Browsing by Author "Cook, Jackie"
Now showing items 2-8 of 8
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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 ... -
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 ... -
Immunophoretic rapid diagnostic tests as a source of immunoglobulins for estimating malaria sero-prevalence and transmission intensity
Williams, Geoffrey S.; Mweya, Clement; Stewart, Laveta; Mtove, George; Reyburn, Hugh T.; Cook, Jackie; Corran, Patrick H.Riley, Eleanor M.Drakeley, Chris J. et al. (2009-07-22)Abstract Background Sero-epidemiological methods are being developed as a tool for rapid assessment of malaria transmission intensity. Simple blood collection methods for use in field settings will make this more feasible. ... -
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, 2018-02-15)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 ... -
Risks of breast or ovarian cancer in BRCA1 or BRCA2 predictive test negatives: findings from the EMBRACE study.
Girardi, Fabio; Barnes, Daniel Robert; Barrowdale, Daniel; Frost, Debra; Brady, Angela F; Miller, Claire; Henderson, AlexDonaldson, AlanMurray, AlexBrewer, CarolePottinger, CarolineEvans, D GarethEccles, DianaEMBRACE,Lalloo, FionaGregory, HelenCook, JackieEason, JacquelineAdlard, JulianBarwell, JulianOng, Kai RenWalker, LisaIzatt, LouiseSide, Lucy EKennedy, M JohnTischkowitz, Marc DerekRogers, Mark TPorteous, Mary EMorrison, Patrick JEeles, RosDavidson, RosemarieSnape, KatieEaston, Douglas FrederickAntoniou, Antonis et al. (Wolters Kluwer Health, 2018-03-22)Purpose. BRCA1/BRCA2 predictive test negatives are proven non-carriers of a BRCA1/BRCA2 mutation that is carried by their relatives. The risk of developing breast cancer (BC) or epithelial ovarian cancer (EOC) in these ...