Low-frequency variation near common germline susceptibility loci are associated with risk of Ewing sarcoma.
Shu-Hong LinJoshua N SampsonThomas G P GrünewaldDidier SurdezStephanie ReynaudOlivier MirabeauEric KarlinsRebeca Alba RubioSakina ZaidiSandrine Grossetête-LalamiStelly BalletEve LapoubleValérie LaurenceJean MichonGaelle PierronHeinrich KovarUdo KontnyAnna González-NeiraJavier AlonsoAna Patino-GarciaNadège CorradiniPerrine Marec BérardJeremy MillerNeal D FreedmanNathaniel RothmanBrian D CarterCasey L DagnallLaurie BurdettKristine JonesMichelle ManningKathleen WyattWeiyin ZhouMeredith YeagerDavid G CoxRobert N HooverJaved KhanGregory T ArmstrongWendy M LeisenringSmita BhatiaLeslie L RobisonAndreas E KulozikJennifer KriebelThomas MeitingerMarkus MetzlerManuela KrumbholzWolfgang HartmannKonstantin StrauchThomas KirchnerUta DirksenLisa MirabelloMargaret A TuckerFranck TirodeLindsay M MortonStephen J ChanockOlivier DelattreMitchell J MachielaPublished in: PloS one (2020)
Motivate future targeted sequencing studies for a comprehensive evaluation of low-frequency and rare variation around common EwS susceptibility loci.