Publications by authors named "Thomas M Morgan"

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Mouse models of patent ductus arteriosus (PDA) and their relevance for human PDA.
Michael T Yarboro, Srirupa H Gopal, Rachel L Su, Thomas M Morgan, Jeff Reese

Dev Dyn· March 2022

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Liver Transplantation in Children with Urea Cycle Disorders: The Importance of Minimizing Waiting Time.
Ioannis A Ziogas, W Kelly Wu, Lea K Matsuoka, Anita K Pai, Einar T Hafberg, Thomas M Morgan

Liver Transpl· December 2021

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Pathogenic variants in USP7 cause a neurodevelopmental disorder with speech delays, altered behavior, and neurologic anomalies.
Michael D Fountain, David S Oleson, Megan E Rech, Lara Segebrecht, Jill V Hunter, Thomas M Morgan

Genet Med· August 2019

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Genomic Screening: The Mutation and the Mustard Seed.
Thomas M Morgan

J Law Med Ethics· June 2018

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Duplicated Enhancer Region Increases Expression of CTSB and Segregates with Keratolytic Winter Erythema in South African and Norwegian Families.
Thandiswa Ngcungcu, Martin Oti, Jan C Sitek, Bjørn I Haukanes, Bolan Linghu, Thomas M Morgan

Am J Hum Genet· May 2017

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USP7 Acts as a Molecular Rheostat to Promote WASH-Dependent Endosomal Protein Recycling and Is Mutated in a Human Neurodevelopmental Disorder.
Yi-Heng Hao, Michael D Fountain, Klementina Fon Tacer, Fan Xia, Weimin Bi, Thomas M Morgan

Mol Cell· September 2015

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Homozygous loss of DIAPH1 is a novel cause of microcephaly in humans.
A Gulhan Ercan-Sencicek, Samira Jambi, Daniel Franjic, Sayoko Nishimura, Mingfeng Li, Thomas M Morgan

Eur J Hum Genet· February 2015

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Neuropathy target esterase impairments cause Oliver-McFarlane and Laurence-Moon syndromes.
Robert B Hufnagel, Gavin Arno, Nichole D Hein, Joshua Hersheson, Megana Prasad, Thomas M Morgan

J Med Genet· February 2015

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Renal teratogens.
Thomas M Morgan, Deborah P Jones, William O Cooper

Clin Perinatol· September 2014

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Brief report: Risk of adverse fetal outcomes associated with immunosuppressive medications for chronic immune-mediated diseases in pregnancy.
William O Cooper, T Craig Cheetham, De-Kun Li, C Michael Stein, S Todd Callahan, Thomas M Morgan

Arthritis Rheumatol· February 2014

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TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensities.
Wojciech Wiszniewski, Jill V Hunter, Neil A Hanchard, Jason R Willer, Chad Shaw, Thomas M Morgan

Am J Hum Genet· August 2013

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Correlation of heart rate and cardiac dysfunction in Duchenne muscular dystrophy.
Tamara O Thomas, Thomas M Morgan, William B Burnette, Larry W Markham

Pediatr Cardiol· October 2012

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A balanced t(10;15) translocation in a male patient with developmental language disorder.
A Gulhan Ercan-Sencicek, Nicole R Davis Wright, Stephan J Sanders, Nicole Oakman, Lianna Valdes, Thomas M Morgan

Eur J Med Genet· February 2012

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Better by the pound: the genetics of birth weight.
Jude J McElroy, Louis J Muglia, Thomas M Morgan

J Pediatr· January 2012

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Genetic risk score does not correlate with body mass index of Latina women in a clinical trial.
Kimberly R Coenen, Sharon M Karp, Sabina B Gesell, Mary S Dietrich, Thomas M Morgan

Clin Transl Sci· October 2011

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Investigation of 95 variants identified in a genome-wide study for association with mortality after acute coronary syndrome.
Thomas M Morgan, John A House, Sharon Cresci, Philip Jones, Hooman Allayee

BMC Med Genet· September 2011

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Common polymorphisms in human lysyl oxidase genes are not associated with the adolescent idiopathic scoliosis phenotype.
Tracy L McGregor, Christina A Gurnett, Matthew B Dobbs, Carol A Wise, Jose A Morcuende, Thomas M Morgan

BMC Med Genet· July 2011

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Vaccines are not associated with metabolic events in children with urea cycle disorders.
Thomas M Morgan, Cameron Schlegel, Kathryn M Edwards, Teresa Welch-Burke, Yuwei Zhu

Pediatrics· May 2011

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Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies.
Themistocles L Assimes, Hilma Hólm, Sekar Kathiresan, Muredach P Reilly, Gudmar Thorleifsson, Thomas M Morgan

J Am Coll Cardiol· November 2010

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Variation in recovery: Role of gender on outcomes of young AMI patients (VIRGO) study design.
Judith H Lichtman, Nancy P Lorenze, Gail D'Onofrio, John A Spertus, Stacy T Lindau, Thomas M Morgan

Circ Cardiovasc Qual Outcomes· November 2010

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L-histidine decarboxylase and Tourette's syndrome.
A Gulhan Ercan-Sencicek, Althea A Stillman, Ananda K Ghosh, Kaya Bilguvar, Brian J O'Roak, Thomas M Morgan

N Engl J Med· May 2010

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Consanguinity mapping of congenital heart disease in a South Indian population.
Tracy L McGregor, Amit Misri, Jackie Bartlett, Guilherme Orabona, Richard D Friedman, Thomas M Morgan

PLoS One· April 2010

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National Institutes of Health State-of-the-Science Conference Statement: Family History and Improving Health.
Alfred O Berg, Macaran A Baird, Jeffrey R Botkin, Deborah A Driscoll, Paul A Fishman, Thomas M Morgan

Ann Intern Med· December 2009

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National Institutes of Health State-of-the-Science Conference Statement: Family History and Improving Health: August 24-26, 2009.
Alfred O Berg, Macaran A Baird, Jeffrey R Botkin, Deborah A Driscoll, Paul A Fishman, Thomas M Morgan

NIH Consens State Sci Statements· August 2009

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Investigation of 89 candidate gene variants for effects on all-cause mortality following acute coronary syndrome.
Thomas M Morgan, Lan Xiao, Patrick Lyons, Bethany Kassebaum, Harlan M Krumholz

BMC Med Genet· July 2008

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