1. Costain, Gregory, Walker, Susan, Argiropoulos, Bob, Vorstman, Jacob A S, Scherer, Stephen W. 2019. Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders. In Journal of neurodevelopmental disorders, 11, 3. doi:10.1186/s11689-019-9263-3. https://pubmed.ncbi.nlm.nih.gov/30732576/
2. Wonkam-Tingang, Edmond, Schrauwen, Isabelle, Esoh, Kevin K, Leal, Suzanne M, Wonkam, Ambroise. 2021. A novel variant in DMXL2 gene is associated with autosomal dominant non-syndromic hearing impairment (DFNA71) in a Cameroonian family. In Experimental biology and medicine (Maywood, N.J.), 246, 1524-1532. doi:10.1177/1535370221999746. https://pubmed.ncbi.nlm.nih.gov/33715530/
3. Gobé, Clara, Elzaiat, Maëva, Meunier, Nicolas, Pailhoux, Eric, Pannetier, Maëlle. 2019. Dual role of DMXL2 in olfactory information transmission and the first wave of spermatogenesis. In PLoS genetics, 15, e1007909. doi:10.1371/journal.pgen.1007909. https://pubmed.ncbi.nlm.nih.gov/30735494/
4. Wahab, Fazal, Drummer, Charis, Schlatt, Stefan, Behr, Rüdiger. 2016. Dynamic Regulation of Hypothalamic DMXL2, KISS1, and RFRP Expression During Postnatal Development in Non-Human Primates. In Molecular neurobiology, 54, 8447-8457. doi:10.1007/s12035-016-0329-x. https://pubmed.ncbi.nlm.nih.gov/27957681/
5. Deberles, Emilie, Durand, Isabelle, Mittre, Hervé, Reznik, Yves, Morera, Julia. 2022. Local aromatase excess with recruitment of unusual promoters of CYP19A1 gene in prepubertal patients with gynecomastia. In Journal of pediatric endocrinology & metabolism : JPEM, 35, 924-930. doi:10.1515/jpem-2021-0757. https://pubmed.ncbi.nlm.nih.gov/35667691/