Corpus 1,285 assessed · 1,186 scored · 647 reproduced ≥75 · 174 flagged ·∅ 73.9/100

Publications 6 Datasets 392.5k Experiments 6.2k

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Filters: DE ✕ University of Zurich ✕ clear all

6 matching publication(s)

Publication	Journal	Year	Score	Verdict
Evaluating genome sequencing strategies: trio, singleton, and standard testing in rare disease diagnosis PMID 40963120	Genome Medicine	2025	88	L1 88/100
Genetic Variants in ARHGEF6 Cause Congenital Anomalies of the Kidneys and Urinary Tract in Humans, Mice, and Frogs. PMID 36414417	—	2023	85	L1 85/100
Ancient variation of the AvrPm17 gene in powdery mildew limits the effectiveness of the introgressed rye Pm17 resistance g PMID 35857869	Proc Natl Acad Sci U S A	2022	80	L1 80/100
treeclimbR pinpoints the data-dependent resolution of hierarchical hypotheses. PMID 34001188	Genome Biol	2021	73	L1 73/100
Reproducible, portable, and efficient ancient genome reconstruction with nf-core/eager. PMID 33777521	PeerJ	2021	95	L1 95/100
Dysregulation of Rho GTPases in the αPix/Arhgef6 mouse model of X-linked intellectual disability is paralleled by impaired structural and synaptic plasticity and cognitive deficits. PMID 21989057	—	2012	—	L1 No computation

Evaluating genome sequencing strategies: trio, singleton, and standard testing in rare disease diagnosis

PMID 40963120 · Genome Medicine · 2025

L1 88/100

Genetic Variants in ARHGEF6 Cause Congenital Anomalies of the Kidneys and Urinary Tract in Humans, Mice, and Frogs.

PMID 36414417 · · 2023

L1 85/100

Ancient variation of the AvrPm17 gene in powdery mildew limits the effectiveness of the introgressed rye Pm17 resistance g

PMID 35857869 · Proc Natl Acad Sci U S A · 2022

L1 80/100

treeclimbR pinpoints the data-dependent resolution of hierarchical hypotheses.

PMID 34001188 · Genome Biol · 2021

L1 73/100

Reproducible, portable, and efficient ancient genome reconstruction with nf-core/eager.

PMID 33777521 · PeerJ · 2021

L1 95/100

Dysregulation of Rho GTPases in the αPix/Arhgef6 mouse model of X-linked intellectual disability is paralleled by impaired structural and synaptic plasticity and cognitive deficits.

PMID 21989057 · · 2012

L1 No computation