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Jaime L. Lopes

Observed names: Jaime L Lopes, Jaime Lopes
ORCID: 0000-0002-9795-1093
Observed ORCID: 0000-0002-9795-1093
OpenAlex ID: A5048885376
Targeted Genotyping in Clinical Pharmacogenomics
2022 · Jaime L. Lopes, Kimberley Harris, et al. · Journal of Molecular Diagnostics · 36
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Germline mutations in apoptosis pathway genes in ovarian cancer; the functional role of a TP53I3 (PIG3) variant in ROS production and DNA repair
2021 · Sophia R. Chaudhry, Jaime Lopes, et al. · Cell Death Discovery · 30
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FANCM, RAD1, CHEK1 and TP53I3 act as BRCA-like tumor suppressors and are mutated in hereditary ovarian cancer
2019 · Jaime L. Lopes, Sophia Chaudhry, et al. · Cancer Genetics · 27
Most noninvasive prenatal screens failing due to inadequate fetal cell free DNA are negative for trisomy when repeated
2020 · Jaime L. Lopes, Guilherme S. Lopes, et al. · Prenatal Diagnosis · 14
Identification of sex-specific genetic associations in response to opioid analgesics in a White, non-Hispanic cohort from Southeast Minnesota
2022 · Guilherme S. Lopes, Jaime L. Lopes, et al. · The Pharmacogenomics Journal · 12
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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
2020 · Jaime L. Lopes, Matthew Webley, et al. · Cancer Genetics · 10
Aminoglycoside induced ototoxicity risk in the cystic fibrosis population: The utility of large‐scale screening
2022 · Jaime Lopes, Noemi Vidal‐Folch, et al. · Pediatric Pulmonology · 5
Uniparental disomy of multiple chromosomes in two cases with a complex phenotype
2023 · Katarzyna Polonis, Jaime L. Lopes, et al. · American Journal of Medical Genetics Part A · 4
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Expanding Access to Genome Sequencing: Higher Diagnostic Yield in Self‐Referred Participants From the CincyKidsSeq Study and Implications for Hybrid Models of Genetic Service Delivery
2025 · Kristin Theobald, Amelle Shillington, et al. · Clinical Genetics · 1
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Genotypic and phenotypic spectrum of hereditary spastic paraplegia 56: insights from novel CYP2U1 variants and a literature review
2026 · Kochakorn Buasri, Kristin Theobald, et al. · BMC Neurology
P262: Transformative care through genome sequencing: Insights from the first 100 patients in the CincyKidsSeq Study
2025 · Kristin Theobald, Farrah Jackson, et al. · Genetics in Medicine Open
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The Innate Immune System Surveillance Biomarker p87 in African Americans and Caucasians with Small High-Grade Dysplastic Adenoma [SHiGDA] and Right-Sided JAK3 Colon Mutations May Explain the Presence of Multiple Cancers Revealing an Important Minority of Patients with JAK3 Mutations and Colorectal Neoplasia
2024 · Martin Tobi, Xiaoqing Zhao, et al. · Gastrointestinal Disorders
P585: Amplification-based nanopore sequencing accurately detects HBA and HBB SNVs, indels, and structural variants in clinical thalassemia samples
2024 · Jaime Lopes, Marcus Cannon, et al. · Genetics in Medicine Open
16. Uniparental disomy (UPD) of multiple chromosomes in two cases with a complex phenotype
2022 · Katarzyna Polonis, Jaime L. Lopes, et al. · Cancer Genetics
Chromosomal microarray analysis offers superior cytogenomic evaluation of products of conception as compared to standard karyotype
2021 · Jaime Lopes, Nicole Hoppman, et al. · Molecular Genetics and Metabolism
35. Frequencies of Turner syndrome abnormalities as detected by high resolution chromosomal microarray in products of conception and postnatal blood samples
2021 · Jaime L. Lopes, Elyse Mitchell, et al. · Cancer Genetics
Unconventional Diagnosis Based on Somatic Findings through Germ Line Whole-Exome Sequencing
2019 · Jaime L Lopes, Kristen J Rasmussen, et al. · Clinical Chemistry
Moss-embroidered electrodes for an ECG monitoring shirt
2017 · Tim Bolle, Jaime L. Lopes, et al. · RWTH Publications (RWTH Aachen)
Works count: 18
Citation count: 139
H-index: 6
I10-index: 6
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