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Nature Medicine|April 15, 2026
Proteomic risk score for early prediction of kidney disease progression in individuals with APOL1 high-risk genotypesChenyu Li, Shola M Richards, Ghazal Quinn, et al.
Neuromuscular Disorders : NMD|January 7, 2018
Diagnosis and management of spinal muscular atrophy: Part 2: Pulmonary and acute care; medications, supplements and immunizations; other organ systems; and ethicsRichard S Finkel, Eugenio Mercuri, Oscar H Meyer, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 28, 2026
Strong intrinsic multiferroism and magnetoelectric coupling in (1-<i>x</i>)BiFeO<sub>3</sub>-(<i>x</i>)BaTiO<sub>3</sub> filmsTae Yeon Kim, Jesse Schimpf, Atanu Paul, et al.
Psychological Medicine|June 8, 2026
The long reach of childhood income inequality: a multinational twin study of gene-environment interplay on adult depressive symptomsAndrew J Petkus, Chandra A Reynolds, Brian K Finch, et al.
Neurology. Genetics|February 25, 2025
The Spastic Paraplegia-Centers of Excellence Research Network (SP-CERN): Clinical Trial Readiness for Hereditary Spastic ParaplegiaLuca Schierbaum, Vicente Quiroz, Kathryn Yang, et al.
JAMA Neurology|May 5, 2015
Association of a Novel ACTA1 Mutation With a Dominant Progressive Scapuloperoneal Myopathy in an Extended FamilyKristen Zukosky, Katherine Meilleur, Bryan J Traynor, et al.
Human Mutation|March 28, 2008
Exon skipping mutations in collagen VI are common and are predictive for severity and inheritanceA K Lampe, Y Zou, D Sudano, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 22, 2013
ΔFosB induction in striatal medium spiny neuron subtypes in response to chronic pharmacological, emotional, and optogenetic stimuliMary Kay Lobo, Samir Zaman, Diane M Damez-Werno, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|December 19, 2025
The Interplay of Genes and Environment Across Multiple Studies (IGEMS) Consortium After Fifteen YearsDeborah Finkel, Brian K Finch, Margaret Gatz, et al.
Neuromuscular Disorders : NMD|February 4, 2026
Refining functional phenotypes in an international cohort of untreated paediatric type 2 and 3 SMA patients using the Revised Hammersmith ScaleE Milev, G Stimpson, D Ramsey, et al.
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