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Child Development|September 1, 2012
A genome-wide association study of autism incorporating autism diagnostic interview-revised, autism diagnostic observation schedule, and social responsiveness scaleJohn J Connolly, Joseph T Glessner, Hakon HakonarsonDiscovery Medicine|February 1, 2011
The genetics of asthma and allergic disordersMichael E March, Patrick M A Sleiman, Hakon HakonarsonBMC Medical Genomics|January 22, 2016
Machine learning derived risk prediction of anorexia nervosaYiran Guo, Zhi Wei, Brendan J Keating, et al.Expert Review of Molecular Diagnostics|March 28, 2008
Classification of genetic profiles of Crohn's disease: a focus on the ATG16L1 geneStruan F A Grant, Robert N Baldassano, Hakon HakonarsonCurrent Topics in Behavioral Neurosciences|January 14, 2012
Rare genomic deletions and duplications and their role in neurodevelopmental disordersJoseph T Glessner, John J M Connolly, Hakon HakonarsonScientific Reports|August 7, 2021
Insights into non-autoimmune type 1 diabetes with 13 novel loci in low polygenic risk score patientsJingchun Qu, Hui-Qi Qu, Jonathan P Bradfield, et al.Communications Biology|July 24, 2021
Genetic architecture of type 1 diabetes with low genetic risk score informed by 41 unreported lociHui-Qi Qu, Jingchun Qu, Jonathan Bradfield, et al.Journal of Paediatrics and Child Health|August 9, 2020
High prevalence of elevated serum liver enzymes in Chinese children suggests metabolic syndrome as a common risk factorJinling Wang, Hui-Qi Qu, Ke Huang, et al.Bone|December 13, 2016
Late-onset hereditary hypophosphatemic rickets with hypercalciuria (HHRH) due to mutation of SLC34A3/NPT2cGauri Dhir, Dong Li, Hakon Hakonarson, et al.Scientific Reports|May 2, 2025
Role of genetic modifiers on pulmonary consequences of cancer therapy in childrenShoshana Leftin Dobkin, Xiao Chang, Frank Mentch, et al.Pageof 93