Kandamurugu Manickam
Biochemistry, Genetics and Molecular Biology · The Ohio State University
Publications
84
Citations
3,584
Est. group size
~1
Recurring co-author estimate
Active years
24
Publishing since 2003
Kandamurugu Manickam's research focuses on medical genetics, particularly identifying genetic causes of rare neurodevelopmental and neurodegenerative conditions in children, and studying how genomic screening can be used in population health and clinical care. Much of the work involves large genome sequencing datasets, biobanks, and electronic health records to find disease-causing gene variants and guide clinical genetics guidelines. The work often involves collaborative consortia such as the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen).
Publication output has been relatively steady at a low-to-moderate rate over the past decade, with a temporary spike in 2021 followed by a decline to roughly 3-4 papers per year in recent years.
Generated by claude-sonnet-5 from public bibliographic data · Jul 20, 2026
- ARID5B mutations cause a neurodevelopmental syndrome with neuroinflammation episodes
bioRxiv (Cold Spring Harbor Laboratory) · 2026
- Biallelic ACER3 Variants Cause Infantile- and Early-Childhood-Onset Neurodegeneration with Leukodystrophy
SSRN Electronic Journal · 2026
- ARID5B mutations cause a neurodevelopmental syndrome with neuroinflammation episodes
eLife · 2026
- ARID5B mutations cause a neurodevelopmental syndrome with neuroinflammation episodes
eLife · 2026
- P602: Developing an actionability framework for population genomic screening
Genetics in Medicine Open · 2025
- The Clinical Genome Resource (ClinGen): Advancing genomic knowledge through global curation
Genetics in Medicine · 2024
- Disorders of Gut-Brain Interaction in a National Cohort of Children With Down Syndrome
Journal of Neurogastroenterology and Motility · 2023
- Quality of life measures in children with Down syndrome with disorders of gut–brain interaction
American Journal of Medical Genetics Part C Seminars in Medical Genetics · 2023
- Exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability: an evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG)
Genetics in Medicine · 2021
- DNA-based screening and population health: a points to consider statement for programs and sponsoring organizations from the American College of Medical Genetics and Genomics (ACMG)
Genetics in Medicine · 2021
- A Genome-First Approach to Characterize <i>DICER1</i> Pathogenic Variant Prevalence, Penetrance, and Phenotype
JAMA Network Open · 2021
- Saturation mutagenesis defines novel mouse models of severe spine deformity
Disease Models & Mechanisms · 2021
- Correction to: Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participants
Genetics in Medicine · 2021
- Biallelic <i>GRM7</i> variants cause epilepsy, microcephaly, and cerebral atrophy
Annals of Clinical and Translational Neurology · 2020
- Healthcare Utilization and Costs after Receiving a Positive BRCA1/2 Result from a Genomic Screening Program
Journal of Personalized Medicine · 2020
- Genetics in Medicine×10
- Molecular Genetics and Metabolism×6
- Figshare×5
- npj Genomic Medicine×3
- bioRxiv (Cold Spring Harbor Laboratory)×3
- Robert C. Green
Biochemistry, Genetics and Molecular Biology · Indiana University
- Kristen Suhrie
Biochemistry, Genetics and Molecular Biology · Indiana University
- Francesco Vetrini
Biochemistry, Genetics and Molecular Biology · Indiana University
- Kayla Treat
Biochemistry, Genetics and Molecular Biology · Indiana University
- Amy Siemon
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