Browsing by Author "Cook, Jackie"

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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 J.Robson, MarkSherman, MarkSpurdle, Amanda B.Wappenschmidt, BarbaraAntoniou, Antonis C.Family Registry, Breast CancerEmbraceCollaborators, GEMO StudyHebonNetwork, Ontario Cancer GeneticsSwe-brcaCimbaOsorio, 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 E. J.Kientz, CarolineWijnen, JuulGomez Garcia, Encarna B.Nelen, Marcel R.Kets, C. MarleenSeynaeve, CarolineTilanus-Linthorst, Madeleine M. A.van der Luijt, Rob B.van Os, Theo A.Rookus, MattiFrost, DebraLongy, MichelJones, J. LouiseEvans, D. GarethLalloo, FionaEeles, RosIzatt, LouiseAdlard, JulianDavidson, RosemarieCook, JackieDonaldson, AlanDorkins, HuwSevenet, NicolasGregory, HelenEason, JacquelineHoughton, CatherineBarwell, JulianSide, Lucy E.McCann, EmmaMurray, AlexPeock, SusanGodwin, AndrewSchmutzler, Rita K.Stoppa-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, AndrewAittomaki, KristiinaBlanco, IgnacioLazaro, ConxiBarkardottir, Rosa B.Soucy, PennyDumont, MartineSimard, JacquesMontagna, MarcoTognazzo, SilviaD'Andrea, EmmaMcGuffog, LesleyFox, StephenYan, MaxRebbeck, Timothy R.Olopade, Olufunmilayo I.Weitzel, Jeffrey N.Lynch, Henry T.Ganz, Patricia A.Tomlinson, Gail E.Wang, XianshuFredericksen, ZacharyHealey, SuePankratz, Vernon S.Lindor, Noralane M.Szabo, CsilaOffit, KennethSakr, RitaGaudet, MiaBhatia, JasmineKauff, NoahSinger, Christian F.Tea, Muy-KhengSinilnikova, Olga M.Gschwantler-Kaulich, DaphneFink-Retter, AnnelieseMai, Phuong L.Greene, Mark H.Imyanitov, EvgenyO'Malley, Frances P.Ozcelik, HilmiGlendon, GordonToland, Amanda E.Gerdes, Anne-MarieJanavicius, RamunasThomassen, MadsKruse, Torben A.Birk Jensen, UffeSkytte, Anne-BineCaligo, Maria A.Soller, MariaHenriksson, Karinvon Wachenfeldt, AnnaArver, BritaStenmark-Askmalm, MarieHansen, Thomas V. O.Karlsson, PerDing, Yuan ChunNeuhausen, Susan L.Beattie, MaryPharoah, Paul D. P.Moysich, Kirsten B.Nathanson, Katherine L.Karlan, Beth Y.Gross, JennyJohn, Esther M.Nielsen, Finn C.Daly, Mary B.Buys, Saundra M.Southey, Melissa C.Hopper, John L.Terry, Mary BethChung, WendyMiron, Alexander F.Goldgar, DavidChenevix-Trench, GeorgiaEaston, Douglas F.Ejlertsen, 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 K.Wappenschmidt, BarbaraEngel, ChristophSchonbuchner, InesDeissler, HelmutMeindl, AlfonsHogervorst, Frans B.Verheus, MartijnHooning, Maartje J.van den Ouweland, Ans M. W.Nelen, Marcel R.Ausems, Margreet G. E. M.Aalfs, Cora M.van Asperen, Christi J.Devilee, PeterGerrits, Monique M.Waisfisz, Quinten(hebon), Hereditary Breast and Ovarian Cancer Research Group NetherlandsSzabo, Csilla I.ModSQuaD, TheEaston, Douglas F.Peock, SusanCook, MargaretOliver, Clare T.Frost, DebraHarrington, PatriciaEvans, D. GarethLalloo, FionaEeles, RosalindIzatt, LouiseChu, CarolDavidson, RosemarieEccles, DianaOng, Kai-RenCook, JackieEmbrace, TheRebbeck, Timothy R.Nathanson, Katherine L.Domchek, Susan M.Singer, Christian F.Gschwantler-Kaulich, DaphneDressler, Anne-CatharinaPfeiler, GeorgGodwin, Andrew K.Heikkinen, TuomasNevanlinna, HeliAgnarsson, Bjarni A.Caligo, Maria AdelaideOlsson, HakanKristoffersson, UlfLiljegren, AnnelieArver, BritaKarlsson, PerMelin, Beatrice(swe-brca), Swedish Breast Cancer StudySinilnikova, Olga M.McGuffog, LesleyAntoniou, Antonis C.Chenevix-Trench, GeorgiaSpurdle, Amanda B.Couch, 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 K.Fernandez-Rodriguez, JuanaImyanitov, Evgeny N.Janavicius, Ramunas(gemo), Groupe Genetique et CancerSinilnikova, Olga M.Stoppa-Lyonnet, DominiqueDavidson, RosemarieMazoyer, SylviePeyrat, Jean-PhilippeVerny-Pierre, CaroleCastera, Laurentde Pauw, AntoineBignon, Yves-JeanVennin, PhilippeFert Ferrer, SandraCollonge-Rame, Marie-AgnesMortemousque, IsabelleRamirez, Maria J.McGuffog, LesleyChenevix-Trench, GeorgiaPereira-Smith, Olivia M.Chu, CarolAntoniou, Antonis C.Renwick, AnthonyCeron, JulianTominaga, KaoruSurralles, JordiPujana, Miguel AngelCastella, MariaRahman, NazneenKuhl, JuliaNeveling, KorneliaSchindler, DetlevHernandez, Gonzalo(embrace), Epidemiological Study of Familial Breast CancersEaston, Douglas F.Peock, SusanCook, MargaretOliver, Clare T.Frost, DebraBlok, Marinus J.Platte, RadkaOng, Kai-RenEvans, D. GarethLalloo, FionaEeles, RosalindIzatt, LouiseCook, JackieDouglas, FionaHodgson, Shirley V.Brewer, CaroleBernard, LorisMorrison, Patrick J.Porteous, MaryPeterlongo, Paolovan Os, Theo A.Manoukian, SiranoushPeissel, BernardZaffaroni, DanielaRoversi, GaiaBarile, MonicaViel, AlessandraRadice, PaoloPasini, BarbaraOttini, LauraPutignano, Anna LauraSavarese, AntonellaHealey, SueSpurdle, Amanda B.Chen, XiaoqingBeesley, Jonathan(kConFab), Kathleen Cuningham Foundation Consortium for ResearchRookus, Matti A.Verhoef, SennoOsorio, AnaTilanus-Linthorst, Madeleine A.Meijers-Heijboer, Hanne E. J.Vreeswijk, Maaike P.Asperen, Christi J.Bodmer, DanielleAusems, Margreet G. E. M.Hogervorst, Frans B.(hebon), Hereditary Breast and Ovarian Cancer Research Group NetherlandsGoldgar, David E.Buys, SaundraLaitman, YaelJohn, Esther M.Miron, AlexanderSouthey, Melissa C.Caldes, 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 M.Nathanson, Katherine L.Rebbeck, Timothy R.Johannsson, Oskar ThorCouch, Fergus J.Wang, XianshuSeal, SheilaFredericksen, Zachary S.Benitez, JavierCuadras, DanielMoreno, VictorPientka, Friederike K.Depping, 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 K.Barjhoux, LaureBelotti, MurielBenitez, JavierBerger, AndreasBojesen, AndersBonanni, BernardoBrewer, CaroleCaldes, TrinidadCaligo, Maria A.Campbell, IanChan, Salina B.Claes, Kathleen B. M.Cohn, David E.Cook, JackieDaly, Mary B.Damiola, FrancescaDavidson, RosemariePauw, Antoine deDelnatte, CapucineDiez, OrlandDomchek, Susan M.Dumont, MartineDurda, KatarzynaDworniczak, BerndEaston, Douglas F.Eccles, DianaEdwinsdotter Ardnor, ChristinaEeles, RosEjlertsen, BentEllis, SteveEvans, D. GarethFeliubadalo, LidiaFostira, FlorentiaFoulkes, William D.Friedman, EitanFrost, DebraGaddam, PragnaGanz, Patricia A.Garber, JudyGarcia-Barberan, VanesaGauthier-Villars, MarionGehrig, AndreaGerdes, Anne-MarieGiraud, SophieGodwin, Andrew K.Goldgar, David E.Hake, Christopher R.Hansen, Thomas V. O.Healey, SueHodgson, ShirleyHogervorst, Frans B. L.Houdayer, ClaudeHulick, Peter J.Imyanitov, Evgeny N.Isaacs, ClaudineIzatt, LouiseIzquierdo, AngelJacobs, LaurenJakubowska, AnnaJanavicius, RamunasJaworska-Bieniek, KatarzynaJensen, Uffe BirkJohn, Esther M.Vijai, JosephKarlan, Beth Y.Kast, KarinInvestigators, KConFabKhan, SofiaKwong, AvaLaitman, YaelLester, JennyLesueur, FabienneLiljegren, AnnelieLubinski, JanMai, Phuong L.Manoukian, SiranoushMazoyer, SylvieMeindl, AlfonsMensenkamp, Arjen R.Montagna, MarcoNathanson, Katherine L.Neuhausen, Susan L.Nevanlinna, HeliNiederacher, DieterOlah, EdithOlopade, Olufunmilayo I.Ong, Kai-renOsorio, AnaPark, Sue KyungPaulsson-Karlsson, YlvaPedersen, Inge SokildePeissel, BernardPeterlongo, PaoloPfeiler, GeorgPhelan, Catherine M.Piedmonte, MarionPoppe, BrucePujana, Miquel AngelRadice, PaoloRennert, GadRodriguez, Gustavo C.Rookus, Matti A.Ross, Eric A.Schmutzler, Rita KatharinaSimard, JacquesSinger, Christian F.Slavin, Thomas P.Soucy, PennySouthey, MelissaSteinemann, DorisStoppa-Lyonnet, DominiqueSukiennicki, GrzegorzSutter, ChristianSzabo, Csilla I.Tea, Muy-KhengTeixeira, Manuel R.Teo, Soo-HwangTerry, Mary BethThomassen, MadsTibiletti, Maria GraziaTihomirova, LaimaTognazzo, Silviavan Rensburg, Elizabeth J.Varesco, LilianaVaron-Mateeva, RaymondaVratimos, AthanassiosWeitzel, Jeffrey N.McGuffog, LesleyKirk, JudyToland, Amanda EwartHamann, UteLindor, NoralaneRamus, Susan J.Greene, Mark H.Couch, Fergus J.Offit, KennethPharoah, Paul D. P.Chenevix-Trench, GeorgiaAntoniou, Antonis C. 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. ...

Browsing by Author "Cook, Jackie"

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. ﻿

Evidence for SMAD3 as a modifier of breast cancer risk in BRCA2 mutation carriers ﻿

Exploring the link between MORF4L1 and risk of breast cancer ﻿

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 ﻿

Immunophoretic rapid diagnostic tests as a source of immunoglobulins for estimating malaria sero-prevalence and transmission intensity ﻿

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.

Evidence for SMAD3 as a modifier of breast cancer risk in BRCA2 mutation carriers

Exploring the link between MORF4L1 and risk of breast cancer

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

Immunophoretic rapid diagnostic tests as a source of immunoglobulins for estimating malaria sero-prevalence and transmission intensity