Author details

Full Name

Eric Karlins

Affiliation

ORCID

Career Start Year

2003

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36787739	Targeted long-read sequencing of the Ewing sarcoma 6p25.1 susceptibility locus identifies germline-somatic interactions with EWSR1-FLI1 binding.	Am J Hum Genet	2023
36991516	DNA methylation age in paired tumor and adjacent normal breast tissue in Chinese women with breast cancer.	Clin Epigenetics	2023
35753512	Clinical exome sequencing of 1000 families with complex immune phenotypes: Toward comprehensive genomic evaluations.	J Allergy Clin Immunol	2022
36166305	Immunogenetics associated with severe coccidioidomycosis.	JCI Insight	2022
32970968	Age-related DNA methylation in paired normal and tumour breast tissue in Chinese breast cancer patients.	Epigenetics	2021
32923912	Subsequent Neoplasm Risk Associated With Rare Variants in DNA Damage Response and Clinical Radiation Sensitivity Syndrome Genes in the Childhood Cancer Survivor Study.	JCO Precis Oncol	2020
32191290	Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in Patients With Osteosarcoma.	JAMA Oncol	2020
32881892	Low-frequency variation near common germline susceptibility loci are associated with risk of Ewing sarcoma.	PLoS One	2020
31101124	Blood DNA methylation and breast cancer risk: a meta-analysis of four prospective cohort studies.	Breast Cancer Res	2019
30910758	Genome-Wide Association Study in Irradiated Childhood Cancer Survivors Identifies HTR2A forÂ Subsequent Basal Cell Carcinoma.	J Invest Dermatol	2019
29510662	Successful use of whole genome amplified DNA from multiple source types for high-density Illumina SNP microarrays.	BMC Genomics	2018
30093639	Genome-wide association study identifies multiple new loci associated with Ewing sarcoma susceptibility.	Nat Commun	2018
29210060	Genome-wide association study identifies the GLDC/IL33 locus associated with survival of osteosarcoma patients.	Int J Cancer	2018
27902461	Whole exome sequencing in 75 high-risk families with validation and replication in independent case-control studies identifies TANGO2, OR5H14, and CHAD as new prostate cancer susceptibility genes.	Oncotarget	2017
28861920	Higher-than-expected population prevalence of potentially pathogenic germline TP53 variants in individuals unselected for cancer history.	Hum Mutat	2017
29033373	Evaluating the Causal Link Between Malaria Infection and Endemic Burkitt Lymphoma in Northern Uganda: A Mendelian Randomization Study.	EBioMedicine	2017
29059430	Genome-Wide Association Study to Identify Susceptibility Loci That Modify Radiation-Related Risk for Breast Cancer After Childhood Cancer.	J Natl Cancer Inst	2017
27087322	Biallelic BRCA2 Mutations Shape the Somatic Mutational Landscape of Aggressive Prostate Tumors.	Am J Hum Genet	2016
27291797	Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome.	Nat Commun	2016
26232412	Comparison against 186 canid whole-genome sequences reveals survival strategies of an ancient clonally transmissible canine tumor.	Genome Res	2015
25767210	Homologous Mutation to Human BRAF V600E Is Common in Naturally Occurring Canine Bladder Cancer--Evidence for a Relevant Model System and Urine-Based Diagnostic Test.	Mol Cancer Res	2015
23555311	A copy number variant at the KITLG locus likely confers risk for canine squamous cell carcinoma of the digit.	PLoS Genet	2013
20332101	Fine scale mapping of the breast cancer 16q12 locus.	Hum Mol Genet	2010
18762813	Association of FGFR4 genetic polymorphisms with prostate cancer risk and prognosis.	Prostate Cancer Prostatic Dis	2009
19223389	FGFR2 variants and breast cancer risk: fine-scale mapping using African American studies and analysis of chromatin conformation.	Hum Mol Genet	2009
19476645	No evidence of BRCA2 mutations in chromosome 13q-linked Utah high-risk prostate cancer pedigrees.	BMC Res Notes	2009
17412960	A single IGF1 allele is a major determinant of small size in dogs.	Science	2007
17700570	Rare germline mutations in the BRCA2 gene are associated with early-onset prostate cancer.	Br J Cancer	2007
16606767	Case-control study of the parkin gene in early-onset Parkinson disease.		2006
17050822	Frequency of LRRK2 mutations in early- and late-onset Parkinson disease.	Neurology	2006
15479945	An intermediate grade of finished genomic sequence suitable for comparative analyses.	Genome Res	2004
12917688	Comparative analyses of multi-species sequences from targeted genomic regions.	Nature	2003