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JAMA|July 21, 1998
Hereditary hemochromatosis: gene discovery and its implications for population-based screeningW Burke, E Thomson, M J Khoury, et al.
Scientific Data|February 22, 2024
Ethnicity data resource in population-wide health records: completeness, coverage and granularity of diversityMarta Pineda-Moncusí, Freya Allery, Antonella Delmestri, et al.
Communications Earth & Environment|June 12, 2026
A long-lived impact-generated hydrothermal system at the Chicxulub impact structureAnnemarie E Pickersgill, Evangelos Christou, Marissa M Tremblay, et al.
Neurology|September 20, 2000
Analysis of EEG and CSF 14-3-3 proteins as aids to the diagnosis of Creutzfeldt-Jakob diseaseI Zerr, M Pocchiari, S Collins, et al.
Genetic Epidemiology|December 24, 2005
Tag SNP selection for Finnish individuals based on the CEPH Utah HapMap databaseCristen J Willer, Laura J Scott, Lori L Bonnycastle, et al.
Human Genetics|September 6, 2005
Mitochondrial polymorphisms and susceptibility to type 2 diabetes-related traits in FinnsKaren L Mohlke, Anne U Jackson, Laura J Scott, et al.
Molecular Genetics and Metabolism|May 1, 1998
11q13 allelotype analysis in 27 northern American MEN1 kindreds identifies two distinct founder chromosomesM R Emmert-Buck, L V Debelenko, S Agarwal, et al.
Human Molecular Genetics|July 16, 2009
Tissue-specific alternative splicing of TCF7L2Ludmila Prokunina-Olsson, Cullan Welch, Ola Hansson, et al.
Journal of Translational Medicine|January 19, 2020
Immune cell phenotyping in low blood volumes for assessment of cardiovascular disease risk, development, and progression: a pilot studyYvonne Baumer, Cristhian A Gutierrez-Huerta, Ankit Saxena, et al.
Diagnostic and Prognostic Research|September 1, 2020
UMBRELLA protocol: systematic reviews of multivariable biomarker prognostic models developed to predict clinical outcomes in patients with heart failureMaria D L A Vazquez-Montes, Thomas P A Debray, Kathryn S Taylor, et al.
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