Circulating tumor DNA as an early cancer detection tool
Campos-Carrillo, Andrea, Weitzel, Jeffrey N., Sahoo, Prativa, Rockne, Russell, Mokhnatkin, Janet V., Murtaza, Muhammed, Gray, Stacy W., Goetz, Laura, Goel, Ajay, Schork, Nicholas, Slavin, Thomas P.
Published in Pharmacology & therapeutics (Oxford) (01.03.2020)
Published in Pharmacology & therapeutics (Oxford) (01.03.2020)
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Personalized circulating tumor DNA analysis to detect residual disease after neoadjuvant therapy in breast cancer
McDonald, Bradon R, Contente-Cuomo, Tania, Sammut, Stephen-John, Odenheimer-Bergman, Ahuva, Ernst, Brenda, Perdigones, Nieves, Chin, Suet-Feung, Farooq, Maria, Mejia, Rosa, Cronin, Patricia A, Anderson, Karen S, Kosiorek, Heidi E, Northfelt, Donald W, McCullough, Ann E, Patel, Bhavika K, Weitzel, Jeffrey N, Slavin, Thomas P, Caldas, Carlos, Pockaj, Barbara A, Murtaza, Muhammed
Published in Science translational medicine (07.08.2019)
Published in Science translational medicine (07.08.2019)
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Evaluation of ACMG-Guideline-Based Variant Classification of Cancer Susceptibility and Non-Cancer-Associated Genes in Families Affected by Breast Cancer
Maxwell, Kara N., Hart, Steven N., Vijai, Joseph, Schrader, Kasmintan A., Slavin, Thomas P., Thomas, Tinu, Wubbenhorst, Bradley, Ravichandran, Vignesh, Moore, Raymond M., Hu, Chunling, Guidugli, Lucia, Wenz, Brandon, Domchek, Susan M., Robson, Mark E., Szabo, Csilla, Neuhausen, Susan L., Weitzel, Jeffrey N., Offit, Kenneth, Couch, Fergus J., Nathanson, Katherine L.
Published in American journal of human genetics (05.05.2016)
Published in American journal of human genetics (05.05.2016)
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Journal Article
The effects of genomic germline variant reclassification on clinical cancer care
Slavin, Thomas P, Manjarrez, Sophia, Pritchard, Colin C, Gray, Stacy, Weitzel, Jeffrey N
Published in Oncotarget (11.01.2019)
Published in Oncotarget (11.01.2019)
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Two-marker association tests yield new disease associations for coronary artery disease and hypertension
Slavin, Thomas P., Feng, Tao, Schnell, Audrey, Zhu, Xiaofeng, Elston, Robert C.
Published in Human genetics (01.12.2011)
Published in Human genetics (01.12.2011)
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Journal Article
Mutation screening of germline TP53 mutations in high-risk Chinese breast cancer patients
Kwong, Ava, Shin, Vivian Yvonne, Ho, Cecilia Y S, Au, Chun Hang, Slavin, Thomas P, Weitzel, Jeffrey N, Chan, Tsun-Leung, Ma, Edmond S K
Published in BMC cancer (02.11.2020)
Published in BMC cancer (02.11.2020)
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The contribution of pathogenic variants in breast cancer susceptibility genes to familial breast cancer risk
Slavin, Thomas P, Maxwell, Kara N, Lilyquist, Jenna, Vijai, Joseph, Neuhausen, Susan L, Hart, Steven N, Ravichandran, Vignesh, Thomas, Tinu, Maria, Ann, Villano, Danylo, Schrader, Kasmintan A, Moore, Raymond, Hu, Chunling, Wubbenhorst, Bradley, Wenz, Brandon M, D'Andrea, Kurt, Robson, Mark E, Peterlongo, Paolo, Bonanni, Bernardo, Ford, James M, Garber, Judy E, Domchek, Susan M, Szabo, Csilla, Offit, Kenneth, Nathanson, Katherine L, Weitzel, Jeffrey N, Couch, Fergus J
Published in NPJ breast cancer (09.06.2017)
Published in NPJ breast cancer (09.06.2017)
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Conversion after laparoscopic cholecystectomy in England
Ballal, M., David, G., Willmott, S., Corless, D. J., Deakin, M., Slavin, J. P.
Published in Surgical endoscopy (01.10.2009)
Published in Surgical endoscopy (01.10.2009)
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Prevalence and characteristics of likely-somatic variants in cancer susceptibility genes among individuals who had hereditary pan-cancer panel testing
Slavin, Thomas P., Coffee, Bradford, Bernhisel, Ryan, Logan, Jennifer, Cox, Hannah C., Marcucci, Guido, Weitzel, Jeffrey, Neuhausen, Susan L., Mancini-DiNardo, Debora
Published in Cancer genetics (01.06.2019)
Published in Cancer genetics (01.06.2019)
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Abnormal body composition is a predictor of adverse outcomes after autologous haematopoietic cell transplantation
Armenian, Saro H., Iukuridze, Aleksi, Teh, Jennifer Berano, Mascarenhas, Kristen, Herrera, Alex, McCune, Jeannine S., Zain, Jasmine M., Mostoufi‐Moab, Sogol, McCormack, Shana, Slavin, Thomas P., Scott, Jessica M., Jones, Lee W., Sun, Can‐Lan, Forman, Stephen J., Wong, F. Lennie, Nakamura, Ryotaro
Published in Journal of cachexia, sarcopenia and muscle (01.08.2020)
Published in Journal of cachexia, sarcopenia and muscle (01.08.2020)
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Genetic associations of relaxin: preterm birth and premature rupture of fetal membranes
Rocha, Frederico G., MD, Slavin, Thomas P., MD, Li, Dongmei, PhD, Tiirikainen, Maarit I., PhD, Bryant-Greenwood, Gillian D., PhD
Published in American journal of obstetrics and gynecology (01.09.2013)
Published in American journal of obstetrics and gynecology (01.09.2013)
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NCCN Guidelines Insights: Genetic/Familial High-Risk Assessment: Colorectal, Version 2.2019
Gupta, Samir, Provenzale, Dawn, Llor, Xavier, Halverson, Amy L, Grady, William, Chung, Daniel C, Haraldsdottir, Sigurdis, Markowitz, Arnold J, Slavin, Jr, Thomas P, Hampel, Heather, Ness, Reid M, Weiss, Jennifer M, Ahnen, Dennis J, Chen, Lee-May, Cooper, Gregory, Early, Dayna S, Giardiello, Francis M, Hall, Michael J, Hamilton, Stanley R, Kanth, Priyanka, Klapman, Jason B, Lazenby, Audrey J, Lynch, Patrick M, Mayer, Robert J, Mikkelson, June, Peter, Shajan, Regenbogen, Scott E, Dwyer, Mary A, Ogba, Ndiya
Published in Journal of the National Comprehensive Cancer Network (01.09.2019)
Published in Journal of the National Comprehensive Cancer Network (01.09.2019)
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Producing Policy-relevant Science by Enhancing Robustness and Model Integration for the Assessment of Global Environmental Change
Warren, R.F., Edwards, N.R., Babonneau, F., Bacon, P.M., Dietrich, J.P., Ford, R.W., Garthwaite, P., Gerten, D., Goswami, S., Haurie, A., Hiscock, K., Holden, P.B., Hyde, M.R., Joshi, S.R., Kanudia, A., Labriet, M., Leimbach, M., Oyebamiji, O.K., Osborn, T., Pizzileo, B., Popp, A., Price, J., Riley, G.D., Schaphoff, S., Slavin, P., Vielle, M., Wallace, C.
Published in Environmental modelling & software : with environment data news (01.01.2019)
Published in Environmental modelling & software : with environment data news (01.01.2019)
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The perinatal presentation of cardiofaciocutaneous syndrome
Wong Ramsey, Kara N., Loichinger, Matthew H., Slavin, Thomas P., Kuo, Sheree, Seaver, Laurie H.
Published in American journal of medical genetics. Part A (01.08.2014)
Published in American journal of medical genetics. Part A (01.08.2014)
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Management of acute gallbladder disease in England
David, G. G., Al-Sarira, A. A., Willmott, S., Deakin, M., Corless, D. J., Slavin, J. P.
Published in British journal of surgery (01.04.2008)
Published in British journal of surgery (01.04.2008)
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Oesophagectomy practice and outcomes in England
Al-Sarira, A. A., David, G., Willmott, S., Slavin, J. P., Deakin, M., Corless, D. J.
Published in British journal of surgery (01.05.2007)
Published in British journal of surgery (01.05.2007)
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Haploinsufficiency of STK11 and neighboring genes cause a contiguous gene syndrome including Peutz–Jeghers phenotype
Scollon, Sarah, McWalter, Kirsty, Abe, Keith, King, Jeremy, Kimata, Kevin, Slavin, Thomas P.
Published in American journal of medical genetics. Part A (01.11.2012)
Published in American journal of medical genetics. Part A (01.11.2012)
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Elevated blood pressure: Our family’s fault?The genetics of essential hypertension
Natekar, Aniket, Olds, Randi L, Lau, Meghann W, Min, Kathleen, Imoto, Karra, Slavin, Thomas P
Published in World journal of cardiology (26.05.2014)
Published in World journal of cardiology (26.05.2014)
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Journal Article
Is Tel Hashomer camptodactyly a distinct clinical entity?
Mochizuki, A., Hyland, J., Brown, T., Slavin, T.P.
Published in American journal of medical genetics. Part A (01.01.2015)
Published in American journal of medical genetics. Part A (01.01.2015)
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Journal Article
Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline CDH1 sequence variants
Lee, Kristy, Krempely, Kate, Roberts, Maegan E., Anderson, Michael J., Carneiro, Fatima, Chao, Elizabeth, Dixon, Katherine, Figueiredo, Joana, Ghosh, Rajarshi, Huntsman, David, Kaurah, Pardeep, Kesserwan, Chimene, Landrith, Tyler, Li, Shuwei, Mensenkamp, Arjen R., Oliveira, Carla, Pardo, Carolina, Pesaran, Tina, Richardson, Matthew, Slavin, Thomas P., Spurdle, Amanda B., Trapp, Mackenzie, Witkowski, Leora, Yi, Charles S., Zhang, Liying, Plon, Sharon E., Schrader, Kasmintan A., Karam, Rachid
Published in Human mutation (01.11.2018)
Published in Human mutation (01.11.2018)
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