Amanote Research

Amanote Research

    RegisterSign In

Discover open access scientific publications

Search, annotate, share and cite publications


Publications by Markus M Nöthen

The CCND1 C.870G>A Polymorphism Is a Risk Factor for T(11;14)(q13;q32) Multiple Myeloma

Nature Genetics
Genetics
2013English

Reproducible Grey Matter Patterns Index a Multivariate, Global Alteration of Brain Structure in Schizophrenia and Bipolar Disorder

Translational Psychiatry
PsychiatryMolecular NeuroscienceBiological PsychiatryMental HealthCellular
2019English

Prediction of Male-Pattern Baldness From Genotypes

European Journal of Human Genetics
Genetics
2015English

First Genotype-Phenotype Study Reveals HLA-DQβ1 Insertion Heterogeneity in High-Resolution Manometry Achalasia Subtypes

United European Gastroenterology Journal
OncologyGastroenterology
2018English

Corrigendum: Loss-Of-Function Mutations of an Inhibitory Upstream ORF in the Human Hairless Transcript Cause Marie Unna Hereditary Hypotrichosis

Nature Genetics
Genetics
2009English

Serotonin Transporter 5HTTLPR Polymorphism and Affective Disorders: No Evidence of Association in a Large European Multicenter Study

European Journal of Human Genetics
Genetics
2004English

Effect of the G72 (DAOA) Putative Risk Haplotype on Cognitive Functions in Healthy Subjects

BMC Psychiatry
PsychiatryMental Health
2009English

Amanote Research

Note-taking for researchers

Follow Amanote

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

Privacy PolicyRefund Policy