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Blood Cancer Journal (5)
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Showing 1–13 of 13 results

Advanced filters: Author: James B. Smadbeck Clear advanced filters

Characterization of TCF3 rearrangements in pediatric B-lymphoblastic leukemia/lymphoma by mate-pair sequencing (MPseq) identifies complex genomic rearrangements and a novel TCF3/TEF gene fusion

Ross A. Rowsey
Stephanie A. Smoley
Jess F. Peterson
ResearchOpen Access01 Oct 2019
Blood Cancer Journal

Volume: 9, P: 1-8
Functional variant rs9344 at 11q13.3 regulates CCND1 expression in multiple myeloma with t(11;14)

Hongwei Tang
Huihuang Yan
Linda B. Baughn
ResearchOpen Access14 Oct 2024
Leukemia

Volume: 39, P: 42-50
Rare coding variant analysis for human diseases across biobanks and ancestries

Gene-based rare variant analyses for 601 diseases across 748,879 individuals from three biobanks identify 363 significant associations and highlight important considerations for multi-ancestry and cross-biobank sequencing studies.

Sean J. Jurgens
Xin Wang
Patrick T. Ellinor
Research29 Aug 2024
Nature Genetics

Volume: 56, P: 1811-1820
Correction: Family history of plasma cell disorders is associated with improved survival in MGUS, multiple myeloma, and systemic AL amyloidosis

Alissa Visram
Celine Vachon
Shaji Kumar
Amendments and Corrections17 Jun 2024
Leukemia

Volume: 38, P: 1865
Mate pair sequencing outperforms fluorescence in situ hybridization in the genomic characterization of multiple myeloma

James Smadbeck
Jess F. Peterson
Linda B. Baughn
ResearchOpen Access16 Dec 2019
Blood Cancer Journal

Volume: 9, P: 1-18
Mass Cytometry reveals unique phenotypic patterns associated with subclonal diversity and outcomes in multiple myeloma

Linda B. Baughn
Erik Jessen
Shaji K. Kumar
ResearchOpen Access22 May 2023
Blood Cancer Journal

Volume: 13, P: 1-9
Family history of plasma cell disorders is associated with improved survival in MGUS, multiple myeloma, and systemic AL amyloidosis

Alissa Visram
Celine Vachon
Shaji Kumar
Research11 Nov 2021
Leukemia

Volume: 36, P: 1058-1065
An analysis and evaluation of the WeFold collaborative for protein structure prediction and its pipelines in CASP11 and CASP12

Chen Keasar
Liam J. McGuffin
Silvia N. Crivelli
ResearchOpen Access02 Jul 2018
Scientific Reports

Volume: 8, P: 1-18
Shared and unique genomic structural variants of different histological components within testicular germ cell tumours identified with mate pair sequencing

Alan H. Bryce
Jan B. Egan
George Vasmatzis
ResearchOpen Access05 Mar 2019
Scientific Reports

Volume: 9, P: 1-9
Quantification of Somatic Chromosomal Rearrangements in Circulating Cell-Free DNA from Ovarian Cancers

Faye R. Harris
Irina V. Kovtun
George Vasmatzis
ResearchOpen Access20 Jul 2016
Scientific Reports

Volume: 6, P: 1-9
Prospective evaluation of genome sequencing to compare conventional cytogenetics in acute myeloid leukemia

Beth A. Pitel
Cinthya Zepeda-Mendoza
Linda B. Baughn
CorrespondenceOpen Access06 Sept 2023
Blood Cancer Journal

Volume: 13, P: 1-5
Myeloid malignancies with 5q and 7q deletions are associated with extreme genomic complexity, biallelic TP53 variants, and very poor prognosis

Beth A. Pitel
Neeraj Sharma
Linda B. Baughn
CorrespondenceOpen Access08 Feb 2021
Blood Cancer Journal

Volume: 11, P: 1-4
Genomic rearrangements in sporadic lymphangioleiomyomatosis: an evolving genetic story

Stephen J Murphy
Simone B Terra
Eva M Carmona
Research23 Jun 2017
Modern Pathology

Volume: 30, P: 1223-1233

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Characterization of TCF3 rearrangements in pediatric B-lymphoblastic leukemia/lymphoma by mate-pair sequencing (MPseq) identifies complex genomic rearrangements and a novel TCF3/TEF gene fusion

Functional variant rs9344 at 11q13.3 regulates CCND1 expression in multiple myeloma with t(11;14)

Rare coding variant analysis for human diseases across biobanks and ancestries

Correction: Family history of plasma cell disorders is associated with improved survival in MGUS, multiple myeloma, and systemic AL amyloidosis

Mate pair sequencing outperforms fluorescence in situ hybridization in the genomic characterization of multiple myeloma

Mass Cytometry reveals unique phenotypic patterns associated with subclonal diversity and outcomes in multiple myeloma

Family history of plasma cell disorders is associated with improved survival in MGUS, multiple myeloma, and systemic AL amyloidosis

An analysis and evaluation of the WeFold collaborative for protein structure prediction and its pipelines in CASP11 and CASP12

Shared and unique genomic structural variants of different histological components within testicular germ cell tumours identified with mate pair sequencing

Quantification of Somatic Chromosomal Rearrangements in Circulating Cell-Free DNA from Ovarian Cancers

Prospective evaluation of genome sequencing to compare conventional cytogenetics in acute myeloid leukemia

Myeloid malignancies with 5q and 7q deletions are associated with extreme genomic complexity, biallelic TP53 variants, and very poor prognosis

Genomic rearrangements in sporadic lymphangioleiomyomatosis: an evolving genetic story

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