Identification of novel noncoding transcripts in telomerase-negative yeast using RNA-seq

Por Niederer, Rachel O., Papadopoulos, Nickolas, Zappulla, David C.
Publicado no Sci Rep (2016)

FAST-SeqS: A Simple and Efficient Method for the Detection of Aneuploidy by Massively Parallel Sequencing

Por Kinde, Isaac, Papadopoulos, Nickolas, Kinzler, Kenneth W., Vogelstein, Bert
Publicado em 2012

The Antisense Transcriptomes of Human Cells

Por He, Yiping, Vogelstein, Bert, Velculescu, Victor E., Papadopoulos, Nickolas, Kinzler, Kenneth W.
Publicado em 2008

Mutation of the TERT promoter, switch to active chromatin, and monoallelic TERT expression in multiple cancers

Por Stern, Josh Lewis, Theodorescu, Dan, Vogelstein, Bert, Papadopoulos, Nickolas, Cech, Thomas R.
Publicado no Genes Dev (2015)

Evaluating the evaluation of cancer driver genes

Por Tokheim, Collin J., Papadopoulos, Nickolas, Kinzler, Kenneth W., Vogelstein, Bert, Karchin, Rachel
Publicado no Proc Natl Acad Sci U S A (2016)

Cancer Genome Landscapes

Por Vogelstein, Bert, Papadopoulos, Nickolas, Velculescu, Victor E., Zhou, Shibin, Diaz, Luis A., Kinzler, Kenneth W.
Publicado em 2013

A panel of isogenic human cancer cells suggests a therapeutic approach for cancers with inactivated p53

Por Sur, Surojit, Pagliarini, Raymond, Bunz, Fred, Rago, Carlo, Diaz, Luis A., Kinzler, Kenneth W., Vogelstein, Bert, Papadopoulos, Nickolas
Publicado em 2009

INTRADUCTAL PAPILLARY MUCINOUS NEOPLASM IN A NEONATE WITH CONGENITAL HYPERINSULINISM AND A DE NOVO GERMLINE SKIL GENE MUTATION

Por Jiao, Yuchen, Lumpkins, Kimberly, Terhune, Julia, Hruban, Ralph H., Klein, Alison, Kinzler, Kenneth W., Papadopoulos, Nickolas, Vogelstein, Bert, Strauch, Eric
Publicado no Pancreatology (2014)

Limited detection of IgH gene rearrangements in plasma of patients with primary central nervous system lymphoma

Por He, Jian, Wu, Jian, Jiao, Yuchen, Rodriguez, Fausto J., Blakeley, Jaishri O., Kinzler, Kenneth W., Papadopoulos, Nickolas, Vogelstein, Bert, Holdhoff, Matthias
Publicado em 2013

Somatic mutations in the transcriptional corepressor gene BCORL1 in adult acute myelogenous leukemia

Por Li, Meng, Collins, Roxane, Jiao, Yuchen, Ouillette, Peter, Bixby, Dale, Erba, Harry, Vogelstein, Bert, Kinzler, Kenneth W., Papadopoulos, Nickolas, Malek, Sami N.
Publicado em 2011

IgH gene rearrangements as plasma biomarkers in Non-Hodgkin's Lymphoma patients

Por He, Jian, Wu, Jian, Jiao, Yuchen, Wagner-Johnston, Nina, Ambinder, Richard F., Diaz, Luis A, Kinzler, Kenneth W, Vogelstein, Bert, Papadopoulos, Nickolas
Publicado em 2011

DETECTION OF CIRCULATING TUMOR DNA IN EARLY AND LATE STAGE HUMAN MALIGNANCIES

Por Bettegowda, Chetan, Sausen, Mark, Leary, Rebecca, Kinde, Isaac, Agrawal, Nishant, Bartlett, Bjarne, Wang, Hao, Luber, Brandon, Kinzler, Kenneth, Vogelstein, Bert, Papadopoulos, Nickolas
Publicado em 2014

Genetic inactivation of AKT1, AKT2, and PDPK1 in human colorectal cancer cells clarifies their roles in tumor growth regulation

Por Ericson, Kajsa, Gan, Christine, Cheong, Ian, Rago, Carlo, Samuels, Yardena, Velculescu, Victor E., Kinzler, Kenneth W., Huso, David L., Vogelstein, Bert, Papadopoulos, Nickolas
Publicado em 2010

Low-grade serous carcinomas of the ovary contain very few point mutations

Por Jones, Siân, Wang, Tian-Li, Kurman, Robert J, Nakayama, Kentaro, Velculescu, Victor E, Vogelstein, Bert, Kinzler, Kenneth W, Papadopoulos, Nickolas, Shih, Ie-Ming
Publicado em 2011

Genome-wide quantification of rare somatic mutations in normal human tissues using massively parallel sequencing

Por Hoang, Margaret L., Kinde, Isaac, Tomasetti, Cristian, McMahon, K. Wyatt, Rosenquist, Thomas A., Grollman, Arthur P., Kinzler, Kenneth W., Vogelstein, Bert, Papadopoulos, Nickolas
Publicado no Proc Natl Acad Sci U S A (2016)

Analysis of masked mutations in familial adenomatous polyposis

Por Laken, Steven J., Papadopoulos, Nickolas, Petersen, Gloria M., Gruber, Stephen B., Hamilton, Stanley R., Giardiello, Francis M., Brensinger, Jill D., Vogelstein, Bert, Kinzler, Kenneth W.
Publicado em 1999

Sequence and expression analysis of gaps in human chromosome 20

Por Minocherhomji, Sheroy, Seemann, Stefan, Mang, Yuan, El-schich, Zahra, Bak, Mads, Hansen, Claus, Papadopoulos, Nickolas, Josefsen, Knud, Nielsen, Henrik, Gorodkin, Jan, Tommerup, Niels, Silahtaroglu, Asli
Publicado em 2012

Characterization of a t(5;8)(q31;q21) translocation in a patient with mental retardation and congenital heart disease: implications for involvement of RUNX1T1 in human brain and he...

Por Zhang, Litu, Tümer, Zeynep, Møllgård, Kjeld, Barbi, Gotthold, Rossier, Eva, Bendsen, Eske, Møller, Rikke Steensbjerre, Ullmann, Reinhard, He, Jian, Papadopoulos, Nickolas, Tommerup, Niels, Larsen, Lars Allan
Publicado em 2009

Heteroplasmic mitochondrial DNA mutations in normal and tumor cells

Por He, Yiping, Wu, Jian, Dressman, Devin C., Iacobuzio-Donahue, Christine, Markowitz, Sanford D., Velculescu, Victor E., Diaz, Luis A., Kinzler, Kenneth W., Vogelstein, Bert, Papadopoulos, Nickolas
Publicado em 2010

Familial and sporadic pancreatic cancer share the same molecular pathogenesis

Por Norris, Alexis L., Roberts, Nicholas J., Jones, Siân, Wheelan, Sarah J., Papadopoulos, Nickolas, Vogelstein, Bert, Kinzler, Kenneth W., Hruban, Ralph H., Klein, Alison P., Eshleman, James R.
Publicado no Fam Cancer (2015)