Amanote Research

Amanote Research

    RegisterSign In

Discover open access scientific publications

Search, annotate, share and cite publications


Publications by Björn Menten

Mutations in KEOPS-complex Genes Cause Nephrotic Syndrome With Primary Microcephaly

Nature Genetics
Genetics
2017English

Shallow Whole-Genome Sequencing of Plasma Cell-Free DNA Accurately Differentiates Small From Non-Small Cell Lung Carcinoma

Genome Medicine
Molecular MedicineGeneticsMolecular Biology
2020English

Complex Genetics of Radial Ray Deficiencies: Screening of a Cohort of 54 Patients

Genetics in Medicine
MedicineGenetics
2012English

Genomic Aberrations of the CACNA2D1 Gene in Three Patients With Epilepsy and Intellectual Disability

European Journal of Human Genetics
Genetics
2014English

Comparative Analysis of Naive, Primed and Ground State Pluripotency in Mouse Embryonic Stem Cells Originating From the Same Genetic Background

Scientific Reports
Multidisciplinary
2018English

Extensive Clinical, Hormonal and Genetic Screening in a Large Consecutive Series of 46,XY Neonates and Infants With Atypical Sexual Development

Orphanet Journal of Rare Diseases
MedicineGeneticsPharmacology
2014English

Disease-Causing 7.4 Kb Cis-Regulatory Deletion Disrupting Conserved Non-Coding Sequences and Their Interaction With the FOXL2 Promotor: Implications for Mutation Screening

PLoS Genetics
EvolutionEcologyGeneticsMolecular BiologyCancer ResearchSystematicsBehavior
2009English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2025 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy