S
Stefan P. Renner
Researcher at University of Erlangen-Nuremberg
Publications - 108
Citations - 2916
Stefan P. Renner is an academic researcher from University of Erlangen-Nuremberg. The author has contributed to research in topics: Endometriosis & Breast cancer. The author has an hindex of 27, co-authored 107 publications receiving 2539 citations. Previous affiliations of Stefan P. Renner include University of Duisburg-Essen.
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Journal ArticleDOI
Clinical aspects of Mayer–Rokitansky–Kuester–Hauser syndrome: recommendations for clinical diagnosis and staging
Peter Oppelt,Stefan P. Renner,A. Kellermann,Sara Y. Brucker,Georges A. Hauser,Kurt S. Ludwig,Pamela L. Strissel,Reiner Strick,Diethelm Wallwiener,Matthias W. Beckmann +9 more
TL;DR: It is shown that associated malformations are present in more than a third of cases and new basic guidelines for standard diagnostic classification involving patients with suspected MRKH are presented.
Journal ArticleDOI
The VCUAM (Vagina Cervix Uterus Adnex-associated Malformation) classification: a new classification for genital malformations.
Peter Oppelt,Stefan P. Renner,Sara Y. Brucker,Pamela L. Strissel,Reiner Strick,Patricia G. Oppelt,Hellmuth G. Doerr,Guenther E. Schott,Juergen Hucke,Diethelm Wallwiener,Matthias W. Beckmann +10 more
TL;DR: The VCUAM classification for the first time makes it possible to reflect even complex malformations in a precise and individual fashion, taking associatedmalformations into account, and makes it easier to provide appropriate clinical care for the affected patients.
Journal ArticleDOI
Epigenetic analysis leads to identification of HNF1B as a subtype-specific susceptibility gene for ovarian cancer
Hui Shen,Brooke L. Fridley,Honglin Song,Kate Lawrenson,Julie M. Cunningham,Susan J. Ramus,Mine S. Cicek,Jonathan Tyrer,Douglas A. Stram,Melissa C. Larson,Martin Köbel,Argyrios Ziogas,Wei Zheng,Hannah P. Yang,Anna H. Wu,Eva Wozniak,Yin Ling Woo,Boris Winterhoff,Elisabeth Wik,Alice S. Whittemore,Nicolas Wentzensen,Rachel Palmieri Weber,Allison F. Vitonis,Daniel Vincent,Robert A. Vierkant,Ignace Vergote,Ignace Vergote,David Van Den Berg,Anne M. van Altena,Shelley S. Tworoger,Pamela J. Thompson,Daniel C. Tessier,Kathryn L. Terry,Soo Hwang Teo,Claire Templeman,Daniel O. Stram,Melissa C. Southey,Weiva Sieh,Nadeem Siddiqui,Yurii B. Shvetsov,Xiao-Ou Shu,Viji Shridhar,Shan Wang-Gohrke,Gianluca Severi,Gianluca Severi,Ira Schwaab,Helga B. Salvesen,Iwona K. Rzepecka,Ingo B. Runnebaum,Mary Anne Rossing,Mary Anne Rossing,Lorna Rodriguez-Rodriguez,Harvey A. Risch,Stefan P. Renner,Elizabeth M. Poole,Malcolm C. Pike,Malcolm C. Pike,Catherine M. Phelan,Liisa M. Pelttari,Tanja Pejovic,James Paul,Irene Orlow,Siti Zawiah Omar,Sara H. Olson,Kunle Odunsi,Stefan Nickels,Heli Nevanlinna,Roberta B. Ness,Steven A. Narod,Toru Nakanishi,Kirsten B. Moysich,Alvaro N.A. Monteiro,Joanna Moes-Sosnowska,Francesmary Modugno,Usha Menon,John R. McLaughlin,Valerie McGuire,Keitaro Matsuo,Noor Azmi Mat Adenan,Leon F.A.G. Massuger,Galina Lurie,Lene Lundvall,Jan Lubinski,Jolanta Lissowska,Douglas A. Levine,Arto Leminen,Alice W. Lee,Nhu D. Le,Sandrina Lambrechts,Sandrina Lambrechts,Diether Lambrechts,Jolanta Kupryjanczyk,Camilla Krakstad,Gottfried E. Konecny,Susanne K. Kjaer,Lambertus A. Kiemeney,Linda E. Kelemen,Linda E. Kelemen,Gary L. Keeney,Beth Y. Karlan,Rod Karevan,Kimberly R. Kalli,Hiroaki Kajiyama,Bu Tian Ji,Allan Jensen,Anna Jakubowska,Edwin S. Iversen,Satoyo Hosono,Claus Høgdall,Estrid Høgdall,Maureen E. Hoatlin,Peter Hillemanns,Florian Heitz,Rebecca Hein,Rebecca Hein,Philipp Harter,Mari K. Halle,Per Hall,Jacek Gronwald,Martin Gore,Marc T. Goodman,Graham G. Giles,Graham G. Giles,Graham G. Giles,Aleksandra Gentry-Maharaj,Montserrat Garcia-Closas,James M. Flanagan,Peter A. Fasching,Peter A. Fasching,Arif B. Ekici,Robert Edwards,Diana Eccles,Douglas F. Easton,Matthias Dürst,Andreas du Bois,Thilo Dörk,Jennifer A. Doherty,Evelyn Despierre,Evelyn Despierre,Agnieszka Dansonka-Mieszkowska,Cezary Cybulski,Daniel W. Cramer,Linda S. Cook,Xiaoqing Chen,Bridget Charbonneau,Jenny Chang-Claude,Ian G. Campbell,Ian G. Campbell,Ralf Bützow,Clareann H. Bunker,Doerthe Brueggmann,Robert S. Brown,Angela Brooks-Wilson,Louise A. Brinton,Natalia Bogdanova,Matthew S. Block,Elizabeth Benjamin,Jonathan Beesley,Matthias W. Beckmann,Elisa V. Bandera,Laura Baglietto,Laura Baglietto,Francois Bacot,Sebastian M. Armasu,Natalia Antonenkova,Hoda Anton-Culver,Katja K.H. Aben,Dong Liang,Xifeng Wu,Karen H. Lu,Michelle A.T. Hildebrandt,Joellen M. Schildkraut,Thomas A. Sellers,David G. Huntsman,Andrew Berchuck,Georgia Chenevix-Trench,Simon A. Gayther,Paul D.P. Pharoah,Peter W. Laird,Ellen L. Goode,Celeste Leigh Pearce +180 more
TL;DR: Different variants in HNF1B associate with risk of serous and clear cell epithelial ovarian cancer; DNA methylation and expression patterns are also notably distinct between these subtypes.
Journal ArticleDOI
Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer
Kristen S. Purrington,Susan L. Slager,Diana Eccles,Drakoulis Yannoukakos,Peter A. Fasching,Peter A. Fasching,Penelope Miron,Jane Carpenter,Jenny Chang-Claude,Nicholas G. Martin,Grant W. Montgomery,Vessela N. Kristensen,Hoda Anton-Culver,Paul J. Goodfellow,William J. Tapper,Sajjad Rafiq,S Gerty,Lorraine Durcan,Irene Konstantopoulou,Florentia Fostira,Athanassios Vratimos,Paraskevi Apostolou,Irene Konstanta,Vassiliki Kotoula,Sotiris Lakis,Meletios A. Dimopoulos,Dimosthenis Skarlos,Dimitrios Pectasides,George Fountzilas,Matthias W. Beckmann,Alexander Hein,Matthias Ruebner,Arif B. Ekici,Arndt Hartmann,Ruediger Schulz-Wendtland,Stefan P. Renner,Wolfgang Janni,Brigitte Rack,Christoph Scholz,Julia Neugebauer,Ulrich Andergassen,Michael P. Lux,Lothar Haeberle,Christine L. Clarke,Nirmala Pathmanathan,Anja Rudolph,Dieter Flesch-Janys,Stefan Nickels,Janet E. Olson,James N. Ingle,Curtis Olswold,Seth W. Slettedahl,Jeanette E. Eckel-Passow,S. Keith Anderson,Daniel W. Visscher,Victoria Cafourek,Hugues Sicotte,Naresh Prodduturi,Elisabete Weiderpass,Leslie Bernstein,Argyrios Ziogas,Jennifer Ivanovich,Graham G. Giles,Laura Baglietto,Melissa C. Southey,Veli-Matti Kosma,Hans Fischer,MW Reed,Simon S. Cross,Sandra Deming-Halverson,Martha J. Shrubsole,Qiuyin Cai,Xiao-Ou Shu,Mary B. Daly,Jo Ellen Weaver,Eric A. Ross,Jennifer R. Klemp,Priyanka Sharma,Diana Torres,Diana Torres,Thomas Rüdiger,Heidrun Wölfing,Hans Ulrich Ulmer,Asta Försti,Asta Försti,Thaer Khoury,Shicha Kumar,Robert Pilarski,Charles L. Shapiro,Dario Greco,Päivi Heikkilä,Kristiina Aittomäki,Carl Blomqvist,Astrid Irwanto,Jianjun Liu,Vernon S. Pankratz,Xianshu Wang,Gianluca Severi,Arto Mannermaa,Douglas F. Easton,Per Hall,Hiltrud Brauch,Angela Cox,Wei Zheng,Andrew K. Godwin,Ute Hamann,Christine B. Ambrosone,Amanda E. Toland,Heli Nevanlinna,Celine M. Vachon,Fergus J. Couch +110 more
TL;DR: A polygenic risk score (PRS) for TN breast cancer based on known breast cancer risk variants showed a 4-fold difference in risk between the highest and lowest PRS quintiles, suggesting that genetic variation may be used for TN Breast cancer risk prediction.
Journal ArticleDOI
Malformations in a cohort of 284 women with Mayer-Rokitansky-Küster-Hauser syndrome (MRKH)
Patricia G. Oppelt,Johannes Lermann,Reiner Strick,Ralf Dittrich,Pamela L. Strissel,I Rettig,C. Schulze,Stefan P. Renner,Matthias W. Beckmann,Sara Y. Brucker,Katharina Rall,Andreas Mueller +11 more
TL;DR: Complete atresia of vagina and cervix were found in all patients, variable malformations were found with uterus and adnexa, and it is recommended that all patients with genital mal Formations should be evaluated for renal abnormalities.