Melanie Lacaria

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 4

Top Topics

Genome Wide Association Study

Circulating Tumor Cells

Top Venues

American journal of medical genetics. Part A

This page only lists publications with an associated author ORCID identifier.

Publications

Aren Elizabeth Marshall, Lauren Brady, Ed Yeh, Alan J Mears, Melanie Lacaria, Pranesh Chakraborty, Mark A Tarnopolsky, Kristin D Kernohan
Next generation sequencing reveals novel compound heterozygous deletions in NDUFAF2 in a child with mitochondrial complex I deficiency, nuclear type 10. American journal of medical genetics. Part A 194 (7) (2024)
Aren Elizabeth Marshall, Lauren Brady, Ed Yeh, Alan J Mears, Melanie Lacaria, Pranesh Chakraborty, Mark A Tarnopolsky, Kristin D Kernohan
Next generation sequencing reveals novel compound heterozygous deletions in NDUFAF2 in a child with mitochondrial complex I deficiency, nuclear type 10. American journal of medical genetics. Part A 194 (7) (2024)
Aren Elizabeth Marshall, Lauren Brady, Ed Yeh, Alan J Mears, Melanie Lacaria, Pranesh Chakraborty, Mark A Tarnopolsky, Kristin D Kernohan
Next generation sequencing reveals novel compound heterozygous deletions in NDUFAF2 in a child with mitochondrial complex I deficiency, nuclear type 10. American journal of medical genetics. Part A (2024)
Melanie Lacaria, Myriam Srour, Jacques L Michaud, Asif Doja, Elka Miller, Jeremy Schwartzentruber, Claire Goldsmith, Jacek Majewski, null null, Kym M Boycott
Expansion of the clinical phenotype of the distal 10q26.3 deletion syndrome to include ataxia and hyperemia of the hands and feet. American journal of medical genetics. Part A 173 (6) (2017)