Prati
Michael C. Adams
Michael C. Adams
Nepoznata afilijacija
Potvrđena adresa e-pošte na med.unc.edu
Naslov
Citirano
Citirano
Godina
A systematic review of the factors affecting accuracy of SUV measurements
MC Adams, TG Turkington, JM Wilson, TZ Wong
American Journal of Roentgenology 195 (2), 310-320, 2010
7002010
An informatics approach to analyzing the incidentalome
JS Berg, M Adams, N Nassar, C Bizon, K Lee, CP Schmitt, KC Wilhelmsen, ...
Genetics in Medicine 15 (1), 36-44, 2013
1792013
The promise and peril of genomic screening in the general population
MC Adams, JP Evans, GE Henderson, JS Berg
Genetics in Medicine 18 (6), 593-599, 2016
662016
Diagnostic utility of exome sequencing in the evaluation of neuromuscular disorders
GT Haskell, MC Adams, Z Fan, K Amin, RJ Guzman Badillo, L Zhou, ...
Neurology: Genetics 4 (1), e212, 2018
552018
Is there evidence that we should screen the general population for Lynch syndrome with genetic testing? A systematic review
AER Prince, RJ Cadigan, GE Henderson, JP Evans, M Adams, ...
Pharmacogenomics and personalized medicine, 49-60, 2017
192017
Look before you leap: genomic screening in obstetrics and gynecology
MC Adams, JS Berg, MD Pearlman, NL Vora
Obstetrics & Gynecology 125 (6), 1299-1305, 2015
122015
P379: Characterizing research on the diagnostic odyssey in the United States: A systematic mapping review
HM Clare, M Waltz, J Berg, B Powell, M Adams, A Kahkoska, KH Lich
Genetics in Medicine Open 1 (1), 2023
12023
P809: Diagnosis and management of pregnant people with inborn errors of metabolism in an adult reproductive genetics and genomics clinic
A Talati, E Hardisty, M Dyke, C Hildebrandt, M Adams, M Calikoglu, ...
Genetics in Medicine Open 2, 2024
2024
P040: Reducing delays of dextrose administration in patients in acute metabolic crisis
M Williams, M Adams, E Colmenares
Genetics in Medicine Open 1 (1), 2023
2023
Quality of care metrics for patients with inborn errors of metabolism
MC Adams, ER Jalazo, CC Hildebrandt, J Wong, SJ Mascaro-Deen, ...
Molecular Genetics and Metabolism 136 (1), 1-3, 2022
2022
Testing and extending strategies for identifying genetic disease–related encounters in pediatric patients
LP Spees, K Hicklin, MC Adams, L Farnan, JT Bensen, DB Gilleskie, ...
Genetics in Medicine 24 (4), 831-838, 2022
2022
eP068: Homozygous SMN1 single nucleotide variant in a patient with SMA type 0
E Jalazo, M Adams, T Felton, T Sneddon, C Powell
Genetics in Medicine 24 (3), S45-S46, 2022
2022
Bi-allelic SPEG variants identified in an infant presenting with severe hypotonia, failure to thrive, and 5-oxoprolinuria
M Adams, E Jalazo, T Felton, S Trau, C Powell
Molecular Genetics and Metabolism 132, S178, 2021
2021
Testing and extending recommended algorithms for identifying genetic disease-related encounters in pediatric patients
L Spees, L Farnan, MC Adams, K Hicklin, J Bensen, J Berg, B Powell, ...
Molecular Genetics and Metabolism 132, S344, 2021
2021
Model of Missense Variation Tolerance to Aid Variant Calling in Whole Exome Sequencing
I King, D Marchuck, M Adams, NT Strande, AK Homstad, JS Berg, ...
JOURNAL OF MOLECULAR DIAGNOSTICS 17 (6), 809-809, 2015
2015
Clarifying Diagnoses: Application of Exome Sequencing for Neuromuscular Disorders
GT Haskell, MC Adams, L Zhou, Z Fan, N Chahin, B Powell, ...
JOURNAL OF MOLECULAR DIAGNOSTICS 17 (6), 757-757, 2015
2015
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