Megan Morand

Publication Activity (10 Years)

Years Active: 2022-2024
Publications (10 Years): 7

Top Topics

African American

Autism Spectrum Disorder

Top Venues

American journal of medical genetics. Part A

Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer

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

Publications

Manjushree Shanmugasundaram, Amanda Wang, Megan Morand, Colin Bixler, Sangeeta Jain, Joseph Ray
Expanded prenatal phenotype of ALG12-associated congenital disorder of glycosylation including bilateral multicystic kidneys. American journal of medical genetics. Part A (2024)
Manjushree Shanmugasundaram, Amanda Wang, Megan Morand, Colin Bixler, Sangeeta Jain, Joseph Ray
Expanded prenatal phenotype of ALG12-associated congenital disorder of glycosylation including bilateral multicystic kidneys. American journal of medical genetics. Part A 194 (9) (2024)
Manjushree Shanmugasundaram, Amanda Wang, Megan Morand, Colin Bixler, Sangeeta Jain, Joseph Ray
Expanded prenatal phenotype of ALG12-associated congenital disorder of glycosylation including bilateral multicystic kidneys. American journal of medical genetics. Part A 194 (9) (2024)
Manjushree Shanmugasundaram, Amanda Wang, Megan Morand, Colin Bixler, Sangeeta Jain, Joseph Ray
Expanded prenatal phenotype of ALG12-associated congenital disorder of glycosylation including bilateral multicystic kidneys. American journal of medical genetics. Part A 194 (9) (2024)
Jack A Colleran, Emily C Daykin, Cindy Hernandez, Joseph Ray, Megan Morand
Novel mosaic TRAF7 likely pathogenic variant in an African American family. American journal of medical genetics. Part A (2023)
Megan Morand, Michael E Roth, Susan K Peterson, Erica M Bednar, Aarti Ramdaney, Jonathan A Livingston, Angela Yarbrough, Jessica L Corredor
Factors impacting adolescent and young adult cancer patients' decision to pursue genetic counseling and testing. Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer 30 (6) (2022)
Aaron Williams, Erin Cooney, Gabrielle Segal, Swetha Narayanan, Megan Morand, Satish Agadi
GABRG1 variant as a potential novel cause of epileptic encephalopathy, hypotonia, and global developmental delay. American journal of medical genetics. Part A 188 (12) (2022)