Melanie Babcock
Biochemistry, Genetics and Molecular Biology · The Ohio State University
Publications
34
Citations
1,111
Est. group size
~4
Recurring co-author estimate
Active years
24
Publishing since 2003
Melanie Babcock works in clinical and cytogenetics research, focusing on chromosomal abnormalities, copy number variants, and genetic testing methods used to diagnose rare diseases, developmental disorders, and pediatric cancers. Much of the work involves analyzing patient case data (such as unusual chromosome rearrangements) and evaluating laboratory testing practices like chromosomal microarray and genome sequencing. This research is clinically oriented, often drawing on case reports and retrospective studies from hospital or laboratory settings.
Publication activity was absent before 2021 but has increased since, with a fairly steady output of several papers per year from 2021 through 2025.
Generated by claude-sonnet-5 from public bibliographic data · Jul 20, 2026
- Unusual Recombinant Chromosome 6 Derived From a Parental Rearrangement With Complex Paracentric Inversions
American Journal of Medical Genetics Part A · 2026
- P726: Provenance/identity testing in genome sequencing: A single institution’s experience
Genetics in Medicine Open · 2025
- O09: Prevalence of germline variants in cancer predisposition genes in patients with pediatric solid tumors using paired tumor-normal exome sequencing
Genetics in Medicine Open · 2025
- Breaking the Mold, A Rare Lung Neoplasm in Childhood
American Journal of Respiratory and Critical Care Medicine · 2025
- Breaking the Mold! A Rare Lung Neoplasm in Childhood
Pediatric Pulmonology · 2025
- ETMR-03. Unique Case of Pontine CNS tumor with BCOR internal tandem duplication (ITD) in an Infant
Neuro-Oncology Pediatrics · 2025
- Clinical Cytogenetics: Current Practices and Beyond
The Journal of Applied Laboratory Medicine · 2024
- 36. Significant copy number variants and loss of heterozygosity in Wilms Tumor: Insights from Nationwide Pediatric Oncology
Cancer Genetics · 2024
- Clinically significant findings in a decade‐long retrospective study of prenatal chromosomal microarray testing
Molecular Genetics & Genomic Medicine · 2024
- P424: An unusual recombinant chromosome 6 derived from a parental double paracentric inversion
Genetics in Medicine Open · 2023
- Chromosome 2q12.3-q13 copy number variants in patients with neurodevelopmental disorders: genotype-phenotype correlation and new hotspots
Psychiatric Genetics · 2022
- 100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report.
UCL Discovery (University College London) · 2021
- Reproductive outcomes in individuals with chromosomal reciprocal translocations
Genetics in Medicine · 2021
- Reproductive outcomes in carriers of chromosomal reciprocal translocations
Molecular Genetics and Metabolism · 2021
- Genetics in Medicine Open×6
- Cancer Genetics×2
- UCL Discovery (University College London)×1
- Genetics in Medicine×1
- The Journal of Applied Laboratory Medicine×1
- Amy M. Breman
Biochemistry, Genetics and Molecular Biology · Indiana University
- Patrícia Dias
Biochemistry, Genetics and Molecular Biology · The Ohio State University
- Theodora Matthews
Biochemistry, Genetics and Molecular Biology · The Ohio State University
- David D. Weaver
Biochemistry, Genetics and Molecular Biology · Indiana University
- Seyed Amir Malekpour
Biochemistry, Genetics and Molecular Biology · The Ohio State University
This profile was generated automatically from public scholarly data (OpenAlex). Group size and activity levels are estimates derived from co-authorship patterns.
Last updated Jul 19, 2026.
Claim or correct this profile