Identification of sex-specific genetic associations in response to opioid analgesics in a White, non-Hispanic cohort from Southeast Minnesota.
Lopes, GS; Lopes, JL; Bielinski, SJ; Armasu, SM; Zhu, Y; Cavanaugh, DC; Moyer, AM; Jacobson, DJ; Wang, L; Jiang, R; et al.
Pharmacogenomics Journal.
2022;
22:117-123.
Germline mutations in apoptosis pathway genes in ovarian cancer; the functional role of a TP53I3 (PIG3) variant in ROS production and DNA repair.
Chaudhry, SR; Lopes, J; Levin, NK; Kalpage, H; Tainsky, MA.
Cell Death Discovery.
2021;
7.
Most noninvasive prenatal screens failing due to inadequate fetal cell free DNA are negative for trisomy when repeated.
Lopes, JL; Lopes, GS; Enninga, EA L; Kearney, HM; Hoppman, NL; Rowsey, RA.
Prenatal Diagnosis.
2020;
40:831-837.
Characterizing false-positive fluorescence in situ hybridization results by mate-pair sequencing in a patient with chronic myeloid leukemia and progression to myeloid blast crisis.
Lopes, JL; Webley, M; Pitel, BA; Pearce, KE; Smadbeck, JB; Johnson, SH; Vasmatzis, G; Sukov, WR; Greipp, PT; Hoppman, NL; et al.
Cancer genetics.
2020;
243:48-51.
Unconventional Diagnosis Based on Somatic Findings through Germ Line Whole-Exome Sequencing.
Lopes, JL; Rasmussen, KJ; Mehta, N; Boczek, NJ; Hasadsri, L.
Clinical Chemistry.
2020;
66:48-51.
Encyclopedia of Evolutionary Psychological Science.
Lopes, J.
.
: Springer International Publishing;
Springer International Publishing;
2020.
FANCM, RAD1, CHEK1 and TP53I3 act as BRCA-like tumor suppressors and are mutated in hereditary ovarian cancer.
Lopes, JL; Chaudhry, S; Lopes, GS; Levin, NK; Tainsky, MA.
Cancer genetics.
2019;
235-236:57-64.
Whole Exome Sequencing: A Necessary Tool for the Future of Clinical Cancer Care.
Chaudhry, S; Lopes, J; Levin, N; Tainsky, M.
2017;
5:1106-1107.