Author

E. B. Klee

Observed names: E Klee, E.B. Klee, Eric Klee, Eric W. Klee

Institution: Mayo Clinic

Observed institutions: Mayo Clinic, University of Glasgow, University of Edinburgh

OpenAlex ID: A5087443352

Viral involvement in Hodgkin's disease: detection of clonal type A Epstein-Barr virus genomes in tumour samples

1991 · S Gledhill, A Gallagher, et al. · British Journal of Cancer · 89

Severe anaemia in pregnancy: a problem of primigravidae in rural Zaire

1991 · D.J. Jackson, E.B. Klee, et al. · Transactions of the Royal Society of Tropical Medicine and Hygiene · 53

Stable seroprevalence of HIV-1 in antenatal women in rural Bas-Zaïre, 1988–1993

1994 · S. D.R. Green, W. A.M. Cutting, et al. · AIDS · 9

Lymphadenopathy and hepatosplenomegaly in the 1st year in children infected by HIV-1 in Zaire

1992 · D. J. Jackson, E. B. Klee, et al. · Annals of Tropical Paediatrics · 8

Biallelic LAMP3 variants in 5 families with interstitial lung disease: Evidence of a disease-gene association

2026 · Laura A. Keehan, Hitomi Ono-Minagi, et al. · Genetics in Medicine · 4

Seroprevalence and Determinants of HIV-1 Infection in Pregnancy in Rural Zaire

1992 · S.D.R. Green, J.K. Mokolo, et al. · 1

Identification of a Novel Missense Homozygous Variant in LINS1 in Two Distinct Iranian Families With Consanguineous Marriage

2026 · Elham Alimoradi, Parham Nejati, et al. · Molecular Genetics & Genomic Medicine

A Pharmacogenomic-Informed Representation Improves Multimodal EHR Survival Prediction

2026 · Mun Hwan Lee, Yang Xiao, et al. · medRxiv

O35: Challenges of RNA sequencing data interpretation for the reclassification of genomic variants of uncertain significance

2026 · Matheus Wilke, Joseph Farris, et al. · Genetics in Medicine Open

P357: Expanding the ADAR-related spectrum: A highly suspicious de novo variant in Aicardi-Goutieres syndrome

2026 · Eva Kahn, Joseph Farris, et al. · Genetics in Medicine Open

P700: A novel LAMA3 splice-site variant in junctional epidermolysis bullosa: Investigating splicing consequences and diagnostic challenges

2026 · Deepak Panwar, Maria O'Connell, et al. · Genetics in Medicine Open

P607: Long-read sequencing enables discovery of disease genes in complex neurological phenotypes

2026 · Angita Jain, Evan Udine, et al. · Genetics in Medicine Open

P687: A novel homozygous MYO9B splice-site variant in a family with Charcot–Marie–Tooth disease: Expanding the emerging gene–disease relationship

2026 · Arash Salmaninejad, Joseph Farris, et al. · Genetics in Medicine Open

P604: Evaluating AI-assisted phenotyping for variant prioritization in clinical laboratory genome/exome workflows

2026 · Sarah Barnett, Anna Essendrup, et al. · Genetics in Medicine Open

Prenatal diagnosis of an FLNB associated skeletal dysplasia

2021 · Myra Wick, Erica Macke, et al. · Molecular Genetics and Metabolism

Works count: 15

Citation count: 164

H-index: 4

I10-index: 2