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Murray Grossman

机构:University of Pennsylvania · ORCID:0000-0002-7447-6218

发表论文 947 篇 · 总被引 62987 次 · h-index 119

代表论文

  • MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association study (2024 · The Lancet Neurology · 被引 24)
  • Reliability and Validity of Smartphone Cognitive Testing for Frontotemporal Lobar Degeneration (2024 · JAMA Network Open · 被引 22)
  • Novel data-driven subtypes and stages of brain atrophy in the ALS–FTD spectrum (2023 · Translational Neurodegeneration · 被引 19)
  • Deciphering distinct genetic risk factors for FTLD-TDP pathological subtypes via whole-genome sequencing (2025 · Nature Communications · 被引 17)
  • CSF Proteomics in Patients With Progressive Supranuclear Palsy (2024 · Neurology · 被引 15)
  • Automated Measures of Syntactic Complexity in Natural Speech Production: Older and Younger Adults as a Case Study (2024 · Journal of Speech Language and Hearing Research · 被引 15)