Holly Laduca

Holly Laduca

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Holly Laduca

Holly Laduca

Publications by authors named "Holly Laduca"

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Genotype-phenotype associations among panel-based TP53+ subjects.

Genet Med 2019 May 20. Epub 2019 May 20.

Department of Medical Oncology, Division of Population Sciences, Dana-Farber Cancer Institute, Boston, MA, USA.

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http://dx.doi.org/10.1038/s41436-019-0541-yDOI Listing
May 2019

Quality of Clinician-Reported Cancer History When Ordering Genetic Testing.

JCO Clin Cancer Inform 2018 12;2:1-11

Holly LaDuca, Stephanie Gutierrez, Amal Yussuf, Nadia Ho, Jonathan Pepper, Patrick Reineke, Kirsten Blanco, Carolyn Horton, Jill S. Dolinsky, Ambry Genetics, Aliso Viejo; Rachel McFarland, University of California Irvine, Irvine, CA; and Taylor Cain, Sarah Lawrence College, Bronxville, NY.

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http://dx.doi.org/10.1200/CCI.18.00014DOI Listing
December 2018

Differences in TP53 Mutation Carrier Phenotypes Emerge From Panel-Based Testing.

J Natl Cancer Inst 2018 08;110(8):863-870

Division of Population Sciences, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.

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http://dx.doi.org/10.1093/jnci/djy001DOI Listing
August 2018

Advances in the diagnosis of hereditary kidney cancer: Initial results of a multigene panel test.

Cancer 2017 Nov 8;123(22):4363-4371. Epub 2017 Aug 8.

Department of Urology, Yale School of Medicine, New Haven, Connecticut.

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http://dx.doi.org/10.1002/cncr.30893DOI Listing
November 2017

Frequency of mutations in a large series of clinically ascertained ovarian cancer cases tested on multi-gene panels compared to reference controls.

Gynecol Oncol 2017 11 7;147(2):375-380. Epub 2017 Sep 7.

Huntsman Cancer Institute, Department of Dermatology, University of Utah School of Medicine, Salt Lake City, UT, USA. Electronic address:

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http://dx.doi.org/10.1016/j.ygyno.2017.08.030DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5801741PMC
November 2017

Exome sequencing covers >98% of mutations identified on targeted next generation sequencing panels.

PLoS One 2017 2;12(2):e0170843. Epub 2017 Feb 2.

Department of Pediatrics, Division of Genetics and Genomic Medicine, University of California Irvine, Irvine, California, United States of America.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0170843PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5289469PMC
August 2017

Multigene Panel Testing Provides a New Perspective on Lynch Syndrome.

J Clin Oncol 2017 Aug 17;35(22):2568-2575. Epub 2017 May 17.

Carin R. Espenschied, Holly LaDuca, Shuwei Li, Rachel McFarland, and Chia-Ling Gau, Ambry Genetics, Clinical Diagnostics, Aliso Viejo, CA; and Heather Hampel, The Ohio State University Comprehensive Cancer Center, Columbus, OH.

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http://dx.doi.org/10.1200/JCO.2016.71.9260DOI Listing
August 2017

Breast cancer risk is similar for CHEK2 founder and non-founder mutation carriers.

Cancer Genet 2016 09 15;209(9):403-407. Epub 2016 Aug 15.

Department of Clinical Diagnostics, Ambry Genetics, 15 Argonaut, Aliso Viejo, CA 92656, USA; Department of Pediatrics, Division of Genetics and Genomic Medicine, University of California, 2054 E. Hewitt Hall, Irvine, CA 92697, USA.

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http://dx.doi.org/10.1016/j.cancergen.2016.08.005DOI Listing
September 2016

Utilization of multigene panels in hereditary cancer predisposition testing: analysis of more than 2,000 patients.

Genet Med 2014 Nov 24;16(11):830-7. Epub 2014 Apr 24.

1] Department of Clinical Diagnostics, Ambry Genetics, Aliso Viejo, California, USA [2] Division of Genetics and Metabolism, Department of Pediatrics, University of California-Irvine, Irvine, California, USA.

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http://www.ambrygen.com/sites/default/files/LaDuca%20et%20al
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http://www.nature.com/doifinder/10.1038/gim.2014.40
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http://dx.doi.org/10.1038/gim.2014.40DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4225457PMC
November 2014

Sapropterin therapy increases stability of blood phenylalanine levels in patients with BH4-responsive phenylketonuria (PKU).

Mol Genet Metab 2010 Oct-Nov;101(2-3):110-4. Epub 2010 Jun 27.

Department of Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, IL 60614, USA.

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http://dx.doi.org/10.1016/j.ymgme.2010.06.015DOI Listing
January 2011