR, Sweet-Cordero EA, Haussler D, Vaske OM. PMID: 32275708; PMCID: PMC7176284.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    62. Gliomas arising in the setting of Li-Fraumeni syndrome stratify into two molecular subgroups with divergent clinicopathologic features. Acta Neuropathol. 2020 05; 139(5):953-957. Sloan EA, Hilz S, Gupta R, Cadwell C, Ramani B, Hofmann J, Kline CN, Banerjee A, Reddy A, Oberheim Bush NA, Chang S, Braunstein S, Chang EF, Raffel C, Gupta N, Sun PP, Kim JYH, Moes G, Alva E, Li R, Bruggers CS, Alashari M, Wetmore C, Garg S, Dishop M, Van Ziffle J, Onodera C, Devine P, Grenert JP, Lee JC, Phillips JJ, Pekmezci M, Tihan T, Bollen AW, Berger MS, Costello JF, Perry A, Solomon DA. PMID: 32157385; PMCID: PMC7183424.
      View in: PubMed   Mentions: 19     Fields:    Translation:Humans
    63. Targeted Therapy and Checkpoint Immunotherapy in Lung Cancer. Surg Pathol Clin. 2020 Mar; 13(1):17-33. Ruiz-Cordero R, Devine WP. PMID: 32005431.
      View in: PubMed   Mentions: 257     Fields:    Translation:Humans
    64. Practical roles for molecular diagnostic testing in ovarian adult granulosa cell tumour, Sertoli-Leydig cell tumour, microcystic stromal tumour and their mimics. Histopathology. 2020 Jan; 76(1):11-24. Rabban JT, Karnezis AN, Devine WP. PMID: 31846522.
      View in: PubMed   Mentions: 13     Fields:    Translation:Humans
    65. Clinicopathologic and molecular features of intracranial desmoplastic small round cell tumors. Brain Pathol. 2020 03; 30(2):213-225. Lee JC, Villanueva-Meyer JE, Ferris SP, Cham EM, Zucker J, Cooney T, Gilani A, Kleinschmidt-DeMasters BK, Trembath D, Mafra M, Chiang J, Ellison DW, Cho SJ, Horvai AE, Van Ziffle J, Onodera C, Devine P, Grenert JP, de Voijs CMA, van Blokland WTM, de Leng WWJ, Ploegmakers MJ, Flucke U, Pekmezci M, Bollen AW, Tihan T, Koelsche C, von Deimling A, Wesseling P, Solomon DA, Perry A. PMID: 31837177; PMCID: PMC7780368.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    66. Next-Generation Sequencing of Retinoblastoma Identifies Pathogenic Alterations beyond RB1 Inactivation That Correlate with Aggressive Histopathologic Features. Ophthalmology. 2020 06; 127(6):804-813. Afshar AR, Pekmezci M, Bloomer MM, Cadenas NJ, Stevers M, Banerjee A, Roy R, Olshen AB, Van Ziffle J, Onodera C, Devine WP, Grenert JP, Bastian BC, Solomon DA, Damato BE. PMID: 32139107; PMCID: PMC7246167.
      View in: PubMed   Mentions: 34     Fields:    Translation:Humans
    67. Myxoid glioneuronal tumor, PDGFRA p.K385-mutant: clinical, radiologic, and histopathologic features. Brain Pathol. 2020 05; 30(3):479-494. Lucas CG, Villanueva-Meyer JE, Whipple N, Oberheim Bush NA, Cooney T, Chang S, McDermott M, Berger M, Cham E, Sun PP, Putnam A, Zhou H, Bollo R, Cheshier S, Poppe MM, Fung KM, Sung S, Glenn C, Fan X, Bannykh S, Hu J, Danielpour M, Li R, Alva E, Johnston J, Van Ziffle J, Onodera C, Devine P, Grenert JP, Lee JC, Pekmezci M, Tihan T, Bollen AW, Perry A, Solomon DA. PMID: 31609499; PMCID: PMC7780370.
      View in: PubMed   Mentions: 34     Fields:    Translation:Humans
    68. Recurrent non-canonical histone H3 mutations in spinal cord diffuse gliomas. Acta Neuropathol. 2019 11; 138(5):877-881. Sloan EA, Cooney T, Oberheim Bush NA, Buerki R, Taylor J, Clarke JL, Torkildson J, Kline C, Reddy A, Mueller S, Banerjee A, Butowski N, Chang S, Mummaneni PV, Chou D, Tan L, Theodosopoulos P, McDermott M, Berger M, Raffel C, Gupta N, Sun PP, Li Y, Shah V, Cha S, Braunstein S, Raleigh DR, Samuel D, Scharnhorst D, Fata C, Guo H, Moes G, Kim JYH, Koschmann C, Van Ziffle J, Onodera C, Devine P, Grenert JP, Lee JC, Pekmezci M, Phillips JJ, Tihan T, Bollen AW, Perry A, Solomon DA. PMID: 31515627; PMCID: PMC6818961.
      View in: PubMed   Mentions: 13     Fields:    Translation:Humans
    69. TP53 structural variants in metastatic prostatic carcinoma. PLoS One. 2019; 14(6):e0218618. Sirohi D, Devine P, Grenert JP, van Ziffle J, Simko JP, Stohr BA. PMID: 31216325; PMCID: PMC6583940.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    70. Heart enhancers with deeply conserved regulatory activity are established early in zebrafish development. Nat Commun. 2018 11 26; 9(1):4977. Yuan X, Song M, Devine P, Bruneau BG, Scott IC, Wilson MD. PMID: 30478328; PMCID: PMC6255839.
      View in: PubMed   Mentions: 35     Fields:    Translation:HumansAnimalsCells
    71. Identification of high-risk human papillomavirus and Rb/E2F pathway genomic alterations in mutually exclusive subsets of colorectal neuroendocrine carcinoma. Mod Pathol. 2019 02; 32(2):290-305. Shamir ER, Devine WP, Pekmezci M, Umetsu SE, Krings G, Federman S, Cho SJ, Saunders TA, Jen KY, Bergsland E, Jones K, Kim GE, Kakar S, Chiu CY, Joseph NM. PMID: 30237525.
      View in: PubMed   Mentions: 28     Fields:    Translation:Humans
    72. A novel reporter allele for monitoring Dll4 expression within the embryonic and adult mouse. Biol Open. 2018 Mar 12; 7(3). Herman AM, Rhyner AM, Devine WP, Marrelli SP, Bruneau BG, Wythe JD. PMID: 29437553; PMCID: PMC5898260.
      View in: PubMed   Mentions: 6     Fields:    
    73. Early patterning and specification of cardiac progenitors in gastrulating mesoderm. Elife. 2014 Oct 08; 3. Devine WP, Wythe JD, George M, Koshiba-Takeuchi K, Bruneau BG. PMID: 25296024; PMCID: PMC4356145.
      View in: PubMed   Mentions: 125     Fields:    Translation:AnimalsCells
    74. ETS factors regulate Vegf-dependent arterial specification. Dev Cell. 2013 Jul 15; 26(1):45-58. Wythe JD, Dang LT, Devine WP, Boudreau E, Artap ST, He D, Schachterle W, Stainier DY, Oettgen P, Black BL, Bruneau BG, Fish JE. PMID: 23830865; PMCID: PMC3754838.
      View in: PubMed   Mentions: 99     Fields:    Translation:HumansAnimalsCells
    75. Refractory lower gastrointestinal bleeding from portal hypertensive colopathy. J Am Coll Surg. 2008 Oct; 207(4):613. Ozgediz D, Devine P, Garcia-Aguilar J, Balibrea JM. PMID: 18926469.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    76. Requirement for chitin biosynthesis in epithelial tube morphogenesis. Proc Natl Acad Sci U S A. 2005 Nov 22; 102(47):17014-9. Devine WP, Lubarsky B, Shaw K, Luschnig S, Messina L, Krasnow MA. PMID: 16287975; PMCID: PMC1283532.
      View in: PubMed   Mentions: 75     Fields:    Translation:Animals
    77. Cortical neurons require Otx1 for the refinement of exuberant axonal projections to subcortical targets. Neuron. 1999 Dec; 24(4):819-31. Weimann JM, Zhang YA, Levin ME, Devine WP, Brûlet P, McConnell SK. PMID: 10624946.
      View in: PubMed   Mentions: 60     Fields:    Translation:AnimalsCells
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