Maria Laura Duque Lasio, MD

Division

• Laboratory & Genomic Medicine

Additional Titles

• Assistant Professor of Pediatrics, Division of Genetics & Genomic Medicine
• Assistant Director of Laboratory Services, St. Louis Children’s Hospital

Education

• Combined Pediatrics and Medical Genetics Residency, St. Louis Children’s Hospital, 2015-2019
• Medical Biochemical Genetics Fellowship, UPMC Children’s Hospital of Pittsburgh, 2019 – 2020
• Clinical Biochemical Genetics Fellowship, University of Utah Health, 2020 – 2022

Board Certifications

• Pediatrics – American Board of Pediatrics
• Clinical Genetics & Genomics – American Board of Medical Genetics & Genomics
• Medical Biochemical Genetics – American Board of Medical Genetics & Genomics

Clinical Interests

Inborn errors of metabolism, newborn screening, medical education

Research Interests

Laboratory test development, newborn screening, pyruvate carboxylase deficiency

Selected Publications

Lines MA, Cuillerier A, Chakraborty P, Naas T, Duque Lasio ML, Michaud J, Pileggi C, Harper ME, Burelle Y, Toler TL, Sondheimer N, Crawford HP, Millan F, Geraghty MT. A recurrent de novo ATP5F1A substitution associated with neonatal complex V deficiency. Eur J Hum Genet. 2021;29(11):1719-1724. PMCID:PMC8560863 PMID:34483339

Guenzel AJ, Turgeon CT, Nickander KK, White AL, Peck DS, Pino GB, Studinski AL, Prasad VK, Kurtzberg J, Escolar ML, Lasio MLD, Pellegrino JE, Sakonju A, Hickey RE, Shallow NM, Ream MA, Orsini JJ, Gelb MH, Raymond K, Gavrilov DK, Oglesbee D, Rinaldo P, Tortorelli S, Matern D. The critical role of psychosine in screening, diagnosis, and monitoring of Krabbe disease. Genet Med. 2020;22(6):1108-1118. PMID:32089546

Kulkarni S, Abro B, Duque Lasio ML, Stoll J, Grange DK, He M. Clinical and Pathological Features of a Newborn With Compound Heterozygous ANKS6 Variants. Pediatr Dev Pathol. 2020;23(3):235-239. PMID:31635528

Duque Lasio ML, Kozel BA. Elastin-driven genetic diseases. Matrix Biol. 2018;71-72:144-160. PMCID:PMC8409172 PMID:29501665