Marc Steffen Raab (German Cancer Research Center / Heidelberg University; ORCID 0000-0003-4181-6922) has an OpenAlex record of 643 works, ~12,996 citations and h-index 56 β but at least three unmerged secondary profiles exist (e.g., "Marc-Steffen Raab": 91 works, 2,467 citations, h 23), so true bibliometric totals are higher than any single profile shows. Output accelerated from ~5β9 works/year (2004β2014) to 26β33/year (2016β2022) and a 182-work spike in 2023 β a pattern typical of consortium/trial authorship rather than a lone-author burst.
His most-cited work spans the full translational arc: a first-authored Lancet seminar on myeloma (697 citations) , co-authorship on the NEJM selinexor trial in triple-class refractory disease , and the 2023 Nature Medicine MagnetisMM-3 elranatamab phase 2 (651 citations). He also co-authors disease-biology genomics, e.g., the Blood study mapping myeloma oncogene dependencies onto primary cytogenetic events (473 citations).
The deepest-dive paper reframes disagreement between hashing-based (HTODemux, MultiSeqDemux) and SNP-based (Souporcell, Vireo) demultiplexers as a structured cell-quality signal, not noise, and ships an open-source Nextflow pipeline. Reported validation across 14 MM donors and AML snMultiome/scRNA/scATAC pools: consensus singlet fraction of only 0.374 at full depth (0.565 with relaxed Vireo-WGS settings); lenient filtering retains 42,970 T cells at 87.1% purity (derived: 100 β 12.9% cross-donor contamination) versus 34,756 cells at 99.2% purity for high-confidence Split-flow, plus 5.3-fold enrichment of VDJdb-confirmed public TCRs. Declared limitations: heuristic thresholds, incomplete genotype ground truth, a fixed toolset, and hematology-only testing. Funding is public (DFG, BMBF, EU) with no competing interests declared β a strong posture for methods work.
A second deep-dive paper shows a different mode: an Amgen-funded observational chart review (435 physicians; 7,635 cross-sectional plus 4,997 retrospective charts; 7 countries) reporting first-line bortezomib 48%, lenalidomide second-line 60% and first-line maintenance 45%, and SCT receipt 31% against 44% eligibility. It is useful real-world evidence, but with disclosed sponsor funding, no multiple-comparison adjustment, and acknowledged selection toward SCT-capable centers β a genre contrast with the independently funded, code-released 2026 work.
The assessment would weaken if Split-flow's purity/TCR enrichment fails replication on non-hematologic tissues, or if concordance tiers merely proxy sequencing depth rather than cell quality; it would strengthen with a merged profile confirming robust first/senior authorship fractions.
Know what changed, what holds up, and what remains uncertain. Every Friday. No ads.