G. Rennert

G. Rennert, F. Lejbkowicz, M. Pinchev, 2009, European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation.

Association of Diabetes and Glycated Hemoglobin With the Risk of Intracerebral Hemorrhage: A Population-Based Cohort Study

N. Gronich, G. Rennert, W. Saliba, 2019, Diabetes Care.

β2‐adrenoceptor agonists and antagonists and risk of Parkinson's disease

N. Gronich, I. Lavi, G. Rennert, 2018, Movement disorders : official journal of the Movement Disorder Society.

Apoptosis, proliferation, and Fas (APO‐1, CD95)/Fas ligand expression in medullary carcinoma of the breast

G. Rennert, L. Maroun, E. Yakirevich, 2000, The Journal of pathology.

Molecular changes in the offspring of liquidators who emigrated to Israel from the Chernobyl disaster area.

G. Rennert, E. Nevo, A. Korol, 1997, Environmental health perspectives.

Association of factor V activity with risk of venous thromboembolism and atherothrombotic cardiovascular events: A retrospective population-based cohort study.

G. Rennert, W. Saliba, N. Stein, 2018, Thrombosis research.

Correction: Common Genetic Variants and Modification of Penetrance of BRCA2-Associated Breast Cancer

M. Daly, D. Altshuler, F. Couch, 2010, PLoS Genetics.

A Recurrent ERCC 3 Truncating Mutation Confers Moderate Risk for Breast Cancer

M. Daly, F. Couch, G. Rennert, 2016 .

Colorectal Polyps in Carriers of the APC I1307K Polymorphism

S. Gruber, G. Rennert, L. Tomsho, 2005, Diseases of the colon and rectum.

BRCA 1 and BRCA 2 Founder Mutations and the Risk of Colorectal Cancer

S. Gruber, G. Rennert, L. Tomsho, 2003 .

Thyroid cancer and multiple primary malignancies in Israel

G. Rennert, A. Kuten, A. Bartal, 1991, Journal of surgical oncology.

Hypothyroidism Is a Risk Factor for New-Onset Diabetes: A Cohort Study

N. Gronich, I. Lavi, G. Rennert, 2015, Diabetes Care.

Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer

Marshall W. Anderson, J. Witte, Y. Bossé, 2022, Nature Genetics.

Transcriptome‐wide association study reveals candidate causal genes for lung cancer

Aurélie A G Gabriel, M. Obeidat, Y. Bossé, 2018, International journal of cancer.

Title: Trans-ethnic genome-wide meta-analysis of 35,732 cases and 34,424 controls identifies novel genomic cross-ancestry loci contributing to lung cancer susceptibility

Aldrich, Mattias, Walsh, 2020 .

Identiﬁcation of four novel susceptibility loci for oestrogen receptor negative breast cancer

Nussbaum, S. Cross, P. Fasching, 2016 .

The risk of all-cause mortality is inversely related to serum 25(OH)D levels.

G. Rennert, H. Rennert, W. Saliba, 2012, The Journal of clinical endocrinology and metabolism.

The relationship between obesity and the increase in serum 25(OH)D levels in response to vitamin D supplementation

G. Rennert, W. Saliba, O. Barnett‐Griness, 2013, Osteoporosis International.

The longitudinal variability of serum 25(OH)D levels.

G. Rennert, W. Saliba, N. Stein, 2012, European journal of internal medicine.

Vitamin D Status in Israeli Subjects before the Initiation and after the Cessation of Vitamin D Supplements

I. Lavi, G. Rennert, H. Rennert, 2011, Calcified Tissue International.

Gene-gene Interaction of AhR With and Within the Wnt Cascade Affects Susceptibility to Lung Cancer

L. Kiemeney, S. Lam, A. Tardón, 2021 .

Identi ﬁ cation of susceptibility pathways for the role of chromosome 15q25.1 in modifying lung cancer risk

L. Wain, M. S. Artigas, Y. Bossé, 2018 .

TITLE: Mendelian randomization of circulating polyunsaturated fatty acids and colorectal cancer risk

Aung Ko Win, C. Ulrich, D. English, 2020 .

Global implementation of genomic medicine: We are not alone

Satoru Miyano, Wasun Chantratita, Andres Metspalu, 2015, Science Translational Medicine.

Dietary indole derivatives induce apoptosis in human breast cancer cells.

G. Rennert, F. Fares, X. Ge, 1998, Advances in experimental medicine and biology.

Genome-wide association study of germline variants and breast cancer-speci ﬁ c mortality

A. Whittemore, M. Beckmann, A. Talhouk, 2019 .

Correction: Corrigendum: Genome-wide association study of colorectal cancer identifies six new susceptibility loci

Christopher P. Fischer, C. Carlson, A. LaCroix, 2015, Nature Communications.

A Large-Scale Genome-Wide Gene-Gene Interaction Study of Lung Cancer Susceptibility in Europeans With a Trans-Ethnic Validation in Asians

L. Kiemeney, Hongbing Shen, A. Tardón, 2022, Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer.

The evaluation of vitamin D status in normocalcemic primary hyperparathyroidism.

I. Lavi, G. Rennert, H. Rennert, 2013, European journal of internal medicine.

Vitamin D status in primary hyperparathyroidism.

I. Lavi, G. Rennert, H. Rennert, 2012, European journal of internal medicine.

Statins use and risk of mortality in patient with Clostridium difficile infection.

G. Rennert, W. Saliba, M. Elias, 2014, Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases.

Quality control in a National Program for the Early Detection of Breast Cancer: women's satisfaction with the mammography process.

G. Rennert, R. Almog, L. Hagoel, 2008, Women's health issues : official publication of the Jacobs Institute of Women's Health.

A novel founder mutation in the RNASEL gene, 471delAAAG, is associated with prostate cancer in Ashkenazi Jews.

G. Rennert, D. Bercovich, L. Kadouri, 2002, American journal of human genetics.

Physical activity, sedentary time and breast cancer risk: a Mendelian randomisation study

Jack A. Taylor, S. Cross, M. Beckmann, 2022, British Journal of Sports Medicine.

APC E1317Q Is Not Associated with Colorectal Cancer in a Population-Based Case-Control Study in Northern Israel

S. Gruber, G. Rennert, L. Rozek, 2006, Cancer Epidemiology Biomarkers & Prevention.

Factor XI deficiency is associated with lower risk for cardiovascular and venous thromboembolism events.

G. Rennert, W. Saliba, N. Stein, 2017, Blood.

University of Southern Denmark Prostate-specific antigen velocity in a prospective prostate cancer screening study of men with genetic predisposition

L. Kiemeney, L. Andrews, R. Eeles, 2018 .

Sustained effect of short-term calcium supplementation on bone mass in adolescent girls with low calcium intake.

G. Rennert, S. Ish-shalom, G. Rozen, 2005, The American journal of clinical nutrition.

ARTICLES BRCA1 and BRCA2 Founder Mutations and the Risk of Colorectal Cancer

S. Gruber, G. Rennert, L. Tomsho, 2004 .

Genome-wide interaction analysis identified low-frequency variants with sex disparity in lung cancer risk

Kristen S Purrington, Y. Bossé, Hongbing Shen, 2021, Human molecular genetics.

Single measurement of serum 25(OH)D: is classification into month-specific cutpoints useful in accounting for seasonal variation?

G. Rennert, W. Saliba, O. Barnett‐Griness, 2012, European Journal of Clinical Nutrition.

Epidemiology of Candidemia – A Nationwide Survey in Israel

G. Rennert, S. Pitlik, H. Rennert, 2000, Infection.

Compliance with mammography screening in Israeli women: the impact of a pre-scheduled appointment and of the letter-style.

G. Rennert, L. Hagoel, L. Ore, 1997, Israel journal of medical sciences.

Cancer Risk following Radioactive Iodine Treatment for Hyperthyroidism: a Cohort Study.

N. Gronich, I. Lavi, G. Rennert, 2019, Thyroid : official journal of the American Thyroid Association.

Clinical outcomes of breast cancer in carriers of BRCA1 and BRCA2 mutations.

Ofra Barnett-Griness, Gad Rennert, G. Rennert, 2007, The New England journal of medicine.

Title Interplay between BRCA 1 and RHAMM regulates epithelial apicobasal polarization and may influence risk of breast cancer

Loris, Fiona, Meindl, 2012 .

Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170

Nicholas A. Sinnott-Armstrong, Richard C. Sallari, S. Cross, 2016, Nature Genetics.

Proband family uptake of familial‐genetic counselling

G. Rennert, R. Almog, L. Hagoel, 2000, Psycho-oncology.

Adiponectin gene and risk of colorectal cancer

S. Gruber, G. Rennert, V. Moreno, 2011, British Journal of Cancer.

Clinical implications of UGT1A1*28 genotype testing in colorectal cancer patients

S. Gruber, G. Rennert, A. Kuten, 2011, Cancer.

Ciliary ultrastructure in primary ciliary dyskinesia and other chronic respiratory conditions: the relevance of microtubular abnormalities.

G. Rennert, J. Rivlin, E. Greenberg, 1992, Ultrastructural pathology.

Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer

C. Carlson, G. Abecasis, H. Kang, 2019, Human Genetics.

Dietary intake of carotenoid isomers in Israel.

S. Gruber, G. Rennert, G. Rozen, 2007, International journal for vitamin and nutrition research. Internationale Zeitschrift fur Vitamin- und Ernahrungsforschung. Journal international de vitaminologie et de nutrition.

Early detection of breast cancer: compromise guidelines for a primary care setting.

G. Rennert, J. Shalom, T. Spenser, 1989, Journal of cancer education : the official journal of the American Association for Cancer Education.

Obesity and Association of Serum 25(OH)D Levels with All-Cause Mortality

G. Rennert, W. Saliba, O. Barnett‐Griness, 2014, Calcified Tissue International.

Diet and cancer: where are we and where are we going?

G. Rennert, 2003, Proceedings of the Nutrition Society.

Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries

Stephanie A. Bien, Anna C. Wu, Aung Ko Win, 2022, Nature Genetics.

Hypothyroidism Is a Risk Factor for New-Onset Diabetes Mellitus: A Cohort Study

N. Gronich, I. Lavi, G. Rennert, 2015 .

Incorporating progesterone receptor expression into the PREDICT breast prognostic model

S. Cross, M. Beckmann, N. Camp, 2022, European journal of cancer.

Prostate-specific antigen velocity in a prospective prostate cancer screening study of men with genetic predisposition

Neil L. Aaronson, L. Kiemeney, L. Andrews, 2018, British Journal of Cancer.

Neurobehavioral and cognitive performances of children exposed to low-dose radiation in the Chernobyl accident: the Israeli Chernobyl Health Effects Study.

D. Reisfeld, G. Rennert, Z. Silman, 2004, American journal of epidemiology.

A genome-wide association study for colorectal cancer identifies a risk locus in 14q23.1

L. Hou, T. Hudson, H. Brenner, 2015, Human Genetics.

BRCA2 germline mutation in a woman with uterine serous papillary carcinoma--case report.

G. Rennert, Y. Cohen, O. Lavie, 2005, Gynecologic oncology.

Catheter ablation of atrial fibrillation is associated with reduced risk of stroke and mortality: A propensity score-matched analysis.

N. Gronich, I. Lavi, G. Rennert, 2017, Heart rhythm.

Cumulative Burden of Colorectal Cancer-Associated Genetic Variants is More Strongly Associated With Early-onset vs Late-onset Cancer.

Stephanie A. Bien, Elizabeth L. Barry, Aung Ko Win, 2019, Gastroenterology.

Shared heritability and functional enrichment across six solid cancers

K. D. Sørensen, Stephanie A. Bien, Ali Amin Al Olama, 2019, Nature Communications.

Ethnic differences in the epidemiological characteristics of severe trauma due to falls from heights among children in northern Israel.

G. Rennert, A. Tamir, G. Bar-Joseph, 2007, The Israel Medical Association journal : IMAJ.

3,3'-Diindolylmethane induces apoptosis in human cancer cells.

G Rennert, G. Rennert, F. Fares, 1996, Biochemical and biophysical research communications.

Cancer Genetics Service Provision: A Comparison of Seven European Centres

G. Rennert, C. V. van Asperen, E. Legius, 2004, Public Health Genomics.

Circulating bilirubin levels and risk of colorectal cancer: serological and Mendelian randomization analyses

A. Peters, C. Ulrich, H. Brenner, 2020, BMC Medicine.

Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes

William S. Bush, Bin Zhu, Angeline S. Andrew, 2017, Nature Genetics.

Coffee Consumption and the Risk of Colorectal Cancer

S. Gruber, G. Rennert, H. Rennert, 2016, Cancer Epidemiology, Biomarkers & Prevention.

Vascular Disorders Preceding Diagnosis of Cancer: Distinguishing the Causal Relationship based on Bradford-Hill Guidelines

Gad Rennert, G. Rennert, D. Yeshurun, 2003, Angiology.

A comparison of the clinical characteristics of second primary and single primary sarcoma: A population based study

A. Neugut, G. Rennert, R. Bar-Deroma, 1992, Journal of surgical oncology.

7.6 – Effect of Ascorbigen on 7,12-Dimethylbenzanthracene-induced Mammary Tumor in Female Sprague-Dawley Rats

G. Rennert, S. Yannai, X. Ge, 2000 .

Association Between ABCG2, ABCB1, ABCC2 Efflux Transporter Single‐Nucleotide Variants and Irinotecan Adverse Effects in Patients With Colorectal Cancer: A Real‐Life Study

N. Gronich, G. Rennert, F. Lejbkowicz, 2022, Clinical pharmacology and therapeutics.

Hormonal and reproductive factors and reduction in the risk of colorectal cancer

S. Gruber, G. Rennert, H. Rennert, 2019, European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation.

Genome-wide association study of germline variants and breast cancer-specific mortality

A. Whittemore, W. Willett, S. Cross, 2019, British Journal of Cancer.

Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants

D. Steinemann, F. Couch, B. Bonanni, 2020, Genetics in Medicine.

Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses

Jack A. Taylor, W. Chung, S. Cross, 2019, bioRxiv.

Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

Michael Jones, Peter Kraft, Arnaud Droit, 2017, Nature Genetics.

Evaluation of Polygenic Risk Scores for Breast and Ovarian Cancer Risk Prediction in BRCA1 and BRCA2 Mutation Carriers

W. Chung, R. Nussbaum, F. Couch, 2017, Journal of the National Cancer Institute.

Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast–ovarian cancer susceptibility locus

A. Whittemore, L. Kiemeney, S. Cross, 2016, Nature Communications.

Fine-Scale Mapping at 9p22.2 Identifies Candidate Causal Variants That Modify Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

D. Steinemann, F. Couch, B. Bonanni, 2016, PloS one.

Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers

R. Nussbaum, D. Steinemann, V. Pankratz, 2014, Breast Cancer Research.

Association of PHB 1630 C>T and MTHFR 677 C>T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter study

V. Pankratz, F. Couch, B. Bonanni, 2012, British Journal of Cancer.

Pooled analysis of p53 mutations in hematological malignancies

V. Rotter, R. Unger, G. Rennert, 1998, Human mutation.

Cancer-driving H3G34V/R/D mutations block H3K36 methylation and H3K36me3–MutSα interaction

G. Rennert, Jun Fang, Haitao Li, 2018, Proceedings of the National Academy of Sciences.

Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry

Jane E. Carpenter, Jack A. Taylor, M. Beckmann, 2023, Genome Medicine.

Transcriptome ‐ wide association study of breast cancer risk by estrogen ‐ receptor status

Jack A. Taylor, W. Chung, S. Cross, 2020 .

Breast cancer risk following bilateral oophorectomy in BRCA1 and BRCA2 mutation carriers: an international case-control study.

T. Rebbeck, J. Klijn, P. Møller, 2005, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

Jane E. Carpenter, Jack A. Taylor, W. Chung, 2019, Nature Genetics.

Alcohol and lung cancer risk among never smokers: A pooled analysis from the international lung cancer consortium and the SYNERGY study

H. Morgenstern, K. Straif, H. Brenner, 2017, International journal of cancer.

BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers.

Dong Liang, Patrick Neven, Harvey Risch, 2016, Journal of the National Cancer Institute.

MicroRNA Polymorphisms and Risk of Colorectal Cancer

M. Shapero, S. Gruber, G. Rennert, 2014, Cancer Epidemiology, Biomarkers & Prevention.

MicroRNA Polymorphisms and Risk of Colorectal

M. Shapero, S. Gruber, G. Rennert, 2014 .

Pathologic Predictors of Microsatellite Instability in Colorectal Cancer

S. Gruber, G. Rennert, L. Tomsho, 2009, The American journal of surgical pathology.

Detecting K-ras mutations in stool from fecal occult blood test cards in multiphasic screening for colorectal cancer.

G. Rennert, H. Rennert, D. Brenner, 2007, Cancer letters.

Prevention and early detection of colorectal cancer--new horizons.

G. Rennert, 2007, Recent results in cancer research. Fortschritte der Krebsforschung. Progres dans les recherches sur le cancer.

K-ras Mutations in Sporadic Colorectal Tumors in Israel: Unusual High Frequency of Codon 13 Mutations and Evidence for Nonhomogeneous Representation of Mutation Subtypes

G. Rennert, A. Lerner, D. Kislitsin, 2002, Digestive Diseases and Sciences.

Phenotype of Microsatellite Unstable Colorectal Carcinomas: Well‐Differentiated and Focally Mucinous Tumors and the Absence of Dirty Necrosis Correlate With Microsatellite Instability

S. Gruber, G. Rennert, J. Greenson, 2003, The American journal of surgical pathology.

Utilization of K‐ras mutations identified in stool DNA for the early detection of colorectal cancer

G. Rennert, A. Lerner, Z. Lev, 2000, Journal of cellular biochemistry. Supplement.

Gene Expression Patterns in Mismatch Repair-Deficient Colorectal Cancers Highlight the Potential Therapeutic Role of Inhibitors of the Phosphatidylinositol 3-Kinase-AKT-Mammalian Target of Rapamycin Pathway

Bhramar Mukherjee, Stephen B Gruber, Rork Kuick, 2009, Clinical Cancer Research.

MRE11 deficiency increases sensitivity to poly(ADP-ribose) polymerase inhibition in microsatellite unstable colorectal cancers.

S. Gruber, G. Rennert, V. Moreno, 2011, Cancer research.

A Transcriptome-Wide Association Study Among 97,898 Women to Identify Candidate Susceptibility Genes for Epithelial Ovarian Cancer Risk.

Harvey Risch, Yian A Chen, Mads Thomassen, 2018, Cancer research.

University of Groningen Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk Couch,

F. Couch, B. Bonanni, O. Olopade, 2013 .

Accurate classification of MLH1/MSH2 missense variants with multivariate analysis of protein polymorphisms–mismatch repair (MAPP‐MMR)

Stephen B Gruber, Hoda Anton-Culver, Jonathan L. Velasquez, 2008, Human mutation.

Genome-wide association meta-analysis identifies pleiotropic risk loci for aerodigestive squamous cell cancers

M. Obeidat, Y. Bossé, L. Kiemeney, 2021, PLoS genetics.

Iam hiQ—a novel pair of accuracy indices for imputed genotypes

L. Kiemeney, A. Tardón, L. Marchand, 2022, BMC Bioinform..

I’am hiQ – A Novel Accuracy Index for Imputed Genotypes

L. Kiemeney, A. Tardón, L. Marchand, 2021 .

FGFR2 Is a Breast Cancer Susceptibility Gene in Jewish and Arab Israeli Populations

Stephen B. Gruber, Gad Rennert, S. Gruber, 2008, Cancer Epidemiology Biomarkers & Prevention.

Smoking attenuates the negative association between carotenoids consumption and colorectal cancer risk

S. Gruber, G. Rennert, G. Rozen, 2009, Cancer Causes & Control.

Common Genetic Variants and Modification of Penetrance of BRCA2-Associated Breast Cancer

M. Daly, D. Altshuler, F. Couch, 2010, PLoS genetics.

Common breast cancer-predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers.

Dieter Niederacher, Ute Hamann, Alfons Meindl, 2008, American journal of human genetics.

RAD51 135G-->C modifies breast cancer risk among BRCA2 mutation carriers: results from a combined analysis of 19 studies.

F. Couch, O. Olopade, T. Rebbeck, 2007, American journal of human genetics.

BRCA1 and BRCA2 founder mutations and the risk of colorectal cancer.

Ronit Almog, Stephen B Gruber, Gad Rennert, 2004, Journal of the National Cancer Institute.

Comprehensive functional annotation of susceptibility variants identifies genetic heterogeneity between lung adenocarcinoma and squamous cell carcinoma

L. Kiemeney, Hongbing Shen, S. Lam, 2020, Frontiers of Medicine.

Rare Variants in the DNA Repair Pathway and the Risk of Colorectal Cancer

S. Gruber, G. Rennert, D. Conti, 2021, Cancer Epidemiology, Biomarkers & Prevention.

Association Analysis of Driver Gene–Related Genetic Variants Identified Novel Lung Cancer Susceptibility Loci with 20,871 Lung Cancer Cases and 15,971 Controls

L. Kiemeney, Hongbing Shen, S. Lam, 2020, Cancer Epidemiology, Biomarkers & Prevention.

Genome‐wide association study of INDELs identified four novel susceptibility loci associated with lung cancer risk

Paul Brennan, John K Field, David C Christiani, 2020, International journal of cancer.

Genetic interaction analysis among oncogenesis-related genes revealed novel genes and networks in lung cancer development

M. S. Artigas, Y. Bossé, L. Kiemeney, 2019, Oncotarget.

Mendelian randomisation study of height and body mass index as modifiers of ovarian cancer risk in 22,588 BRCA1 and BRCA2 mutation carriers

W. Chung, D. Steinemann, F. Couch, 2019, British Journal of Cancer.

Human papillomavirus is not associated with colorectal cancer in a large international study

S. Gruber, T. Giordano, G. Rennert, 2010, Cancer Causes & Control.

Pleiotropy of genetic variants on obesity and smoking phenotypes: Results from the Oncoarray Project of The International Lung Cancer Consortium

Tao Wang, Yun-Chul Hong, John K Field, 2017, PloS one.

Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer

Jane E. Carpenter, Jack A. Taylor, W. Chung, 2019, Nature Communications.

Gene–gene interaction of AhRwith and within the Wntcascade affects susceptibility to lung cancer

L. Kiemeney, A. Tardón, A. Cox, 2022, European Journal of Medical Research.

Lung Cancer Risk in Never-Smokers of European Descent is Associated With Genetic Variation in the 5p15.33 TERT-CLPTM1Ll Region.

H. Morgenstern, L. Kiemeney, H. Brenner, 2019, Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer.

Systematic analyses of regulatory variants in DNase I hypersensitive sites identified two novel lung cancer susceptibility loci.

L. Kiemeney, Hongbing Shen, S. Lam, 2019, Carcinogenesis.

Novel Common Genetic Susceptibility Loci for Colorectal Cancer

Stephanie A. Bien, Elizabeth L. Barry, Aung Ko Win, 2018, Journal of the National Cancer Institute.

Genome-wide association study of colorectal cancer identifies six new susceptibility loci

Christopher P. Fischer, C. Carlson, A. LaCroix, 2015, Nature Communications.

Meta-analysis of new genome-wide association studies of colorectal cancer risk

C. Carlson, Lin S. Chen, A. LaCroix, 2011, Human Genetics.

Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers

Joshua M. Korn, M. Daly, D. Altshuler, 2011, Human Genetics.

RNASEL Mutation Screening and Association Study in Ashkenazi and Non-Ashkenazi Prostate Cancer Patients

G. Rennert, D. Bercovich, L. Kadouri, 2006, Cancer Epidemiology Biomarkers & Prevention.

Genetic anthropology of the colorectal cancer-susceptibility allele APC I1307K: evidence of genetic drift within the Ashkenazim.

J. Long, S. Gruber, G. Rennert, 2003, American journal of human genetics.

Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer

Jane E. Carpenter, A. Whittemore, W. Chung, 2016, Nature Communications.

Clinical Phenotype of Families with Longevity

G. Rennert, N. Barzilai, G. Atzmon, 2004, Journal of the American Geriatrics Society.

Genetic architectures of proximal and distal colorectal cancer are partly distinct

Richard T. Barfield, Stephanie A. Bien, G. Abecasis, 2020, Gut.

Long term follow-up of EGFR mutated NSCLC cases

N. Gronich, G. Rennert, H. Nechushtan, 2020, Translational oncology.

Artificial intelligence for detection of microsatellite instability in colorectal cancer—a multicentric analysis of a pre-screening tool for clinical application

T. Brinker, H. Grabsch, J. Chang-Claude, 2022, ESMO open.

Tumor immune infiltration estimated from gene expression profiles predicts colorectal cancer relapse

S. Gruber, G. Rennert, C. Amos, 2021, Oncoimmunology.

Immune-mediated genetic pathways resulting in pulmonary function impairment increase lung cancer susceptibility

J. Witte, M. Obeidat, Y. Bossé, 2019, Nature Communications.

Assessing Lung Cancer Absolute Risk Trajectory Based on a Polygenic Risk Model

L. Kiemeney, S. Lam, A. Tardón, 2021, Cancer Research.

Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk

Jane E. Carpenter, M. Beckmann, A. Børresen-Dale, 2020, Scientific Reports.

CDX2 polymorphisms, RNA expression, and risk of colorectal cancer.

David E. Misek, R. Kuick, S. Hanash, 2005, Cancer research.

The MLH1 D132H variant is associated with susceptibility to sporadic colorectal cancer

F. Collins, S. Gruber, G. Rennert, 2004, Nature Genetics.

PTPRJ Haplotypes and Colorectal Cancer Risk

S. Gruber, G. Rennert, L. Rozek, 2008, Cancer Epidemiology Biomarkers & Prevention.

Risk of colorectal cancer in self‐reported inflammatory bowel disease and modification of risk by statin and NSAID use

S. Gruber, G. Rennert, J. Greenson, 2011, Cancer.

Genetic variation in 8q24 associated with risk of colorectal cancer

S. Gruber, T. Giordano, G. Rennert, 2007, Cancer biology & therapy.

Protein-altering germline mutations implicate novel genes related to lung cancer development

M. S. Artigas, M. Obeidat, Y. Bossé, 2020, Nature Communications.

Targeted Prostate Cancer Screening in BRCA1 and BRCA2 Mutation Carriers: Results from the Initial Screening Round of the IMPACT Study

L. Kiemeney, R. Eeles, Z. Kote-Jarai, 2014, European urology.

Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment

Jaana M. Hartikainen, S. Cross, M. Beckmann, 2021, Breast Cancer Research.

A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers

Jane E. Carpenter, Jack A. Taylor, W. Chung, 2021, Nature Communications.

No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer.

Sandra L. Halverson, A. Whittemore, L. Kiemeney, 2016, Gynecologic oncology.

Mendelian randomization analysis of C-reactive protein on colorectal cancer risk.

James Y. Dai, P. Schrotz-King, H. Brenner, 2018, International journal of epidemiology.

The association between obesity and urinary tract infection.

G. Rennert, W. Saliba, O. Barnett‐Griness, 2013, European journal of internal medicine.

BLM Heterozygosity and the Risk of Colorectal Cancer

P. Gregersen, S. Gruber, J. Satagopan, 2002, Science.

A prospective study evaluating the usefulness of continuous supplemental oxygen in various endoscopic procedures.

G. Rennert, H. Rennert, R. Reshef, 1996, Israel journal of medical sciences.

Functional annotation of the 2q35 breast cancer risk locus implicates a structural variant in influencing activity of a long-range enhancer element

Jack A. Taylor, S. Cross, M. Beckmann, 2021, American journal of human genetics.

Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

Lara E Sucheston-Campbell, Simon G. Coetzee, Dennis J. Hazelett, 2017, Nature Genetics.

Common variants in breast cancer risk loci predispose to distinct tumor subtypes

Jack A. Taylor, S. Cross, P. Fasching, 2022, Breast cancer research : BCR.

Common breast cancer risk loci predispose to distinct tumor subtypes

Jack A. Taylor, S. Cross, P. Fasching, 2019, bioRxiv.

The predictive ability of the 313 variant–based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant

W. Chung, F. Couch, O. Olopade, 2021, Genetics in Medicine.

Physical activity and risks of breast and colorectal cancer: a Mendelian randomisation analysis

C. Ulrich, H. Brenner, J. Chang-Claude, 2020, Nature Communications.

Spontaneous and therapeutic abortions and the risk of breast cancer among BRCA mutation carriers

O. Olopade, B. Karlan, P. Møller, 2006, Breast Cancer Research.

Common Genetic Variants and Modification of Penetrance of BRCA2-Associated Breast Cancer

Joshua M. Korn, Debra, M. Daly, 2010, PLoS genetics.

Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers.

Mads Thomassen, Nina Ditsch, Dieter Niederacher, 2009, Human molecular genetics.

Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

Jane E. Carpenter, A. Whittemore, S. Cross, 2016, Breast Cancer Research.

A prospective prostate cancer screening programme for men with pathogenic variants in mismatch repair genes (IMPACT): initial results from an international prospective study

R. Eeles, Z. Kote-Jarai, F. Hamdy, 2021, The Lancet. Oncology.

Association of breast cancer risk in BRCA 1 and BRCA 2 mutation carriers with genetic variants showing differential allelic expression

R. Nussbaum, F. Couch, O. Olopade, 2016 .

An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers

W. Chung, R. Nussbaum, D. Steinemann, 2015, Breast Cancer Research.

Assessing Associations between the AURKA-HMMR-TPX2-TUBG1 Functional Module and Breast Cancer Risk in BRCA1/2 Mutation Carriers

W. Chung, R. Nussbaum, D. Steinemann, 2015, PloS one.

Germline variants and breast cancer survival in patients with distant metastases at primary breast cancer diagnosis

M. Beckmann, P. Fasching, A. Olshan, 2021, Scientific Reports.

Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21

I. Deary, T. Hudson, C. Greenwood, 2008, Nature Genetics.

Interplay between BRCA1 and RHAMM Regulates Epithelial Apicobasal Polarization and May Influence Risk of Breast Cancer

Marc Vidal, Dieter Niederacher, Roderic Guigó, 2011, PLoS biology.

Two truncating variants in FANCC and breast cancer risk

Jane E. Carpenter, M. Beckmann, P. Fasching, 2019, Scientific Reports.

Red meat and processed meat intake and risk of colorectal cancer: a population-based case–control study

S. Gruber, N. Gronich, G. Rennert, 2019, European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation.

Genotype-phenotype analysis of the Crohn’s disease susceptibility haplotype on chromosome 5q31

D. Jewell, S. Gruber, J. Struewing, 2003, Gut.

The role of CHADS2 and CHA2DS2‐VASc scores in the prediction of stroke in individuals without atrial fibrillation: a population‐based study

N. Gronich, G. Rennert, W. Saliba, 2016, Journal of thrombosis and haemostasis : JTH.

Antithrombotic therapy for prevention of stroke in clinical practice in the ED.

G. Rennert, A. Tamir, A. Kogan, 2007, The American journal of emergency medicine.

Usefulness of CHADS2 and CHA2DS2-VASc Scores in the Prediction of New-Onset Atrial Fibrillation: A Population-Based Study.

N. Gronich, G. Rennert, W. Saliba, 2016, The American journal of medicine.

Neutrophil to lymphocyte ratio and risk of a first episode of stroke in patients with atrial fibrillation: a cohort study

G. Rennert, W. Saliba, M. Elias, 2015, Journal of thrombosis and haemostasis : JTH.

Glycated hemoglobin and risk of first episode stroke in diabetic patients with atrial fibrillation: A cohort study.

G. Rennert, W. Saliba, M. Elias, 2015, Heart rhythm.

CHA2DS2-VASc score is directly associated with the risk of pulmonary embolism in patients with atrial fibrillation.

G. Rennert, W. Saliba, 2014, The American journal of medicine.

Association of statin use with spontaneous intracerebral hemorrhage

N. Gronich, G. Rennert, H. Rennert, 2018, Neurology.

A Genome-Wide Gene-Based Gene–Environment Interaction Study of Breast Cancer in More than 90,000 Women

James M. Hodge, Jack A. Taylor, K. Czene, 2022, Cancer research communications.

Mendelian randomisation study of smoking exposure in relation to breast cancer risk

Jack A. Taylor, S. Cross, M. Beckmann, 2021, British Journal of Cancer.

Combining Asian-European Genome-Wide Association Studies of Colorectal Cancer Improves Risk Prediction Across Race and Ethnicity

Christopher R. Gignoux, Peter T Campbell, D. Bishop, 2023, medRxiv.

Very high mutation rate in offspring of Chernobyl accident liquidators

H S Weinberg, A B Korol, V M Kirzhner, 2001, Proceedings of the Royal Society of London. Series B: Biological Sciences.

The value of mammography in different ethnic groups in Israel--analysis of mortality reduction and costs using CAN*TROL.

G. Rennert, 1991, Cancer detection and prevention.

Lymphocytic infiltration in stage II microsatellite stable colorectal tumors: A retrospective prognosis biomarker analysis

R. Emerson, M. Vignali, S. Gruber, 2020, PLoS medicine.

Breast Cancer Risk Factors and Survival by Tumor Subtype: Pooled Analyses from the Breast Cancer Association Consortium

S. Cross, M. Beckmann, P. Fasching, 2021, Cancer Epidemiology, Biomarkers & Prevention.

Tumor-Infiltrating Lymphocytes, Crohn's-Like Lymphoid Reaction, and Survival From Colorectal Cancer.

Stephen B Gruber, Gad Rennert, Stephanie L Schmit, 2016, Journal of the National Cancer Institute.

Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk.

S. Cross, M. Beckmann, P. Fasching, 2020, American journal of human genetics.

Fully transformer-based biomarker prediction from colorectal cancer histology: a large-scale multicentric study

Jakob Nikolas Kather, H. Grabsch, M. Hoffmeister, 2023, ArXiv.

The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

W. Chung, M. Beckmann, P. Fasching, 2019, npj Breast Cancer.

CYP3A7*1C allele: linking premenopausal oestrone and progesterone levels with risk of hormone receptor-positive breast cancers

Jane E. Carpenter, Jack A. Taylor, S. Cross, 2021, British Journal of Cancer.

Gynecologic malignancies in Ashkenazi families with the MSH2 A636P founder mutation.

S. Gruber, G. Rennert, F. Lejbkowicz, 2008, American journal of obstetrics and gynecology.

Associated Links Among Smoking, Chronic Obstructive Pulmonary Disease, and Small Cell Lung Cancer: A Pooled Analysis in the International Lung Cancer Consortium.

H. Morgenstern, L. Kiemeney, Hongbing Shen, 2015, EBioMedicine.

Are we getting closer to molecular population screening for colorectal cancer?

G. Rennert, 2009, Journal of the National Cancer Institute.

Protein-altering germline mutations implicate novel genes related to lung cancer development

M. S. Artigas, M. Obeidat, Y. Bossé, 2020, Nature Communications.

The pattern of diagnosis of a second primary tumor in the breast

A. Neugut, G. Rennert, E. Robinson, 2004, Breast Cancer Research and Treatment.

Tests for gene‐environment interaction from case‐control data: a novel study of type I error, power and designs

Jaeil Ahn, Bhramar Mukherjee, Nilanjan Chatterjee, 2008, Genetic epidemiology.

Clinical characteristics of non-Hodgkin's lymphoma as a second primary tumor: a population-based survey.

A. Neugut, G. Rennert, R. Epelbaum, 1996, Leukemia & lymphoma.

Association between myelofibrosis and thromboembolism: A population‐based retrospective cohort study

G. Rennert, W. Saliba, E. Mishchenko, 2020, Journal of thrombosis and haemostasis : JTH.

The EUROMED CANCER network: state-of-art of cancer screening programmes in non-EU Mediterranean countries.

L. Bisanti, G. Rennert, J. Espinàs, 2016, European journal of public health.

Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCA1/BRCA2 (CIMBA)

G Rennert, N Weerasooriya, K Offit, 2009, British Journal of Cancer.

Associated Links Among Smoking, Chronic Obstructive Pulmonary Disease, and Small Cell Lung Cancer: A Pooled Analysis in the International Lung Cancer Consortium

H. Morgenstern, L. Kiemeney, Hongbing Shen, 2015, EBioMedicine.

Associations of obesity and circulating insulin and glucose with breast cancer risk: a Mendelian randomization analysis.

Jeffery M. Meyer, Jack A. Taylor, A. Whittemore, 2018, International journal of epidemiology.

Candidate Genetic Modifiers for Breast and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

W. Chung, R. Nussbaum, D. Steinemann, 2014, Cancer Epidemiology, Biomarkers & Prevention.

Beyond aspirin—cancer prevention with statins, metformin and bisphosphonates

N. Gronich, G. Rennert, 2013, Nature Reviews Clinical Oncology.

Use of metformin and risk of breast and colorectal cancer.

S. Gruber, N. Gronich, G. Rennert, 2020, Diabetes research and clinical practice.

Risk-Reducing (Chemopreventive) Agents in Breast Cancer Prevention

N. Gronich, G. Rennert, 2016 .

Genetic Variation in 3-Hydroxy-3-Methylglutaryl CoA Reductase Modifies the Chemopreventive Activity of Statins for Colorectal Cancer

Stephen B Gruber, Gad Rennert, Victor Moreno, 2010, Cancer Prevention Research.

Causal relationships between body mass index, smoking and lung cancer: Univariable and multivariable Mendelian randomization

L. Kiemeney, Hongbing Shen, S. Lam, 2020, International journal of cancer.

Salicylic Acid and Risk of Colorectal Cancer: A Two-Sample Mendelian Randomization Study

David A. Drew, C. Ulrich, D. Bishop, 2021, medRxiv.

A network analysis to identify mediators of germline-driven differences in breast cancer prognosis

Gary D Bader, S. Cross, M. Beckmann, 2020, Nature Communications.

Oral Bisphosphonates and Improved Survival of Breast Cancer

N. Gronich, I. Lavi, G. Rennert, 2016, Clinical Cancer Research.

A novel colorectal cancer risk locus at 4q32.2 identified from an international genome-wide association study.

S. Gruber, J. Hopper, G. Rennert, 2014, Carcinogenesis.

A genome-wide association study for colorectal cancer identifies a risk locus in 14q23.1

L. Hou, J. Chang-Claude, M. Hoffmeister, 2015, Human Genetics.

Mendelian Randomization of Circulating Polyunsaturated Fatty Acids and Colorectal Cancer Risk

Aung Ko Win, C. Ulrich, D. English, 2020, Cancer Epidemiology, Biomarkers & Prevention.

Mendelian randomisation study of age at menarche and age at menopause and the risk of colorectal cancer

James Y. Dai, Aung Ko Win, C. Ulrich, 2018, British Journal of Cancer.

Tyrosine kinase-targeting drugs-associated heart failure

G Rennert, D R Abernethy, N. Gronich, 2017, British Journal of Cancer.

A network analysis to identify mediators of germline-driven differences in breast cancer prognosis

Gary D. Bader, Christine L. Clarke, Gary D Bader, 2020, Nature Communications.

Clustering Women’s Health Behaviors

G. Rennert, L. Hagoel, E. Neter, 2002, Health education & behavior : the official publication of the Society for Public Health Education.

Women ’ s Health Behaviors Clustering Women ’ s Health Behaviors

G. Rennert, Ma, L. Hagoel, 2001 .

Alcohol consumption and lung cancer risk: A pooled analysis from the International Lung Cancer Consortium and the SYNERGY study.

H. Morgenstern, K. Straif, H. Brenner, 2019, Cancer epidemiology.

The founder mutation MSH2*1906G-->C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish population.

P. Gregersen, M. King, C. Greenwood, 2002, American journal of human genetics.

Low Allele Frequency of MLH1 D132H in American Colorectal and Endometrial Cancer Patients

S. Gruber, G. Rennert, P. Goodfellow, 2005, Diseases of the colon and rectum.

Characterization of two Ashkenazi Jewish founder mutations in MSH6 gene causing Lynch syndrome

S. Gruber, S. Thibodeau, W. Foulkes, 2011, Clinical genetics.

Red cell distribution width and all-cause mortality in patients with atrial fibrillation: A cohort study

G. Rennert, W. Saliba, O. Barnett‐Griness, 2016, Journal of arrhythmia.

The association between red cell distribution width and stroke in patients with atrial fibrillation.

G. Rennert, W. Saliba, M. Elias, 2015, The American journal of medicine.

Rare germline copy number variants (CNVs) and breast cancer risk

Jack A. Taylor, S. Cross, M. Beckmann, 2022, Communications Biology.

Development of APE1 enzymatic DNA repair assays: low APE1 activity is associated with increase lung cancer risk

G. Rennert, T. Paz-Elizur, Z. Livneh, 2015, Carcinogenesis.

associated with increase lung cancer risk

G. Rennert, T. Paz-Elizur, Z. Livneh, 2015 .

Enzymatic MPG DNA repair assays for two different oxidative DNA lesions reveal associations with increased lung cancer risk.

G. Rennert, T. Paz-Elizur, Z. Livneh, 2014, Carcinogenesis.

Low Integrated DNA Repair Score and Lung Cancer Risk

G. Rennert, T. Paz-Elizur, Z. Livneh, 2013, Cancer Prevention Research.

N-Methylpurine DNA Glycosylase and OGG1 DNA Repair Activities: Opposite Associations With Lung Cancer Risk

G. Rennert, T. Paz-Elizur, Z. Livneh, 2012, Journal of the National Cancer Institute.

Recreational Physical Activity Modifies the Association Between a Common GH1 Polymorphism and Colorectal Cancer Risk

S. Gruber, G. Rennert, H. Rennert, 2008, Cancer Epidemiology Biomarkers & Prevention.

Wife's level of education and husband's risk of primary cardiac arrest.

D. Siscovick, G. Rennert, N. Weiss, 1988, American journal of public health.

Association between vaccination with the BNT162b2 mRNA COVID-19 vaccine and Bell's palsy: a population-based study

N. Gronich, G. Rennert, I. Doweck, 2021, The Lancet Regional Health - Europe.

Smoking, Gender, and Ethnicity Predict Somatic BRAF Mutations in Colorectal Cancer

S. Gruber, G. Rennert, V. Moreno, 2010, Cancer Epidemiology, Biomarkers & Prevention.

Nongenetic Determinants of Risk for Early-Onset Colorectal Cancer

Aung Ko Win, H. Brenner, J. Chang-Claude, 2021, JNCI cancer spectrum.

High prevalence of MUTYH associated polyposis among minority populations in Israel, due to rare founder pathogenic variants.

G. Rennert, K. Weiss, Y. Goldberg, 2023, Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver.

Laypersons' views of material incentives for enhancing colorectal cancer screening

G. Rennert, P. Feder-Bubis, L. Hagoel, 2015, Health expectations : an international journal of public participation in health care and health policy.

Screening with faecal occult blood test (FOBT) for colorectal cancer: assessment of two methods that attempt to improve compliance

G Rennert, I. Lavi, G. Rennert, 2001, European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation.

Calcium Intake and Bone Mass Development Among Israeli Adolescent Girls

G. Rennert, G. Rozen, H. Rennert, 2001, Journal of the American College of Nutrition.

Physical activity and risks of breast and colorectal cancer: a Mendelian randomisation analysis

C. Ulrich, J. Chang-Claude, M. Hoffmeister, 2020, Nature Communications.

Common MUTYH mutations and colorectal cancer risk in multiethnic populations

S. Gruber, G. Rennert, Ilana Cohen, 2012, Familial Cancer.

Political interpretation of scientific evidence--case study of breast cancer screening policies around the world.

G. Rennert, 2002, Recent results in cancer research. Fortschritte der Krebsforschung. Progres dans les recherches sur le cancer.

Ischemic stroke and myocardial ischemia in clopidogrel users and the association with CYP2C19 loss-of-function homozygocity: a real-world study

N. Gronich, I. Lavi, G. Rennert, 2021, The Pharmacogenomics Journal.

Polymorphisms in Alcohol Metabolism Genes ADH1B and ALDH2, Alcohol Consumption and Colorectal Cancer

G. Rennert, D. Cordero, M. Crous-Bou, 2013, PloS one.

Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21

Zanke, I. Deary, T. Hudson, 2008, Nature Genetics.

Beyond GWAS of Colorectal Cancer: Evidence of Interaction with Alcohol Consumption and Putative Causal Variant for the 10q24.2 Region.

Stephanie A. Bien, David A. Drew, A. Kundaje, 2022, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

Targeted prostate cancer screening in men with mutations in BRCA1 and BRCA2 detects aggressive prostate cancer: preliminary analysis of the results of the IMPACT study

Katherine M. Tucker, L. Kiemeney, H. Grönberg, 2011, BJU international.

From the bench to public health: population-level implementation intentions in colorectal cancer screening.

G. Rennert, L. Hagoel, E. Neter, 2014, American journal of preventive medicine.

Harnessing the Question-Behavior Effect to Enhance Colorectal Cancer Screening in an mHealth Experiment.

G. Rennert, L. Hagoel, E. Neter, 2016, American journal of public health.

Lower lung cancer rates in Jewish smokers in Israel and the USA

M. Spitz, G. Rennert, J. Muscat, 2015, International journal of cancer.

Fecal occult blood screening--trial evidence, practice and beyond.

G. Rennert, 2003, Recent results in cancer research. Fortschritte der Krebsforschung. Progres dans les recherches sur le cancer.

Population colorectal cancer screening with fecal occult blood test.

G Rennert, G. Rennert, H. Rennert, 2001, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

Genome-wide association study of lung adenocarcinoma in East Asia and comparison with a European population

L. Kiemeney, Y. Miyagi, B. Qian, 2023, Nature communications.

Rare copy number variants (CNVs) and breast cancer risk

Jack A. Taylor, S. Cross, M. Beckmann, 2021, bioRxiv.

Gene Expression Differences between Colon and Rectum Tumors

S. Gruber, T. Giordano, G. Rennert, 2011, Clinical Cancer Research.

CDX 2 Polymorphisms , RNA Expression , and Risk of Colorectal Cancer

David E. Misek, R. Kuick, S. Hanash, 2005 .

Lung cancer histology in Jews and Arabs in Israel, 1962-1982.

G. Rennert, H. Rennert, L. Epstein, 1991, The American review of respiratory disease.

Lung cancer in Israel, 1962–1982 I. Jews and Arabs

G. Rennert, A. Tamir, R. Steinitz, 1988, European Journal of Epidemiology.

Lung cancer histology in major ethnic groups among the Jews. Israel, 1962–1982

G. Rennert, H. Rennert, L. Epstein, 2004, European Journal of Epidemiology.

**Israel Cancer Registry, Ministry of Health, State of Israel Key words: Lung cancer - Incidence - Israel - Jews - Arabs The magnitude and dynamics of lung cancer incidence in Jews and Arabs in Israel between the years

G. Rennert, A. Tamir, L. Katz, 2004 .

Identification of susceptibility pathways for the role of chromosome 15q25.1 in modifying lung cancer risk

L. Wain, M. S. Artigas, M. Obeidat, 2018, Nature Communications.

Genetic modifiers of radon-induced lung cancer risk: a genome-wide interaction study in former uranium miners

S. Lam, A. Tardón, C. Haiman, 2018, International Archives of Occupational and Environmental Health.

Probing the diabetes and colorectal cancer relationship using gene – environment interaction analyses

Stephanie A. Bien, Peter T Campbell, A. Kundaje, 2022, British Journal of Cancer.

Breast cancer screening in 21 countries: delivery of services, notification of results and outcomes ascertainment.

S. Shapiro, G. Rennert, E. Paci, 1999, European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation.

Cancer prevention: from public health interventions to individual tailoring.

Gad Rennert, G. Rennert, 2007, European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation.

Handling Individuals with High Cancer Risk: One Size Doesn't Fit All.

G. Rennert, 2016, The Israel Medical Association journal : IMAJ.

Fecal DNA biomarkers for the detection of colorectal neoplasia: attractive, but is it feasible?

G. Rennert, D. Brenner, 2005, Journal of the National Cancer Institute.

High risk of colorectal and endometrial cancer in Ashkenazi families with the MSH2 A636P founder mutation.

S. Gruber, G. Rennert, V. Moreno, 2011, Gastroenterology.

Getting out of a wheelchair: an uncommon insertion mutation in exon 19 of EGFR responsive to erlotinib

G. Rennert, O. Kaidar-Person, J. Bar, 2014, SpringerPlus.

Selective serotonin reuptake inhibitors associated with increased mortality risk in breast cancer patients in Northern Israel.

G. Rennert, H. Rennert, Avital Fischer, 2022, International journal of epidemiology.

Distinct reproductive risk profiles for intrinsic-like breast cancer subtypes: pooled analysis of population-based studies.

C. Perou, A. Olshan, C. Vachon, 2022, Journal of the National Cancer Institute.

Discovery of common and rare genetic risk variants for colorectal cancer

Stephanie A. Bien, Aung Ko Win, Sarah C. Nelson, 2018, Nature Genetics.

Understanding the genetic complexity of puberty timing across the allele frequency spectrum

M. P. Concas, M. Jarvelin, E. Demerath, 2023, medRxiv.

Evaluation of European-based polygenic risk score for breast cancer in Ashkenazi Jewish women in Israel

S. Rosset, W. He, S. Cross, 2023, Journal of Medical Genetics.

Common variants in breast cancer risk loci predispose to distinct tumor subtypes

Jane E. Carpenter, Jack A. Taylor, S. Cross, 2022, Breast Cancer Research.

Preoperative direct oral anticoagulants treatment and all-cause mortality in elderly patients with hip fracture: A retrospective cohort study.

G. Rennert, W. Saliba, Shai Cohen, 2020, Thrombosis research.

Association between myelofibrosis and risk of non-hematologic malignancies: a population-based retrospective cohort study

G. Rennert, W. Saliba, E. Mishchenko, 2020, Annals of Hematology.

A Genetic Locus within the FMN1/GREM1 Gene Region Interacts with Body Mass Index in Colorectal Cancer Risk

Stephanie A. Bien, David A. Drew, Elizabeth L. Barry, 2023, Cancer research.

Cancer risk and overall survival in APC I1307K carriers.

S. Gruber, G. Rennert, L. Tomsho, 2020 .

Physical activity and risks of breast and colorectal cancer: A Mendelian randomization analysis

C. Ulrich, H. Brenner, J. Chang-Claude, 2019, bioRxiv.

Breast cancer risk variants at 6 q 25 display different phenotype associations and regulate ESR 1 , RMND 1 and CCDC 170

Wei Zheng, Mads Thomassen, Nicholas A. Sinnott-Armstrong, 2016 .

A genome-wide gene-environment interaction study of breast cancer risk for women of European ancestry

Jack A. Taylor, S. Cross, C. Vachon, 2023, Breast Cancer Research.

Risk Stratification for Early-Onset Colorectal Cancer Using a Combination of Genetic and Environmental Risk Scores: An International Multi-Center Study.

D. Bishop, J. Chang-Claude, M. Hoffmeister, 2022, Journal of the National Cancer Institute.

The gradient in mammography screening behavior: a lifestyle marker.

G. Rennert, L. Hagoel, E. Neter, 1999, Social science & medicine.

Transcriptome‐wide association study reveals candidate causal genes for lung cancer

Aurélie A G Gabriel, M. Obeidat, Y. Bossé, 2019, International journal of cancer.

Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes

Jin Hee Kim, L. Wain, M. Obeidat, 2017, Nature Genetics.

Transformer-based biomarker prediction from colorectal cancer histology: A large-scale multicentric study

Jakob Nikolas Kather, P. A. van den Brandt, H. Grabsch, 2023, Cancer cell.

Translational Research in Cancer Screening: Long-Term Population-Action Bridges to Diffuse Adherence

G. Rennert, L. Hagoel, E. Neter, 2021, International journal of environmental research and public health.

Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

Jane E. Carpenter, A. Whittemore, S. Cross, 2016, Breast Cancer Research.

The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

Jane E. Carpenter, W. Chung, M. Beckmann, 2019, npj Breast Cancer.

Genome-wide interaction analysis of folate for colorectal cancer risk.

Stephanie A. Bien, A. Kundaje, J. Wang, 2023, The American journal of clinical nutrition.

Excellent performance of Hemoccult Sensa in organised colorectal cancer screening.

G. Rennert, F. Lejbkowicz, A. Flugelman, 2013, European journal of cancer.

Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: implications for risk prediction.

V. Pankratz, F. Couch, O. Olopade, 2010, Cancer research.

Mendelian randomisation study of age at menarche and age at menopause and the risk of colorectal cancer

Stephanie A. Bien, James Y. Dai, Aung Ko Win, 2018, British Journal of Cancer.

Differences in the characteristics of families with BRCA1 and BRCA2 mutations in Israel

G. Rennert, H. Rennert, F. Fares, 2005, European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation.

University of Groningen Identification of a BRCA 2-Specific Modifier Locus at 6 p 24 Related to Breast Cancer

D. Altshuler, V. Pankratz, F. Couch, 2017 .

Identification of susceptibility pathways for the role of chromosome 15q25.1 in modifying lung cancer risk

L. Wain, M. Obeidat, Y. Bossé, 2018, Nature Communications.

Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

A. Whittemore, S. Cross, R. Nussbaum, 2016, Breast Cancer Research.

A Germline Variant on Chromosome 4q31.1 Associates with Susceptibility to Developing Colon Cancer Metastasis

M. Adams, R. Elston, S. Gruber, 2016, PLoS ONE.

Reply: Allelic imbalance of TGFBR1 is not a major contributor to the genetic predisposition to colorectal cancer

S. Gruber, G. Rennert, V. Moreno, 2011, British Journal of Cancer.

Obesity, metabolic factors and risk of different histological types of lung cancer: A Mendelian randomization study

Hongbing Shen, A. Tardón, L. Marchand, 2017, PloS one.

No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer.

Sandra L. Halverson, A. Whittemore, L. Kiemeney, 2016, Gynecologic oncology.

Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes

Kristen S Purrington, Jack A. Taylor, A. Whittemore, 2018, American Journal of Human Genetics.

Identification of six new susceptibility loci for invasive epithelial ovarian cancer

Yurii B. Shvetsov, Simon G. Coetzee, Dennis J. Hazelett, 2014, Nature Genetics.

A Transcriptome-Wide Association Study Among 97,898 Women to Identify Candidate Susceptibility Genes for Epithelial Ovarian Cancer Risk.

L. Kiemeney, P. Fasching, R. Nussbaum, 2018, Cancer research.

Aspirin and NSAID use and lung cancer risk: a pooled analysis in the International Lung Cancer Consortium (ILCCO)

V. McCormack, A. Tjønneland, L. Marchand, 2011, Cancer Causes & Control.

Genetic Epidemiology

K. Humphreys, O. Olopade, B. Karlan, 2011, Methods in Molecular Biology.

Oral contraceptives and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers.

F. Couch, O. Olopade, J. Klijn, 2002, Journal of the National Cancer Institute.

Genome-wide association study of germline variants and breast cancer-specific mortality

A. Whittemore, W. Willett, S. Cross, 2019, British Journal of Cancer.

Combining Asian and European genome-wide association studies of colorectal cancer improves risk prediction across racial and ethnic populations

Peter T Campbell, A. Zauber, A. Wolk, 2023, Nature communications.

Better Ask Than Tell: Responses to mHealth Interrogative Reminders and Associations With Colorectal Cancer Screening Subsequent Uptake in a Prospective Cohort Intervention

G. Rennert, L. Hagoel, E. Neter, 2019, JMIR mHealth and uHealth.

Inference of the Haplotype Effect in a Matched Case-Control Study Using Unphased Genotype Data

S. Gruber, S. Sinha, G. Rennert, 2008, The international journal of biostatistics.

A Likelihood Ratio Approach for Utilizing Case-Control Data in the Clinical Classification of Rare Sequence Variants: Application to BRCA1 and BRCA2

Jack A. Taylor, C. Vachon, K. Czene, 2023, Human Mutation.

Prostate-specific antigen velocity in a prospective prostate cancer screening study of men with genetic predisposition

L. Kiemeney, L. Andrews, R. Eeles, 2018, British Journal of Cancer.

High risk of colorectal and endometrial cancer in Ashkenazi families with the MSH2 A636P founder mutation.

S. Gruber, G. Rennert, V. Moreno, 2011, Gastroenterology.

Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers.

F. Couch, B. Bonanni, J. Benítez, 2009, Human molecular genetics.

Genetic Epidemiology

K. Humphreys, O. Olopade, B. Karlan, 2020, Methods in Molecular Biology.

Genetic variation in IGF-1 and breast cancer risk in Ashkenazi carriers and noncarriers of BRCA1/2 mutations

G. Rennert, F. Lejbkowicz, M. Pinchev, 2009, European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation.

Heterozygote advantage at HLA class I and II loci and reduced risk of colorectal cancer

G. Rennert, R. Sanz-Pamplona, J. Greenson, 2023, Frontiers in immunology.

Laypersons' views of material incentives for enhancing colorectal cancer screening

G. Rennert, P. Feder-Bubis, L. Hagoel, 2015, Health expectations : an international journal of public participation in health care and health policy.

International comparison of performance measures for screening mammography: can it be done?

G. Rennert, B. Yankaskas, J. Bulliard, 2004, Journal of medical screening.

Implications of Russian immigration on mortality patterns in Israel.

G. Rennert, 1994, International journal of epidemiology.

Genetic risk impacts the association of menopausal hormone therapy with colorectal cancer risk

Stephanie A. Bien, A. Kundaje, S. Larsson, 2024, British journal of cancer.

PTPRJ Haplotypes and Colorectal Cancer Risk

S. Gruber, G. Rennert, L. Rozek, 2008, Cancer Epidemiology Biomarkers & Prevention.

Transcriptome-wide association study of breast cancer risk by estrogen-receptor status

Jack A. Taylor, S. Cross, C. Vachon, 2020, Genetic epidemiology.

Enzymatic MPG DNA repair assays for two different oxidative DNA lesions reveal associations with increased lung cancer risk.

G. Rennert, T. Paz-Elizur, Z. Livneh, 2014, Carcinogenesis.

Large-scale alternative polyadenylation (APA)-wide association studies to identify putative susceptibility genes in human common cancers

G. Rennert, G. Casey, Q. Cai, 2023, medRxiv.

Germline genetic regulation of the colorectal tumor immune microenvironment

G. Rennert, R. Sanz-Pamplona, J. Greenson, 2024, BMC genomics.

Lung Cancer in Ever- and Never-Smokers: Findings from Multi-Population GWAS Studies

Kristen S Purrington, Y. Bossé, L. Kiemeney, 2024, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.