1. Siguero-Álvarez, Marcos, Salguero-Jiménez, Alejandro, Grego-Bessa, Joaquim, Gimeno-Blanes, Juan R, de la Pompa, José Luis. 2022. A Human Hereditary Cardiomyopathy Shares a Genetic Substrate With Bicuspid Aortic Valve. In Circulation, 147, 47-65. doi:10.1161/CIRCULATIONAHA.121.058767. https://pubmed.ncbi.nlm.nih.gov/36325906/
2. Takahashi, Meiko, Fujita, Manabu, Furukawa, Yoichi, Ogawa, Michio, Nakamura, Yusuke. . Isolation of a novel human gene, APCDD1, as a direct target of the beta-Catenin/T-cell factor 4 complex with probable involvement in colorectal carcinogenesis. In Cancer research, 62, 5651-6. doi:. https://pubmed.ncbi.nlm.nih.gov/12384519/
3. Neupane, Sanjiv, Sohn, Wern-Joo, Gwon, Gi-Jeong, Lee, Youngkyun, Kim, Jae-Young. 2015. The role of APCDD1 in epithelial rearrangement in tooth morphogenesis. In Histochemistry and cell biology, 144, 377-87. doi:10.1007/s00418-015-1345-z. https://pubmed.ncbi.nlm.nih.gov/26170146/
4. Lee, Hyun Kyoung, Laug, Dylan, Zhu, Wenyi, Mohila, Carrie, Deneen, Benjamin. 2015. Apcdd1 stimulates oligodendrocyte differentiation after white matter injury. In Glia, 63, 1840-9. doi:10.1002/glia.22848. https://pubmed.ncbi.nlm.nih.gov/25946682/
5. Shimomura, Yutaka, Agalliu, Dritan, Vonica, Alin, Barres, Ben A, Christiano, Angela M. . APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex. In Nature, 464, 1043-7. doi:10.1038/nature08875. https://pubmed.ncbi.nlm.nih.gov/20393562/
6. Skopelitou, Diamanto, Miao, Beiping, Srivastava, Aayushi, Försti, Asta, Bandapalli, Obul Reddy. 2021. Whole Exome Sequencing Identifies APCDD1 and HDAC5 Genes as Potentially Cancer Predisposing in Familial Colorectal Cancer. In International journal of molecular sciences, 22, . doi:10.3390/ijms22041837. https://pubmed.ncbi.nlm.nih.gov/33673279/
7. Han, Weifeng, Liu, Junpeng. 2017. Epigenetic silencing of the Wnt antagonist APCDD1 by promoter DNA hyper-methylation contributes to osteosarcoma cell invasion and metastasis. In Biochemical and biophysical research communications, 491, 91-97. doi:10.1016/j.bbrc.2017.07.049. https://pubmed.ncbi.nlm.nih.gov/28698141/