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European Journal of Human Genetics : EJHG|April 1, 2004
Refined genetic mapping of autosomal recessive chronic distal spinal muscular atrophy to chromosome 11q13.3 and evidence of linkage disequilibrium in European familiesLouis Viollet, Mohammed Zarhrate, Isabelle Maystadt, et al.
Molecular Psychiatry|October 27, 2018
Genome-wide association study of brain amyloid deposition as measured by Pittsburgh Compound-B (PiB)-PET imagingQi Yan, Kwangsik Nho, Jorge L Del-Aguila, et al.
Frontiers in Neurology|January 9, 2019
A Novel Compound Targeting Protease Receptor 1 Activators for the Treatment of GlioblastomaEfrat Shavit-Stein, Ehud Sheinberg, Valery Golderman, et al.
Stigma and Health|September 2, 2025
Sexual and Gender Minority Status Predicts Additional Variance in PTSD Symptoms After Accounting for Conventional Trauma ExposureScott McKernan, Wendy D'Andrea, Amanda Collier, et al.
Oncogene|October 2, 2019
Bile acid-induced "Minority MOMP" promotes esophageal carcinogenesis while maintaining apoptotic resistance via Mcl-1Yuan Xu, Deborah R Surman, Laurence Diggs, et al.
American Journal on Intellectual and Developmental Disabilities|November 14, 2018
Associations Between Medical History, Cognition, and Behavior in Youth With Down Syndrome: A Report From the Down Syndrome Cognition ProjectTracie C Rosser, Jamie O Edgin, George T Capone, et al.
Human Genetics|November 7, 2014
Effects of enamel matrix genes on dental caries are moderated by fluoride exposuresJohn R Shaffer, Jenna C Carlson, Brooklyn O C Stanley, et al.
The Journal of Investigative Dermatology|April 23, 2004
Peroxisome proliferator-activated receptor (PPAR)-beta/delta stimulates differentiation and lipid accumulation in keratinocytesMatthias Schmuth, Christopher M Haqq, William J Cairns, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|July 21, 2019
Early outcomes for low-risk pediatric heart transplant recipients and steroid avoidance: A multicenter cohort study (Clinical Trials in Organ Transplantation in Children - CTOTC-04)Jacqueline M Lamour, Kristen L Mason, Daphne T Hsu, et al.
American Journal of Human Genetics|September 26, 2003
Mutations in the gene encoding capillary morphogenesis protein 2 cause juvenile hyaline fibromatosis and infantile systemic hyalinosisSandra Hanks, Sarah Adams, Jenny Douglas, et al.
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