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JAMA Network Open|September 8, 2025
Long-Term Survival Among Children With Trisomy 13 and Trisomy 18 by Cytogenetic StatusKatherine L Ludorf, Renata H Benjamin, Charles J Shumate, et al.
Molecular Therapy. Methods & Clinical Development|April 14, 2025
Precise measurement of CRISPR genome editing outcomes through single-cell DNA sequencingNechama Kalter, Saurabh Gulati, Michael Rosenberg, et al.
Drug Safety|July 5, 2021
Prevalence, Nature, Severity and Preventability of Adverse Drug Events in Mental Health Settings: Findings from the MedicAtion relateD harm in mEntal health hospitals (MADE) StudyGhadah H Alshehri, Darren M Ashcroft, Joanne Nguyen, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|June 26, 2004
Effective dosing regimen of 1-aminobenzotriazole for inhibition of antipyrine clearance in guinea pigs and mice using serial samplingSuresh K Balani, Ping Li, Joanne Nguyen, et al.
Birth Defects Research|November 18, 2022
Factors associated with nonsyndromic anotia and microtia, Texas, 1999-2014Jeremy M Schraw, J P Woodhouse, Renata H Benjamin, et al.
Cancer|October 3, 2023
Pediatric cancer incidence among individuals with overgrowth syndromes and overgrowth features: A population-based assessment in seven million childrenGillean K Connolly, Rachel D Harris, Charles Shumate, et al.
Birth Defects Research|November 25, 2024
Epidemiology of Macrocephaly in the Texas Birth Defects Registry, 1999-2019Rachel P Allred, J Aguilar-Martinez, R Howell, et al.
Clinical Pharmacology in Drug Development|April 28, 2016
Pharmacokinetic drug-drug interaction assessment of LCZ696 (an angiotensin receptor neprilysin inhibitor) with omeprazole, metformin or levonorgestrel-ethinyl estradiol in healthy subjectsLu Gan, Xuemin Jiang, Anisha Mendonza, et al.
Genome Medicine|September 30, 2022
Sequencing individual genomes with recurrent genomic disorder deletions: an approach to characterize genes for autosomal recessive rare disease traitsBo Yuan, Katharina V Schulze, Nurit Assia Batzir, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 10, 2023
Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infectionsLauren Jeffries, Emily K Mis, Kirsty McWalter, et al.
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