The Influence of Smoking and Occupational Risk Factors on DNA Methylation in the AHRR and F2RL3 Genes
Pelland-St-Pierre, Laura, Pham, Michael C, Nguyen, Alice Quynh Huong, Pasquet, Romain, Taylor, Sherryl A, Bosson-Rieutort, Delphine, Koushik, Anita, Ho, Vikki
Published in Cancer epidemiology, biomarkers & prevention (06.02.2024)
Published in Cancer epidemiology, biomarkers & prevention (06.02.2024)
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A cross-sectional study of global DNA methylation and risk of colorectal adenoma
King, Will D, Ashbury, Janet E, Taylor, Sherryl A, Tse, M Yat, Pang, Stephen C, Louw, Jacob A, Vanner, Stephen J
Published in BMC cancer (07.07.2014)
Published in BMC cancer (07.07.2014)
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Journal Article
Paternal transmission of fragile X syndrome
Zeesman, Susan, Zwaigenbaum, Lonnie, Whelan, Donald T., Hagerman, Randi J., Tassone, Flora, Taylor, Sherryl A.M.
Published in American journal of medical genetics. Part A (30.08.2004)
Published in American journal of medical genetics. Part A (30.08.2004)
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Journal Article
A model for GFRα4 function and a potential modifying role in multiple endocrine neoplasia 2
VANHORNE, Judith B, ANDREW, Scott D, HARRISON, Karen J, TAYLOR, Sherryl A. M, THOMAS, Bradley, MCDONALD, Thomas J, AINSWORTH, Peter J, MULLIGAN, Lois M
Published in Oncogene (03.02.2005)
Published in Oncogene (03.02.2005)
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Biomarkers measured in buccal and blood leukocyte DNA as proxies for colon tissue global methylation
Ashbury, Janet E, Taylor, Sherryl A, Tse, M Yat, Pang, Stephen C, Louw, Jacob A, Vanner, Stephen J, King, Will D
Published in International journal of molecular epidemiology and genetics (01.01.2014)
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Published in International journal of molecular epidemiology and genetics (01.01.2014)
Journal Article
Boy with 47,XXY,del(15)(q11.2q13) karyotype and Prader–Willi syndrome: A new case and review of the literature
Nowaczyk, Małgorzata J.M., Zeesman, Susan, Kam, April, Taylor, Sherryl A.M., Carter, Ronald F., Whelan, Donald T.
Published in American journal of medical genetics. Part A (15.02.2004)
Published in American journal of medical genetics. Part A (15.02.2004)
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A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes
MacDonald, Marcy E., Ambrose, Christine M., Duyao, Mabel P., Myers, Richard H., Lin, Carol, Srinidhi, Lakshmi, Barnes, Glenn, Taylor, Sherryl A., James, Marianne, Groot, Nicolet, MacFarlane, Heather, Jenkins, Barbara, Anderson, Mary Anne, Wexler, Nancy S., Gusella, James F., Bates, Gillian P., Baxendale, Sarah, Hummerich, Holger, Kirby, Susan, North, Mike, Youngman, Sandra, Mott, Richard, Zehetner, Gunther, Sedlacek, Zdenek, Poustka, Annemarie, Frischauf, Anna-Maria, Lehrach, Hans, Buckler, Alan J., Church, Deanna, Doucette-Stamm, Lynn, O'Donovan, Michael C., Riba-Ramirez, Laura, Shah, Manish, Stanton, Vincent P., Strobel, Scott A., Draths, Karen M., Wales, Jennifer L., Dervan, Peter, Housman, David E., Altherr, Michael, Shiang, Rita, Thompson, Leslie, Fielder, Thomas, Wasmuth, John J., Tagle, Danilo, Valdes, John, Elmer, Lawrence, Allard, Marc, Castilla, Lucio, Swaroop, Manju, Blanchard, Kris, Collins, Francis S., Snell, Russell, Holloway, Tracey, Gillespie, Kathleen, Datson, Nicole, Shaw, Duncan, Harper, Peter S.
Published in Cell (26.03.1993)
Published in Cell (26.03.1993)
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Quantitative neuropathological changes in presymptomatic Huntington's disease
Gómez-Tortosa, Estrella, MacDonald, Marcy E., Friend, Julia C., Taylor, Sherryl A.M., Weiler, Larry J., Cupples, L. Adrienne, Srinidhi, Jayalakshmi, Gusella, James F., Bird, Edward D., Vonsattel, Jean-Paul, Myers, Richard H.
Published in Annals of neurology (01.01.2001)
Published in Annals of neurology (01.01.2001)
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Journal Article
Genetic basis of familial Meniere's disease
Fung, Kevin, Xie, Y, Hall, Stephen F, Lillicrap, David P, Taylor, Sherryl A M
Published in Journal of otolaryngology (01.02.2002)
Published in Journal of otolaryngology (01.02.2002)
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Journal Article
A model for GFR alpha 4 function and a potential modifying role in multiple endocrine neoplasia 2
Vanhorne, Judith B, Andrew, Scott D, Harrison, Karen J, Taylor, Sherryl A M, Thomas, Bradley, McDonald, Thomas J, Ainsworth, Peter J, Mulligan, Lois M
Published in Oncogene (03.02.2005)
Published in Oncogene (03.02.2005)
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Journal Article
Mutation of RET codon 768 is associated with the FMTC phenotype
Boccia, Lara M., Green, Jane S., Joyce, Carol, Eng, Charts, Taylor, Sherryl A. M., Mulligan, Lois M.
Published in Clinical genetics (01.02.1997)
Published in Clinical genetics (01.02.1997)
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Journal Article
Severe haemophilia A in a female resulting from two de novo factor VIII mutations
Windsor, S, Lyng, A, Taylor, S A, Ewenstein, B M, Neufeld, E J, Lillicrap, D
Published in British journal of haematology (01.08.1995)
Published in British journal of haematology (01.08.1995)
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Journal Article
A past mutation at isoleucine 397 is now a common cause of moderate/mild haemophilia B
Bottema, C D, Koeberl, D D, Ketterling, R P, Bowie, E J, Taylor, S A, Lillicrap, D, Shapiro, A, Gilchrist, G, Sommer, S S
Published in British journal of haematology (01.06.1990)
Published in British journal of haematology (01.06.1990)
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Characterization of the original Christmas disease mutation (cysteine 206----serine): from clinical recognition to molecular pathogenesis
Taylor, S A, Duffin, J, Cameron, C, Teitel, J, Garvey, B, Lillicrap, D P
Published in Thrombosis and haemostasis (23.01.1992)
Published in Thrombosis and haemostasis (23.01.1992)
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A model for GFR 4 function and a potential modifying role in multiple endocrine neoplasia 2
Vanhorne, Judith B, Andrew, Scott D, Harrison, Karen J, Sherryl AM Taylor, Bradley, Thomas, McDonald, Thomas J, Ainsworth, Peter J, Mulligan, Lois M
Published in Oncogene (03.02.2005)
Published in Oncogene (03.02.2005)
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Journal Article
Multiple Xba I polymorphisms in haemophilia A
Published in British journal of haematology
(01.06.1990)
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