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Simon Glerup

5PUBLICATIONS

41CO-AUTHORS

Infant and child healthDevelopmental genetics (incl. sex determination)Cellular immunologyMolecular targetsMajor global burdens of disease

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Publications (5)

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|Nov 12, 2025

Rare genetic variants confer a high risk of ADHD and implicate neuronal biology.

Ditte Demontis, Jinjie Duan, Yu-Han H Hsu

|Sep 18, 2025

A low frequency damaging SORCS2 variant identified in a family with ADHD compromises receptor stability and quenches activity.

Mathias Kaas, Sarah Broholt Dinesen, Ole Ahlgreen

|Jun 12, 2025

Rare missense variants of the leukocyte common antigen related receptor (LAR) display reduced activity in transcellular adhesion and synapse formation.

Mathias Kaas, Nicolas Chofflet, Deniz Bicer

|Nov 18, 2024

Lack of renoprotective effects by long-term PCSK9 and SGLT2 inhibition using alirocumab and empagliflozin in obese ZSF1 rats.

Sandra Hummelgaard, Henning Hvid, Henrik Birn

|Jan 26, 2021

Altered dopaminergic firing pattern and novelty response underlie ADHD-like behavior of SorCS2-deficient mice.

Ditte Olsen, Niels Wellner, Mathias Kaas

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Frequent Collaborators

3 joint publications

Ditte Demontis

3 joint publications

Jinjie Duan

3 joint publications

Anders D Børglum

2 joint publications

Barbara Franke

2 joint publications

Andreas Reif

2 joint publications

Søren Thirup

2 joint publications

Mathias Ollendorff

2 joint publications

Thomas Werge

1 joint publications

Anders Nykjaer

1 joint publications

Henrik Birn

Frequent Collaborators

3 joint publications

Ditte Demontis

3 joint publications

Jinjie Duan

3 joint publications

Anders D Børglum

2 joint publications

Barbara Franke

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