Clinically relevant subsets identified by gene expression patterns support a revised ontogenic model of Wilms tumor: A Children's Oncology Group study

Samantha Gadd; Vicki Huff; Chiang Ching Huang; E. Cristy Ruteshouser; Jeffrey S. Dome; Paul E. Grundy; Norman Breslow; Lawrence Jennings; Daniel M. Green; J. Bruce Beckwith; Elizabeth J. Perlman

doi:10.1593/neo.12714

Clinically relevant subsets identified by gene expression patterns support a revised ontogenic model of Wilms tumor: A Children's Oncology Group study

Samantha Gadd, Vicki Huff, Chiang Ching Huang, E. Cristy Ruteshouser, Jeffrey S. Dome, Paul E. Grundy, Norman Breslow, Lawrence Jennings, Daniel M. Green, J. Bruce Beckwith, Elizabeth J. Perlman

Pathology Division

Research output: Contribution to journal › Article › peer-review

Original language	English
Pages (from-to)	742-756
Number of pages	15
Journal	Neoplasia (United States)
Volume	14
Issue number	8
DOIs	https://doi.org/10.1593/neo.12714
State	Published - Aug 2012

ASJC Scopus Subject Areas

Cancer Research

Access to Document

10.1593/neo.12714

OpenUrl availability

Full text

Cite this

Gadd, S., Huff, V., Huang, C. C., Cristy Ruteshouser, E., Dome, J. S., Grundy, P. E., Breslow, N., Jennings, L., Green, D. M., Bruce Beckwith, J., & Perlman, E. J. (2012). Clinically relevant subsets identified by gene expression patterns support a revised ontogenic model of Wilms tumor: A Children's Oncology Group study. Neoplasia (United States), 14(8), 742-756. https://doi.org/10.1593/neo.12714

Gadd, S, Huff, V, Huang, CC, Cristy Ruteshouser, E, Dome, JS, Grundy, PE, Breslow, N, Jennings, L, Green, DM, Bruce Beckwith, J & Perlman, EJ 2012, 'Clinically relevant subsets identified by gene expression patterns support a revised ontogenic model of Wilms tumor: A Children's Oncology Group study', Neoplasia (United States), vol. 14, no. 8, pp. 742-756. https://doi.org/10.1593/neo.12714

@article{2282451e0e32400fa0eb6c695d7a0677,

title = "Clinically relevant subsets identified by gene expression patterns support a revised ontogenic model of Wilms tumor: A Children's Oncology Group study",

author = "Samantha Gadd and Vicki Huff and Huang, {Chiang Ching} and {Cristy Ruteshouser}, E. and Dome, {Jeffrey S.} and Grundy, {Paul E.} and Norman Breslow and Lawrence Jennings and Green, {Daniel M.} and {Bruce Beckwith}, J. and Perlman, {Elizabeth J.}",

note = "Funding Information: Abbreviations: WT, Wilms tumor; ICR1, imprint control region 1; ICR2, imprint control region 2; MM, metanephric mesenchyme; LOI, loss of imprinting; LOH, loss of heterozygosity; ROI, retention of imprinting; UPD, uniparental disomy Address all correspondence to: Elizabeth J. Perlman, MD, Children{\textquoteright}s Memorial Hospital, 2300 Children{\textquoteright}s Plaza, Box 17, Chicago, IL 60614. E-mail: [email protected] 1This work is supported by grants from the National Institutes of Health: U10CA42326 (N.B., D.M.G., E.J.P.). U10CA98543 ( J.S.D., P.E.G., E.J.P.), UO1CA88131 (E.J.P., C.C.H.), CA34936 (V.H.), DK069599 (V.H.), CA16672 (V.H.), RP100329 (V.H.), and RP110324 (V.H.). 2This article refers to supplementary materials, which are designated by Tables W1 and W2 and are available online at www.neoplasia.com. Received 23 April 2012; Revised 28 June 2012; Accepted 4 July 2012 Copyright {\textcopyright} 2012 Neoplasia Press, Inc. All rights reserved 1522-8002/12/$25.00 DOI 10.1593/neo.12714",

year = "2012",

month = aug,

doi = "10.1593/neo.12714",

language = "English",

volume = "14",

pages = "742--756",

journal = "Neoplasia (United States)",

issn = "1522-8002",

number = "8",

}

TY - JOUR

T1 - Clinically relevant subsets identified by gene expression patterns support a revised ontogenic model of Wilms tumor

T2 - A Children's Oncology Group study

AU - Gadd, Samantha

AU - Huff, Vicki

AU - Huang, Chiang Ching

AU - Cristy Ruteshouser, E.

AU - Dome, Jeffrey S.

AU - Grundy, Paul E.

AU - Breslow, Norman

AU - Jennings, Lawrence

AU - Green, Daniel M.

AU - Bruce Beckwith, J.

AU - Perlman, Elizabeth J.

N1 - Funding Information: Abbreviations: WT, Wilms tumor; ICR1, imprint control region 1; ICR2, imprint control region 2; MM, metanephric mesenchyme; LOI, loss of imprinting; LOH, loss of heterozygosity; ROI, retention of imprinting; UPD, uniparental disomy Address all correspondence to: Elizabeth J. Perlman, MD, Children’s Memorial Hospital, 2300 Children’s Plaza, Box 17, Chicago, IL 60614. E-mail: [email protected] 1This work is supported by grants from the National Institutes of Health: U10CA42326 (N.B., D.M.G., E.J.P.). U10CA98543 ( J.S.D., P.E.G., E.J.P.), UO1CA88131 (E.J.P., C.C.H.), CA34936 (V.H.), DK069599 (V.H.), CA16672 (V.H.), RP100329 (V.H.), and RP110324 (V.H.). 2This article refers to supplementary materials, which are designated by Tables W1 and W2 and are available online at www.neoplasia.com. Received 23 April 2012; Revised 28 June 2012; Accepted 4 July 2012 Copyright © 2012 Neoplasia Press, Inc. All rights reserved 1522-8002/12/$25.00 DOI 10.1593/neo.12714

PY - 2012/8

Y1 - 2012/8

UR - http://www.scopus.com/inward/record.url?scp=84865245097&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84865245097&partnerID=8YFLogxK

U2 - 10.1593/neo.12714

DO - 10.1593/neo.12714

M3 - Article

C2 - 22952427

AN - SCOPUS:84865245097

SN - 1522-8002

VL - 14

SP - 742

EP - 756

JO - Neoplasia (United States)

JF - Neoplasia (United States)

IS - 8

ER -

Clinically relevant subsets identified by gene expression patterns support a revised ontogenic model of Wilms tumor: A Children's Oncology Group study

ASJC Scopus Subject Areas

Access to Document

OpenUrl availability

Other files and links

Cite this