Human Molecular Genetics

Published by: Oxford University Press  

People

  1. Offit
    Offit
  2. Joseph
    Joseph
  3. Bajorin
    Bajorin
  4. Dogan
    Dogan
  5. Furberg-Barnes
    Furberg-Barnes
  6. Nafa
    Nafa
  7. Robson
    Robson
  8. Zelenetz
    Zelenetz

Groups

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

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People
  1. Kenneth Offit (9)
  2. Vijai Joseph (6)
  3. Tomas Kirchhoff (3)
  4. Ahmet Dogan (1)
  5. Andrew Zelenetz (1)
  6. Anna Furberg-Barnes (1)

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  1. 2021 (1)
  2. 2020 (1)
  3. 2016 (2)
  4. 2015 (2)
  5. 2011 (2)
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Publishers
  1. Oxford University Press (10)

Results (10)


Citation style sort is year ascending, and then by author or title. Author ascending is default.
  • Sequencing at lymphoid neoplasm susceptibility loci maps six myeloma risk genes
    Journal Article

    Griffin Waller, R.; Klein, R. J.; Vijai, J.; McKay, J. D.; Clay-Gilmour, A.; Wei, X.; Madsen, M. J.; Sborov, D. W.; Curtin, K.; Slager, S. L.; more...
    Human Molecular Genetics (2021)

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  • Inherited variants at 3q13.33 and 3p24.1 are associated with risk of diffuse large B-cell lymphoma and implicate immune pathways
    Journal Article

    Kleinstern, G.; Yan, H.; Hildebrandt, M. A. T.; Vijai, J.; Berndt, S. I.; Ghesquiè€res, H.; McKay, J.; Wang, S. S.; Nieters, A.; Ye, Y.; more...
    Human Molecular Genetics (2020)

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  • Genetically predicted longer telomere length is associated with increased risk of B-cell lymphoma subtypes
    Journal Article

    Machiela, M. J.; Lan, Q.; Slager, S. L.; Vermeulen, R. C. H.; Teras, L. R.; Camp, N. J.; Cerhan, J. R.; Spinelli, J. J.; Wang, S. S.; Nieters, A.; more...
    Human Molecular Genetics (2016)

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  • Identification of a novel susceptibility locus at 13q34 and refinement of the 20p12.2 region as a multi-signal locus associated with bladder cancer risk in individuals of European ancestry
    Journal Article

    Figueroa, J. D.; Middlebrooks, C. D.; Banday, A. R.; Ye, Y.; Garcia-Closas, M.; Chatterjee, N.; Koutros, S.; Kiemeney, L. A.; Rafnar, T.; Bishop, T.; more...
    Human Molecular Genetics (2016)

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  • FANCM c.5791C > T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor
    Journal Article

    Peterlongo, P.; Catucci, I.; Colombo, M.; Caleca, L.; Mucaki, E.; Bogliolo, M.; Marin, M.; Damiola, F.; Bernard, L.; Pensotti, V.; more...
    Human Molecular Genetics (2015)

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  • Cell-type-specific enrichment of risk-associated regulatory elements at ovarian cancer susceptibility loci
    Journal Article

    Coetzee, S. G.; Shen, H. C.; Hazelett, D. J.; Lawrenson, K.; Kuchenbaecker, K.; Tyrer, J.; Rhie, S. K.; Levanon, K.; Karst, A.; Drapkin, R.; more...
    Human Molecular Genetics (2015)

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  • Associations of common variants at 1p11.2 and 14q24.1 (RAD51l1) with breast cancer risk and heterogeneity by tumor subtype: Findings from the Breast Cancer Association Consortium
    Journal Article

    Figueroa, J. D.; Garcia-Closas, M.; Humphreys, M.; Platte, R.; Hopper, J. L.; Southey, M. C.; Apicella, C.; Hammet, F.; Schmidt, M. K.; Broeks, A.; more...
    Human Molecular Genetics (2011)

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  • Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers
    Journal Article

    Antoniou, A. C.; Kartsonaki, C.; Sinilnikova, O. M.; Soucy, P.; McGuffog, L.; Healey, S.; Lee, A.; Peterlongo, P.; Manoukian, S.; Peissel, B.; more...
    Human Molecular Genetics (2011)

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  • Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers
    Journal Article

    Antoniou, A. C.; Sinilnikova, O. M.; McGuffog, L.; Healey, S.; Nevanlinna, H.; Heikkinen, T.; Simard, J.; Spurdle, A. B.; Beesley, J.; Chen, X. Q.; more...
    Human Molecular Genetics (2009)

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  • Functional and genomic approaches reveal an ancient CHEK2 allele associated with breast cancer in the Ashkenazi Jewish population
    Journal Article

    Shaag, A.; Walsh, T.; Renbaum, P.; Kirchhoff, T.; Nafa, K.; Shiovitz, S.; Mandell, J. B.; Welcsh, P.; Lee, M. K.; Ellis, N.; more...
    Human Molecular Genetics (2005)

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    • Human Molecular Genetics – authorized name for:

    Name ISSN / ISBN Publisher
    Human Molecular Genetics 0964-6906 Oxford University Press
    Human Molecular Genetics 0964-6906 Oxford University Press
    Human Molecular Genetics 0964-6906 Oxford University Press
    Human Molecular Genetics 0964-6906 Oxford University Press
    Human Molecular Genetics 09646906 Unknown
    Human Molecular Genetics 0964-6906 Oxford University Press
    Human Molecular Genetics 0964-6906 Oxford University Press
    Human Molecular Genetics 09646906 Oxford University Press
    Human Molecular Genetics 0964-6906 Unknown
    Human Molecular Genetics 1460-2083 Oxford University Press
    Human Molecular Genetics 09646906 Oxford University Press
    Human Molecular Genetics 09646906 The Author 2012
    Human Molecular Genetics 09646906 Oxford University Press
    Human Molecular Genetics 09646906 The Author 2008
    Human molecular genetics 1460-2083 Oxford University Press
    Human Molecular Genetics 09646906 Oxford University Press
    Human Molecular Genetics 09646906 The Author 2005
    Human molecular genetics 1460-2083 Oxford University Press
    Human Molecular Genetics 0964-6906 Oxford University Press