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Genomics|May 14, 2011
Next generation genome-wide association tool: design and coverage of a high-throughput European-optimized SNP arrayThomas J Hoffmann, Mark N Kvale, Stephanie E Hesselson, et al.Nature Genetics|May 5, 2009
Narcolepsy is strongly associated with the T-cell receptor alpha locusJoachim Hallmayer, Juliette Faraco, Ling Lin, et al.Pediatrics|January 19, 2017
Newborn Sequencing in Genomic Medicine and Public HealthJonathan S Berg, Pankaj B Agrawal, Donald B Bailey, et al.Nature Genetics|April 12, 2022
Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophreniaDuncan S Palmer, Daniel P Howrigan, Sinéad B Chapman, et al.Nature Genetics|December 9, 2008
Loci influencing lipid levels and coronary heart disease risk in 16 European population cohortsYurii S Aulchenko, Samuli Ripatti, Ida Lindqvist, et al.Clinical Trials (London, England)|July 3, 2013
The epilepsy phenome/genome project, Bassel Abou-Khalil, Brian Alldredge, et al.Nature Genetics|December 21, 2010
Common variants in P2RY11 are associated with narcolepsyBirgitte R Kornum, Minae Kawashima, Juliette Faraco, et al.Nature|August 1, 2008
Large recurrent microdeletions associated with schizophreniaHreinn Stefansson, Dan Rujescu, Sven Cichon, et al.Molecular Psychiatry|January 23, 2021
Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorderXiaoming Jia, Fernando S Goes, Adam E Locke, et al.Biorxiv : the Preprint Server for Biology|September 16, 2024
A blended genome and exome sequencing method captures genetic variation in an unbiased, high-quality, and cost-effective mannerToni A Boltz, Benjamin B Chu, Calwing Liao, et al.Pageof 24