M. J. Thomas

发表

Genetic counseling for congenital heart disease – Practice resource of the National Society of Genetic Counselors

S. Fitzgerald-Butt, L. Meyers, B. Helm, 2021, Journal of genetic counseling.

COVID-19 scenario modelling for the mitigation of capacity-dependent deaths in intensive care

C. Vasilakis, C. McWilliams, C. Bourdeaux, 2020, medRxiv.

First report: Rare RNF213 variant associated with familial moyamoya disease in an African American family.

B. Worrall, M. J. Thomas, N. Sunmonu, 2021, Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association.

2013 Review and Update of the Genetic Counseling Practice Based Competencies by a Task Force of the Accreditation Council for Genetic Counseling

D. L. Doyle, K. Ormond, E. Petty, 2016, Journal of Genetic Counseling.

α1-Syntrophin Variant Identified in Drug-Induced Long QT Syndrome Increases Late Sodium Current

G. Pitt, M. J. Thomas, Chaojian Wang, 2016, PloS one.

Mortality and postoperative care after emergency laparotomy

T. Cook, C. Peden, A. Clarke, 2011, European journal of anaesthesiology.

Risk profiles and one-year outcomes of patients with newly diagnosed atrial fibrillation in India: Insights from the GARFIELD-AF Registry

Mehrad Amin Eskandari, J. F. Tinto, A. Capucci, 2018, Indian heart journal.

PR interval: a comparison of electrical and mechanical methods in the fetus.

Salome Oseku-Afful, H. Gardiner, M. Roughton, 2007, Early human development.

Something Old, Something New: Using Family History and Genetic Testing to Diagnose and Manage Athletes with Inherited Cardiovascular Disease.

R. Battle, M. J. Thomas, 2015, Clinics in sports medicine.

The Value of Triage during Periods of Intense COVID-19 Demand: Simulation Modeling Study

R. Booton, C. Vasilakis, C. McWilliams, 2021, Medical decision making : an international journal of the Society for Medical Decision Making.

A machine learning approach to intensive care discharge

Daniel J. Lawson, Iain D Gilchrist, Raul Santos-Rodriguez, 2018, bioRxiv.

Simultaneous fzd4 and lrp5 mutation in autosomal dominant familial exudative vitreoretinopathy.

C. Shields, E. Say, B. C. Carter, 2013, Retinal cases & brief reports.

Increasing compliance with low tidal volume ventilation in the ICU with two nudge-based interventions: evaluation through intervention time-series analyses

Iain D Gilchrist, Gaurav Malhotra, Andreas Jarvstad, 2016, BMJ Open.

A classifier for the SNP-based inference of ancestry.

T. Frudakis, K. Venkateswarlu, S. Gunturi, 2003, Journal of forensic sciences.