Works: 27; citations ≈1.0–1.3k; h-index ≈15–16. Appears as recurring co-author on high-impact protein-design papers (Nature, Science, Nat. Chem. Biol., JACS) showing strength in computational protein design and enzyme engineering, often as mid-author in lab-led consortia — i.e., technical contributor in strong teams rather than lone PI leading multiple independent landmark studies.
Representative high-impact contributions include the 2023 Nature luciferase design (large multi-author team) and a 2012 Nature Chemical Biology enzyme redesign paper demonstrating sustained relevance in enzyme design across >10 years of work.
Sources: OpenAlex author metrics and representative papers below.Interpretation: modest publication count with above-average citation reach (≈1.0–1.3k), indicating high-impact co-authorships rather than a large independent corpus.
Interpretation: episodic publication activity with large citation spikes in 2012, 2023, and 2024 consistent with high-impact collaborative works (e.g., 2012 enzyme redesign and 2023 luciferase design).
Strengths: Repeated co-authorship on experimental + computational enzyme/protein-design studies published in top-tier journals (Nature, Science, Nat Commun, JACS, NChemBio) indicates strong technical competence in computational protein design and participation in high-quality experimental validation pipelines; citation spikes correspond to community-valued contributions ().
Limitations / red flags: Low independent paper count and frequent middle-author placement suggest role as a technical collaborator rather than an independent group leader publishing many first-/last-author papers; author affiliation metadata is sparse in the provided data (no consistent primary institution listed), which complicates assessing leadership, lab resources, and independent reproducibility work. Some highly-cited collaborative papers are recent; long-term reproducibility and follow-up outside the originating teams remain to be seen ().
Potential biases & blindspots considered: collaborative, high-impact labs can obscure individual contribution; publication bias toward positive engineering outcomes in protein design; possible sponsor/industry ties in translational works (not shown explicitly here); many papers are method-development + demonstration — risk of overgeneralization if results are not reproduced in independent labs.
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