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Plos One|August 14, 2013
Two variants of the C-reactive protein gene are associated with risk of pre-eclampsia in an American Indian populationLyle G Best, Richa Saxena, Cindy M Anderson, et al.
Schizophrenia Research|February 7, 2016
Genome-wide investigation of schizophrenia associated plasma Ndel1 enzyme activityAry Gadelha, Jonathan Coleman, Gerome Breen, et al.
Pediatric Blood & Cancer|August 30, 2025
Expansion of the Phenotype of Lymphatic Anomalies Caused by Somatic Activating BRAF VariantMichael D Fox, Sumukh Kumar, Allison D Britt, et al.
Scientific Reports|December 22, 2015
Genome-wide association study reveals two loci for serum magnesium concentrations in European-American childrenXiao Chang, Joseph Glessner, Adrienne Tin, et al.
International Heart Journal|January 18, 2021
FLNC and MYLK2 Gene Mutations in a Chinese Family with Different Phenotypes of CardiomyopathyXianyu Qin, Ping Li, Hui-Qi Qu, et al.
Molecular Autism|February 26, 2014
Variability in the common genetic architecture of social-communication spectrum phenotypes during childhood and adolescenceBeate St Pourcain, David H Skuse, William P Mandy, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 21, 2011
Loss-of-function DNA sequence variant in the CLCNKA chloride channel implicates the cardio-renal axis in interindividual heart failure risk variationThomas P Cappola, Scot J Matkovich, Wei Wang, et al.
Genes|August 6, 2021
Genome-Wide Association Studies of Conotruncal Heart Defects with Normally Related Great Vessels in the United StatesOmobola O Oluwafemi, Fadi I Musfee, Laura E Mitchell, et al.
Pediatric Research|March 5, 2022
Treatment of severe Kaposiform lymphangiomatosis positive for NRAS mutation by MEK inhibitionGuy Chowers, Gadi Abebe-Campino, Hana Golan, et al.
The Journal of Clinical Investigation|February 21, 2018
CYP3A4 mutation causes vitamin D-dependent rickets type 3Jeffrey D Roizen, Dong Li, Lauren O'Lear, et al.
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