Publications by authors named "Angela Fay"

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Foods and Nutritional Characteristics Associated With Addictive-Like Eating.
Kirstie M Herb Neff, Angela Fay, Karen K Saules

Psychol Rep· August 2022

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Positive Germline Selection in Pedigrees With Multiple Endocrine Neoplasia Type 2 Carrying V804M Mutation in the RET Gene.
Leema Reddy Peddareddygari, Angela Musial Fay, Alexander L Shifrin, Raji P Grewal

World J Oncol· December 2016

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Neuroendocrine thymic carcinoma metastatic to the parathyroid gland that was reimplanted into the forearm in patient with multiple endocrine neoplasia type 1 syndrome: a challenging management dilemma.
Alexander L Shifrin, Virginia A LiVolsi, Min Zheng, Danielle E Lann, Svetlana Fomin, Angela M Fay

Endocr Pract· July 2014

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NSGC practice guideline: risk assessment and genetic counseling for hereditary breast and ovarian cancer.
Janice L Berliner, Angela Musial Fay, Shelly A Cummings, Brittany Burnett, Todd Tillmanns

J Genet Couns· April 2013

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Response to "Single nucleotide polymorphisms and development of hereditary medullary thyroid cancer in V804M RET families: disease modification or linkage disequilibrium?".
Alexander L Shifrin, Angela Fay, Yen-Hong Kuo, Jennifer Ogilvie

Surgery· June 2012

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Single nucleotide polymorphisms act as modifiers and correlate with the development of medullary and simultaneous medullary/papillary thyroid carcinomas in 2 large, non-related families with the RET V804M proto-oncogene mutation.
Alexander L Shifrin, Jennifer B Ogilvie, Michael T Stang, Angela Musial Fay, Yen-Hong Kuo

Surgery· December 2010

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One hundred and seven member family with the rearranged during transfection V804M proto-oncogene mutation presenting with simultaneous medullary and papillary thyroid carcinomas, rare primary hyperparathyroidism, and no pheochromocytomas: Is this a new syndrome-MEN 2C?
Alexander L Shifrin, Angela M Fay, Cristina Z Xenachis, Jerome J Vernick

Surgery· September 2010

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One hundred and seven family members with the rearranged during transfection V804M proto-oncogene mutation presenting with simultaneous medullary and papillary thyroid carcinomas, rare primary hyperparathyroidism, and no pheochromocytomas: is this a new syndrome--MEN 2C?
Alexander L Shifrin, Cristina Xenachis, Angela Fay, Theodore J Matulewicz, Yen-Hong Kuo

Surgery· December 2009

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Risk assessment and genetic counseling for hereditary breast and ovarian cancer: recommendations of the National Society of Genetic Counselors.
Janice L Berliner, Angela Musial Fay,

J Genet Couns· June 2007

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