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American Journal of Human Genetics|December 4, 2018
OUTRIDER: A Statistical Method for Detecting Aberrantly Expressed Genes in RNA Sequencing DataFelix Brechtmann, Christian Mertes, Agnė Matusevičiūtė, et al.American Journal of Human Genetics|December 1, 1988
Type II achondrogenesis-hypochondrogenesis: morphologic and immunohistopathologic studiesM Godfrey, D R Keene, E Blank, et al.American Journal of Human Genetics|January 1, 2019
Heterozygous RNF13 Gain-of-Function Variants Are Associated with Congenital Microcephaly, Epileptic Encephalopathy, Blindness, and Failure to ThriveSimon Edvardson, Claudia M Nicolae, Grace J Noh, et al.American Journal of Human Genetics|January 2, 2019
Human-Disease Phenotype Map Derived from PheWAS across 38,682 IndividualsAnurag Verma, Lisa Bang, Jason E Miller, et al.American Journal of Human Genetics|December 18, 2018
Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer SubtypesNasim Mavaddat, Kyriaki Michailidou, Joe Dennis, et al.American Journal of Human Genetics|January 5, 2019
Integrating Genomics into Healthcare: A Global ResponsibilityZornitza Stark, Lena Dolman, Teri A Manolio, et al.American Journal of Human Genetics|January 5, 2019
Mutations in NCAPG2 Cause a Severe Neurodevelopmental Syndrome that Expands the Phenotypic Spectrum of CondensinopathiesTahir N Khan, Kamal Khan, Azita Sadeghpour, et al.American Journal of Human Genetics|October 1, 1988
A resolution of the ascertainment sampling problem. III. PedigreesN C Shute, W J EwensAmerican Journal of Human Genetics|October 1, 1988
Fanconi anemia mutation causes cellular susceptibility to ambient oxygenD Schindler, H HoehnAmerican Journal of Human Genetics|October 1, 1988
Molecular analysis of male-viable deletions and duplications allows ordering of 52 DNA probes on proximal XqF P Cremers, T J van de Pol, B Wieringa, et al.Pageof 981