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Exon scanning by reverse transcriptase–polymerase chain reaction for detection of known and novel EML4–ALK fusion variants in non–small cell lung cancer

Cancer genetics, 2011, Vol.204 (1), p.45-52

2011

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Recurrent t(2;2) and t(2;8) translocations in rhabdomyosarcoma without the canonical PAX-FOXO1 fuse PAX3 to members of the nuclear receptor transcriptional coactivator family

Genes chromosomes & cancer, 2010-03, Vol.49 (3), p.224-236

2010

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Incidence and patterns of ALK FISH abnormalities seen in a large unselected series of lung carcinomas

Molecular cytogenetics, 2012, Vol.5 (1), p.44-44

2012

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Trisomies 8 and 20 Characterize a Subgroup of Benign Fibrous Lesions Arising in Both Soft Tissue and Bone

The American journal of pathology, 1999-03, Vol.154 (3), p.729-733

1999

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Synchronous development of acute myeloid leukemia in recipient and donor after allogeneic bone marrow transplantation: report of a case with comments on donor evaluation

Transfusion (Philadelphia, Pa.), 2009-03, Vol.49 (3), p.555-562

2009

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Recurrent (2;2) and (2;8) Translocations in Rhabdomyosarcoma without the Canonical PAX-FOXO1 fuse PAX3 to Members of the Nuclear Receptor Transcriptional Coactivator (NCOA) Family

Genes chromosomes & cancer, 2010-03, Vol.49 (3), p.224-236

2010

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Bilateral synchronous tibial periosteal osteosarcoma with familial incidence

Skeletal radiology, 2012-08, Vol.41 (8), p.1005-1009

2012

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Reviews of Chromosome Studies in Urological Tumors. III. Cytogenetics and Genes in Testicular Tumors

The Journal of urology, 1996-05, Vol.155 (5), p.1531-1556

1996

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Misexpression of disrupted HMGI architectural factors activates alternative pathways of tumorigenesis

Cancer research (Chicago, Ill.), 1997-06, Vol.57 (11), p.2276-2280

1997

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Hepatic undifferentiated (embryonal) sarcoma arising in a mesenchymal hamartoma

The American journal of surgical pathology, 1997-10, Vol.21 (10), p.1248-1254

1997

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Gastric cancer: Classification, histology and application of molecular pathology

Journal of gastrointestinal oncology, 2012-09, Vol.3 (3), p.251-261

2012

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Blastic Plasmacytoid Dendritic Cell Neoplasm (BPDCN)

Atlas of genetics and cytogenetics in oncology and haematology, 2018-11 (6)

Meloni-Ehrig, Aurelia

2018

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t(7;11)(p15;p15) NUP98/HOXA13

Atlas of genetics and cytogenetics in oncology and haematology, 2018-10 (10)

Meloni-Ehrig, Aurelia M

2018

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t(X;14)(q28;q11.2) TRA-TRD/MTCP1

Atlas of genetics and cytogenetics in oncology and haematology, 2018-04 (12)

Meloni-Ehrig, Aurelia M

2018

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Plasmablastic lymphoma with MYC translocation: evidence for a common pathway in the generation of plasmablastic features

Modern pathology, 2010-07, Vol.23 (7), p.991-999

2010

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Plasmablastic lymphoma (PBL)

Atlas of genetics and cytogenetics in oncology and haematology, 2018-07 (2)

2018

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Benign chronic neutropenia with abnormalities involving 16q22, affecting mother and daughter

American journal of hematology, 2006-04, Vol.81 (4), p.262-270

2006

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Cloning of a breakpoint cluster region on chromosome 14 in uterine leiomyoma

Cancer letters, 1998-04, Vol.126 (2), p.119-126

1998

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Second case of t(2;21)(q11.2;q22.3) in a child with T-cell acute lymphoblastic leukemia 30

Atlas of genetics and cytogenetics in oncology and haematology, 2018-06 (1)

2018

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Renal cancer: Cytogenetic and molecular genetic aspects

American journal of medical genetics, 2002-10, Vol.115 (3), p.164-172

Meloni-Ehrig, Aurelia M.

2002

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The der(17)t(x;17)(p11;q25) of human alveolar soft part sarcoma fuses the TFE3 transcription factor gene to ASPL, a novel gene at 17q25

Oncogene, 2001-01, Vol.20 (1), p.48-57

2001

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36. Quadruple-hit B-cell lymphoma with simultaneous BCL2, BCL6, CCND1, and MYC rearrangements: Two new cases

Cancer genetics, 2020-06, Vol.244, p.14-14

2020

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A case of lipoblastoma with seven copies of chromosome 8

Cancer genetics and cytogenetics, 2009-04, Vol.190 (1), p.49-51

2009

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Commentary on ISCN 2005

Cancer genetics and cytogenetics, 2007-06, Vol.175 (2), p.89-90

2007

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Exon scanning by reverse transcriptase–polymerase chain reaction for detection of known and novel EML4–ALK fusion variants in non–small cell lung cancer

Recurrent t(2;2) and t(2;8) translocations in rhabdomyosarcoma without the canonical PAX-FOXO1 fuse PAX3 to members of the nuclear receptor transcriptional coactivator family

Incidence and patterns of ALK FISH abnormalities seen in a large unselected series of lung carcinomas

Trisomies 8 and 20 Characterize a Subgroup of Benign Fibrous Lesions Arising in Both Soft Tissue and Bone

Synchronous development of acute myeloid leukemia in recipient and donor after allogeneic bone marrow transplantation: report of a case with comments on donor evaluation

Recurrent (2;2) and (2;8) Translocations in Rhabdomyosarcoma without the Canonical PAX-FOXO1 fuse PAX3 to Members of the Nuclear Receptor Transcriptional Coactivator (NCOA) Family

Bilateral synchronous tibial periosteal osteosarcoma with familial incidence

Reviews of Chromosome Studies in Urological Tumors. III. Cytogenetics and Genes in Testicular Tumors

Misexpression of disrupted HMGI architectural factors activates alternative pathways of tumorigenesis

Hepatic undifferentiated (embryonal) sarcoma arising in a mesenchymal hamartoma

Gastric cancer: Classification, histology and application of molecular pathology

Blastic Plasmacytoid Dendritic Cell Neoplasm (BPDCN)

t(7;11)(p15;p15) NUP98/HOXA13

t(X;14)(q28;q11.2) TRA-TRD/MTCP1

Plasmablastic lymphoma with MYC translocation: evidence for a common pathway in the generation of plasmablastic features

Plasmablastic lymphoma (PBL)

Benign chronic neutropenia with abnormalities involving 16q22, affecting mother and daughter

Cloning of a breakpoint cluster region on chromosome 14 in uterine leiomyoma

High BAALC expression associates with other molecular prognostic markers, poor outcome, and a distinct gene-expression signature in cytogenetically normal patients younger than 60 years with acute myeloid leukemia: a Cancer and Leukemia Group B (CALGB) study

Second case of t(2;21)(q11.2;q22.3) in a child with T-cell acute lymphoblastic leukemia 30

Renal cancer: Cytogenetic and molecular genetic aspects

The der(17)t(x;17)(p11;q25) of human alveolar soft part sarcoma fuses the TFE3 transcription factor gene to ASPL, a novel gene at 17q25

36. Quadruple-hit B-cell lymphoma with simultaneous BCL2, BCL6, CCND1, and MYC rearrangements: Two new cases

A case of lipoblastoma with seven copies of chromosome 8

Commentary on ISCN 2005

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