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American Journal of Human Genetics|April 14, 2015
Lupus Risk Variant Increases pSTAT1 Binding and Decreases ETS1 ExpressionXiaoming Lu, Erin E Zoller, Matthew T Weirauch, et al.American Journal of Human Genetics|April 22, 2021
Engagement and return of results preferences among a primarily African American genomic sequencing research cohortKatie L Lewis, Erin Turbitt, Priscilla A Chan, et al.American Journal of Human Genetics|April 3, 2021
30 years of repeat expansion disorders: What have we learned and what are the remaining challenges?Christel Depienne, Jean-Louis MandelAmerican Journal of Human Genetics|October 1, 1989
Parental origin of the extra chromosome in trisomy 18K G Kupke, U MüllerAmerican Journal of Human Genetics|March 30, 2023
Bi-allelic variants in the ESAM tight-junction gene cause a neurodevelopmental disorder associated with fetal intracranial hemorrhageMauro Lecca, Davut Pehlivan, Damià Heine Suñer, et al.American Journal of Human Genetics|June 1, 1988
A segregation and linkage study of classical and nonclassical 21-hydroxylase deficiencyS L Sherman, C E Aston, N E Morton, et al.American Journal of Human Genetics|April 23, 2021
Somatic MAP3K3 mutation defines a subclass of cerebral cavernous malformationJiancong Weng, Yingxi Yang, Dong Song, et al.American Journal of Human Genetics|July 5, 2001
Localization of a susceptibility gene for familial nonmedullary thyroid carcinoma to chromosome 2q21J D McKay, F Lesueur, L Jonard, et al.American Journal of Human Genetics|July 10, 2001
Schizophrenia and affective disorders--cosegregation with a translocation at chromosome 1q42 that directly disrupts brain-expressed genes: clinical and P300 findings in a familyD H Blackwood, A Fordyce, M T Walker, et al.American Journal of Human Genetics|September 1, 1975
Inheritance of very low serum dopamine-beta-hydroxylase activityR M Weinshilboum, H G Schorott, F A Raymond, et al.Pageof 979