SMARCB1/INI1 Alterations and Hepatoblastoma: Another Extrarenal Rhabdoid Tumor Revealed?

Por Russo, Pierre, Biegel, Jaclyn A.
Publicado em 2009

The role of SMARCB1/INI1 in development of rhabdoid tumor

Por Roberts, Charles W.M., Biegel, Jaclyn A.
Publicado em 2009

SWI/SNF Chromatin Remodeling Complexes and Cancer

Por Biegel, Jaclyn A, Busse, Tracy M., Weissman, Bernard E.
Publicado no Am J Med Genet C Semin Med Genet (2014)

Educational paper: Screening in cancer predisposition syndromes: guidelines for the general pediatrician

Por Teplick, Alexis, Kowalski, Megan, Biegel, Jaclyn A., Nichols, Kim E.
Publicado em 2011

Mutation of the INI1 gene in composite rhabdoid tumor of the endometrium

Por Donner, Ludvik R., Wainwright, Luanne M., Zhang, Fan, Biegel, Jaclyn A.
Publicado em 2007

Atypical teratoid/rhabdoid tumor evolving from an optic pathway ganglioglioma: Case study

Por Allen, Jeffrey C., Judkins, Alexander R., Rosenblum, Marc K., Biegel, Jaclyn A.
Publicado em 2006

Spectrum of SMARCB1/INI1 Mutations in Familial and Sporadic Rhabdoid Tumors

Por Eaton, Katherine W., Tooke, Laura S., Wainwright, Luanne M., Judkins, Alexander R., Biegel, Jaclyn A.
Publicado em 2011

Epithelioid sarcoma is associated with a high percentage of SMARCB1 deletions

Por Sullivan, Lisa M., Folpe, Andrew L., Pawel, Bruce R., Judkins, Alexander R., Biegel, Jaclyn A.
Publicado em 2012

Atypical teratoid/rhabdoid tumors—current concepts, advances in biology, and potential future therapies

Por Frühwald, Michael C., Biegel, Jaclyn A., Bourdeaut, Franck, Roberts, Charles W.M., Chi, Susan N.
Publicado no Neuro Oncol (2016)

Clinicopathologic Comparison of Familial Versus Sporadic Atypical Teratoid/Rhabdoid Tumors (AT/RT) of the Central Nervous System

Por Bruggers, Carol S., Bleyl, Steven B., Pysher, Theodore, Barnette, Philip, Afify, Zeinab, Walker, Marion, Biegel, Jaclyn A.
Publicado em 2010

Proximal-type Epithelioid Sarcoma of the Head and Neck (HN): A Study with Immunohistochemical and Molecular Analysis of SMARCB1

Por Frank, Renee, Sadri, Navid, Bhatti, Tricia, Biegel, Jaclyn A, LiVolsi, Virginia A, Zhang, Paul J
Publicado em 2013

Whole Chromosome 7 Gain Predicts Higher Risk of Recurrence in Pediatric Pilocytic Astrocytomas Independently From KIAA1549-BRAF Fusion Status

Por Roth, Jacquelyn J., Fierst, Tamara M., Waanders, Angela J., Yimei, Li, Biegel, Jaclyn A., Santi, Mariarita
Publicado no J Neuropathol Exp Neurol (2016)

Mixed Phenotype Acute Leukemia with Low Hypodiploidy in a Pediatric Patient

Por Salazar, Elizabeth G., Wertheim, Gerald B., Biegel, Jaclyn A., Hwang, William, Tasian, Sarah K., Rheingold, Susan R.
Publicado no J Pediatr Oncol (2015)

Acquired copy number neutral loss of heterozygosity of chromosome 7 associated with clonal haematopoiesis in a patient with Shwachman-Diamond syndrome

Por Parikh, Shefali, Perdigones, Nieves, Paessler, Michelle, Greenbaum, Barbara, Tooke, Laura S., Biegel, Jaclyn A., Mason, Philip J., Bessler, Monica
Publicado em 2012

Microdeletions and Microduplications in Patients with Congenital Heart Disease and Multiple Congenital Anomalies

Por Goldmuntz, Elizabeth, Paluru, Prasuna, Glessner, Joseph, Hakonarson, Hakon, Biegel, Jaclyn A., White, Peter S., Gai, Xiaowu, Shaikh, Tamim H.
Publicado no Congenit Heart Dis (2011)

Atypical teratoid/ rhabdoid tumor of the central nervous system in an 18-year-old patient

Por Samaras, Vassilis, Stamatelli, Angeliki, Samaras, Efstathios, Stergiou, Ioanna, Konstantopoulou, Paraskevi, Varsos, Vassilis, Judkins, Alexander R., Biegel, Jaclyn A., Barbatis, Calypso
Publicado em 2009

Loss of INI1 expression defines a unique subset of pediatric undifferentiated soft tissue sarcomas

Por Kreiger, Portia A, Judkins, Alexander R, Russo, Pierre A, Biegel, Jaclyn A, Lestini, Brian J, Assanasen, Chatchawin, Pawel, Bruce R
Publicado em 2008

Claudin-6 is a Non-Specific Marker for Malignant Rhabdoid and Other Pediatric Tumors

Por Sullivan, Lisa M., Yankovich, Theresa, Le, Paul, Martinez, Daniel, Santi, Mariarita, Biegel, Jaclyn A., Pawel, Bruce R., Judkins, Alexander R.
Publicado em 2012

Diagnostic application of high resolution single nucleotide polymorphism array analysis for children with brain tumors

Por Roth, Jacquelyn J., Santi, Mariarita, Rorke-Adams, Lucy B., Harding, Brian N., Busse, Tracy M., Tooke, Laura S., Biegel, Jaclyn A.
Publicado em 2014

Chromosome Band 7q34 Deletions Resulting in KIAA 1549‐ BRAF and FAM 131 B ‐ BRAF Fusions in Pediatric Low‐Grade Gliomas

Por Roth, Jacquelyn J., Santi, Mariarita, Pollock, Avrum N., Harding, Brian N., Rorke‐Adams, Lucy B., Tooke, Laura S., Biegel, Jaclyn A.
Publicado no Brain Pathol (2014)