MichaelJKeoghMD

Cardiology • Reno, NV

Adult Congenital Heart Disease

Physician

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Office
975 Kirman Ave
Reno, NV 89502
Phone+1 702-341-3020
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Education & Training

San Antonio Uniformed Services Health Education ConsortiumFellowship, Cardiovascular Disease, 1988 - 1991
San Antonio Uniformed Services Health Education ConsortiumResidency, Internal Medicine, 1985 - 1988
Rutgers Robert Wood Johnson Medical SchoolClass of 1985

Certifications & Licensure

CA State Medical License 2012 - 2025
NC State Medical License 2010 - 2024
WI State Medical License 1993 - 1997
PA State Medical License 1990 - 1994
American Board of Internal Medicine Internal Medicine

Awards, Honors, & Recognition

Fellow (FACC) American College of Cardiology

Publications & Presentations

PubMed

1 citations
Disappearing "Myxoma": Left Atrial Thrombus Masquerading as a Myxoma.
Daniel Antwi-Amoabeng, Charles E. Willyard, Nageshwara Gullapalli, Michael Keogh> ;Cureus. 2020 Jun 9
22 citations
A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longe...
Sven J van der Lee, Olivia J Conway, Iris Jansen, Minerva M Carrasquillo, Luca Kleineidam, Erik van den Akker, Isabel Hernández, Kristel R van Eijk, Najada Stringa, Ja...> ;Acta Neuropathologica. 2019 Aug 1
127 citations
Germline selection shapes human mitochondrial DNA diversity.
Wei Wei, Salih Tuna, Michael J. Keogh, Katherine R. Smith, Timothy J. Aitman, PL Beales, David L.H. Bennett, Daniel P. Gale, Bitner-Glindzicz Mak., Graeme C.M. Black, ...> ;Science. 2019 May 24
44 citations
Somatic variants in autosomal dominant genes are a rare cause of sporadic Alzheimer's disease
Gaël Nicolas, Rocio Acuna-Hidalgo, Michael J. Keogh, Olivier Quenez, Marloes Steehouwer, Stefan H. Lelieveld, Stéphane Rousseau, Anne-Claire Richard, Manon S. Oud, Flo...> ;Alzheimer's & Dementia. 2018 Dec 1
44 citations
High prevalence of focal and multi-focal somatic genetic variants in the human brain
Michael J. Keogh, Wei Wei, Juvid Aryaman, Lauren Walker, Jelle van den Ameele, Jon Coxhead, Ian J. Wilson, Matthew Bashton, Jon Beck, John A. West, Richard Chen, Chris...> ;Nature Communications. 2018 Oct 15
14 citations
Frequency and signature of somatic variants in 1461 human brain exomes.
Wei Wei, Michael J. Keogh, Juvid Aryaman, Zoe J. Golder, Peter J. Kullar, Ian J. Wilson, Kevin Talbot, Martin R Turner, Chris-Anne McKenzie, Claire Troakes, Johannes A...> ;Genetics in Medicine. 2019 Apr 1
16 citations
Oligogenic genetic variation of neurodegenerative disease genes in 980 postmortem human brains.
Michael J. Keogh, Wei Wei, Juvid Aryaman, Ian J. Wilson, Kevin Talbot, Martin R Turner, Chris-Anne McKenzie, Claire Troakes, Johannes Attems, Colin Smith, Safa Al Sarr...> ;Journal of Neurology, Neurosurgery, and Psychiatry. 2018 Jan 13
PLP1 mutations and central demyelination: Evidence from electrophysiologic phenotyping in female manifesting carriers
Michael J. Keogh, Stephan R. Jaiser, Hannah E. Steele, Rita Horvath, Patrick F. Chinnery, Mark R. Baker> ;Neurology. Clinical Practice. 2017 Oct 1
Response to Simon et al.
Wei Wei, Michael J. Keogh, James W. Ironside, Patrick F. Chinnery> ;Acta Neuropathologica Communications. 2017 Apr 29
75 citations
Amyloid-β accumulation in the CNS in human growth hormone recipients in the UK
Diane Ritchie, Peter Adlard, Alexander Peden, Suzanne Lowrie, Margaret Le Grice, Kimberley Burns, Rosemary J. Jackson, Helen Yull, Michael J. Keogh, Wei Wei, Patrick F...> ;Acta Neuropathologica. 2017 Mar 27
13 citations
Erratum to: Mitochondrial DNA point mutations and relative copy number in 1363 disease and control human brains.
Wei Wei, Michael J Keogh, Ian Wilson, Jonathan Coxhead, Sarah Ryan, Sara Rollinson, Helen Griffin, Marzena Kurzawa-Akanbi, Mauro Santibanez-Koref, Kevin Talbot, Martin...> ;Acta Neuropathologica Communications. 2017 Feb 22
36 citations
Mitochondrial DNA point mutations and relative copy number in 1363 disease and control human brains.
Wei Wei, Michael J Keogh, Ian Wilson, Jonathan Coxhead, Sarah Ryan, Sara Rollinson, Helen Griffin, Marzena Kurzawa-Akanbi, Mauro Santibanez-Koref, Kevin Talbot, Martin...> ;Acta Neuropathologica Communications. 2017 Feb 2
39 citations
Genetic compendium of 1511 human brains available through the UK Medical Research Council Brain Banks Network Resource.
Michael J. Keogh, Wei Wei, Ian J. Wilson, Jon Coxhead, Sarah Ryan, Sara Rollinson, Helen Griffin, Marzena Kurzawa-Akanbi, Mauro Santibanez-Koref, Kevin Talbot, Martin ...> ;Genome Research. 2017 Jan 1
57 citations
HDBR Expression: A Unique Resource for Global and Individual Gene Expression Studies during Early Human Brain Development
Susan Lindsay, Yaobo Xu, Steven Lisgo, Lauren F. Harkin, Andrew J. Copp, Dianne Gerrelli, Gavin J. Clowry, Aysha Talbot, Michael J. Keogh, Jonathan Coxhead, Mauro Sant...> ;Frontiers in Neuroanatomy. 2016 Oct 26
30 citations
SCP2 mutations and neurodegeneration with brain iron accumulation.
Rita Horvath, David Lewis-Smith, Konstantinos Douroudis, Jennifer Duff, Michael J. Keogh, Angela Pyle, Nicholas A. Fletcher, Patrick F. Chinnery> ;Neurology. 2015 Nov 24
101 citations
Mitochondrial DNA mutations in neurodegeneration
Michael J. Keogh, Patrick F. Chinnery> ;Biochimica Et Biophysica Acta. 2015 Nov 1
22 citations
Prevalence of neurogenetic disorders in the North of England
David Bargiela, Patrick Yu-Wai-Man, Michael J. Keogh, Rita Horvath, Patrick F. Chinnery> ;Neurology. 2015 Oct 6
3 citations
Reply: Evaluation of exome sequencing variation in undiagnosed ataxias.
Angela Pyle, Helen Griffin, Michael J. Keogh, Rita Horvath, Patrick F. Chinnery> ;Brain. 2015 Oct 1
13 citations
Clinical heterogeneity of primary familial brain calcification due to a novel mutation in PDGFB
Michael J. Keogh, Angela Pyle, Daniyal Daud, Helen Griffin, Konstantinos Douroudis, Gail Eglon, James Miller, Rita Horvath, Patrick F. Chinnery> ;Neurology. 2015 Apr 28
33 citations
LRRK2 exonic variants and risk of multiple system atrophy.
Michael G. Heckman, Lucia Schottlaender, Alexandra I. Soto-Ortolaza, N. N. Diehl, Sruti Rayaprolu, Kotaro Ogaki, Shinsuke Fujioka, Melissa E. Murray, William P. Cheshi...> ;Neurology. 2014 Dec 9
30 citations
A novel de novo STXBP1 mutation is associated with mitochondrial complex I deficiency and late-onset juvenile-onset parkinsonism
Michael J. Keogh, Daniyal Daud, Angela Pyle, Jennifer Duff, Helen Griffin, Langping He, Charlotte L. Alston, Hannah E. Steele, S. Taggart, Anna Basu, Robert W. Taylor,...> ;Neurogenetics. 2015 Jan 1
Exome sequencing: how to understand it.
Keogh MJ, Daud D, Chinnery PF> ;Pract Neurol. 2013-12-01
29 citations
Hereditary mtDNA Heteroplasmy: A Baseline for Aging?
Michael J. Keogh, Patrick F. Chinnery> ;Cell Metabolism. 2013 Oct 1
Awareness of venous thromboembolism prophylaxis must be increased
John M. Findlay, Michael J Keogh, E Tatman, Simon Leach> ;British Journal of Hospital Medicine. 2013 Sep 27
7 citations
Early neuropsychiatry features in neuroferritinopathy
Michael J. Keogh, Baldev Singh, Patrick F. Chinnery> ;Movement Disorders. 2013 Aug 1
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