Maher ER - Search Results

1

A comprehensive next generation sequencing-based genetic testing strategy to improve diagnosis of inherited pheochromocytoma and paraganglioma.

Rattenberry E, Vialard L, Yeung A, Bair H, McKay K, Jafri M, Canham N, Cole TR, Denes J, Hodgson SV, Irving R, Izatt L, Korbonits M, Kumar AV, Lalloo F, Morrison PJ, Woodward ER, Macdonald F, Wallis Y, Maher ER. Rattenberry E, et al. Among authors: maher er. J Clin Endocrinol Metab. 2013 Jul;98(7):E1248-56. doi: 10.1210/jc.2013-1319. Epub 2013 May 10. J Clin Endocrinol Metab. 2013. PMID: 23666964

2

Phenotypic variation in hereditary nonpolyposis colon cancer syndrome. Association with infiltrative fibromatosis (desmoid tumor).

Maher ER, Morson B, Beach R, Hodgson SV. Maher ER, et al. Cancer. 1992 Apr 15;69(8):2049-51. doi: 10.1002/1097-0142(19920415)69:8<2049::aid-cncr2820690807>3.0.co;2-6. Cancer. 1992. PMID: 1544113

3

Genetics of familial and non-familial skull base tumours.

Irving RM, Moffat DA, Maher ER. Irving RM, et al. Among authors: maher er. Clin Otolaryngol Allied Sci. 1995 Feb;20(1):5-11. doi: 10.1111/j.1365-2273.1995.tb00003.x. Clin Otolaryngol Allied Sci. 1995. PMID: 7788935 Review.

4

Molecular genetic analysis of the mechanism of tumorigenesis in acoustic neuroma.

Irving RM, Moffat DA, Hardy DG, Barton DE, Xuereb JH, Maher ER. Irving RM, et al. Among authors: maher er. Arch Otolaryngol Head Neck Surg. 1993 Nov;119(11):1222-8. doi: 10.1001/archotol.1993.01880230066011. Arch Otolaryngol Head Neck Surg. 1993. PMID: 8217082

5

Genetic predisposition to phaeochromocytoma: analysis of candidate genes GDNF, RET and VHL.

Woodward ER, Eng C, McMahon R, Voutilainen R, Affara NA, Ponder BA, Maher ER. Woodward ER, et al. Among authors: maher er. Hum Mol Genet. 1997 Jul;6(7):1051-6. doi: 10.1093/hmg/6.7.1051. Hum Mol Genet. 1997. PMID: 9215674

6

Somatic neurofibromatosis type 2 gene mutations and growth characteristics in vestibular schwannoma.

Irving RM, Harada T, Moffat DA, Hardy DG, Whittaker JL, Xuereb JH, Maher ER. Irving RM, et al. Among authors: maher er. Am J Otol. 1997 Nov;18(6):754-60. Am J Otol. 1997. PMID: 9391673

7

Molecular genetic analysis of von Hippel-Lindau disease.

Richards FM, Webster AR, McMahon R, Woodward ER, Rose S, Maher ER. Richards FM, et al. Among authors: maher er. J Intern Med. 1998 Jun;243(6):527-33. doi: 10.1046/j.1365-2796.1998.00334.x. J Intern Med. 1998. PMID: 9681854 Free article. Review.

8

Germline E-cadherin gene (CDH1) mutations predispose to familial gastric cancer and colorectal cancer.

Richards FM, McKee SA, Rajpar MH, Cole TR, Evans DG, Jankowski JA, McKeown C, Sanders DS, Maher ER. Richards FM, et al. Among authors: maher er. Hum Mol Genet. 1999 Apr;8(4):607-10. doi: 10.1093/hmg/8.4.607. Hum Mol Genet. 1999. PMID: 10072428

9

Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlation.

Lam WW, Hatada I, Ohishi S, Mukai T, Joyce JA, Cole TR, Donnai D, Reik W, Schofield PN, Maher ER. Lam WW, et al. Among authors: maher er. J Med Genet. 1999 Jul;36(7):518-23. J Med Genet. 1999. PMID: 10424811 Free PMC article.

10

Differences in allelic distribution of two polymorphisms in the VHL-associated gene CUL2 in pheochromocytoma patients without somatic CUL2 mutations.

Duerr EM, Gimm O, Neuberg DS, Kum JB, Clifford SC, Toledo SP, Maher ER, Dahia PL, Eng C. Duerr EM, et al. Among authors: maher er. J Clin Endocrinol Metab. 1999 Sep;84(9):3207-11. doi: 10.1210/jcem.84.9.5961. J Clin Endocrinol Metab. 1999. PMID: 10487688

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