Publications for Diana Benn
Publications for Diana Benn
2016
Flynn, A., Dwight, T., Harris, J., Benn, D., Zhou,
L., Hogg, A., Catchpoole, D., James, P., Duncan,
E., Trainer, A., Gill, A., et al (2016). Pheo-Type:
A Diagnostic Gene-expression Assay for the
Classification of Pheochromocytoma and
Paraganglioma. Journal of Clinical
Endocrinology and Metabolism, 101(4),
1034-1043. <a
href="http://dx.doi.org/10.1210/jc.2015-3889">[
More Information]</a>
2015
Benn, D., Robinson, B., Clifton-Bligh, R. (2015).
15 Years of Paraganglioma: Clinical
manifestations of paraganglioma syndromes
types 1-5. Endocrine-Related Cancer, 22(4),
T91-T103. <a
href="http://dx.doi.org/10.1530/ERC-15-0268">[
More Information]</a>
Kim, E., Rath, E., Tsang, V., Duff, A., Robinson,
B., Church, W., Benn, D., Dwight, T.,
Clifton-Bligh, R. (2015). Structural and
functional consequences of succinate
dehydrogenase subunit B mutations.
Endocrine-Related Cancer, 22(3), 387-397. <a
href="http://dx.doi.org/10.1530/ERC-15-0099">[
More Information]</a>
Flynn, A., Benn, D., Clifton-Bligh, R., Robinson,
B., Trainer, A., James, P., Hogg, A., Waldeck,
K., George, J., Li, J., Gill, A., et al (2015). The
genomic landscape of phaeochromocytoma.
Journal of Pathology, 236(1), 78-89. <a
href="http://dx.doi.org/10.1002/path.4503">[Mo
re Information]</a>
2014
Pillai, U., Phillips, K., Wilkins, G., Baxter, R.,
Benn, D., Parker, N., Smith, R., Marsh, D.
(2014). Factors that may influence the
willingness of cancer patients to consent for
biobanking. Biopreservation and Biobanking,
12(6), 409-414. <a
href="http://dx.doi.org/10.1089/bio.2014.0039">
[More Information]</a>
Tsang, V., Dwight, T., Benn, D.,
Meyer-Rochow, G., Gill, A., Sywak, M., Sidhu,
S., Veivers, D., Sue, C., Robinson, B.,
Clifton-Bligh, R., Parker, N. (2014).
Overexpression of miR-210 is associated with
SDH-related pheochromocytomas,
paragangliomas, and gastrointestinal stromal
tumours. Endocrine-Related Cancer, 21(3),
415-426. <a
href="http://dx.doi.org/10.1530/ERC-13-0519">[
More Information]</a>
Paik, J., Toon, C., Benn, D., High, H., Hasovitz,
C., Pavlakis, N., Clifton-Bligh, R., Gill, A.
(2014). Renal Carcinoma Associated With
Succinate Dehydrogenase B Mutation: A New
and Unique Subtype of Renal Carcinoma.
Journal of Clinical Oncology, 32(6), e10-e13. <a
href="http://dx.doi.org/10.1200/JCO.2012.47.26
47">[More Information]</a>
Gill, A., Hes, O., Papathomas, T., Šedivcová, M.,
Tan, P., Agaimy, A., Andresen, P., Kedziora, A.,
Clarkson, A., Toon, C., Sioson, L., Clifton-Bligh,
R., Robinson, B., Benn, D., et al (2014).
Succinate dehydrogenase (SDH)-deficient renal
carcinoma: A morphologically distinct entity: A
clinicopathologic series of 36 tumors from 27
patients. The American Journal of Surgical
Pathology, 38(12), 1588-1602. <a
href="http://dx.doi.org/10.1097/PAS.000000000
0000292">[More Information]</a>
Gill, A., Toon, C., Clarkson, A., Sioson, L.,
Chou, A., Winship, I., Robinson, B., Benn, D.,
Clifton-Bligh, R., Dwight, T. (2014). Succinate
dehydrogenase deficiency is rare in pituitary
adenomas. American Journal of Surgical
Pathology, 38(4), 560-566. <a
href="http://dx.doi.org/10.1097/PAS.000000000
0000149">[More Information]</a>
Holt, D., Henthorn, P., Howell, V., Robinson, B.,
Benn, D. (2014). Succinate Dehydrogenase
Subunit D and A Succinate Dehydrogenase
Subunit B Mutation Analysis in Canine
Phaeochromocytoma and Paraganglioma.
Journal of Comparative Pathology, 151(1),
25-34. <a
href="http://dx.doi.org/10.1016/j.jcpa.2014.03.00
7">[More Information]</a>
McInerney-Leo, A., Marshall, M., Gardiner, B.,
Benn, D., McFarlane, J., Robinson, B., Brown,
M., Leo, P., Clifton-Bligh, R., Duncan, E.
(2014). Whole exome sequencing is an efficient
and sensitive method for detection of germline
mutations in patients with phaeochromcytomas
and paragangliomas. Clinical Endocrinology,
80(1), 25-33. <a
href="http://dx.doi.org/10.1111/cen.12331">[Mo
re Information]</a>
2013
Soon, P., Kim, E., Pon, C., Gill, A., Moore, K.,
Spillane, A., Benn, D., Baxter, R. (2013). Breast
cancer-associated fibroblasts induce
epithelial-to-mesenchymal transition in breast
cancer cells. Endocrine-Related Cancer, 20(1),
1-12. <a
href="http://dx.doi.org/10.1530/ERC-12-0227">[
More Information]</a>
Dwight, T., Mann, K., Benn, D., Robinson, B.,
McKelvie, P., Gill, A., Winship, I.,
Clifton-Bligh, R. (2013). Familial SDHA
Mutation Associated With Pituitary Adenoma
Publications for Diana Benn
and Pheochromocytoma/Paraganglioma. Journal
of Clinical Endocrinology and Metabolism,
98(6), E1103-E1108. <a
href="http://dx.doi.org/10.1210/jc.2013-1400">[
More Information]</a>
Gill, A., Lipton, L., Taylor, J., Benn, D.,
Richardson, A., Frydenberg, M., Shapiro, J.,
Clifton-Bligh, R., Chow, C., Bogwitz, M. (2013).
Germline SDHC mutation presenting as
recurrent SDH deficient GIST and renal
carcinoma. Pathology, 45(7), 689-691. <a
href="http://dx.doi.org/10.1097/PAT.000000000
0000018">[More Information]</a>
Dwight, T., Benn, D., Clarkson, A., Vilain, R.,
Lipton, L., Robinson, B., Clifton-Bligh, R., Gill,
A. (2013). Loss of SDHA Expression Identifies
SDHA Mutations in Succinate
Dehydrogenase-deficient Gastrointestinal
Stromal Tumors. The American Journal of
Surgical Pathology, 37(2), 226-233. <a
href="http://dx.doi.org/10.1097/PAS.0b013e318
2671155">[More Information]</a>
2012
Tsang, V., Parker, N., Cassano, J., Dwight, T.,
Sue, C., Veivers, D., Robinson, B., Benn, D.,
Clifton-Bligh, R. (2012). Interaction between
hypoxia and mutations in the SDH subunit genes
associated with
phaeochromocytoma/paragangliomas. 2012
Annual Scientific Meeting of the Endocrine
Society of Australia and the Society for
Reproductive Biology, Gold Coast, Queensland,
Australia.
2011
Gill, A., Pachter, N., Clarkson, A., Tucker, K.,
Winship, I., Benn, D., Robinson, B.,
Clifton-Bligh, R. (2011). Renal tumors and
hereditary pheochromocytoma-paraganglioma
syndrome type 4. The New England Journal of
Medicine, 364(9), 885-886. <a
href="http://dx.doi.org/10.1056/NEJMc1012357
">[More Information]</a>
Gill, A., Pachter, N., Chou, A., Young, B.,
Clarkson, A., Tucker, K., Winship, I., Earls, P.,
Benn, D., Robinson, B., Clifton-Bligh, R., et al
(2011). Renal Tumors Associated With Germline
SDHB Mutation Show Distinctive Morphology.
American Journal of Surgical Pathology, 35(10),
1578-1585. <a
href="http://dx.doi.org/10.1097/PAS.0b013e318
227e7f4">[More Information]</a>
2010
Gill, A., Chou, A., Vilain, R., Clarkson, A., Lui,
M., Jin, R., Tobias, V., Samra, J., Goldstein, D.,
Smith, C., Smith, R., Sywak, M., Sidhu, S.,
Robinson, B., Eckstein, R., Benn, D.,
Clifton-Bligh, R., et al (2010).
Immunohistochemistry for SDHB Divides
Gastrointestinal Stromal Tumors (GISTs) into 2
Distinct Types. American Journal of Surgical
Pathology, 34(5), 636-644. <a
href="http://dx.doi.org/10.1097/PAS.0b013e318
1d6150d">[More Information]</a>
Gill, A., Benn, D., Chou, A., Clarkson, A.,
Muljono, A., Meyer-Rochow, G., Richardson,
A., Sidhu, S., Robinson, B., Clifton-Bligh, R.
(2010). Immunohistochemistry for SDHB triages
genetic testing of SDHB, SDHC, and SDHD in
paraganglioma-pheochromocytoma syndromes.
Human Pathology, 41(6), 805-814. <a
href="http://dx.doi.org/10.1016/j.humpath.2009.
12.005">[More Information]</a>
Meyer-Rochow, G., Jackson, N., Conaglen, J.,
Whittle, D., Kunnimalaiyaan, M., Chen, H.,
Westin, G., Sandgren, J., Stalberg, P.,
Khanafshar, E., Gill, A., Clifton-Bligh, R.,
Robinson, B., Benn, D., Sidhu, S., et al (2010).
MicroRNA profiling of benign and malignant
pheochromocytoma identifies novel diagnostic
and therapeutic targets. Endocrine-Related
Cancer, 17(3), 835-846. <a
href="http://dx.doi.org/10.1677/ERC-10-0142">[
More Information]</a>
Meyer-Rochow, G., Schembri, G., Benn, D.,
Sywak, M., Delbridge, L., Robinson, B., Roach,
P., Sidhu, S. (2010). The Utility of
Metaiodobenzylguanidine Single Photon
Emission Computed Tomography/Computed
Tomography (MIBG SPECT/CT) for the
Diagnosis of Pheochromocytoma. Annals of
Surgical Oncology, 17(2), 392-400. <a
href="http://dx.doi.org/10.1245/s10434-009-085
0-5">[More Information]</a>
2009
Neumann, H., Erlic, Z., Boedeker, C., Rybicki,
L., Robledo, M., Hermsen, M., Schiavi, F.,
Falcioni, M., Kwok, P., Benn, D., Robinson, B.,
Learoyd, D., et al (2009). Clinical Predictors for
Germline Mutations in Head and Neck
Paraganglioma Patients: Cost Reduction Strategy
in Genetic Diagnostic Process as Fall-Out.
Cancer Research, 69(8), 3650-3656. <a
href="http://dx.doi.org/10.1158/0008-5472.CAN
-08-4057">[More Information]</a>
Meyer-Rochow, G., Smith, J., Richardson, A.,
Marsh, D., Sidhu, S., Robinson, B., Benn, D.
(2009). Denaturing High Performance Liquid
Chromatography Detection of SDHB, SDHD,
and VHL Germline Mutations in
Pheochromocytoma. Journal of Surgical
Research, 157, 55-62. <a
href="http://dx.doi.org/10.1016/j.jss.2008.07.043
">[More Information]</a>
Soon, P., Gill, A., Benn, D., Clarkson, A.,
Publications for Diana Benn
Robinson, B., McDonald, K., Sidhu, S. (2009).
Microarray gene expression and
immunohistochemistry analyses of
adrenocortical tumours identify IGF2 and Ki-67
as useful in differentiating carcinomas from
adenomas. Endocrine-Related Cancer, 16(2),
573-583. <a
href="http://dx.doi.org/10.1677/ERC-08-0237">[
More Information]</a>
2008
Soon, P., Libe, R., Benn, D., Gill, A., Shaw, J.,
Sywak, M., Groussin, L., Bertagna, X., Gicquel,
C., Bertherat, J., McDonald, K., Sidhu, S.,
Robinson, B. (2008). Loss of Heterozygosity of
17p13, With Possible
Involvement of ACADVL and ALOX15B, in the
Pathogenesis of Adrenocortical Tumors. Annals
of Surgery, 247(1), 157-164. <a
href="http://dx.doi.org/10.1097/SLA.0b013e318
153ff55">[More Information]</a>
Kim, L., Holland, A., Srinivasan, S., Cowell, C.,
Benn, D., Robinson, B. (2008). Paediatric
bilateral adrenal phaeochromocytomas in
association with a novel mutation in the von
Hippel Lindau gene. Journal of Paediatrics and
Child Health, 44(9), 514-516. <a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=18928468">[More Information]</a>
Addler, J., Meyer-Rochow, G., Chen, H., Benn,
D., Robinson, B., Sippel, R., Sidhu, S. (2008).
Pheochromocytoma: current approaches and
future directions. The Oncologist, 13(7),
779-793. <a
href="http://dx.doi.org/10.1634/theoncologist.20
08-0043">[More Information]</a>
2007
Benn, D., Robinson, B. (2007). Editorial:
Pheochromocytoma - quo vadis? Nature clinical
practice: Endocrinology and metabolism, 3(5),
377.
Soon, P., Benn, D., Gill, A., Robinson, B.,
McDonald, K. (2007). Es07 microarray gene
expression analysis of human adrenocortical
tumours. ANZ Journal of Surgery, 77(Suppl.1),
A22-A22. <a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=17490064">[More Information]</a>
Benn, D., Robinson, B. (2007).
Pheochromocytoma - quo vadis? Nature clinical
practice: Endocrinology and metabolism, 3(5),
377-377. <a
href="http://dx.doi.org/10.1038/ncpendmet0498"
>[More Information]</a>
2006
Elston, M., Benn, D., Robinson, B., Conaglen, J.
(2006). An apparently sporadic paraganglioma
with an SDHB gene germline mutation
presenting at age 68 years. Internal Medicine
Journal, 36, 129-131.
Benn, D., Robinson, B. (2006). Genetic basis of
phaeochromocytoma and paraganglioma. Best
Practice and Research: Clinical Endocrinology
and Metabolism, 20(3), 435-450. <a
href="http://dx.doi.org/10.1016/j.beem.2006.07.0
05">[More Information]</a>
Benn, D., Marsh, D., Robinson, B., Riches, J.
(2006). Genetic testing in pheochromocytomaand paraganglioma-associated syndromes.
Annals of the New York Academy of Sciences,
1073, 104-111. <a
href="http://dx.doi.org/10.1196/annals.1353.011
">[More Information]</a>
Bolland, M., Benn, D., Croxson, M., McCall, J.,
Shaw, J., Baillie, T., Robinson, B. (2006). Letter
to the Editor: Gastrointestinal stromal tumour in
succinate dehydrogenase subunit B
mutation-associated familial
phaeochromocytoma/paraganglioma. ANZ
Journal of Surgery, 76, 763-765.
2005
Dahia, P., Ross, K., Wright, M., Hayashida, C.,
Santagata, S., Barontini, M., Kung, A., Sanso,
G., Powers, J., Benn, D., Marsh, D., Robinson,
B., et al (2005). A HIF1-alpha Regulatory Loop
Links Hypoxia
and Mitochondrial Signals in
Pheochromocytomas. PLoS Genetics, 1(1),
72-80. <a
href="http://dx.doi.org/10.1371/journal.pgen.001
0008">[More Information]</a>
Benn, D., Gimenez-Roqueplo, A., Reilly, J.,
Bertherat, J., Burgess, J., Byth Wilson, K.,
Croxson, M., Dahia, P., Elston, M., Gimm, O.,
Marsh, D., Robinson, B., et al (2005). Clinical
presentation and penetrance of
Pheochromocytoma/ Paraganglioma syndromes.
Journal of Clinical Endocrinology and
Metabolism, 91(3), 827-836. <a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=16317055">[More Information]</a>
Alderazi, Y., Yeh, M., Robinson, B., Benn, D.,
Sywak, M., Learoyd, D., Delbridge, L., Sidhu, S.
(2005). Phaeochromocytoma: current concepts.
Medical Journal of Australia, 183(4), 201-204.
<a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=16097921">[More Information]</a>
Marsh, D., Benn, D. (2005). Von Hippel-Lindau
Disease. In Fuchs J and Podda M (Eds.),
Publications for Diana Benn
Encyclopaedia of Diagnostics Genomics and
Proteomics, (pp. 1329-1333). New York, USA:
Marcel Dekker.
2004
McDonnell, C., Benn, D., Marsh, D., Robinson,
B., Zacharin, M. (2004). K40E: A Novel
Succinate Dehydrogenase (Sdh)B Mutation
Causing Familial Phaeochromocytoma And
Paraganglioma. Clinical Endocrinology, 61(4),
510-514.
2003
Benn, D., Croxson, M., Tucker, K., Bambach,
C., Richardson, A., Delbridge, L., Pullan, P.,
Hammond, J., Marsh, D., Robinson, B. (2003).
Novel succinate dehydrogenase subunit B
(SDHB) mutations in familial
phaeochromocytomas and paragangliomas, but
an absence of somatic SDHB mutations in
sporatid phaeochromaocytomas. Oncogene,
22(9), 1358-1364.
2002
Benn, D., Marsh, D., Robinson, B. (2002).
Genetics of pheochromocytoma and
paraganglioma. Current Opinion in
Endocrinology, Diabetes and Obesity, 9(1),
79-86.
2001
Marsh, D., Howell, V., Benn, D., Robinson, B.,
Theodosopoulos, G., Riches, J., Proos, A., Eng,,
C. (2001). Rapid mutation scanning of genes
associated with familial cancer syndromes using
denaturing high-performance liquid
chromatography. Neoplasia (Spanish Edition):
oncologia multidisciplinaria, 3, 236-244.