Author details

Full Name

Xinjie Xu

Affiliation

Mayo Clinic

ORCID

Career Start Year

2011

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36373660	CIViCdb 2022: evolution of an open-access cancer variant interpretation knowledgebase.	Nucleic Acids Res	2023
37634651	Follicular lymphoma and diffuse large B-cell lymphoma with BCL2 and IRF4 rearrangements in adult patients.	Hum Pathol	2023
37673866	Prospective evaluation of genome sequencing to compare conventional cytogenetics in acute myeloid leukemia.	Blood Cancer J	2023
36627146	A <i>TRIP11:: FLT3</i> gene fusion in a patient with myeloid/lymphoid neoplasm with eosinophilia and tyrosine kinase gene fusions: a case report and review of the literature.	Cold Spring Harb Mol Case Stud	2023
34781094	Utilizing next-generation sequencing to characterize a case of acute myeloid leukemia with t(4;12)(q12;p13) in the absence of ETV6/CHIC2 and ETV6/PDGFRA gene fusions.	Cancer Genet	2022
35771717	Characterization of unusual iAMP21 B-lymphoblastic leukemia (iAMP21-ALL) from the Mayo Clinic and Children's Oncology Group.	Genes Chromosomes Cancer	2022
35506873	Apparent coexistence of <i>ETV6::RUNX1</i> and <i>KMT2A::MLLT3</i> fusions due to a nonproductive <i>KMT2A</i> rearrangement in B-ALL.	Leuk Lymphoma	2022
35344861	Identification of EWSR1 rearrangements in patients with immature hematopoietic neoplasms: A case series and review of literature.	Ann Diagn Pathol	2022
35639830	Typical, atypical and cryptic t(15;17)(q24;q21) (PML::RARA) observed in acute promyelocytic leukemia: A retrospective review of 831 patients with concurrent chromosome and PML::RARA dual-color dual-fusion FISH studies.	Genes Chromosomes Cancer	2022
35624339	A community approach to the cancer-variant-interpretation bottleneck.	Nat Cancer	2022
36063163	Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC).	Genet Med	2022
35101336	Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC).	Genet Med	2022
35217871	A Novel USP25::PDGFRA Gene Fusion in a 78 Year Old Patient with a Myeloid Neoplasm.	Lab Med	2022
35167654	Guiding the global evolution of cytogenetic testing for hematologic malignancies.	Blood	2022
34791328	Identification of a Cryptic t(8;20;21)(q22;p13;q22) Resulting in RUNX1T1/RUNX1 Fusion in a Patient with Newly Diagnosed Acute Myeloid Leukemia.	Lab Med	2022
33078871	Identification of a novel KMT2A/GIMAP8 gene fusion in a pediatric patient with acute undifferentiated leukemia.	Genes Chromosomes Cancer	2021
33563889	Myeloid malignancies with 5q and 7q deletions are associated with extreme genomic complexity, biallelic TP53 variants, and very poor prognosis.	Blood Cancer J	2021
34819491	MYC break-apart FISH probe set reveals frequent unbalanced patterns of uncertain significance when evaluating aggressive B-cell lymphoma.	Blood Cancer J	2021
33991782	Clinical utility of next generation sequencing to detect IGH/IL3 rearrangements [t(5;14)(q31.1;q32.1)] in B-lymphoblastic leukemia/lymphoma.	Ann Diagn Pathol	2021
34297047	Genomic and clinical characterization of early T-cell precursor lymphoblastic lymphoma.	Blood Adv	2021
33145596	Detection of a Cryptic EP300/ZNF384 Gene Fusion by Chromosomal Microarray and Next-Generation Sequencing Studies in a Pediatric Patient with B-Lymphoblastic Leukemia.	Lab Med	2021
32196814	Cryptic and atypical KMT2A-USP2 and KMT2A-USP8 rearrangements identified by mate pair sequencing in infant and childhood leukemia.	Genes Chromosomes Cancer	2020
32836179	Siblings with ETV6/RUNX1-positive B-lymphoblastic leukemia: A single site experience and review of the literature.	Ann Diagn Pathol	2020
32408254	Detection of cryptic CCND1 rearrangements in mantle cell lymphoma by next generation sequencing.	Ann Diagn Pathol	2020
30649724	Genome-Wide Copy Number Variation Detection Using NGS: Data Analysis and Interpretation.	Methods Mol Biol	2019
31798590	Mechanisms of Relapse After CD19 CAR T-Cell Therapy for Acute Lymphoblastic Leukemia and Its Prevention and Treatment Strategies.	Front Immunol	2019
29197855	Detection of genome-wide copy number variants in myeloid malignancies using next-generation sequencing.	J Clin Pathol	2018
30138724	OncoKids: A Comprehensive Next-Generation Sequencing Panel for Pediatric Malignancies.	J Mol Diagn	2018
30377088	Assessing copy number aberrations and copy neutral loss of heterozygosity across the genome as best practice: An evidence based review of clinical utility from the cancer genomics consortium (CGC) working group for myelodysplastic syndrome, myelodysplastic/myeloproliferative and myeloproliferative neoplasms.	Cancer Genet	2018
30344013	Assessing copy number abnormalities and copy-neutral loss-of-heterozygosity across the genome as best practice in diagnostic evaluation of acute myeloid leukemia: An evidence-based review from the cancer genomics consortium (CGC) myeloid neoplasms working group.	Cancer Genet	2018
28103116	Acute Leukemia and Concurrent Mediastinal Germ Cell Tumor: Case Report and Literature Review.	Fetal Pediatr Pathol	2017
26728869	Concurrent detection of targeted copy number variants and mutations using a myeloid malignancy next generation sequencing panel allows comprehensive genetic analysis using a single testing strategy.	Br J Haematol	2016
27614666	Genomic Copy Number Analysis of HER2-Equivocal Breast Cancers.	Am J Clin Pathol	2016
24269304	The advantage of using SNP array in clinical testing for hematological malignancies--a comparative study of three genetic testing methods.	Cancer Genet	2013
22581475	Typical renal-coloboma syndrome phenotype in a patient with a submicroscopic deletion of the PAX2 gene.	Am J Med Genet A	2012
21063078	Duplication 5q and deletion 9p due to a t(5;9)(q34;p23) in 2 cousins with features of Hunter-McAlpine syndrome and hypothyroidism.	Cytogenet Genome Res	2011

1 - 36 of 36

Aparna Pallavajjala

Johns Hopkins University School of Medicine

Career Start Year 2014

Number of shared co-authors 0

David Shabsovich

university of california los angeles Medical Center

Career Start Year 2013

Number of shared co-authors 0

Yanara Marincevic-Zuniga

Uppsala University

Career Start Year 2012

Number of shared co-authors 0

David Wu

University of Washington

Career Start Year 2010

Number of shared co-authors 5

Christopher A Miller

Washington University School of Medicine

Career Start Year 2009

Number of shared co-authors 19

Daniela S Gerhard

National Cancer Institute

Career Start Year 2009

Number of shared co-authors 8

Jennifer Dunlap

Oregon Health & Science University

Career Start Year 2008

Number of shared co-authors 1

Don??t Alp??r

Semmelweis University

Career Start Year 2006

Number of shared co-authors 0

Emmanuelle Clappier

Saint-Louis Hospital

Career Start Year 2005

Number of shared co-authors 0

Jill M Hagenkord

Color Genomics Inc.

Career Start Year 2004

Number of shared co-authors 1

Alexander Kohlmann

Oncology R&D

Career Start Year 2002

Number of shared co-authors 0

Fei Yang

Oregon Health & Science University

Career Start Year 2002

Number of shared co-authors 1

Gudrun G??hring

Hannover Medical School

Career Start Year 2002

Number of shared co-authors 2

Fady M Mikhail

University of Alabama at Birmingham

Career Start Year 2002

Number of shared co-authors 10

Jeffery M Klco

St. Jude Children's Research Hospital

Career Start Year 2000

Number of shared co-authors 19

Guang Fan

Oregon Health and Science University

Career Start Year 2000

Number of shared co-authors 2

Marilyn M Li

Children's Hospital of Philadelphia

Career Start Year 2000

Number of shared co-authors 15

Karoly Szuhai

Leiden University Medical Center

Career Start Year 1997

Number of shared co-authors 1

Charles G Mullighan

St Jude Children's Research Hospital

Career Start Year 1996

Number of shared co-authors 13

Stefan Fr??hling

German Cancer Research Center (DKFZ), National Center for Tumor Diseases (NCT)

Career Start Year 1996

Number of shared co-authors 5

Michael Baudis

University of Zurich

Career Start Year 1995

Number of shared co-authors 17

Doris Steinemann

Hannover Medical School

Career Start Year 1994

Number of shared co-authors 1

Jean Soulier

University of Paris

Career Start Year 1993

Number of shared co-authors 6

Seishi Ogawa

Kyoto University

Career Start Year 1993

Number of shared co-authors 1

Julie M Gastier-Foster

Baylor College of Medicine

Career Start Year 1992

Number of shared co-authors 15

Christopher D Gocke

Johns Hopkins University School of Medicine

Career Start Year 1992

Number of shared co-authors 2

Claude Preudhomme

Lille University Hospital, INSERM UMR-S7, CNRS UMR9020, Lille University.

Career Start Year 1989

Number of shared co-authors 0

Mark J Routbort

University of Texas MD Anderson Cancer Center

Career Start Year 1989

Number of shared co-authors 6

Krzysztof Mr??zek

The Ohio State Comprehensive Cancer Center

Career Start Year 1988

Number of shared co-authors 7

Torsten Haferlach

Taussig Cancer Institute, Cleveland Clinic

Career Start Year 1983

Number of shared co-authors 5

row(s) 1 - 30 of 30

Gordana Raca

Children's Hospital Los Angeles

Co-authored papers 10

Beth A Pitel

Mayo Clinic

Co-authored papers 7

Rashmi Kanagal-Shamanna

The University of Texas MD Anderson Cancer Center

Co-authored papers 7

Yassmine Akkari

Association for Molecular Pathology

Co-authored papers 5

Peter Horak

German Cancer Research Center (DKFZ) and National Center for Tumor Diseases (NCT)

Co-authored papers 4

Subha Madhavan

Innovation Center for Biomedical Informatics, Georgetown University Medical Center

Co-authored papers 4

Alex H Wagner

Iowa State University, Mayo Clinic, Nationwide Children's Hospital, The Ohio State University College of Medicine, University of Iowa, Washington University in Saint Louis

Co-authored papers 4

Shruti Rao

Innovation Center for Biomedical Informatics, Georgetown University Medical Center

Co-authored papers 4

Kilannin Krysiak

Washington University School of Medicine

Co-authored papers 4

Deborah I Ritter

Baylor College of Medicine

Co-authored papers 4

Malachi Griffith

Washington University