Thomas S. Jacques - Publications

Affiliations: 
Institute of Child Health University College London, London, United Kingdom 

67 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Ritzmann TA, Rogers HA, Paine SML, Storer LCD, Jacques TS, Chapman RJ, Ellison D, Donson AM, Foreman NK, Grundy RG. A retrospective analysis of recurrent pediatric ependymoma reveals extremely poor survival and ineffectiveness of current treatments across central nervous system locations and molecular subgroups. Pediatric Blood & Cancer. e28426. PMID 32614133 DOI: 10.1002/Pbc.28426  0.324
2020 Clarke M, Mackay A, Ismer B, Pickles JC, Tatevossian RG, Newman S, Bale TA, Stoler I, Izquierdo E, Temelso S, Carvalho DM, Molinari V, Burford A, Howell L, Virasami A, ... ... Jacques TS, et al. Infant high grade gliomas comprise multiple subgroups characterized by novel targetable gene fusions and favorable outcomes. Cancer Discovery. PMID 32238360 DOI: 10.1158/2159-8290.Cd-19-1030  0.308
2020 Pickles JC, Stone TJ, Jacques TS. Methylation-based algorithms for diagnosis: experience from neuro-oncology. The Journal of Pathology. PMID 32057098 DOI: 10.1002/Path.5397  0.307
2019 Wefers AK, Stichel D, Schrimpf D, Coras R, Pages M, Tauziède-Espariat A, Varlet P, Schwarz D, Söylemezoglu F, Pohl U, Pimentel J, Meyer J, Hewer E, Japp A, Joshi A, ... ... Jacques TS, et al. Isomorphic diffuse glioma is a morphologically and molecularly distinct tumour entity with recurrent gene fusions of MYBL1 or MYB and a benign disease course. Acta Neuropathologica. PMID 31563982 DOI: 10.1007/S00401-019-02078-W  0.326
2019 Panagopoulou P, Sattar S, Aquilina K, Jan W, Jacques T, Slater O. Challenges in the Diagnosis of Medulloblastoma Recurrence at an Unusual Site in a Patient With Prader-Willi Syndrome. Journal of Pediatric Hematology/Oncology. PMID 31306337 DOI: 10.1097/Mph.0000000000001555  0.323
2019 Carreno G, Boult JKR, Apps JR, Gonzalez-Meljem JM, Haston S, Guiho R, Stache C, Danielson LS, Koers A, Smith LS, Virasami A, Panousopoulos L, Buchfelder M, Jacques TS, Chesler L, et al. SHH pathway inhibition is protumourigenic in adamantinomatous craniopharyngioma. Endocrine-Related Cancer. PMID 30645190 DOI: 10.1530/Erc-18-0538  0.307
2019 Benova B, Jacques TS. Genotype-phenotype correlations in focal malformations of cortical development: a pathway to integrated pathological diagnosis in epilepsy surgery. Brain Pathology. 29: 473-484. PMID 30485578 DOI: 10.1111/Bpa.12686  0.322
2019 Ritzmann T, Rogers H, Paine S, Jacques T, Donson A, Phipps K, Foreman N, Grundy R. G537 A retrospective analysis of recurrent paediatric ependymoma: poor survival and ineffective therapy necessitates a better understanding of relapse biology to develop improved therapeutic approaches Archives of Disease in Childhood. 104. DOI: 10.1136/Archdischild-2019-Rcpch.520  0.343
2019 Smolicz I, Fairchild A, Pickles J, Stone T, Chalker J, Zapata JG, Wilkhu L, Yasin S, Merve A, Harding B, Hargrave D, Sebire N, Jacques T. 49 The biology of paediatric central nervous system tumours at post-mortem Archives of Disease in Childhood. 104. DOI: 10.1136/Archdischild-2019-Gosh.49  0.347
2018 Blümcke I, Coras R, Wefers AK, Capper D, Aronica E, Becker A, Honavar M, Stone TJ, Jacques TS, Miyata H, Mühlebner A, Pimentel J, Söylemezoğlu F, Thom M. Challenges in the histopathological classification of ganglioglioma and DNT: microscopic agreement studies and a preliminary genotype-phenotype analysis. Neuropathology and Applied Neurobiology. PMID 30326153 DOI: 10.1111/Nan.12522  0.337
2018 Sa M, Green L, Abdel-Mannan O, Chong W', Jacques T, Clarke A, Childs AM, Lim M, Hemingway C, Hacohen Y. Is chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids (CLIPPERS) in children the same condition as in adults? Developmental Medicine and Child Neurology. PMID 30146710 DOI: 10.1111/Dmcn.13997  0.31
2018 Sa M, Hacohen Y, Alderson L, Chong WKK, Anderson G, Jacques TS, Neubauer D, Szczepanik E, Lim M, Kaliakatsos M. Immunotherapy-responsive childhood neurodegeneration with systemic and central nervous system inflammation. European Journal of Paediatric Neurology : Ejpn : Official Journal of the European Paediatric Neurology Society. PMID 29759327 DOI: 10.1016/J.Ejpn.2018.04.010  0.308
2018 Apps JR, Carreno G, Gonzalez-Meljem JM, Haston S, Guiho R, Cooper JE, Manshaei S, Jani N, Hölsken A, Pettorini B, Beynon RJ, Simpson DM, Fraser HC, Hong Y, Hallang S, ... ... Jacques TS, et al. Tumour compartment transcriptomics demonstrates the activation of inflammatory and odontogenic programmes in human adamantinomatous craniopharyngioma and identifies the MAPK/ERK pathway as a novel therapeutic target. Acta Neuropathologica. PMID 29541918 DOI: 10.1007/S00401-018-1830-2  0.319
2018 Capper D, Jones DTW, Sill M, Hovestadt V, Schrimpf D, Sturm D, Koelsche C, Sahm F, Chavez L, Reuss DE, Kratz A, Wefers AK, Huang K, Pajtler KW, Schweizer L, ... ... Jacques TS, et al. DNA methylation-based classification of central nervous system tumours. Nature. PMID 29539639 DOI: 10.1038/Nature26000  0.311
2018 Burford A, Mackay A, Popov S, Vinci M, Carvalho D, Clarke M, Izquierdo E, Avery A, Jacques TS, Ingram WJ, Moore AS, Frawley K, Hassall TE, Robertson T, Jones C. The ten-year evolutionary trajectory of a highly recurrent paediatric high grade neuroepithelial tumour with MN1:BEND2 fusion. Scientific Reports. 8: 1032. PMID 29348602 DOI: 10.1038/S41598-018-19389-9  0.357
2018 Stone TJ, Rowell R, Jayasekera BAP, Cunningham MO, Jacques TS. Molecular characteristics of long-term epilepsy-associated tumours (LEATs) and mechanisms for tumour-related epilepsy (TRE). Neuropathology and Applied Neurobiology. PMID 29315734 DOI: 10.1111/Nan.12459  0.304
2018 Finetti MA, Selby Mp, Pons Ad, Batting S, Wood JA, Barker JM, Smith A, Crosier S, Bashton M, Pickles JC, Fairchild AR, Avery A, O’Hare P, Pizer B, Brennan B, ... ... Jacques TS, et al. Atrt-23. Smarcb1-Dependencies In Atypical Teratoid/Rhabdoid Tumours: A Strategy For Pre-Clinical Therapeutic Target Identification In The Absence Of Actionable Mutations Neuro-Oncology. 20. DOI: 10.1093/Neuonc/Noy059.021  0.302
2018 Grabovska Y, Finetti M, Selby MP, Schwalbe EC, Smith A, Crosier S, Pickles JC, Fairchild AR, Avery A, O’Hare P, Pizer B, Brennan B, Hargrave D, Anderson J, Jacques TS, et al. Atrt-20. Intra- And Extra-Cranial Malignant Rhabdoid Tumours Share Common Location-Independent Clinical And Molecular Disease Characteristics Neuro-Oncology. 20. DOI: 10.1093/Neuonc/Noy059.018  0.323
2017 Izquierdo E, Yuan L, George S, Hubank M, Jones C, Proszek P, Shipley J, Gatz SA, Stinson C, Moore AS, Clifford SC, Hicks D, Lindsey JC, Hill RM, Jacques TS, et al. Development of a targeted sequencing approach to identify prognostic, predictive and diagnostic markers in paediatric solid tumours. Oncotarget. 8: 112036-112050. PMID 29340109 DOI: 10.18632/Oncotarget.23000  0.301
2017 Tan AP, Jacques TS, Mankad K, James G, Jeelani O, Slater O, D'Arco F. Melanotic neuroectodermal tumour of infancy: A case report and differential diagnosis. The Neuroradiology Journal. 1971400917741770. PMID 29125038 DOI: 10.1177/1971400917741770  0.324
2017 Stone TJ, Keeley A, Virasami A, Harkness W, Tisdall M, Izquierdo Delgado E, Gutteridge A, Brooks T, Kristiansen M, Chalker J, Wilkhu L, Mifsud W, Apps J, Thom M, Hubank M, ... ... Jacques TS, et al. Comprehensive molecular characterisation of epilepsy-associated glioneuronal tumours. Acta Neuropathologica. PMID 29058119 DOI: 10.1007/S00401-017-1773-Z  0.348
2017 Pickles JC, Hawkins C, Pietsch T, Jacques TS. CNS embryonal tumours: WHO 2016 and beyond. Neuropathology and Applied Neurobiology. PMID 28949028 DOI: 10.1111/Nan.12443  0.344
2017 Wesseling P, Jacques TS. Taxonomy of CNS Tumours; A Series of Three Short Reviews on the WHO 2016 Classification and Beyond. Neuropathology and Applied Neurobiology. PMID 28944505 DOI: 10.1111/Nan.12442  0.316
2017 Liu J, Reeves C, Jacques T, McEvoy A, Miserocchi A, Thompson P, Sisodiya S, Thom M. Nestin-expressing cell types in the temporal lobe and hippocampus: Morphology, differentiation, and proliferative capacity. Glia. PMID 28925561 DOI: 10.1002/Glia.23211  0.305
2017 Thom M, Liu J, Bongaarts A, Reinten RJ, Paradiso B, Jäger HR, Reeves C, Somani A, An S, Marsdon D, McEvoy A, Miserocchi A, Thorne L, Newman F, Bucur S, ... ... Jacques T, et al. MULTINODULAR AND VACUOLATING NEURONAL TUMOURS IN EPILEPSY: DYSPLASIA OR NEOPLASIA? Brain Pathology (Zurich, Switzerland). PMID 28833756 DOI: 10.1111/Bpa.12555  0.354
2017 Shelmerdine SC, Hutchinson JC, Sebire NJ, Jacques TS, Arthurs OJ. Post-mortem magnetic resonance (PMMR) imaging of the brain in fetuses and children with histopathological correlation. Clinical Radiology. PMID 28821323 DOI: 10.1016/J.Crad.2017.07.015  0.31
2017 Schwalbe EC, Lindsey JC, Nakjang S, Crosier S, Smith AJ, Hicks D, Rafiee G, Hill RM, Iliasova A, Stone T, Pizer B, Michalski A, Joshi A, Wharton SB, Jacques TS, et al. Novel molecular subgroups for clinical classification and outcome prediction in childhood medulloblastoma: a cohort study. The Lancet. Oncology. PMID 28545823 DOI: 10.1016/S1470-2045(17)30243-7  0.304
2017 Hikmat O, Tzoulis C, Chong WK, Chentouf L, Klingenberg C, Fratter C, Carr LJ, Prabhakar P, Kumaraguru N, Gissen P, Cross JH, Jacques TS, Taanman JW, Bindoff LA, Rahman S. The clinical spectrum and natural history of early-onset diseases due to DNA polymerase gamma mutations. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 28471437 DOI: 10.1038/Gim.2017.35  0.35
2017 Kinsler VA, O'Hare P, Jacques T, Hargrave D, Slater O. MEK inhibition appears to improve symptom control in primary NRAS-driven CNS melanoma in children. British Journal of Cancer. 116: 990-993. PMID 28253523 DOI: 10.1038/Bjc.2017.49  0.332
2017 Bryant VA, Booth J, Palm L, Ashworth M, Jacques TS, Sebire NJ. Childhood neoplasms presenting at autopsy: A 20-year experience. Pediatric Blood & Cancer. 64. PMID 28164435 DOI: 10.1002/Pbc.26474  0.307
2017 Kinsler VA, O'Hare P, Bulstrode N, Calonje JE, Chong WK, Hargrave D, Jacques T, Lomas D, Sebire NJ, Slater O. Melanoma in congenital melanocytic naevi. The British Journal of Dermatology. PMID 28078671 DOI: 10.1111/Bjd.15301  0.315
2017 Al-Olabi L, Polubothu S, Dowsett K, Andrews KA, Stadnik P, Joseph AP, Knox R, Pittman A, Clark G, Baird W, Bulstrode N, Glover M, Gordon K, Hargrave D, Huson SM, ... Jacques T, et al. C2.2 Postzygotic activating variants in mapk pathway genes cause intracranial and extracranial vascular malformations that respond to targeted inhibition Archives of Disease in Childhood. 102. DOI: 10.1136/Archdischild-2017-084620.30  0.302
2017 Schwalbe E, Lindsey J, Nakjang S, Crosier S, Smith A, Hicks D, Rafiee G, Hill R, Iliasova A, Stone T, Pizer B, Michalski A, Joshi A, Robson K, Wharton S, ... Jacques T, et al. Medu-06: Novel Molecular Subgroups Improve Clinical Classification And Outcome Prediction For Childhood Medulloblastoma Neuro-Oncology. 19. DOI: 10.1093/Neuonc/Nox083.157  0.307
2017 Yasin SA, Schutz PW, Deakin CT, Sag E, Varsani H, Simou S, Tansley S, McHugh N, Holton JL, Wedderburn LR, Jacques TS. Biopsy pathology in a large cohort of juvenile dermatomyositis is heterogeneous and, for the most part, independent of autoantibody phenotype Canadian Journal of Neurological Sciences. 44. DOI: 10.1017/Cjn.2017.17  0.306
2017 Apps J, Carreno G, Boult J, Gutteridge A, Danielson L, Jani N, Tossell K, Forshew T, Hargrave D, Chesler L, Robinson S, Jacques T, Williams H, Martinez-Barbera JP. Molecular profiling and preclinical targeted therapeutic testing in adamantinomatous craniopharyngioma The Lancet. 389. DOI: 10.1016/S0140-6736(17)30418-X  0.335
2016 Blümcke I, Aronica E, Becker A, Capper D, Coras R, Honavar M, Jacques TS, Kobow K, Miyata H, Mühlebner A, Pimentel J, Söylemezoğlu F, Thom M. Low-grade epilepsy-associated neuroepithelial tumours - the 2016 WHO classification. Nature Reviews. Neurology. 12: 732-740. PMID 27857123 DOI: 10.1038/Nrneurol.2016.173  0.331
2016 Reid ES, Papandreou A, Drury S, Boustred C, Yue WW, Wedatilake Y, Beesley C, Jacques TS, Anderson G, Abulhoul L, Broomfield A, Cleary M, Grunewald S, Varadkar SM, Lench N, et al. Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes. Brain : a Journal of Neurology. PMID 27604308 DOI: 10.1093/Brain/Aww221  0.327
2016 Rajakulendran S, Pitceathly RD, Taanman JW, Costello H, Sweeney MG, Woodward CE, Jaunmuktane Z, Holton JL, Jacques TS, Harding BN, Fratter C, Hanna MG, Rahman S. A Clinical, Neuropathological and Genetic Study of Homozygous A467T POLG-Related Mitochondrial Disease. Plos One. 11: e0145500. PMID 26735972 DOI: 10.1371/Journal.Pone.0145500  0.307
2016 Apps JR, Jani N, Carreno G, Gonzalez-Meljem JM, Tossell K, Stone TJ, Ungless MA, Williams HJ, Jacques TS, Martinez-Barbera J. Abstract 1804: Expression analysis of adamantinomatous craniopharyngioma suggests two subtypes associated withCTNNB1mutational frequency and highlights potential therapeutic targets Cancer Research. 76: 1804-1804. DOI: 10.1158/1538-7445.Am2016-1804  0.303
2016 Hicks D, Rafiee G, Schwalbe E, Howell C, Lindsey J, Hill R, Smith A, Crosier S, Joshi A, Robson K, Wharton S, Jacques T, Williamson D, Bailey S, Clifford aS. Mb-63Subgroup-Directed Stratification Of Risk In Infant Medulloblastoma Neuro-Oncology. 18. DOI: 10.1093/Neuonc/Now076.59  0.306
2015 Angelini P, Chalker J, Austin N, Hing S, Paine SM, Mankad K, Hargrave D, Jacques TS. Genetic heterogeneity for SMARCB1, H3F3A and BRAF in a malignant childhood brain tumour: genetic-pathological correlation. Neuropathology and Applied Neurobiology. 41: 832-6. PMID 26084471 DOI: 10.1111/Nan.12257  0.35
2015 Moraitis E, Foley AR, Pilkington CA, Manzur AY, Quinlivan R, Jacques TS, Phadke R, Compeyrot-Lacassagne S. Infantile-onset LMNA-associated Muscular Dystrophy Mimicking Juvenile Idiopathic Inflammatory Myopathy. The Journal of Rheumatology. 42: 1064-6. PMID 26034236 DOI: 10.3899/Jrheum.140554  0.304
2015 Hill RM, Kuijper S, Lindsey JC, Petrie K, Schwalbe EC, Barker K, Boult JK, Williamson D, Ahmad Z, Hallsworth A, Ryan SL, Poon E, Robinson SP, Ruddle R, Raynaud FI, ... ... Jacques TS, et al. Combined MYC and P53 defects emerge at medulloblastoma relapse and define rapidly progressive, therapeutically targetable disease. Cancer Cell. 27: 72-84. PMID 25533335 DOI: 10.1016/J.Ccell.2014.11.002  0.314
2015 Amarasinghe SG, Ben-Ali H, Jacques TS, Hatfield RH, Leach PA. A rare case of multicystic disseminated astrocytoma with pilomyxoid characteristics in a 4-year-old child. Child's Nervous System : Chns : Official Journal of the International Society For Pediatric Neurosurgery. 31: 625-9. PMID 25348811 DOI: 10.1007/S00381-014-2566-5  0.319
2015 Carvalho D, Taylor K, Burford A, Nowak I, Mackay A, Vinci M, Bjerke L, Molinari V, Nandhabalan M, Ingram W, Jury A, Natrajan R, Jones D, Pfister S, Shats L, ... ... Jacques T, et al. HG-09 * INFANTILE GLIOBLASTOMA WITH SARCOMATOUS HISTOLOGY DRIVEN BY ETV6:NTRK3 FUSIONS ARE SENSITIVE TO TRK INHIBITION BY PHA-848125 Neuro-Oncology. 17: iii12-iii12. DOI: 10.1093/Neuonc/Nov061.46  0.357
2014 Tansley SL, Betteridge ZE, Gunawardena H, Jacques TS, Owens CM, Pilkington C, Arnold K, Yasin S, Moraitis E, Wedderburn LR, McHugh NJ. Anti-MDA5 autoantibodies in juvenile dermatomyositis identify a distinct clinical phenotype: a prospective cohort study. Arthritis Research & Therapy. 16: R138. PMID 24989778 DOI: 10.1186/Ar4600  0.304
2014 Eggens VR, Barth PG, Niermeijer JM, Berg JN, Darin N, Dixit A, Fluss J, Foulds N, Fowler D, Hortobágyi T, Jacques T, King MD, Makrythanasis P, Máté A, Nicoll JA, et al. EXOSC3 mutations in pontocerebellar hypoplasia type 1: novel mutations and genotype-phenotype correlations. Orphanet Journal of Rare Diseases. 9: 23. PMID 24524299 DOI: 10.1186/1750-1172-9-23  0.3
2014 Yasin SA, Arnold K, Sag E, Tansley S, Moraitis E, Jacques TS, Holton JL, Owens C, McHugh N, Pilkington C, Wedderburn LR. Sub-phenotyping of juvenile dermatomyositis: can it assist clinical decisions? Pediatric Rheumatology. 12: 1-2. DOI: 10.1186/1546-0096-12-S1-O18  0.302
2014 Hill RM, Kuijper S, Lindsey J, Schwalbe EC, Barker K, Boult J, Williamson D, Ahmad Z, Hallsworth A, Ryan S, Poon E, Robinson S, Ruddle R, Raynaud F, Howell L, ... ... Jacques T, et al. MYC and TP53 defects interact at medulloblastoma relapse to define rapidly progressive disease and can be targeted therapeutically Cancer Research. 74. DOI: 10.1158/1538-7445.Am2014-Lb-201  0.356
2014 McTague A, Appleton R, Cross JH, Jacques TS, Meyer E, Poduri A, Scheffer I, Kneen R, Kurian MA. Migrating partial seizures of infancy: delineation of the clinical and genetic features in a national patient cohort The Lancet. 383. DOI: 10.1016/S0140-6736(14)60277-4  0.346
2013 Schwalbe EC, Hayden JT, Rogers HA, Miller S, Lindsey JC, Hill RM, Nicholson SL, Kilday JP, Adamowicz-Brice M, Storer L, Jacques TS, Robson K, Lowe J, Williamson D, Grundy RG, et al. Histologically defined central nervous system primitive neuro-ectodermal tumours (CNS-PNETs) display heterogeneous DNA methylation profiles and show relationships to other paediatric brain tumour types. Acta Neuropathologica. 126: 943-6. PMID 24212602 DOI: 10.1007/S00401-013-1206-6  0.365
2013 McTague A, Appleton R, Avula S, Cross JH, King MD, Jacques TS, Bhate S, Cronin A, Curran A, Desurkar A, Farrell MA, Hughes E, Jefferson R, Lascelles K, Livingston J, et al. Migrating partial seizures of infancy: expansion of the electroclinical, radiological and pathological disease spectrum. Brain : a Journal of Neurology. 136: 1578-91. PMID 23599387 DOI: 10.1093/Brain/Awt073  0.328
2013 Dlamini N, Josifova DJ, Paine SM, Wraige E, Pitt M, Murphy AJ, King A, Buk S, Smith F, Abbs S, Sewry C, Jacques TS, Jungbluth H. Clinical and neuropathological features of X-linked spinal muscular atrophy (SMAX2) associated with a novel mutation in the UBA1 gene. Neuromuscular Disorders : Nmd. 23: 391-8. PMID 23518311 DOI: 10.1016/J.Nmd.2013.02.001  0.328
2013 Scoto M, Cullup T, Cirak S, Yau S, Manzur AY, Feng L, Jacques TS, Anderson G, Abbs S, Sewry C, Jungbluth H, Muntoni F. Nebulin (NEB) mutations in a childhood onset distal myopathy with rods and cores uncovered by next generation sequencing. European Journal of Human Genetics : Ejhg. 21: 1249-52. PMID 23443021 DOI: 10.1038/Ejhg.2013.31  0.316
2013 Thurston B, Gunny R, Anderson G, Paine S, Thompson D, Jacques T, Ternier J. Fourth ventricle rosette-forming glioneuronal tumour in children: An unusual presentation in an 8-year-old patient, discussion and review of the literature Child's Nervous System. 29: 839-847. PMID 23239254 DOI: 10.1007/S00381-012-1993-4  0.323
2012 Coras R, de Boer OJ, Armstrong D, Becker A, Jacques TS, Miyata H, Thom M, Vinters HV, Spreafico R, Oz B, Marucci G, Pimentel J, Mühlebner A, Zamecnik J, Buccoliero AM, et al. Good interobserver and intraobserver agreement in the evaluation of the new ILAE classification of focal cortical dysplasias. Epilepsia. 53: 1341-8. PMID 22642611 DOI: 10.1111/J.1528-1167.2012.03508.X  0.306
2012 Andoniadou CL, Gaston-Massuet C, Reddy R, Schneider RP, Blasco MA, Le Tissier P, Jacques TS, Pevny LH, Dattani MT, Martinez-Barbera JP. Identification of novel pathways involved in the pathogenesis of human adamantinomatous craniopharyngioma. Acta Neuropathologica. 124: 259-71. PMID 22349813 DOI: 10.1007/S00401-012-0957-9  0.305
2012 Kinsler VA, Paine SM, Anderson GW, Wijesekara DS, Sebire NJ, Chong WK, Harkness W, Aylett SE, Jacques TS. Neuropathology of neurocutaneous melanosis: histological foci of melanotic neurones and glia may be undetectable on MRI. Acta Neuropathologica. PMID 22294043 DOI: 10.1007/S00401-012-0945-0  0.307
2012 Pryce JW, Paine SM, Weber MA, Harding B, Jacques TS, Sebire NJ. Role of routine neuropathological examination for determining cause of death in sudden unexpected deaths in infancy (SUDI). Journal of Clinical Pathology. 65: 257-61. PMID 22135027 DOI: 10.1136/Jclinpath-2011-200264  0.304
2012 Holme H, Ghara N, Jacques TS, Humphries P, Daw S, Shankar A. Isolated intracranial relapse of hodgkin lymphoma in a child International Journal of Case Reports and Images. 3: 12-15. DOI: 10.5348/Ijcri-2012-10-190-Cr-3  0.325
2011 Catarino CB, Liu JY, Liagkouras I, Gibbons VS, Labrum RW, Ellis R, Woodward C, Davis MB, Smith SJ, Cross JH, Appleton RE, Yendle SC, McMahon JM, Bellows ST, Jacques TS, et al. Dravet syndrome as epileptic encephalopathy: evidence from long-term course and neuropathology. Brain : a Journal of Neurology. 134: 2982-3010. PMID 21719429 DOI: 10.1093/Brain/Awr129  0.313
2011 Menghi F, Jacques TS, Barenco M, Schwalbe EC, Clifford SC, Hubank M, Ham J. Genome-wide analysis of alternative splicing in medulloblastoma identifies splicing patterns characteristic of normal cerebellar development. Cancer Research. 71: 2045-55. PMID 21248070 DOI: 10.1158/0008-5472.Can-10-2519  0.314
2010 Lawson AR, Tatevossian RG, Phipps KP, Picker SR, Michalski A, Sheer D, Jacques TS, Forshew T. RAF gene fusions are specific to pilocytic astrocytoma in a broad paediatric brain tumour cohort. Acta Neuropathologica. 120: 271-3. PMID 20454969 DOI: 10.1007/S00401-010-0693-Y  0.349
2010 Jacques TS, Swales A, Brzozowski MJ, Henriquez NV, Linehan JM, Mirzadeh Z, O' Malley C, Naumann H, Alvarez-Buylla A, Brandner S. Combinations of genetic mutations in the adult neural stem cell compartment determine brain tumour phenotypes. The Embo Journal. 29: 222-35. PMID 19927122 DOI: 10.1038/Emboj.2009.327  0.302
2006 Jacques TS, Eldridge C, Patel A, Saleem NM, Powell M, Kitchen ND, Thom M, Revesz T. Mixed glioneuronal tumour of the fourth ventricle with prominent rosette formation. Neuropathology and Applied Neurobiology. 32: 217-20. PMID 16599951 DOI: 10.1111/J.1365-2990.2005.00692.X  0.336
2006 Vujovic S, Henderson S, Presneau N, Odell E, Jacques TS, Tirabosco R, Boshoff C, Flanagan AM. Brachyury, a crucial regulator of notochordal development, is a novel biomarker for chordomas. The Journal of Pathology. 209: 157-65. PMID 16538613 DOI: 10.1002/Path.1969  0.307
2005 Clarke AJ, Jacques TS, Galloway MJ, Thom M, Kitchen ND, Plant GT. ALK positive inflammatory myofibroblastic tumour of the pineal region. Journal of Clinical Pathology. 58: 981-3. PMID 16126883 DOI: 10.1136/Jcp.2004.022947  0.316
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