Fady M Mikhail
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Explore the profile of Fady M Mikhail including associated specialties, affiliations and a list of published articles.
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70
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1272
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Recent Articles
1.
Gao M, Chen Y, Lertwilaiwittaya P, Hurst A, Al-Beshri A, Carroll A, et al.
Am J Med Genet A
. 2024 Dec;
197(4):e63951.
PMID: 39622782
Aplastic anemia, characterized by pancytopenia and hypoplastic bone marrow, is associated with various acquired cytogenetic abnormalities, including trisomy 8, in 4%-15% of patients. Constitutional mosaic trisomy 8 notably increases the...
2.
Deignan J, Aggarwal V, Bale A, Bellissimo D, Booker J, Cao Y, et al.
Genet Med Open
. 2024 Aug;
2.
PMID: 39175871
Purpose: The specialty of Laboratory Genetics and Genomics (LGG) was created in 2017 in an effort to reflect the increasing convergence in technologies and approaches between clinical molecular genetics and...
3.
Akkari Y, Baughn L, Kim A, Karaca E, Raca G, Shao L, et al.
Genet Med
. 2024 Feb;
26(4):101054.
PMID: 38349293
Cytogenomic analyses of acquired clonal chromosomal abnormalities in neoplastic blood, bone marrow, and/or lymph nodes are instrumental in the clinical management of patients with hematologic neoplasms. Cytogenetic analyses assist in...
4.
Chen Y, Karaca E, Robin N, Goodloe D, Al-Beshri A, Dean S, et al.
Genet Med
. 2023 Oct;
26(1):101010.
PMID: 37860969
Purpose: Multiple studies suggest an association between DLG2 and neurodevelopmental disorders and indicate the haploinsufficiency of this gene; however, few cases have been thoroughly described. We performed additional studies to...
5.
Blackburn P, McGee R, Mostafavi R, Carroll A, Mikhail F, Armstrong G, et al.
Genes Chromosomes Cancer
. 2023 Aug;
63(1):e23195.
PMID: 37548271
Rhabdoid Tumor Predisposition Syndrome 1 (RTPS1) confers an increased risk of developing rhabdoid tumors and is caused by germline mutations in SMARCB1. RTPS1 should be evaluated in all individuals with...
6.
Dunn-Valadez S, Bathini S, Purdy K, Bachiashvili K, Bhatia R, Jamy O, et al.
Leuk Lymphoma
. 2023 Jul;
64(10):1673-1680.
PMID: 37493540
Significant variations exist related to the end of induction practices in the management of Acute Promyelocytic Leukemia (APL). These variations include all-trans retinoic acid (ATRA)-arsenic trioxide (ATO) in fixed doses...
7.
Belnap N, Price-Smith A, Ramsey K, Leka K, Abraham A, Lieberman E, et al.
Clin Genet
. 2023 Jul;
104(5):607-609.
PMID: 37491870
Pedigree showing the autosomal dominant inheritance pattern of CSNK21 variants in families presenting with OCNDS. (A) Maternal inheritance to two daughters in Family 1, (B) Paternal inheritance to a daughter...
8.
Stackhouse C, Anderson J, Yue Z, Nguyen T, Eustace N, Langford C, et al.
JCI Insight
. 2022 Jul;
7(16).
PMID: 35852875
Key molecular regulators of acquired radiation resistance in recurrent glioblastoma (GBM) are largely unknown, with a dearth of accurate preclinical models. To address this, we generated 8 GBM patient-derived xenograft...
9.
Shao L, Akkari Y, Cooley L, Miller D, Seifert B, Wolff D, et al.
Genet Med
. 2021 Jun;
23(10):1818-1829.
PMID: 34131312
Chromosomal microarray technologies, including array comparative genomic hybridization and single-nucleotide polymorphism array, are widely applied in the diagnostic evaluation for both constitutional and neoplastic disorders. In a constitutional setting, this...
10.
Li G, Holly T, Kelly D, Reddy V, Mikhail F, Carroll A, et al.
J Pediatr Hematol Oncol
. 2021 Feb;
44(1):e109-e113.
PMID: 33625084
Therapy-related myeloid neoplasm (t-MN) in the pediatric population is not well characterized. We studied 12 pediatric patients diagnosed with t-MN in our institution since 2006. The median age at the...