Michael J. Macera
Morgan Stanley Children's Hospital(US)
Publications by Year
Research Areas
Genomic variations and chromosomal abnormalities, Prenatal Screening and Diagnostics, Chromosomal and Genetic Variations, Chronic Myeloid Leukemia Treatments, Acute Myeloid Leukemia Research
Most-Cited Works
- → The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies(2016)350 cited
- → Structural Chromosomal Rearrangements Require Nucleotide-Level Resolution: Lessons from Next-Generation Sequencing in Prenatal Diagnosis(2016)97 cited
- → Atypical 18p- syndrome associated with partial trisomy 16p in a chromosomally unbalanced child of consanguineous parents with an identical balanced translocation(2005)75 cited
- → Clinical manifestations of trisomy 4p syndrome(1995)47 cited
- → Localization of the gene coding for ventricular myosin regulatory light chain (MYL2) to human chromosome 12q23-q24.3(1992)39 cited
- → Prenatal diagnosis of chromothripsis, with nine breaks characterized by karyotyping, FISH, microarray and whole‐genome sequencing(2014)38 cited
- Molecular topography of the secondary constriction region (qh) of human chromosome 9 with an unusual euchromatic band.(1993)
- → Mechanisms of the origin of a G-positive band within the secondary constriction region of human chromosome 9(1995)28 cited
- → Inversion‐duplication of bands q13→q21 of human chromosome 9(1991)24 cited
- → Intensity heteromorphisms of human chromosome 15p by DA/DAPI technique(1986)21 cited