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Journal of Medical Genetics|March 3, 2018
Practice guideline: joint CCMG-SOGC recommendations for the use of chromosomal microarray analysis for prenatal diagnosis and assessment of fetal loss in CanadaChristine M Armour, Shelley Danielle Dougan, Jo-Ann Brock, et al.
Environmental Science & Technology|January 28, 2021
Oxidative Dissolution of Sulfide Minerals in Single and Mixed Sulfide Systems under Simulated Acid and Metalliferous Drainage ConditionsGujie Qian, Rong Fan, Jianyin Huang, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 27, 2015
Alternating hypoglycemia and hyperglycemia in a toddler with a homozygous p.R1419H ABCC8 mutation: an unusual clinical pictureShira Harel, Ana S A Cohen, Khalid Hussain, et al.
International Journal of Cancer|August 24, 2019
Randomized trial of weight loss in primary breast cancer: Impact on body composition, circulating biomarkers and tumor characteristicsWendy Demark-Wahnefried, Laura Q Rogers, Justin T Gibson, et al.
Medrxiv : the Preprint Server for Health Sciences|June 10, 2024
The Polygenic Score Catalog: new functionality and tools to enable FAIR researchSamuel A Lambert, Benjamin Wingfield, Joel T Gibson, et al.
Journal of Medical Genetics|May 30, 2025
Using long-read sequencing to detect and subtype a case with Temple syndromeSarah Dada, Vahid Akbari, Duha Hejla, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|May 20, 2020
Reactive Compression Molding Post-Inverse Vulcanization: A Method to Assemble, Recycle, and Repurpose Sulfur Polymers and CompositesNicholas A Lundquist, Alfrets D Tikoalu, Max J H Worthington, et al.
Scientific Reports|February 18, 2022
Genotype-phenotype correlations for COL4A3-COL4A5 variants resulting in Gly substitutions in Alport syndromeJoel T Gibson, Mary Huang, Marina Shenelli Croos Dabrera, et al.
European Heart Journal|December 15, 2025
Combined clinical, metabolomic, and polygenic scores for cardiovascular risk predictionScott C Ritchie, Xilin Jiang, Lisa Pennells, et al.
American Journal of Medical Genetics. Part A|September 13, 2017
Compound heterozygous TRPV4 mutations in two siblings with a complex phenotype including severe intellectual disability and neuropathyMy Linh Thibodeau, Colin H Peters, Katelin N Townsend, et al.
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