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MSc: Molecular Genetics of Human Disease, University College London, UK, 2012-2013.
PhD: Molecular Genetics and Genomics, Wayne State State University, Detroit, MI, 2014-2018.
Fellowship: Laboratory Genetics and genomics, Mayo Clinic, Rochester, MN, 2018-2021.
Molecular and cytogenetics
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.
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.
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.
Unconventional Diagnosis Based on Somatic Findings through Germ Line Whole-Exome Sequencing.
Lopes, JL; Rasmussen, KJ; Mehta, N; Boczek, NJ; Hasadsri, L.
Encyclopedia of Evolutionary Psychological Science.
: Springer International Publishing;
Springer International Publishing;
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.
Whole Exome Sequencing: A Necessary Tool for the Future of Clinical Cancer Care.
Chaudhry, S; Lopes, J; Levin, N; Tainsky, M.
Reanalysis of BRCA1/2 negative high risk ovarian cancer patients reveals novel germline risk loci and insights into missing heritability.
Stafford, JL; Dyson, G; Levin, NK; Chaudhry, S; Rosati, R; Kalpage, H; Wernette, C; Petrucelli, N; Simon, MS; Tainsky, MA.
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