Publications by authors named "Donald W Hadley"

48Publications

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

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

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