Associated Papers
The intricate dance of RNA-binding proteins: unveiling the mechanisms behind male infertility.
Gao Y et al.
Human Reproduction Update, 2026
Frequency enrichment of coding variants in a French-Canadian founder population and its implication for inflammatory bowel diseases.
Bhérer C et al.
Medrxiv : the Preprint Server for Health Sciences, 2025
40791678 (PubMed )
Supplement: media-2.xlsx › Table_S12_ClinVar_PLP_variants
Profile of DHX37 gene defects in human genetic diseases: 46,XY disorders of sex development.
Peng H et al.
Frontiers in Endocrinology, 2025
NR5A1/SF-1 Collaborates with Inhibin α and the Androgen Receptor.
Naamneh Elzenaty R et al.
International Journal of Molecular Sciences, 2024
39337600 (PubMed )
Supplement: ijms-25-10109-s001.zip › ijms-3175587-supplementary.pdf
Identification and functional analysis of a rare variant of gene DHX37 in a patient with 46,XY disorders of sex development.
Jiang W et al.
Molecular Genetics & Genomic Medicine, 2024
DHX37 and the Implications in Disorders of Sex Development: An Update Review.
de Oliveira FR et al.
Hormone Research in Paediatrics, 2024
DHX37 and NR5A1 Variants Identified in Patients with 46,XY Partial Gonadal Dysgenesis.
de Oliveira FR et al.
Life (basel, Switzerland), 2023
Monogenic Forms of DSD: An Update.
McElreavey K et al.
Hormone Research in Paediatrics, 2023
Whole-exome sequencing of a Saudi epilepsy cohort reveals association signals in known and potentially novel loci.
Al Anazi AH et al.
Human Genomics, 2022
36539902 (PubMed )
Supplement: 40246_2022_444_MOESM2_ESM.xlsx › Epilepsy_Uncertain_variants
DHX37 and 46,XY DSD: A New Ribosomopathy?
McElreavey K et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation, 2022
Paralog Studies Augment Gene Discovery: DDX and DHX Genes.
Paine I et al.
American Journal of Human Genetics, 2019
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