Rolf W. Stottmann
Biochemistry, Genetics and Molecular Biology · The Ohio State University
Publications
136
Citations
2,735
Est. group size
~1
Recurring co-author estimate
Active years
29
Publishing since 1998
Rolf W. Stottmann's research uses mouse and other model organisms (including C. elegans) to study how genetic mutations disrupt embryonic development, with a particular focus on brain, craniofacial, and neural crest development. His work often connects specific gene variants found in human patients with developmental disorders to their functional effects in animal models, aiming to understand the genetic basis of congenital anomalies and neurodevelopmental conditions.
Publication output has grown over the last decade, rising from roughly 5-7 papers per year earlier on to a peak of 16 in 2025, indicating an increasingly active and productive research program.
Generated by claude-sonnet-5 from public bibliographic data · Jul 20, 2026
- Genetic dissection of the role of Piga and Pgap2 in the embryonic mouse brain
iScience · 2026
- Recessive AARS1 variants perturb human and mouse development
Human Genetics and Genomics Advances · 2026
- Microtubule-stabilizing drugs suppress convulsions in a C. elegans model of CAMSAP disorders
Epilepsy Research · 2026
- Genetic dissection of the role of <i>Piga</i> and <i>Pgap2</i> in the embryonic mouse brain.
PubMed · 2026
- Differential contribution of P73+ Cajal-Retzius cells and Reelin to cortical morphogenesis
Development · 2025
- Mouse variants in Taf1c result in reduced survival to birth
Developmental Biology · 2025
- Genetic analysis and functional assessment of a TGFBR2 variant in micrognathia and cleft palate
PLoS ONE · 2025
- Perdurant TTC21B protein in the early mouse embryo is required for proper forebrain neural progenitor proliferation
bioRxiv (Cold Spring Harbor Laboratory) · 2025
- <i>NUBP2</i> deficiency disrupts the centrosome-check point in the brain and causes primary microcephaly
medRxiv · 2025
- The Society for Craniofacial Genetics and Developmental Biology 47th Annual Meeting
American Journal of Medical Genetics Part A · 2025
- <i>Cse1l</i> Regulates Neural Crest Cell Survival and is Critical for Craniofacial and Cardiac Development
bioRxiv (Cold Spring Harbor Laboratory) · 2025
- De Novo Heterozygous <scp> <i>ZFX</i> </scp> Frameshift Variant in a Female With an X‐Linked Neurodevelopmental Disorder
American Journal of Medical Genetics Part A · 2025
- Detection of the Heterozygous Recurrent <scp> <i>MAX</i> </scp> p.( <scp>Arg60Gln</scp> ) Variant in Two Females Confirms and Expands the Phenotypic Spectrum of Polydactyly–Macrocephaly Syndrome
Clinical Genetics · 2025
- Dmxl1 is required for survival in the mouse to organogenesis stages of development
Differentiation · 2025
- Challenges and opportunities for understanding the genetic causes of congenital anomalies
Developmental Biology · 2025
- bioRxiv (Cold Spring Harbor Laboratory)×18
- American Journal of Medical Genetics Part A×11
- The American Journal of Human Genetics×4
- Development×4
- Human Genetics and Genomics Advances×4
- Kirk Mykytyn
Biochemistry, Genetics and Molecular Biology · The Ohio State University
- Mariana Moraes de Lima Perini
Biochemistry, Genetics and Molecular Biology · Indiana University
- Douglas Landsittel
Biochemistry, Genetics and Molecular Biology · Indiana University
- Erin Ables
Biochemistry, Genetics and Molecular Biology · Indiana University
- Bonnie L. Blazer‐Yost
Biochemistry, Genetics and Molecular Biology · Indiana 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.
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