Publications by authors named "Bruce Korf"

100Publications

mutation featuring Charcot-Marie-Tooth disease, joint hyperlaxity, and scoliosis.

Neurol Genet 2020 Aug 25;6(4):e476. Epub 2020 Jun 25.

Department of Neurology (M.K., M.B., E.E.U.), University of Alabama at Birmingham (UAB); Department of Pediatrics (M.A.L., M.B.), Children's of Alabama | UAB; HudsonAlpha Institute for Biotechnology (K.B., G.S.B., G.M.C.), Huntsville, AL; and Department of Genetics (B.R.K., A.C.E.H.), UAB.

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http://dx.doi.org/10.1212/NXG.0000000000000476DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7413605PMC
August 2020

Mutation-Directed Therapeutics for Neurofibromatosis Type I.

Mol Ther Nucleic Acids 2020 Jun 29;20:739-753. Epub 2020 Apr 29.

Department of Genetics, University of Alabama at Birmingham, Birmingham, AL 35294, USA. Electronic address:

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http://dx.doi.org/10.1016/j.omtn.2020.04.012DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7225739PMC
June 2020

An Update on Neurofibromatosis Type 1-Associated Gliomas.

Cancers (Basel) 2020 Jan 1;12(1). Epub 2020 Jan 1.

Division of Neuro Oncology, Department of Neurology, University of Alabama at Birmingham, 510 20th Street South, Faculty Office Tower suite 1020 Birmingham, Birmingham, AL 35294, USA.

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http://dx.doi.org/10.3390/cancers12010114DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7017116PMC
January 2020

Clinical spectrum of individuals with pathogenic NF1 missense variants affecting p.Met1149, p.Arg1276, and p.Lys1423: genotype-phenotype study in neurofibromatosis type 1.

Authors:
Magdalena Koczkowska Tom Callens Yunjia Chen Alicia Gomes Alesha D Hicks Angela Sharp Eric Johns Kim Armfield Uhas Linlea Armstrong Katherine Armstrong Bosanko Dusica Babovic-Vuksanovic Laura Baker Donald G Basel Mario Bengala James T Bennett Chelsea Chambers Lola K Clarkson Maurizio Clementi Fanny M Cortés Mitch Cunningham M Daniela D'Agostino Martin B Delatycki Maria C Digilio Laura Dosa Silvia Esposito Stephanie Fox Mary-Louise Freckmann Christine Fauth Teresa Giugliano Sandra Giustini Allison Goetsch Yael Goldberg Robert S Greenwood Cristin Griffis Karen W Gripp Punita Gupta Eric Haan Rachel K Hachen Tamara L Haygarth Concepción Hernández-Chico Katelyn Hodge Robert J Hopkin Louanne Hudgins Sandra Janssens Kory Keller Geraldine Kelly-Mancuso Aaina Kochhar Bruce R Korf Andrea M Lewis Jan Liebelt Angie Lichty Robert H Listernick Michael J Lyons Isabelle Maystadt Mayra Martinez Ojeda Carey McDougall Lesley K McGregor Daniela Melis Nancy Mendelsohn Malgorzata J M Nowaczyk June Ortenberg Karin Panzer John G Pappas Mary Ella Pierpont Giulio Piluso Valentina Pinna Eniko K Pivnick Dinel A Pond Cynthia M Powell Caleb Rogers Noa Ruhrman Shahar S Lane Rutledge Veronica Saletti Sarah A Sandaradura Claudia Santoro Ulrich A Schatz Allison Schreiber Daryl A Scott Elizabeth A Sellars Ruth Sheffer Elizabeth Siqveland John M Slopis Rosemarie Smith Alberto Spalice David W Stockton Haley Streff Amy Theos Gail E Tomlinson Grace Tran Pamela L Trapane Eva Trevisson Nicole J Ullrich Jenneke Van den Ende Samantha A Schrier Vergano Stephanie E Wallace Michael F Wangler David D Weaver Kaleb H Yohay Elaine Zackai Jonathan Zonana Vickie Zurcher Kathleen B M Claes Marica Eoli Yolanda Martin Katharina Wimmer Alessandro De Luca Eric Legius Ludwine M Messiaen

Hum Mutat 2020 01 26;41(1):299-315. Epub 2019 Oct 26.

Department of Genetics, University of Alabama at Birmingham, Birmingham, Albama.

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http://dx.doi.org/10.1002/humu.23929DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6973139PMC
January 2020

Child Neurology: Spastic paraparesis and dystonia with a novel mutation.

Neurology 2019 09;93(11):510-514

From the Departments of Neurology (M.D., D.G.S.) and Genetics (L.M., B.R.K.) and Division of Pediatric Neurology, Department of Pediatrics (S.R.), University of Alabama at Birmingham; and HudsonAlpha Institute for Biotechnology (G.M.C., M.D.A.), Huntsville, AL.

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http://www.neurology.org/lookup/doi/10.1212/WNL.000000000000
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http://dx.doi.org/10.1212/WNL.0000000000008089DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6746208PMC
September 2019

Affinity Purification of NF1 Protein-Protein Interactors Identifies Keratins and Neurofibromin Itself as Binding Partners.

Genes (Basel) 2019 08 28;10(9). Epub 2019 Aug 28.

Department of Genetics, The University of Alabama at Birmingham, Birmingham, AL 35294, USA.

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http://dx.doi.org/10.3390/genes10090650DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6770187PMC
August 2019

Return of raw data in genomic testing and research: ownership, partnership, and risk-benefit.

Genet Med 2020 01 17;22(1):12-14. Epub 2019 Jul 17.

HudsonAlpha Institute for Biotechnology, Huntsville, AL, USA.

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http://dx.doi.org/10.1038/s41436-019-0607-xDOI Listing
January 2020

A YWHAZ Variant Associated With Cardiofaciocutaneous Syndrome Activates the RAF-ERK Pathway.

Front Physiol 2019 8;10:388. Epub 2019 Apr 8.

Department of Cell, Developmental and Integrative Biology, The University of Alabama at Birmingham, Birmingham, AL, United States.

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https://www.frontiersin.org/article/10.3389/fphys.2019.00388
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http://dx.doi.org/10.3389/fphys.2019.00388DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6465419PMC
April 2019

Multi-Omics Profiling for NF1 Target Discovery in Neurofibromin (NF1) Deficient Cells.

Proteomics 2019 06;19(11):e1800334

Department of Genetics, University of Alabama at Birmingham, 35294, Birmingham, AL, USA.

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http://dx.doi.org/10.1002/pmic.201800334DOI Listing
June 2019

Response to Hannah-Shmouni and Stratakis.

Genet Med 2019 05 4;21(5):1256. Epub 2018 Oct 4.

Department of Neurology, New York University School of Medicine, New York, NY, USA.

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http://www.nature.com/articles/s41436-018-0313-0
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http://dx.doi.org/10.1038/s41436-018-0313-0DOI Listing
May 2019

Correction: Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype-phenotype correlation.

Genet Med 2019 03;21(3):764-765

Department of Genetics, University of Alabama at Birmingham, Birmingham, AL, USA.

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http://www.nature.com/articles/s41436-018-0326-8
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http://dx.doi.org/10.1038/s41436-018-0326-8DOI Listing
March 2019

Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype-phenotype correlation.

Genet Med 2019 04 7;21(4):867-876. Epub 2018 Sep 7.

Department of Genetics, University of Alabama at Birmingham, Birmingham, Alabama, USA.

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http://dx.doi.org/10.1038/s41436-018-0269-0DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6752285PMC
April 2019

Epilepsy treatment patterns among patients with tuberous sclerosis complex.

J Neurol Sci 2018 08 15;391:104-108. Epub 2018 Jun 15.

Texas Scottish Rite Hospital for Children, 2222 Wellborn St, Dallas, TX 75219, United States.

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https://linkinghub.elsevier.com/retrieve/pii/S0022510X183026
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http://dx.doi.org/10.1016/j.jns.2018.06.011DOI Listing
August 2018

Care of adults with neurofibromatosis type 1: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).

Genet Med 2018 07 26;20(7):671-682. Epub 2018 Apr 26.

Department of Neurology, New York University School of Medicine, New York, New York, USA.

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http://www.nature.com/articles/gim201828
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http://dx.doi.org/10.1038/gim.2018.28DOI Listing
July 2018

Clinical trial design for cutaneous neurofibromas.

Neurology 2018 07;91(2 Suppl 1):S31-S37

From the Department of Genetics (A.C., B.K.), University of Alabama at Birmingham; BioPharm Tech (K.J.), San Mateo, CA; Pediatric Oncology Branch (B.C.W.) and Dermatology Branch, Center for Cancer Research (D.C.P.), National Cancer Institute, NIH, Bethesda; Division of Oncology Products (D.C.) and Division of Dermatology and Dental Products (H.-S.K.), Food and Drug Administration, Silver Spring; and Department of Neurology (J.O.B., S.K.V.), The Neurofibromatosis Therapeutic Acceleration Program, The Johns Hopkins University School of Medicine, Baltimore, MD.

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http://dx.doi.org/10.1212/WNL.0000000000005790DOI Listing
July 2018

Cutaneous neurofibromas: Current clinical and pathologic issues.

Neurology 2018 07;91(2 Suppl 1):S5-S13

From the Departments of Pathology (N.O.) and Dermatology (P.W.), French Referral Center for Neurofibromatoses, Henri-Mondor Hospital, AP-HP, University Paris Est Créteil, France; Department of Neurology (J.O.B., S.K.V.), Johns Hopkins University School of Medicine, The Neurofibromatosis Therapuetic Acceleration Program, Baltimore, MD; University of Alabama at Birmingham (B.K.); Cancer Center and Department of Neurology (S.R.P.) and Department of Pathology, Division of Neuropathology (A.S.-R.), Massachusetts General Hospital, Boston; The Neurofibromatosis Institute (V.M.R.), La Crescenta, CA; Department of Pathology & Anatomical Sciences (D.C.M.), University of Missouri School of Medicine, Columbia; Manchester Centre for Genomic Medicine (S.H.), Central Manchester University Hospitals NHS Foundation Trust, Manchester Academic Health Science Centre, UK; Institute of Biomedicine (J.P.), University of Turku, Finland; Department of Pathology and Laboratory Medicine (A.R.), Jackson Memorial Hospital/University of Miami Miller School of Medicine, FL; Department of Pathology and Laboratory Medicine (S.L.C.), Medical University of South Carolina, Charleston; Clinics and Polyclinics of Neurology (V.M.), University Hospital Hamburg-Eppendorf, Hamburg, Germany; and Division of Cancer and Genetics (M.U.), Institute of Medical Genetics, Cardiff University, UK.

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http://dx.doi.org/10.1212/WNL.0000000000005792DOI Listing
July 2018

Unusual presentation of hereditary leiomyomatosis mimicking neurofibromatosis.

JAAD Case Rep 2018 Jun 30;4(5):440-441. Epub 2018 Apr 30.

Department of Dermatology, University of Alabama at Birmingham, Birmingham, Alabama.

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http://dx.doi.org/10.1016/j.jdcr.2017.12.013DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6031563PMC
June 2018

Neurofibromin (NF1) genetic variant structure-function analyses using a full-length mouse cDNA.

Hum Mutat 2018 06 10;39(6):816-821. Epub 2018 Apr 10.

Department of Genetics, University of Alabama at Birmingham, Birmingham, AL.

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http://dx.doi.org/10.1002/humu.23421DOI Listing
June 2018

Cutaneous neurofibromas in Neurofibromatosis type I: a quantitative natural history study.

Orphanet J Rare Dis 2018 02 7;13(1):31. Epub 2018 Feb 7.

Department of Genetics, University of Alabama, 720 20th Street South, Birmingham, AL, 35294, USA.

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http://dx.doi.org/10.1186/s13023-018-0772-zDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5803843PMC
February 2018

Genotype-Phenotype Correlation in NF1: Evidence for a More Severe Phenotype Associated with Missense Mutations Affecting NF1 Codons 844-848.

Am J Hum Genet 2018 01 28;102(1):69-87. Epub 2017 Dec 28.

Department of Genetics, University of Alabama at Birmingham, Birmingham, AL 35294, USA. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2017.12.001DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5777934PMC
January 2018

Neurofibromatosis Clinical Trial Consortium.

J Child Neurol 2018 Jan;33(1):82-91

5 University of Alabama at Birmingham, Birmingham, AL, USA.

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http://journals.sagepub.com/doi/10.1177/0883073817739196
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http://dx.doi.org/10.1177/0883073817739196DOI Listing
January 2018

Report on the Banbury Summit Meeting on medical genetics training in the genomic era, 23-26 February 2014.

Genet Med 2017 09 27;19(9). Epub 2017 Apr 27.

American College of Medical Genetics and Genomics, Bethesda, Maryland, USA.

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http://dx.doi.org/10.1038/gim.2017.38DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5589971PMC
September 2017

Overview of Genetic Diagnosis in Cancer.

Curr Protoc Hum Genet 2017 04 6;93:10.1.1-10.1.9. Epub 2017 Apr 6.

Department of Genetics, University of Alabama at Birmingham, Birmingham, Alabama.

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http://dx.doi.org/10.1002/cphg.36DOI Listing
April 2017

Neurocutaneous Disorders in Children.

Pediatr Rev 2017 Mar;38(3):119-128

Neurology and Pediatrics, University of Alabama at Birmingham, Birmingham, AL.

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http://dx.doi.org/10.1542/pir.2015-0118DOI Listing
March 2017

Neurofibromatosis type 1.

Nat Rev Dis Primers 2017 Feb 23;3:17004. Epub 2017 Feb 23.

Master of Public Health Program, Brown School, St. Louis, Missouri, USA.

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http://www.nature.com/articles/nrdp20174
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http://dx.doi.org/10.1038/nrdp.2017.4DOI Listing
February 2017

Randomized placebo-controlled study of lovastatin in children with neurofibromatosis type 1.

Neurology 2016 Dec 9;87(24):2575-2584. Epub 2016 Nov 9.

From the Murdoch Children's Research Institute (J.M.P., S.J.C.H., K.N.N.), Royal Children's Hospital; Department of Paediatrics (J.M.P., K.N.N.), Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne; Children's Hospital Education Research Institute (B.B.), Children's Hospital at Westmead; Discipline of Paediatrics and Child Health (B.B.), University of Sydney, Australia; Department of Neurology (N.J.U., C.R.-C.), Boston Children's Hospital, MA; Department of Preventative Medicine (A.C.), School of Public Health (G.C.), Department of Psychology (J.D.A.), and Department of Genetics (B.K.), University of Alabama at Birmingham; Department of Neurology (T.R., S.H.O.), Children's Hospital of Los Angeles, CA; Center for Neuroscience and Behavioral Medicine (K.S.W., G.A.G., R.J.P., M.T.A.), Children's National Health System, Washington, DC; Pediatric Oncology Branch Center for Cancer Research (P.L.W.), National Cancer Institute, Bethesda, MD; Division of Neurology (J.T., S.J.H.), University of Chicago Medicine Comer Children's Hospital, IL; Human Genetics (E.S.) and Division of Neurology (A.W.B.), Cincinnati Children's Hospital Medical Center, OH; Department of Genetics (D.V.), University of Utah, Salt Lake City; Department of Pediatrics (L.K.), University of Texas Southwestern Medical Center, Dallas; Division of Oncology (M.F., C.L.A.), Children's Hospital of Philadelphia, PA; Department of Neurology (D.H.G., J.I.), Washington University School of Medicine in St Louis, MO; Gonda Neuroscience and Genetics Center (A.J.S.), University of California Los Angeles; Primary Children's Hospital (N.L.C.), Salt Lake City, UT; and University of Texas MD Anderson Cancer Center (P.L.S.), Houston.

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http://dx.doi.org/10.1212/WNL.0000000000003435DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5207004PMC
December 2016

Clinical relevance of small copy-number variants in chromosomal microarray clinical testing.

Genet Med 2017 04 15;19(4):377-385. Epub 2016 Sep 15.

Department of Genetics, University of Alabama at Birmingham, Birmingham, Alabama, USA.

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http://dx.doi.org/10.1038/gim.2016.132DOI Listing
April 2017

Current status and recommendations for biomarkers and biobanking in neurofibromatosis.

Neurology 2016 Aug;87(7 Suppl 1):S40-8

From Plymouth University (C.O.H.), Peninsula Schools of Medicine and Dentistry, The Institute of Translational and Stratified Medicine, Plymouth, UK; Department of Neurology (J.O.B.), Johns Hopkins University Medical School, Baltimore, MD; Department of Pediatrics (F.P.N.) and Department of Pediatrics, School of Medicine (K.R., M.F.), Indiana University; Tailored Therapeutics (F.P.N.), Eli Lilly and Company, Indianapolis, IN; Department of Pathology (A.S.-R.), Neuro-oncology (S.R.P.), Massachusetts General Hospital, Boston; Neurologische Klinik (V.M.), Uniklinik Eppendorf, Hamburg; Berlin-Brandenburg Center for Regenerative Therapies (A.K.), Charité Universitätsmedizin Berlin, Germany; Seoul National University (A.K.), College of Veterinary Medicine and Research Institute for Veterinary Science, Republic of Korea; NCI (B.C.W.), Pediatric Oncology Branch, Bethesda, MD; Genomic Medicine (D.G.E.), University of Manchester, UK; National Neurofibromatosis Service (R.F.), Department of Neurology, Guy's and St. Thomas' NHS Foundation Trust, London UK; Department of Pathology and Laboratory Medicine (S.L.C.), Medical University of South Carolina, Charleston; and Heflin Center for Genomic Sciences (B.K.), University of Alabama at Birmingham; Dermatology (P.W.), GHU Henri Mondor, Paris, France; Children's Tumor Foundation (P.K.), New York.

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http://dx.doi.org/10.1212/WNL.0000000000002932DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5578360PMC
August 2016

Overview of Clinical Cytogenetics.

Curr Protoc Hum Genet 2016 Apr 1;89:8.1.1-8.1.13. Epub 2016 Apr 1.

Department of Genetics, University of Alabama at Birmingham, Birmingham, Alabama.

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http://doi.wiley.com/10.1002/0471142905.hg0801s89
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http://dx.doi.org/10.1002/0471142905.hg0801s89DOI Listing
April 2016

High Incidence of Noonan Syndrome Features Including Short Stature and Pulmonic Stenosis in Patients carrying NF1 Missense Mutations Affecting p.Arg1809: Genotype-Phenotype Correlation.

Hum Mutat 2015 Nov 21;36(11):1052-63. Epub 2015 Aug 21.

Department of Genetics, Medical Genomics Laboratory, University of Alabama at Birmingham, Birmingham, Alabama.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5049609PMC
http://dx.doi.org/10.1002/humu.22832DOI Listing
November 2015

How to know when physicians are ready for genomic medicine.

Sci Transl Med 2015 May;7(287):287fs19

Department of Medicine, Harvard Medical School, Boston, MA 02115, USA. Division of Genetics, Department of Medicine, Brigham and Women's Hospital, Boston, MA 02115, USA.

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http://stm.sciencemag.org/lookup/doi/10.1126/scitranslmed.aa
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http://dx.doi.org/10.1126/scitranslmed.aaa2401DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4519005PMC
May 2015

Partial trisomy 21: a fifty-year follow-up visit.

Am J Med Genet A 2015 Jul 5;167(7):1610-3. Epub 2015 May 5.

Department of Genetics at the University of Alabama at Birmingham, Birmingham, Alabama.

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http://dx.doi.org/10.1002/ajmg.a.37031DOI Listing
July 2015

Spinal neurofibromatosis and phenotypic heterogeneity in NF1.

Authors:
Bruce R Korf

Clin Genet 2015 May;87(5):399-400

Department of Genetics, University of Alabama at Birmingham, Birmingham, AL, USA.

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http://dx.doi.org/10.1111/cge.12532DOI Listing
May 2015

Pushing the envelope in genomics education.

Authors:
Bruce R Korf

Genet Med 2015 Nov 19;17(11):857-8. Epub 2015 Mar 19.

Department of Genetics, University of Alabama at Birmingham, Birmingham, Alabama, USA.

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http://dx.doi.org/10.1038/gim.2015.20DOI Listing
November 2015

Clinical response to bevacizumab in schwannomatosis.

Neurology 2014 Nov 22;83(21):1986-7. Epub 2014 Oct 22.

From The Johns Hopkins Hospital (J.O.B., K.C.S., A.L.B., A.J.B.), Baltimore, MD; St. Mary's Hospital (D.G.E.), Manchester, UK; University of Alabama at Birmingham (B.K.); and NYU Langone Medical Center (D.Z., M.A.K.), New York.

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http://dx.doi.org/10.1212/WNL.0000000000000997DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4248457PMC
November 2014

Sirolimus for progressive neurofibromatosis type 1-associated plexiform neurofibromas: a neurofibromatosis Clinical Trials Consortium phase II study.

Neuro Oncol 2015 Apr 14;17(4):596-603. Epub 2014 Oct 14.

Division of Oncology, Cincinnati Children's Hospital Medical Center, Cancer and Blood Diseases Institute, Cincinnati, Ohio (B.W., J.P.); Division of Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio (E.S.); Division of Clinical Pharmacology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio (A.V.); National Cancer Institute, Pediatric Oncology Branch, Bethesda, Maryland (B.C.W, E.D., P.W.); Department of Genetics, University of Alabama at Birmingham, Birmingham, Alabama (B.K.); Department of Preventitive Medicine, University of Alabama at Birmingham, Birmingham, Alabama (A.C.); Department of Neurology, Boston Children's Hospital, Boston, Massachusetts (N.U.); Department of Neurology, Washington University, St. Louis, Missouri (D.H.G.); Children's National Health System, Center for Neuroscience and Behavioral Medicine, Washington, DC (R.J.P.); Division of Oncology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania (M.J.F.); Division of Genetics, Primary Children's Hospital, Salt Lake City, Utah (D.V.); Division of Neurology, The University of Chicago Medicine Comer Children's Hospital, Chicago, Illinois (J.T.).

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http://dx.doi.org/10.1093/neuonc/nou235DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4483073PMC
April 2015

The medical genetics residency milestones.

Authors:
Bruce R Korf

J Grad Med Educ 2014 Mar;6(1 Suppl 1):87-90

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http://dx.doi.org/10.4300/JGME-06-01s1-31DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3966601PMC
March 2014

Phase 2 randomized, flexible crossover, double-blinded, placebo-controlled trial of the farnesyltransferase inhibitor tipifarnib in children and young adults with neurofibromatosis type 1 and progressive plexiform neurofibromas.

Neuro Oncol 2014 May 4;16(5):707-18. Epub 2014 Feb 4.

Pediatric Oncology Branch, National Cancer Institute, Bethesda, Maryland (B.W., E.D., A.G., P.W., S.M., E.F., F.B.); Cancer Therapy Evaluation Program, Investigational Drug Branch, National Cancer Institute, Bethesda, Maryland (J.W.); Biostatistics and Data Management Section, National Cancer Institute, Bethesda, Maryland (S.S.); Diagnostic Radiology Department, National Institutes of Health, Bethesda, Maryland (N.P.); The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania (J.B., E.F., F.B.); Ann and Robert H. Lurie Children's Hospital, Chicago, Illinois (S.G.); Department of Genetics, University of Alabama at Birmingham, South Birmingham, Alabama (B.K.); Expert Image Analysis LC, Potomac, Maryland (J.S.); Dana-Farber/Children's Hospital Cancer Center, Boston, Massachusetts (M.K.); Cincinnati Children's Hospital, Cincinnati, Ohio (J.P.); Children's National Medical Center, Washington, DC (A.K.); US Army Medical Research and Material Command, Fort Detrick, Maryland (W.S.); Children's Hospital of Alabama, Birmingham, Alabama (A.R.).

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http://dx.doi.org/10.1093/neuonc/nou004DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3984559PMC
May 2014

Genomic medicine: educational challenges.

Authors:
Bruce R Korf

Mol Genet Genomic Med 2013 Sep;1(3):119-22

Department of Genetics, University of Alabama at Birmingham Birmingham, Alabama, 35294.

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http://dx.doi.org/10.1002/mgg3.38DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3865578PMC
September 2013

Prenatal whole-genome sequencing--is the quest to know a fetus's future ethical?

N Engl J Med 2014 Jan;370(3):195-7

From Harvard Medical School (I.R.Y.) and the Center for Bioethics, Brigham and Women's Hospital (L.S.L.) - both in Boston; and the Department of Genetics, University of Alabama at Birmingham, Birmingham (B.R.K.).

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http://dx.doi.org/10.1056/NEJMp1215536DOI Listing
January 2014

Genetic literacy and competency.

Pediatrics 2013 Dec;132(Suppl 3):S224-30

FAAP, FACMG, University of Colorado School of Medicine, 13001 East 17th Pl, Rm E1330, Aurora, CO 80045.

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http://dx.doi.org/10.1542/peds.2013-1032GDOI Listing
December 2013

Recommendations for imaging tumor response in neurofibromatosis clinical trials.

Neurology 2013 Nov;81(21 Suppl 1):S33-40

From the Pediatric Oncology Branch (E.D., B.C.W.), National Cancer Institute, Bethesda, MD; Department of Neurology (S.L.A.-H.), The Children's Hospital at Westmead, Sydney, Australia; Department of Medical Genetics (D. B.-V.), Mayo Clinic, Rochester, MN; Neurosurgical Service (F.G.B.), Department of Radiology (G.J.H.), and Department of Neurology and Cancer Center (S.R.P.), Massachusetts General Hospital, Boston, MA; Department of Neuroradiology (S.C.), King's College Hospital, London, UK; Department of Genetic Medicine (D.G.E.), MAHSC, St Mary's Hospital, Manchester, UK; Division of Oncology (M.J.F.) and Department of Radiology (D.J.), The Children's Hospital of Philadelphia; Department of Pediatrics (M.J.F.), The Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA; Department of Neurosurgery (S.G.), Hôpital Beaujon, Clichy, France; Division of Pediatric Hematology/Oncology and NYU Cancer Institute (M.A.K.), NYU Langone Medical Center, New York, NY; Department of Genetics (B.R.K.), University of Alabama at Birmingham, Birmingham, AL; Department of Neurology (V.M.), University Medical Center Hamburg-Eppendorf, Hamburg, Germany; Department of Radiology (T.Y.P.), Boston Children's Hospital, Boston, MA; and Department of Pediatrics (K.R., C.-S.S.), Riley Hospital for Children, Indianapolis, IN.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3908340PMC
November 2013

Integration of genomics into medical practice.

Authors:
Bruce R Korf

Discov Med 2013 Nov;16(89):241-8

Department of Genetics, University of Alabama at Birmingham, 1720 2nd Ave. South, Kaul 230, Birmingham, Alabama 35294, USA.

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November 2013

Response to Townsend et al.

Authors:
Bruce Korf

Genet Med 2013 Sep;15(9):752-3

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September 2013

Neurofibromatosis.

Authors:
Bruce R Korf

Handb Clin Neurol 2013 ;111:333-40

Department of Genetics, University of Alabama at Birmingham, Birmingham, AL, USA. Electronic address:

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April 2014

Genomic privacy in the information age.

Authors:
Bruce R Korf

Clin Chem 2013 Aug 19;59(8):1148-50. Epub 2013 Apr 19.

Department of Genetics, University of Alabama at Birmingham, Birmingham, AL, USA.

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August 2013

New approaches to molecular diagnosis.

JAMA 2013 Apr;309(14):1511-21

Department of Genetics, University of Alabama at Birmingham, 1720 Second Ave S, Kaul 230, Birmingham, AL 35294, USA.

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April 2013

Optimizing biologically targeted clinical trials for neurofibromatosis.

Expert Opin Investig Drugs 2013 Apr 21;22(4):443-62. Epub 2013 Feb 21.

Washington University School of Medicine, Department of Neurology and Washington University Neurofibromatosis Center, 660 South Euclid Avenue, St. Louis, MO 63110, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4009992PMC
April 2013

Genetic and genomic competency in medical practice.

Authors:
Bruce Korf

Virtual Mentor 2012 Aug 1;14(8):622-6. Epub 2012 Aug 1.

Wayne H. and Sara Crews Finley Professor of Medical Genetics, Department of Genetics, and Heflin Center for Genomic Sciences at University of Alabama at Birmingham, USA.

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August 2012

Overview of molecular genetic diagnosis.

Curr Protoc Hum Genet 2013 ;Chapter 9:Unit9.1

University of Alabama at Birmingham, USA.

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June 2013

Biochemical genetics. Introduction.

Curr Protoc Hum Genet 2012 Apr;Chapter 17:Unit 17.0.1

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April 2012

Genetics and genomics education: the next generation.

Authors:
Bruce R Korf

Genet Med 2011 Mar;13(3):201-2

Department of Genetics, University of Alabama at Birmingham, Alabama, USA.

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March 2011

Phenotypic variability among café-au-lait macules in neurofibromatosis type 1.

J Am Acad Dermatol 2010 Sep 3;63(3):440-7. Epub 2010 Jun 3.

Department of Dermatology, University of Alabama at Birmingham, Birmingham, Alabama, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2922676PMC
September 2010

Neurofibromatosis type 1.

J Am Acad Dermatol 2009 Jul;61(1):1-14; quiz 15-6

Departments of Dermatology and Genetics, University of Alabama at Birmingham, 1530 3rd Ave S., Birmingham, AL 35294-0009, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2716546PMC
July 2009

AsktheGeneticist: five years of online experience.

Genet Med 2009 Apr;11(4):294-304

Department of Human Genetics, Emory University, Atlanta, Georgia 30322, USA.

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April 2009

Neurofibromatosis type 1 revisited.

Pediatrics 2009 Jan;123(1):124-33

Department of Pediatrics, Medical University of South Carolina, Charleston, SC 29425, USA.

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January 2009

Statins, bone, and neurofibromatosis type 1.

Authors:
Bruce R Korf

BMC Med 2008 Jul 31;6:22. Epub 2008 Jul 31.

Department of Genetics, University of Alabama at Birmingham, 1530 Third Avenue South, Kaul 230, Birmingham, AL, USA.

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July 2008