Germline and somatic SMARCA4 mutations characterize small cell carcinoma of the ovary, hypercalcemic type (Q39012911)

8 September 2017

Germline and somatic SMARCA4 mutations characterize small cell carcinoma of the ovary, hypercalcemic type (English)

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8 September 2017

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William David Foulkes

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Somayyeh Fahiminiya

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8 September 2017

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Martin Hasselblatt

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Ester Castellsagué

Ester Castellsagué

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Emmanouil Saloustros

Emmanouil Saloustros

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Barbara Rivera

Barbara Rivera

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Blaise A Clarke

Blaise A Clarke

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Reiner Siebert

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Reiner Siebert

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Marc Tischkowitz

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Andrew Berchuck

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W Glenn McCluggage

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Leora Witkowski

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Jian Carrot-Zhang

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Steffen Albrecht

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Nancy Hamel

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Eva Tomiak

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David Grynspan

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Javad Nadaf

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Catherine Gilpin

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Rachel Silva-Smith

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François Plourde

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Mona Wu

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Avi Saskin

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Madeleine Arseneault

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Rouzan G Karabakhtsian

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Elizabeth A Reilly

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Frederick R Ueland

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Anna Margiolaki

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Kitty Pavlakis

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Sharon M Castellino

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Janez Lamovec

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Helen J Mackay

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Lawrence M Roth

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Thomas M Ulbright

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Tracey A Bender

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Vassilis Georgoulias

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Michel Longy

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Inga Nagel

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Colin J R Stewart

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Jocelyne Arseneau

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Yasser Riazalhosseini

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Jacek Majewski

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8 September 2017

language of work or name

English

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publication date

23 March 2014

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438-443

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https://scigraph.springernature.com/pub.10.1038/ng.2931

8 September 2017

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Ovarian small cell carcinoma of the hypercalcemic type in children and adolescents: a prognostically unfavorable but curable disease

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Residual complexes containing SMARCA2 (BRM) underlie the oncogenic drive of SMARCA4 (BRG1) mutation

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An immunohistochemical analysis of ovarian small cell carcinoma of hypercalcemic type

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Ovarian small cell carcinoma of hypercalcemic type - evidence of germline origin and SMARCA4 gene inactivation. a pilot study

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Clinical correlations of mutations affecting six components of the SWI/SNF complex: detailed description of 21 patients and a review of the literature

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Small cell carcinoma of the ovary of hypercalcemic type: a case report.

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Current FIGO staging for cancer of the vagina, fallopian tube, ovary, and gestational trophoblastic neoplasia

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Germline nonsense mutation and somatic inactivation of SMARCA4/BRG1 in a family with rhabdoid tumor predisposition syndrome

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Loss-of-function mutations in SMARCE1 cause an inherited disorder of multiple spinal meningiomas

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Primary ovarian small cell carcinoma of pulmonary type. A clinicopathologic, immunohistologic, and flow cytometric analysis of 11 cases

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Nonsense Mutation and Inactivation of SMARCA4 (BRG1) in an Atypical Teratoid/Rhabdoid Tumor Showing Retained SMARCB1 (INI1) Expression

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Selected miscellaneous ovarian lesions: small cell carcinomas, mesothelial lesions, mesenchymal and mixed neoplasms, and non-neoplastic lesions

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Familial cluster of ovarian small cell carcinoma: a new mendelian entity?

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12 December 2020

Small cell carcinoma of the ovary, hypercalcemic type. A clinicopathological analysis of 150 cases

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Poorly differentiated (small cell) carcinoma of the ovary in young women: evidence supporting a germ cell origin

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12 December 2020

Small cell carcinoma of the ovary of the hypercalcaemic type: an analysis of clinical and prognostic aspects of a rare disease on the basis of cases published in the literature

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ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

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Familial occurrence of small-cell carcinoma of the ovary

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12 December 2020

Identifiers

DOI

10.1038/NG.2931

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8 September 2017

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