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Journal of Medical Genetics|May 27, 2019
Pathogenic variants in PLOD3 result in a Stickler syndrome-like connective tissue disorder with vascular complicationsLisa Jean Ewans, Alison Colley, Carles Gaston-Massuet, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
Lymphatic constraint of germinal centers optimizes protective antibody responsesTenny Mudianto, Gabrielle R Berman, Kimberly Zaldana, et al.
BMJ Open Respiratory Research|August 3, 2023
Cross-sectional study evaluating the impact of SARS-CoV-2 variants on Long COVID outcomes in UK hospital survivorsAnita Saigal, Camila Nagoda Niklewicz, Sindhu Bhaarrati Naidu, et al.
The Journal of Allergy and Clinical Immunology|August 14, 2013
Environmental assessment and exposure reduction of cockroaches: a practice parameterJay Portnoy, Ginger L Chew, Wanda Phipatanakul, et al.
Cancer & Metabolism|February 7, 2017
Mitochondrial mutations and metabolic adaptation in pancreatic cancerRae-Anne Hardie, Ellen van Dam, Mark Cowley, et al.
Annals of Vascular Surgery|December 29, 2020
Higher Risk for Reintervention in Patients after Stenting for Radiation-Induced Internal Carotid Artery Stenosis: A Single-Center Analysis and Systematic ReviewYoung Erben, Camila Franco-Mesa, David Miller, et al.
Neurosurgery|January 8, 2024
Trends in the Utilization of Surgical Modalities for the Treatment of Drug-Resistant Epilepsy: A Comprehensive 10-Year Analysis Using the National Inpatient SampleAbdul Karim Ghaith, Victor Gabriel El-Hajj, Jesus E Sanchez-Garavito, et al.
Nature Genetics|November 25, 2014
Mutations in the voltage-gated potassium channel gene KCNH1 cause Temple-Baraitser syndrome and epilepsyCas Simons, Lachlan D Rash, Joanna Crawford, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 30, 2018
Whole-exome sequencing reanalysis at 12 months boosts diagnosis and is cost-effective when applied early in Mendelian disordersLisa J Ewans, Deborah Schofield, Rupendra Shrestha, et al.
American Journal of Human Genetics|April 16, 2013
A de novo mutation in the β-tubulin gene TUBB4A results in the leukoencephalopathy hypomyelination with atrophy of the basal ganglia and cerebellumCas Simons, Nicole I Wolf, Nathan McNeil, et al.
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