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Nature Communications|December 6, 2022
Subduction-related oxidation of the sublithospheric mantle evidenced by ferropericlase and magnesiowüstite diamond inclusionsEkaterina S Kiseeva, Nester Korolev, Iuliia Koemets, et al.
Journal of the International Neuropsychological Society : JINS|September 20, 2024
Psychometric and adherence considerations for high-frequency, smartphone-based cognitive screening protocols in older adultsLouisa I Thompson, Alyssa N De Vito, Zachary J Kunicki, et al.
Kidney International|June 17, 2020
Mutation of complement factor B causing massive fluid-phase dysregulation of the alternative complement pathway can result in atypical hemolytic uremic syndromeYuzhou Zhang, Robin A Kremsdorf, C John Sperati, et al.
Journal of Assisted Reproduction and Genetics|January 5, 2026
The spermatozoon neck role in infertility and intracytoplasmic sperm injection outcomesDerek F Kluczynski, Isabel Nester, Haley Prine, et al.
The CRISPR Journal|January 6, 2025
Monitoring the Land and Sea: Enhancing Efficiency Through CRISPR-Cas Driven Depletion and Enrichment of Environmental DNAAnya Kardailsky, Benjamín Durán-Vinet, Georgia Nester, et al.
Molecular Immunology|April 7, 2015
Atypical aHUS: State of the artCarla M Nester, Thomas Barbour, Santiago Rodriquez de Cordoba, et al.
Prosthetics and Orthotics International|August 8, 2025
A scoping review of digital fabrication techniques applied to prosthetics & orthotics: Part 2 of 2-orthoticsBen M Oldfrey, Dafne Z Morgado Ramirez, Catherine Holloway, et al.
JCO Global Oncology|June 21, 2024
Stigma in Pediatric Cancer: An Exploratory Study of Osteosarcoma and Retinoblastoma in Guatemala, Jordan, and ZimbabweDylan E Graetz, Thelma Velasquez, Inam Chitsike, et al.
Kidney International|December 20, 2016
Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a "Kidney Disease: Improving Global Outcomes" (KDIGO) Controversies ConferenceTimothy H J Goodship, H Terence Cook, Fadi Fakhouri, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 4, 2011
Phenotypical spectrum of cerebellar ataxia associated with a novel mutation in the CA8 gene, encoding carbonic anhydrase (CA) VIIINamik Kaya, Hesham Aldhalaan, Banan Al-Younes, et al.
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