Search Results - "Greene, Mark H."

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    Malignancies and survival patterns in the National Cancer Institute inherited bone marrow failure syndromes cohort study by Alter, Blanche P., Giri, Neelam, Savage, Sharon A., Peters, June A., Loud, Jennifer T., Leathwood, Lisa, Carr, Ann G., Greene, Mark H., Rosenberg, Philip S.

    Published in British journal of haematology (01-07-2010)
    “…Summary Fanconi anaemia (FA), dyskeratosis congenita (DC), Diamond‐Blackfan anaemia (DBA), and Shwachman‐Diamond syndrome (SDS) comprise major inherited bone…”
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    Diabetes, metformin and cancer risk in myotonic dystrophy type I by Alsaggaf, Rotana, Pfeiffer, Ruth M., Wang, Youjin, St. George, Diane Marie M., Zhan, Min, Wagner, Kathryn R., Amr, Sania, Greene, Mark H., Gadalla, Shahinaz M.

    Published in International journal of cancer (01-08-2020)
    “…Myotonic dystrophy type I (DM1) is an autosomal dominant multisystem disorder characterized by myotonia and muscle weakness. Type 2 diabetes (T2D) and cancer…”
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    Cancer phenotype in myotonic dystrophy patients: Results from a meta‐analysis by Emparanza, Jose I., López de Munain, Adolfo, Greene, Mark H., Matheu, Ander, Fernández‐Torrón, Roberto, Gadalla, Shahinaz M.

    Published in Muscle & nerve (01-10-2018)
    “…ABSTRACT Introduction: Recent studies have provided evidence that patients with myotonic dystrophy (DM) are at excess risk of cancer. However, inconsistencies…”
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    In their own words: treating very young BRCA1/2 mutation-positive women with care and caution by Hoskins, Lindsey M, Werner-Lin, Allison, Greene, Mark H

    Published in PloS one (28-02-2014)
    “…Young women who have been identified as carrying a deleterious mutation in BRCA1 or BRCA2 face a unique set of challenges related to managing cancer risk…”
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    Does bilateral salpingectomy with ovarian retention warrant consideration as a temporary bridge to risk-reducing bilateral oophorectomy in BRCA1/2 mutation carriers? by Greene, Mark H., MD, Mai, Phuong L., MD, MS, Schwartz, Peter E., MD

    “…Risk-reducing salpingo-oophorectomy (RRSO) is the most definitive surgical intervention for ovarian cancer risk reduction among BRCA1/2 mutation carriers. For…”
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    Mosaic chromosome Y loss and testicular germ cell tumor risk by Machiela, Mitchell J, Dagnall, Casey L, Pathak, Anand, Loud, Jennifer T, Chanock, Stephen J, Greene, Mark H, McGlynn, Katherine A, Stewart, Douglas R

    Published in Journal of human genetics (01-06-2017)
    “…Studies have suggested mosaic loss of chromosome Y (mLOY) in blood-derived DNA is common in older men. Cohort studies investigating mLOY and mortality have…”
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    Peritoneal carcinomatosis after risk‐reducing surgery in BRCA1/2 mutation carriers by Harmsen, Marline G., Piek, Jurgen M. J., Bulten, Johan, Casey, Murray J., Rebbeck, Timothy R., Mourits, Marian J., Greene, Mark H., Slangen, Brigitte F. M., van Beurden, Marc, Massuger, Leon F. A. G., Hoogerbrugge, Nicoline, de Hullu, Joanne A.

    Published in Cancer (01-03-2018)
    “…BACKGROUND Risk‐reducing salpingo‐oophorectomy (RRSO) is recommended for BRCA1/2 mutation carriers because of their increased risk of ovarian carcinoma…”
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    Potential Usefulness of Single Nucleotide Polymorphisms to Identify Persons at High Cancer Risk: An Evaluation of Seven Common Cancers by PARK, Ju-Hyun, GAIL, Mitchell H, GREENE, Mark H, CHATTERJEE, Nilanjan

    Published in Journal of clinical oncology (10-06-2012)
    “…To estimate the likely number and predictive strength of cancer-associated single nucleotide polymorphisms (SNPs) that are yet to be discovered for seven…”
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    Quantifying cancer absolute risk and cancer mortality in the presence of competing events after a myotonic dystrophy diagnosis by Gadalla, Shahinaz M, Pfeiffer, Ruth M, Kristinsson, Sigurdur Y, Björkholm, Magnus, Hilbert, James E, Moxley, 3rd, Richard T, Landgren, Ola, Greene, Mark H

    Published in PloS one (13-11-2013)
    “…Recent studies show that patients with myotonic dystrophy (DM) have an increased risk of specific malignancies, but estimates of absolute cancer risk…”
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    Challenges related to developing serum-based biomarkers for early ovarian cancer detection by Mai, Phuong L, Wentzensen, Nicolas, Greene, Mark H

    “…In this issue of the journal, Cramer and colleagues and Zhu and colleagues report carefully designed phase 3 assessments of candidate ovarian cancer screening…”
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    Familial testicular germ cell tumors in adults: 2010 summary of genetic risk factors and clinical phenotype by Greene, Mark H, Kratz, Christian P, Mai, Phuong L, Mueller, Christine, Peters, June A, Bratslavsky, Gennady, Ling, Alex, Choyke, Peter M, Premkumar, Ahalya, Bracci, Janet, Watkins, Rissah J, McMaster, Mary Lou, Korde, Larissa A

    Published in Endocrine-related cancer (01-06-2010)
    “…Familial aggregations of testicular germ cell tumor (FTGCT) have been well described, suggesting the existence of a hereditary TGCT subset. Approximately 1.4%…”
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    Prophylactic Oophorectomy Reduces Breast Cancer Penetrance During Prospective, Long-Term Follow-Up of BRCA1 Mutation Carriers by KRAMER, Joan L, VELAZQUEZ, Isela A, CHEN, Bingshu E, ROSENBERG, Philip S, STRUEWING, Jeffery P, GREENE, Mark H

    Published in Journal of clinical oncology (01-12-2005)
    “…Breast cancer penetrance estimates in BRCA1 mutation carriers have varied from 40% to 85%; this heterogeneity has been attributed to variations in risk among…”
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    Hypothesis: neoplasms in myotonic dystrophy by Mueller, Christine M, Hilbert, James E, Martens, William, Thornton, Charles A, Moxley, Richard T. III, Greene, Mark H

    Published in Cancer causes & control (01-12-2009)
    “…Tumorigenesis is a multi-step process due to an accumulation of genetic mutations in multiple genes in diverse pathways which ultimately lead to loss of…”
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    LINE-1 methylation is inherited in familial testicular cancer kindreds by Mirabello, Lisa, Savage, Sharon A, Korde, Larissa, Gadalla, Shahinaz M, Greene, Mark H

    Published in BMC medical genetics (17-05-2010)
    “…Testicular germ cell tumors (TGCT) are the most frequent cancers among young men. There is a clear familial component to TGCT etiology, but no high-penetrance…”
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    Cancer Risk in Myotonic Dystrophy Type I: Evidence of a Role for Disease Severity by Alsaggaf, Rotana, St. George, Diane Marie M, Zhan, Min, Pfeiffer, Ruth M, Wang, Youjin, Wagner, Kathryn R, Greene, Mark H, Amr, Sania, Gadalla, Shahinaz M

    Published in JNCI cancer spectrum (01-10-2018)
    “…Abstract Background Myotonic dystrophy type 1 (DM1) is an inherited trinucleotide repeat disorder in which specific cancers have been implicated as part of the…”
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