Cancer Genetics

1

Molecular identification of a TPR-FGFR1 fusion transcript in an adult with myeloproliferative neoplasm, T-lymphoblastic lymphoma, and a t(1;8)(q25;p11.2)

Kim, Seon Young, Kim, Ji-Eun, Park, Seonyang, Kim, Hyun Kyung

Journal:

Cancer Genetics

Year:

2014

Language:

english

File:

PDF, 357 KB

english, 2014

2

ABL1 gene involvement within a complex three-way translocation (2;9;4) in perineurioma characterized by molecular cytogenetic methods

Duff, Deiter J., Guzman, Miguel A., Batanian, Jacqueline R.

Journal:

Cancer Genetics

Year:

2014

Language:

english

File:

PDF, 102 KB

english, 2014

3

From chromosomal abnormalities to the identification of target genes in mouse models of breast cancer

Fabris, Victoria T.

Journal:

Cancer Genetics

Year:

2014

Language:

english

File:

PDF, 1.04 MB

english, 2014

4

Whole Genome Copy Number Analysis of Formalin Fixed Paraffin Embedded Samples Identifies Major Genomic Aberrations in Medulloblastoma

Robison, Nathan J., Margol, Ashley S., Shukla, Anju, Kennedy, Rebekah J., Fung, Eric, Judkins, Alexander R., Asgharzadeh, Shahab

Journal:

Cancer Genetics

Year:

2014

Language:

english

File:

PDF, 37 KB

english, 2014

5

Microarray Detects Variation in Deletions of IGH (14q32) Gene Region in CLL

Utter, Rachel A., Pickering, Diane L., Stevens, Jadd M., Althof, Pamela A., Sanger, Warren G., Dave, Bhavana J.

Journal:

Cancer Genetics

Year:

2014

Language:

english

File:

PDF, 41 KB

english, 2014

6

What you are missing could matter: a rare, complex BRAF mutation affecting codons 599, 600, and 601 uncovered by next generation sequencing

Wilson, Melissa A., Morrissette, Jennifer J.D., McGettigan, Suzanne, Roth, David, Elder, David, Schuchter, Lynn M., Daber, Robert D.

Journal:

Cancer Genetics

Year:

2014

Language:

english

File:

PDF, 808 KB

english, 2014

7

My Cancer Genome

Micheel, Christine M., Lovly, Christine M., Levy, Mia A.

Journal:

Cancer Genetics

Year:

2014

Language:

english

File:

PDF, 38 KB

english, 2014

8

KRAS Amplification in a 73-Year-Old Man with Adenocarcinoma of Lung

Chen, Hui, Singh, Rajesh R., Abraham, Ronald, Mehrotra, Meenakshi, Mishra, Bal Mukund, Roy-Chowdhuri, Sinchita, Routbort, Mark, Aldape, Kenneth, Broaddus, Russell, Patel, Keyur P., Luthra, Rajyalakshm

Journal:

Cancer Genetics

Year:

2014

Language:

english

File:

PDF, 51 KB

english, 2014

9

Non-invasive Cell-free Tumor DNA-based Detection of Breast Cancer-related Copy Number Variations

Zimmermann, Bernhard G., Kirkizlar, Eser, Hill, Matthew, Constantin, Tudor, Sigurjonsson, Styrmir, Hoanga, Bin, Chopra, Nikhil, Rabinowitz, Matthew

Journal:

Cancer Genetics

Year:

2014

Language:

english

File:

PDF, 81 KB

english, 2014

10

Clinical Utility of DNA Arrays in Detecting Chromosomal Aberrations Associated with High-Risk Philadelphia-Like Acute Lymphoblastic Leukemia

Raca, Gordana, Zhang, Zhiyu, Sukhanova, Madina, Li, Zejuan, Gurbuxani, Sandeep, Stock, Wendy

Journal:

Cancer Genetics

Year:

2014

Language:

english

File:

PDF, 117 KB

english, 2014

11

Integrative Copy Number and Mutational Analysis Improves Glioma Diagnostics

Ramkissoon, Shakti H., Bi, Wenya L., Schumacher, Steven E., Ramkissoon, Lori A., Haidar, Sam, Dubuc, Adrian M., Brown, Loreal, Burns, Margot, Cryan, Jane, Reardon, David A., Lee, Eudocia Q., Rinne, Mi

Journal:

Cancer Genetics

Year:

2014

Language:

english

File:

PDF, 52 KB

english, 2014

12

Genome-Wide Microarray Analysis Improves Routine Diagnosis of Hematological Malignancies

Shao, Lina, Miller, Sue, Roulston, Diane

Journal:

Cancer Genetics

Year:

2014

Language:

english

File:

PDF, 103 KB

english, 2014

13

Secondary Philadelphia chromosome and erythrophagocytosis in a relapsed acute myeloid leukemia after hematopoietic cell transplantation

Kelemen, Katalin, Galani, Komal, Conley, Christopher R., Greipp, Patricia T.

Journal:

Cancer Genetics

Year:

2014

Language:

english

File:

PDF, 773 KB

english, 2014

14

Extraskeletal myxoid chondrosarcoma with a t(9;16)(q22;p11.2) resulting in a NR4A3-FUS fusion

Broehm, Cory J., Wu, Jin, Gullapalli, Rama R., Bocklage, Thèrése

Journal:

Cancer Genetics

Year:

2014

Language:

english

File:

PDF, 1.27 MB

english, 2014

15

Validation of Affymetrix Cytoscan HD: Children's Mercy Hospital Experience with Neoplastic Samples

Cooley, Linda D., Fiedler, Stephanie D., Joyce, Julie M., Mouron, Barbara, Nick, Jessica, Repnikova, Elena, Thakor, Preeti V., Zhang, Lei

Journal:

Cancer Genetics

Year:

2014

Language:

english

File:

PDF, 103 KB

english, 2014

16

Multiple Segmental Chromosomal Aberrations in Low-Risk Neuroblastoma are Associated with Metastatic Relapse

Mayfield, Jodi R., Raca, Gordana, Sukhanova, Madina, Bagatell, Rochelle, Irwin, Meredith, Little, Anthony, Rawwas, Jawhar, Cohn, Susan L.

Journal:

Cancer Genetics

Year:

2014

Language:

english

File:

PDF, 51 KB

english, 2014

17

Detection of Copy Number Variations in Breast Cancer Samples Using Single-nucleotide Polymorphism-targeted Massively Multiplexed PCR

Babiarz, Joshua E., Zimmermann, Bernhard G., Constantin, Tudor, Swenerton, Ryan, Kirkizlar, Eser, Wayham, Nicholas, Rabinowitz, Matthew, Hill, Matthew

Journal:

Cancer Genetics

Year:

2014

Language:

english

File:

PDF, 51 KB

english, 2014

18

A Novel 1p35.1p34.3 Microdeletion in a Baby Boy with Multiple Congenital Anomalies and Developmental Delay

Kantarci, Sibel

Journal:

Cancer Genetics

Year:

2014

Language:

english

File:

PDF, 37 KB

english, 2014

19

Old Dog, New Tricks: Novel Application of Whole Genome SNP Microarray for Chimerism Studies in Allogeneic Bone Marrow Transplant Patients

Znoyko, Iya Y., Wolff, Daynna J.

Journal:

Cancer Genetics

Year:

2014

Language:

english

File:

PDF, 41 KB

english, 2014

20

Rare Complete and Partial Monosomy 7 Mosaicism Detected in a Case with FTT and Borderline Motor Delay, Subsequently Diagnosed with Juvenile MDS: An Exposition of this Case and Other Interesting Mosaic Cancer Case Studies

Bickley, Vivienne M., Parker, Elsa M., Taylor, Jill C., Watt, Jane E., Robertson, Monique D., Doudney, Kit W.E., Cross, Siobhan, Townsend, Janine, Kidd, Alexa M.J., George, Peter M.

Journal:

Cancer Genetics

Year:

2014

Language:

english

File:

PDF, 42 KB

english, 2014

21

aCGH+SNP as a Promising Analytical Tool for the Detection of Chromosomal Abnormalities in Acute Leukemia

Chen, Chuanfei, Tiong Lim, Alvin Soon, Lim, Tse Hui, Lau, Lai Ching, Teng, Li Min, Tien, Sim Leng

Journal:

Cancer Genetics

Year:

2014

Language:

english

File:

PDF, 34 KB

english, 2014

22

Effects of TSP-1 -696 C/T polymorphism on bladder cancer susceptibility and clinicopathologic features

Gu, Jinbao, Tao, Jun, Yang, Xiao, Li, Pengchao, Yang, Xuejian, Qin, Chao, Cao, Qiang, Cai, Hongzhou, Zhang, Zhengdong, Wang, Meilin, Gu, Min, Lu, Qiang, Yin, Changjun

Journal:

Cancer Genetics

Year:

2014

Language:

english

File:

PDF, 228 KB

english, 2014

23

Detection of Genomic Imbalances Involved in Common Chromosomal Rearrangements of Acute Leukemia by Cytogenomic SNP Microarray Analysis

Yenamandra, A., Wheeler, F.C., Hollis, A.B., Barba, L., Wang, Y., Geng, L.

Journal:

Cancer Genetics

Year:

2014

Language:

english

File:

PDF, 56 KB

english, 2014

24

Cover 1

Journal:

Cancer Genetics

Year:

2014

File:

PDF, 693 KB

2014

25

Recurrent Genetic Alterations in Hepatitis C-Associated Hepatocellular Carcinoma Detected by Genomic Microarray and Their correlation with Histology and Clinical Outcome

Liu, Yajuan, Zhou, Yang, Yeh, Matthew

Journal:

Cancer Genetics

Year:

2014

Language:

english

File:

PDF, 33 KB

english, 2014

26

Molecular Characterization of WNT5B as a Candidate Gene for Developmental Delay Associated with 12p13.13 Microdeletions

Omorodion, Jacklyn, Carter, Ronald, Carter, Teresa, Tarnopolsky, Mark, McCready, Elizabeth

Journal:

Cancer Genetics

Year:

2014

Language:

english

File:

PDF, 39 KB

english, 2014

27

Translocation t(2;7)(p11.2;q21.2): a rare genetic aberration associated with B-cell lymphoproliferative disorders of marginal-zone origin

Xochelli, Aliki, Baliakas, Panagiotis, Moore, Sarah, Sole, Francesc, Wickham, Nicholas, Salido, Marta, Athanasiadou, Anastasia, Oscier, David, Stamatopoulos, Kostas

Journal:

Cancer Genetics

Year:

2014

Language:

english

File:

PDF, 168 KB

english, 2014

28

A Mosaic Copy Number Gain of 5p15.3p13.3

Valle, Stephanie E., Tafe, Laura J., Reader, Elizabeth I., Bao, Liming, Dinulos, Mary Beth P., Tsongalis, Gregory J., Lefferts, Joel A.

Journal:

Cancer Genetics

Year:

2014

Language:

english

File:

PDF, 73 KB

english, 2014

29

Editorial Board

Journal:

Cancer Genetics

Year:

2014

File:

PDF, 102 KB

2014

30

Volume 207; Issue 6

Molecular identification of a TPR-FGFR1 fusion transcript in an adult with myeloproliferative neoplasm, T-lymphoblastic lymphoma, and a t(1;8)(q25;p11.2)

ABL1 gene involvement within a complex three-way translocation (2;9;4) in perineurioma characterized by molecular cytogenetic methods

From chromosomal abnormalities to the identification of target genes in mouse models of breast cancer

Whole Genome Copy Number Analysis of Formalin Fixed Paraffin Embedded Samples Identifies Major Genomic Aberrations in Medulloblastoma

Microarray Detects Variation in Deletions of IGH (14q32) Gene Region in CLL

What you are missing could matter: a rare, complex BRAF mutation affecting codons 599, 600, and 601 uncovered by next generation sequencing

My Cancer Genome

KRAS Amplification in a 73-Year-Old Man with Adenocarcinoma of Lung

Non-invasive Cell-free Tumor DNA-based Detection of Breast Cancer-related Copy Number Variations

Clinical Utility of DNA Arrays in Detecting Chromosomal Aberrations Associated with High-Risk Philadelphia-Like Acute Lymphoblastic Leukemia

Integrative Copy Number and Mutational Analysis Improves Glioma Diagnostics

Genome-Wide Microarray Analysis Improves Routine Diagnosis of Hematological Malignancies

Secondary Philadelphia chromosome and erythrophagocytosis in a relapsed acute myeloid leukemia after hematopoietic cell transplantation

Extraskeletal myxoid chondrosarcoma with a t(9;16)(q22;p11.2) resulting in a NR4A3-FUS fusion

Validation of Affymetrix Cytoscan HD: Children's Mercy Hospital Experience with Neoplastic Samples

Multiple Segmental Chromosomal Aberrations in Low-Risk Neuroblastoma are Associated with Metastatic Relapse

Detection of Copy Number Variations in Breast Cancer Samples Using Single-nucleotide Polymorphism-targeted Massively Multiplexed PCR

A Novel 1p35.1p34.3 Microdeletion in a Baby Boy with Multiple Congenital Anomalies and Developmental Delay

Old Dog, New Tricks: Novel Application of Whole Genome SNP Microarray for Chimerism Studies in Allogeneic Bone Marrow Transplant Patients

Rare Complete and Partial Monosomy 7 Mosaicism Detected in a Case with FTT and Borderline Motor Delay, Subsequently Diagnosed with Juvenile MDS: An Exposition of this Case and Other Interesting Mosaic Cancer Case Studies

aCGH+SNP as a Promising Analytical Tool for the Detection of Chromosomal Abnormalities in Acute Leukemia

Effects of TSP-1 -696 C/T polymorphism on bladder cancer susceptibility and clinicopathologic features

Detection of Genomic Imbalances Involved in Common Chromosomal Rearrangements of Acute Leukemia by Cytogenomic SNP Microarray Analysis

Cover 1

Recurrent Genetic Alterations in Hepatitis C-Associated Hepatocellular Carcinoma Detected by Genomic Microarray and Their correlation with Histology and Clinical Outcome

Molecular Characterization of WNT5B as a Candidate Gene for Developmental Delay Associated with 12p13.13 Microdeletions

Translocation t(2;7)(p11.2;q21.2): a rare genetic aberration associated with B-cell lymphoproliferative disorders of marginal-zone origin

A Mosaic Copy Number Gain of 5p15.3p13.3

Editorial Board

Table of Contents