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: IT ✕ Universität Hamburg ✕ clear all

6 matching publication(s)

Publication	Journal	Year	Score	Verdict
Pleiotropic effects of MORC2 derive from its epigenetic signature PMID 40302207	—	2025	—	L1 No data access
TFEB deficiency attenuates mitochondrial degradation upon brown adipose tissue whitening at thermoneutrality PMID 33516944	Molecular Metabolism 47:101173	2021	—	L1 No computation
The role of the multidisciplinary health care team in the management of patients with Marfan syndrome. PMID 27843325	—	2016	—	L1 No computation
Mutations of the mitochondrial holocytochrome c-type synthase in X-linked dominant microphthalmia with linear skin defects syndrome. PMID 17033964	—	2006	75	L1 75/100
Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome. PMID 18834967	—	2008	70	L1 70/100
Duplication of Glu37 in the switch I region of HRAS impairs effector/GAP binding and underlies Costello syndrome by promoting enhanced growth factor-dependent MAPK and AKT activation. PMID 19995790	—	2010	—	L1 No computation

Pleiotropic effects of MORC2 derive from its epigenetic signature

PMID 40302207 · · 2025

L1 No data access

TFEB deficiency attenuates mitochondrial degradation upon brown adipose tissue whitening at thermoneutrality

PMID 33516944 · Molecular Metabolism 47:101173 · 2021

L1 No computation

The role of the multidisciplinary health care team in the management of patients with Marfan syndrome.

PMID 27843325 · · 2016

L1 No computation

Mutations of the mitochondrial holocytochrome c-type synthase in X-linked dominant microphthalmia with linear skin defects syndrome.

PMID 17033964 · · 2006

L1 75/100

Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.

PMID 18834967 · · 2008

L1 70/100

Duplication of Glu37 in the switch I region of HRAS impairs effector/GAP binding and underlies Costello syndrome by promoting enhanced growth factor-dependent MAPK and AKT activation.

PMID 19995790 · · 2010

L1 No computation