Phenotypic expansion and variable expressivity in individuals with JARID2 ‐related intellectual disability: A case series

Nager syndrome in patient lacking acrofacial dysostosis: Expanding the phenotypic spectrum of SF3B4 ‐related disease

(2021) Maxime Cadieux‐Dion et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

JARID2 haploinsufficiency is associated with a clinically distinct neurodevelopmental syndrome

(2020) Eline A. Verberne et al.   GENETICS IN MEDICINE

Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen)

(2019) Erin Rooney Riggs et al.   GENETICS IN MEDICINE

Brazilian multicenter study of association between polymorphisms inCRISPLD2andJARID2and non-syndromic oral clefts

(2016) Ana Camila Messetti et al.   JOURNAL OF ORAL PATHOLOGY & MEDICINE

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology

(2015) Sue Richards et al.   GENETICS IN MEDICINE

Association ofJARID2polymorphisms with non-syndromic orofacial clefts in northern Chinese Han population

(2014) Yanru Hao et al.   JOURNAL OF ORAL PATHOLOGY & MEDICINE

Effectiveness of exome and genome sequencing guided by acuity of illness for diagnosis of neurodevelopmental disorders

(2014) S. E. Soden et al.   Science Translational Medicine

Expression and association data strongly support JARID2 involvement in nonsyndromic cleft lip with or without cleft palate

(2010) Luca Scapoli et al.   HUMAN MUTATION

JARID2 regulates binding of the Polycomb repressive complex 2 to target genes in ES cells

(2010) Diego Pasini et al.   NATURE