Harvard Catalyst Profiles

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Sina Neyazi, M.D.


Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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  1. Kresbach C, Dottermusch M, Eckhardt A, Ristow I, Paplomatas P, Altendorf L, Wefers AK, Bockmayr M, Belakhoua S, Tran I, Pohl L, Neyazi S, Bode H, Farschtschi S, Well L, Friedrich RE, Reuss D, Snuderl M, Hagel C, Mautner VF, Schüller U. Atypical Neurofibromas reveal distinct epigenetic features with proximity to benign peripheral nerve sheath tumor entities. Neuro Oncol. 2023 Mar 02. PMID: 36866403.
    Citations:    Fields:    
  2. Neyazi S, Altendorf L, Schwetje D, Göbel C, Schoof M, Holdhof D, Schüller U. Generation of new transgenic SMARCA4-deficient mouse models results in neuromuscular weakness and paralysis of limbs. Brain Pathol. 2022 Dec 29; e13146. PMID: 36582072.
    Citations:    Fields:    
  3. Neyazi S, Ng M, Heckl D, Klusmann JH. Long noncoding RNAs as regulators of pediatric acute myeloid leukemia. Mol Cell Pediatr. 2022 May 20; 9(1):10. PMID: 35596093; PMCID: PMC9123150.
  4. Kresbach C, Neyazi S, Schüller U. Updates in the classification of ependymal neoplasms: The 2021 WHO Classification and beyond. Brain Pathol. 2022 07; 32(4):e13068. PMID: 35307892; PMCID: PMC9245931.
    Citations: 3     Fields:    Translation:Humans
  5. Mawrin C, Koch R, Waldt N, Sandalcioglu IE, Braunsdorf WEK, Warnke JP, Goehre F, Meisel HJ, Ewald C, Neyazi S, Schüller U, Kirches E. A new amplicon-based gene panel for next generation sequencing characterization of meningiomas. Brain Pathol. 2022 03; 32(2):e13046. PMID: 35213080; PMCID: PMC8877726.
    Citations: 4     Fields:    Translation:Humans
  6. Al-Kershi S, Golnik R, Flasinski M, Waack K, Rasche M, Creutzig U, Dworzak M, Reinhardt D, Klusmann JH. Recommendations for Diagnosis and Treatment of Children with Transient Abnormal Myelopoiesis (TAM) and Myeloid Leukemia in Down Syndrome (ML-DS). Klin Padiatr. 2021 Nov; 233(6):267-277. PMID: 34407551.
    Citations: 2     Fields:    Translation:Humans
  7. Schoof M, Kordes U, Volk AE, Al-Kershi S, Kresbach C, Schüller U. Malignant gliomas with H3F3A G34R mutation or MYCN amplification in pediatric patients with Li Fraumeni syndrome. Acta Neuropathol. 2021 09; 142(3):591-593. PMID: 34264394; PMCID: PMC8357758.
    Citations: 1     Fields:    Translation:Humans
  8. Holdhof D, Schoof M, Al-Kershi S, Spohn M, Kresbach C, Göbel C, Hellwig M, Indenbirken D, Moreno N, Kerl K, Schüller U. Brahma-related gene 1 has time-specific roles during brain and eye development. Development. 2021 05 15; 148(10). PMID: 34042968.
    Citations: 2     Fields:    Translation:AnimalsCells
  9. Al-Kershi S, Bhayadia R, Ng M, Verboon L, Emmrich S, Gack L, Schwarzer A, Strowig T, Heckl D, Klusmann JH. The stem cell-specific long noncoding RNA HOXA10-AS in the pathogenesis of KMT2A-rearranged leukemia. Blood Adv. 2019 12 23; 3(24):4252-4263. PMID: 31867596; PMCID: PMC6929382.
    Citations: 10     Fields:    Translation:HumansAnimalsCells
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.