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American Journal of Human Genetics|October 9, 2021
Detecting cryptic clinically relevant structural variation in exome-sequencing data increases diagnostic yield for developmental disordersEugene J Gardner, Alejandro Sifrim, Sarah J Lindsay, et al.
American Journal of Human Genetics|April 22, 2022
Combining evidence from Mendelian randomization and colocalization: Review and comparison of approachesVerena Zuber, Nastasiya F Grinberg, Dipender Gill, et al.
American Journal of Human Genetics|April 23, 2022
Powerful and robust inference of complex phenotypes' causal genes with dependent expression quantitative loci by a median-based Mendelian randomizationLin Jiang, Lin Miao, Guorong Yi, et al.
American Journal of Human Genetics|January 1, 1979
Mapping of the structural gene for the second component of complement with respect to the human major histocompatibility complexD Raum, D Glass, C B Carpenter, et al.
American Journal of Human Genetics|June 18, 2019
Genes for Good: Engaging the Public in Genetics Research via Social MediaKatharine Brieger, Gregory J M Zajac, Anita Pandit, et al.
American Journal of Human Genetics|June 4, 2019
Geographic Variation and Bias in the Polygenic Scores of Complex Diseases and Traits in FinlandSini Kerminen, Alicia R Martin, Jukka Koskela, et al.
American Journal of Human Genetics|November 1, 1978
A new allele of human alpha1-antitrypsin: PiNhamptonP Arnaud, R M Galbraith, G M Galbraith, et al.
American Journal of Human Genetics|February 1, 1988
Penetrance of von Recklinghausen neurofibromatosis: a distinction between predecessors and descendantsV M Riccardi, R A Lewis
American Journal of Human Genetics|July 2, 2019
Paralog Studies Augment Gene Discovery: DDX and DHX GenesIngrid Paine, Jennifer E Posey, Christopher M Grochowski, et al.
American Journal of Human Genetics|April 8, 2022
Germline variants in tumor suppressor FBXW7 lead to impaired ubiquitination and a neurodevelopmental syndromeSarah E M Stephenson, Gregory Costain, Laura E R Blok, et al.
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