Year |
Citation |
Score |
Low-probability matches (unlikely to be authored by this person) |
2018 |
Herman AM, Rhyner AM, Devine WP, Marrelli SP, Bruneau BG, Wythe JD. A novel reporter allele for monitoringexpression within the embryonic and adult mouse. Biology Open. PMID 29437553 DOI: 10.1242/Bio.026799 |
0.282 |
|
2020 |
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, et al. Hydra: A mixture modeling framework for subtyping pediatric cancer cohorts using multimodal gene expression signatures. Plos Computational Biology. 16: e1007753. PMID 32275708 DOI: 10.1371/Journal.Pcbi.1007753 |
0.217 |
|
2022 |
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. De novo heterozygous variants in SLC30A7 are a candidate cause for Joubert syndrome. American Journal of Medical Genetics. Part A. PMID 35751429 DOI: 10.1002/ajmg.a.62872 |
0.192 |
|
2013 |
Wythe JD, Dang LT, Devine WP, Boudreau E, Artap ST, He D, Schachterle W, Stainier DY, Oettgen P, Black BL, Bruneau BG, Fish JE. ETS factors regulate Vegf-dependent arterial specification. Developmental Cell. 26: 45-58. PMID 23830865 DOI: 10.1016/J.Devcel.2013.06.007 |
0.156 |
|
2022 |
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, ... ... Devine WP, et al. EMILIN1 deficiency causes arterial tortuosity with osteopenia and connects impaired elastogenesis with defective collagen fibrillogenesis. American Journal of Human Genetics. PMID 36351433 DOI: 10.1016/j.ajhg.2022.10.010 |
0.153 |
|
2021 |
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, et al. New Cases that Expand the Genotypic and Phenotypic Spectrum of Congenital NAD Deficiency Disorder. Human Mutation. PMID 33942433 DOI: 10.1002/humu.24211 |
0.133 |
|
2020 |
Rabban JT, Karnezis AN, Devine WP. Practical roles for molecular diagnostic testing in ovarian adult granulosa cell tumour, Sertoli-Leydig cell tumour, microcystic stromal tumour and their mimics. Histopathology. 76: 11-24. PMID 31846522 DOI: 10.1111/his.13978 |
0.125 |
|
1999 |
Weimann JM, Zhang YA, Levin ME, Devine WP, Brûlet P, McConnell SK. Cortical neurons require Otx1 for the refinement of exuberant axonal projections to subcortical targets. Neuron. 24: 819-31. PMID 10624946 DOI: 10.1016/S0896-6273(00)81030-2 |
0.12 |
|
2014 |
Devine WP, Wythe JD, George M, Koshiba-Takeuchi K, Bruneau BG. Early patterning and specification of cardiac progenitors in gastrulating mesoderm. Elife. 3. PMID 25296024 DOI: 10.7554/Elife.03848 |
0.086 |
|
2023 |
Apsel Winger B, Devine WP, Hsiao EC, Zapala M, Van Ziffle J, Gupta N, Frieden IJ, Shimano KA. EML4::ALK fusions in complex lymphatic malformations. Pediatric Blood & Cancer. e30516. PMID 37377128 DOI: 10.1002/pbc.30516 |
0.073 |
|
2020 |
Ruiz-Cordero R, Devine WP. Targeted Therapy and Checkpoint Immunotherapy in Lung Cancer. Surgical Pathology Clinics. 13: 17-33. PMID 32005431 DOI: 10.1016/j.path.2019.11.002 |
0.071 |
|
2019 |
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. Next-Generation Sequencing of Retinoblastoma Identifies Pathogenic Alterations beyond RB1 Inactivation That Correlate with Aggressive Histopathologic Features. Ophthalmology. PMID 32139107 DOI: 10.1016/J.Ophtha.2019.12.005 |
0.033 |
|
2005 |
Devine WP, Lubarsky B, Shaw K, Luschnig S, Messina L, Krasnow MA. Requirement for chitin biosynthesis in epithelial tube morphogenesis. Proceedings of the National Academy of Sciences of the United States of America. 102: 17014-9. PMID 16287975 DOI: 10.1073/Pnas.0506676102 |
0.014 |
|
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