| Year |
Citation |
Score |
| 2024 |
Macagno N, Kervarrec T, Thanguturi S, Sohier P, Pissaloux D, Mescam L, Jullie ML, Frouin E, Osio A, Faisant M, Le Loarer F, Cribier B, Calonje E, Luna EVE, Massi D, et al. SOX10-internal tandem duplications and PLAG1 or HMGA2 fusions segregate eccrine-type and apocrine-type cutaneous mixed tumors. Modern Pathology : An Official Journal of the United States and Canadian Academy of Pathology, Inc. 100430. PMID 38266920 DOI: 10.1016/j.modpat.2024.100430 |
0.341 |
|
| 2023 |
Kervarrec T, Tallet A, Macagno N, de la Fouchardière A, Pissaloux D, Tirode F, Bravo IG, Nicolas A, Baulande S, Sohier P, Balme B, Osio A, Jullie ML, Moulonguet I, Bonsang B, et al. Sweat Gland Tumors Arising on Acral Sites: A Molecular Survey. The American Journal of Surgical Pathology. PMID 37505808 DOI: 10.1097/PAS.0000000000002098 |
0.325 |
|
| 2023 |
Kervarrec T, Imbeaud S, Veyer D, Pere H, Puech J, Pekár-Lukacs A, Markiewicz D, Coutts M, Tallet A, Collin C, Berthon P, Bravo IG, Seris A, Jouary T, Macagno N, et al. Digital Papillary Adenocarcinoma in Nonacral Skin: Clinicopathologic and Genetic Characterization of 5 Cases. The American Journal of Surgical Pathology. PMID 37505796 DOI: 10.1097/PAS.0000000000002096 |
0.339 |
|
| 2023 |
Trecourt A, Macagno N, Ngo C, Philip CA, Lopez J, Ferreira J, Alves-Vale C, Ray-Coquard I, Genestie C, Agaimy A, Devouassoux-Shisheboran M. CREB fusion-associated epithelioid mesenchymal neoplasms of the female adnexa: three cases documenting a novel location of an emerging entity and further highlighting an ambiguous misleading immunophenotype. Virchows Archiv : An International Journal of Pathology. PMID 37097347 DOI: 10.1007/s00428-023-03546-1 |
0.403 |
|
| 2022 |
Marechal E, Poliard A, Henry K, Moreno M, Legrix M, Macagno N, Mondielli G, Fauquier T, Barlier A, Etchevers HC. Multiple congenital malformations arise from somatic mosaicism for constitutively active Pik3ca signaling. Frontiers in Cell and Developmental Biology. 10: 1013001. PMID 36353506 DOI: 10.3389/fcell.2022.1013001 |
0.323 |
|
| 2022 |
Picard C, Macagno N, Corradini N, Marec-Bérard P, Cabet S, Guibaud L, Viremouneix L, Raux S, Chotel F, Weinbreck N, Meurgey A, Karanian M, Pissaloux D, Tirode F, Dijoud F. Identification of a novel translocation producing an in-frame fusion of TAF15 and ETV4 in a case of extraosseous Ewing sarcoma revealed in the prenatal period. Virchows Archiv : An International Journal of Pathology. 481: 665-669. PMID 35527322 DOI: 10.1007/s00428-022-03335-2 |
0.316 |
|
| 2022 |
Thanguturi S, Tallet A, Miquelestorena-Standley E, Coco C, Le Corre Y, Hainaut-Wierzbicka E, Blom A, Saiag P, Beneton N, Bens G, Zaragoza J, Nardin C, Aubin F, Dinulescu M, Machet MC, ... ... Macagno N, et al. Investigation of the RB1-SOX2 axis constitutes a tool for viral status determination and diagnosis in Merkel cell carcinoma. Virchows Archiv : An International Journal of Pathology. PMID 35412101 DOI: 10.1007/s00428-022-03315-6 |
0.368 |
|
| 2022 |
de la Fouchardiere A, Tirode F, Castillo C, Buisson A, Boivin F, Macagno N, Pissaloux D. Attempting to Solve the Pigmented Epithelioid Melanocytoma (PEM) Conundrum: PRKAR1A Inactivation Can Occur in Different Genetic Backgrounds (Common, Blue, and Spitz Subgroups) With Variation in Their Clinicopathologic Characteristics. The American Journal of Surgical Pathology. 46: 1106-1115. PMID 35319526 DOI: 10.1097/PAS.0000000000001888 |
0.483 |
|
| 2022 |
Macagno N, Sohier P, Kervarrec T, Pissaloux D, Jullie ML, Cribier B, Battistella M. Recent Advances on Immunohistochemistry and Molecular Biology for the Diagnosis of Adnexal Sweat Gland Tumors. Cancers. 14. PMID 35158743 DOI: 10.3390/cancers14030476 |
0.371 |
|
| 2021 |
Molines E, Haffner A, Fina F, Malissen N, Ouafik L, Grob JJ, Macagno N. [BRAF mutation evolution in melanoma: Myth or reality?] Annales De Pathologie. 42: 113-118. PMID 34865880 DOI: 10.1016/j.annpat.2021.11.001 |
0.428 |
|
| 2021 |
de la Fouchardière A, Boivin F, Etchevers HC, Macagno N. Cutaneous Melanomas Arising during Childhood: An Overview of the Main Entities. Dermatopathology (Basel, Switzerland). 8: 301-314. PMID 34449585 DOI: 10.3390/dermatopathology8030036 |
0.555 |
|
| 2021 |
Gaudy-Marqueste C, Macagno N, Loundou A, Pellegrino E, Ouafik L, Budden T, Mundra P, Gremel G, Akhras V, Lin L, Cook M, Kumar R, Grob JJ, Nagore E, Marais R, et al. Molecular characterization of fast-growing melanomas. Journal of the American Academy of Dermatology. PMID 34280484 DOI: 10.1016/j.jaad.2021.07.011 |
0.352 |
|
| 2021 |
Macagno N, Kervarrec T, Sohier P, Poirot B, Haffner A, Carlotti A, Balme B, Castillo C, Jullie ML, Osio A, Lehmann-Che J, Frouin E, Battistella M. NUT Is a Specific Immunohistochemical Marker for the Diagnosis of YAP1-NUTM1-rearranged Cutaneous Poroid Neoplasms. The American Journal of Surgical Pathology. 45: 1221-1227. PMID 33739783 DOI: 10.1097/PAS.0000000000001693 |
0.401 |
|
| 2020 |
Le Corroller T, Macagno N, Nihous H, Champsaur P, Bouvier C. Acral FibroChondroMyxoid tumor: imaging features of a new entity. Skeletal Radiology. PMID 32844242 DOI: 10.1007/S00256-020-03592-9 |
0.309 |
|
| 2020 |
Macagno N, Pissaloux D, Etchevers H, Haddad V, Vergier B, Sierra-Fortuny S, Tirode F, de la Fouchardière A. Cutaneous Melanocytic Tumors With Concomitant NRASQ61R and IDH1R132C Mutations: A Report of 6 Cases. The American Journal of Surgical Pathology. PMID 32732488 DOI: 10.1097/Pas.0000000000001500 |
0.564 |
|
| 2020 |
Nihous H, Macagno N, Baud-Massière J, Haffner A, Jouve JL, Gentet JC, Touzery C, Le Loarer F, Bouvier C. Genetic variant of SRF-rearranged myofibroma with a misleading nuclear expression of STAT6 and STAT6 involvement as 3' fusion partner. Virchows Archiv : An International Journal of Pathology. PMID 32529351 DOI: 10.1007/S00428-020-02859-9 |
0.348 |
|
| 2020 |
Bouvier C, Le Loarer F, Macagno N, Aubert S, Audard V, Geneste D, Gomez-Brouchet A, Guinebretière JM, Larousserie F, Pissaloux D, Marie B, Tirode F, Baud J, De Pinieux G. Recurrent novel THBS1-ADGRF5 gene fusion in a new tumor subtype "Acral FibroChondroMyxoid Tumors". Modern Pathology : An Official Journal of the United States and Canadian Academy of Pathology, Inc. PMID 32047233 DOI: 10.1038/S41379-020-0493-4 |
0.315 |
|
| 2019 |
Vogels R, Macagno N, Griewank K, Groenen P, Verdijk M, Fonville J, Kusters B, Figarella-Branger D, Wesseling P, Bouvier C, Flucke U. Prognostic significance of NAB2-STAT6 fusion variants and TERT promotor mutations in solitary fibrous tumors/hemangiopericytomas of the CNS: not (yet) clear. Acta Neuropathologica. PMID 30761420 DOI: 10.1007/S00401-019-01968-3 |
0.38 |
|
| 2018 |
Trucco LD, Mundra PA, Hogan K, Garcia-Martinez P, Viros A, Mandal AK, Macagno N, Gaudy-Marqueste C, Allan D, Baenke F, Cook M, McManus C, Sanchez-Laorden B, Dhomen N, Marais R. Ultraviolet radiation-induced DNA damage is prognostic for outcome in melanoma. Nature Medicine. PMID 30510256 DOI: 10.1038/s41591-018-0265-6 |
0.33 |
|
| 2018 |
Appay R, Fina F, Macagno N, Padovani L, Colin C, Barets D, Ordioni J, Scavarda D, Giangaspero F, Badiali M, Korshunov A, M Pfister S, T W Jones D, Figarella-Branger D. Duplications of KIAA1549 and BRAF screening by Droplet Digital PCR from formalin-fixed paraffin-embedded DNA is an accurate alternative for KIAA1549-BRAF fusion detection in pilocytic astrocytomas. Modern Pathology : An Official Journal of the United States and Canadian Academy of Pathology, Inc. PMID 29802359 DOI: 10.1038/S41379-018-0050-6 |
0.312 |
|
| 2018 |
Appay R, Tabouret E, Macagno N, Touat M, Carpentier C, Colin C, Ducray F, Idbaih A, Mokhtari K, Uro-Coste E, Dehais C, Figarella-Branger D. IDH2 mutations are commonly associated with 1p/19q codeletion in diffuse adult gliomas. Neuro-Oncology. PMID 29522183 DOI: 10.1093/Neuonc/Noy014 |
0.379 |
|
| 2018 |
Delteil C, Malissen N, Appay R, Magis Q, Aubert S, Bouvier C, Richard MA, Macagno N. [Chordoma cutis, an unusual clinical presentation of a rare neoplasm: Chordoma]. Annales De Pathologie. PMID 29449046 DOI: 10.1016/J.Annpat.2018.01.004 |
0.329 |
|
| 2018 |
Macagno N, Etchevers HC, Malissen N, Rome A, Hesse S, Mallet S, Degardin N, Gaudy C. Reduced H3K27me3 Expression is Common in Nodular Melanomas of Childhood Associated With Congenital Melanocytic Nevi But Not in Proliferative Nodules. The American Journal of Surgical Pathology. 42: 701-704. PMID 29369061 DOI: 10.1097/Pas.0000000000001026 |
0.515 |
|
| 2018 |
Etchevers HC, Rose C, Kahle B, Vorbringer H, Fina F, Heux P, Berger I, Schwarz B, Zaffran S, Macagno N, Krengel S. Giant congenital melanocytic nevus with vascular malformation and epidermal cysts associated with a somatic activating mutation in BRAF. Pigment Cell & Melanoma Research. PMID 29316280 DOI: 10.1111/Pcmr.12685 |
0.543 |
|
| 2017 |
Brandone N, Okhremchuk I, Rojat-Habib MC, Blanc AL, Essamet W, Agostini A, Macagno N. [An ovarian tumor can hide another one]. Annales De Pathologie. PMID 29169834 DOI: 10.1016/j.annpat.2017.10.001 |
0.311 |
|
| 2017 |
Benyamine A, Bernard-Guervilly F, Tummino C, Macagno N, Daniel L, Valleix S, Granel B. Hereditary lysozyme amyloidosis with sicca syndrome, digestive, arterial, and tracheobronchial involvement: case-based review. Clinical Rheumatology. PMID 28963698 DOI: 10.1007/S10067-017-3839-7 |
0.315 |
|
| 2017 |
Le Guellec S, Macagno N, Velasco V, Lamant L, Lae M, Filleron T, Malissen N, Cassagnau E, Terrier P, Chevreau C, Ranchere-Vince D, Coindre JM. Loss of H3K27 trimethylation is not suitable for distinguishing malignant peripheral nerve sheath tumor from melanoma: a study of 387 cases including mimicking lesions. Modern Pathology : An Official Journal of the United States and Canadian Academy of Pathology, Inc. 30: 1677-1687. PMID 28752843 DOI: 10.1038/modpathol.2017.91 |
0.32 |
|
| 2017 |
Appay R, Macagno N, Padovani L, Korshunov A, Kool M, André N, Scavarda D, Pietsch T, Figarella-Branger D. HGNET-BCOR Tumors of the Cerebellum: Clinicopathologic and Molecular Characterization of 3 Cases. The American Journal of Surgical Pathology. PMID 28704208 DOI: 10.1097/Pas.0000000000000866 |
0.381 |
|
| 2017 |
Macagno N, Fuentes S, de Pinieux G, Maues de Paula A, Salas S, Mattéi JC, Dupuis C, Appay R, Aurias A, Dufour H, Figarella-Branger D, Bouvier C. Paravertebral Well-Differentiated Liposarcoma with Low-Grade Osteosarcomatous Component: Case Report with 11-Year Follow-Up, Radiological, Pathological, and Genetic Data, and Literature Review. Case Reports in Pathology. 2017: 2346316. PMID 28377828 DOI: 10.1155/2017/2346316 |
0.362 |
|
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