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Genome Biology|July 14, 2026
CIT-Lasso: a scalable approach beyond guilty by association for identifying causal variants from genome-wide summary statisticsZihuai He, Benjamin Chu, James Yang, et al.
Biorxiv : the Preprint Server for Biology|March 11, 2024
Beyond guilty by association at scale: searching for causal variants on the basis of genome-wide summary statisticsZihuai He, Benjamin Chu, James Yang, et al.
JAMA Psychiatry|February 14, 2014
Multisystem component phenotypes of bipolar disorder for genetic investigations of extended pedigreesScott C Fears, Susan K Service, Barbara Kremeyer, et al.
American Journal of Obstetrics & Gynecology MFM|July 18, 2026
Incremental yield of genome sequencing after exome sequencing for nonimmune hydrops fetalis spectrumRozlyn Ct Boutin, Billie R Lianoglou, Nuriye N Sahin Hodoglugil, et al.
Human Molecular Genetics|April 21, 2011
Phenotype mining in CNV carriers from a population cohortOlli P H Pietiläinen, Karola Rehnström, Eveliina Jakkula, et al.
Human Molecular Genetics|May 22, 2020
Analysis of putative cis-regulatory elements regulating blood pressure variationPriyanka Nandakumar, Dongwon Lee, Thomas J Hoffmann, et al.
Genome Biology|November 26, 2009
Ancestry-related assortative mating in Latino populationsNeil Risch, Shweta Choudhry, Marc Via, et al.
American Journal of Hypertension|December 13, 2006
Genome-wide linkage analysis of lipids in nondiabetic Chinese and Japanese from the SAPPHIRe family studyChin-Fu Hsiao, Yen-Feng Chiu, Fu-Tien Chiang, et al.
NPJ Genomic Medicine|January 3, 2024
Genetic ancestry and diagnostic yield of exome sequencing in a diverse populationYusuph Mavura, Nuriye Sahin-Hodoglugil, Ugur Hodoglugil, et al.
American Journal of Hypertension|February 1, 2003
A meta-analysis of genome-wide linkage scans for hypertension: the National Heart, Lung and Blood Institute Family Blood Pressure ProgramMichael A Province, Sharon L R Kardia, Koustubh Ranade, et al.
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