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Nature Genetics|April 28, 2015
Analysis of loss-of-function variants and 20 risk factor phenotypes in 8,554 individuals identifies loci influencing chronic diseaseAlexander H Li, Alanna C Morrison, Christie Kovar, et al.
Biorxiv : the Preprint Server for Biology|January 8, 2024
Tryptophan Metabolites And Their Predicted Microbial Sources In Fecal Samples From Healthy IndividualsCynthia L Chappell, Kristi L Hoffman, Philip L Lorenzi, et al.
BMC Health Services Research|April 4, 2025
Does a waiting room increase same-day treatment for sexually transmitted infections among pregnant women? A quality improvement study at South African primary healthcare facilitiesRanjana M S Gigi, Mandisa M Mdingi, Lukas Bütikofer, et al.
Medrxiv : the Preprint Server for Health Sciences|February 24, 2025
Does a waiting room increase same-day treatment for sexually transmitted infections among pregnant women? A quality improvement study at South African primary healthcare facilitiesRanjana M S Gigi, Mandisa M Mdingi, Lukas Bütikofer, et al.
Frontiers in Molecular Biosciences|January 26, 2023
Modeling nonsegmented negative-strand RNA virus (NNSV) transcription with ejective polymerase collisions and biased diffusionFelipe-Andrés Piedra, David Henke, Anubama Rajan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 24, 2018
Phenotypic expansion illuminates multilocus pathogenic variationEnder Karaca, Jennifer E Posey, Zeynep Coban Akdemir, et al.
Communications Biology|November 20, 2025
Single cell long read whole genome sequencing reveals somatic transposon activity in human brainMichal B Izydorczyk, Ester Kalef-Ezra, Dominic W Horner, et al.
BMJ Open|February 5, 2024
Microbial interactions among <i>Gardnerella</i>, <i>Prevotella</i> and <i>Fannyhessea</i> prior to incident bacterial vaginosis: protocol for a prospective, observational studyChristina A Muzny, Jacob H Elnaggar, Lúcia G V Sousa, et al.
Human Mutation|September 9, 2011
Whole-exome sequencing identifies ALMS1, IQCB1, CNGA3, and MYO7A mutations in patients with Leber congenital amaurosisXia Wang, Hui Wang, Ming Cao, et al.
Journal of Thrombosis and Haemostasis : JTH|May 8, 2013
Next-generation sequencing study finds an excess of rare, coding single-nucleotide variants of ADAMTS13 in patients with deep vein thrombosisL A Lotta, G Tuana, J Yu, et al.
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