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Frontiers in Genetics|June 8, 2026
Identification and molecular functional analysis of genes associated with addiction using integrated genetic web-based programs and databasesWaheeda A Hossain, Merlin G Butler
International Journal of Molecular Sciences|January 21, 2023
Chromosomal Microarray Study in Prader-Willi SyndromeMerlin G Butler, Waheeda A Hossain, Neil Cowen, et al.
BMC Medical Genomics|August 2, 2022
Clinical genetics evaluation and testing of connective tissue disorders: a cross-sectional studyOlivia J Veatch, Jacob Steinle, Waheeda A Hossain, et al.
American Journal of Medical Genetics. Part A|October 6, 2018
Preliminary observations of mitochondrial dysfunction in Prader-Willi syndromeMerlin G Butler, Waheeda A Hossain, Robert Tessman, et al.
American Journal of Medical Genetics. Part A|February 14, 2018
Three siblings with Prader-Willi syndrome caused by imprinting center microdeletions and reviewSamantha N Hartin, Waheeda A Hossain, Nicolette Weisensel, et al.
American Journal of Medical Genetics. Part A|December 28, 2020
ADAMTSL2 gene variant in patients with features of autosomal dominant connective tissue disordersJacob Steinle, Waheeda A Hossain, Scott Lovell, et al.
International Journal of Molecular Sciences|February 13, 2025
ZEB2 Gene Pathogenic Variants Across Protein-Coding Regions and Impact on Clinical Manifestations: A ReviewWaheeda A Hossain, Caroline St Peter, Scott Lovell, et al.
American Journal of Medical Genetics. Part A|July 29, 2022
Next-generation sequencing and analysis of consecutive patients referred for connective tissue disordersJacob Steinle, Waheeda A Hossain, Olivia J Veatch, et al.
International Journal of Molecular Sciences|March 13, 2024
Mowat-Wilson Syndrome: Case Report and Review of <i>ZEB2</i> Gene Variant Types, Protein Defects and Molecular InteractionsCaroline St Peter, Waheeda A Hossain, Scott Lovell, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 19, 2022
Central adrenal insufficiency screening with morning plasma cortisol and ACTH levels in Prader-Willi syndromeMoris A Angulo, Merlin G Butler, Waheeda A Hossain, et al.
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