Jennelle C Hodge

Jennelle C Hodge

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Jennelle C Hodge

Jennelle C Hodge

Publications by authors named "Jennelle C Hodge"

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Molecular and pathologic characterization of AML with double Inv(3)(q21q26.2).

Cancer Genet 2019 01 16;230:28-36. Epub 2018 Nov 16.

Pathology and Laboratory Medicine Institute, Cleveland Clinic, Cleveland, OH, USA; Department of Pathology, UH Cleveland Medical Center, 10524 Euclid Ave, Cleveland, OH 44106, USA. Electronic address:

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http://dx.doi.org/10.1016/j.cancergen.2018.08.007DOI Listing
January 2019

The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies.

Authors:
Claire Redin Harrison Brand Ryan L Collins Tammy Kammin Elyse Mitchell Jennelle C Hodge Carrie Hanscom Vamsee Pillalamarri Catarina M Seabra Mary-Alice Abbott Omar A Abdul-Rahman Erika Aberg Rhett Adley Sofia L Alcaraz-Estrada Fowzan S Alkuraya Yu An Mary-Anne Anderson Caroline Antolik Kwame Anyane-Yeboa Joan F Atkin Tina Bartell Jonathan A Bernstein Elizabeth Beyer Ian Blumenthal Ernie M H F Bongers Eva H Brilstra Chester W Brown Hennie T Brüggenwirth Bert Callewaert Colby Chiang Ken Corning Helen Cox Edwin Cuppen Benjamin B Currall Tom Cushing Dezso David Matthew A Deardorff Annelies Dheedene Marc D'Hooghe Bert B A de Vries Dawn L Earl Heather L Ferguson Heather Fisher David R FitzPatrick Pamela Gerrol Daniela Giachino Joseph T Glessner Troy Gliem Margo Grady Brett H Graham Cristin Griffis Karen W Gripp Andrea L Gropman Andrea Hanson-Kahn David J Harris Mark A Hayden Rosamund Hill Ron Hochstenbach Jodi D Hoffman Robert J Hopkin Monika W Hubshman A Micheil Innes Mira Irons Melita Irving Jessie C Jacobsen Sandra Janssens Tamison Jewett John P Johnson Marjolijn C Jongmans Stephen G Kahler David A Koolen Jerome Korzelius Peter M Kroisel Yves Lacassie William Lawless Emmanuelle Lemyre Kathleen Leppig Alex V Levin Haibo Li Hong Li Eric C Liao Cynthia Lim Edward J Lose Diane Lucente Michael J Macera Poornima Manavalan Giorgia Mandrile Carlo L Marcelis Lauren Margolin Tamara Mason Diane Masser-Frye Michael W McClellan Cinthya J Zepeda Mendoza Björn Menten Sjors Middelkamp Liya R Mikami Emily Moe Shehla Mohammed Tarja Mononen Megan E Mortenson Graciela Moya Aggie W Nieuwint Zehra Ordulu Sandhya Parkash Susan P Pauker Shahrin Pereira Danielle Perrin Katy Phelan Raul E Piña Aguilar Pino J Poddighe Giulia Pregno Salmo Raskin Linda Reis William Rhead Debra Rita Ivo Renkens Filip Roelens Jayla Ruliera Patrick Rump Samantha L P Schilit Ranad Shaheen Rebecca Sparkes Erica Spiegel Blair Stevens Matthew R Stone Julia Tagoe Joseph V Thakuria Bregje W van Bon Jiddeke van de Kamp Ineke van Der Burgt Ton van Essen Conny M van Ravenswaaij-Arts Markus J van Roosmalen Sarah Vergult Catharina M L Volker-Touw Dorothy P Warburton Matthew J Waterman Susan Wiley Anna Wilson Maria de la Concepcion A Yerena-de Vega Roberto T Zori Brynn Levy Han G Brunner Nicole de Leeuw Wigard P Kloosterman Erik C Thorland Cynthia C Morton James F Gusella Michael E Talkowski

Nat Genet 2017 01 14;49(1):36-45. Epub 2016 Nov 14.

Molecular Neurogenetics Unit, Center for Human Genetic Research, Department of Neurology, Massachusetts General Hospital, Boston, Massachusetts, USA.

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http://dx.doi.org/10.1038/ng.3720DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5307971PMC
January 2017

Molecular Cytogenetic Analysis of JAZF1, PHF1, and YWHAE in Endometrial Stromal Tumors: Discovery of Genetic Complexity by Fluorescence in Situ Hybridization.

J Mol Diagn 2016 07 4;18(4):516-26. Epub 2016 May 4.

Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota.

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http://dx.doi.org/10.1016/j.jmoldx.2016.02.001DOI Listing
July 2016

Analysis of MDM2 Amplification in 43 Endometrial Stromal Tumors: A Potential Diagnostic Pitfall.

Int J Gynecol Pathol 2015 Nov;34(6):576-83

Department of Laboratory Medicine and Pathology (J.K.S., A.P.S., P.T.G., J.C.H., G.L.K.), Mayo Clinic, Rochester, Minnesota Department of Pathology (P.D.C., M.R.N.), Division of Women's and Perinatal Pathology, Brigham and Women's Hospital, Boston, Massachusetts.

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https://insights.ovid.com/crossref?an=00004347-201511000-000
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http://dx.doi.org/10.1097/PGP.0000000000000187DOI Listing
November 2015

Paired-Duplication Signatures Mark Cryptic Inversions and Other Complex Structural Variation.

Am J Hum Genet 2015 Jul 18;97(1):170-6. Epub 2015 Jun 18.

Molecular Neurogenetics Unit and Psychiatric and Neurodevelopmental Genetics Unit, Center for Human Genetic Research, Massachusetts General Hospital, Boston, MA 02114, USA; Department of Neurology, Harvard Medical School, Boston, MA 02114, USA; Program in Medical and Population Genetics and Genomics Platform, Broad Institute of Harvard and MIT, Cambridge, MA 02141, USA. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2015.05.012DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4571023PMC
July 2015

The phenotype spectrum of X-linked ichthyosis identified by chromosomal microarray.

J Am Acad Dermatol 2015 Apr 7;72(4):617-27. Epub 2015 Feb 7.

Department of Medical Genetics, Mayo Clinic, Rochester, Minnesota; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota; Department of Pathology and Laboratory Medicine, Cedars-Sinai Medical Center, Los Angeles, California.

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http://dx.doi.org/10.1016/j.jaad.2014.12.020DOI Listing
April 2015

High-grade endometrial stromal sarcomas: a clinicopathologic study of a group of tumors with heterogenous morphologic and genetic features.

Am J Surg Pathol 2014 Sep;38(9):1161-72

*Department of Laboratory Medicine and Pathology, Division of Anatomic Pathology †Department of Laboratory Medicine and Pathology, Division of Laboratory Genetics, Mayo Clinic, Rochester, MN.

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http://dx.doi.org/10.1097/PAS.0000000000000256DOI Listing
September 2014

Uterine cellular leiomyomata with chromosome 1p deletions represent a distinct entity.

Am J Obstet Gynecol 2014 Jun 8;210(6):572.e1-7. Epub 2014 Jan 8.

Department of Obstetrics and Gynecology and Surgery, Mayo Clinic, Rochester, MN.

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http://dx.doi.org/10.1016/j.ajog.2014.01.011DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4040311PMC
June 2014

Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes.

Hum Mol Genet 2014 May 30;23(10):2752-68. Epub 2013 Dec 30.

The Centre for Applied Genomics.

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http://dx.doi.org/10.1093/hmg/ddt669DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3990173PMC
May 2014

Reciprocal deletion and duplication at 2q23.1 indicates a role for MBD5 in autism spectrum disorder.

Eur J Hum Genet 2014 Jan 1;22(1):57-63. Epub 2013 May 1.

1] Department of Human and Molecular Genetics, Virginia Commonwealth University School of Medicine, Richmond, VA, USA [2] Department of Pediatrics, Virginia Commonwealth University School of Medicine, Richmond, VA, USA [3] Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.

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http://dx.doi.org/10.1038/ejhg.2013.67DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3865402PMC
January 2014

ALK alterations in adult renal cell carcinoma: frequency, clinicopathologic features and outcome in a large series of consecutively treated patients.

Mod Pathol 2012 Nov 29;25(11):1516-25. Epub 2012 Jun 29.

Department of Laboratory Medicine & Pathology, Mayo Clinic, Rochester, MN 55905, USA.

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http://dx.doi.org/10.1038/modpathol.2012.107DOI Listing
November 2012

A cytogenetic analysis of 2 cases of phosphaturic mesenchymal tumor of mixed connective tissue type.

Hum Pathol 2012 Aug 11;43(8):1334-8. Epub 2012 Apr 11.

Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN 55905, USA.

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http://dx.doi.org/10.1016/j.humpath.2011.11.020DOI Listing
August 2012

Array CGH on unstimulated blood does not detect all cases of Pallister-Killian syndrome: a skin biopsy should remain the diagnostic gold standard.

Am J Med Genet A 2012 Mar 7;158A(3):669-73. Epub 2012 Feb 7.

Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota 55905, USA.

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http://dx.doi.org/10.1002/ajmg.a.35209DOI Listing
March 2012

In-frame multi-exon deletion of SMC1A in a severely affected female with Cornelia de Lange Syndrome.

Am J Med Genet A 2012 Jan 21;158A(1):193-8. Epub 2011 Nov 21.

Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.

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http://dx.doi.org/10.1002/ajmg.a.34360DOI Listing
January 2012

Uterine leiomyomata and decreased height: a common HMGA2 predisposition allele.

Hum Genet 2009 Apr 9;125(3):257-63. Epub 2009 Jan 9.

Department of Obstetrics, Gynecology and Reproductive Biology, Brigham and Women's Hospital, Boston, MA 02115, USA.

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http://dx.doi.org/10.1007/s00439-008-0621-6DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2839499PMC
April 2009

Molecular and cytogenetic characterization of plexiform leiomyomata provide further evidence for genetic heterogeneity underlying uterine fibroids.

Am J Pathol 2008 May 10;172(5):1403-10. Epub 2008 Apr 10.

Brigham and Women's Hospital, Department of Obstetrics and Gynecology and Reproductive Biology, 77 Avenue Louis Pasteur, Boston, MA 02115, USA.

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http://dx.doi.org/10.2353/ajpath.2008.071102DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2329848PMC
May 2008

Genetic heterogeneity among uterine leiomyomata: insights into malignant progression.

Hum Mol Genet 2007 Apr;16 Spec No 1:R7-13

Department of Obstetrics, Gynecology and Reproductive Biology, Harvard Medical School, Brigham and Women's Hospital, Boston, MA 02115, USA.

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http://dx.doi.org/10.1093/hmg/ddm043DOI Listing
April 2007

Lysophosphatidic acid stimulates PC-3 prostate cancer cell Matrigel invasion through activation of RhoA and NF-kappaB activity.

Mol Carcinog 2006 Jul;45(7):518-29

Department of Pathology, Northwestern University, Feinberg School of Medicine, Chicago, Illinois 60611, USA.

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http://doi.wiley.com/10.1002/mc.20183
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http://dx.doi.org/10.1002/mc.20183DOI Listing
July 2006

Requirement of RhoA activity for increased nuclear factor kappaB activity and PC-3 human prostate cancer cell invasion.

Cancer Res 2003 Mar;63(6):1359-64

Department of Pathology, Northwestern University, The Feinberg School of Medicine, Chicago, Illinois 60611, USA.

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March 2003