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Corticotroph cells give rise to aggressive and rare pituitary neoplasms comprising ACTH-producing adenomas resulting in Cushing disease (CD), clinically silent ACTH adenomas (SCA), Crooke cell adenomas (CCA) and ACTH-producing carcinomas (CA). The molecular pathogenesis of these tumors is still poorly understood. To better understand the genomic landscape of all the lesions of the corticotroph lineage, we sequenced the whole exome of three SCA, one CCA, four ACTH-secreting PA causing CD, one corticotrophinoma occurring in a CD patient who developed Nelson syndrome after adrenalectomy and one patient with an ACTH-producing CA. The ACTH-producing CA was the lesion with the highest number of single nucleotide variants (SNV) in genes such as <i>USP8</i>, <i>TP53, AURKA, EGFR, HSD3B1</i> and <i>CDKN1A</i>. The <i>USP8</i> variant was found only in the ACTH-CA and in the corticotrophinoma occurring in a patient with Nelson syndrome. In CCA, SNV in <i>TP53, EGFR, HSD3B1</i> and <i>CDKN1A</i> SNV were present. <i>HSD3B1</i> and <i>CDKN1A</i> SNVs were present in all three SCA, whereas in two of these tumors SNV in <i>TP53, AURKA</i> and <i>EGFR</i> were found. None of the analyzed tumors showed SNV in <i>USP48, BRAF, BRG1</i> or <i>CABLES1</i>. The amplification of 17q12 was found in all tumors, except for the ACTH-producing carcinoma. The four clinically functioning ACTH adenomas and the ACTH-CA shared the amplification of 10q11.22 and showed more copy-number variation (CNV) gains and single-nucleotide variations than the nonfunctioning tumors.