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Biological Psychiatry|December 16, 2011
Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autismThomas V Fernandez, Stephan J Sanders, Ilana R Yurkiewicz, et al.Pediatric Nephrology (Berlin, Germany)|January 14, 2026
APOL1 kidney risk variants and outcomes in children with congenital anomalies of the kidney and urinary tractLisanne M Vendrig, Juntao Ke, Michael W T Tanck, et al.American Journal of Human Genetics|March 3, 2009
Diverse genome-wide association studies associate the IL12/IL23 pathway with Crohn DiseaseKai Wang, Haitao Zhang, Subra Kugathasan, 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|November 13, 2015
Genetic predisposition to neuroblastoma mediated by a LMO1 super-enhancer polymorphismDerek A Oldridge, Andrew C Wood, Nina Weichert-Leahey, et al.Circulation Research|September 11, 2014
Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence dataJoseph T Glessner, Alexander G Bick, Kaoru Ito, et al.Scientific Reports|October 29, 2023
Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infectionKathleen Ferar, Taryn O Hall, Dana C Crawford, 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 Psychiatric Research|May 17, 2014
The role of leptin, melanocortin, and neurotrophin system genes on body weight in anorexia nervosa and bulimia nervosaZeynep Yilmaz, Allan S Kaplan, Arun K Tiwari, et al.Human Molecular Genetics|May 21, 2014
Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypesVladimir Vacic, Laurie J Ozelius, Lorraine N Clark, et al.Pageof 91