Margo Thelander
John Muir Health
1 Papers
Margo Thelander is an academic researcher from John Muir Health. The author has contributed to research in topics: Single-nucleotide polymorphism & Haplotype. The author has an hindex of 1, co-authored 1 publications.
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Papers
An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers
Sophie Blein,Claire Bardel,Claire Bardel,Vincent Danjean,Vincent Danjean,Lesley McGuffog,Sue Healey,Daniel Barrowdale,Andrew Lee,Joe Dennis,Karoline Kuchenbaecker,Penny Soucy,Mary Beth Terry,Wendy K. Chung,David E. Goldgar,Saundra S. Buys,Ramunas Janavicius,Laima Tihomirova,Nadine Tung,Cecilia M. Dorfling,Elizabeth J. van Rensburg,Susan L. Neuhausen,Yuan Chun Ding,Anne-Marie Gerdes,Bent Ejlertsen,Finn Cilius Nielsen,Thomas Hansen,Ana Osorio,Javier Benitez,Raquel Andrés Conejero,Ena Segota,Ena Segota,Jeffrey N. Weitzel,Margo Thelander,Paolo Peterlongo,Paolo Radice,Valeria Pensotti,Riccardo Dolcetti,Bernardo Bonanni,Bernard Peissel,Daniela Zaffaroni,Giulietta Scuvera,Siranoush Manoukian,Liliana Varesco,Gabriele Lorenzo Capone,Laura Papi,Laura Ottini,Drakoulis Yannoukakos,Irene Konstantopoulou,Judy Garber,Ute Hamann,Alan Donaldson,Angela F. Brady,Carole Brewer,Claire Foo,D. Gareth Evans,Debra Frost,Diana Eccles,Fiona Douglas,Jackie Cook,Julian Adlard,Julian Barwell,Lisa Walker,Louise Izatt,Lucy Side,M. John Kennedy,M. John Kennedy,Marc Tischkowitz,Mark T. Rogers,Mary Porteous,Patrick J. Morrison,Patrick J. Morrison,Radka Platte,Ros Eeles,Rosemarie Davidson,Shirley Hodgson,Trevor Cole,Andrew K. Godwin,Claudine Isaacs,Kathleen Claes,Kim De Leeneer,Alfons Meindl,Andrea Gehrig,Barbara Wappenschmidt,Christian Sutter,Christoph Engel,Dieter Niederacher,Doris Steinemann,Hansjoerg Plendl,Karin Kast,Kerstin Rhiem,Nina Ditsch,Norbert Arnold,Raymonda Varon-Mateeva,Rita K. Schmutzler,Sabine Preisler-Adams,Nadja Bogdanova Markov,Shan Wang-Gohrke,Antoine De Pauw,Cédrick Lefol,Christine Lasset,Dominique Leroux,Dominique Leroux,Etienne Rouleau,Francesca Damiola,Hélène Dreyfus,Hélène Dreyfus,Laure Barjhoux,Lisa Golmard,Nancy Uhrhammer,Valérie Bonadona,Valérie Sornin,Yves-Jean Bignon,Jonathan Carter,Linda Van Le,Marion Piedmonte,Paul DiSilvestro,Miguel de la Hoya,Trinidad Caldés,Heli Nevanlinna,Kristiina Aittomäki,Agnes Jager,Ans M.W. van den Ouweland,Carolien M. Kets,Cora M. Aalfs,Flora E. van Leeuwen,Frans B. L. Hogervorst,Hanne Meijers-Heijboer,Jan C. Oosterwijk,Kees E. P. van Roozendaal,Matti A. Rookus,Peter Devilee,Rob B. van der Luijt,Edith Olah,Orland Diez,Alex Teulé,Conxi Lázaro,Ignacio Blanco,Jesús del Valle,Anna Jakubowska,Grzegorz Sukiennicki,Jacek Gronwald,Jan Lubinski,Katarzyna Durda,Katarzyna Jaworska-Bieniek,Bjarni A. Agnarsson,Christine Maugard,Alberto Amadori,Marco Montagna,Manuel R. Teixeira,Amanda B. Spurdle,William D. Foulkes,Curtis Olswold,Noralane M. Lindor,Vernon S. Pankratz,Csilla Szabo,Anne Lincoln,Lauren Jacobs,Marina Corines,Mark E. Robson,Joseph Vijai,Andreas Berger,Anneliese Fink-Retter,Christian F. Singer,Christine Rappaport,Daphne Geschwantler Kaulich,Georg Pfeiler,Muy-Kheng Tea,Mark H. Greene,Phuong L. Mai,Gad Rennert,Gad Rennert,Evgeny N. Imyanitov,Anna Marie Mulligan,Anna Marie Mulligan,Gord Glendon,Gord Glendon,Irene L. Andrulis,Irene L. Andrulis,Sandrine Tchatchou,Amanda E. Toland,Inge Søkilde Pedersen,Mads Thomassen,Torben A Kruse,Uffe Birk Jensen,Maria A. Caligo,Eitan Friedman,Jamal Zidan,Yael Laitman,Annika Lindblom,Beatrice Melin,Brita Arver,Niklas Loman,Richard Rosenquist,Olufunmilayo I. Olopade,Robert L. Nussbaum,Susan J. Ramus,Katherine L. Nathanson,Susan M. Domchek,Timothy R. Rebbeck,Banu Arun,Gillian Mitchell,Gillian Mitchell,Beth Y. Karlan,Jenny Lester,Sandra Orsulic,Dominique Stoppa-Lyonnet,Dominique Stoppa-Lyonnet,Gilles Thomas,Jacques Simard,Fergus J. Couch,Kenneth Offit,Douglas F. Easton,Georgia Chenevix-Trench,Antonis C. Antoniou,Sylvie Mazoyer,Catherine M. Phelan,Olga M. Sinilnikova,David G. Cox +218 more
TL;DR: This study illustrates how original approaches such as the phylogeny-based method used can empower classical molecular epidemiological studies aimed at identifying association or risk modification effects.