PTEN Hamartoma Tumor Syndrome: A Clinical Overview

per Pilarski, Robert
Publicat a Cancers (Basel) (2019)

Mutation Screening in Juvenile Polyposis Syndrome

per Pyatt, Robert E., Pilarski, Robert, Prior, Thomas W.
Publicat 2006

Characterization of BRCA1 Ring Finger Variants of Uncertain Significance

per Sweet, Kevin, Senter, Leigha, Pilarski, Robert, Wei, Lai, Toland, Amanda Ewart
Publicat a Breast Cancer Res Treat (2009)

Impact of previous genetic counseling and objective numeracy on accurate interpretation of a pharmacogenetics test report

per Drelles, Kelly, Pilarski, Robert, Manickam, Kandamurugu, Shoben, Abigail B., Toland, Amanda Ewart
Publicat a Public Health Genomics (2021)

Distinct Expression Profiles for PTEN Transcript and Its Splice Variants in Cowden Syndrome and Bannayan-Riley-Ruvalcaba Syndrome

per Sarquis, Marta S., Agrawal, Shipra, Shen, Lei, Pilarski, Robert, Zhou, Xiao-Ping, Eng, Charis
Publicat 2006

Mutation-Positive and Mutation-Negative Patients with Cowden and Bannayan-Riley-Ruvalcaba Syndromes Associated with Distinct 10q Haplotypes

per Pezzolesi, Marcus G., Li, Yan, Zhou, Xiao-Ping, Pilarski, Robert, Shen, Lei, Eng, Charis
Publicat 2006

Germline BAP1 mutations misreported as somatic based on tumor-only testing

per Abdel-Rahman, Mohamed H., Rai, Karan, Pilarski, Robert, Davidorf, Frederick H., Cebulla, Colleen M.
Publicat a Fam Cancer (2016)

Concurrent germline BRCA1, BRCA2, and CHEK2 pathogenic variants in hereditary breast cancer: a case series

per Sukumar, Jasmine, Kassem, Mahmoud, Agnese, Doreen, Pilarski, Robert, Ramaswamy, Bhuvaneswari, Sweet, Kevin, Sardesai, Sagar
Publicat a Breast Cancer Res Treat (2021)

Colonic manifestations of PTEN hamartoma tumor syndrome: Case series and systematic review

per Stanich, Peter P, Pilarski, Robert, Rock, Jonathan, Frankel, Wendy L, El-Dika, Samer, Meyer, Marty M
Publicat 2014

Atypical Choroidal Nevus in a Subject with a Germline PALB2 Pathogenic Variant

per Grosel, Timothy W., Karl, Matthew, Pilarski, Robert T., Davidorf, Frederick H., Abdel-Rahman, Mohamed H., Cebulla, Colleen M.
Publicat a Fam Cancer (2022)

Risk factors for anthracycline-associated cardiotoxicity

per Reinbolt, Raquel E., Patel, Roshan, Pan, Xueliang, Timmers, Cynthia Dawn, Pilarski, Robert, Shapiro, Charles L., Lustberg, Maryam B.
Publicat a Support Care Cancer (2015)

Fhit, Wwox and AP2γ expression levels correlate with basal phenotype in breast cancer

per Guler, Gulnur, Huebner, Kay, Himmetoglu, Cigdem, Jimenez, Rafael E., Costinean, Stefan, Volinia, Stefano, Pilarski, Robert T., Hayran, Mutlu, Shapiro, Charles L.
Publicat 2009

IL-6 variant is associated with metastasis in breast cancer patients

per Abana, Chike O., Bingham, Brian S., Cho, Ju Hwan, Graves, Amy J., Koyama, Tatsuki, Pilarski, Robert T., Chakravarthy, A. Bapsi, Xia, Fen
Publicat a PLoS One (2017)

Analysis of the Exome Aggregation Consortium (ExAC) database suggests that the BAP1-tumor predisposition syndrome is underreported in cancer patients

per Massengill, James B., Sample, Klarke M., Pilarski, Robert, McElroy, Joseph, Davidorf, Frederick H., Cebulla, Colleen M., Abdel-Rahman, Mohamed H.
Publicat a Genes Chromosomes Cancer (2018)

Germline BAP1 mutation predisposes to uveal melanoma, lung adenocarcinoma, meningioma, and other cancers

per Abdel-Rahman, Mohamed H, Pilarski, Robert, Cebulla, Colleen M, Massengill, James B, Christopher, Benjamin N, Boru, Getachew, Hovland, Peter, Davidorf, Frederick H
Publicat 2011

KIAA0101 interacts with BRCA1 and regulates centrosome number

per Kais, Zeina, Barsky, Sanford H., Mathsyaraja, Haritha, Zha, Alicia, Ransburgh, Derek J.R., He, Gang, Pilarski, Robert T., Shapiro, Charles L., Huang, Kun, Parvin, Jeffrey D.
Publicat 2011

Analysis of BAP1 Germline Gene Mutation in Young Uveal Melanoma Patients

per Cebulla, Colleen M., Binkley, Elaine M., Pilarski, Robert, Massengill, James B., Rai, Karan, Liebner, David A., Marino, Meghan J., Singh, Arun D., Abdel-Rahman, Mohamed H.
Publicat a Ophthalmic Genet (2015)

Expanding the Clinical Phenotype of Hereditary BAP1 Cancer Predisposition Syndrome, Reporting Three New Cases

per Pilarski, Robert, Cebulla, Colleen M., Massengill, James B., Rai, Karan, Rich, Thereasa, Strong, Louise, McGillivray, Barbara, Asrat, Mary-Jill, Davidorf, Frederick H, Abdel-Rahman, Mohamed H.
Publicat 2013

Genomic risk prediction of aromatase inhibitor‐related arthralgia in patients with breast cancer using a novel machine‐learning algorithm

per Reinbolt, Raquel E., Sonis, Stephen, Timmers, Cynthia D., Fernández‐Martínez, Juan Luis, Cernea, Ana, de Andrés‐Galiana, Enrique J., Hashemi, Sepehr, Miller, Karin, Pilarski, Robert, Lustberg, Maryam B.
Publicat a Cancer Med (2017)

Germline BAP1 Alterations in Familial Uveal Melanoma

per Rai, Karan, Pilarski, Robert, Boru, Getachew, Rehman, Muneeb, Saqr, Ahmad H., Massengill, James B., Singh, Arun, Marino, Meghan J., Davidorf, Frederick H., Cebulla, Colleen M., Abdel-Rahman, Mohamed H.
Publicat a Genes Chromosomes Cancer (2016)