Columbia University Medical Center-ko ikertzaileekin lankidetzan egindako argitalpenak (9)

2024

  1. MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association study

    The Lancet Neurology, Vol. 23, Núm. 5, pp. 487-499

2023

  1. Sphingolipid desaturase DEGS1 is essential for mitochondria-associated membrane integrity

    The Journal of clinical investigation, Vol. 133, Núm. 10

2022

  1. New insights into the genetic etiology of Alzheimer's disease and related dementias

    Nature genetics, Vol. 54, Núm. 4, pp. 412-436

2021

  1. Common variants in Alzheimer's disease and risk stratification by polygenic risk scores

    Nature communications, Vol. 12, Núm. 1, pp. 3417

  2. Lipidomic traits of plasma and cerebrospinal fluid in amyotrophic lateral sclerosis correlate with disease progression

    Brain Communications, Vol. 3, Núm. 3

2019

  1. Large expert-curated database for benchmarking document similarity detection in biomedical literature search

    Database, Vol. 2019, pp. 1-67

2013

  1. Prognostic relevance of integrated genetic profiling in adult T-cell acute lymphoblastic leukemia

    Blood, Vol. 122, Núm. 1, pp. 74-82

2011

  1. ETV6 mutations in early immature human T cell leukemias

    Journal of Experimental Medicine, Vol. 208, Núm. 13, pp. 2571-2579

2007

  1. The Smc5-Smc6 complex and SUMO modification of Rad52 regulates recombinational repair at the ribosomal gene locus

    Nature Cell Biology, Vol. 9, Núm. 8, pp. 923-931