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Human Molecular Genetics|April 19, 2017
P4HA1 mutations cause a unique congenital disorder of connective tissue involving tendon, bone, muscle and the eyeYaqun Zou, Sandra Donkervoort, Antti M Salo, et al.
American Journal of Public Health|May 20, 2016
From Design to Dissemination: Implementing Community-Based Participatory Research in Postdisaster CommunitiesMaureen Lichtveld, Suzanne Kennedy, Rebecca Z Krouse, et al.
Gynecologic Oncology|September 13, 2005
The efficacy of adjuvant platinum-based chemotherapy in Stage I uterine papillary serous carcinoma (UPSC)C S Dietrich, S C Modesitt, P D DePriest, et al.
CMAJ Open|October 13, 2021
SARS-CoV-2 antibodies in Ontario health care workers during and after the first wave of the pandemic: a cohort studyMichelle Science, Shelly Bolotin, Michael Silverman, et al.
Nature Communications|November 27, 2025
Mutations in the β-tubulin TUBB impair ciliogenesis and are associated with ciliopathy-like phenotypesAntonio Mollica, Safia Omer, Georgiana Forguson, et al.
Arthritis and Rheumatism|January 13, 2012
Prevalence and sociodemographic correlates of antinuclear antibodies in the United StatesMinoru Satoh, Edward K L Chan, Lindsey A Ho, et al.
Science (New York, N.Y.)|April 8, 2006
Losartan, an AT1 antagonist, prevents aortic aneurysm in a mouse model of Marfan syndromeJennifer P Habashi, Daniel P Judge, Tammy M Holm, et al.
NPJ Genomic Medicine|July 2, 2025
Assessing the diagnostic impact of blood transcriptome profiling in a pediatric cohort previously assessed by genome sequencingHuayun Hou, Kyoko E Yuki, Gregory Costain, et al.
The New England Journal of Medicine|December 1, 2006
CD4+ count-guided interruption of antiretroviral treatment, W M El-Sadr, J D Lundgren, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 29, 2020
Cell-based analysis of CAD variants identifies individuals likely to benefit from uridine therapyFrancisco Del Caño-Ochoa, Bobby G Ng, Malak Abedalthagafi, et al.
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