Jamie K Teer

Jamie K Teer

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Jamie K Teer

Jamie K Teer

Publications by authors named "Jamie K Teer"

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Geographic variation in molecular subtype for gastric adenocarcinoma.

Gut 2019 07 29;68(7):1340-1341. Epub 2018 Jun 29.

Hunan Key Laboratory of Pharmacogenetics, Department of Clinical Pharmacology, Institute of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, Hunan, China.

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http://dx.doi.org/10.1136/gutjnl-2018-316605DOI Listing
July 2019

Repurposing EGFR Inhibitor Utility in Colorectal Cancer in Mutant and Subpopulations.

Cancer Epidemiol Biomarkers Prev 2019 Jul 23;28(7):1141-1152. Epub 2019 Apr 23.

Gibbs Cancer Center & Research Institute, Spartanburg, South Carolina.

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http://dx.doi.org/10.1158/1055-9965.EPI-18-1383DOI Listing
July 2019

An Interactive Resource to Probe Genetic Diversity and Estimated Ancestry in Cancer Cell Lines.

Cancer Res 2019 Apr 20;79(7):1263-1273. Epub 2019 Mar 20.

Department of Biostatistics and Bioinformatics, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.

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http://dx.doi.org/10.1158/0008-5472.CAN-18-2747DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6445675PMC
April 2019

Genome-scale analysis identifies SERPINE1 and SPARC as diagnostic and prognostic biomarkers in gastric cancer.

Onco Targets Ther 2018 15;11:6969-6980. Epub 2018 Oct 15.

Hunan Key Laboratory of Pharmacogenetics, Department of Clinical Pharmacology, Institute of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, Hunan, China,

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http://dx.doi.org/10.2147/OTT.S173934DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6199229PMC
October 2018

A Transcriptome-Wide Association Study Among 97,898 Women to Identify Candidate Susceptibility Genes for Epithelial Ovarian Cancer Risk.

Authors:
Yingchang Lu Alicia Beeghly-Fadiel Lang Wu Xingyi Guo Bingshan Li Joellen M Schildkraut Hae Kyung Im Yian A Chen Jennifer B Permuth Brett M Reid Jamie K Teer Kirsten B Moysich Irene L Andrulis Hoda Anton-Culver Banu K Arun Elisa V Bandera Rosa B Barkardottir Daniel R Barnes Javier Benitez Line Bjorge James Brenton Ralf Butzow Trinidad Caldes Maria A Caligo Ian Campbell Jenny Chang-Claude Kathleen B M Claes Fergus J Couch Daniel W Cramer Mary B Daly Anna deFazio Joe Dennis Orland Diez Susan M Domchek Thilo Dörk Douglas F Easton Diana M Eccles Peter A Fasching Renée T Fortner George Fountzilas Eitan Friedman Patricia A Ganz Judy Garber Graham G Giles Andrew K Godwin David E Goldgar Marc T Goodman Mark H Greene Jacek Gronwald Ute Hamann Florian Heitz Michelle A T Hildebrandt Claus K Høgdall Antoinette Hollestelle Peter J Hulick David G Huntsman Evgeny N Imyanitov Claudine Isaacs Anna Jakubowska Paul James Beth Y Karlan Linda E Kelemen Lambertus A Kiemeney Susanne K Kjaer Ava Kwong Nhu D Le Goska Leslie Fabienne Lesueur Douglas A Levine Amalia Mattiello Taymaa May Lesley McGuffog Iain A McNeish Melissa A Merritt Francesmary Modugno Marco Montagna Susan L Neuhausen Heli Nevanlinna Finn C Nielsen Liene Nikitina-Zake Robert L Nussbaum Kenneth Offit Edith Olah Olufunmilayo I Olopade Sara H Olson Håkan Olsson Ana Osorio Sue K Park Michael T Parsons Petra H M Peeters Tanja Pejovic Paolo Peterlongo Catherine M Phelan Miquel Angel Pujana Susan J Ramus Gad Rennert Harvey Risch Gustavo C Rodriguez Cristina Rodríguez-Antona Isabelle Romieu Matti A Rookus Mary Anne Rossing Iwona K Rzepecka Dale P Sandler Rita K Schmutzler Veronica W Setiawan Priyanka Sharma Weiva Sieh Jacques Simard Christian F Singer Honglin Song Melissa C Southey Amanda B Spurdle Rebecca Sutphen Anthony J Swerdlow Manuel R Teixeira Soo H Teo Mads Thomassen Marc Tischkowitz Amanda E Toland Antonia Trichopoulou Nadine Tung Shelley S Tworoger Elizabeth J van Rensburg Adriaan Vanderstichele Ana Vega Digna Velez Edwards Penelope M Webb Jeffrey N Weitzel Nicolas Wentzensen Emily White Alicja Wolk Anna H Wu Drakoulis Yannoukakos Kristin K Zorn Simon A Gayther Antonis C Antoniou Andrew Berchuck Ellen L Goode Georgia Chenevix-Trench Thomas A Sellers Paul D P Pharoah Wei Zheng Jirong Long

Cancer Res 2018 09 27;78(18):5419-5430. Epub 2018 Jul 27.

Division of Epidemiology, Department of Medicine, Vanderbilt Epidemiology Center, Vanderbilt-Ingram Cancer Center, Vanderbilt University School of Medicine, Nashville, Tennessee.

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http://dx.doi.org/10.1158/0008-5472.CAN-18-0951DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6139053PMC
September 2018

Genomic analysis of a case of agminated Spitz nevi and congenital-pattern nevi arising in extensive nevus spilus.

J Cutan Pathol 2018 Feb 17;45(2):180-183. Epub 2017 Dec 17.

Department of Anatomic Pathology, Moffitt Cancer Center, Tampa, Florida.

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http://dx.doi.org/10.1111/cup.13082DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5768454PMC
February 2018

The genomic landscape of malignant peripheral nerve sheath tumors: diverse drivers of Ras pathway activation.

Sci Rep 2017 11 8;7(1):14992. Epub 2017 Nov 8.

Sarcoma Department, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.

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http://www.nature.com/articles/s41598-017-15183-1
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http://dx.doi.org/10.1038/s41598-017-15183-1DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5678116PMC
November 2017

Evaluating somatic tumor mutation detection without matched normal samples.

Hum Genomics 2017 09 4;11(1):22. Epub 2017 Sep 4.

Department of Biostatistics and Bioinformatics, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, 33612, USA.

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http://dx.doi.org/10.1186/s40246-017-0118-2DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5584341PMC
September 2017

Mutational heterogeneity in non-serous ovarian cancers.

Sci Rep 2017 08 29;7(1):9728. Epub 2017 Aug 29.

Cancer Epidemiology Program, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, 33612, USA.

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http://dx.doi.org/10.1038/s41598-017-10432-9DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5574976PMC
August 2017

Discordance of Somatic Mutations Between Asian and Caucasian Patient Populations with Gastric Cancer.

Mol Diagn Ther 2017 04;21(2):179-185

Institute for Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, China.

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http://dx.doi.org/10.1007/s40291-016-0250-zDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5357153PMC
April 2017

Key Lessons Learned from Moffitt's Molecular Tumor Board: The Clinical Genomics Action Committee Experience.

Oncologist 2017 02 8;22(2):144-151. Epub 2017 Feb 8.

DeBartolo Family Personalized Medicine Institute, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, USA.

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http://dx.doi.org/10.1634/theoncologist.2016-0195DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5330702PMC
February 2017

Increased incidence of FBXW7 and POLE proofreading domain mutations in young adult colorectal cancers.

Cancer 2016 09 31;122(18):2828-35. Epub 2016 May 31.

Department of Surgery, University of Tennessee Health Science Center, Memphis, Tennessee.

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http://dx.doi.org/10.1002/cncr.30082DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5014625PMC
September 2016

Genetic Investigation of Uterine Carcinosarcoma: Case Report and Cohort Analysis.

Cancer Control 2016 Jan;23(1):61-6

Department of Thoracic Oncology, Moffitt Cancer Center, Tampa, FL 33612, USA.

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http://journals.sagepub.com/doi/10.1177/107327481602300111
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http://dx.doi.org/10.1177/107327481602300111DOI Listing
January 2016

Overexpression of major CDKN3 transcripts is associated with poor survival in lung adenocarcinoma.

Br J Cancer 2015 Dec 10;113(12):1735-43. Epub 2015 Nov 10.

Department of Molecular Oncology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL 33612, USA.

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http://dx.doi.org/10.1038/bjc.2015.378DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4701993PMC
December 2015

Adaptive responses to dasatinib-treated lung squamous cell cancer cells harboring DDR2 mutations.

Cancer Res 2014 Dec 27;74(24):7217-7228. Epub 2014 Oct 27.

Department of Thoracic Oncology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL 33612.

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http://dx.doi.org/10.1158/0008-5472.CAN-14-0505DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4326029PMC
December 2014

An improved understanding of cancer genomics through massively parallel sequencing.

Authors:
Jamie K Teer

Transl Cancer Res 2014 Jun;3(3):243-259

, H. Lee Moffitt Cancer Center and Research Institute, 12902 Magnolia Dr., Tampa, FL 33612, Tel: 813-745-2650.

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http://dx.doi.org/10.3978/j.issn.2218-676X.2014.05.05DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4486294PMC
June 2014

Using exome data to identify malignant hyperthermia susceptibility mutations.

Anesthesiology 2013 Nov;119(5):1043-53

* Research Associate, † Clinical Specialty Consultant, ‡ Staff Scientist, ‡‡ Branch Chief, Genetic Disease Research Branch, †† Director, National Institutes of Health Intramural Sequencing Center, National Human Genome Research Institute (NHGRI), National Institutes of Health, Bethesda, Maryland. # Research Associate, ** Professor of Human Molecular Genetics, Institute of Medical Genetics, School of Medicine, Cardiff University, Heath Park, Cardiff, United Kingdom. § Postdoctoral Fellow, Genome Technology Branch, National Human Genome Research Institute, National Institutes of Health. Current position: Assistant Member, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida. ‖ Members of the National Institutes of Health Intramural Sequencing Center group are listed in the appendix.

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http://dx.doi.org/10.1097/ALN.0b013e3182a8a8e7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4077354PMC
November 2013

JAK1 truncating mutations in gynecologic cancer define new role of cancer-associated protein tyrosine kinase aberrations.

Sci Rep 2013 Oct 24;3:3042. Epub 2013 Oct 24.

Department of Molecular Oncology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, USA.

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http://dx.doi.org/10.1038/srep03042DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3807107PMC
October 2013

Interpreting secondary cardiac disease variants in an exome cohort.

Circ Cardiovasc Genet 2013 Aug 16;6(4):337-46. Epub 2013 Jul 16.

Genetic Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.1161/CIRCGENETICS.113.000039DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3887521PMC
August 2013

Comparative exome sequencing of metastatic lesions provides insights into the mutational progression of melanoma.

BMC Genomics 2012 Sep 24;13:505. Epub 2012 Sep 24.

The Cancer Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.1186/1471-2164-13-505DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3500261PMC
September 2012

Secondary variants in individuals undergoing exome sequencing: screening of 572 individuals identifies high-penetrance mutations in cancer-susceptibility genes.

Am J Hum Genet 2012 Jul 14;91(1):97-108. Epub 2012 Jun 14.

Genetic Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.1016/j.ajhg.2012.05.021DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3397257PMC
July 2012

Incidental medical information in whole-exome sequencing.

Pediatrics 2012 Jun 14;129(6):e1605-11. Epub 2012 May 14.

Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland 20892, USA.

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http://dx.doi.org/10.1542/peds.2011-0080DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3362899PMC
June 2012

VarSifter: visualizing and analyzing exome-scale sequence variation data on a desktop computer.

Bioinformatics 2012 Feb 30;28(4):599-600. Epub 2011 Dec 30.

National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.1093/bioinformatics/btr711DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3278764PMC
February 2012

The phenotype of a germline mutation in PIGA: the gene somatically mutated in paroxysmal nocturnal hemoglobinuria.

Am J Hum Genet 2012 Feb 2;90(2):295-300. Epub 2012 Feb 2.

Genetic Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.

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http://dx.doi.org/10.1016/j.ajhg.2011.11.031DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3276655PMC
February 2012

Exome sequencing identifies GRIN2A as frequently mutated in melanoma.

Nat Genet 2011 May 15;43(5):442-6. Epub 2011 Apr 15.

The Cancer Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.

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http://dx.doi.org/10.1038/ng.810DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3161250PMC
May 2011

Exome sequencing: the sweet spot before whole genomes.

Hum Mol Genet 2010 Oct 12;19(R2):R145-51. Epub 2010 Aug 12.

Genetic Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, 5625 Fishers Lane, Bethesda, MD 20892, USA.

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https://academic.oup.com/hmg/article-lookup/doi/10.1093/hmg/
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http://dx.doi.org/10.1093/hmg/ddq333DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2953745PMC
October 2010

Human Cdt1 lacking the evolutionarily conserved region that interacts with MCM2-7 is capable of inducing re-replication.

J Biol Chem 2008 Mar 8;283(11):6817-25. Epub 2008 Jan 8.

Biological and Biomedical Sciences Program, Harvard Medical School, Boston, Massachusetts 02115, USA.

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http://www.jbc.org/lookup/doi/10.1074/jbc.M708767200
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http://dx.doi.org/10.1074/jbc.M708767200DOI Listing
March 2008

Regulation of S phase.

Results Probl Cell Differ 2006 ;42:31-63

Biological and Biomedical Sciences Program, Harvard Medical School, Boston, MA 02115, USA.

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September 2006

Acute reduction of an origin recognition complex (ORC) subunit in human cells reveals a requirement of ORC for Cdk2 activation.

J Biol Chem 2005 Jul 7;280(30):27624-30. Epub 2005 Jun 7.

Department of Biochemistry and Molecular Genetics, University of Virginia School of Medicine, Charlottesville, Virginia 22908, USA.

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http://www.jbc.org/lookup/doi/10.1074/jbc.M502615200
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http://dx.doi.org/10.1074/jbc.M502615200DOI Listing
July 2005