Response to “Germline Mosaicism in Cornelia de Lange Syndrome: Dilemmas and Risk Figures” by Mariani et al

Por Slavin, Thomas P., Krantz, Ian
Publicado em 2013

SAT-315 SDHC Germline Mutation Carrier with Primary Paraganglioma of the Thyroid Gland

Por Lee, Hyunju, Slavin, Thomas, Salehian, Behrouz
Publicado no J Endocr Soc (2019)

Increased Reach of Genetic Cancer Risk Assessment as a Tool for Precision Management of Hereditary Breast Cancer

Por Blazer, Kathleen R., Slavin, Thomas, Weitzel, Jeffrey N.
Publicado no JAMA Oncol (2016)

Two-marker association tests yield new disease associations for coronary artery disease and hypertension

Por Slavin, Thomas P., Feng, Tao, Schnell, Audrey, Zhu, Xiaofeng, Elston, Robert C.
Publicado em 2011

The effects of genomic germline variant reclassification on clinical cancer care

Por Slavin, Thomas P., Manjarrez, Sophia, Pritchard, Colin C., Gray, Stacy, Weitzel, Jeffrey N.
Publicado no Oncotarget (2019)

Isolated Skeletal Malformations in a Child With a Small Mosaic Ring Microduplication of 18 p11.21q11.2: Genotype–Phenotype Correlations

Por Slavin, Thomas P., Kuruvilla, Kevin, Curtis, Christine A., Christ, Laurie A., Mitchell, Anna L.
Publicado no Am J Med Genet A (2011)

Bilateral Radial Ulnar Synostosis and Vertebral Anomalies in a Child with a De Novo 16p13.3 Interstitial Deletion

Por Tam, Allison, Lee, Kit Shan, Lee, Sansan, Burkhalter, William, Pascua, Lucio U., Slavin, Thomas P.
Publicado em 2013

Genetic associations of relaxin: preterm birth and premature rupture of fetal membranes

Por ROCHA, Frederico G., SLAVIN, Thomas P., LI, Dongmei, TIIRIKAINEN, Maarit I., BRYANT-GREENWOOD, Gillian D.
Publicado em 2013

Elevated blood pressure: Our family’s fault? The genetics of essential hypertension

Por Natekar, Aniket, Olds, Randi L, Lau, Meghann W, Min, Kathleen, Imoto, Karra, Slavin, Thomas P
Publicado em 2014

Genetics of gastric cancer: what do we know about the genetic risks?

Por Slavin, Thomas Paul, Weitzel, Jeffrey N., Neuhausen, Susan L., Schrader, Kasmintan A., Oliveira, Carla, Karam, Rachid
Publicado no Transl Gastroenterol Hepatol (2019)

Novel candidates in early-onset familial colorectal cancer

Por Jansen, Anne ML, Ghosh, Pradipta, Dakal, Tikam Chand, Slavin, Thomas Paul, Boland, C. Richard, Goel, Ajay
Publicado no Fam Cancer (2019)

Clinical Application of Multigene Panels: Challenges of Next-Generation Counseling and Cancer Risk Management

Por Slavin, Thomas Paul, Niell-Swiller, Mariana, Solomon, Ilana, Nehoray, Bita, Rybak, Christina, Blazer, Kathleen R., Weitzel, Jeffrey N.
Publicado no Front Oncol (2015)

Corrigendum: Clinical Application of Multigene Panels: Challenges of Next-Generation Counseling and Cancer Risk Management

Por Slavin, Thomas Paul, Niell-Swiller, Mariana, Solomon, Ilana, Nehoray, Bita, Rybak, Christina, Blazer, Kathleen R., Weitzel, Jeffrey N.
Publicado no Front Oncol (2015)

The State of the Art in Colorectal Cancer Molecular Biomarker Testing

Por Pillai, Raju K., Lopategui, Jean, Dhall, Deepti, Guindi, Maha, Slavin, Thomas, Lofton-Day, Catherine E., Patterson, Scott D.
Publicado no Adv Anat Pathol (2016)

Systematic misclassification of missense variants in BRCA1 and BRCA2 “coldspots”

Por Dines, Jennifer N., Shirts, Brian H., Slavin, Thomas P., Walsh, Tom, King, Mary-Claire, Fowler, Douglas M., Pritchard, Colin C.
Publicado no Genet Med (2020)

Prevalence and characteristics of likely-somatic variants in cancer susceptibility genes among individuals who had hereditary pan-cancer panel testing

Por Slavin, Thomas P., Coffee, Bradford, Bernhisel, Ryan, Logan, Jennifer, Cox, Hannah C., Marcucci, Guido, Weitzel, Jeffrey, Neuhausen, Susan L., Mancini-DiNardo, Debora
Publicado no Cancer Genet (2019)

Older breast cancer survivors may harbor hereditary cancer predisposition pathogenic variants and are at risk for clonal hematopoiesis.

Por Slavin, Thomas P., Sun, Can-Lan, Chavarri-Guerra, Yanin, Sedrak, Mina S., Katheria, Vani, Castillo, Danielle, Herzog, Josef, Dale, William, Hurria, Arti, Weitzel, Jeffrey N.
Publicado no J Geriatr Oncol (2019)

Circulating tumor DNA as an early cancer detection tool

Por 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.
Publicado no Pharmacol Ther (2019)

Experience Gained from the Development and Execution of a Multidisciplinary Multi-Syndrome Hereditary Colon Cancer Family Conference

Por Solomon, Ilana, Rybak, Christina, Van Tongeren, Lily, Kuzmich, Lili, Blazer, Kathleen, Nehoray, Bita, Niell-Swiller, Mariana, Bray, Shawnie, Bray, Travis H., Hurley, Karen, Weitzel, Jeffrey N., Slavin, Thomas P.
Publicado no J Cancer Educ (2019)

Clinical Report: Germline Mosaicism in Cornelia de Lange Syndrome

Por Slavin, Thomas P., Lazebnik, Noam, Clark, Dinah M., Vengoechea, Jaime, Cohen, Leslie, Kaur, Maninder, Konczal, Laura, Crowe, Carol A., Corteville, Jane E., Nowaczyk, Malgorzata J., Byrne, Janice L., Jackson, Laird G., Krantz, Ian D.
Publicado em 2012