Publications by authors named "Donald Hadley"

84Publications

Uptake and predictors of colonoscopy use in family members not participating in cascade genetic testing for Lynch syndrome.

Sci Rep 2020 09 29;10(1):15959. Epub 2020 Sep 29.

Social Networks Methods Section, Social and Behavioral Research Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.

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September 2020

The first pancreatic neuroendocrine tumor in Li-Fraumeni syndrome: a case report.

BMC Cancer 2020 Mar 30;20(1):256. Epub 2020 Mar 30.

Surgical Oncology Program, Center for Cancer Research, National Cancer Institute, National Institutes of Health, 10 Center Drive, Building 10, Room 4-5952, Bethesda, MD, 20892, USA.

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March 2020

An International Summit in Human Genetics and Genomics: Empowering clinical practice and research in developing countries.

Mol Genet Genomic Med 2019 01;7(1):e00599

National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland.

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January 2019

Challenging issues arising in counseling families experiencing holoprosencephaly.

Am J Med Genet C Semin Med Genet 2018 06;178(2):238-245

Human Development Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland.

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June 2018

Heart disease risk information, encouragement, and physical activity among Mexican-origin couples: Self- or spouse-driven change?

Transl Behav Med 2018 01;8(1):95-104

Social and Behavioral Research Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.

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January 2018

Medical genetics and genomic medicine in the United States of America. Part 1: history, demographics, legislation, and burden of disease.

Mol Genet Genomic Med 2017 Jul 16;5(4):307-316. Epub 2017 Jul 16.

National Human Genome Research InstituteNational Institutes of HealthBethesdaMaryland.

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July 2017

SIX3 deletions and incomplete penetrance in families affected by holoprosencephaly.

Congenit Anom (Kyoto) 2018 Jan 1;58(1):29-32. Epub 2017 Aug 1.

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

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January 2018

KCNQ1 Gene Variants in Large Asymptomatic Populations: Considerations for Genomic Screening of Military Cohorts.

Mil Med 2017 03;182(3):e1795-e1800

Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, 35 Convent Drive, Room 1B207, Bethesda, MD 20894.

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March 2017

Circulating tumour necrosis factor is highly correlated with brainstem serotonin transporter availability in humans.

Brain Behav Immun 2016 Jan 6;51:29-38. Epub 2015 Aug 6.

Sackler Institute of Psychobiological Research, Institute of Health and Wellbeing, University of Glasgow, United Kingdom. Electronic address:

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January 2016

Executive Function and Adaptive Behavior in Muenke Syndrome.

J Pediatr 2015 Aug 28;167(2):428-34. Epub 2015 May 28.

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

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August 2015

Expanding the phenotypic expression of Sonic Hedgehog mutations beyond holoprosencephaly.

J Craniofac Surg 2015 Jan;26(1):3-5

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

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January 2015

Analysis of renal anomalies in VACTERL association.

Birth Defects Res A Clin Mol Teratol 2014 Oct 5;100(10):801-5. Epub 2014 Sep 5.

Department of Pediatrics, Walter Reed National Military Medical Center-Bethesda, Maryland; Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland.

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October 2014

Exploring psychological responses to genetic testing for Lynch Syndrome within the family context.

Psychooncology 2014 Nov 28;23(11):1292-9. Epub 2014 May 28.

National Human Genome Research Institute, Bethesda, MD, USA.

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November 2014

Analysis of cardiac anomalies in VACTERL association.

Birth Defects Res A Clin Mol Teratol 2013 Dec;97(12):792-7

Department of Pediatrics, Walter Reed National Military Medical Center-Bethesda, Maryland; Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland.

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December 2013

The role of religious and existential well-being in families with Lynch syndrome: prevention, family communication, and psychosocial adjustment.

J Genet Couns 2013 Aug 25;22(4):482-91. Epub 2013 Jan 25.

Social and Behavioral Research Branch, National Human Genome Research Institute, Bethesda, MD, USA.

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August 2013

Crossed cerebellar diaschisis: insights into oxygen challenge MRI.

J Cereb Blood Flow Metab 2012 Dec 10;32(12):2114-7. Epub 2012 Oct 10.

Institute of Neurosciences and Psychology, School of Medicine, University of Glasgow, Glasgow, UK.

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December 2012

Patients within the Broad Holoprosencephaly Spectrum have Distinct and Subtle Ophthalmologic Anomalies: Response to Khan.

Am J Med Genet A 2012 May 7;158A(5):1244-1245. Epub 2012 Feb 7.

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

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May 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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June 2012

Biodistribution and dosimetry of ¹²³I-mZIENT: a novel ligand for imaging serotonin transporters.

Eur J Nucl Med Mol Imaging 2012 May;39(5):786-91

Department of Nuclear Medicine, Southern General Hospital, NHS Greater Glasgow & Clyde, 1345 Govan Rd, Glasgow G51 4TF, UK.

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May 2012

A broad range of ophthalmologic anomalies is part of the holoprosencephaly spectrum.

Am J Med Genet A 2011 Nov 4;155A(11):2713-20. Epub 2011 Oct 4.

Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland 20814, USA.

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November 2011

Willingness of Mexican-American adults to share family health history with healthcare providers.

Am J Prev Med 2011 Jun;40(6):633-6

Social and Behavioral Research Branch, National Human Genome Research Institute/NIH, 31 Center Drive, Bethesda, MD 20892, USA.

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June 2011

Atypical adult medulloblastoma.

Acta Neurochir (Wien) 2011 Jul 9;153(7):1511-7; discussion 1517. Epub 2011 May 9.

Department of Neurosurgery, Institute of Neurological Sciences, Southern General Hospital, Glasgow G51 4TF, UK.

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July 2011

Generation after generation: exploring the psychological impact of providing genetic services through a cascading approach.

Genet Med 2010 Dec;12(12):808-15

Social and Behavioral Research Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland 20892-2073, USA.

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December 2010

Long-term outcomes of adults with features of VACTERL association.

Eur J Med Genet 2011 Jan-Feb;54(1):34-41. Epub 2010 Oct 1.

Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Building 35, Room 1B207, 35 Convent Drive MSC 3717, Bethesda, MD 20892-3717, USA.

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June 2011

T2*-weighted magnetic resonance imaging with hyperoxia in acute ischemic stroke.

Ann Neurol 2010 Jul;68(1):37-47

Division of Clinical Neurosciences, University of Glasgow, Institute of Neurological Sciences, Southern General Hospital, Glasgow, UK.

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July 2010

Randomized, controlled trial of insulin for acute poststroke hyperglycemia.

Ann Neurol 2010 May;67(5):570-8

Division of Clinical Neurosciences, University of Glasgow, Glasgow, Scotland, UK.

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May 2010

Accuracy of Parkinson's disease diagnosis in 610 general practice patients in the West of Scotland.

Mov Disord 2009 Dec;24(16):2379-85

Department of Neurology, Institute of Neurological Sciences, Southern General Hospital, Glasgow, UK.

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December 2009

Communication, encouragement, and cancer screening in families with and without mutations for hereditary nonpolyposis colorectal cancer: a pilot study.

Genet Med 2009 Oct;11(10):728-34

Social and Behavioral Research Branch, National Human Genome Research Institute, National Institutes of Health Bethesda, Maryland, USA.

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October 2009

Colon cancer screening practices and disclosure after receipt of positive or inconclusive genetic test results for hereditary nonpolyposis colorectal cancer.

Cancer 2009 Sep;115(18):4071-9

Social and Behavioral Research Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland 20892-2073, USA.

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September 2009

Localisation of regions of intense pleasure response evoked by soccer goals.

Psychiatry Res 2009 Jan 11;171(1):33-43. Epub 2008 Dec 11.

The Sackler Institute of Psychobiological Research, Institute of Neurological Sciences, Glasgow, G51 4TF, UK.

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January 2009

Perceptions of cancer risks and predictors of colon and endometrial cancer screening in women undergoing genetic testing for Lynch syndrome.

J Clin Oncol 2008 Feb;26(6):948-54

Social & Behavioral Research Branch, National Institutes of Health, 31 Center Drive, MSC 2073, Building 31, Room B1B37F, Bethesda, MD 20892-2073, USA.

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February 2008

Serial postmortem relaxometry in the normal rat brain and following stroke.

J Magn Reson Imaging 2008 Mar;27(3):469-75

Department of Medical Physics and Bioengineering, St James's Hospital, Dublin 8, Ireland.

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March 2008

Magnetic resonance imaging technology in transtibial socket research: a pilot study.

J Rehabil Res Dev 2006 Nov-Dec;43(7):883-90

National Centre for Training and Education in Prosthetics and Orthotics, University of Strathclyde, Glasgow, Scotland G4 0LS.

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March 2008

Two-year follow-up in 150 consecutive cases with normal dopamine transporter imaging.

Nucl Med Commun 2006 Dec;27(12):933-7

Department of Neurology, Institute of Neurological Sciences, Southern General Hospital, Glasgow, UK.

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December 2006

Successful antiparkinsonian medication withdrawal in patients with Parkinsonism and normal FP-CIT SPECT.

Mov Disord 2006 Dec;21(12):2247-50

Department of Neurology, Institute of Neurological Sciences, Southern General Hospital, Glasgow, United Kingdom.

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December 2006

Family history: the three-generation pedigree.

Am Fam Physician 2005 Aug;72(3):441-8

Department of Family Medicine, Uniformed Services University of the Health Sciences, F. Edward Hébert School of Medicine, Bethesda, Maryland, USA.

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August 2005

Measurement of tumor "size" in recurrent malignant glioma: 1D, 2D, or 3D?

AJNR Am J Neuroradiol 2005 Apr;26(4):770-6

Department of Clinical Physics, Institute of Neurological Sciences, Southern General Hospital, Glasgow.

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April 2005

Evaluating the impact of genetic counseling and testing with signal detection methods.

J Genet Couns 2005 Feb;14(1):17-27

Department of Psychiatry and Biobehavioral Sciences, University of California, Los Angeles, California, USA.

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February 2005

BRCA1/2 testing in hereditary breast and ovarian cancer families II: impact on relationships.

Am J Med Genet A 2005 Mar;133A(2):165-9

Medical Genetics Branch, National Human Genome Research Institute/NIH, Bldg. 10, 10 Center Drive, Bethesda, MD 20892, USA.

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March 2005

Genetic testing in Parkinson's disease.

Mov Disord 2005 Jan;20(1):1-10

Social and Behavioral Research Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland 20952, USA.

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January 2005

Are there gender-specific neural substrates of route learning from different perspectives?

Cereb Cortex 2004 Nov 13;14(11):1207-13. Epub 2004 May 13.

Department of Clinical Physics, Institute of Neurological Sciences, Southern General Hospital, Glasgow G51 4TF, UK.

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November 2004

Colon cancer screening practices after genetic counseling and testing for hereditary nonpolyposis colorectal cancer.

J Clin Oncol 2004 Jan;22(1):39-44

Genetic Counseling Research Unit, Medical Genetics Branch, National Human Genome Research Institute/NIH, 10 Center Drive, MSC 1852, Bldg 10/Room 10 C103, Bethesda, MD 20892-1852, USA.

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January 2004

Perceptions of reproductive risk and carrier testing among adolescent sisters of males with chronic granulomatous disease.

Am J Med Genet C Semin Med Genet 2003 May;119C(1):60-9

Division of Cardiology, Johns Hopkins Medical Institutions, Baltimore, Maryland 21287-0409, USA.

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May 2003

The reliability of "Analyze" software in measuring orbital volume utilizing CT-derived data.

J Craniomaxillofac Surg 2003 Apr;31(2):88-91

West of Scotland Regional Maxillofacial Unit, Southern General Hospital, Glasgow, UK.

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April 2003

Genetic counseling and testing in families with hereditary nonpolyposis colorectal cancer.

Arch Intern Med 2003 Mar;163(5):573-82

Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, 10 Center Dr, MSC 1852, Building 10, Room 10C103, Bethesda, MD 20892-1852, USA.

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March 2003

MRI safety review.

Semin Ultrasound CT MR 2002 Oct;23(5):392-401

Institute of Neurological Sciences, Southern General Hospital, Glasgow, Scotland, UK.

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October 2002

The Chiari malformations.

Authors:
Donald M Hadley

J Neurol Neurosurg Psychiatry 2002 Jun;72 Suppl 2:ii38-ii40

Department of Neuroradiology, Institute of Neurological Sciences, Southern General Hospital, Glasgow, UK.

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June 2002

Genetic heterogeneity of syndromic X-linked recessive microphthalmia-anophthalmia: is Lenz microphthalmia a single disorder?

Am J Med Genet 2002 Jul;110(4):308-14

Medical Genetics Branch, NHGRI, National Institutes of Health, Bethesda, Maryland 20892-4472, USA.

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July 2002

Case 47: dural ectasia associated with Marfan syndrome.

Radiology 2002 Jun;223(3):767-71

Section of Human Genetics and Integrative Medicine, National Institute on Aging, National Institutes of Health, Bethesda, MD, USA.

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June 2002

MR findings in intralabyrinthine schwannomas.

Clin Radiol 2002 May;57(5):355-8

Department of Neuro-Otology, Institute of Neurological Sciences, Southern General Hospital, Glasgow, U.K.

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May 2002

SPECT imaging in head injury interpreted with statistical parametric mapping.

J Nucl Med 2002 Apr;43(4):476-83

Department of Psychology, University of Stirling, Stirling, Scotland, United Kingdom.

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April 2002