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Select item 100275061.

Waldenström macroglobulinemia whole genome reveals prolonged germinal center activity and late copy number aberrations

Kylee H. Maclachlan, Tina Bagratuni, Efstathios Kastritis, Bachisio Ziccheddu, Sydney Lu, Venkata Yellapantula, Chris Famulare, Kimon Argyropoulos, Andriy Derkach, Elli Papaemmanuil, Ahmet Dogan, Alexander Lesokhin, Saad Z. Usmani, C. Ola Landgren, Lia M. Palomba, Francesco Maura, Meletios A. Dimopoulos

Blood Adv. 2023 Mar 28; 7(6): 971–981. Published online 2022 Nov 6. doi: 10.1182/bloodadvances.2022008876

PMCID:: PMC10027506

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Select item 82605832.

Neofunctionalisation of the Sli gene leads to self-compatibility and facilitates precision breeding in potato

Ernst-Jan Eggers, Ate van der Burgt, Sjaak A. W. van Heusden, Michiel E. de Vries, Richard G. F. Visser, Christian W. B. Bachem, Pim Lindhout

Nat Commun. 2021; 12: 4141. Published online 2021 Jul 6. doi: 10.1038/s41467-021-24267-6

PMCID:: PMC8260583

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Select item 72891403.

Report From the International Society of Urological Pathology (ISUP) Consultation Conference on Molecular Pathology of Urogenital Cancers: IV: Current and Future Utilization of Molecular-Genetic Tests for Testicular Germ Cell Tumors

Leendert H.J. Looijenga, Theodorus H. Van der Kwast, David Grignon, Lars Egevad, Glen Kristiansen, Chia-Sui Kao, Muhammad T. Idrees

Am J Surg Pathol. 2020 Jul; 44(7): e66–e79. Published online 2020 Mar 20. doi: 10.1097/PAS.0000000000001465

PMCID:: PMC7289140

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Select item 69423764.

12q14 microduplication: a new clinical entity reciprocal to the microdeletion syndrome?

Sofia Dória, Daniela Alves, Maria João Pinho, Joel Pinto, Miguel Leão

BMC Med Genomics. 2020; 13: 2. Published online 2020 Jan 3. doi: 10.1186/s12920-019-0653-x

PMCID:: PMC6942376

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Select item 68053985.

Inter- and intra-breed genome-wide copy number diversity in a large cohort of European equine breeds

Marina Solé, Michela Ablondi, Amrei Binzer-Panchal, Brandon D. Velie, Nina Hollfelder, Nadine Buys, Bart J. Ducro, Liesbeth François, Steven Janssens, Anouk Schurink, Åsa Viklund, Susanne Eriksson, Anders Isaksson, Hanna Kultima, Sofia Mikko, Gabriella Lindgren

BMC Genomics. 2019; 20: 759. Published online 2019 Oct 22. doi: 10.1186/s12864-019-6141-z

PMCID:: PMC6805398

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Select item 67560246.

SH2B3 inactivation through CN-LOH 12q is uniquely associated with B-cell precursor ALL with iAMP21 or other chromosome 21 gain

Paul B. Sinclair, Sarra Ryan, Matthew Bashton, Shaun Hollern, Rebecca Hanna, Marian Case, Edward C. Schwalbe, Claire J. Schwab, Ruth E. Cranston, Brian D. Young, Julie A. E. Irving, Ajay J. Vora, Anthony V. Moorman, Christine J. Harrison

Leukemia. 2019; 33(8): 1881–1894. Published online 2019 Feb 28. doi: 10.1038/s41375-019-0412-1

PMCID:: PMC6756024

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Select item 63068797.

Advanced forms of MPNs are accompanied by chromosomal abnormalities that lead to dysregulation of TP53

Bridget K. Marcellino, Ronald Hoffman, Joseph Tripodi, Min Lu, Heidi Kosiorek, John Mascarenhas, Raajit K. Rampal, Amylou Dueck, Vesna Najfeld

Blood Adv. 2018 Dec 26; 2(24): 3581–3589. Published online 2018 Dec 18. doi: 10.1182/bloodadvances.2018024018

PMCID:: PMC6306879

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Select item 62889858.

Combined Genetic and Chromosomal Characterization of Wilms Tumors Identifies Chromosome 12 Gain as a Potential New Marker Predicting a Favorable Outcome

Masayuki Haruta, Yasuhito Arai, Hajime Okita, Yukichi Tanaka, Tetsuya Takimoto, Ryuichi P. Sugino, Yasuhiro Yamada, Takehiko Kamijo, Takaharu Oue, Masahiro Fukuzawa, Tsugumichi Koshinaga, Yasuhiko Kaneko

Neoplasia. 2019 Jan; 21(1): 117–131. Published online 2018 Dec 6. doi: 10.1016/j.neo.2018.10.007

PMCID:: PMC6288985

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Select item 60102319.

Combined somatic mutation and copy number analysis in the survival of familial CLL

Weiyin Zhou, Lynn Goldin, Mingyi Wang, Mary L. McMaster, Kristine Jones, Laurie Burdett, Stephen J. Chanock, Meredith Yeager, Michael Dean, Neil Caporaso

Br J Haematol. Author manuscript; available in PMC 2019 Jun 1.

Published in final edited form as: Br J Haematol. 2018 Jun; 181(5): 604–613. Published online 2018 Apr 24. doi: 10.1111/bjh.15239

PMCID:: PMC6010231

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Select item 497083710.

Genetic variation frequencies in Wilms' tumor: A meta‐analysis and systematic review

Changkai Deng, Rong Dai, Xuliang Li, Feng Liu

Cancer Sci. 2016 May; 107(5): 690–699. Published online 2016 Mar 18. doi: 10.1111/cas.12910

PMCID:: PMC4970837

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Select item 485454111.

Methylation and expression analyses of Pallister-Killian syndrome reveal partial dosage compensation of tetrasomy 12p and hypomethylation of gene-poor regions on 12p

Josef Davidsson, Bertil Johansson

Epigenetics. 2016 Mar; 11(3): 194–204. Published online 2016 Feb 18. doi: 10.1080/15592294.2016.1146854

PMCID:: PMC4854541

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Select item 468036612.

Amplification of chromosome 8q21-qter associated with the acquired paclitaxel resistance of nasopharyngeal caricinoma cells

Wei Li, Yating You, Xiaowei Zhang, Yexun Song, Hong Xiang, Xiaowei Peng, Jiangbo Qin, Guolin Tan

Int J Clin Exp Pathol. 2015; 8(10): 12346–12356. Published online 2015 Oct 1.

PMCID:: PMC4680366

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Select item 464333013.

A LIN28B-RAN-AURKA Signaling Network Promotes Neuroblastoma Tumorigenesis

Robert W. Schnepp, Priya Khurana, Edward F. Attiyeh, Pichai Raman, Sara E. Chodosh, Derek A. Oldridge, Maria E. Gagliardi, Karina L. Conkrite, Shahab Asgharzadeh, Robert C. Seeger, Blair B. Madison, Anil K. Rustgi, John M. Maris, Sharon J. Diskin

Cancer Cell. Author manuscript; available in PMC 2016 Nov 9.

Published in final edited form as: Cancer Cell. 2015 Nov 9; 28(5): 599–609. Published online 2015 Oct 17. doi: 10.1016/j.ccell.2015.09.012

PMCID:: PMC4643330

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Select item 461595814.

Novel Genomic Aberrations in Testicular Germ Cell Tumors by Array-CGH, and Associated Gene Expression Changes

Rolf I. Skotheim, Reija Autio, Guro E. Lind, Sigrid M. Kraggerud, Peter W. Andrews, Outi Monni, Olli Kallioniemi, Ragnhild A. Lothe

Cell Oncol. 2006; 28(5-6): 315–326. Published online 2006 Dec 12. doi: 10.1155/2006/219786

PMCID:: PMC4615958

Abstract PDF–378K Cite

Select item 436915415.

The tyrosine kinase adaptor protein FRS2 is oncogenic and amplified in high-grade serous ovarian cancer

Leo Y. Luo, Eejung Kim, Hiu Wing Cheung, Barbara A. Weir, Gavin P. Dunn, Rhine R. Shen, William C. Hahn

Mol Cancer Res. Author manuscript; available in PMC 2016 Mar 1.

Published in final edited form as: Mol Cancer Res. 2015 Mar; 13(3): 502–509. Published online 2014 Nov 3. doi: 10.1158/1541-7786.MCR-14-0407

PMCID:: PMC4369154

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Select item 433854616.

Whole-exome sequencing reveals the mutational spectrum of testicular germ cell tumours

Kevin Litchfield, Brenda Summersgill, Shawn Yost, Razvan Sultana, Karim Labreche, Darshna Dudakia, Anthony Renwick, Sheila Seal, Reem Al-Saadi, Peter Broderick, Nicholas C. Turner, Richard S. Houlston, Robert Huddart, Janet Shipley, Clare Turnbull

Nat Commun. 2015; 6: 5973. Published online 2015 Jan 22. doi: 10.1038/ncomms6973

PMCID:: PMC4338546

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Select item 427500317.

Imbalances of Chromosomes 4, 9, and 12 are Recurrent in the Thecoma-Fibroma Group of Ovarian Stromal Tumors

Renae C. Streblow, Alicia J. Dafferner, Marilu Nelson, Mavis Fletcher, William W. West, Rachel K. Stevens, Zoran Gatalica, Deborah Novak, Julia A. Bridge

Cancer Genet Cytogenet. Author manuscript; available in PMC 2014 Dec 23.

Published in final edited form as: Cancer Genet Cytogenet. 2007 Oct 15; 178(2): 135–140. doi: 10.1016/j.cancergencyto.2007.07.009