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Maria Rasmussen

6PUBLICATIONS

2CO-AUTHORS

Medical devicesCardiology (incl. cardiovascular diseases)Characterisation of biological macromoleculesNeonatologyNeurogenetics

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Publications (6)

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|Jan 09, 2025

<i>MUC1</i>-associated autosomal dominant tubulointerstitial kidney disease: prevalence in kidney failure of undetermined aetiology and clinical insights from Danish families.

Jeff Granhøj, Dorte L Lildballe, Katja V Pedersen

|Jul 18, 2024

The role of genomic disorders in chronic kidney failure of undetermined aetiology ≤50 years.

Jeff Granhøj, Katja Venborg Pedersen, Mads Malik Aagaard

|Nov 10, 2021

Functional megalin is expressed in renal cysts in a mouse model of adult polycystic kidney disease.

Marlene L Nielsen, Mia C Mundt, Dorte L Lildballe

|Jul 05, 2021

Total Anomalous Pulmonary Venous Connection in Mother and Son with a Central 22q11.2 Microdeletion.

Signe Faurschou, Dorte L Lildballe, Lisa L Maroun

|Feb 24, 2021

<i>PAX2</i> variant associated with bilateral kidney agenesis and broad intrafamilial disease variability.

Maria Rasmussen, Marlene Louise Nielsen, J Robert Manak

|Dec 02, 2017

Targeted gene sequencing and whole-exome sequencing in autopsied fetuses with prenatally diagnosed kidney anomalies.

M Rasmussen, L Sunde, M L Nielsen

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Frequent Collaborators

1 joint publications

Marlene L Nielsen

1 joint publications

Lone Sunde

Frequent Collaborators

1 joint publications

Marlene L Nielsen

1 joint publications

Lone Sunde

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