Public Library of Science

SHERPA: Unknown

People

  1. Joseph
    Joseph
  2. Offit
    Offit
  3. Stadler
    Stadler
  4. Balachandran
    Balachandran
  5. Capanu
    Capanu
  6. Cheguri
    Cheguri
  7. Dutra-Clarke
    Dutra-Clarke
  8. Gaddam
    Gaddam
  9. Goldgur
    Goldgur
  10. Gonen
    Gonen

Groups

  1. Center for Pancreatic Cancer Research (6)
  2. GSK Faculty (4)
  3. Epidemiology and Biostatistics (3)
  4. Biostatistics Service (2)
  5. Center for Hematologic Malignancies (2)
  6. Clinical Genetics Service (2)
  7. Department of Medicine (2)
  8. Population Sciences Research Program (2)
  9. Solid Tumor Oncology Division (2)
  10. Survivorship Research (2)
Search Within
  1. "Center for Pancreatic Cancer Research"
Formats
  1. Journal Article (6)
Groups
  1. Center for Pancreatic Cancer Research (6)
  2. GSK Faculty (4)
  3. Epidemiology and Biostatistics (3)
  4. Biostatistics Service (2)
  5. Center for Hematologic Malignancies (2)
  6. Clinical Genetics Service (2)

More Groups

People
  1. Kenneth Offit (2)
  2. Vijai Joseph (2)
  3. Zsofia Stadler (2)
  4. Agnes Viale (1)
  5. Ana Virginia Dutra-Clarke (1)
  6. Andrew Zelenetz (1)

More People

Years
  1. 2021 (1)
  2. 2015 (1)
  3. 2014 (3)
  4. 2013 (1)
Publications
  1. PLoS Genetics (4)
  2. PLoS Computational Biology (2)

Results (6)


Citation style sort is year ascending, and then by author or title. Author ascending is default.
  • Probing T-cell response by sequence-based probabilistic modeling
    Journal Article

    Bravi, B.; Balachandran, V. P.; Greenbaum, B. D.; Walczak, A. M.; Mora, T.; Monasson, R.; Cocco, S.
    PLoS Computational Biology (2021)

    Fulltext@MSK | Save
  • Germline ETV6 mutations confer susceptibility to acute lymphoblastic leukemia and thrombocytopenia
    Journal Article

    Topka, S.; Vijai, J.; Walsh, M. F.; Jacobs, L.; Maria, A.; Villano, D.; Gaddam, P.; Wu, G.; McGee, R. B.; Quinn, E.; more...
    PLoS Genetics (2015)

    Fulltext@MSK | Save
  • Identification of rare causal variants in sequence-based studies: Methods and applications to VPS13B, a gene involved in Cohen syndrome and autism
    Journal Article

    Ionita-Laza, I.; Capanu, M.; De Rubeis, S.; McCallum, K.; Buxbaum, J. D.
    PLoS Genetics (2014)

    Fulltext@MSK | Save
  • Histone modifications are associated with transcript isoform diversity in normal and cancer cells
    Journal Article

    Podlaha, O.; De, S.; Gonen, M.; Michor, F.
    PLoS Computational Biology (2014)

    Fulltext@MSK | Save
  • Loss of function mutation in the palmitoyl-transferase HHAT leads to syndromic 46,XY disorder of sex development by impeding hedgehog protein palmitoylation and signaling
    Journal Article

    Callier, P.; Calvel, P.; Matevossian, A.; Makrythanasis, P.; Bernard, P.; Kurosaka, H.; Vannier, A.; Thauvin-Robinet, C.; Borel, C.; Mazaud-Guittot, S.; more...
    PLoS Genetics (2014)

    Fulltext@MSK | Save
  • Susceptibility Loci Associated with Specific and Shared Subtypes of Lymphoid Malignancies
    Journal Article

    Vijai, J.; Kirchhoff, T.; Schrader, K. A.; Brown, J.; Dutra Clarke, A. V.; Manschreck, C.; Hansen, N.; Rau-Murthy, R.; Sarrel, K.; Przybylo, J.; more...
    PLoS Genetics (2013)

    Fulltext@MSK | Save

    • Public Library of Science – authorized name for: