Abdallah F. Elias

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论文共 51 篇作者统计合作学者相似作者

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Long-Read Sequencing is Required for Precision Diagnosis of Incontinentia Pigmenti

Monica H Wojcik, Robin D Clark,Abdallah F Elias,Casie A Genetti,Jill A Madden, Dana Simpson, Linda Golkar,Miranda Pg Zalusky,Angela L Miller, Araceli Rodriguez,Joy Goffena, Camille A Dash,Nikhita Damaraju, Sophia B Gibson, Sophia Hr Storz, Zach Anderson,Jonas A Gustafson,Isabelle Thiffault,Emily G Farrow,Tomi Pastinen,Jasmine Lin, Jennifer Huang, Alan H Beggs,Pankaj B Agrawal, Genomics Research to Elucidate the Genetics of Rare Diseases (GREGoR) Consortium, David T Miller,Danny E Miller

Research square (2025)

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Prenatally Detected Maternally Inherited Partial Duplication of 11p15.5 ICR1 Results in Phenotypes Overlapping Russell-Silver Syndrome in Infancy

Amanda Thomas-Wilson,Mythily Ganapathi, Nina Harkavy,Corbin Schwanke, Jessica Giordano,Abdallah F Elias,Ronald J Wapner,Vaidehi Jobanputra

Prenatal diagnosis (2025)

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Non-Mosaic Trisomy 9: Further Delineation of the Clinical Phenotype

Courtney P Verscaj, Michael Gordon, Bradley D Holbrook, Olivia Maher Trocki, Tabitha Poorvu, Christina Miller,Tammy Schwalbe, Maija Trout, Amy Zearfoss, Angela Welker,Monica H Wojcik,Abdallah F Elias

American journal of medical genetics Part App.e64087-e64087, (2025)

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Autosomal Dominant HK1-related Neurodevelopmental Disorder with Visual Defects and Brain Anomalies (NEDVIBA): an Emerging Mitochondrial Disorder

Bobby G Ng,Erik A Eklund, Jill A Rosenfeld,Abdallah F Elias, Aya Abu-El-Haija,Celine Bris,Magalie Barth,Jong-Hee Chae,Murim Choi, Holly A Dubbs,Carl Fratter,Nicola Foulds,Candace Gamble,Ralitza H Gavrilova, Jaclyn Haven, Trevor L Hoffman,Jill V Hunter,Austin Larson, Timothy Edward Lotze, Pilar Magoulas, Emily C Magness, Debra M Bootin, Eric D Marsh, Victoria Nesbitt, Matthew T Pastore, Joanna Poulton,Shamima Rahman,Fernando Scaglia, Chaya Murali, Jennifer Posey,Joshua Rotenberg, Betsy Schmalz,Deepali N Shinde, Zöe Powis, Rivka Sukenik-Halevy, Kristen V Truxal, Tami Uster, Matheus Vernet Machado Bressan Wilke, Erik Klee,Hyewon Woo, Donald Younkin, Jianhua Zhao, Jorge Granadillo, Seema Lalani,David Chitayat, Wendy K Chung, Hudson H Freeze, Volkan Okur

Genetics in medicine open (2025): 103425-103425

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P775: Maternally Inherited 11p15 Duplication Involving Only Part of the ICR1 H19/IGF2 Domain: Unraveling Mild Russell-Silver Syndrome Phenotype