Author details

Full Name

Darryl Nousome

Affiliation

ORCID

Career Start Year

2012

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37534375	Immunologic Assessment of Tumors from a Race-matched Military Cohort Identifies Mast Cell Depletion as a Marker of Prostate Cancer Progression.		2023
37922907	Sequencing-based functional assays for classification of BRCA2 variants in mouse ESCs.		2023
37713444	Saturation genome editing of 11 codons and exon 13 of BRCA2 coupled with chemotherapeutic drug response accurately determines pathogenicity of variants.	PLoS Genet	2023
37707375	Early Immune Changes Support Signet Ring Cell Dormancy in CDH1-Driven Hereditary Diffuse Gastric Carcinogenesis.	Mol Cancer Res	2023
37034649	Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.	medRxiv	2023
37343085	overexpression as a predictive biomarker for CHK1 inhibitor response in PARP inhibitor-resistant -mutant ovarian cancer.		2023
36705597	Phase I Study and Cell-Free DNA Analysis of T-DM1 and Metronomic Temozolomide for Secondary Prevention of HER2-Positive Breast Cancer Brain Metastases.	Clin Cancer Res	2023
37239075	Association of <i>TP53</i> Single Nucleotide Polymorphisms with Prostate Cancer in a Racially Diverse Cohort of Men.	Biomedicines	2023
36609596	Five-year survival of patients with late-stage prostate cancer: comparison of the Military Health System and the U.S. general population.	Br J Cancer	2023
34428537	Impact of Age and Race on Health-Related Quality of Life Outcomes in Patients Undergoing Radical Prostatectomy for Localized Prostate Cancer.	Urology	2022
35638719	Race-specific prostate cancer outcomes in a cohort of military health care beneficiaries undergoing surgery: 1990-2017.	Cancer Med	2022
36268164	Erratum: Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium.	HGG Adv	2022
35616266	Race-specific prostate cancer outcomes in a cohort of low and favorable-intermediate risk patients who underwent external beam radiation therapy from 1990 to 2017.	Cancer Med	2022
35551307	Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.	Nat Genet	2022
35399580	Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium.	HGG Adv	2022
36733941	Identification of a dysfunctional exon-skipping splice variant in / causal for renal hypouricemia type 2.		2022
35292633	Germline mutation landscape of DNA damage repair genes in African Americans with prostate cancer highlights potentially targetable RAD genes.	Nat Commun	2022
33217471	Retinal Nerve Fiber Layer Thickness in Healthy Eyes of Black, Chinese, and Latino Americans: A Population-Based Multiethnic Study.	Ophthalmology	2021
33575208	Age and Tumor Differentiation-Associated Gene Expression Based Analysis of Non-Familial Prostate Cancers.	Front Oncol	2021
32821522	A Mitochondrial Genome-Wide Association Study of Cataract in a Latino Population.	Transl Vis Sci Technol	2020
30487263	Multiethnic Genome-Wide Association Study of Diabetic Retinopathy Using Liability Threshold Modeling of Duration of Diabetes and Glycemic Control.	Diabetes	2019
25145691	Serum anti-MÃ¼llerian hormone levels in reproductive-age women with relapsing-remitting multiple sclerosis.	Multiple Sclerosis Journal	2015
25518914	Brain Tumor Epidemiology - A Hub within Multidisciplinary Neuro-oncology. Report on the 15th Brain Tumor Epidemiology Consortium (BTEC) Annual Meeting, Vienna, 2014.	Clin Neuropathol	2015
24586730	Genome-wide methylation analyses in glioblastoma multiforme.	PLoS One	2014
23433810	Maternal and offspring xenobiotic metabolism haplotypes and the risk of childhood acute lymphoblastic leukemia.	Leukemia Research	2013
24367687	Using a Bayesian hierarchical model for identifying single nucleotide polymorphisms associated with childhood acute lymphoblastic leukemia risk in case-parent triads.	PLoS ONE	2013
23059057	A GCH1 haplotype and risk of neural tube defects in the National Birth Defects Prevention Study.	Mol Genet Metab	2012
22941668	A case-parent triad assessment of folate metabolic genes and the risk of childhood acute lymphoblastic leukemia.	Cancer Causes and Control	2012
22994552	Maternal variation in EPHX1, a xenobiotic metabolism gene, is associated with childhood medulloblastoma: an exploratory case-parent triad study.	Pediatr Hematol Oncol	2012