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American Journal of Medical Genetics. Part A|September 9, 2016
Autosomal and X chromosome structural variants are associated with congenital heart defects in Turner syndrome: The NHLBI GenTAC registrySiddharth K Prakash, Carolyn A Bondy, Cheryl L Maslen, et al.
Cell Death and Differentiation|January 8, 2011
Clusterin secreted by astrocytes enhances neuronal differentiation from human neural precursor cellsO Cordero-Llana, S A Scott, S L Maslen, et al.
European Journal of Human Genetics : EJHG|January 21, 2011
ALK2 mutation in a patient with Down's syndrome and a congenital heart defectIrene C Joziasse, Kelly A Smith, Sonja Chocron, et al.
G3 (Bethesda, Md.)|November 17, 2017
Analysis of Copy Number Variants on Chromosome 21 in Down Syndrome-Associated Congenital Heart DefectsBenjamin L Rambo-Martin, Jennifer G Mulle, David J Cutler, et al.
The Journal of Heart Valve Disease|October 10, 2014
Valve-sparing aortic root replacement in patients with Marfan syndrome enrolled in the National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular ConditionsHoward K Song, Liliana R Preiss, Cheryl L Maslen, et al.
Molecular Cell|August 1, 2024
The V-ATPase/ATG16L1 axis is controlled by the V1H subunitLewis Timimi, Antoni G Wrobel, George N Chiduza, et al.
The Annals of Thoracic Surgery|October 1, 2019
Open Thoracoabdominal Aortic Repair in Patients With Heritable Aortic Disease in the GenTAC RegistryWilliam C Frankel, Howard K Song, Rita K Milewski, et al.
Clinical Genetics|July 26, 2022
Identification of novel rare copy number variants associated with sporadic tetralogy of Fallot and clinical implicationsGuo-Wei He, Cheryl L Maslen, Huan-Xin Chen, et al.
Plos One|August 20, 2011
Drug-resistant genotypes and multi-clonality in Plasmodium falciparum analysed by direct genome sequencing from peripheral blood of malaria patientsTimothy Robinson, Susana G Campino, Sarah Auburn, et al.
Molecular Cell|November 8, 2022
ATG9A and ATG2A form a heteromeric complex essential for autophagosome formationAlexander R van Vliet, George N Chiduza, Sarah L Maslen, et al.
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