Publications by authors named "Athena M Cherry"

56Publications

Acute leukemia in a patient with 15q overgrowth syndrome.

Am J Med Genet A 2019 06 12;179(6):1025-1029. Epub 2019 Mar 12.

Division of Medical Genetics, Department of Pediatrics, Stanford University, Stanford, California.

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http://dx.doi.org/10.1002/ajmg.a.61115DOI Listing
June 2019

Immune checkpoint blockade as a potential therapeutic strategy for undifferentiated malignancies.

Hum Pathol 2018 12 7;82:39-45. Epub 2018 Jul 7.

Department of Pathology, Stanford University School of Medicine, Stanford, CA 94305, USA. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S00468177183025
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http://dx.doi.org/10.1016/j.humpath.2018.06.034DOI Listing
December 2018

A Clinicopathologic and Molecular Analysis of 34 Mediastinal Germ Cell Tumors Suggesting Different Modes of Teratoma Development.

Am J Surg Pathol 2018 12;42(12):1662-1673

Department of Pathology & Laboratory Medicine, Indiana University School of Medicine, Indianapolis, IN.

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http://dx.doi.org/10.1097/PAS.0000000000001164DOI Listing
December 2018

Investigating human placentation and pregnancy using first trimester chorionic villi.

Placenta 2018 05 21;65:65-75. Epub 2018 Mar 21.

Department of Genetics, Stanford University School of Medicine, Stanford, CA, United States. Electronic address:

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http://dx.doi.org/10.1016/j.placenta.2018.03.005DOI Listing
May 2018

A novel TRIP11-FLT3 fusion in a patient with a myeloid/lymphoid neoplasm with eosinophilia.

Cancer Genet 2017 Oct 10;216-217:10-15. Epub 2017 May 10.

Department of Pathology, Stanford University School of Medicine, Stanford, CA 94305, USA. Electronic address:

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http://dx.doi.org/10.1016/j.cancergen.2017.05.001DOI Listing
October 2017

Section E6.1-6.4 of the ACMG technical standards and guidelines: chromosome studies of neoplastic blood and bone marrow-acquired chromosomal abnormalities.

Genet Med 2016 06 28;18(6):635-42. Epub 2016 Apr 28.

Department of Pathology and Laboratory Medicine, Children's Mercy Hospital, University of Missouri Kansas City Medical School, Kansas City, Missouri, USA.

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http://dx.doi.org/10.1038/gim.2016.50DOI Listing
June 2016

Reply: To PMID 25843063.

Am J Obstet Gynecol 2015 Oct 9;213(4):596. Epub 2015 Jun 9.

Stanford University School of Medicine, Palo Alto, CA.

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http://dx.doi.org/10.1016/j.ajog.2015.06.007DOI Listing
October 2015

Noninvasive prenatal screening for aneuploidy: positive predictive values based on cytogenetic findings.

Am J Obstet Gynecol 2015 Aug 3;213(2):214.e1-5. Epub 2015 Apr 3.

Department of Pathology, Stanford University School of Medicine, Palo Alto, CA.

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http://dx.doi.org/10.1016/j.ajog.2015.04.001DOI Listing
August 2015

Reply: To PMID 23529082.

Am J Obstet Gynecol 2014 Jul 10;211(1):81. Epub 2014 Jan 10.

Stanford University School of Medicine, Palo Alto, CA.

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http://dx.doi.org/10.1016/j.ajog.2014.01.015DOI Listing
July 2014

Hidden mastocytosis in acute myeloid leukemia with t(8;21)(q22;q22).

Am J Clin Pathol 2013 Oct;140(4):525-35

Dept of Pathology, Stanford University School of Medicine, 300 Pasteur Dr, MC 5324, Stanford, CA 94086; e-mail:

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https://ajcp.oxfordjournals.org/content/ajcpath/140/4/525.fu
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http://ajcp.ascpjournals.org/cgi/doi/10.1309/AJCP1Q0YSXEAHNK
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http://dx.doi.org/10.1309/AJCP1Q0YSXEAHNKKDOI Listing
October 2013

B-cell transcription factor expression and immunoglobulin gene rearrangement frequency in acute myeloid leukemia with t(8;21)(q22;q22).

Am J Clin Pathol 2013 Sep;140(3):355-62

Department of Pathology, Stanford University School of Medicine, 300 Pasteur Dr, Stanford, CA 94305, USA.

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http://dx.doi.org/10.1309/AJCPFBCFXP94AKWJDOI Listing
September 2013

Still a screening test: more attention needed to noninvasive prenatal test false-positive rates.

Am J Obstet Gynecol 2013 Aug 11;209(2):160-1. Epub 2013 Apr 11.

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http://dx.doi.org/10.1016/j.ajog.2013.04.021DOI Listing
August 2013

Is it time to sound an alarm about false-positive cell-free DNA testing for fetal aneuploidy?

Am J Obstet Gynecol 2013 Nov 22;209(5):415-9. Epub 2013 Mar 22.

Department of Obstetrics and Gynecology, Perelman School of Medicine, University of Pennsylvania, Philadelphia PA; Prenatal Cytogenetic Laboratory, Perelman School of Medicine, University of Pennsylvania, Philadelphia PA.

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http://dx.doi.org/10.1016/j.ajog.2013.03.027DOI Listing
November 2013

ACMG Policy Statement. Risk categorization for oversight of laboratory-developed tests for inherited conditions.

Genet Med 2013 Apr 24;15(4):314-5. Epub 2013 Jan 24.

Department of Medical Genetics, Henry Ford Health System, Detroit, Michigan, USA.

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http://dx.doi.org/10.1038/gim.2012.178DOI Listing
April 2013

Report of two patients and further characterization of interstitial 9p13 deletion--a rare but recurrent microdeletion syndrome?

Am J Med Genet A 2012 Sep 7;158A(9):2328-35. Epub 2012 Aug 7.

Department of Pediatrics, Division of Medical Genetics, Stanford University School of Medicine, Stanford, California 94305, USA.

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http://dx.doi.org/10.1002/ajmg.a.35536DOI Listing
September 2012

Short tandem repeat and human leukocyte antigen mutations or losses confound engraftment and typing analysis in hematopoietic stem cell transplants.

Hum Immunol 2011 Jun 2;72(6):503-9. Epub 2011 Apr 2.

Clinical Research Division, Department of Laboratory Medicine, University of Washington, Seattle, WA 98109, USA.

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http://dx.doi.org/10.1016/j.humimm.2011.03.003DOI Listing
June 2011

Loss of SMARCB1/INI1 expression in poorly differentiated chordomas.

Acta Neuropathol 2010 Dec 30;120(6):745-53. Epub 2010 Oct 30.

Department of Pathology, Stanford University School of Medicine, Palo Alto, CA 94305, USA.

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http://dx.doi.org/10.1007/s00401-010-0767-xDOI Listing
December 2010

A pediatric B lineage leukemia with coincident MYC and MLL translocations.

J Pediatr Hematol Oncol 2011 Mar;33(2):158-60

Department of Pediatrics, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.

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http://dx.doi.org/10.1097/MPH.0b013e3181e65c39DOI Listing
March 2011

Feeder-free derivation of induced pluripotent stem cells from adult human adipose stem cells.

Proc Natl Acad Sci U S A 2009 Sep 8;106(37):15720-5. Epub 2009 Sep 8.

Department of Radiology, Stanford University School of Medicine, Stanford, CA 94305, USA.

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http://dx.doi.org/10.1073/pnas.0908450106DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2739869PMC
September 2009

Complete remission of primary plasma cell leukemia with bortezomib, doxorubicin, and dexamethasone: a case report.

Cases J 2009 Feb 4;2(1):121. Epub 2009 Feb 4.

Division of Hematology, Department of Medicine, Stanford University School of Medicine, Stanford, CA, USA.

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http://dx.doi.org/10.1186/1757-1626-2-121DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2644294PMC
February 2009

Array-based comparative genomic hybridization: clinical contexts for targeted and whole-genome designs.

Genet Med 2007 Sep;9(9):553-9

Department of Pathology, Stanford University School of Medicine, Palo Alto, California, USA.

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http://dx.doi.org/10.1097/gim.0b013e318149e354DOI Listing
September 2007

Gliosarcoma with melanocytic differentiation.

Acta Neuropathol 2008 Mar 20;115(3):357-61. Epub 2007 Jul 20.

Department of Pathology, Stanford University Medical Center, 300 Pasteur Drive, Stanford, CA 94305, USA.

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http://dx.doi.org/10.1007/s00401-007-0232-7DOI Listing
March 2008

Whole-genome array-CGH identifies novel contiguous gene deletions and duplications associated with developmental delay, mental retardation, and dysmorphic features.

Am J Med Genet A 2007 Jul;143A(13):1431-41

Department of Pathology, Stanford University School of Medicine, Stanford, California, USA.

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http://dx.doi.org/10.1002/ajmg.a.31773DOI Listing
July 2007

Molecular analysis of chromosomal rearrangements in mammalian cells after phiC31-mediated integration.

Hum Gene Ther 2006 Nov;17(11):1077-94

Department of Pediatrics, School of Medicine, Stanford University, Stanford, CA 94305, USA.

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http://dx.doi.org/10.1089/hum.2006.17.1077DOI Listing
November 2006

Evaluation of Her-2/neu status in carcinomas with amplified chromosome 17 centromere locus.

Am J Clin Pathol 2006 Nov;126(5):709-16

Department of Pathology, Oregon Health & Science University, Portland, OR 97239, USA.

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http://dx.doi.org/10.1309/9EYM-6VE5-8F2Y-CD9FDOI Listing
November 2006

Utility of interphase FISH to stratify patients into cytogenetic risk categories at diagnosis of AML in an Eastern Cooperative Oncology Group (ECOG) clinical trial (E1900).

Leuk Res 2007 May 22;31(5):605-9. Epub 2006 Sep 22.

Medical and Molecular Genetics, Indiana University School of Medicine, 975 W. Walnut Street IB 264, Indianapolis, IN 46202, USA.

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http://dx.doi.org/10.1016/j.leukres.2006.07.026DOI Listing
May 2007

Overexpression of the anaphase promoting complex/cyclosome inhibitor Emi1 leads to tetraploidy and genomic instability of p53-deficient cells.

Cell Cycle 2006 Jul 17;5(14):1569-73. Epub 2006 Jul 17.

Department of Pathology, Stanford University, Stanford, California 94305, USA.

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https://www.tandfonline.com/doi/full/10.4161/cc.5.14.2925
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http://dx.doi.org/10.4161/cc.5.14.2925DOI Listing
July 2006

Identification of novel Runx1 (AML1) translocation partner genes SH3D19, YTHDf2, and ZNF687 in acute myeloid leukemia.

Genes Chromosomes Cancer 2006 Oct;45(10):918-32

Department of Pathology, Stanford University, Stanford, CA, USA.

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http://dx.doi.org/10.1002/gcc.20355DOI Listing
October 2006

Nablus mask-like facial syndrome is caused by a microdeletion of 8q detected by array-based comparative genomic hybridization.

Am J Med Genet A 2006 Jun;140(12):1267-73

Department of Pediatrics, Division of Medical Genetics, Stanford University School of Medicine, Stanford, California 94305-5208, USA.

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http://dx.doi.org/10.1002/ajmg.a.31262DOI Listing
June 2006

CTCF mediates interchromosomal colocalization between Igf2/H19 and Wsb1/Nf1.

Science 2006 Apr;312(5771):269-72

Medical Service, Department of Veterans Affairs, Palo Alto Health Care System, and Department of Medicine, Stanford University, Palo Alto, CA 94304, USA.

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http://dx.doi.org/10.1126/science.1123191DOI Listing
April 2006

Triplication of 8p22-8p23 in a patient with features similar to Kabuki syndrome.

Am J Med Genet A 2006 Jan;140(2):170-3

Department of Pediatrics, Division of Medical Genetics, Stanford University School of Medicine, Stanford, California 94305-5208, USA.

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http://dx.doi.org/10.1002/ajmg.a.31036DOI Listing
January 2006

Fluorescence in situ hybridization investigation of cutaneous lesions in acute promyelocytic leukemia.

Mod Pathol 2005 Dec;18(12):1569-76

Department of Pathology, Stanford University School of Medicine, Stanford, CA 94305-5627, USA.

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http://dx.doi.org/10.1038/modpathol.3800465DOI Listing
December 2005

Low-grade B-Cell lymphomas with plasmacytic differentiation lack PAX5 gene rearrangements.

J Mol Diagn 2005 Aug;7(3):346-51

Department of Pathology, Stanford University Medical Center, 300 Pasteur Dr., Room H1501B, MC 5627, Stanford, CA 94305-5627, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1867539PMC
http://dx.doi.org/10.1016/S1525-1578(10)60563-6DOI Listing
August 2005

A report of three patients with an interstitial deletion of chromosome 15q24.

Am J Med Genet A 2005 Aug;137(1):65-71

Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, 46202, USA.

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http://dx.doi.org/10.1002/ajmg.a.30836DOI Listing
August 2005

Cytologic diagnosis of Burkitt lymphoma.

Cancer 2005 Oct;105(5):310-8

Department of Pathology, Stanford University Medical Center, Stanford, California 94305, USA.

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http://dx.doi.org/10.1002/cncr.21307DOI Listing
October 2005

Terminal deletion of 6p results in a recognizable phenotype.

Am J Med Genet A 2005 Jul;136(2):162-8

Department of Pediatrics, Division of Medical Genetics, Stanford University School of Medicine, CA 94305, USA.

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http://dx.doi.org/10.1002/ajmg.a.30784DOI Listing
July 2005

Mild developmental delay in terminal chromosome 6p deletion.

Am J Med Genet A 2004 Aug;129A(2):201-5

Department of Pediatrics, Division of Medical Genetics, Stanford University, School of Medicine, Stanford, California 94305-5208, USA.

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http://dx.doi.org/10.1002/ajmg.a.30127DOI Listing
August 2004

Terminal 22q deletion syndrome: a newly recognized cause of speech and language disability in the autism spectrum.

Pediatrics 2004 Aug;114(2):451-7

Department of Pediatrics, Division of Medical Genetics, H-315, Stanford University School of Medicine, Stanford, California 94305-5208, USA.

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http://dx.doi.org/10.1542/peds.114.2.451DOI Listing
August 2004

Preferential expression of a mutant allele of the amplified MDR1 (ABCB1) gene in drug-resistant variants of a human sarcoma.

Genes Chromosomes Cancer 2002 08;34(4):372-83

Oncology Division, Department of Medicine, Stanford University School of Medicine, 269 Campus Drive, Stanford, CA 94305-5151, USA.

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http://doi.wiley.com/10.1002/gcc.10067
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http://dx.doi.org/10.1002/gcc.10067DOI Listing
August 2002

FISHing for answers: the use of molecular cytogenetic techniques in adolescent medicine practice.

Adolesc Med 2002 Jun;13(2):305-13, vi

Division of Medical Genetics, Department of Pediatrics, Stanford University School of Medicine, California 94305-5208, USA.

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June 2002