Publications by authors named "Donald Hadley"

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An exploration of knowledge, risk perceptions, and communication in a family with multiple genetic risks for Parkinson's disease.
Emily C Daykin, Chelsie N Poffenberger, Jenny Do, Emory Ryan, Nahid Tayebi, Donald W Hadley

J Genet Couns· June 2023

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The structure of emotional support networks in families affected by Lynch syndrome.
Christopher Steven Marcum, Dawn Lea, Dina Eliezer, Donald W Hadley, Laura M Koehly

Netw Sci (Camb Univ Press)· December 2020

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Uptake and predictors of colonoscopy use in family members not participating in cascade genetic testing for Lynch syndrome.
Donald W Hadley, Dina Eliezer, Yonit Addissie, Andrea Goergen, Sato Ashida

Sci Rep· September 2020

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A novel frameshift mutation in SOX10 causes Waardenburg syndrome with peripheral demyelinating neuropathy, visual impairment and the absence of Hirschsprung disease.
Elizabeth A Burke, Kyle E Reichard, Lynne A Wolfe, Brian P Brooks, John J DiGiovanna, Donald W Hadley

Am J Med Genet A· May 2020

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The first pancreatic neuroendocrine tumor in Li-Fraumeni syndrome: a case report.
John G Aversa, Francine Blumental De Abreu, Sho Yano, Liqiang Xi, Donald W Hadley

BMC Cancer· March 2020

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An International Summit in Human Genetics and Genomics: Empowering clinical practice and research in developing countries.
Manjit Kaur, Donald W Hadley, Maximilian Muenke, P Suzanne Hart

Mol Genet Genomic Med· January 2019

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Challenging issues arising in counseling families experiencing holoprosencephaly.
Donald W Hadley, Paul Kruszka, Maximilian Muenke

Am J Med Genet C Semin Med Genet· June 2018

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In-depth investigations of adolescents and adults with holoprosencephaly identify unique characteristics.
Karin Weiss, Paul Kruszka, Maria J Guillen Sacoto, Yonit A Addissie, Donald W Hadley

Genet Med· January 2018

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SIX3 deletions and incomplete penetrance in families affected by holoprosencephaly.
Bethany Stokes, Seth I Berger, Beth A Hall, Karin Weiss, Ariel F Martinez, Donald W Hadley

Congenit Anom (Kyoto)· January 2018

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Heart disease risk information, encouragement, and physical activity among Mexican-origin couples: Self- or spouse-driven change?
Kaley F Skapinsky, Susan Persky, Megan Lewis, Andrea Goergen, Sato Ashida, Donald Hadley

Transl Behav Med· January 2018

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Medical genetics and genomic medicine in the United States. Part 2: Reproductive genetics, newborn screening, genetic counseling, training, and registries.
Debra S Regier, Carlos R Ferreira, Suzanne Hart, Donald W Hadley, Maximilian Muenke

Mol Genet Genomic Med· November 2017

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Medical genetics and genomic medicine in the United States of America. Part 1: history, demographics, legislation, and burden of disease.
Carlos R Ferreira, Debra S Regier, Donald W Hadley, P Suzanne Hart, Maximilian Muenke

Mol Genet Genomic Med· July 2017

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KCNQ1 Gene Variants in Large Asymptomatic Populations: Considerations for Genomic Screening of Military Cohorts.
Paul Kruszka, Karin Weiss, Donald W Hadley

Mil Med· March 2017

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Muenke syndrome: An international multicenter natural history study.
Paul Kruszka, Yonit A Addissie, Colin M P Yarnell, Donald W Hadley, Maria J Guillen Sacoto

Am J Med Genet A· April 2016

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Circulating tumour necrosis factor is highly correlated with brainstem serotonin transporter availability in humans.
Rajeev Krishnadas, Alice Nicol, Jen Sassarini, Navesh Puri, A David Burden, Donald Hadley

Brain Behav Immun· January 2016

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Executive Function and Adaptive Behavior in Muenke Syndrome.
Colin M P Yarnell, Yonit A Addissie, Donald W Hadley, Maria J Guillen Sacoto, Nneamaka B Agochukwu

J Pediatr· August 2015

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Expanding the phenotypic expression of Sonic Hedgehog mutations beyond holoprosencephaly.
Paul Kruszka, Rachel A Hart, Donald W Hadley, Maximilian Muenke, Mutaz B Habal

J Craniofac Surg· January 2015

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Exploring psychological responses to genetic testing for Lynch Syndrome within the family context.
Dina Eliezer, Donald W Hadley, Laura M Koehly

Psychooncology· November 2014

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Analysis of renal anomalies in VACTERL association.
Bridget K Cunningham, Alina Khromykh, Ariel F Martinez, Tyler Carney, Donald W Hadley

Birth Defects Res A Clin Mol Teratol· October 2014

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Pathogenic mutations in GLI2 cause a specific phenotype that is distinct from holoprosencephaly.
Kelly A Bear, Benjamin D Solomon, Sonir Antonini, Ivo J P Arnhold, Marcela M França, Donald W Hadley

J Med Genet· June 2014

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An approach to the identification of anomalies and etiologies in neonates with identified or suspected VACTERL (vertebral defects, anal atresia, tracheo-esophageal fistula with esophageal atresia, cardiac anomalies, renal anomalies, and limb anomalies) association.
Benjamin D Solomon, Linda A Baker, Kelly A Bear, Bridget K Cunningham, Philip F Giampietro, Donald W Hadley

J Pediatr· March 2014

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Analysis of cardiac anomalies in VACTERL association.
Bridget K Cunningham, Donald W Hadley, Hwaida Hannoush, Andrew C Meltzer, Nickie Niforatos

Birth Defects Res A Clin Mol Teratol· December 2013

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The role of religious and existential well-being in families with Lynch syndrome: prevention, family communication, and psychosocial adjustment.
Bronwyn A Morris, Donald W Hadley, Laura M Koehly

J Genet Couns· August 2013

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Clinical and imaging services for TIA and minor stroke: results of two surveys of practice across the UK.
Miriam Brazzelli, Kirsten Shuler, Zahid Quayyum, Donald Hadley, Keith Muir

BMJ Open· August 2013

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Crossed cerebellar diaschisis: insights into oxygen challenge MRI.
Krishna A Dani, Celestine Santosh, David Brennan, Donald M Hadley, Keith W Muir

J Cereb Blood Flow Metab· December 2012

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