Fady M. Mikhail

Rearrangement of CRLF2 in B-progenitor– and Down syndrome–associated acute lymphoblastic leukemia

Charles G. Mullighan, J. Racquel Collins-Underwood, Letha A. Phillips et al. · Nature Genetics · 2009 · 615 citations · Full text

Hematological Malignancy, Chromatin, Mixed-phenotype Acute Leukemia +8

Rearrangement of CRLF2 is associated with mutation of JAK kinases, alteration of IKZF1, Hispanic/Latino ethnicity, and a poor outcome in pediatric B-progenitor acute lymphoblastic leukemia

Richard C. Harvey, Charles G. Mullighan, I‐Ming Chen et al. · Blood · 2010 · 569 citations · Full text

Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay

Rachel D. Burnside, Romela Pasion, Fady M. Mikhail et al. · Human Genetics · 2011 · 251 citations · Full text

Neurodevelopmental Disorders, Molecular Neuroscience, Proximal 15Q11.2 +11

Clinically relevant single gene or intragenic deletions encompassing critical neurodevelopmental genes in patients with developmental delay, mental retardation, and/or autism spectrum disorders

Fady M. Mikhail, Edward J. Lose, Nathaniel H. Robin et al. · American Journal of Medical Genetics Part A · 2011 · 169 citations

Mosaic type-1 NF1 microdeletions as a cause of both generalized and segmental neurofibromatosis type-1 (NF1)

Ludwine M. Messiaen, J. Vogt, Kathrin Bengesser et al. · Human Mutation · 2010 · 115 citations · Full text

Neuro-oncology, Nf1 Deletions, Segmental Neurofibromatosis Type-1 +13