Improving survival prediction for melanoma

por Artomov, Mykyta
Publicado no eLife (2019)

Only signaling modules that discriminate sharply between stimulatory and nonstimulatory inputs require basal signaling for fast cellular responses

por Artomov, Mykyta, Kardar, Mehran, Chakraborty, Arup K.
Publicado em 2010

Classifying melanoma by TERT promoter mutational status

por Shaughnessy, Michael, Njauw, Ching-Ni, Artomov, Mykyta, Tsao, Hensin
Publicado no J Invest Dermatol (2019)

Gender Disparity and Mutation Burden in Metastatic Melanoma

por Gupta, Sameer, Artomov, Mykyta, Goggins, William, Daly, Mark, Tsao, Hensin
Publicado no J Natl Cancer Inst (2015)

Mosaic mutations in blood DNA sequence are associated with solid tumor cancers

por Artomov, Mykyta, Rivas, Manuel A., Genovese, Giulio, Daly, Mark J.
Publicado no NPJ Genom Med (2017)

Burden of unique and low prevalence somatic mutations correlates with cancer survival

por Klebanov, Nikolai, Artomov, Mykyta, Goggins, William B., Daly, Emma, Daly, Mark J., Tsao, Hensin
Publicado no Sci Rep (2019)

Cancer risks associated with the germline MITF(E318K) variant

por Guhan, Samantha M., Artomov, Mykyta, McCormick, Shelley, Njauw, Ching -Ni, Stratigos, Alexander J., Shannon, Kristen, Ellisen, Leif W., Tsao, Hensin
Publicado no Sci Rep (2020)

Use of Targeted Next-Generation Sequencing to Identify Activating Hot Spot Mutations in Cherry Angiomas

por Klebanov, Nikolai, Lin, William M., Artomov, Mykyta, Shaughnessy, Michael, Njauw, Ching-Ni, Bloom, Romi, Eterovic, Agda Karina, Chen, Ken, Kim, Tae-Beom, Tsao, Sandy S., Tsao, Hensin
Publicado no JAMA Dermatol (2019)

A role for genetic susceptibility in sporadic focal segmental glomerulosclerosis

por Yu, Haiyang, Artomov, Mykyta, Brähler, Sebastian, Stander, M. Christine, Shamsan, Ghaidan, Sampson, Matthew G., White, J. Michael, Kretzler, Matthias, Miner, Jeffrey H., Jain, Sanjay, Winkler, Cheryl A., Mitra, Robi D., Kopp, Jeffrey B., Daly, Mark J., Shaw, Andrey S.
Publicado no J Clin Invest (2016)

A role for genetic susceptibility in sporadic focal segmental glomerulosclerosis

por Yu, Haiyang, Artomov, Mykyta, Brähler, Sebastian, Stander, M. Christine, Shamsan, Ghaidan, Sampson, Matthew G., White, J. Michael, Kretzler, Matthias, Miner, Jeffrey H., Jain, Sanjay, Winkler, Cheryl A., Mitra, Robi D., Kopp, Jeffrey B., Daly, Mark J., Shaw, Andrey S.
Publicado no J Clin Invest (2016)

Assessment of genetic variant burden in epilepsy-associated brain lesions

por Niestroj, Lisa-Marie, May, Patrick, Artomov, Mykyta, Kobow, Katja, Coras, Roland, Pérez-Palma, Eduardo, Altmüller, Janine, Thiele, Holger, Nürnberg, Peter, Leu, Costin, Palotie, Aarno, Daly, Mark J., Klein, Karl Martin, Beschorner, Rudi, Weber, Yvonne G., Blümcke, Ingmar, Lal, Dennis
Publicado no Eur J Hum Genet (2019)

Case–control analysis identifies shared properties of rare germline variation in cancer predisposing genes

por Artomov, Mykyta, Joseph, Vijai, Tiao, Grace, Thomas, Tinu, Schrader, Kasmintan, Klein, Robert J., Kiezun, Adam, Gupta, Namrata, Margolin, Lauren, Stratigos, Alexander J., Kim, Ivana, Shannon, Kristen, Ellisen, Leif W., Haber, Daniel, Getz, Gad, Tsao, Hensin, Lipkin, Steven M., Altshuler, David, Offit, Kenneth, Daly, Mark J.
Publicado no Eur J Hum Genet (2019)

Rare Variant, Gene-Based Association Study of Hereditary Melanoma Using Whole-Exome Sequencing

por Artomov, Mykyta, Stratigos, Alexander J, Kim, Ivana, Kumar, Raj, Lauss, Martin, Reddy, Bobby Y, Miao, Benchun, Daniela Robles-Espinoza, Carla, Sankar, Aravind, Njauw, Ching-Ni, Shannon, Kristen, Gragoudas, Evangelos S, Marie Lane, Anne, Iyer, Vivek, Newton-Bishop, Julia A, Timothy Bishop, D, Holland, Elizabeth A, Mann, Graham J, Singh, Tarjinder, Daly, Mark J, Tsao, Hensin
Publicado no J Natl Cancer Inst (2017)

Haplotype Sharing Provides Insights into Fine-Scale Population History and Disease in Finland

por Martin, Alicia R., Karczewski, Konrad J., Kerminen, Sini, Kurki, Mitja I., Sarin, Antti-Pekka, Artomov, Mykyta, Eriksson, Johan G., Esko, Tõnu, Genovese, Giulio, Havulinna, Aki S., Kaprio, Jaakko, Konradi, Alexandra, Korányi, László, Kostareva, Anna, Männikkö, Minna, Metspalu, Andres, Perola, Markus, Prasad, Rashmi B., Raitakari, Olli, Rotar, Oxana, Salomaa, Veikko, Groop, Leif, Palotie, Aarno, Neale, Benjamin M., Ripatti, Samuli, Pirinen, Matti, Daly, Mark J.
Publicado no Am J Hum Genet (2018)

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

por Satterstrom, F. Kyle, Kosmicki, Jack A., Wang, Jiebiao, Breen, Michael S., De Rubeis, Silvia, An, Joon-Yong, Peng, Minshi, Collins, Ryan, Grove, Jakob, Klei, Lambertus, Stevens, Christine, Reichert, Jennifer, Mulhern, Maureen S., Artomov, Mykyta, Gerges, Sherif, Sheppard, Brooke, Xu, Xinyi, Bhaduri, Aparna, Norman, Utku, Brand, Harrison, Schwartz, Grace, Nguyen, Rachel, Guerrero, Elizabeth E., Dias, Caroline, Betancur, Catalina, Cook, Edwin H., Gallagher, Louise, Gill, Michael, Sutcliffe, James S., Thurm, Audrey, Zwick, Michael E., Børglum, Anders D., State, Matthew W., Cicek, A. Ercument, Talkowski, Michael E., Cutler, David J., Devlin, Bernie, Sanders, Stephan J., Roeder, Kathryn, Daly, Mark J., Buxbaum, Joseph D.
Publicado no Cell (2020)

Germline Lysine-Specific Demethylase 1 (LSD1/KDM1A) Mutations Confer Susceptibility to Multiple Myeloma

por Wei, Xiaomu, Calvo-Vidal, M. Nieves, Chen, Siwei, Wu, Gang, Revuelta, Maria V., Sun, Jian, Zhang, Jinghui, Walsh, Michael F., Nichols, Kim E., Joseph, Vijai, Snyder, Carrie, Vachon, Celine M., McKay, James D., Wang, Shu-Ping, Jayabalan, David S., Jacobs, Lauren M., Becirovic, Dina, Waller, Rosalie G., Artomov, Mykyta, Viale, Agnes, Patel, Jayeshkumar, Phillip, Jude, Chen-Kiang, Selina, Curtin, Karen, Salama, Mohamed, Atanackovic, Djordje, Niesvizky, Ruben, Landgren, Ola, Slager, Susan L., Godley, Lucy A., Churpek, Jane, Garber, Judy E., Anderson, Kenneth C., Daly, Mark J., Roeder, Robert G., Dumontet, Charles, Lynch, Henry T., Mullighan, Charles G., Camp, Nicola J., Offit, Ken, Klein, Robert J., Yu, Haiyuan, Cerchietti, Leandro, Lipkin, Steven M.
Publicado no Cancer Res (2018)