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Eckel‐Passow, Jeanette E.

https://orcid.org/0000-0002-6113-1114

Mayo Clinic

Mayo Clinic

Citations 164

Transcriptome-Wide Association Study Identifies New Candidate Susceptibility Genes for Glioma
Atkins, Isabelle, Kinnersley, Ben , Ostrom, Quinn T. , Labrèche, Karim , Il’yasova, Dora , Armstrong, Georgina , Eckel‐Passow, Jeanette E. , Schoemaker, Minouk J. , Nöthen, Markus M. , Barnholtz‐Sloan, Jill S. , Simon, Matthias , Rajaraman, Preetha , Shildkraut, Joellen, Bernstein, Jonine L. , Jöckel, Karl‐Heinz, Lai, Rose , Claus, Elizabeth B. , Johansen, Christoffer , Wrensch, Margaret , Melin, Beatrice , Jenkins, Robert B. , Sanson, Marc , Bondy, Melissa L. , Houlston, Richard S. , Swerdlow, Anthony J , Houlston, Richard S , Barnholtz-Sloan, Jill S , Nöthen, Markus M , Sanson, Marc , Schoemaker, Minouk J , Armstrong, Georgina , Swerdlow, Anthony J. , Chanock, Stephen Jacob , Hoffmann, Per , Olson, Sara H. , Ostrom, Quinn T

Cancer Research | February 1, 2019 | Volume: 79 | Issue: 8 | Pages: 2065-2071

10.1158/0008-5472.can-18-2888 Get It

Abstract Genome-wide association studies (GWAS) have so far identified 25 loci associated with glioma risk, with most showing specificity for either glioblastoma (GBM) or non-GBM tumors. The majority of these GWAS susceptibility variants reside in noncoding regions and the causal genes underlying the associations are largely unknown. Here we performed a transcriptome-wide association study to search for novel risk loci and candidate causal genes at known GWAS loci using Genotype-Tissue Expression Project (GTEx) data to predict cis-predicted gene expression in relation to GBM and non-GBM risk in conjunction with GWAS summary statistics on 12,488 glioma cases (6,183 GBM and 5,820 non-GBM) and 18,169 controls. Imposing a Bonferroni-corrected significance level of P < 5.69 × 10−6, we identified 31 genes, including GALNT6 at 12q13.33, as a candidate novel risk locus for GBM (mean Z = 4.43; P = 5.68 × 10−6). GALNT6 resides at least 55 Mb away from any previously identified glioma risk variant, while all other 30 significantly associated genes were located within 1 Mb of known GWAS-identified loci and were not significant after conditioning on the known GWAS-identified variants. These data identify a novel locus (GALNT6 at 12q13.33) and 30 genes at 12 known glioma risk loci associated with glioma risk, providing further insights into glioma tumorigenesis. Significance: This study identifies new genes associated with glioma risk, increasing understanding of how these tumors develop.
Loss of BAP1 and PBRM1 expression in non-clear cell renal cell carcinomas compared to clear cell renal cell carcinomas.
Serie, Daniel, Eckel‐Passow, Jeanette E. , Parasramka, Mansi, Cheville, John C. , Parker, Alexander S. , Ho, Thai H. , Kapur, Payal , Joseph, Richard W. , Brugarolas, James

Journal of Clinical Oncology | January 3, 2019 | Volume: 32 | Issue: 15_suppl | Pages: 4529-4529

10.1200/jco.2014.32.15_suppl.4529 Get It

Association of genomic analysis of immune function genes and clinical outcome in the NCCTG (Alliance) N9831 adjuvant trastuzumab trial.
Perez, Edith A. , Thompson, E. Aubrey , Anderson, S. Keith , Asmann, Yan W. , Eckel‐Passow, Jeanette E. , Tenner, Kathleen , Jen, Jin , Fan, Jian‐Bing , Geiger, Xochiquetzal J., McCullough, Ann E. , Chen, Beiyun, Zschunke, Michael A., Jenkins, Robert B. , Reinholz, Monica M., Kalari, Krishna R. , Dueck, Amylou C. , Sledge, George W. , Winer, Eric P. , Gralow, Julie R. , Ballman, Karla V.

Journal of Clinical Oncology | January 3, 2019 | Volume: 32 | Issue: 15_suppl | Pages: 509-509

10.1200/jco.2014.32.15_suppl.509 Get It

Association of loss of BAP1 expression in cell renal cell carcinomas with PDL1 expression.
Serie, Daniel, Cheville, John C. , Eckel‐Passow, Jeanette E. , Parasramka, Mansi, Kwon, Eugene D., Thompson, R. Houston, Parker, Alexander S. , Joseph, Richard W. , Kapur, Payal , Ho, Thai H. , Brugarolas, James

Journal of Clinical Oncology | January 3, 2019 | Volume: 32 | Issue: 15_suppl | Pages: 4530-4530

10.1200/jco.2014.32.15_suppl.4530 Get It

COMP-05. EVALUATION OF A DEEP LEARNING ARCHITECTURE FOR MRI PREDICTION OF IDH, 1p19q AND TERT IN GLIOMA PATIENTS
Korfiatis, Panagiotis , Buckner, Jan C. , Eckel‐Passow, Jeanette E. , Decker, Paul A. , Jenkins, Robert B. , Wrensch, Margaret , Wiencke, John, Hansen, Helen, Rice, Terri, McCoy, Lucie , Nelson, Sarah J. , Clarke, Jennifer , Taylor, Jennie , Luks, Tracy , Lachance, Daniel Honore , Parney, Ian F. , Decker, Paul A. , Wiencke, John K. , Hansen, Helen M. , Erickson, Bradley J.

Neuro-Oncology | November 5, 2018 | Volume: 20 | Issue: suppl_6 | Pages: vi64-vi64

10.1093/neuonc/noy148.260 Get It

GENE-29. DLL3 AND ETV1 ARE INACTIVATED/METHYLATED IN CIC WILD-TYPE, IDH-MUTATED, 1p/19q-CODELETED GLIOMA
Kosel, Matthew , Decker, Paul A. , Caron, Alissa, Sarkar, Gobinda , Halder, Chandralekha, Tian, Shulan , Eckel‐Passow, Jeanette E. , Jenkins, Robert B. , Lachance, Daniel Honore , Decker, Paul A. , Kollmeyer, Thomas M. , Drucker, Kristen , Knight, Andrew, Abyzov, Alexej , Burns, Terry C. , Giannini, Caterina

Neuro-Oncology | November 5, 2018 | Volume: 20 | Issue: suppl_6 | Pages: vi109-vi109

10.1093/neuonc/noy148.455 Get It

TMOD-18. THE PATIENT DERIVED XENOGRAFT NATIONAL RESOURCE: A COMPREHENSIVE COLLECTION OF HIGH-GRADE GLIOMA MODELS FOR PRE-CLINICAL AND TRANSLATIONAL STUDIES
Tian, Shulan , Peng, Sen, Carlson, Brett L. , Kitange, Gaspar J. , Evers, Lisa, Decker, Paul A. , Kosel, Matthew , Klee, Eric W. , James, C. David , Eckel‐Passow, Jeanette E. , Verhaak, Roel G.W. , Jenkins, Robert B. , Vaubel, Rachael A. , Remonde, Dioval , Schroeder, Mark A. , Kollmeyer, Thomas M. , Mladek, Ann C. , Daniel, J. , Decker, Paul A. , Berens, Michael E. , Califano, Andrea , Lachance, Daniel Honore , Sulman, Erik P. , Tran, Nhan L. , Giannini, Caterina , Parney, Ian F. , Sarkaria, Jann N.

Neuro-Oncology | November 5, 2018 | Volume: 20 | Issue: suppl_6 | Pages: vi272-vi272

10.1093/neuonc/noy148.1130 Get It