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Human Molecular Genetics|September 1, 2017
Whole-genome sequencing study of serum peptide levels: the Atherosclerosis Risk in Communities studyPaul S de Vries, Bing Yu, Elena V Feofanova, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 9, 2011
Copy number variation detection in whole-genome sequencing data using the Bayesian information criterionRuibin Xi, Angela G Hadjipanayis, Lovelace J Luquette, et al.
The Journal of Chemical Physics|July 1, 2025
Detecting ion pairing in sodium fluoride solutions with dielectric spectroscopyMichael Woodcox, Sarah R Evans, Aaron M Hagerstrom, et al.
Immunogenetics|July 20, 2019
MHC genotyping from rhesus macaque exome sequencesJohn R Caskey, Roger W Wiseman, Julie A Karl, et al.
Cold Spring Harbor Molecular Case Studies|May 6, 2016
A t(5;16) translocation is the likely driver of a syndrome with ambiguous genitalia, facial dysmorphism, intellectual disability, and speech delayAyşegül Ozantürk, Erica E Davis, Aniko Sabo, et al.
Comparative Medicine|November 30, 2018
Spontaneous Spongiform Brainstem Degeneration in a Young Mouse Lemur (<i>Microcebus murinus</i>) with Conspicuous Behavioral, Motor, Growth, and Ocular PathologiesDaniel Schmidtke, Charlotte Lempp, Marko Dubicanac, et al.
Medrxiv : the Preprint Server for Health Sciences|July 16, 2021
Transmission event of SARS-CoV-2 Delta variant reveals multiple vaccine breakthrough infectionsTimothy Farinholt, Harsha Doddapaneni, Xiang Qin, et al.
Neuro-Oncology|August 31, 2018
Elucidating the molecular pathogenesis of glioma: integrated germline and somatic profiling of a familial glioma case seriesDaniel I Jacobs, Kazutaka Fukumura, Matthew N Bainbridge, et al.
Scientific Reports|April 18, 2024
Somatic mutations of esophageal adenocarcinoma: a comparison between Black and White patientsHyeyeun Lim, Marie-Claude Gingras, Jing Zhao, et al.
Clinical Genetics|December 12, 2017
Phenotype expansion and development in Kosaki overgrowth syndromeP Gawliński, M Pelc, E Ciara, et al.
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