Felicitas Lacbawan

Felicitas Lacbawan

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Felicitas Lacbawan

Felicitas Lacbawan

Publications by authors named "Felicitas Lacbawan"

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32Publications

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Traceback: A Proposed Framework to Increase Identification and Genetic Counseling of BRCA1 and BRCA2 Mutation Carriers Through Family-Based Outreach.

J Clin Oncol 2017 Jul 11;35(20):2329-2337. Epub 2017 Apr 11.

Goli Samimi, Charlisse F. Caga-anan, Michael Dean, Leah E. Mechanic, Lori M. Minasian, and Mark E. Sherman, National Cancer Institute; Lawrence C. Brody, National Human Genome Research Institute, Bethesda, MD; Marcus Q. Bernardini, Stephanie Lheureux, Patricia A. Shaw, Princess Margaret Cancer Centre, Toronto, Ontario; Janice S. Kwon, University of British Columbia; British Columbia Cancer Agency, Vancouver, British Columbia, Canada; Ian G. Campbell, Paul A. James, Masataka Takenaka, and David D. Bowtell, Peter MacCallum Cancer Centre; David D. Bowtell, University of Melbourne, Melbourne, Victoria; Georgia Chenevix-Trench, QIMR Berghofer Medical Research Institute, Brisbane, Queensland; Michael Friedlander, The Prince of Wales Hospital; Susan J. Ramus, University of New South Wales; Susan J. Ramus and David D. Bowtell, Garvan Institute of Medical Research, Sydney, New South Wales, Australia; Fergus J. Couch, Mayo Clinic, Rochester, MN; Joanne A. de Hullu and Marline G. Harmsen, Radboud University Medical Center, Nijmegen, the Netherlands; Susan M. Domchek and Ronny Drapkin, University of Pennsylvania, Philadelphia; Phuong L. Mai, Magee-Women's Hospital of the University of Pittsburgh Medical Center, Pittsburgh, PA; Heather Spencer Feigelson, Kaiser Permanente Institute for Health Research, Denver, CO; Mia M. Gaudet, American Cancer Society, Atlanta, GA; Karen Hurley and Mark E. Robson, Memorial Sloan Kettering Cancer Center; Mark E. Robson, Weill Cornell Medical College, New York, NY; Felicitas Lacbawan, Quest Diagnostics Nichols Institute, San Juan Capistrano; Thomas P. Slavin, City of Hope, Duarte, CA; Evan R. Myers, Duke University Medical Center, Durham, NC; Lisa F. Rezende, FORCE: Facing Our Risk of Cancer Empowered, Tampa; Mark E. Sherman, Mayo Clinic, Jacksonville, FL; and Elizabeth M. Swisher, University of Washington Medical Center, Seattle, WA.

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http://dx.doi.org/10.1200/JCO.2016.70.3439DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5501360PMC
July 2017

A Case in Point: When Extended Genotyping of α-1 Antitrypsin (SERPINA1) is Indicated.

Appl Immunohistochem Mol Morphol 2015 Nov-Dec;23(10):744

*Robert J. Tomsich Pathology and Laboratory Medicine Institute ‡Education and Respiratory Institutes, Cleveland Clinic †Case Western Reserve University School of Medicine Cleveland, OH.

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http://dx.doi.org/10.1097/PAI.0000000000000101DOI Listing
August 2016

Adult autoinflammatory disease frequency and our diagnostic experience in an adult autoinflammatory clinic.

Semin Arthritis Rheum 2016 Apr 29;45(5):633-7. Epub 2015 Oct 29.

Biostatistics, Cleveland Clinic, Cleveland, OH.

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http://dx.doi.org/10.1016/j.semarthrit.2015.10.012DOI Listing
April 2016

NOD2-associated autoinflammatory disease: a large cohort study.

Rheumatology (Oxford) 2015 Oct 11;54(10):1904-12. Epub 2015 Jun 11.

Department of Gastroenterology/Hepatology, Cleveland Clinic, Cleveland, OH, USA.

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https://academic.oup.com/rheumatology/article-lookup/doi/10.
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http://dx.doi.org/10.1093/rheumatology/kev207DOI Listing
October 2015

Improving Molecular Genetic Test Utilization through Order Restriction, Test Review, and Guidance.

J Mol Diagn 2015 May 27;17(3):225-9. Epub 2015 Feb 27.

Department of Laboratory Medicine, Robert J. Tomsich Pathology and Laboratory Medicine Institute, Cleveland Clinic, Cleveland, Ohio; Section of Molecular Pathology, Robert J. Tomsich Pathology and Laboratory Medicine Institute, Cleveland Clinic, Cleveland, Ohio. Electronic address:

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http://dx.doi.org/10.1016/j.jmoldx.2015.01.003DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5707195PMC
May 2015

Molecular testing for the BRCA1 and BRCA2 Ashkenazi Jewish founder mutations: a report on the College of American Pathologists proficiency testing surveys.

Genet Med 2015 Jan 19;17(1):58-62. Epub 2014 Jun 19.

Department of Molecular Pathology, Robert J Tomsich Pathology and Laboratory Medicine Institute, Cleveland Clinic, Cleveland, Ohio, USA.

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http://dx.doi.org/10.1038/gim.2014.77DOI Listing
January 2015

Cleveland Clinic's Center for personalized healthcare: setting the stage for value-based care.

Pharmacogenomics 2014 Apr;15(5):587-91

Center for Personalized Healthcare, Internal Medicine, Cleveland Clinic, 9500 Euclid Ave, NE50, Cleveland, OH 44195, USA.

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http://dx.doi.org/10.2217/pgs.14.31DOI Listing
April 2014

Three-year experience of a CAP/ACMG methods-based external proficiency testing program for laboratories offering DNA sequencing for rare inherited disorders.

Genet Med 2014 Jan 23;16(1):25-32. Epub 2013 May 23.

Detroit Medical Center and Departments of Pathology and Pediatrics and Center for Molecular Medicine and Genetics, Wayne State University, Detroit, Michigan, USA.

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http://dx.doi.org/10.1038/gim.2013.65DOI Listing
January 2014

Verification of performance specifications of a molecular test: cystic fibrosis carrier testing using the Luminex liquid bead array.

Arch Pathol Lab Med 2012 Jan;136(1):14-9

Department of Pathology, State University of New York Downstate Medical Center, Brooklyn, 11203, USA.

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http://www.archivesofpathology.org/doi/abs/10.5858/arpa.2010
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http://dx.doi.org/10.5858/arpa.2010-0536-OADOI Listing
January 2012

Unique phenotype in a patient with CHARGE syndrome.

Int J Pediatr Endocrinol 2011 Oct 13;2011:11. Epub 2011 Oct 13.

State University of New York Downstate Medical Center, Children's Hospital at Downstate, Department of Pediatrics, Division of Pediatric Endocrinology, Brooklyn, NY 11203 USA.

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http://dx.doi.org/10.1186/1687-9856-2011-11DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3216247PMC
October 2011

Holoprosencephaly in a family segregating novel variants in ZIC2 and GLI2.

Am J Med Genet A 2011 Apr 17;155A(4):860-4. Epub 2011 Mar 17.

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

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http://dx.doi.org/10.1002/ajmg.a.33903DOI Listing
April 2011

Truncating loss-of-function mutations of DISP1 contribute to holoprosencephaly-like microform features in humans.

Hum Genet 2009 May 31;125(4):393-400. Epub 2009 Jan 31.

Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, 35 Convent Drive-MSC 3717, Building 35, Bethesda, MD 20892-3717, USA.

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http://dx.doi.org/10.1007/s00439-009-0628-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2774849PMC
May 2009

A novel SIX3 mutation segregates with holoprosencephaly in a large family.

Am J Med Genet A 2009 May;149A(5):919-25

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

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http://dx.doi.org/10.1002/ajmg.a.32813DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2737713PMC
May 2009

Mutations in the human SIX3 gene in holoprosencephaly are loss of function.

Hum Mol Genet 2008 Dec 12;17(24):3919-28. Epub 2008 Sep 12.

1Medical Genetics Branch, National Human Genome Research Institute, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.1093/hmg/ddn294DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2733808PMC
December 2008

Brain-derived neurotrophic factor and obesity in the WAGR syndrome.

N Engl J Med 2008 Aug;359(9):918-27

Unit on Growth and Obesity, Program in Developmental Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892-1103, USA.

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http://dx.doi.org/10.1056/NEJMoa0801119DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2553704PMC
August 2008

Functional analysis of mutations in TGIF associated with holoprosencephaly.

Mol Genet Metab 2007 Jan 7;90(1):97-111. Epub 2006 Sep 7.

Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892-3717, USA.

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http://dx.doi.org/10.1016/j.ymgme.2006.07.011DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1820763PMC
January 2007

A female infant with duplication of chromosome 2q33 to 2q37.3.

Clin Dysmorphol 2003 Oct;12(4):251-6

Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland 20892-4472, USA.

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http://dx.doi.org/10.1097/01.mcd.0000081307.64648.5dDOI Listing
October 2003

Central nervous system embryogenesis and its failures.

Pediatr Dev Pathol 2002 Sep-Oct;5(5):425-47. Epub 2002 Sep 4.

Department of Medical Genetics, Children's National Medical Center, 111 Michigan Avenue NW, Washington, DC 20010, USA.

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http://dx.doi.org/10.1007/s10024-002-0003-3DOI Listing
March 2003

Report of a child with aortic aneurysm, orofacial clefting, hemangioma, upper sternal defect, and marfanoid features: possible PHACE syndrome.

Am J Med Genet 2002 Jul;110(3):283-8

Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland 20892-4472, USA.

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http://dx.doi.org/10.1002/ajmg.10455DOI Listing
July 2002