Author details

Full Name

Thomas M Morgan

Affiliation

ORCID

Career Start Year

2001

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
34350653	Mouse models of patent ductus arteriosus (PDA) and their relevance for human PDA.	Developmental Dynamics	2022
30679821	Pathogenic variants in USP7 cause a neurodevelopmental disorder with speech delays, altered behavior, and neurologic anomalies.	Genet Med	2019
31956451	Two Cases of Oculofaciocardiodental (OFCD) Syndrome due to X-Linked BCOR Mutations Presenting with Infantile Hemangiomas: Phenotypic Overlap with PHACE Syndrome.	Case Rep Genet	2019
28457472	Duplicated Enhancer Region Increases Expression of CTSB and Segregates with Keratolytic Winter Erythema in South African and Norwegian Families.	Am J Hum Genet	2017
24781755	Homozygous loss of DIAPH1 is a novel cause of microcephaly in humans.	Eur J Hum Genet	2015
25480986	Neuropathy target esterase impairments cause Oliver-McFarlane and Laurence-Moon syndromes.	J Med Genet	2015
26365382	USP7 Acts as a Molecular Rheostat to Promote WASH-Dependent Endosomal Protein Recycling and Is Mutated in a Human Neurodevelopmental Disorder.	Mol Cell	2015
25155731	Renal teratogens.	Clin Perinatol	2014
24504818	Brief report: Risk of adverse fetal outcomes associated with immunosuppressive medications for chronic immune-mediated diseases in pregnancy.	Arthritis Rheumatol	2014
23723048	Expansion of genetic services utilizing a general genetic counseling clinic.	J Genet Couns	2014
23810381	TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensities.	Am J Hum Genet	2013
22266071	A balanced t(10;15) translocation in a male patient with developmental language disorder.	European Journal of Medical Genetics	2012
22434508	Correlation of heart rate and cardiac dysfunction in Duchenne muscular dystrophy.	Pediatric Cardiology	2012
21740577	Common polymorphisms in human lysyl oxidase genes are not associated with the adolescent idiopathic scoliosis phenotype.	BMC Med Genet	2011
21482610	Vaccines are not associated with metabolic events in children with urea cycle disorders.	Pediatrics	2011
21957892	Investigation of 95 variants identified in a genome-wide study for association with mortality after acute coronary syndrome.	BMC Med Genet	2011
22029802	Genetic risk score does not correlate with body mass index of Latina women in a clinical trial.	Clin Transl Sci	2011
20445167	L-histidine decarboxylase and Tourette's syndrome.	N Engl J Med	2010
21081748	Variation in recovery: Role of gender on outcomes of young AMI patients (VIRGO) study design.	Circ Cardiovasc Qual Outcomes	2010
20933357	Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies.	J Am Coll Cardiol	2010
20351724	Additional support for the association of SLITRK1 var321 and Tourette syndrome.	Mol Psychiatry	2010
20422016	Consanguinity mapping of congenital heart disease in a South Indian population.	PLoS One	2010
19198609	Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.	Nat Genet	2009
18179895	Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders.	Am J Hum Genet	2008
18620593	Investigation of 89 candidate gene variants for effects on all-cause mortality following acute coronary syndrome.	BMC Med Genet	2008
18551756	Disruption of Contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome.	Am J Hum Genet	2008
17426274	Nonvalidation of reported genetic risk factors for acute coronary syndrome in a large-scale replication study.	JAMA	2007
17708142	Turner syndrome: diagnosis and management.	American Family Physician	2007
16224024	Sequence variants in SLITRK1 are associated with Tourette's syndrome.	Science	2005
14698017	Reporting of model validation procedures in human studies of genetic interactions.	Nutrition	2004
15514396	Autism in a 15-month-old child.	American Journal of Psychiatry	2004
15131760	Acute effects of nicotine on serum glucose insulin growth hormone and cortisol in healthy smokers.	Metabolism	2004
15106122	Disruption of contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome.	Am J Hum Genet	2004
12791034	Overestimation of genetic risks owing to small sample sizes in cardiovascular studies.	Clin Genet	2003
12911258	The education and medical practice of Dr. James McCune Smith (1813-1865), first black American to hold a medical degree.	Journal of the National Medical Association	2003
12682296	Epigenetic abnormalities associated with a chromosome 18(q21-q22) inversion and a Gilles de la Tourette syndrome phenotype.	Proc Natl Acad Sci U S A	2003
11674911	The economic impact of wasted prescription medication in an outpatient population of older adults.	Journal of Family Practice	2001