Author

Melek Firat Altay

Observed names: Altay, Melek Firat, Firat Altay

Institutions: University of Bern, University Hospital of Bern, Stanford University

Observed institutions: University of Bern, University Hospital of Bern, Stanford Medicine, École Polytechnique Fédérale de Lausanne, Stanford University

ORCID: 0000-0002-8174-5631

Observed ORCID: 0000-0002-8174-5631

OpenAlex ID: A5009739790

Prominent astrocytic alpha-synuclein pathology with unique post-translational modification signatures unveiled across Lewy body disorders

2022 · Melek Firat Altay, Alan King Lun Liu, et al. · Acta Neuropathologica Communications · 86

Revisiting the specificity and ability of phospho-S129 antibodies to capture alpha-synuclein biochemical and pathological diversity

2022 · Hilal A. Lashuel, Anne-Laure Mahul-Mellier, et al. · npj Parkinson s Disease · 65

Development and validation of an expanded antibody toolset that captures alpha-synuclein pathological diversity in Lewy body diseases

2023 · Melek Firat Altay, Senthil T. Kumar, et al. · npj Parkinson s Disease · 51

Pathological Relevance of Post-Translationally Modified Alpha-Synuclein (pSer87, pSer129, nTyr39) in Idiopathic Parkinson’s Disease and Multiple System Atrophy

2022 · Berkiye Sonustun, Melek Firat Altay, et al. · Cells · 44

The making of a Lewy body: the role of alpha-synuclein post-fibrillization modifications in regulating the formation and the maturation of pathological inclusions.

2018 · Anne-Laure Mahul-Mellier, Firat Altay, et al. · bioRxiv (Cold Spring Harbor Laboratory) · 42

Pathological substrate of memory impairment in multiple system atrophy

2022 · Yasuo Miki, Kunikazu Tanji, et al. · Neuropathology and Applied Neurobiology · 24

Differential role of C-terminal truncations on alpha-synuclein pathology and Lewy body formation

2025 · Anne-Laure Mahul-Mellier, Melek Firat Altay, et al. · npj Parkinson s Disease · 22

Heterozygous loss of SRRM1 may be associated with neurodevelopmental phenotypes and anomalies in cell growth and neurite morphology

2025 · Melek Firat Altay, Anne Gregor, et al. · European Journal of Human Genetics · 3

Author Correction: Development and validation of an expanded antibody toolset that captures alpha-synuclein pathological diversity in Lewy body diseases

2024 · Melek Firat Altay, Senthil T. Kumar, et al. · npj Parkinson s Disease · 2

SysNDD: A Systematic Database for Neurodevelopmental Disorders

2026 · Bernt Popp, Simon Frueh, et al. · bioRxiv (Cold Spring Harbor Laboratory) · 1

Heterozygous loss of SRRM1 may be associated with neurodevelopmental phenotypes and anomalies in cell growth and neurite morphology

2026 · Altay, Melek Firat, Gregor, Anne, et al. · Zurich Open Repository and Archive (University of Zurich)

Works count: 15

Citation count: 340

H-index: 7

I10-index: 7