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Human Molecular Genetics|November 22, 2002
A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applicationsPatrick G Buckley, Kiran K Mantripragada, Magdalena Benetkiewicz, et al.Journal of Nephrology|March 3, 2025
Polygenic risk scores for eGFR are associated with age at kidney failureKane E Collins, Edmund Gilbert, Vincent Mauduit, et al.The New England Journal of Medicine|October 29, 2025
A Randomized Trial of Physical Therapy for Meniscal Tear and Knee PainJeffrey N Katz, Jamie E Collins, Leslie Bisson, et al.Journal of Nephrology|January 30, 2025
The impact of a secondary, rare, non-pathogenic PKD1 variant on disease progression in autosomal dominant polycystic kidney diseaseElhussein A E Elhassan, Kane E Collins, Sophia Heneghan, et al.Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|August 3, 2016
The Trichoptera barcode initiative: a strategy for generating a species-level Tree of LifeXin Zhou, Paul B Frandsen, Ralph W Holzenthal, et al.Osteoarthritis and Cartilage Open|December 10, 2025
Corrigendum to "The PIKASO trial (Preventing Injured Knees from Osteoarthritis: Severity Outcomes): Rationale and design features for a randomized controlled trial" [Osteoarthr Cartil Open 7 (2025) 100563]Cale A Jacobs, Morgan H Jones, Jamie E Collins, et al.Osteoarthritis and Cartilage Open|January 27, 2025
The PIKASO trial (Preventing Injured Knees from Osteoarthritis: Severity Outcomes): Rationale and design features for a randomized controlled trialCale A Jacobs, Morgan H Jones, Jamie E Collins, et al.Philosophical Transactions. Series A, Mathematical, Physical, and Engineering Sciences|May 1, 2025
Multi-messenger gravitational lensingGraham P Smith, Tessa Baker, Simon Birrer, et al.Nature Medicine|January 19, 2023
Complex I inhibitor of oxidative phosphorylation in advanced solid tumors and acute myeloid leukemia: phase I trialsTimothy A Yap, Naval Daver, Mikhila Mahendra, et al.Nature Genetics|April 2, 2014
Gain-of-function mutations in IFIH1 cause a spectrum of human disease phenotypes associated with upregulated type I interferon signalingGillian I Rice, Yoandris Del Toro Duany, Emma M Jenkinson, et al.Pageof 239