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Cell Metabolism|November 21, 2025
Endothelial senescent-cell-specific clearance alleviates metabolic dysfunction in obese miceMasayoshi Suda, Selim Chaib, Larissa G P Langhi Prata, et al.
Nanoimpact|August 22, 2022
Analytical and toxicological aspects of nanomaterials in different product groups: Challenges and opportunitiesHarald R Tschiche, Frank S Bierkandt, Otto Creutzenberg, et al.
Alzheimer Disease and Associated Disorders|August 10, 2023
Visuospatial and Verbal Memory Differences in Amish Individuals With Alzheimer Disease and Related DementiasMichael B Prough, Andrew Zaman, Laura J Caywood, et al.
The Review of Scientific Instruments|November 2, 2010
Diagnostics design for steady-state operation of the Wendelstein 7-X stellaratorR König, J Baldzuhn, W Biel, et al.
HGG Advances|September 24, 2023
Founder population-specific weights yield improvements in performance of polygenic risk scores for Alzheimer disease in the Midwestern AmishMichael D Osterman, Yeunjoo E Song, Audrey Lynn, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 23, 2024
Examination of MGMT as a risk gene for dementia in the AmishLeighanne R Main, Yeunjoo E Song, Audrey Lynn, et al.
Epilepsia|November 18, 2025
Cognitive stagnation and executive function deficits in young children with SCN1A+ Dravet syndrome: Detailed characterization of onset, progression, and impact in the ENVISION natural history studyJoseph Sullivan, M Scott Perry, Ingrid E Scheffer, et al.
Epilepsia|December 4, 2023
Severe communication delays are independent of seizure burden and persist despite contemporary treatments in SCN1A+ Dravet syndrome: Insights from the ENVISION natural history studyM Scott Perry, Ingrid E Scheffer, Joseph Sullivan, et al.
Medrxiv : the Preprint Server for Health Sciences|January 3, 2024
Genetic analysis of cognitive preservation in the midwestern Amish reveals a novel locus on chromosome 2Leighanne R Main, Yeunjoo E Song, Audrey Lynn, et al.
Genome Research|June 21, 2013
The complex SNP and CNV genetic architecture of the increased risk of congenital heart defects in Down syndromeM Reza Sailani, Periklis Makrythanasis, Armand Valsesia, et al.
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