Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 2 (of 2 Records) |
Query Trace: Meningioma[original query] |
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Common variation at 10p12.31 near MLLT10 influences meningioma risk.
Nature genetics 2011 Sep 43 (9): 825-7. Dobbins Sara E, Broderick Peter, Melin Beatrice, Feychting Maria, Johansen Christoffer, Andersson Ulrika, Brännström Thomas, Schramm Johannes, Olver Bianca, Lloyd Amy, Ma Yussanne P, Hosking Fay J, Lönn Stefan, Ahlbom Anders, Henriksson Roger, Schoemaker Minouk J, Hepworth Sarah J, Hoffmann Per, Mühleisen Thomas W, Nöthen Markus M, Moebus Susanne, Eisele Lewin, Kosteljanetz Michael, Muir Kenneth, Swerdlow Anthony, Simon Matthias, Houlston Richard |
Genome-wide association analysis identifies a meningioma risk locus at 11p15.5.
Neuro-oncology 2018 May . Claus Elizabeth B, Cornish Alex J, Broderick Peter, Schildkraut Joellen M, Dobbins Sara E, Holroyd Amy, Calvocoressi Lisa, Lu Lingeng, Hansen Helen M, Smirnov Ivan, Walsh Kyle M, Schramm Johannes, Hoffmann Per, Nöthen Markus M, Jöckel Karl-Heinz, Swerdlow Anthony, Larsen Signe Benzon, Johansen Christoffer, Simon Matthias, Bondy Melissa, Wrensch Margaret, Houlston Richard, Wiemels Joseph |
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