D
Drakoulis Yannoukakos
Researcher at Aristotle University of Thessaloniki
Publications - 159
Citations - 12099
Drakoulis Yannoukakos is an academic researcher from Aristotle University of Thessaloniki. The author has contributed to research in topics: Breast cancer & Cancer. The author has an hindex of 43, co-authored 151 publications receiving 10048 citations. Previous affiliations of Drakoulis Yannoukakos include American Cancer Society & Institute of Cancer Research.
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Journal ArticleDOI
RAD51B in Familial Breast Cancer
Liisa M. Pelttari,Sofia Khan,Mikko Vuorela,Johanna I. Kiiski,Sara Vilske,Viivi Nevanlinna,Salla Ranta,Johanna Schleutker,Johanna Schleutker,Johanna Schleutker,Robert Winqvist,Anne Kallioniemi,Thilo Dörk,Natalia Bogdanova,Jonine Figueroa,Paul D.P. Pharoah,Marjanka K. Schmidt,Alison M. Dunning,Montserrat Garcia-Closas,Manjeet K. Bolla,Joe Dennis,Kyriaki Michailidou,Qin Wang,John L. Hopper,Melissa C. Southey,Efraim H. Rosenberg,Peter A. Fasching,Peter A. Fasching,Matthias W. Beckmann,Julian Peto,Isabel dos-Santos-Silva,Elinor J. Sawyer,Ian Tomlinson,Barbara Burwinkel,Barbara Burwinkel,Harald Surowy,Harald Surowy,Pascal Guénel,Thérèse Truong,Stig E. Bojesen,Stig E. Bojesen,Børge G. Nordestgaard,Børge G. Nordestgaard,Javier Benitez,Anna González-Neira,Susan L. Neuhausen,Hoda Anton-Culver,Hermann Brenner,Volker Arndt,Alfons Meindl,Rita K. Schmutzler,Hiltrud Brauch,Hiltrud Brauch,Hiltrud Brauch,Thomas Brüning,Annika Lindblom,Sara Margolin,Arto Mannermaa,Jaana M. Hartikainen,Georgia Chenevix-Trench,kConFab,kConFab,Aocs Investigators,Laurien Van Dyck,Hilde Janssen,Hilde Janssen,Jenny Chang-Claude,Anja Rudolph,Paolo Radice,Paolo Peterlongo,Emily Hallberg,Janet E. Olson,Janet E. Olson,Graham G. Giles,Graham G. Giles,Roger L. Milne,Christopher A. Haiman,Fredrick Schumacher,Jacques Simard,Martine Dumont,Martine Dumont,Vessela N. Kristensen,Vessela N. Kristensen,Anne Lise Børresen-Dale,Wei Zheng,Alicia Beeghly-Fadiel,Mervi Grip,Mervi Grip,Irene L. Andrulis,Gord Glendon,Peter Devilee,Caroline Seynaeve,Maartje J. Hooning,Margriet Collée,Angela Cox,Simon S. Cross,Mitul Shah,Robert Luben,Ute Hamann,Ute Hamann,Diana Torres,Anna Jakubowska,Jan Lubinski,Fergus J. Couch,Drakoulis Yannoukakos,Nick Orr,Anthony J. Swerdlow,Hatef Darabi,Jingmei Li,Kamila Czene,Per Hall,Douglas F. Easton,Johanna Mattson,Carl Blomqvist,Kristiina Aittomäki,Heli Nevanlinna +115 more
TL;DR: It is suggested that loss-of-function mutations in RAD 51B are rare, but common variation at the RAD51B region is significantly associated with familial breast cancer risk.
Journal ArticleDOI
MicroRNA related polymorphisms and breast cancer risk
Sofia Khan,Dario Greco,Dario Greco,Kyriaki Michailidou,Roger L. Milne,Roger L. Milne,Taru A. Muranen,Tuomas Heikkinen,Kirsimari Aaltonen,Joe Dennis,Manjeet K. Bolla,Jianjun Liu,Per Hall,Astrid Irwanto,Keith Humphreys,Jingmei Li,Kamila Czene,Jenny Chang-Claude,Rebecca Hein,Anja Rudolph,Petra Seibold,Dieter Flesch-Janys,Olivia Fletcher,Julian Peto,Isabel dos Santos Silva,Nichola Johnson,Lorna Gibson,Zoe Aitken,John L. Hopper,Helen Tsimiklis,Minh Bui,Enes Makalic,Daniel F. Schmidt,Melissa C. Southey,Carmel Apicella,Jennifer Stone,Quinten Waisfisz,Hanne Meijers-Heijboer,Muriel A. Adank,Rob B. van der Luijt,Alfons Meindl,Rita K. Schmutzler,Bertram Müller-Myhsok,Peter Lichtner,Clare Turnbull,Nazneen Rahman,Stephen J. Chanock,David J. Hunter,Angela Cox,Simon S. Cross,Malcolm W.R. Reed,Marjanka K. Schmidt,Annegien Broeks,Laura Van't Veer,Frans B. L. Hogervorst,Peter A. Fasching,Michael G. Schrauder,Arif B. Ekici,Matthias W. Beckmann,Stig E. Bojesen,Børge G. Nordestgaard,Sune F. Nielsen,Henrik Flyger,Javier Benitez,Pilar Zamora,Jose Ignacio Arias Perez,Christopher A. Haiman,Brian E. Henderson,Fredrick R. Schumacher,Loic Le Marchand,Paul D.P. Pharoah,Alison M. Dunning,Mitul Shah,Robert Luben,Judith E. Brown,Fergus J. Couch,Xianshu Wang,Celine M. Vachon,Janet E. Olson,Diether Lambrechts,Matthieu Moisse,Robert Paridaens,Marie-Rose Christiaens,Pascal Guénel,Thérèse Truong,Pierre Laurent-Puig,Claire Mulot,F Marmé,Barbara Burwinkel,Andreas Schneeweiss,Christof Sohn,Elinor J. Sawyer,Ian Tomlinson,Michael J. Kerin,Nicola Miller,Irene L. Andrulis,Julia A. Knight,Sandrine Tchatchou,Anna Marie Mulligan,Thilo Dörk,Natalia Bogdanova,Natalia Antonenkova,Hoda Anton-Culver,Hatef Darabi,Mikael Eriksson,Montserrat Garcia-Closas,Jonine D. Figueroa,Jolanta Lissowska,Louise A. Brinton,Peter Devilee,Robert A.E.M. Tollenaar,Caroline Seynaeve,Christi J. van Asperen,Vessela N. Kristensen,Susan L. Slager,Amanda E. Toland,Christine B. Ambrosone,Drakoulis Yannoukakos,Annika Lindblom,Sara Margolin,Paolo Radice,Paolo Peterlongo,Monica Barile,Paolo Mariani,Maartje J. Hooning,John W.M. Martens,J. Margriet Collée,Agnes Jager,Anna Jakubowska,Jan Lubinski,Katarzyna Jaworska-Bieniek,Katarzyna Durda,Graham G. Giles,Catriona McLean,Hiltrud Brauch,Thomas Brüning,Yon-Dschun Ko,Hermann Brenner,Aida Karina Dieffenbach,Volker Arndt,Christa Stegmaier,Anthony J. Swerdlow,Alan Ashworth,Nick Orr,Michael Jones,Jacques Simard,Mark S. Goldberg,Martine Dumont,Robert Winqvist,Katri Pylkäs,Arja Jukkola-Vuorinen,Mervi Grip,Vesa Kataja,Veli-Matti Kosma,Jaana M. Hartikainen,Arto Mannermaa,Ute Hamann,Georgia Chenevix-Trench,Carl Blomqvist,Kristiina Aittomäki,Douglas F. Easton,Heli Nevanlinna +161 more
TL;DR: Five miRNA binding site SNPs associated significantly with breast cancer risk are located in the 3′ UTR of CASP8, HDDC3, DROSHA, MUSTN1, and MYCL1, respectively, which belongs to miRNA machinery genes and has a central role in initial miRNA processing.
Journal ArticleDOI
Breast-Cancer Risk in Families with Mutations in PALB2
Antonis C. Antoniou,Silvia Casadei,Tuomas Heikkinen,Daniel Barrowdale,Katri Pylkäs,Jonathan Roberts,Andy C. H. Lee,D. Subramanian,K De Leeneer,Florentia Fostira,Eva Tomiak,Susan L. Neuhausen,Zhi Ling Teo,Sofia Khan,Kristiina Aittomäki,Jukka S. Moilanen,Clare Turnbull,Sheila Seal,Arto Mannermaa,Anne Kallioniemi,Geoffrey J. Lindeman,Saundra S. Buys,Irene L. Andrulis,Paolo Radice,Carlo Tondini,Siranoush Manoukian,Amanda E. Toland,Penelope Miron,J. N. Weitzel,Susan M. Domchek,Bruce Poppe,Kathleen Claes,Drakoulis Yannoukakos,Patrick Concannon,Jonine L. Bernstein,Paul A. James,Douglas F. Easton,David E. Goldgar,John L. Hopper,Nazneen Rahman,Paolo Peterlongo,Heli Nevanlinna,Mary Claire King,Fergus J. Couch,Melissa C. Southey,Robert Winqvist,William D. Foulkes,Marc Tischkowitz +47 more
TL;DR: The data suggest the breast-cancer risk for PALB2 mutation carriers may overlap with that for BRCA1 mutation carriers, and loss-of-function mutations in PALB1 are an important cause of hereditary breast cancer.
Journal ArticleDOI
Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes
Nasim Mavaddat,Kyriaki Michailidou,Kyriaki Michailidou,Joe Dennis,Michael Lush,Laura Fachal,Andrew Lee,Jonathan Tyrer,Ting Huei Chen,Qin Wang,Manjeet K. Bolla,Xin Yang,Muriel A. Adank,Thomas U. Ahearn,Kristiina Aittomäki,Jamie Allen,Irene L. Andrulis,Irene L. Andrulis,Hoda Anton-Culver,Natalia Antonenkova,Volker Arndt,Kristan J. Aronson,Paul L. Auer,Paul L. Auer,Päivi Auvinen,Myrto Barrdahl,Laura E. Beane Freeman,Matthias W. Beckmann,Sabine Behrens,Javier Benitez,Marina Bermisheva,Leslie Bernstein,Carl Blomqvist,Carl Blomqvist,Natalia Bogdanova,Stig E. Bojesen,Stig E. Bojesen,Bernardo Bonanni,Anne Lise Børresen-Dale,Anne Lise Børresen-Dale,Hiltrud Brauch,Hiltrud Brauch,Hiltrud Brauch,Michael Bremer,Hermann Brenner,Adam R. Brentnall,Ian W. Brock,Angela Brooks-Wilson,Angela Brooks-Wilson,Sara Y. Brucker,Thomas Brüning,Barbara Burwinkel,Barbara Burwinkel,Daniele Campa,Daniele Campa,Brian D. Carter,Jose E. Castelao,Stephen J. Chanock,Rowan T. Chlebowski,Hans Christiansen,Christine L. Clarke,J. Margriet Collée,Emilie Cordina-Duverger,Sten Cornelissen,Fergus J. Couch,Angela Cox,Simon S. Cross,Kamila Czene,Mary B. Daly,Peter Devilee,Thilo Dörk,Isabel dos-Santos-Silva,Martine Dumont,Lorraine Durcan,Miriam Dwek,Diana Eccles,Arif B. Ekici,A. Heather Eliassen,A. Heather Eliassen,Carolina Ellberg,Christoph Engel,Mikael Eriksson,D. Gareth Evans,Peter A. Fasching,Peter A. Fasching,Jonine D. Figueroa,Jonine D. Figueroa,Olivia Fletcher,Henrik Flyger,Asta Försti,Asta Försti,Lin Fritschi,Marike Gabrielson,Manuela Gago-Dominguez,Susan M. Gapstur,José A. García-Sáenz,Mia M. Gaudet,Vassilios Georgoulias,Graham G. Giles,Graham G. Giles,Graham G. Giles,I. R. Gilyazova,I. R. Gilyazova,Gord Glendon,Mark S. Goldberg,David E. Goldgar,Anna González-Neira,Grethe I. Grenaker Alnæs,Mervi Grip,Jacek Gronwald,Anne Grundy,Pascal Guénel,Lothar Haeberle,Eric Hahnen,Christopher A. Haiman,Niclas Håkansson,Ute Hamann,Susan E. Hankinson,Elaine F. Harkness,Elaine F. Harkness,Steven N. Hart,Wei He,Alexander Hein,Jane Heyworth,Peter Hillemanns,Antoinette Hollestelle,Maartje J. Hooning,Robert N. Hoover,John L. Hopper,Anthony Howell,Guanmengqian Huang,Keith Humphreys,David J. Hunter,David J. Hunter,Milena Jakimovska,Anna Jakubowska,Anna Jakubowska,Wolfgang Janni,Esther M. John,Nichola Johnson,Michael Jones,Arja Jukkola-Vuorinen,Audrey Y. Jung,Rudolf Kaaks,Katarzyna Kaczmarek,Vesa Kataja,Renske Keeman,Michael J. Kerin,Elza Khusnutdinova,Elza Khusnutdinova,Johanna I. Kiiski,Julia A. Knight,Julia A. Knight,Yon-Dschun Ko,Veli-Matti Kosma,Stella Koutros,Vessela N. Kristensen,Vessela N. Kristensen,Ute Krüger,Tabea Kühl,Diether Lambrechts,Loic Le Marchand,Eunjung Lee,Flavio Lejbkowicz,Jenna Lilyquist,Annika Lindblom,Sara Lindström,Sara Lindström,Jolanta Lissowska,Wing-Yee Lo,Wing-Yee Lo,Sibylle Loibl,Jirong Long,Jan Lubinski,Michael P. Lux,Robert J. MacInnis,Robert J. MacInnis,Tom Maishman,Enes Makalic,Ivana Maleva Kostovska,Arto Mannermaa,Siranoush Manoukian,Sara Margolin,John W.M. Martens,Maria Elena Martinez,Dimitrios Mavroudis,Catriona McLean,Alfons Meindl,Usha Menon,Pooja Middha,Pooja Middha,Nicola Miller,Fernando Salvador Moreno,Anna Marie Mulligan,Anna Marie Mulligan,Claire Mulot,Victor Muñoz-Garzón,Susan L. Neuhausen,Heli Nevanlinna,Patrick Neven,William G. Newman,Sune F. Nielsen,Børge G. Nordestgaard,Børge G. Nordestgaard,Aaron D. Norman,Kenneth Offit,Janet E. Olson,Håkan Olsson,Nick Orr,V. Shane Pankratz,Tjoung-Won Park-Simon,Jose Ignacio Arias Perez,Clara Pérez-Barrios,Paolo Peterlongo,Julian Peto,Mila Pinchev,Dijana Plaseska-Karanfilska,Eric C. Polley,Ross L. Prentice,Nadege Presneau,Darya Prokofyeva,Kristen S. Purrington,Katri Pylkäs,Brigitte Rack,Paolo Radice,Rohini Rau-Murthy,Gad Rennert,Hedy S. Rennert,Valerie Rhenius,Mark E. Robson,Atocha Romero,Kathryn J. Ruddy,Matthias Ruebner,Emmanouil Saloustros,Dale P. Sandler,Elinor J. Sawyer,Daniel F. Schmidt,Daniel F. Schmidt,Rita K. Schmutzler,Andreas Schneeweiss,Minouk J. Schoemaker,Fredrick R. Schumacher,Peter Schürmann,Lukas Schwentner,Christopher G. Scott,Rodney J. Scott,Rodney J. Scott,Caroline Seynaeve,Mitul Shah,Mark E. Sherman,Martha J. Shrubsole,Xiao-Ou Shu,Susan L. Slager,Ann Smeets,Christof Sohn,Penny Soucy,Melissa C. Southey,Melissa C. Southey,John J. Spinelli,Christa Stegmaier,Jennifer Stone,Jennifer Stone,Anthony J. Swerdlow,Rulla M. Tamimi,Rulla M. Tamimi,William J. Tapper,Jack A. Taylor,Mary Beth Terry,Kathrin Thöne,Rob A. E. M. Tollenaar,Ian Tomlinson,Ian Tomlinson,Thérèse Truong,Maria Tzardi,Hans-Ulrich Ulmer,Michael Untch,Celine M. Vachon,Elke M van Veen,Joseph Vijai,Clarice R. Weinberg,Camilla Wendt,Alice S. Whittemore,Hans Wildiers,Walter C. Willett,Walter C. Willett,Robert Winqvist,Alicja Wolk,Alicja Wolk,Xiaohong R. Yang,Drakoulis Yannoukakos,Yan Zhang,Wei Zheng,Argyrios Ziogas,Alison M. Dunning,Deborah J. Thompson,Georgia Chenevix-Trench,Jenny Chang-Claude,Jenny Chang-Claude,Marjanka K. Schmidt,Per Hall,Roger L. Milne,Roger L. Milne,Roger L. Milne,Paul D.P. Pharoah,Antonis C. Antoniou,Nilanjan Chatterjee,Nilanjan Chatterjee,Peter Kraft,Montserrat Garcia-Closas,Jacques Simard,Douglas F. Easton +310 more
TL;DR: This PRS, optimized for prediction of estrogen receptor (ER)-specific disease, from the largest available genome-wide association dataset is developed and empirically validated and is a powerful and reliable predictor of breast cancer risk that may improve breast cancer prevention programs.
Journal ArticleDOI
Inherited Mutations in 17 Breast Cancer Susceptibility Genes Among a Large Triple-Negative Breast Cancer Cohort Unselected for Family History of Breast Cancer
Fergus J. Couch,Steven N. Hart,Priyanka Sharma,Amanda E. Toland,Xianshu Wang,Penelope Miron,Janet E. Olson,Andrew K. Godwin,V. Shane Pankratz,Curtis Olswold,Seth W. Slettedahl,Emily Hallberg,Lucia Guidugli,Jaime I. Davila,Matthias W. Beckmann,Wolfgang Janni,Brigitte Rack,Arif B. Ekici,Dennis J. Slamon,Irene Konstantopoulou,Florentia Fostira,Athanassios Vratimos,George Fountzilas,Liisa M. Pelttari,William J. Tapper,Lorraine Durcan,Simon S. Cross,Robert Pilarski,Charles L. Shapiro,Jennifer R. Klemp,Song Yao,Judy Garber,Angela Cox,Hiltrud Brauch,Christine B. Ambrosone,Heli Nevanlinna,Drakoulis Yannoukakos,Susan L. Slager,Celine M. Vachon,Diana Eccles,Peter A. Fasching,Peter A. Fasching +41 more
TL;DR: Mutation prevalence estimates suggest that patients with TNBC, regardless of age at diagnosis or family history of cancer, should be considered for germline genetic testing of BRCA1 and BRCa2.