J
Jeanette E. Eckel-Passow
Researcher at Mayo Clinic
Publications - 160
Citations - 8247
Jeanette E. Eckel-Passow is an academic researcher from Mayo Clinic. The author has contributed to research in topics: Glioma & Clear cell renal cell carcinoma. The author has an hindex of 43, co-authored 146 publications receiving 6674 citations. Previous affiliations of Jeanette E. Eckel-Passow include Virginia Commonwealth University & Medical University of South Carolina.
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Journal ArticleDOI
Glioma Groups Based on 1p/19q, IDH, and TERT Promoter Mutations in Tumors
Jeanette E. Eckel-Passow,Daniel H. Lachance,Annette M. Molinaro,Kyle M. Walsh,Paul A. Decker,Hugues Sicotte,Melike Pekmezci,Terri Rice,Matt L. Kosel,Ivan Smirnov,Gobinda Sarkar,Alissa Caron,Thomas M. Kollmeyer,Corinne Praska,Anisha R. Chada,Chandralekha Halder,Helen M. Hansen,Lucie McCoy,Paige M. Bracci,Roxanne Marshall,Shichun Zheng,Gerald F. Reis,Alexander R. Pico,Brian P. O'Neill,Jan C. Buckner,Caterina Giannini,Jason T. Huse,Arie Perry,Tarik Tihan,Mitchell S. Berger,Susan M. Chang,Michael D. Prados,Joseph L. Wiemels,John K. Wiencke,Margaret Wrensch,Robert B. Jenkins +35 more
TL;DR: The five glioma molecular groups had different ages at onset, overall survival, and associations with germline variants, which implies that they are characterized by distinct mechanisms of pathogenesis.
Journal ArticleDOI
A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population
Antonis C. Antoniou,Xianshu Wang,Zachary S. Fredericksen,Lesley McGuffog,Robert F. Tarrell,Olga M. Sinilnikova,Sue Healey,Jonathan J. Morrison,Christiana Kartsonaki,Timothy G. Lesnick,Maya Ghoussaini,Daniel Barrowdale,Susan Peock,Margaret Cook,Clare Oliver,Debra Frost,Diana Eccles,D. Gareth Evans,Ros Eeles,Louise Izatt,Carol Chu,Fiona Douglas,Joan Paterson,Dominique Stoppa-Lyonnet,Claude Houdayer,Sylvie Mazoyer,Sophie Giraud,Christine Lasset,Audrey Remenieras,Olivier Caron,Agnès Hardouin,Pascaline Berthet,Frans B. L. Hogervorst,Matti A. Rookus,Agnes Jager,Ans M.W. van den Ouweland,Nicoline Hoogerbrugge,Rob B. van der Luijt,Hanne Meijers-Heijboer,Encarna B. Gomez Garcia,Peter Devilee,Maaike P.G. Vreeswijk,Jan Lubinski,Anna Jakubowska,Jacek Gronwald,Tomasz Huzarski,Tomasz Byrski,Bohdan Górski,Cezary Cybulski,Amanda B. Spurdle,Helene Holland,David E. Goldgar,Esther M. John,John L. Hopper,Melissa C. Southey,Saundra S. Buys,Mary B. Daly,Mary Beth Terry,Rita K. Schmutzler,Barbara Wappenschmidt,Christoph Engel,Alfons Meindl,Sabine Preisler-Adams,Norbert Arnold,Dieter Niederacher,Christian Sutter,Susan M. Domchek,Katherine L. Nathanson,Timothy R. Rebbeck,Joanne L. Blum,Marion Piedmonte,Gustavo C. Rodriguez,Katie Wakeley,John F. Boggess,Jack Basil,Stephanie V. Blank,Eitan Friedman,Bella Kaufman,Yael Laitman,Roni Milgrom,Irene L. Andrulis,Irene L. Andrulis,Gord Glendon,Hilmi Ozcelik,Tomas Kirchhoff,Tomas Kirchhoff,Joseph Vijai,Joseph Vijai,Mia M. Gaudet,David Altshuler,Candace Guiducci,Niklas Loman,Katja Harbst,Johanna Rantala,Hans Ehrencrona,Anne-Marie Gerdes,Mads Thomassen,Lone Sunde,Paolo Peterlongo,Siranoush Manoukian,Bernardo Bonanni,Alessandra Viel,Paolo Radice,Trinidad Caldés,Miguel de la Hoya,Christian F. Singer,Anneliese Fink-Retter,Mark H. Greene,Phuong L. Mai,Jennifer T. Loud,Lucia Guidugli,Noralane M. Lindor,Thomas Hansen,Finn Cilius Nielsen,Ignacio Blanco,Conxi Lázaro,Judy Garber,Susan J. Ramus,Simon A. Gayther,Catherine M. Phelan,Stephen Narod,Csilla Szabo,Javier Benitez,Ana Osorio,Heli Nevanlinna,Tuomas Heikkinen,Maria A. Caligo,Mary S. Beattie,Ute Hamann,Andrew K. Godwin,Marco Montagna,Cinzia Casella,Susan L. Neuhausen,Beth Y. Karlan,Nadine Tung,Amanda E. Toland,Jeffrey N. Weitzel,O. I. Olopade,Jacques Simard,Penny Soucy,Wendy S. Rubinstein,Adalgeir Arason,Gad Rennert,Nicholas G. Martin,Grant W. Montgomery,Jenny Chang-Claude,Dieter Flesch-Janys,Hiltrud Brauch,Hiltrud Brauch,Gianluca Severi,Laura Baglietto,Angela Cox,Simon S. Cross,Penelope Miron,Sue Gerty,William J. Tapper,Drakoulis Yannoukakos,George Fountzilas,Peter A. Fasching,Matthias W. Beckmann,Isabel dos Santos Silva,Julian Peto,Diether Lambrechts,Robert Paridaens,Thomas Ruediger,Asta Foersti,Robert Winqvist,Katri Pylkaes,Robert B. Diasio,Adam M. Lee,Jeanette E. Eckel-Passow,Celine M. Vachon,Fiona M. Blows,Kristy Driver,Alison M. Dunning,Alison M. Dunning,Paul D.P. Pharoah,Kenneth Offit,V. Shane Pankratz,Hakon Hakonarson,Georgia Chenevix-Trench,Douglas F. Easton,Fergus J. Couch +182 more
TL;DR: Five SNPs on 19p13 were associated with breast cancer risk and an association with estrogen receptor–positive disease in the opposite direction was identified andotyping these SNPs in 6,800 population-based breast cancer cases and 6,613 controls identified a similar association.
Journal ArticleDOI
Association of Maximal Extent of Resection of Contrast-Enhanced and Non-Contrast-Enhanced Tumor With Survival Within Molecular Subgroups of Patients With Newly Diagnosed Glioblastoma.
Annette M. Molinaro,Shawn L. Hervey-Jumper,Ramin A. Morshed,Jacob S. Young,Seunggu J. Han,Pranathi Chunduru,Yalan Zhang,Joanna J. Phillips,Anny Shai,Marisa Lafontaine,Jason C. Crane,Ankush Chandra,Patrick M. Flanigan,Arman Jahangiri,Gino Cioffi,Quinn T. Ostrom,John E. Anderson,John E. Anderson,Chaitra Badve,Chaitra Badve,Jill S. Barnholtz-Sloan,Jill S. Barnholtz-Sloan,Andrew E. Sloan,Andrew E. Sloan,Bradley J. Erickson,Paul A. Decker,Matthew L. Kosel,Daniel H. Lachance,Jeanette E. Eckel-Passow,Robert B. Jenkins,Javier Villanueva-Meyer,Terri Rice,Margaret Wrensch,John K. Wiencke,Nancy Ann Oberheim Bush,Jennie Taylor,Nicholas Butowski,Michael D. Prados,Jennifer Clarke,Susan M. Chang,Edward F. Chang,Manish K. Aghi,Philip V. Theodosopoulos,Michael W. McDermott,Mitchel S. Berger +44 more
TL;DR: An association between maximal resection of CE tumor and OS in patients with glioblastoma is confirmed across all subgroups and was associated with longer OS in younger patients, regardless of IDH status, and among patients with IDH-wild-type gliOBlastoma regardless of the methylation status of the promoter region of the DNA repair enzyme O6-methylguanine-DNA methyltransferase.
Journal ArticleDOI
Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors
Beatrice Melin,Jill S. Barnholtz-Sloan,Margaret Wrensch,Christoffer Johansen,Dora Il'yasova,Dora Il'yasova,Ben Kinnersley,Quinn T. Ostrom,Karim Labreche,Karim Labreche,Yanwen Chen,Georgina Armstrong,Yanhong Liu,Jeanette E. Eckel-Passow,Paul A. Decker,Marianne Labussière,Ahmed Idbaih,Khê Hoang-Xuan,Anna Luisa Di Stefano,Karima Mokhtari,Jean-Yves Delattre,Peter Broderick,Pilar Galan,Konstantinos Gousias,Johannes Schramm,Minouk J. Schoemaker,Sarah Fleming,Stefan Herms,Stefanie Heilmann,Markus M. Nöthen,Heinz-Erich Wichmann,Heinz-Erich Wichmann,Stefan Schreiber,Anthony J. Swerdlow,Anthony J. Swerdlow,Mark Lathrop,Matthias Simon,Marc Sanson,Ulrika Andersson,Preetha Rajaraman,Stephen J. Chanock,Martha S. Linet,Zhaoming Wang,Meredith Yeager,John K. Wiencke,Helen M. Hansen,Lucie McCoy,Terri Rice,Matthew L. Kosel,Hugues Sicotte,Christopher I. Amos,Jonine L. Bernstein,Faith G. Davis,Dan Lachance,Ching C. Lau,Ryan Merrell,Joellen Shildkraut,Francis Ali-Osman,Siegal Sadetzki,Siegal Sadetzki,Michael E. Scheurer,Sanjay Shete,Rose Lai,Elizabeth B. Claus,Elizabeth B. Claus,Sara H. Olson,Robert B. Jenkins,Richard S. Houlston,Melissa L. Bondy +68 more
TL;DR: A meta-analysis of existing GWAS and two new GWAS substantiate that genetic susceptibility to GBM and non-GBM tumors are highly distinct, which likely reflects different etiology.
Journal ArticleDOI
Adult infiltrating gliomas with WHO 2016 integrated diagnosis: additional prognostic roles of ATRX and TERT.
Melike Pekmezci,Terri Rice,Annette M. Molinaro,Kyle M. Walsh,Paul A. Decker,Helen M. Hansen,Hugues Sicotte,Thomas M. Kollmeyer,Lucie McCoy,Gobinda Sarkar,Arie Perry,Caterina Giannini,Tarik Tihan,Mitchel S. Berger,Joseph L. Wiemels,Paige M. Bracci,Jeanette E. Eckel-Passow,Daniel H. Lachance,Jennifer Leigh Clarke,Jennie Taylor,Tracy Luks,John K. Wiencke,Robert B. Jenkins,Margaret Wrensch +23 more
TL;DR: Evidence is presented that in certain WHO 2016 diagnostic groups, testing for TERT promoter mutations or ATRX alterations may provide additional useful prognostic information.