Stefan P. Renner

ORCID: 0000-0003-2057-1268
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About
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Research Areas
  • Endometriosis Research and Treatment
  • Uterine Myomas and Treatments
  • Endometrial and Cervical Cancer Treatments
  • Gynecological conditions and treatments
  • Ovarian cancer diagnosis and treatment
  • Reproductive System and Pregnancy
  • Medical and Health Sciences Research
  • Health and Medical Studies
  • Urological Disorders and Treatments
  • BRCA gene mutations in cancer
  • Intestinal and Peritoneal Adhesions
  • Cancer Risks and Factors
  • Global Cancer Incidence and Screening
  • Social and Demographic Issues in Germany
  • Reproductive Biology and Fertility
  • Breast Cancer Treatment Studies
  • Cervical Cancer and HPV Research
  • Prenatal Screening and Diagnostics
  • HER2/EGFR in Cancer Research
  • Mobile Health and mHealth Applications
  • Intraperitoneal and Appendiceal Malignancies
  • Pelvic floor disorders treatments
  • Ectopic Pregnancy Diagnosis and Management
  • Genital Health and Disease
  • Urologic and reproductive health conditions

Friedrich-Alexander-Universität Erlangen-Nürnberg
2012-2025

Klinikum Sindelfingen-Böblingen
2018-2025

Klinikverbund Südwest
2018-2024

Zentrum für Seelische Gesundheit
2022

Klinik für Frauenheilkunde
2021

Hewlett-Packard (Germany)
2021

Universitätsklinikum Erlangen
2011-2020

Comprehensive Cancer Center Erlangen
2012-2020

Bayreuth Medical Center
2019

Olgahospital
2015-2016

The Mayer-Rokitansky-Kuester-Hauser (MRKH) syndrome is a malformation of the female genitals (occurring in one 4000 live births) as result interrupted embryonic development Müllerian (paramesonephric) ducts. This retrospective study examined issue associated malformations, subtyping, and frequency distribution subtypes MRKH syndrome.Fifty-three patients were investigated using newly developed standardized questionnaire. Together with results clinical diagnostic examinations, classified into...

10.1093/humrep/dei381 article EN Human Reproduction 2005-11-11
Hui Shen Brooke L. Fridley Honglin Song Kate Lawrenson Julie M. Cunningham and 95 more Susan J. Ramus Mine S. Cicek Jonathan P. Tyrer Douglas Stram Melissa C. Larson Martin Köbel Argyrios Ziogas Wei Zheng Hannah 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 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 Ira Schwaab Helga B. Salvesen Iwona K. Rzepecka Ingo B. Runnebaum Mary Anne Rossing Lorna Rodríguez-Rodríguez Harvey A. Risch Stefan P. Renner Elizabeth M. Poole Malcolm C. Pike Catherine M. Phelan Liisa M. Pelttari Tanja Pejović 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 Álvaro N.A. Monteiro Joanna Moes-Sosnowska Francesmary Modugno Usha Menon Esther M. John Valerie McGuire Keitaro Matsuo Noor Azmi Mat Adenan Leon F.A.G. Massuger Galina Lurie Lene Lundvall Jan Lubiński Jolanta Lissowska Douglas A. Levine Arto Leminen Alice W. Lee Nhu D. Le Sandrina Lambrechts Diether Lambrechts Jolanta Kupryjańczyk Camilla Krakstad Gottfried E. Konecny Susanne K. Kjær Lambertus A. Kiemeney Linda E. Kelemen Gary L. Keeney Beth Y. Karlan Rod Karevan Kimberly R. Kalli Hiroaki Kajiyama Bu‐Tian Ji Allan Jensen Anna Jakubowska

HNF1B is overexpressed in clear cell epithelial ovarian cancer, and we observed epigenetic silencing serous leading us to hypothesize that variation this gene differentially associates with cancer risk according histological subtype. Here comprehensively map respect analyse DNA methylation expression profiles across subtypes. Different single-nucleotide polymorphisms associate invasive (rs7405776 odds ratio (OR)=1.13, P=3.1 × 10−10) (rs11651755 OR=0.77, P=1.6 10−8) cancer. Risk alleles for...

10.1038/ncomms2629 article EN cc-by-nc-nd Nature Communications 2013-03-27
Kristen S. Purrington Susan Slager Diana Eccles Drakoulis Yannoukakos Peter A. Fasching and 95 more Penelope Miron Jane Carpenter Jenny Chang‐Claude Nicholas G. Martin Grant W. Montgomery Vessela Kristensen Hoda Anton‐Culver Paul J. Goodfellow William Tapper Sajjad Rafiq Susan M. Gerty Lorraine Durcan Irene Konstantopoulou Florentia Fostira Athanassios Vratimos Paraskevi Apostolou Irene Konstanta Vassiliki Kotoula Sotiris Lakis Meletios Α. Dimopoulos Dimosthenis Skarlos Dimitrios Pectasides George Fountzilas Matthias W. Beckmann Alexander Hein Matthias Ruebner Arif B. Ekici Arndt Hartmann R. 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 H.-P. Fischer Malcolm Reed Simon S. Cross Sandra Deming-Halverson Martha J. Shrubsole Qiuyin Cai Xiao‐Ou Shu Mary B. Daly JoEllen Weaver Eric A. Ross Jennifer R. Klemp Priyanka Sharma Diana Torres Thomas Rüdiger Heidrun Wölfing Hans-Ulrich Ulmer Asta Försti Thaer Khoury Shicha Kumar Robert Pilarski Charles L. Shapiro Dario Greco Päivi Heikkilä Kristiina Aittomäki Carl Blomqvist Astrid Irwanto Jianjun Liu V. Shane Pankratz Xianshu Wang Gianluca Severi Graham J. Mann Douglas F. Easton Per Hall Hiltrud Brauch Angela Cox

Triple-negative (TN) breast cancer is an aggressive subtype of associated with a unique set epidemiologic and genetic risk factors. We conducted two-stage genome-wide association study TN (stage 1: 1529 cases, 3399 controls; stage 2: 2148 1309 controls) to identify loci that influence risk. Variants in the 19p13.1 PTHLH showed significant associations (P < 5 × 10−8) 1 2 combined. Results also suggested substantial enrichment significantly variants among single nucleotide polymorphisms (SNPs)...

10.1093/carcin/bgt404 article EN Carcinogenesis 2013-12-09

ObjectiveTo harmonize standard operating procedures (SOPs) and standardize the recording of associated data for collection, processing, storage human tissues relevant to endometriosis.DesignAn international collaboration involving 34 clinical/academic centers three industry collaborators from 16 countries on five continents.SettingIn 2013, two workshops were conducted followed by global consultation, bringing together 54 leaders in endometriosis research sample processing around...

10.1016/j.fertnstert.2014.07.1209 article EN cc-by Fertility and Sterility 2014-09-23

Abstract Background The aim of this retrospective study was to describe the spectrum genital and associated malformations in women with Mayer-Rokitansky-Küster-Hauser syndrome using evaluated diagnostic procedures Vagina Cervix Uterus Adnex – Malformation classification system (VCUAM). Methods 290 MRKH were clinically clinical examinations, abdominal perineal/rectal ultrasound, MRI, laparoscopy. Results Classification female malformation according possible 284 (97.9%). Complete atresia (V5b)...

10.1186/1477-7827-10-57 article EN cc-by Reproductive Biology and Endocrinology 2012-08-20

<h3>Background</h3> Congenital malformations involving the Müllerian ducts are observed in around 5% of infertile women. Complete aplasia uterus, cervix, and upper vagina, also termed or Mayer–Rokitansky–Kuster–Hauser (MRKH) syndrome, occurs with an incidence 1 4500 female births, both isolated syndromic forms. Previous reports have suggested that a proportion cases, especially caused by variation copy number at different genomic loci. <h3>Methods</h3> In order to obtain overview...

10.1136/jmg.2010.082412 article EN Journal of Medical Genetics 2011-01-28

Abstract STUDY QUESTION Does linzagolix administered orally once daily for up to 3 months at a dose of 75 mg alone or 200 in combination with add-back therapy (ABT) (1.0 estradiol; 0.5 norethindrone acetate, also known as norethisterone acetate [NETA]) demonstrate better efficacy than placebo the management endometriosis-related dysmenorrhea and non-menstrual pelvic pain? SUMMARY ANSWER Combining ABT was found significantly reduce pain therapy, while yielded significant decrease only months....

10.1093/humrep/deae076 article EN cc-by Human Reproduction 2024-04-22

In this guideline, recommendations and standards for optimum diagnosis treatment of endometriosis are presented. They based on the analysis available scientific evidence as published in prospective randomized retrospective studies well systematic reviews. The guideline working group consisted experts from Austria, Germany, Switzerland, Czech Republic.

10.1055/s-0034-1383187 article EN other-oa Geburtshilfe und Frauenheilkunde 2014-12-23

Abstract Blood lipids have been associated with the development of a range cancers, including breast, lung and colorectal cancer. For endometrial cancer, observational studies reported inconsistent associations between blood cancer risk. To reduce biases from unmeasured confounding, we performed bidirectional, two‐sample Mendelian randomization analysis to investigate relationship levels three (low‐density lipoprotein [LDL] high‐density [HDL] cholesterol, triglycerides) Genetic variants each...

10.1002/ijc.33206 article EN International Journal of Cancer 2020-07-13

Abstract Aims The aim of this official guideline published and coordinated by the German Society Gynaecology Obstetrics (DGGG) in cooperation with Austrian for (OEGGG) Swiss (SGGG) was to provide consensus-based recommendations diagnosis treatment endometriosis based on an evaluation relevant literature. Methods This S2k represents structured consensus a representative panel experts different professional backgrounds commissioned Guideline Committee DGGG, OEGGG SGGG. Recommendations...

10.1055/a-1380-3693 article EN Geburtshilfe und Frauenheilkunde 2021-04-01

To evaluate blood-based biomarkers to detect endometriosis and/or adenomyosis across nine European centers (June 2014-April 2018).This prospective, non-interventional study assessed the diagnostic accuracy of 54 biomarker immunoassays in samples from 919 women (aged 18-45 years) with suspicion versus symptomatic controls. Endometriosis was stratified by revised American Society for Reproductive Medicine stage. Symptomatic controls were "pathologic controls" or "pathology-free controls". The...

10.1002/ijgo.15062 article EN cc-by International Journal of Gynecology & Obstetrics 2023-08-28
Jodie N. Painter Tracy A. O’Mara Jyotsna Batra Timothy Cheng Felicity Lose and 95 more Joe Dennis Kyriaki Michailidou Jonathan P. Tyrer Shahana Ahmed Kaltin Ferguson Catherine S. Healey Susanne Kaufmann Kristine M. Hillman Carina Walpole Leire Moya Pamela M. Pollock Angela Jones Kimberley Howarth Lynn Martin Maggie Gorman Shirley Hodgson Ma. Magdalena Echeverry de Polanco Mónica Sans Ángel Carracedo Sergi Castellvı́-Bel Augusto Rojas-Martı́nez Érika Maria Monteiro Santos Manuel R. Teixeira Luis G. Carvajal‐Carmona Xiao‐Ou Shu Jirong Long Wei Zheng Yong‐Bing Xiang Grant W. Montgomery Penelope M. Webb Rodney J. Scott Mark McEvoy John Attia Elizabeth Holliday Nicholas G. Martin Dale R. Nyholt Anjali K. Henders Peter A. Fasching Alexander Hein Matthias W. Beckmann Stefan P. Renner Thilo Dörk Peter Hillemanns Matthias Dürst Ingo B. Runnebaum Diether Lambrechts Lieve Coenegrachts Stefanie Schrauwen Frédéric Amant Boris Winterhoff Sean C. Dowdy Ellen L. Goode Attila Teoman Helga B. Salvesen Jone Trovik Tormund S. Njølstad Henrica M.J. Werner Katie A. Ashton Tony Proietto Geoffrey Otton Gerasimos Tzortzatos Miriam Mints Emma Tham Per Hall Kamila Czene Jianjun Liu Jingmei Li John L. Hopper Melissa C. Southey Arif B. Ekici Matthias Ruebner Nicola Johnson Julian Peto Barbara Burwinkel Frederik Marmé Hermann Brenner Aida Karina Dieffenbach Thomas Ind Hiltrud Brauch Annika Lindblom Jeroen Depreeuw Matthieu Moisse Jenny Chang‐Claude Anja Rudolph Fergus J. Couch Janet E. Olson Graham G. Giles Fiona Bruinsma Julie M. Cunningham Brooke L. Fridley Anne‐Lise Børresen‐Dale Vessela N. Kristensen Angela Cox Anthony J. Swerdlow Nick Orr

Common variants in the hepatocyte nuclear factor 1 homeobox B (HNF1B) gene are associated with risk of Type II diabetes and multiple cancers. Evidence to date indicates that cancer may be mediated via genetic or epigenetic effects on HNF1B expression. We previously found single-nucleotide polymorphisms (SNPs) at locus endometrial cancer, now report extensive fine-mapping silico laboratory analyses this locus. Analysis 1184 genotyped imputed SNPs 6608 Caucasian cases 37 925 controls, 895...

10.1093/hmg/ddu552 article EN Human Molecular Genetics 2014-11-06

The appropriate surgical technique to treat patients with uterine fibroids is still a matter of debate as the potential risk incorrect treatment if histological examination detects sarcoma instead fibroids. published epidemiology for set against incidence accidental findings during surgery International comments on this topic are discussed and incorporated into assessment by German Society Gynecology Obstetrics (DGGG). ICD-O-3 version 2003 was used anatomical topographical coding sarcomas,...

10.1055/s-0035-1545684 article EN other-oa Geburtshilfe und Frauenheilkunde 2015-03-16

The advantages and disadvantages of the various surgical techniques for hysterectomy are currently a topic debate, with particular controversy over leaving cervix in situ laparoscopic supracervical (LASH) procedure.In retrospective single-center study, medical history clinical characteristics were compared patients who had undergone benign disease period 2002-2008 at Department Obstetrics Gynecology, Erlangen University Hospital. Postoperative satisfaction frequency secondary operations...

10.3238/arztebl.2010.0353 article EN Deutsches Ärzteblatt international 2010-05-21
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