2009

• Meyer-Rochow, G., Smith, J., Richardson, A., Marsh, D., Sidhu, S., Robinson, B., Benn, D. Denaturing High Performance Liquid Chromatography Detection of SDHB, SDHD, and VHL Germline Mutations in Pheochromocytoma. The Journal of surgical research. 2009; 157:55-62. [Abstract]
• Hahn, M., McDonnell, J., Marsh, D. The effect of disease-associated HRPT2 mutations on splicing. Journal of Endocrinology. 2009; 201:387-396. [Abstract]
• Howell, V., Gill, A., Clarkson, A., Nelson, A., Dunne, R., Delbridge, L., Robinson, B., Teh, B., Gimm, O., Marsh, D. Accuracy of combined protein gene product 9.5 and parafibromin markers for immunohistochemical diagnosis of parathyroid carcinoma. The Journal of clinical endocrinology and metabolism. 2009; 94:434-41. [Abstract]

2008

• Marsh, D., Trahair, T., Martin, J., Chee, W., Walker, J., Kirk, E., Baxter, R., Marshall, G. Rapamycin treatment for a child with germline PTEN mutation. Nature clinical practice. Oncology. 2008; 5:357-61. [Abstract]
• Marsh, D., Zori, R. Cowden Syndrome. In: Encyclopedia of Cancer, Vol. 1. Germany: Springer 2008. p. 0.

2007

• Hahn, M., Marsh, D. Nucleolar localization of parafibromin is mediated by three nucleolar localization signals. FEBS letters. 2007; 581:5070-4. [Abstract]
• Marsh, D., Hahn, M., Howell, V., Gill, A. Molecular diagnosis of primary hyperparathyroidism in familial cancer syndromes. Expert Opinion on Medical Diagnostics. 2007; 1:377-392.

2006

• Howell, V., Cardinal, J., Richardson, A., Gimm, O., Robinson, B., Marsh, D. Rapid Mutation Screening for HRPT2 and MEN1 Mutations Associated with Familial and Sporadic Primary Hyperparathyroidism. The Journal of molecular diagnostics : JMD. 2006; 8:559-66. [Abstract]
• Gill, A., Clarkson, A., Gimm, O., Keil, J., Dralle, H., Howell, V., Marsh, D. Loss of Nuclear Expression of Parafibromin Distinguishes Parathyroid Carcinomas and Hyperparathyroidism-Jaw Tumor (HPT-JT) Syndrome-related Adenomas From Sporadic Parathyroid Adenomas and Hyperplasias. The American journal of surgical pathology. 2006; 30:1140-1149. [Abstract]
• Benn, D., Richardson, A., Marsh, D., Robinson, B. Genetic testing in pheochromocytoma- and paraganglioma-associated syndromes. Annals of the New York Academy of Sciences. 2006; 1073:104-11. [Abstract]
• Benn, D., Gimenez-Roqueplo, A., Reilly, J., Bertherat, J., Burgess, J., Byth, K., Croxson, M., Dahia, P., Elston, M., Gimm, O., Henley, D., Herman, P., Murday, V., Niccoli-Sire, P., Pasieka, J., Rohmer, V., Tucker, K., Jeunemaitre, X., Marsh, D., Plouin, P., Robinson, B. Clinical presentation and penetrance of Pheochromocytoma/ Paraganglioma syndromes. The Journal of clinical endocrinology and metabolism. 2006; 91:827-36. [Abstract]
• Benn, D., Gimenez-Roqueplo, A., Reilly, J., Bertherat, J., Burgess, J., Byth, K., Croxson, M., Dahia, P., Elston, M., Gimm, O., Henley, D., Herman, P., Murday, V., Niccoli-Sire, P., Pasieka, J., Rohmer, V., Tucker, K., Jeunemaitre, X., Marsh, D., Plouin, P., Robinson, B. Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes. Journal of Clinical Endocrinology and Metabolism. 2006; 91:827-836. [Abstract]
• Moscova, M., Marsh, D., Baxter, R. Protein chip discovery of secreted proteins regulated by the phosphatidylinositol 3-kinase pathway in ovarian cancer cell lines. Cancer research. 2006; 66:1376-83. [Abstract]
• Gimm, O., Lorenz, K., Nguyen Thanh, P., Schneyer, U., Bloching, M., Howell, V., Marsh, D., Teh, B., Krause, U., Dralle, H. [Prophylactic parathyroidectomy for familial parathyroid carcinoma]. Der Chirurg; Zeitschrift fur alle Gebiete der operativen Medizen. 2006; 77:15-24. [Abstract]

2005

• Moscova, M., Marsh, D., Baxter, R. Identification of Cytokines regulated by phosphatidylinositol-3 kinase in ovarian cancer. Clinical Cancer Research. 2005; 11:8977S-8977S. [Abstract]
• Hahn, M., Marsh, D. Identification of a functional bipartite nuclear localization signal in the tumor suppressor parafibromin. Oncogene. 2005; 24:6241-8. [Abstract]
• Dahia, P., Ross, K., Wright, M., Hayashida, C., Santagata, S., Barontini, M., Kung, A., Sanso, G., Powers, J., Tischler, A., Hodin, R., Heitritter, S., Moore, F., Dluhy, R., Sosa, J., Ocal, I., Benn, D., Marsh, D., Robinson, B., Schneider, K., Garber, J., Arum, S., Korbonits, M., Grossman, A., Pigny, P., Toledo, S., Nose, V., Li, C., Stiles, C. A HIF1 alpha regulatory loop links hypoxia and mitochondrial signals in pheochromocytomas. Plos Genetics. 2005; 1:72-80. [Abstract]
• Marsh, D., Benn, D. Von Hippel-Lindau Disease. In: Encyclopedia of Diagnostics Genomics and Proteomics. New York: Marcel Dekker 2005. p. 1329-1333.
• Marsh, D., Zori, R. Cowden Syndrome. In: Encyclopaedia of Diagnostics Genomics and Proteomics. New York: Marcel Dekker Inc. 2005. p. 301-304.

2004

• Haven, C., Howell, V., Eilers, P., Dunne, R., Takahashi, M., van Puijenbroek, M., Furge, K., Kievit, J., Tan, M., Fleuren, G., Robinson, B., Delbridge, L., Philips, J., Nelson, A., Krause, U., Dralle, H., Hoang-Vu, C., Gimm, O., Morreau, H., Marsh, D., Teh, B. Gene expression of parathyroid tumors: molecular subclassification and identification of the potential malignant phenotype. Cancer research. 2004; 64:7405-11. [Abstract]
• Howell, V., Zori, R., Stalker, H., Williams, C., Jesse, N., Nelson, A., Robinson, B., Marsh, D. A molecular diagnosis of hyperparathyroidism-jaw tumor syndrome in an adolescent with recurrent kidney stones. The Journal of pediatrics. 2004; 145:567. [Abstract]
• McDonnell, C., Benn, D., Marsh, D., Robinson, B., Zacharin, M. K40E: a novel succinate dehydrogenase (SDH)B mutation causing familial phaeochromocytoma and paraganglioma. Clinical endocrinology. 2004; 61:510-4. [Abstract]
• Kirk, E., Smith, J., Field, M., Marshall, G., Marsh, D. Diagnosis of Proteus syndrome was correct. American Journal of Medical Genetics. Part A. 2004. p. 214-5; author reply 216-7. [Abstract]
• Marsh, D., Morreau, H., Teh, B. HRPT2 and parathyroid cancer. The lancet oncology. 2004. p. 78. [Abstract]
• Teh, B., Howell, V., Haven, C., Kahnoski, K., Khoo, S., Petillo, D., Chen, J., Fleuren, G., Robinson, B., Delbridge, L., Philips, J., Nelson, A., Krause, U., Hammje, K., Dralle, H., Hoang-Vu, C., Gimm, O., Marsh, D., Morreau, H. Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome. Human genetics. 2004; 114:221-224. [Abstract]

2003

• Zhou, X., Marsh, D., Morrison, C., Chaudhury, A., Maxwell, M., Reifenberger, G., Eng, C. Germline inactivation of PTEN and dysregulation of the phosphoinositol-3-kinase/Akt pathway cause human Lhermitte-Duclos disease in adults. American journal of human genetics. 2003; 73:1191-1198. [Abstract]
• Howell, V., Haven, C., Kahnoski, K., Khoo, S., Petillo, D., Chen, J., Fleuren, G., Robinson, B., Delbridge, L., Philips, J., Nelson, A., Krause, U., Hammje, K., Dralle, H., Hoang-Vu, C., Gimm, O., Marsh, D., Morreau, H., Teh, B. HRPT2 mutations are associated with malignancy in sporadic parathyroid tumours. Journal of medical genetics. 2003; 40:657-63. [Abstract]
• Gimm, O., Marsh, D. Does a somatic deletion in RET clarify the sporadic nature of medullary thyroid carcinoma?. Journal of endocrinological investigation. 2003. p. 381-383. [Abstract]
• Marsh, D., Theodosopoulos, G., Martin-Schulte, K., Richardson, A., Philips, J., Röher, H., Delbridge, L., Robinson, B. Genome-wide copy number imbalances identified in familial and sporadic medullary thyroid carcinoma. The Journal of clinical endocrinology and metabolism. 2003; 88:1866-72. [Abstract]
• Benn, D., Croxson, M., Tucker, K., Bambach, C., Richardson, A., Delbridge, L., Pullan, P., Hammond, J., Marsh, D., Robinson, B. Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas. Oncogene. 2003; 22:1358-64. [Abstract]
• Bernard, M., Sidhu, S., Berger, N., Peix, J., Marsh, D., Robinson, B., Gaston, V., Le Bouc, Y., Gicquel, C. A case report in favor of a multistep adrenocortical tumorigenesis. The Journal of clinical endocrinology and metabolism. 2003; 88:998-1001. [Abstract]
• Marsh, D. Endocrine Tumors - book review. Cancer Forum. 2003; 27(3):1810-181.