Browsing by Author "Domchek, Susan M"
Now showing items 1-14 of 14
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Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3.
Hamdi, Yosr; Soucy, Penny; Kuchenbaeker, Karoline B; Pastinen, Tomi; Droit, Arnaud; Lemaçon, Audrey; Adlard, JulianAittomäki, KristiinaAndrulis, Irene LArason, AdalgeirArnold, NorbertArun, Banu KAzzollini, JacopoBane, AnitaBarjhoux, LaureBarrowdale, DanielBenitez, JavierBerthet, PascalineBlok, Marinus JBobolis, KristieBonadona, ValérieBonanni, BernardoBradbury, Angela RBrewer, CaroleBuecher, BrunoBuys, Saundra SCaligo, Maria AChiquette, JocelyneChung, Wendy KClaes, Kathleen BMDaly, Mary BDamiola, FrancescaDavidson, RosemarieDe, la Hoya MiguelDe, Leeneer KimDiez, OrlandDing, Yuan ChunDolcetti, RiccardoDomchek, Susan MDorfling, Cecilia MEccles, DianaEeles, RosEinbeigi, ZakariaEjlertsen, BentEMBRACE,,Engel, ChristophGareth, Evans DFeliubadalo, LidiaForetova, LenkaFostira, FlorentiaFoulkes, William DFountzilas, GeorgeFriedman, EitanFrost, DebraGanschow, PamelaGanz, Patricia AGarber, JudyGayther, Simon AGEMO, Study CollaboratorsGerdes, Anne-MarieGlendon, GordGodwin, Andrew KGoldgar, David EGreene, Mark HGronwald, JacekHahnen, EricHamann, UteHansen, Thomas VOHart, StevenHays, John LHEBON,,Hogervorst, Frans BLHulick, Peter JImyanitov, Evgeny NIsaacs, ClaudineIzatt, LouiseJakubowska, AnnaJames, PaulJanavicius, RamunasJensen, Uffe BirkJohn, Esther MJoseph, VijaiJust, WalterKaczmarek, KatarzynaKarlan, Beth YKConFab, InvestigatorsKets, Carolien MKirk, JudyKriege, MiekeLaitman, YaelLaurent, MaïtéLazaro, ConxiLeslie, GoskaLester, JennyLesueur, FabienneLiljegren, AnnelieLoman, NiklasLoud, Jennifer TManoukian, SiranoushMariani, MilenaMazoyer, SylvieMcGuffog, LesleyMeijers-Heijboer, Hanne EJMeindl, AlfonsMiller, AustinMontagna, MarcoMulligan, Anna MarieNathanson, Katherine LNeuhausen, Susan LNevanlinna, HeliNussbaum, Robert LOlah, EdithOlopade, Olufunmilayo IOng, Kai-RenOosterwijk, Jan COsorio, AnaPapi, LauraPark, Sue KyungPedersen, Inge SokildePeissel, BernardSegura, Pedro PerezPeterlongo, PaoloPhelan, Catherine MRadice, PaoloRantala, JohannaRappaport-Fuerhauser, ChristineRennert, GadRichardson, AndreaRobson, MarkRodriguez, Gustavo CRookus, Matti ASchmutzler, Rita KatharinaSevenet, NicolasShah, Payal DSinger, Christian FSlavin, Thomas PSnape, KatieSokolowska, JohannaSønderstrup, Ida Marie HeeholmSouthey, MelissaSpurdle, Amanda BStadler, ZsofiaStoppa-Lyonnet, DominiqueSukiennicki, GrzegorzSutter, ChristianTan, YenTea, Muy-KhengTeixeira, Manuel RTeulé, AlexTeo, Soo-HwangTerry, Mary BethThomassen, MadsTihomirova, LaimaTischkowitz, Marc DerekTognazzo, SilviaToland, Amanda EwartTung, Nadinevan, den Ouweland Ans MWvan, der Luijt Rob Bvan, Engelen Klaartjevan, Rensburg Elizabeth JVaron-Mateeva, RaymondaWappenschmidt, BarbaraWijnen, Juul TRebbeck, TimothyChenevix-Trench, GeorgiaOffit, KennethCouch, Fergus JNord, SiljeEaston, Douglas FrederickAntoniou, AntonisSimard, Jacques et al. (Springer, 2017-01)$\textit{Purpose}$ $\textit{Cis}$-acting regulatory SNPs resulting in differential allelic expression (DAE) may, in part, explain the underlying phenotypic variation associated with many complex diseases. To investigate ... -
Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers
Kuchenbaecker, Karoline Bernhardine; Neuhausen, Susan L; Robson, Mark; Barrowdale, Daniel; McGuffog, Lesley; Mulligan, Anna Marie; Andrulis, Irene LSpurdle, Amanda BSchmidt, Marjanka KSchmutzler, Rita KEngel, ChristophWappenschmidt, BarbaraNevanlinna, HeliThomassen, MadsSouthey, MelissaRadice, PaoloRamus, Susan JDomchek, Susan MNathanson, Katherine LLee, Andrew JohnHealey, SueNussbaum, Robert LRebbeck, Timothy RArun, Banu KJames, PaulKarlan, Beth YLester, JennyCass, IlanaBreast, Cancer Family RegistryTerry, Mary BethDaly, Mary BGoldgar, David EBuys, Saundra SJanavicius, RamunasTihomirova, LaimaTung, NadineDorfling, Cecilia Mvan, Rensburg Elizabeth JSteele, LindaHansen, Thomas VOEjlertsen, BentGerdes, Anne-MarieNielsen, Finn CDennis, JoeCunningham, JulieHart, StevenSlager, SusanOsorio, AnaBenitez, JavierDuran, MercedesWeitzel, Jeffrey NTafur, IsaacHander, MaryPeterlongo, PaoloManoukian, SiranoushPeissel, BernardRoversi, GaiaScuvera, GiuliettaBonanni, BernardoMariani, PaoloVolorio, SaraDolcetti, RiccardoVaresco, LilianaPapi, LauraTibiletti, Maria GraziaGiannini, GiuseppeFostira, FlorentiaKonstantopoulou, IreneGarber, JudyHamann, UteDonaldson, AlanBrewer, CaroleFoo, ClaireEvans, D GarethFrost, DebraEccles, DianaEMBRACE,Douglas, FionaBrady, AngelaCook, JackieTischkowitz, Marc DerekAdlard, JulianBarwell, JulianOng, Kai-renWalker, LisaIzatt, LouiseSide, Lucy EKennedy, M JohnRogers, Mark TPorteous, Mary EMorrison, Patrick JPlatte, RadkaEeles, RosDavidson, RosemarieHodgson, ShirleyEllis, SteveGodwin, Andrew KRhiem, KerstinMeindl, AlfonsDitsch, NinaArnold, NorbertPlendl, HansjoergNiederacher, DieterSutter, ChristianSteinemann, DorisBogdanova-Markov, NadjaKast, KarinVaron-Mateeva, RaymondaWang-Gohrke, ShanGehrig, AndreaMarkiefka, BirgidBuecher, BrunoLefol, CédrickStoppa-Lyonnet, DominiqueRouleau, EtiennePrieur, FabienneDamiola, FrancescaGEMO, Study CollaboratorsBarjhoux, LaureFaivre, LaurenceLongy, MichelSevenet, NicolasSinilnikova, Olga MMazoyer, SylvieBonadona, ValérieCaux-Moncoutier, VirginieIsaacs, ClaudineVan, Maerken TomClaes, KathleenPiedmonte, MarionAndrews, LesleyHays, JohnRodriguez, Gustavo CCaldes, Trinidadde, la Hoya MiguelKhan, SofiaHogervorst, Frans BLAalfs, Cora Mde, Lange JLMeijers-Heijboer, Hanne EJvan, der Hout Annemarie HWijnen, Juul Tvan, Roozendaal KEPMensenkamp, Arjen Rvan, den Ouweland Ans MWvan, Deurzen Carolien HMvan, der Luijt Rob BHEBON,Olah, EdithDiez, OrlandLazaro, ConxiBlanco, IgnacioTeulé, AlexMenendez, MireiaJakubowska, AnnaLubinski, JanCybulski, CezaryGronwald, JacekJaworska-Bieniek, KatarzynaDurda, KatarzynaArason, AdalgeirMaugard, ChristineSoucy, PennyMontagna, MarcoAgata, SimonaTeixeira, Manuel RKConFab, InvestigatorsOlswold, CurtisLindor, NoralanePankratz, Vernon SHallberg, EmilyWang, XianshuSzabo, Csilla IVijai, JosephJacobs, LaurenCorines, MarinaLincoln, AnneBerger, AndreasFink-Retter, AnnelieseSinger, Christian FRappaport, ChristineKaulich, Daphne GschwantlerPfeiler, GeorgTea, Muy-KhengPhelan, Catherine MMai, Phuong LGreene, Mark HRennert, GadImyanitov, Evgeny NGlendon, GordToland, Amanda EwartBojesen, AndersPedersen, Inge SokildeJensen, Uffe BirkCaligo, Maria AFriedman, EitanBerger, RaananLaitman, YaelRantala, JohannaArver, BritaLoman, NiklasBorg, AkeEhrencrona, HansOlopade, Olufunmilayo ISimard, JacquesEaston, Douglas FrederickChenevix-Trench, GeorgiaOffit, KennethCouch, Fergus JAntoniou, AntonisCIMBA, et al. (BioMed Central, 2014-12-31)Introduction: More than 70 common alleles are known to be involved in breast cancer (BC) susceptibility and several exhibit significant heterogeneity in their associations with different BC subtypes. Although there are ... -
Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170
Dunning, Alison Margaret; Michailidou, Kyriaki; Kuchenbaecker, Karoline Bernhardine; Thompson, Deborah Jane; French, Juliet D; Beesley, Jonathan; Healey, Catherine SKar, SiddharthaPooley, Karen AnneLopez-Knowles, ElenaDicks, EdBarrowdale, DanielSinnott-Armstrong, Nicholas ASallari, Richard CHillman, Kristine MKaufmann, SusanneSivakumaran, HaranMarjaneh, Mahdi MoradiLee, Jason SHills, MargaretJarosz, MonikaDrury, SuzieCanisius, SanderBolla, Manjeet KDennis, JoeWang, QinHopper, John LSouthey, Melissa CBroeks, AnnegienSchmidt, Marjanka KLophatananon, ArtitayaMuir, KennethBeckmann, Matthias WFasching, Peter Ados-Santos-Silva, IsabelPeto, JulianSawyer, Elinor JTomlinson, IanBurwinkel, BarbaraMarme, FrederikGuénel, PascalTruong, ThérèseBojesen, Stig EFlyger, HenrikGonzález-Neira, AnnaPerez, Jose IAAnton-Culver, HodaEunjung, LeeArndt, VolkerBrenner, HermannMeindl, AlfonsSchmutzler, Rita KBrauch, HiltrudHamann, UteAittomäki, KristiinaBlomqvist, CarlIto, HidemiMatsuo, KeitaroBogdanova, NatashaDörk, ThiloLindblom, AnnikaMargolin, SaraKosma, Veli-MattiMannermaa, ArtoTseng, ChiuchenWu, Anna HLambrechts, DietherWildiers, HansChang-Claude, JennyRudolph, AnjaPeterlongo, PaoloRadice, PaoloOlson, Janet EGiles, Graham GMilne, Roger LHaiman, Christopher AHenderson, Brian EGoldberg, Mark STeo, Soo HYip, Cheng HarNord, SiljeBorresen-Dale, Anne-LiseKristensen, VesselaLong, JirongZheng, WeiPylkäs, KatriWinqvist, RobertAndrulis, Irene LKnight, Julia ADevilee, PeterSeynaeve, CarolineFigueroa, JonineSherman, Mark ECzene, KamilaDarabi, HatefHollestelle, Antoinettevan, den Ouweland Ans MWHumphreys, KeithGao, Yu-TangShu, Xiao-OuCox, AngelaCross, Simon SBlot, WilliamCai, QiuyinGhoussaini, MayaPerkins, Barbara JShah, Mitulkumar NandlalChoi, Ji-YeobKang, DaeheeLee, Soo ChinHartman, MikaelKabisch, MariaTorres, DianaJakubowska, AnnaLubinski, JanBrennan, PaulSangrajrang, SuleepornAmbrosone, Christine BToland, Amanda EShen, Chen-YangWu, Pei-EiOrr, NickSwerdlow, AnthonyMcGuffog, LesleyHealey, SueLee, Andrew JohnKapuscinski, MiroslavJohn, Esther MTerry, Mary BethDaly, Mary BGoldgar, David EBuys, Saundra SJanavicius, RamunasTihomirova, LaimaTung, NadineDorfling, Cecilia Mvan, Rensburg Elizabeth JNeuhausen, Susan LEjlertsen, BentHansen, Thomas VOOsorio, AnaBenitez, JavierRando, RachelWeitzel, Jeffrey NBonanni, BernardoPeissel, BernardManoukian, SiranoushPapi, LauraOttini, LauraKonstantopoulou, IreneApostolou, ParaskeviGarber, JudyRashid, Muhammad UsmanFrost, DebraEMBRACE,Izatt, LouiseEllis, SteveGodwin, Andrew KArnold, NorbertNiederacher, DieterRiem, KerstinBogdanova-Markov, NadjaSagne, CharlotteStoppa-Lyonnet, DominiqueDamiola, FrancescaGEMO, Study CollaboratorsSinilnikova, Olga MMazoyer, SylvieIsaacs, ClaudineClaes, Kathleen BMDe, Leeneer Kimde, la Hoya MiguelCaldes, TrinidadNevanlinna, HeliKhan, SofiaMensenkamp, Arjen RHEBON,Hooning, Maartje JRookus, Matti AKwong, AvaOlah, EdithDiez, OrlandBrunet, JoanPujana, Miquel AngelGronwald, JacekHuzarski, TomaszBarkardottir, Rosa BLaframboise, RachelSoucy, PennyMontagna, MarcoAgata, SimonaTeixeira, Manuel RkConFab, InvestigatorsPark, Sue KyungLindor, NoralaneCouch, Fergus JTischkowitz, Marc DerekForetova, LenkaVijai, JosephOffit, KennethSinger, Christian FRappaport, ChristinePhelan, Catherine MGreene, Mark HMai, Phuong LRennert, GadImyanitov, Evgeny NHulick, Peter JPhillips, Kelly-AnnePiedmonte, MarionMulligan, Anna MarieGlendon, GordBojesen, AndersThomassen, MadsCaligo, Maria AYoon, Sook-YeeFriedman, EitanLaitman, YaelBorg, Akevon, Wachenfeldt AnnaEhrencrona, HansRantala, JohannaOlopade, Olufunmilayo IGanz, Patricia ANussbaum, Robert LGayther, Simon ANathanson, Katherine LDomchek, Susan MArun, Banu KMitchell, GillianKarlan, Beth YLester, JennyMaskarinec, GertraudWoolcott, ChristyScott, ChristopherStone, JenniferApicella, CarmelTamimi, RullaLuben, RobertKhaw, Kay-TeeHelland, ÅslaugHaakensen, VildeDowsett, MitchPharoah, Paul DavidSimard, JacquesHall, PerGarcía-Closas, MontserratVachon, CelineChenevix-Trench, GeorgiaAntoniou, AntonisEaston, Douglas FrederickEdwards, Stacey L et al. (Nature Publishing Group, 2016)We analysed 3872 common genetic variants across the ESR1 locus (encoding estrogen receptor–alpha) in 118,816 subjects from three international consortia. We found evidence for at least five independent causal variants, ... -
Common breast cancer susceptibility alleles are associated with tumor subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2.
Mulligan, Anna Marie; Couch, Fergus J; Barrowdale, Daniel; Domchek, Susan M; Eccles, Diana; Nevanlinna, Heli; Ramus, Susan JRobson, MarkSherman, MarkSpurdle, Amanda BWappenschmidt, BarbaraAntoniou, AntonisFamily, Registry Breast CancerEmbrace,Collaborators, GEMO StudyHebon,Network, Ontario Cancer GeneticsSwe-brca,Cimba,Osorio, AnaMunoz-Repeto, IvanCoupier, IsabelleDuran, MercedesGodino, JavierPertesi, MaroulioBenitez, JavierPeterlongo, PaoloManoukian, SiranoushPeissel, BernardZaffaroni, DanielaCattaneo, ElisaBonanni, BernardoLebrun, MarineViel, AlessandraPasini, BarbaraPapi, LauraOttini, LauraSavarese, AntonellaBernard, LorisRadice, PaoloHamann, UteVerheus, MartijnMeijers-Heijboer, Hanne EJKientz, CarolineWijnen, JuulGomez, Garcia Encarna BNelen, Marcel RKets, C MarleenSeynaeve, CarolineTilanus-Linthorst, Madeleine MAvan, der Luijt Rob Bvan, Os Theo ARookus, MattiFrost, DebraLongy, MichelJones, J LouiseEvans, D GarethLalloo, FionaEeles, RosIzatt, LouiseAdlard, JulianDavidson, RosemarieCook, JackieDonaldson, AlanDorkins, HuwSevenet, NicolasGregory, HelenEason, JacquelineHoughton, CatherineBarwell, JulianSide, Lucy EMcCann, EmmaMurray, AlexPeock, SusanGodwin, AndrewSchmutzler, Rita KStoppa-Lyonnet, DominiqueRhiem, KerstinEngel, ChristophMeindl, AlfonsRuehl, InaArnold, NorbertNiederacher, DieterSutter, ChristianDeissler, HelmutGadzicki, DorotheaKast, KarinIsaacs, ClaudinePreisler-Adams, SabineVaron-Mateeva, RaymondaSchoenbuchner, InesFiebig, BrittaHeinritz, WolframSchafer, DieterGevensleben, HeidrunCaux-Moncoutier, VirginieFassy-Colcombet, MarionCornelis, FrancoisCaldes, TrinidadMazoyer, SylvieLeone, MelanieBoutry-Kryza, NadiaHardouin, AgnesBerthet, PascalineMuller, DanieleFricker, Jean-PierreMortemousque, IsabellePujol, Pascalde, al Hoya MiguelHeikkinen, TuomasLee, Andrew JohnAittomaki, KristiinaBlanco, IgnacioLazaro, ConxiBarkardottir, Rosa BSoucy, PennyDumont, MartineSimard, JacquesMontagna, MarcoTognazzo, SilviaD'Andrea, EmmaMcGuffog, LesleyFox, StephenYan, MaxRebbeck, Timothy ROlopade, Olufunmilayo IWeitzel, Jeffrey NLynch, Henry TGanz, Patricia ATomlinson, Gail EWang, XianshuFredericksen, ZacharyHealey, SuePankratz, Vernon SLindor, Noralane MSzabo, CsilaOffit, KennethSakr, RitaGaudet, MiaBhatia, JasmineKauff, NoahSinger, Christian FTea, Muy-KhengSinilnikova, Olga MGschwantler-Kaulich, DaphneFink-Retter, AnnelieseMai, Phuong LGreene, Mark HImyanitov, EvgenyO'Malley, Frances POzcelik, HilmiGlendon, GordonToland, Amanda EGerdes, Anne-MarieJanavicius, RamunasThomassen, MadsKruse, Torben ABirk, Jensen UffeSkytte, Anne-BineCaligo, Maria ASoller, MariaHenriksson, Karinvon, Wachenfeldt AnnaArver, BritaStenmark-Askmalm, MarieHansen, Thomas VOKarlsson, PerDing, Yuan ChunNeuhausen, Susan LBeattie, MaryPharoah, Paul DavidMoysich, Kirsten BNathanson, Katherine LKarlan, Beth YGross, JennyJohn, Esther MNielsen, Finn CDaly, Mary BBuys, Saundra MSouthey, Melissa CHopper, John LTerry, Mary BethChung, WendyMiron, Alexander FGoldgar, DavidChenevix-Trench, GeorgiaEaston, Douglas FrederickEjlertsen, BentAndrulis, Irene L et al. (2011-11-02)Abstract Introduction Previous studies have demonstrated that common breast cancer susceptibility alleles are differentially associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers. It is currently ... -
Effects of BRCA2 cis-regulation in normal breast and cancer risk amongst BRCA2 mutation carriers
Maia, Ana Teresa; Antoniou, Antonis; O'Reilly, Martin; Samarajiwa, Shamith Anusha; Dunning, Mark James; Kartsonaki, Christiana; Chin, Suet FeungCurtis, Christina NMcGuffog, LesleyDomchek, Susan MEmbrace, EmbraceEaston, Douglas FrederickPeock, SusanFrost, DebraEvans, D GarethEeles, RosIzatt, LouiseAdlard, JulianEccles, DianaGemo, GemoSinilnikova, Olga MMazoyer, SylvieStoppa-Lyonnet, DominiqueGauthier-Villars, MarionFaivre, LaurenceVenat-Bouvet, LaurenceDelnatte, CapucineNevanlinna, HeliCouch, Fergus JGodwin, Andrew KCaligo, Maria AdelaideSwe-brca, Swe-brcaBarkardottir, Rosa BkConFab, kConFabChen, XiaoqingBeesley, JonathanHealey, SueCaldas, Carlos ManuelChenevix-Trench, GeorgiaPonder, Bruce Anthony et al. (2012-04-18)Abstract Introduction Cis-acting regulatory single nucleotide polymorphisms (SNPs) at specific loci may modulate penetrance of germline mutations at the same loci by introducing different levels of expression of the wild-type ... -
Evidence for SMAD3 as a modifier of breast cancer risk in BRCA2 mutation carriers
Walker, Logan C; Fredericksen, Zachary S; Wang, Xianshu; Tarrell, Robert; Pankratz, Vernon Shane; Lindor, Noralane M; Beesley, JonathanHealey, SueChen, Xiaoqing(kConFab), Kathleen Cuningham Foundation Consortium for ResearchStoppa-Lyonnet, DominiqueTirapo, CaroleGiraud, SophieMazoyer, SylvieMuller, DanieleFricker, Jean-PierreDelnatte, Capucine(gemo), Groupe Genetique et CancerSchmutzler, Rita KWappenschmidt, BarbaraEngel, ChristophSchonbuchner, InesDeissler, HelmutMeindl, AlfonsHogervorst, Frans BVerheus, MartijnHooning, Maartje Jvan, den Ouweland Ans MWNelen, Marcel RAusems, Margreet GEMAalfs, Cora Mvan, Asperen Christi JDevilee, PeterGerrits, Monique MWaisfisz, Quinten(hebon), Hereditary Breast and Ovarian Cancer Research Group NetherlandsSzabo, Csilla IModSQuaD, TheEaston, Douglas FrederickPeock, SusanCook, MargaretOliver, Clare TFrost, DebraHarrington, PatriciaEvans, D GarethLalloo, FionaEeles, RosalindIzatt, LouiseChu, CarolDavidson, RosemarieEccles, DianaOng, Kai-RenCook, JackieEmbrace, TheRebbeck, Timothy RNathanson, Katherine LDomchek, Susan MSinger, Christian FGschwantler-Kaulich, DaphneDressler, Anne-CatharinaPfeiler, GeorgGodwin, Andrew KHeikkinen, TuomasNevanlinna, HeliAgnarsson, Bjarni ACaligo, Maria AdelaideOlsson, HakanKristoffersson, UlfLiljegren, AnnelieArver, BritaKarlsson, PerMelin, Beatrice(swe-brca), Swedish Breast Cancer StudySinilnikova, Olga MMcGuffog, LesleyAntoniou, AntonisChenevix-Trench, GeorgiaSpurdle, Amanda BCouch, Fergus J et al. (2010-11-29)Abstract Introduction Current attempts to identify genetic modifiers of BRCA1 and BRCA2 associated risk have focused on a candidate gene approach, based on knowledge of gene functions, or the development of large genome-wide ... -
Exploring the link between MORF4L1 and risk of breast cancer
Martrat, Griselda; Maxwell, Christopher A; Tominaga, Emiko; Porta, Montserrat; Bonifaci, Nuria; Gomez-Baldo, Laia; Bogliolo, MassimoLazaro, ConxiBlanco, IgnacioBrunet, JoanAguilar, HelenaUhrhammer, NancyTorres, DianaCaligo, Maria AdelaideGodwin, Andrew KFernandez-Rodriguez, JuanaImyanitov, Evgeny NJanavicius, Ramunas(gemo), Groupe Genetique et CancerSinilnikova, Olga MStoppa-Lyonnet, DominiqueDavidson, RosemarieMazoyer, SylviePeyrat, Jean-PhilippeVerny-Pierre, CaroleCastera, Laurentde, Pauw AntoineBignon, Yves-JeanVennin, PhilippeFert, Ferrer SandraCollonge-Rame, Marie-AgnesMortemousque, IsabelleRamirez, Maria JMcGuffog, LesleyChenevix-Trench, GeorgiaPereira-Smith, Olivia MChu, CarolAntoniou, AntonisRenwick, AnthonyCeron, JulianTominaga, KaoruSurralles, JordiPujana, Miguel AngelCastella, MariaRahman, NazneenKuhl, JuliaNeveling, KorneliaSchindler, DetlevHernandez, Gonzalo(embrace), Epidemiological Study of Familial Breast CancersEaston, Douglas FrederickPeock, SusanCook, MargaretOliver, Clare TFrost, DebraBlok, Marinus JPlatte, RadkaOng, Kai-RenEvans, D GarethLalloo, FionaEeles, RosalindIzatt, LouiseCook, JackieDouglas, FionaHodgson, Shirley VBrewer, CaroleBernard, LorisMorrison, Patrick JPorteous, MaryPeterlongo, Paolovan, Os Theo AManoukian, SiranoushPeissel, BernardZaffaroni, DanielaRoversi, GaiaBarile, MonicaViel, AlessandraRadice, PaoloPasini, BarbaraOttini, LauraPutignano, Anna LauraSavarese, AntonellaHealey, SueSpurdle, Amanda BChen, XiaoqingBeesley, Jonathan(kConFab), Kathleen Cuningham Foundation Consortium for ResearchRookus, Matti AVerhoef, SennoOsorio, AnaTilanus-Linthorst, Madeleine AMeijers-Heijboer, Hanne EJVreeswijk, Maaike PAsperen, Christi JBodmer, DanielleAusems, Margreet GEMHogervorst, Frans B(hebon), Hereditary Breast and Ovarian Cancer Research Group NetherlandsGoldgar, David EBuys, SaundraLaitman, YaelJohn, Esther MMiron, AlexanderSouthey, Melissa CCaldes, TrinidadDaly, Mary B(bcfr), Breast Cancer Family Registry(swe-brca), Swedish Breast Cancer StudyHarbst, KatjaBorg, AkeRantala, JohannaMilgrom, RoniBarbany-Bustinza, GiselaEhrencrona, HansStenmark-Askmalm, MarieKaufman, BellaFriedman, EitanDomchek, Susan MNathanson, Katherine LRebbeck, Timothy RJohannsson, Oskar ThorCouch, Fergus JWang, XianshuSeal, SheilaFredericksen, Zachary SBenitez, JavierCuadras, DanielMoreno, VictorPientka, Friederike KDepping, ReinhardBueren, JuanHeikkinen, TuomasNevanlinna, HeliHamann, Ute et al. (2011-04-05)Abstract Introduction Proteins encoded by Fanconi anemia (FA) and/or breast cancer (BrCa) susceptibility genes cooperate in a common DNA damage repair signaling pathway. To gain deeper insight into this pathway and its ... -
Fine-Scale Mapping at 9p22.2 Identifies Candidate Causal Variants That Modify Ovarian Cancer Risk in $\small \textit{BRCA1}$ and $\small \textit{BRCA2}$ Mutation Carriers
Vigorito, Elena; Kuchenbaecker, Karoline B; Beesley, Jonathan; Adlard, Julian; Agnarsson, Bjarni A; Andrulis, Irene L; Arun, Banu KBarjhoux, LaureBelotti, MurielBenitez, JavierBerger, AndreasBojesen, AndersBonanni, BernardoBrewer, CaroleCaldes, TrinidadCaligo, Maria ACampbell, IanChan, Salina BClaes, Kathleen BMCohn, David ECook, JackieDaly, Mary BDamiola, FrancescaDavidson, RosemariePauw, Antoine deDelnatte, CapucineDiez, OrlandDomchek, Susan MDumont, MartineDurda, KatarzynaDworniczak, BerndEaston, Douglas FrederickEccles, DianaEdwinsdotter, Ardnor ChristinaEeles, RosEjlertsen, BentEllis, Stephen DavidEvans, D GarethFeliubadalo, LidiaFostira, FlorentiaFoulkes, William DFriedman, EitanFrost, DebraGaddam, PragnaGanz, Patricia AGarber, JudyGarcia-Barberan, VanesaGauthier-Villars, MarionGehrig, AndreaGerdes, Anne-MarieGiraud, SophieGodwin, Andrew KGoldgar, David EHake, Christopher RHansen, Thomas VOHealey, SueHodgson, ShirleyHogervorst, Frans BLHoudayer, ClaudeHulick, Peter JImyanitov, Evgeny NIsaacs, ClaudineIzatt, LouiseIzquierdo, AngelJacobs, LaurenJakubowska, AnnaJanavicius, RamunasJaworska-Bieniek, KatarzynaJensen, Uffe BirkJohn, Esther MVijai, JosephKarlan, Beth YKast, KarinInvestigators, KConFabKhan, SofiaKwong, AvaLaitman, YaelLester, JennyLesueur, FabienneLiljegren, AnnelieLubinski, JanMai, Phuong LManoukian, SiranoushMazoyer, SylvieMeindl, AlfonsMensenkamp, Arjen RMontagna, MarcoNathanson, Katherine LNeuhausen, Susan LNevanlinna, HeliNiederacher, DieterOlah, EdithOlopade, Olufunmilayo IOng, Kai-renOsorio, AnaPark, Sue KyungPaulsson-Karlsson, YlvaPedersen, Inge SokildePeissel, BernardPeterlongo, PaoloPfeiler, GeorgPhelan, Catherine MPiedmonte, MarionPoppe, BrucePujana, Miquel AngelRadice, PaoloRennert, GadRodriguez, Gustavo CRookus, Matti ARoss, Eric ASchmutzler, Rita KatharinaSimard, JacquesSinger, Christian FSlavin, Thomas PSoucy, PennySouthey, MelissaSteinemann, DorisStoppa-Lyonnet, DominiqueSukiennicki, GrzegorzSutter, ChristianSzabo, Csilla ITea, Muy-KhengTeixeira, Manuel RTeo, Soo-HwangTerry, Mary BethThomassen, MadsTibiletti, Maria GraziaTihomirova, LaimaTognazzo, Silviavan, Rensburg Elizabeth JVaresco, LilianaVaron-Mateeva, RaymondaVratimos, AthanassiosWeitzel, Jeffrey NMcGuffog, LesleyKirk, JudyToland, Amanda EwartHamann, UteLindor, NoralaneRamus, Susan JGreene, Mark HCouch, Fergus JOffit, KennethPharoah, Paul DavidChenevix-Trench, GeorgiaAntoniou, Antonis et al. (Public Library of Science, 2016-07-27)Population-based genome wide association studies have identified a locus at 9p22.2 associated with ovarian cancer risk, which also modifies ovarian cancer risk in $\small \textit{BRCA1}$ and $\small \textit{BRCA2}$ mutation ... -
Functional Mechanisms Underlying Pleiotropic Risk Alleles at the 19p13.1 Breast-Ovarian Cancer Susceptibility Locus
Lawrenson, Kate; Kar, Siddhartha; McCue, Karen; Kuchenbaeker, Karoline; Michailidou, Kyriaki; Tyrer, Jonathan; Beesley, JonathanRamus, Susan JLi, QiyuanDelgado, Melissa KLee, Janet MAittomäki, KristiinaAndrulis, Irene LAnton-Culver, HodaArndt, VolkerArun, Banu KArver, BritaBandera, Elisa VBarile, MonicaBarkardottir, Rosa BBarrowdale, DanielBeckmann, Matthias WBenitez, JavierBerchuck, AndrewBisogna, MariaBjorge, LineBlomqvist, CarlBlot, WilliamBogdanova, NataliaBojesen, AndersBojesen, Stig EBolla, Manjeet KBonanni, BernardoBorresen-Dale, Anne-LiseBrauch, HiltrudBrennan, PaulBrenner, HermannBruinsma, FionaBrunet, JoanBuhari, Shaik AhmadBurwinkel, BarbaraButzow, RalfBuys, Saundra SCai, QiuyinCaldes, TrinidadCampbell, IanCanniotto, RikkiChang-Claude, JennyChiquette, JocelyneChoi, Ji-YeobClaes, Kathleen BMGEMO, Study CollaboratorsCook, Linda SCox, AngelaCramer, Daniel WCross, Simon SCybulski, CezaryCzene, KamilaDaly, Mary BDamiola, FrancescaDansonka-Mieszkowska, AgnieszkaDarabi, HatefDennis, JoeDevilee, PeterDiez, OrlandDoherty, Jennifer ADomchek, Susan MDorfling, Cecilia MDörk, ThiloDumont, MartineEhrencrona, HansEjlertsen, BentEllis, SteveEMBRACE,Engel, ChristophLee, EunjungEvans, D GarethFasching, Peter AFeliubadalo, LidiaFigueroa, JonineFlesch-Janys, DieterFletcher, OliviaFlyger, HenrikForetova, LenkaFostira, FlorentiaFoulkes, William DFridley, Brooke LFriedman, EitanFrost, DebraGambino, GaetanaGanz, Patricia AGarber, JudyGarcía-Closas, MontserratGentry-Maharaj, AleksandraGhoussaini, MayaGiles, Graham GGlasspool, RosalindGodwin, Andrew KGoldberg, Mark SGoldgar, David EGonzález-Neira, AnnaGoode, Ellen LGoodman, Marc TGreene, Mark HGronwald, JacekGuénel, PascalHaiman, Christopher AHall, PerHallberg, EmilyHamann, UteHansen, Thomas VOHarrington, Patricia AHartman, MikaelHassan, NorhashimahHealey, SueHEBON,Heitz, FlorianHerzog, JosefHøgdall, EstridHøgdall, Claus KHogervorst, Frans BLHollestelle, AntoinetteHopper, John LHulick, Peter JHuzarski, TomaszImyanitov, Evgeny NKConFab, InvestigatorsAustralian, Ovarian Cancer Study GroupIsaacs, ClaudineIto, HidemiJakubowska, AnnaJanavicius, RamunasJensen, AllanJohn, Esther MJohnson, NicholaKabisch, MariaKang, DaeheeKapuscinski, MiroslavKarlan, Beth YKhan, SofiaKiemeney, Lambertus AKjaer, Susanne KrugerKnight, Julia AKonstantopoulou, IreneKosma, Veli-MattiKristensen, VesselaKupryjanczyk, JolantaKwong, AvaHoya, Miguel de laLaitman, YaelLambrechts, DietherLe, NhuLeeneer, Kim DeLester, JennyLevine, Douglas ALi, JingmeiLindblom, AnnikaLong, JirongLophatananon, ArtitayaLoud, Jennifer TLu, KarenLubinski, JanMannermaa, ArtoManoukian, SiranoushMarchand, Loic LeMargolin, SaraMarme, FrederikMassuger, Leon FAGMatsuo, KeitaroMazoyer, SylvieMcGuffog, LesleyMcLean, CatrionaMcNeish, IainMeindl, AlfonsMenon, UshaMensenkamp, Arjen RMilne, Roger LMontagna, MarcoMoysich, Kirsten BMuir, KennethMulligan, Anna MarieNathanson, Katherine LNess, Roberta BNeuhausen, Susan LNevanlinna, HeliNord, SiljeNussbaum, Robert LOdunsi, KunleOffit, KennethOlah, EdithOlopade, Olufunmilayo IOlson, Janet EOlswold, CurtisO’Malley, DavidOrlow, IreneOrr, NickOsorio, AnaPark, Sue KyungPearce, Celeste LPejovic, TanjaPeterlongo, PaoloPfeiler, GeorgPhelan, Catherine MPoole, Elizabeth MPylkäs, KatriRadice, PaoloRantala, JohannaRashid, Muhammad UsmanRennert, GadRhenius, ValerieRhiem, KerstinRisch, Harvey ARodriguez, GusRossing, Mary AnneRudolph, AnjaSalvesen, Helga BSangrajrang, SuleepornSawyer, Elinor JSchildkraut, Joellen MSchmidt, Marjanka KSchmutzler, Rita KSellers, Thomas ASeynaeve, CarolineShah, Mitulkumar NandlalShen, Chen-YangShu, Xiao-OuSieh, WeivaSinger, Christian FSinilnikova, Olga MSlager, SusanSong, HonglinSoucy, PennySouthey, Melissa CStenmark-Askmalm, MarieStoppa-Lyonnet, DominiqueSutter, ChristianSwerdlow, AnthonyTchatchou, SandrineTeixeira, Manuel RTeo, Soo HTerry, Kathryn LTerry, Mary BethThomassen, MadsTibiletti, Maria GraziaTihomirova, LaimaTognazzo, SilviaToland, Amanda EwartTomlinson, IanTorres, DianaTruong, ThérèseTseng, Chiu-chenTung, NadineTworoger, Shelley SVachon, CelineOuweland, Ans MW van denDoorn, Helena C vanRensburg, Elizabeth J vanVeer, Laura J Van'tVanderstichele, AdriaanVergote, IgnaceVijai, JosephWang, QinWang-Gohrke, ShanWeitzel, Jeffrey NWentzensen, NicolasWhittemore, Alice SWildiers, HansWinqvist, RobertWu, Anna HYannoukakos, DrakoulisYoon, Sook-YeeYu, Jyh-CherngZheng, WeiZheng, YingKhanna, Kum KumSimard, JacquesMonteiro, Alvaro NFrench, Juliet DCouch, Fergus JFreedman, Matthew LEaston, Douglas FrederickDunning, Alison MargaretPharoah, Paul DavidEdwards, Stacey LChenevix-Trench, GeorgiaAntoniou, AntonisGayther, Simon A et al. (Nature Publishing Group, 2016)A locus at 19p13 is associated with breast cancer (BC) and ovarian cancer (OC) risk. We analyzed 438 SNPs in this region in 46,451 BC and 15,438 OC cases, 15,252 BRCA1 mutation carriers and 73,444 controls and identified ... -
Gene-Panel Sequencing and the Prediction of Breast-Cancer Risk
Easton, Douglas Frederick; Pharoah, Paul David; Antoniou, Antonis; Tischkowitz, Marc Derek; Tavtigian, Sean V; Nathanson, Katherine L; Devilee, PeterMeindl, AlfonsCouch, Fergus JSouthey, MelissaGoldgar, David EEvans, Gareth RChenevix-Trench, GeorgiaRahman, NazneenRobson, MarkDomchek, Susan MFoulkes, William D et al. (Massachusetts Medical Society, 2015-06-04)Advances in sequencing technology have made multigene testing, or “panel testing,” a practical option when looking for genetic variants that may be associated with a risk of breast cancer. In June 2013, the U.S. Supreme ... -
Identification of four novel susceptibility loci for estrogen receptor negative breast cancer
Couch, Fergus J; Kuchenbaecker, Karoline B; Michailidou, Kyriaki; Mendoza-Fandino, Gustavo A; Nord, Silje; Lilyquist, Janna; Olswold, CurtisHallberg, EmilyAgata, SimonaAhsan, HabibulAittomäki, KristiinaAmbrosone, ChristineAndrulis, Irene LAnton-Culver, HodaArndt, VolkerArun, Banu KArver, BritaBarile, MonicaBarkardottir, Rosa BBarrowdale, DanielBeckmann, LarsBeckmann, Matthias WBenitez, JavierBlank, Stephanie VBlomqvist, CarlBogdanova, Natalia VBojesen, Stig EBolla, Manjeet KBonanni, BernardoBrauch, HiltrudBrenner, HermannBurwinkel, BarbaraBuys, Saundra SCaldes, TrinidadCaligo, Maria ACanzian, FedericoCarpenter, JaneChang-Claude, JennyChanock, Stephen JChung, Wendy KClaes, Kathleen BMCox, AngelaCross, Simon SCunningham, Julie MCzene, KamilaDaly, Mary BDamiola, FrancescaDarabi, Hatefde, la Hoya MiguelDevilee, PeterDiez, OrlandDing, Yuan CDolcetti, RiccardoDomchek, Susan MDorfling, Cecilia Mdos-Santos-Silva, IsabelDumont, MartineDunning, Alison MargaretEccles, Diana MEhrencrona, HansEkici, Arif BEliassen, HeatherEllis, Stephen DavidFasching, Peter AFigueroa, JonineFlesch-Janys, DieterFörsti, AstaFostira, FlorentiaFoulkes, William DFriebel, TaraFriedman, EitanFrost, DebraGabrielson, MarikeGammon, Marilie DGanz, Patricia AGapstur, Susan MGarber, JudyGaudet, Mia MGayther, Simon AGerdes, Anne-MarieGhoussaini, MayaGiles, Graham GGlendon, GordGodwin, Andrew KGoldberg, Mark SGoldgar, David EGonzález-Neira, AnnaGreene, Mark HGronwald, JacekGuénel, PascalGunter, MarcHaeberle, LotharHaiman, Christopher AHamann, UteHansen, Thomas VOHart, StevenHealey, SueHeikkinen, TuomasHenderson, Brian EHerzog, JosefHogervorst, Frans BLHollestelle, AntoinetteHooning, Maartje JHoover, Robert NHopper, John LHumphreys, KeithHunter, David JHuzarski, TomaszImyanitov, Evgeny NIsaacs, ClaudineJakubowska, AnnaJames, PaulJanavicius, RamunasJensen, Uffe BirkJohn, Esther MJones, MichaelKabisch, MariaKar, SiddarthaKarlan, Beth YKhan, SofiaKhaw, Kay-TeeKibriya, Muhammad GKnight, Julia AKo, Yon-DschunKonstantopoulou, IreneKosma, Veli-MattiKristensen, VesselaKwong, AvaLaitman, YaelLambrechts, DietherLazaro, ConxiLee, EunjungMarchand, Loic LeLester, JennyLindblom, AnnikaLindor, NoralaneLindstrom, SaraLiu, JianjunLong, JirongLubinski, JanMai, Phuong LMakalic, EnesMalone, Kathleen EMannermaa, ArtoManoukian, SiranoushMargolin, SaraMarme, FrederikMartens, John WMMcGuffog, LesleyMeindl, AlfonsMiller, AustinMilne, Roger LMiron, PenelopeMontagna, MarcoMazoyer, SylvieMulligan, Anna MMuranen, Taru ANathanson, Katherine LNeuhausen, Susan LNevanlinna, HeliNordestgaard, Børge GNussbaum, Robert LOffit, KennethOlah, EdithOlopade, Olufunmilayo IOlson, Janet EOsorio, AnaPark, Sue KPeeters, Petra HPeissel, BernardPeterlongo, PaoloPeto, JulianPhelan, Catherine MPilarski, RobertPoppe, BrucePylkäs, KatriRadice, PaoloRahman, NazneenRantala, JohannaRappaport, ChristineRennert, GadRichardson, AndreaRobson, MarkRomieu, IsabelleRudolph, AnjaRutgers, Emiel JSanchez, Maria-JoseSantella, Regina MSawyer, Elinor JSchmidt, Daniel FSchmidt, Marjanka KSchmutzler, Rita KSchumacher, FredrickScott, RodneySenter, LeighaSharma, PriyankaSimard, JacquesSinger, Christian FSinilnikova, Olga MSoucy, PennySouthey, MelissaSteinemann, DorisStenmark-Askmalm, MarieStoppa-Lyonnet, DominiqueSwerdlow, AnthonySzabo, Csilla ITamimi, RullaTapper, WilliamTeixeira, Manuel RTeo, Soo-HwangTerry, Mary BThomassen, MadsThompson, Deborah JaneTihomirova, LaimaToland, Amanda ETollenaar, Robert AEMTomlinson, IanTruong, ThérèseTsimiklis, HelenTeulé, AlexTumino, RosarioTung, NadineTurnbull, ClareUrsin, Giskivan, Deurzen Carolien HMvan, Rensburg Elizabeth JVaron-Mateeva, RaymondaWang, ZhaomingWang-Gohrke, ShanWeiderpass, ElisabeteWeitzel, Jeffrey NWhittemore, AliceWildiers, HansWinqvist, RobertYang, Xiaohong RYannoukakos, DrakoulisYao, SongZamora, M PilarZheng, WeiHall, PerKraft, PeterVachon, CelineSlager, SusanChenevix-Trench, GeorgiaPharoah, Paul DavidMonteiro, Alvaro ANGarcía-Closas, MontserratEaston, Douglas FrederickAntoniou, Antonis et al. (Nature Publishing Group, 2016)Common variants in 94 loci have been associated with breast cancer including 15 loci with genome wide significant associations (P<5x10-8) with estrogen receptor (ER)-negative breast cancer and BRCA1-associated breast cancer ... -
Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus
Zeng, Chenjie; Guo, Xingyi; Long, Jirong; Kuchenbaecker, Karoline B; Droit, Arnaud; Michailidou, Kyriaki; Ghoussaini, MayaKar, SiddharthaFreeman, AdamHopper, John LMilne, Roger LBolla, Manjeet KWang, QinDennis, JoeAgata, SimonaAhmed, ShahanaAittomäki, KristiinaAndrulis, Irene LAnton-Culver, HodaAntonenkova, Natalia NArason, AdalgeirArndt, VolkerArun, Banu KArver, BritaBacot, FrancoisBarrowdale, DanielBaynes, CarolineBeeghly-Fadiel, AliciaBenitez, JavierBermisheva, MarinaBlomqvist, CarlBlot, William JBogdanova, Natalia VBojesen, Stig EBonanni, BernardoBorresen-Dale, Anne-LiseBrand, Judith SBrauch, HiltrudBrennan, PaulBrenner, HermannBroeks, AnnegienBrüning, ThomasBurwinkel, BarbaraBuys, Saundra SCai, QiuyinCaldes, TrinidadCampbell, IanCarpenter, JaneChang-Claude, JennyChoi, Ji-YeobClaes, Kathleen BMClarke, ChristineCox, AngelaCross, Simon SCzene, KamilaDaly, Mary Bde, la Hoya MiguelDe, Leeneer KimDevilee, PeterDiez, OrlandDomchek, Susan MDoody, MicheleDorfling, Cecilia MDörk, Thilodos-Santos-Silva, IsabelDumont, MartineDwek, MiriamDworniczak, BerndEgan, KathleenEilber, UrsulaEinbeigi, ZakariaEjlertsen, BentEllis, Stephen DavidFrost, DebraLalloo, FionaEMBRACE2,Fasching, Peter AFigueroa, JonineFlyger, HenrikFriedlander, MichaelFriedman, EitanGambino, GaetanaGao, Yu-TangGarber, JudyGarcía-Closas, MontserratGehrig, AndreaDamiola, FrancescaLesueur, FabienneMazoyer, SylvieStoppa-Lyonnet, DominiqueGEMO, StudyGiles, Graham GGodwin, Andrew KGoldgar, David EGonzález-Neira, AnnaGreene, Mark HGuénel, PascalHaeberle, LotharHaiman, Christopher AHallberg, EmilyHamann, UteHansen, Thomas VOHart, StevenHartikainen, Jaana MHartman, MikaelHassan, NorhashimahHealey, SueHogervorst, Frans BLVerhoef, SennoHEBON106,Hendricks, Carolyn BHillemanns, PeterHollestelle, AntoinetteHulick, Peter JHunter, David JImyanitov, Evgeny NIsaacs, ClaudineIto, HidemiJakubowska, AnnaJanavicius, RamunasJaworska-Bieniek, KatarzynaJensen, Uffe BirkJohn, Esther MBeauparlant, Charles JolyJones, MichaelKabisch, MariaKang, DaeheeKarlan, Beth YKauppila, SailaKerin, Michael JKhan, SofiaKhusnutdinova, ElzaKnight, Julia AKonstantopoulou, IreneKraft, PeterKwong, AvaLaitman, YaelLambrechts, DietherLazaro, ConxiMarchand, Loic LeLee, Chuen NengLee, Min HyukLester, JennyLi, JingmeiLiljegren, AnnelieLindblom, AnnikaLophatananon, ArtitayaLubinski, JanMai, Phuong LMannermaa, ArtoManoukian, SiranoushMargolin, SaraMarme, FrederikMatsuo, KeitaroMcGuffog, LesleyMeindl, AlfonsMenegaux, FlorenceMontagna, MarcoMuir, KennethMulligan, Anna MarieNathanson, Katherine LNeuhausen, Susan LNevanlinna, HeliNewcomb, Polly ANord, SiljeNussbaum, Robert LOffit, KennethOlah, EdithOlopade, Olufunmilayo IOlswold, CurtisOsorio, AnaPapi, LauraPark-Simon, Tjoung-WonPaulsson-Karlsson, YlvaPeeters, StephaniePeissel, BernardPeterlongo, PaoloPeto, JulianPfeiler, GeorgPhelan, Catherine MPresneau, NadegeRadice, PaoloRahman, NazneenRamus, Susan JRashid, Muhammad UsmanRennert, GadRhiem, KerstinRudolph, AnjaSalani, RituSangrajrang, SuleepornSawyer, Elinor JSchmidt, Marjanka KSchmutzler, Rita KSchoemaker, Minouk JSchürmann, PeterSeynaeve, CarolineShen, Chen-YangShrubsole, Martha JShu, Xiao-OuSigurdson, AliceSinger, Christian FSlager, SusanSoucy, PennySouthey, MelissaSteinemann, DorisSwerdlow, AnthonySzabo, Csilla ITchatchou, SandrineTeixeira, Manuel RTeo, Soo HTerry, Mary BethTessier, Daniel CTeulé, AlexThomassen, MadsTihomirova, LaimaTischkowitz, Marc DerekToland, Amanda ETung, NadineTurnbull, Clarevan, den Ouweland Ans MWvan, Rensburg Elizabeth Jven, den Berg DavidVijai, JosephWang-Gohrke, ShanWeitzel, Jeffrey NWhittemore, Alice SWinqvist, RobertWong, Tien YWu, Anna HYannoukakos, DrakoulisYu, Jyh-CherngPharoah, Paul DavidHall, PerChenevix-Trench, GeorgiaKConFab,AOCS, InvestigatorsDunning, Alison MargaretSimard, JacquesCouch, Fergus JAntoniou, AntonisEaston, Douglas FrederickZheng, Wei et al. (BioMed Central, 2016)Background Multiple recent genome-wide association studies (GWAS) have identified a single nucleotide polymorphism (SNP), rs10771399, at 12p11 that is associated with breast cancer risk. Method We performed a fine-scale ... -
Identification of six new susceptibility loci for invasive epithelial ovarian cancer
Kuchenbaecker, Karoline Bernhardine; Ramus, Susan J; Tyrer, Jonathan; Lee, Andrew; Shen, Howard C; Beesley, Jonathan; Lawrenson, KateMcGuffog, LesleyHealey, SueLee, Janet MSpindler, Tassja JLin, Yvonne GPejovic, TanjaBean, YukieLi, QiyuanCoetzee, SimonHazelett, DennisMiron, AlexanderSouthey, MelissaTerry, Mary BethGoldgar, David EBuys, Saundra SJanavicius, RamunasDorfling, Cecilia MRensburg, Elizabeth J vanNeuhausen, Susan LDing, Yuan ChunHansen, Thomas VOJonson, LarsGerdes, Anne-MarieEjlertsen, BentBarrowdale, DanielDennis, JosephBenitez, JavierOsorio, AnaGarcia, Maria JoseKomenaka, IanWeitzel, Jeffrey NGanschow, PamelaPeterlongo, PaoloBernard, LorisViel, AlessandraBonanni, BernardoPeissel, BernardManoukian, SiranoushRadice, PaoloPapi, LauraOttini, LauraFostira, FlorentiaKonstantopoulou, IreneGarber, JudyFrost, DebraPerkins, JoPlatte, RadkaEllis, Stephen DavidEMBRACE,Godwin, Andrew KSchmutzler, Rita KatharinaMeindl, AlfonsEngel, ChristophSutter, ChristianSinilnikova, Olga MGEMO, Study CollaboratorsDamiola, FrancescaMazoyer, SylvieStoppa-Lyonnet, DominiqueClaes, KathleenLeeneer, Kim DeKirk, JudyRodriguez, Gustavo CPiedmonte, MarionO'Malley, David MHoya, Miguel de laCaldes, TrinidadAittomaki, KristiinaNevanlinna, HeliCollee, J MargrietRookus, Matti AOosterwijk, Jan CBreast, Cancer Family RegistryTihomirova, LaimaTung, NadineHamann, UteIsaccs, ClaudineTischkowitz, Marc DerekImyanitov, Evgeny NCaligo, Maria ACampbell, Ian GHogervorst, Frans BLHEBON,Olah, EdithDiez, OrlandBlanco, IgnacioBrunet, JoanLazaro, ConxiPujana, Miquel AngelJakubowska, AnnaGronwald, JacekLubinski, JanSukiennicki, GrzegorzBarkardottir, Rosa BPlante, MarieSimard, JacquesSoucy, PennyMontagna, MarcoTognazzo, SilviaTeixeira, Manuel RKConFab, InvestigatorsPankratz, Vernon SWang, XianshuLindor, NoralaneSzabo, Csilla IKauff, NoahVijai, JosephAghajanian, Carol APfeiler, GeorgBerger, AndreasSinger, Christian FTea, Muy-KhengPhelan, Catherine MGreene, Mark HMai, Phuong LRennert, GadMulligan, Anna MarieTchatchou, SandrineAndrulis, Irene LGlendon, GordToland, Amanda EwartJensen, Uffe BirkKruse, Torben AThomassen, MadsBojesen, AndersZidan, JamalFriedman, EitanLaitman, YaelSoller, MariaLiljegren, AnnelieArver, BritaEinbeigi, ZakariaStenmark-Askmalm, MarieOlopade, Olufunmilayo INussbaum, Robert LRebbeck, Timothy RNathanson, Katherine LDomchek, Susan MLu, Karen HKarlan, Beth YWalsh, ChristineLester, JennyAustralian, Cancer Study (Ovarian Cancer Investigators)Australian, Ovarian Cancer Study GroupHein, AlexanderEkici, Arif BBeckmann, Matthias WFasching, Peter ALambrechts, DietherNieuwenhuysen, Els vanVergote, IgnaceLambrechts, SandrinaDicks, EdDoherty, Jennifer AWicklund, Kristine GRossing, Mary AnneRudolph, AnjaChang-Claude, JennyWang-Gohrke, ShanEilber, UrsulaMoysich, Kirsten BOdunsi, KunleSucheston, LaraLele, ShashiWilkens, Lynne RGoodman, Marc TThompson, Pamela JShvetsov, Yurii BRunnebaum, Ingo BDurst, MatthiasHillemanns, PeterDork, ThiloAntonenkova, NataliaBogdanova, NataliaLeminen, ArtoPelttari, Liisa MButzow, RalfModugno, FrancesmaryKelley, Joseph LEdwards, Robert PNess, Roberta BBois, Andreas duHeitz, FlorianSchwaab, IraHarter, PhilippMatsuo, KeitaroHosono, SatoyoOrsulic, SandraJensen, AllanKjaer, Susanne KrugerHogdall, EstridHasmad, Hanis NazihahAzmi, Mat Adenan NoorTeo, Soo-HwangWoo, Yin-LingFridley, Brooke LGoode, Ellen LCunningham, Julie MVierkant, Robert ABruinsma, FionaGiles, Graham GLiang, DongHildebrandt, Michelle ATWu, XifengLevine, Douglas ABisogna, MariaBerchuck, AndrewIversen, Edwin SSchildkraut, Joellen MConcannon, PatrickWeber, Rachel PalmieriCramer, Daniel WTerry, Kathryn LPoole, Elizabeth MTworoger, Shelley SBandera, Elisa VOrlow, IreneOlson, Sara HKrakstad, CamillaSalvesen, Helga BTangen, Ingvild LBjorge, LineAltena, Anne M vanAben, Katja KHKiemeney, Lambertus AMassuger, Leon FAGKellar, MelissaBrooks-Wilson, AngelaKelemen, Linda ECook, Linda SLe, Nhu DCybulski, CezaryYang, HannahLissowska, JolantaBrinton, Louise AWentzensen, NicolasHogdall, ClausLundvall, LeneNedergaard, LotteBaker, HelenSong, HonglinEccles, DianaMcNeish, IanPaul, JamesCarty, KarenSiddiqui, NadeemGlasspool, RosalindWhittemore, Alice SRothstein, Joseph HMcGuire, ValerieSieh, WeivaJi, Bu-TianZheng, WeiShu, Xiao-OuGao, Yu-TangRosen, BarryRisch, Harvey AMcLaughlin, John RNarod, Steven AMonteiro, Alvaro NChen, AnnLin, Hui-YiPermuth-Wey, JennySellers, Thomas ATsai, Ya-YuChen, ZhihuaZiogas, ArgyriosAnton-Culver, HodaGentry-Maharaj, AleksandraMenon, UshaHarrington, PatriciaLee, Andrew JohnWu, Anna HPearce, Celeste LCoetzee, GerryPike, Malcolm CDansonka-Mieszkowska, AgnieszkaTimorek, AgnieszkaRzepecka, Iwona KKupryjanczyk, JolantaFreedman, MattNoushmehr, HoutanEaston, Douglas FrederickOffit, KennethCouch, Fergus JGayther, SimonPharoah, Paul DavidAntoniou, AntonisChenevix-Trench, GeorgiaConsortium, of Investigators of Modifiers of BRCA1 and BRCA2 et al. (2015-01-12)Genome-wide association studies (GWAS) have identified 12 epithelial ovarian cancer (EOC) susceptibility alleles. The pattern of association at these loci is consistent in BRCA1 and BRCA2 mutation carriers who are at high ... -
Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations.
Rebbeck, Timothy R; Friebel, Tara M; Friedman, Eitan; Hamann, Ute; Huo, Dezheng; Kwong, Ava; Olah, EdithOlopade, Olufunmilayo ISolano, Angela RTeo, Soo-HwangThomassen, MadsWeitzel, Jeffrey NChan, TLCouch, Fergus JGoldgar, David EKruse, Torben APalmero, Edenir InêzPark, Sue KyungTorres, Dianavan Rensburg, Elizabeth JMcGuffog, LesleyParsons, Michael TLeslie, GoskaAalfs, Cora MAbugattas, JulioAdlard, JulianAgata, SimonaAittomäki, KristiinaAndrews, LesleyAndrulis, Irene LArason, AdalgeirArnold, NorbertArun, Banu KAsseryanis, EllaAuerbach, LeoAzzollini, JacopoBalmaña, JudithBarile, MonicaBarkardottir, Rosa BBarrowdale, DanielBenitez, JavierBerger, AndreasBerger, RaananBlanco, Amie MBlazer, Kathleen RBlok, Marinus JBonadona, ValérieBonanni, BernardoBradbury, Angela RBrewer, CaroleBuecher, BrunoBuys, Saundra SCaldes, TrinidadCaliebe, AlmuthCaligo, Maria ACampbell, IanCaputo, Sandrine MChiquette, JocelyneChung, Wendy KClaes, Kathleen BMCollée, J MargrietCook, JackieDavidson, Rosemariede la Hoya, MiguelDe Leeneer, Kimde Pauw, AntoineDelnatte, CapucineDiez, OrlandDing, Yuan ChunDitsch, NinaDomchek, Susan MDorfling, Cecilia MVelazquez, CarolinaDworniczak, BerndEason, JacquelineEaston, Douglas FrederickEeles, RosEhrencrona, HansEjlertsen, BentEMBRACE,Engel, ChristophEngert, StefanieEvans, D GarethFaivre, LaurenceFeliubadaló, LidiaFerrer, Sandra FertForetova, LenkaFowler, JeffreyFrost, DebraGalvão, Henrique CRGanz, Patricia AGarber, JudyGauthier-Villars, MarionGehrig, AndreaGEMO Study Collaborators,Gerdes, Anne-MarieGesta, PaulGiannini, GiuseppeGiraud, SophieGlendon, GordGodwin, Andrew KGreene, Mark HGronwald, JacekGutierrez-Barrera, AngelicaHahnen, EricHauke, JanHEBON,Henderson, AlexHentschel, JuliaHogervorst, Frans BLHonisch, EllenImyanitov, Evgeny NIsaacs, ClaudineIzatt, LouiseIzquierdo, AngelJakubowska, AnnaJames, PaulJanavicius, RamunasJensen, Uffe BirkJohn, Esther MVijai, JosephKaczmarek, KatarzynaKarlan, Beth YKast, KarinInvestigators, KConFabKim, Sung-WonKonstantopoulou, IreneKorach, JacobLaitman, YaelLasa, AdrianaLasset, ChristineLázaro, ConxiLee, Andrew JohnLee, Min HyukLester, JennyLesueur, FabienneLiljegren, AnnelieLindor, Noralane MLongy, MichelLoud, Jennifer TLu, Karen HLubinski, JanMachackova, EvaManoukian, SiranoushMari, VéroniqueMartínez-Bouzas, CristinaMatrai, ZoltanMebirouk, NouraMeijers-Heijboer, Hanne EJMeindl, AlfonsMensenkamp, Arjen RMickys, UgniusMiller, AustinMontagna, MarcoMoysich, Kirsten BMulligan, Anna MarieMusinsky, JacobNeuhausen, Susan LNevanlinna, HeliNgeow, JoanneNguyen, Huu PhucNiederacher, DieterNielsen, Henriette RoedNielsen, Finn CiliusNussbaum, Robert LOffit, KennethÖfverholm, AnnaOng, Kai-RenOsorio, AnaPapi, LauraPapp, JanosPasini, BarbaraPedersen, Inge SokildePeixoto, AnaPeruga, NinaPeterlongo, PaoloPohl, EstherPradhan, NishaPrajzendanc, KarolinaPrieur, FabiennePujol, PascalRadice, PaoloRamus, Susan JRantala, JohannaRashid, Muhammad UsmanRhiem, KerstinRobson, MarkRodriguez, Gustavo CRogers, Mark TRudaitis, ViliusSchmidt, Ane YSchmutzler, Rita KatharinaSenter, LeighaShah, Payal DSharma, PriyankaSide, Lucy ESimard, JacquesSinger, Christian FSkytte, Anne-BineSlavin, Thomas PSnape, KatieSobol, HagaySouthey, MelissaSteele, LindaSteinemann, DorisSukiennicki, GrzegorzSutter, ChristianSzabo, Csilla ITan, Yen YTeixeira, Manuel RTerry, Mary BethTeulé, AlexThomas, AbigailThull, Darcy LTischkowitz, Marc DerekTognazzo, SilviaToland, Amanda EwartTopka, SabineTrainer, Alison HTung, Nadinevan Asperen, Christi Jvan der Hout, Annemieke Hvan der Kolk, Lizet Evan der Luijt, Rob BVan Heetvelde, MattiasVaresco, LilianaVaron-Mateeva, RaymondaVega, AnaVillarreal-Garza, Cynthiavon Wachenfeldt, AnnaWalker, LisaWang-Gohrke, ShanWappenschmidt, BarbaraWeber, Bernhard HFYannoukakos, DrakoulisYoon, Sook-YeeZanzottera, CristinaZidan, JamalZorn, Kristin KHutten Selkirk, Christina GHulick, Peter JChenevix-Trench, GeorgiaSpurdle, Amanda BAntoniou, AntonisNathanson, Katherine L et al. (Wiley-Blackwell, 2018-05)The prevalence and spectrum of germline mutations in BRCA1 and BRCA2 have been reported in single populations, with the majority of reports focused on Caucasians in Europe and North America. The Consortium of Investigators ...