BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

164 related articles for article (PubMed ID: 35042965)

  • 1. Rare germline copy number variants (CNVs) and breast cancer risk.
    Dennis J; Tyrer JP; Walker LC; Michailidou K; Dorling L; Bolla MK; Wang Q; Ahearn TU; Andrulis IL; Anton-Culver H; Antonenkova NN; Arndt V; Aronson KJ; Freeman LEB; Beckmann MW; Behrens S; Benitez J; Bermisheva M; Bogdanova NV; Bojesen SE; Brenner H; Castelao JE; Chang-Claude J; Chenevix-Trench G; Clarke CL; ; Collée JM; ; Couch FJ; Cox A; Cross SS; Czene K; Devilee P; Dörk T; Dossus L; Eliassen AH; Eriksson M; Evans DG; Fasching PA; Figueroa J; Fletcher O; Flyger H; Fritschi L; Gabrielson M; Gago-Dominguez M; García-Closas M; Giles GG; González-Neira A; Guénel P; Hahnen E; Haiman CA; Hall P; Hollestelle A; Hoppe R; Hopper JL; Howell A; ; ; Jager A; Jakubowska A; John EM; Johnson N; Jones ME; Jung A; Kaaks R; Keeman R; Khusnutdinova E; Kitahara CM; Ko YD; Kosma VM; Koutros S; Kraft P; Kristensen VN; Kubelka-Sabit K; Kurian AW; Lacey JV; Lambrechts D; Larson NL; Linet M; Ogrodniczak A; Mannermaa A; Manoukian S; Margolin S; Mavroudis D; Milne RL; Muranen TA; Murphy RA; Nevanlinna H; Olson JE; Olsson H; Park-Simon TW; Perou CM; Peterlongo P; Plaseska-Karanfilska D; Pylkäs K; Rennert G; Saloustros E; Sandler DP; Sawyer EJ; Schmidt MK; Schmutzler RK; Shibli R; Smeets A; Soucy P; Southey MC; Swerdlow AJ; Tamimi RM; Taylor JA; Teras LR; Terry MB; Tomlinson I; Troester MA; Truong T; Vachon CM; Wendt C; Winqvist R; Wolk A; Yang XR; Zheng W; Ziogas A; Simard J; Dunning AM; Pharoah PDP; Easton DF
    Commun Biol; 2022 Jan; 5(1):65. PubMed ID: 35042965
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Increased genomic burden of germline copy number variants is associated with early onset breast cancer: Australian breast cancer family registry.
    Walker LC; Pearson JF; Wiggins GA; Giles GG; Hopper JL; Southey MC
    Breast Cancer Res; 2017 Mar; 19(1):30. PubMed ID: 28302160
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Germline copy number variations are associated with breast cancer risk and prognosis.
    Kumaran M; Cass CE; Graham K; Mackey JR; Hubaux R; Lam W; Yasui Y; Damaraju S
    Sci Rep; 2017 Nov; 7(1):14621. PubMed ID: 29116104
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Copy Number Variants Are Ovarian Cancer Risk Alleles at Known and Novel Risk Loci.
    DeVries AA; Dennis J; Tyrer JP; Peng PC; Coetzee SG; Reyes AL; Plummer JT; Davis BD; Chen SS; Dezem FS; Aben KKH; Anton-Culver H; Antonenkova NN; Beckmann MW; Beeghly-Fadiel A; Berchuck A; Bogdanova NV; Bogdanova-Markov N; Brenton JD; Butzow R; Campbell I; Chang-Claude J; Chenevix-Trench G; Cook LS; DeFazio A; Doherty JA; Dörk T; Eccles DM; Eliassen AH; Fasching PA; Fortner RT; Giles GG; Goode EL; Goodman MT; Gronwald J; ; ; Håkansson N; Hildebrandt MAT; Huff C; Huntsman DG; Jensen A; Kar S; Karlan BY; Khusnutdinova EK; Kiemeney LA; Kjaer SK; Kupryjanczyk J; Labrie M; Lambrechts D; Le ND; Lubiński J; May T; Menon U; Milne RL; Modugno F; Monteiro AN; Moysich KB; Odunsi K; Olsson H; Pearce CL; Pejovic T; Ramus SJ; Riboli E; Riggan MJ; Romieu I; Sandler DP; Schildkraut JM; Setiawan VW; Sieh W; Song H; Sutphen R; Terry KL; Thompson PJ; Titus L; Tworoger SS; Van Nieuwenhuysen E; Edwards DV; Webb PM; Wentzensen N; Whittemore AS; Wolk A; Wu AH; Ziogas A; Freedman ML; Lawrenson K; Pharoah PDP; Easton DF; Gayther SA; Jones MR
    J Natl Cancer Inst; 2022 Nov; 114(11):1533-1544. PubMed ID: 36210504
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genome-wide association and targeted analysis of copy number variants with psoriatic arthritis in German patients.
    Uebe S; Ehrlicher M; Ekici AB; Behrens F; Böhm B; Homuth G; Schurmann C; Völker U; Jünger M; Nauck M; Völzke H; Traupe H; Krawczak M; Burkhardt H; Reis A; Hüffmeier U
    BMC Med Genet; 2017 Aug; 18(1):92. PubMed ID: 28835222
    [TBL] [Abstract][Full Text] [Related]  

  • 6. copy number variation analysis in familial BRCA1/2-negative Finnish breast and ovarian cancer.
    Kuusisto KM; Akinrinade O; Vihinen M; Kankuri-Tammilehto M; Laasanen SL; Schleutker J
    PLoS One; 2013; 8(8):e71802. PubMed ID: 23967248
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A Genome-Wide Association Study to Identify Potential Germline Copy Number Variants for Sporadic Breast Cancer Susceptibility.
    Sapkota Y; Narasimhan A; Kumaran M; Sehrawat BS; Damaraju S
    Cytogenet Genome Res; 2016; 149(3):156-164. PubMed ID: 27668787
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Germline copy number variants are not associated with globally acquired copy number changes in familial breast tumours.
    Walker LC; Krause L; ; Spurdle AB; Waddell N
    Breast Cancer Res Treat; 2012 Aug; 134(3):1005-11. PubMed ID: 22434526
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genome-wide rare copy number variation screening in ulcerative colitis identifies potential susceptibility loci.
    Saadati HR; Wittig M; Helbig I; Häsler R; Anderson CA; Mathew CG; Kupcinskas L; Parkes M; Karlsen TH; Rosenstiel P; Schreiber S; Franke A
    BMC Med Genet; 2016 Apr; 17():26. PubMed ID: 27037036
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Breast cancer associated germline structural variants harboring small noncoding RNAs impact post-transcriptional gene regulation.
    Kumaran M; Krishnan P; Cass CE; Hubaux R; Lam W; Yasui Y; Damaraju S
    Sci Rep; 2018 May; 8(1):7529. PubMed ID: 29760470
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder.
    Jarick I; Volckmar AL; Pütter C; Pechlivanis S; Nguyen TT; Dauvermann MR; Beck S; Albayrak Ö; Scherag S; Gilsbach S; Cichon S; Hoffmann P; Degenhardt F; Nöthen MM; Schreiber S; Wichmann HE; Jöckel KH; Heinrich J; Tiesler CM; Faraone SV; Walitza S; Sinzig J; Freitag C; Meyer J; Herpertz-Dahlmann B; Lehmkuhl G; Renner TJ; Warnke A; Romanos M; Lesch KP; Reif A; Schimmelmann BG; Hebebrand J; Scherag A; Hinney A
    Mol Psychiatry; 2014 Jan; 19(1):115-21. PubMed ID: 23164820
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Germline DNA copy number variation in familial and early-onset breast cancer.
    Krepischi AC; Achatz MI; Santos EM; Costa SS; Lisboa BC; Brentani H; Santos TM; Gonçalves A; Nóbrega AF; Pearson PL; Vianna-Morgante AM; Carraro DM; Brentani RR; Rosenberg C
    Breast Cancer Res; 2012 Feb; 14(1):R24. PubMed ID: 22314128
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Identification of rare germline copy number variations over-represented in five human cancer types.
    Park RW; Kim TM; Kasif S; Park PJ
    Mol Cancer; 2015 Feb; 14():25. PubMed ID: 25644941
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genome-wide Burden of Rare Short Deletions Is Enriched in Major Depressive Disorder in Four Cohorts.
    Zhang X; Abdellaoui A; Rucker J; de Jong S; Potash JB; Weissman MM; Shi J; Knowles JA; Pato C; Pato M; Sobell J; Smit JH; Hottenga JJ; de Geus EJC; Lewis CM; Buttenschøn HN; Craddock N; Jones I; Jones L; McGuffin P; Mors O; Owen MJ; Preisig M; Rietschel M; Rice JP; Rivera M; Uher R; Gejman PV; Sanders AR; Boomsma D; Penninx BWJH; Breen G; Levinson DF
    Biol Psychiatry; 2019 Jun; 85(12):1065-1073. PubMed ID: 31003785
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Breast cancer in East Africa: Prevalence and spectrum of germline SNV/indel and CNVs in BRCA1 and BRCA2 genes among breast cancer patients in Tanzania.
    Rweyemamu LP; Gültaşlar BK; Akan G; Dharsee N; Namkinga LA; Lyantagaye SL; Yazıcı H; Atalar F
    Cancer Med; 2023 Feb; 12(3):3395-3409. PubMed ID: 35908255
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hereditary breast and ovarian cancer: assessment of point mutations and copy number variations in Brazilian patients.
    Silva FC; Lisboa BC; Figueiredo MC; Torrezan GT; Santos EM; Krepischi AC; Rossi BM; Achatz MI; Carraro DM
    BMC Med Genet; 2014 May; 15():55. PubMed ID: 24884479
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Rare CNVs in Suicide Attempt include Schizophrenia-Associated Loci and Neurodevelopmental Genes: A Pilot Genome-Wide and Family-Based Study.
    Sokolowski M; Wasserman J; Wasserman D
    PLoS One; 2016; 11(12):e0168531. PubMed ID: 28030616
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of novel candidate disease genes from de novo exonic copy number variants.
    Gambin T; Yuan B; Bi W; Liu P; Rosenfeld JA; Coban-Akdemir Z; Pursley AN; Nagamani SCS; Marom R; Golla S; Dengle L; Petrie HG; Matalon R; Emrick L; Proud MB; Treadwell-Deering D; Chao HT; Koillinen H; Brown C; Urraca N; Mostafavi R; Bernes S; Roeder ER; Nugent KM; Bader PI; Bellus G; Cummings M; Northrup H; Ashfaq M; Westman R; Wildin R; Beck AE; Immken L; Elton L; Varghese S; Buchanan E; Faivre L; Lefebvre M; Schaaf CP; Walkiewicz M; Yang Y; Kang SL; Lalani SR; Bacino CA; Beaudet AL; Breman AM; Smith JL; Cheung SW; Lupski JR; Patel A; Shaw CA; Stankiewicz P
    Genome Med; 2017 Sep; 9(1):83. PubMed ID: 28934986
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The impact of coding germline variants on contralateral breast cancer risk and survival.
    Morra A; Mavaddat N; Muranen TA; Ahearn TU; Allen J; Andrulis IL; Auvinen P; Becher H; Behrens S; Blomqvist C; Bojesen SE; Bolla MK; Brauch H; Camp NJ; Carvalho S; Castelao JE; Cessna MH; Chang-Claude J; Chenevix-Trench G; ; Czene K; Decker B; Dennis J; Dörk T; Dorling L; Dunning AM; Ekici AB; Eriksson M; Evans DG; Fasching PA; Figueroa JD; Flyger H; Gago-Dominguez M; García-Closas M; Geurts-Giele WRR; Giles GG; Guénel P; Gündert M; Hahnen E; Hall P; Hamann U; Harrington PA; He W; Heikkilä P; Hooning MJ; Hoppe R; Howell A; Humphreys K; ; Jakubowska A; Jung AY; Keeman R; Kristensen VN; Lubiński J; Mannermaa A; Manoochehri M; Manoukian S; Margolin S; Mavroudis D; Milne RL; Mulligan AM; Newman WG; Park-Simon TW; Peterlongo P; Pharoah PDP; Rhenius V; Saloustros E; Sawyer EJ; Schmutzler RK; Shah M; Spurdle AB; Tomlinson I; Truong T; van Veen EM; Vreeswijk MPG; Wang Q; Wendt C; Yang XR; Nevanlinna H; Devilee P; Easton DF; Schmidt MK
    Am J Hum Genet; 2023 Mar; 110(3):475-486. PubMed ID: 36827971
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Breast cancer patients suggestive of Li-Fraumeni syndrome: mutational spectrum, candidate genes, and unexplained heredity.
    Penkert J; Schmidt G; Hofmann W; Schubert S; Schieck M; Auber B; Ripperger T; Hackmann K; Sturm M; Prokisch H; Hille-Betz U; Mark D; Illig T; Schlegelberger B; Steinemann D
    Breast Cancer Res; 2018 Aug; 20(1):87. PubMed ID: 30086788
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.