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Inflammatory Bowel Diseases|June 20, 2020
Colonoids From Patients With Pediatric Inflammatory Bowel Disease Exhibit Decreased Growth Associated With Inflammation Severity and Durable Upregulation of Antigen Presentation GenesJudith R Kelsen, Noor Dawany, Maire A Conrad, et al.
Nature Genetics|May 5, 2009
Common variations in BARD1 influence susceptibility to high-risk neuroblastomaMario Capasso, Marcella Devoto, Cuiping Hou, et al.
Obesity Reviews : an Official Journal of the International Association for the Study of Obesity|September 5, 2023
Design, analysis, and interpretation of treatment response heterogeneity in personalized nutrition and obesity treatment researchRoger S Zoh, Bridget H Esteves, Xiaoxin Yu, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 29, 2024
Human mutations in high-confidence Tourette disorder genes affect sensorimotor behavior, reward learning, and striatal dopamine in miceCara Nasello, Lauren A Poppi, Junbing Wu, et al.
Biorxiv : the Preprint Server for Biology|December 11, 2023
Human mutations in high-confidence Tourette disorder genes affect sensorimotor behavior, reward learning, and striatal dopamine in miceCara Nasello, Lauren A Poppi, Junbing Wu, et al.
Human Genetics|October 20, 2005
Localization of PSORS1 to a haplotype block harboring HLA-C and distinct from corneodesmosin and HCRCynthia Helms, Nancy L Saccone, Li Cao, et al.
Nature Communications|March 19, 2015
A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in femalesSwarkar Sharma, Douglas Londono, Walter L Eckalbar, et al.
The New England Journal of Medicine|May 9, 2008
Chromosome 6p22 locus associated with clinically aggressive neuroblastomaJohn M Maris, Yael P Mosse, Jonathan P Bradfield, et al.
Nature|June 19, 2009
Copy number variation at 1q21.1 associated with neuroblastomaSharon J Diskin, Cuiping Hou, Joseph T Glessner, et al.
Journal of the American Academy of Dermatology|March 12, 2005
Germline fumarate hydratase mutations and evidence for a founder mutation underlying multiple cutaneous and uterine leiomyomataGary S Chuang, Amalia Martinez-Mir, Adam Geyer, et al.
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