Andrea Gsur

ORCID: 0000-0002-9795-1528
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About
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Research Areas
  • Genetic factors in colorectal cancer
  • Genetic Associations and Epidemiology
  • Fibroblast Growth Factor Research
  • Colorectal Cancer Screening and Detection
  • Cancer Genomics and Diagnostics
  • Cancer, Lipids, and Metabolism
  • Colorectal Cancer Treatments and Studies
  • Prostate Cancer Treatment and Research
  • Hormonal and reproductive studies
  • Epigenetics and DNA Methylation
  • Digestive system and related health
  • Nutrition, Genetics, and Disease
  • Sexual Differentiation and Disorders
  • Drug Transport and Resistance Mechanisms
  • RNA modifications and cancer
  • Gut microbiota and health
  • Metabolomics and Mass Spectrometry Studies
  • Folate and B Vitamins Research
  • Cancer-related molecular mechanisms research
  • Diet and metabolism studies
  • Liver Disease Diagnosis and Treatment
  • Tryptophan and brain disorders
  • DNA Repair Mechanisms
  • Acute Myeloid Leukemia Research
  • Glutathione Transferases and Polymorphisms

Medical University of Vienna
2016-2025

Comprehensive Cancer Center Vienna
2011-2025

Institute of Cancer Research
2005-2023

Center for Cancer Research
2023

University of Vienna
1995-2022

Imperial College London
2021

Broad Institute
2021

Massachusetts General Hospital
2021

Harvard University
2021

Huntsman Cancer Institute
2019

Abstract Physical activity has been associated with lower risks of breast and colorectal cancer in epidemiological studies; however, it is unknown if these associations are causal or confounded. In two-sample Mendelian randomisation analyses, using summary genetic data from the UK Biobank GWA consortia, we found that a one standard deviation increment average acceleration was (odds ratio [OR]: 0.51, 95% confidence interval [CI]: 0.27 to 0.98, P-value = 0.04) (OR: 0.66, CI: 0.48 0.90, 0.01)....

10.1038/s41467-020-14389-8 article EN cc-by Nature Communications 2020-01-30
Stephanie L. Schmit Christopher K. Edlund Fredrick R. Schumacher Jian Gong Tabitha A. Harrison and 95 more Jeroen R. Huyghe Chenxu Qu Marilena Melas David Van Den Berg Hansong Wang Stephanie Tring Sarah J. Plummer Demetrius Albanes M. Henar Alonso Christopher I. Amos Kristen Anton Aaron K. Aragaki Volker Arndt Elizabeth L. Barry Sonja I. Berndt Stéphane Bézieau Stephanie A. Bien Amanda M. Bloomer Juergen Boehm Marie‐Christine Boutron‐Ruault Hermann Brenner Stefanie Brezina Daniel D. Buchanan Katja Butterbach Bette J. Caan Peter T. Campbell Christopher S. Carlson Jose E. Castelao Andrew T. Chan Jenny Chang‐Claude Stephen J. Chanock Iona Cheng Ya‐Wen Cheng Lee Soo Chin James M. Church Timothy R. Church Gerhard A. Coetzee Michelle Cotterchio Marcia Cruz Correa Keith R. Curtis David Duggan Douglas F. Easton Dallas R. English Edith J. M. Feskens Rocky Fischer Liesel M. FitzGerald Barbara K. Fortini Lars G. Fritsche Charles S. Fuchs Manuela Gago‐Dominguez Manish Gala Steven Gallinger W. James Gauderman Graham G. Giles Edward L. Giovannucci Stephanie M. Gogarten Clicerio González‐Villalpando Elena M. Gonzalez-Villalpando William M. Grady Joel K. Greenson Andrea Gsur Marc J. Gunter Christopher A. Haiman Jochen Hampe Sophia Harlid John F. Harju Richard B. Hayes Philipp Hofer Michael Hoffmeister John L. Hopper Shu-Chen Huang José María Huerta Thomas J. Hudson David J. Hunter Gregory Idos Motoki Iwasaki Rebecca D. Jackson Eric J. Jacobs Sun Ha Jee Mark A. Jenkins Wei-Hua Jia Shuo Jiao Amit D. Joshi Laurence N. Kolonel Suminori Kono Charles Kooperberg Vittorio Krogh Tilman Küehn Sébastien Küry Andrea Z. LaCroix Cecelia Laurie Flavio Lejbkowicz Mathieu Lemire Heinz‐Josef Lenz David Levine

Abstract Background Previous genome-wide association studies (GWAS) have identified 42 loci (P < 5 × 10−8) associated with risk of colorectal cancer (CRC). Expanded consortium efforts facilitating the discovery additional susceptibility may capture unexplained familial risk. Methods We conducted a GWAS in European descent CRC cases and control subjects using discovery–replication design, followed by examination novel findings multiethnic sample (cumulative n = 163 315). In stage (36 948...

10.1093/jnci/djy099 article EN JNCI Journal of the National Cancer Institute 2018-04-30
Minta Thomas Lori C. Sakoda Michael Hoffmeister Elisabeth A. Rosenthal Jeffrey K. Lee and 92 more Fränzel J.B. van Duijnhoven Elizabeth A. Platz Anna H. Wu Christopher H. Dampier Albert de la Chapelle Alicja Wolk Amit D. Joshi Andrea N. Burnett‐Hartman Andrea Gsur Annika Lindblom Antoni Castells Aung Ko Win Bahram Namjou Bethany Van Guelpen Catherine M. Tangen Qianchuan He Christopher I. Li Clemens Schafmayer Corinne E. Joshu Cornelia M. Ulrich D. Timothy Bishop Daniel D. Buchanan Daniel J. Schaid David A. Drew David C. Muller David Duggan David R. Crosslin Demetrius Albanes Edward L. Giovannucci Eric B. Larson Flora Qu Frank Mentch Graham G. Giles Hákon Hákonarson Heather Hampel Ian B. Stanaway Jane C. Figueiredo Jeroen R. Huyghe Jessica Minnier Jenny Chang‐Claude Jochen Hampe John B. Harley Kala Visvanathan Keith R. Curtis Kenneth Offit Li Li Loı̈c Le Marchand Ludmila Vodičková Marc J. Gunter Mark A. Jenkins Martha L. Slattery Mathieu Lemire Michael O. Woods Mingyang Song Neil Murphy Noralane M. Lindor Ozan Dikilitas Paul D.P. Pharoah Peter T. Campbell Polly A. Newcomb Roger L. Milne Robert J. MacInnis Sergi Castellví‐Bel Shuji Ogino Sonja I. Berndt Stéphane Bézieau Stephen N. Thibodeau Steven Gallinger Syed Hassan Ejaz Zaidi Tabitha A. Harrison Temitope O. Keku Thomas J. Hudson Veronika Vymetalková Vı́ctor Moreno Vicente Martín Volker Arndt Wei‐Qi Wei Wendy K. Chung Yu‐Ru Su Richard B. Hayes Emily White Pavel Vodička Graham Casey Stephen B. Gruber Robert E. Schoen Andrew T. Chan John D. Potter Hermann Brenner Gail P. Jarvik Douglas A. Corley Ulrike Peters Li Hsu

10.1016/j.ajhg.2020.07.006 article EN publisher-specific-oa The American Journal of Human Genetics 2020-08-05
Alexi Archambault Yu‐Ru Su Jihyoun Jeon Minta Thomas Yi Lin and 95 more David V. Conti Aung Ko Win Lori C. Sakoda Iris Lansdorp‐Vogelaar Elisabeth F. P. Peterse Ann G. Zauber David Duggan Andreana N. Holowatyj Jeroen R. Huyghe Hermann Brenner Michelle Cotterchio Stéphane Bézieau Stephanie L. Schmit Christopher K. Edlund Melissa C. Southey Robert J. MacInnis Peter T. Campbell Jenny Chang‐Claude Martha L. Slattery Andrew T. Chan Amit D. Joshi Mingyang Song Yin Cao Michael O. Woods Emily White Stephanie J. Weinstein Cornelia M. Ulrich Michael Hoffmeister Stephanie A. Bien Tabitha A. Harrison Jochen Hampe Christopher I. Li Clemens Schafmayer Kenneth Offit Paul D.P. Pharoah Vı́ctor Moreno Annika Lindblom Alicja Wolk Anna H. Wu Li Li Marc J. Gunter Andrea Gsur Temitope O. Keku Rachel Pearlman D. Timothy Bishop Sergi Castellví‐Bel Leticia Moreira Pavel Vodička Ellen Kampman Graham G. Giles Demetrius Albanes John A. Baron Sonja I. Berndt Stefanie Brezina Stephan Buch Daniel D. Buchanan Antonia Trichopoulou Gianluca Severi María‐Dolores Chirlaque María‐José Sánchez Domenico Palli Tilman Kühn Neil Murphy Amanda J. Cross Andrea N. Burnett‐Hartman Stephen J. Chanock Albert de la Chapelle Douglas F. Easton Faye Elliott Dallas R. English Edith J. M. Feskens Liesel M. FitzGerald Phyllis J. Goodman John L. Hopper Thomas J. Hudson David J. Hunter Eric J. Jacobs Corinne E. Joshu Sébastien Küry Sanford D. Markowitz Roger L. Milne Elizabeth A. Platz Gad Rennert Hedy S. Rennert Fredrick R. Schumacher Robert S. Sandler Daniela Seminara Catherine M. Tangen Stephen N. Thibodeau Amanda E. Toland Fränzel J.B. van Duijnhoven Kala Visvanathan Ludmila Vodičková John D. Potter Satu Männistö

10.1053/j.gastro.2019.12.012 article EN Gastroenterology 2019-12-19

Abstract Background Higher adiposity increases the risk of colorectal cancer (CRC), but whether this relationship varies by anatomical sub-site or sex is unclear. Further, metabolic alterations mediating effects on CRC are not fully understood. Methods We examined sex- and site-specific associations with adiposity-associated metabolites explain CRC. Genetic variants from genome-wide association studies body mass index (BMI) waist-to-hip ratio (WHR, unadjusted for BMI; N = 806,810), 123...

10.1186/s12916-020-01855-9 article EN cc-by BMC Medicine 2020-12-01

Background & AimsHuman studies examining associations between circulating levels of insulin-like growth factor 1 (IGF1) and binding protein 3 (IGFBP3) colorectal cancer risk have reported inconsistent results. We conducted complementary serologic Mendelian randomization (MR) analyses to determine whether alterations in IGF1 or IGFBP3 are associated with development.MethodsSerum were measured blood samples collected from 397,380 participants the UK Biobank, 2006 through 2010. Incident cases...

10.1053/j.gastro.2019.12.020 article EN cc-by-nc-nd Gastroenterology 2019-12-27

Epidemiological studies have linked lifestyle, cardiometabolic, reproductive, developmental, and inflammatory factors to the risk of colorectal cancer. However, which specific affect strength these effects are unknown. We aimed examine relationship between potentially modifiable

10.1016/s2468-1253(19)30294-8 article EN cc-by ˜The œLancet. Gastroenterology & hepatology 2019-10-24

Diverticular disease is a common complex disorder characterised by mucosal outpouchings of the colonic wall that manifests through complications such as diverticulitis, perforation and bleeding. We report to date largest genome-wide association study (GWAS) identify genetic risk factors for diverticular disease.Discovery GWAS analysis was performed on UK Biobank imputed genotypes using 31 964 cases 419 135 controls European descent. Associations were replicated in sample 3893 2829...

10.1136/gutjnl-2018-317619 article EN Gut 2019-01-19

Disease-specific alterations of the cell-free DNA methylation status are frequently found in serum samples and currently considered to be suitable biomarkers. Candidate markers were identified by bisulfite conversion-based genome-wide screening lung tissue from cancer, fibrotic ILD, COPD. cfDNA 400 μl (n = 204) served test diagnostic performance these markers. Following methylation-sensitive restriction enzyme digestion enrichment methylated via targeted amplification (multiplexed MSRE...

10.1016/j.ebiom.2015.06.025 article EN cc-by-nc-nd EBioMedicine 2015-07-04

Colorectal cancer (CRC) is a biologically heterogeneous disease. To characterize its mutational profile, we conduct targeted sequencing of 205 genes for 2,105 CRC cases with survival data. Our data shows several findings in addition to enhancing the existing knowledge CRC. We identify PRKCI, SPZ1, MUTYH, MAP2K4, FETUB, and TGFBR2 as additional significantly mutated find that among hypermutated tumors, an increased mutation burden associated improved CRC-specific (HR = 0.42, 95% CI:...

10.1038/s41467-020-17386-z article EN cc-by Nature Communications 2020-07-20

Background Epidemiological studies have reported conflicting findings on the potential adverse effects of long-term antihypertensive medication use cancer risk. Naturally occurring variation in genes encoding drug targets can be used as proxies for these to examine effect their therapeutic inhibition disease outcomes. Methods and We performed a mendelian randomization analysis association between genetically proxied 3 risk 4 common cancers (breast, colorectal, lung, prostate)....

10.1371/journal.pmed.1003897 article EN public-domain PLoS Medicine 2022-02-03
Zhishan Chen Xingyi Guo Ran Tao Jeroen R. Huyghe Philip Law and 95 more Ceres Fernández‐Rozadilla Jie Ping Guochong Jia Jirong Long Chao Li Quanhu Shen Yuhan Xie Maria Timofeeva Minta Thomas Stephanie L. Schmit Virginia Díez‐Obrero Matthew A.M. Devall Ferrán Moratalla-Navarro Juan Fernández‐Tajes Claire Palles Kitty Sherwood Sarah Briggs Victoria Svinti Kevin Donnelly Susan M. Farrington James P. Blackmur P G Vaughan-Shaw Xiao‐Ou Shu Yingchang Lu Peter Broderick James B. Studd Tabitha A. Harrison David V. Conti Fredrick R. Schumacher Marilena Melas Gad Rennert Mireia Obón‐Santacana Vicente Martín Jae Hwan Oh Jeongseon Kim Sun Ha Jee Keum Ji Jung Sun-Seog Kweon Min‐Ho Shin Aesun Shin Yoon‐Ok Ahn Dong-Hyun Kim Isao Oze Wanqing Wen Keitaro Matsuo Koichi Matsuda Chizu Tanikawa Zefang Ren Yu‐Tang Gao Wei‐Hua Jia John L. Hopper Mark A. Jenkins Aung Ko Win Rish K. Pai Jane C. Figueiredo Robert W. Haile Steven Gallinger Michael O. Woods Polly A. Newcomb David Duggan Jeremy P. Cheadle Richard Kaplan Rachel Kerr David Kerr Iva Kirac Jan Böhm Jukka‐Pekka Mecklin Pekka Jousilahti Paul Knekt Lauri A. Aaltonen Harri Rissanen ­Eero Pukkala Johan G. Eriksson Tatiana Cajuso Ulrika A. Hänninen Johanna Kondelin Kimmo Palin Tomas Tanskanen Laura Renkonen‐Sinisalo Satu Männistö Demetrius Albanes Stephanie J. Weinstein Edward A. Ruiz‐Narváez Julie R. Palmer Daniel D. Buchanan Elizabeth A. Platz Kala Visvanathan Cornelia M. Ulrich Erin M. Siegel Stefanie Brezina Andrea Gsur Peter T. Campbell Jenny Chang‐Claude Michael Hoffmeister Hermann Brenner

Abstract Genome-wide association studies (GWAS) have identified more than 200 common genetic variants independently associated with colorectal cancer (CRC) risk, but the causal and target genes are mostly unknown. We sought to fine-map all known CRC risk loci using GWAS data from 100,204 cases 154,587 controls of East Asian European ancestry. Our stepwise conditional analyses revealed 238 independent signals each a set credible (CCVs), which 28 had single CCV. cis-eQTL/mQTL colocalization...

10.1038/s41467-024-47399-x article EN cc-by Nature Communications 2024-04-26

CYP17 encodes the enzyme cytochrome P-450c17 alpha, which mediates both 17 alpha-hydroxylase and 17,20-lyase in steroid biosynthesis pathway. A polymorphism 5; promoter region of gene has been described. Steroid hormones, especially androgens, are believed to play a key role etiology prostate cancer. Therefore, polymorphisms genes involved androgen metabolism may affect risk We conducted case-control study 63 patients with untreated histologically proven cancer 126 age-matched control men...

10.1002/1097-0215(20000801)87:3<434::aid-ijc19>3.0.co;2-g article EN International Journal of Cancer 2000-01-01

Several polymorphic glutathione-S-transferase (GST) enzymes are involved in the metabolism of a number potential prostate carcinogens and thought to engage transport steroid hormones. A case-control study was conducted determine association GSTP1, GSTM1 GSTT1 polymorphisms prostate-cancer risk. The population consisted 166 patients with previously untreated, histologically proven cancer age-matched control benign prostatic hyperplasia (BPH), all them Caucasians. In GSTP1 gene, 2 alleles,...

10.1002/1097-0215(20010520)95:3<152::aid-ijc1026>3.0.co;2-s article EN International Journal of Cancer 2001-01-01

Colorectal cancer is known to arise from multiple tumorigenic pathways; however, the underlying mechanisms remain not completely understood. Metabolomics becoming an increasingly popular tool in assessing biological processes. Previous metabolomics research focusing on colorectal limited by sample size and did replicate findings independent study populations verify robustness of reported findings. Here, we performed a ultrahigh performance liquid chromatography‐quadrupole time‐of‐flight mass...

10.1002/ijc.32146 article EN cc-by International Journal of Cancer 2019-01-21

10.1053/j.gastro.2020.08.062 article EN Gastroenterology 2020-10-12
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